Aryltetrahydropyridine compound and pest control agent

Abstract

The present invention relates to an aryltetrahydropyridine compound or a salt thereof, the aryltetrahydropyridine compound being represented by formula (1). In formula (1), Q is Q-3 or the like, J is J-1 or the like, G is G-3 or the like, R2 is a hydrogen atom or the like, R3 is a hydrogen atom or the like, X is an oxygen atom or the like, and Y is an oxygen atom or the like.

Description

Aryltetrahydropyridine compounds and pest control agents

[0001] The present invention relates to novel aryltetrahydropyridine compounds and salts thereof, production intermediates thereof, and pest control agents, agricultural chemicals, control agents, insecticides or miticides, seed treatment agents and soil treatment agents each containing the compound and / or its salt as an active ingredient.

[0002] Certain aryltetrahydropyridine compounds are known to exhibit pesticidal activity (for example, Patent Documents 1 to 3).

[0003] International Publication No. 2021 / 261562 International Publication No. 2023 / 127806 International Publication No. 2024 / 048778

[0004] However, long-term use of insecticides can lead to the emergence of pests and harmful organisms that have acquired resistance to existing insecticides, and therefore there is a constant demand for the development of new pesticides with excellent pest control effects.

[0005] The present inventors have conducted extensive research aimed at solving the above problems, and as a result have found that the novel aryltetrahydropyridine compounds according to the present invention, represented by the following formula (1), exhibit excellent pest control activity, particularly excellent insecticidal and acaricidal activity, and have thus completed the present invention.

[0006] That is, the present invention relates to an aryltetrahydropyridine compound represented by the following formula (1) or a salt thereof. Formula (1): wherein Q is Q-A, Q-B or Q-C, and (i) when Q is Q-A, Q-A is C １ ~C ６ Alkyl, R １７ (C １ ~C ６ ) alkyl, —N(R １８ ) R １９ , -OR ６２ or Q-1 to Q-82; R １７ is a halogen atom, C １ ~C ６represents alkoxy or E-1 to E-83; R １８ is a hydrogen atom, C １ ~C ６ Alkyl or C ２ ~C ６ represents alkenyloxycarbonyl, R １９ are E-1 to E-63, E-65 to E-70, E-72 to E-80, C １ ~C ６ Alkyl, C １ ~C ６ Alkylcarbonyl, C １ ~C ６ Alkoxycarbonyl, C １ ~C ６ Alkylsulfonyl or R ２０ (C １ ~C ６ ) alkyl, R ２０ represents E-1 to E-83, and R ６２ is a hydrogen atom or C １ ~C ６ represents alkyl; Z １ is a halogen atom, C １ ~C ６ Alkyl, C ２ ~C ６ Alkenyl, C ２ ~C ６ Alkynyl, halo(C １ ~C ６ ) alkyl, halo (C ２ ~C ６ ) alkenyl, halo(C ２ ~C ６ ) alkynyl, C １ ~C ６ Alkoxy, halo (C １ ~C ６ ) alkoxy, C ２ ~C ６ Alkenyloxy, halo(C ２ ~C ６ ) alkenyloxy, C ２ ~C ６ Alkynyloxy, halo(C ２ ~C ６ ) alkynyloxy, hydroxy, C １ ~C６ Alkylcarbonyloxy, C １ ~C ６ Alkoxycarbonyloxy, C １ ~C ６ Alkyl sulfonyloxy, halo(C １ ~C ６ ) alkylsulfonyloxy, —OC(O)N(R ２６ ) R ２７ , C １ ~C ６ Alkylthio, C １ ~C ６ Alkylsulfinyl, C １ ~C ６ Alkyl sulfonyl, halo(C １ ~C ６ ) alkylthio, halo(C １ ~C ６ ) alkylsulfinyl, halo(C １ ~C ６ ) alkylsulfonyl, C ２ ~C ６ Alkenylthio, C ２ ~C ６ Alkenylsulfinyl, C ２ ~C ６ Alkenylsulfonyl, halo(C ２ ~C ６ ) alkenylthio, halo(C ２ ~C ６ ) alkenylsulfinyl, halo(C ２ ~C ６ ) alkenylsulfonyl, C ２ ~C ６ Alkynylthio, C ２ ~C ６ Alkynylsulfinyl, C ２ ~C ６ Alkynylsulfonyl, halo(C ２ ~C ６ ) alkynylthio, halo(C ２ ~C ６ ) alkynylsulfinyl, halo(C ２ ~C ６ ) alkynylsulfonyl, —SO ３ H, -S(O) ２ N (R ２８ ) R ２９, -SC≡N, -S(O)(=NR ３０ ) R ３１ , -SF ５ , -N(R ３２ ) R ３３ , -N=S(O)(R ５４ ) R ５５ , formyl, carboxy, C １ ~C ６ Alkylcarbonyl, halo(C １ ~C ６ ) alkylcarbonyl, C １ ~C ６ Alkoxycarbonyl, halo(C １ ~C ６ ) alkoxycarbonyl, —C(O)N(R ３５ ) R ３６ , -C(=NOR １２ ) R １３ , Tori (C １ ~C ６ ) alkylsilyl, R ７ (C １ ~C ６ ) alkyl, R １６ (C １ ~C ６ ) alkoxy, C ３ ~C ６ Cycloalkyl, R ５８ (C ３ ~C ６ ) cycloalkyl, cyano, nitro, E-1 to E-56, E-61 to E-83, -O-(E-1) to -O-(E-63), -O-(E-65) to -O-(E-70), -O-(E-72) to -O-(E-80), -S-(E-1) to -S-(E-63), -S-(E-65) to -S-(E-70), -S-(E-72) to -S-(E-80), -S(O)-(E-1) to -S(O)-(E-83), -S(O) ２ -(E-1)~-S(O) ２ -(E-83), -C(O)-(E-1) to -C(O)-(E-83), -N=N-(E-1) to -N=N-(E-63), -N=N-(E-65) to -N=N-(E-70), or -N=N-(E-72) to -N=N-(E-80), Z １In the above relationship, when t2 represents an integer of 2, t3 represents an integer of 2 or 3, t4 represents an integer of 2, 3 or 4, and t5 represents an integer of 2, 3, 4 or 5, each of Z １ may be the same as or different from each other, １ is a halogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl, C １ ~C ６ Alkoxy, C １ ~C ６ Alkylthio, halo(C １ ~C ６ ) alkylthio, C １ ~C ６ Alkylsulfinyl, C １ ~C ６ represents alkylsulfonyl or cyano; １ In the above relationship, when t2 represents an integer of 2, t3 represents an integer of 2 or 3, t4 represents an integer of 2, 3 or 4, and t5 represents an integer of 2, 3, 4 or 5, each E １ may be the same as or different from each other, ３ is a hydrogen atom, C １ ~C ６ Alkyl or halo(C １ ~C ６ ) alkyl, R ７ is C １ ~C ６ Alkoxy (C １ ~C ６ ) alkoxy, cyano, C １ ~C ６ Alkoxy, C １ ~C ６ Alkylcarbonyloxy, carboxy, C １ ~C ６ Alkylcarbonyl, C １ ~C ６ Alkoxycarbonyl, —C(O)N(R ３７ ) R ３８ , -N(R ３９ ) R ４０ , C １ ~C ６Alkylthio, C １ ~C ６ alkylsulfonyl or E-1 to E-83, １６ is C １ ~C ６ Alkylthio, C １ ~C ６ Alkylsulfinyl, C １ ~C ６ Alkylsulfonyl, —C(O)N(R ４１ ) R ４２ , C １ ~C ６ Alkoxy, halo (C １ ~C ６ ) alkoxy, C １ ~C ６ Alkoxy (C １ ~C ６ ) alkoxy, E-1 to E-83, or —C(O)—(E-1) to —C(O)—(E-83), R １２ is a hydrogen atom, C １ ~C ６ Alkyl or halo(C １ ~C ６ ) alkyl, R １３ is a hydrogen atom, C １ ~C ６ Alkyl or halo(C １ ~C ６ ) alkyl; Z ３ is a hydrogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl, C １ ~C ６ Alkoxy (C １ ~C ６ ) alkyl, C １ ~C ６ Alkylcarbonyl, halo(C １ ~C ６ ) alkylcarbonyl, C １ ~C ６ Alkoxycarbonyl or halo(C １ ~C ６ ) alkoxycarbonyl; R ２６ is a hydrogen atom or C １ ~C ６represents alkyl, R ２７ is a hydrogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl or C ３ ~C ６ represents cycloalkyl, R ２８ is a hydrogen atom or C １ ~C ６ represents alkyl, R ２９ is a hydrogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl, C ３ ~C ６ Cycloalkyl, C １ ~C ６ Alkylcarbonyl, halo(C １ ~C ６ ) alkylcarbonyl or C １ ~C ６ represents an alkoxycarbonyl; R ３０ is a hydrogen atom, C １ ~C ６ Alkyl or halo(C １ ~C ６ ) alkyl, R ３１ is C １ ~C ６ Alkyl or halo(C １ ~C ６ ) alkyl, R ３２ is a hydrogen atom or C １ ~C ６ represents alkyl, R ３３ is a hydrogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl, C １ ~C ６ Alkylcarbonyl, halo(C １ ~C ６ ) alkylcarbonyl, C １ ~C ６ Alkoxycarbonyl, halo(C １ ~C ６ ) alkoxycarbonyl, C １ ~C６ Alkylaminocarbonyl, di(C １ ~C ６ ) alkylaminocarbonyl, —C(O)NHC(O)OR ３４ , -C(S)NHC(O)OR ３４ or C １ ~C ６ represents alkylsulfonyl, R ３４ is C １ ~C ６ represents alkyl, R ３５ is a hydrogen atom or C １ ~C ６ represents alkyl, R ３６ is a hydrogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl or C ３ ~C ６ represents cycloalkyl, R ３７ is a hydrogen atom or C １ ~C ６ represents alkyl, R ３８ is a hydrogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl or C ３ ~C ６ represents cycloalkyl, R ３９ is a hydrogen atom, C １ ~C ６ Alkyl or halo(C １ ~C ６ ) alkyl, R ４０ is a hydrogen atom, C １ ~C ６ Alkyl, C １ ~C ６ Alkylcarbonyl or C １ ~C ６ represents an alkoxycarbonyl; R ４１ is a hydrogen atom or C １ ~C ６ represents alkyl, R ４２ is a hydrogen atom, C １ ~C ６ Alkyl, halo (C １ ~C６ ) alkyl or C ３ ~C ６ represents cycloalkyl, R ５４ is C １ ~C ６ represents alkyl, R ５５ is C １ ~C ６ represents alkyl, R ５８ is a halogen atom, C １ ~C ６ alkoxy or cyano, J represents J-1 to J-52, Z ５ is a hydrogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl, C １ ~C ６ Alkoxy (C １ ~C ６ ) alkyl, C １ ~C ６ Alkylcarbonyl, halo(C １ ~C ６ ) alkylcarbonyl, C １ ~C ６ Alkoxycarbonyl, halo(C １ ~C ６ ) alkoxycarbonyl, C １ ~C ６ Alkyl sulfonyl or halo(C １ ~C ６ ) alkylsulfonyl; G represents G-1 to G-65; Z ２ is a halogen atom, C １ ~C ６ Alkyl, C ２ ~C ６ Alkenyl, C ２ ~C ６ Alkynyl, halo(C １ ~C ６ ) alkyl, halo (C ２ ~C ６ ) alkenyl, halo(C ２ ~C ６ ) alkynyl, C １ ~C ６Alkoxy, halo (C １ ~C ６ ) alkoxy, C ２ ~C ６ Alkenyloxy, halo(C ２ ~C ６ ) alkenyloxy, C ２ ~C ６ Alkynyloxy, halo(C ２ ~C ６ ) alkynyloxy, hydroxy, C １ ~C ６ Alkylcarbonyloxy, C １ ~C ６ Alkoxycarbonyloxy, C １ ~C ６ Alkyl sulfonyloxy, halo(C １ ~C ６ ) alkylsulfonyloxy, —OC(O)N(R ６０ ) R ６１ , C １ ~C ６ Alkylthio, C １ ~C ６ Alkylsulfinyl, C １ ~C ６ Alkyl sulfonyl, halo(C １ ~C ６ ) alkylthio, halo(C １ ~C ６ ) alkylsulfinyl, halo(C １ ~C ６ ) alkylsulfonyl, C ２ ~C ６ Alkenylthio, C ２ ~C ６ Alkenylsulfinyl, C ２ ~C ６ Alkenylsulfonyl, halo(C ２ ~C ６ ) alkenylthio, halo(C ２ ~C ６ ) alkenylsulfinyl, halo(C ２ ~C ６ ) alkenylsulfonyl, C ２ ~C ６ Alkynylthio, C ２ ~C ６ Alkynylsulfinyl, C２ ~C ６ Alkynylsulfonyl, halo(C ２ ~C ６ ) alkynylthio, halo(C ２ ~C ６ ) alkynylsulfinyl, halo(C ２ ~C ６ ) alkynylsulfonyl, —SO ３ H, -S(O) ２ N (R ４８ ) R ４９ , -SC≡N, -S(O)(=NR ５２ ) R ５３ , -SF ５ , -N(R ４４ ) R ４５ , -N=S(O)(R ５６ ) R ５７ , formyl, carboxy, C １ ~C ６ Alkylcarbonyl, halo(C １ ~C ６ ) alkylcarbonyl, C １ ~C ６ Alkoxycarbonyl, halo(C １ ~C ６ ) alkoxycarbonyl, —C(O)N(R ４６ ) R ４７ , -C(=NOR １４ ) R １５ , Tori (C １ ~C ６ ) alkylsilyl, R ２４ (C １ ~C ６ ) alkyl, R ２５ (C １ ~C ６ ) alkoxy, C ３ ~C ６ Cycloalkyl, R ５９ (C ３ ~C ６ ) represents cycloalkyl, cyano, nitro, M-1 to M-56, M-61 to M-82, —O-(M-1) to —O-(M-63), —O-(M-65) to —O-(M-70), or —O-(M-72) to —O-(M-80); Z ２In the above relationship, when t2 represents an integer of 2, t3 represents an integer of 2 or 3, t4 represents an integer of 2, 3 or 4, and t5 represents an integer of 2, 3, 4 or 5, each of Z ２ may be the same as or different from each other, R ２４ is C １ ~C ６ Alkoxy, hydroxy or -N(R ５０ ) R ５１ represents R ２５ is C １ ~C ６ represents alkoxy or M-1 to M-82, １ is a halogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl, C １ ~C ６ Alkoxy, C １ ~C ６ Alkylthio, halo(C １ ~C ６ ) alkylthio, C １ ~C ６ Alkylsulfinyl, C １ ~C ６ represents alkylsulfonyl or cyano; M １ In the above relationship, when t2 represents an integer of 2, t3 represents an integer of 2 or 3, t4 represents an integer of 2, 3 or 4, and t5 represents an integer of 2, 3, 4 or 5, each of M １ may be the same as or different from each other, M ３ is a hydrogen atom, C １ ~C ６ Alkyl or halo(C １ ~C ６ ) alkyl, R １４ is a hydrogen atom, C １ ~C ６ Alkyl or halo(C １ ~C ６ ) alkyl, R １５ is a hydrogen atom, C １ ~C ６ Alkyl or halo(C １~C ６ ) alkyl; Z ４ is a hydrogen atom, C １ ~C ６ Alkyl, C １ ~C ６ Alkylcarbonyl, C １ ~C ６ Alkoxycarbonyl, C １ ~C ６ Alkoxy (C １ ~C ６ ) alkyl or C １ ~C ６ represents alkylsulfonyl, R ４４ is a hydrogen atom, C １ ~C ６ Alkyl or halo(C １ ~C ６ ) alkyl, R ４５ is a hydrogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl, C １ ~C ６ Alkylcarbonyl, halo(C １ ~C ６ ) alkylcarbonyl, C １ ~C ６ Alkoxycarbonyl, halo(C １ ~C ６ ) alkoxycarbonyl, C １ ~C ６ Alkyl sulfonyl or halo(C １ ~C ６ ) represents alkylsulfonyl, R ４６ is a hydrogen atom or C １ ~C ６ represents alkyl, R ４７ is a hydrogen atom, C １ ~C ６ Alkyl or halo(C １ ~C ６ ) alkyl, R ４８ is a hydrogen atom, C １ ~C ６ Alkyl or halo(C １ ~C ６ ) alkyl, R ４９is a hydrogen atom, C １ ~C ６ Alkyl or halo(C １ ~C ６ ) alkyl, R ５０ is a hydrogen atom or C １ ~C ６ represents alkyl, R ５１ is a hydrogen atom, C １ ~C ６ Alkyl, C １ ~C ６ Alkylcarbonyl, halo(C １ ~C ６ ) alkylcarbonyl, C １ ~C ６ Alkoxycarbonyl, halo(C １ ~C ６ ) alkoxycarbonyl, C １ ~C ６ Alkyl sulfonyl or halo(C １ ~C ６ ) represents alkylsulfonyl, R ５２ is a hydrogen atom or C １ ~C ６ represents alkyl, R ５３ is C １ ~C ６ represents alkyl, R ５６ is C １ ~C ６ represents alkyl, R ５７ is C １ ~C ６ represents alkyl, R ５９ is a halogen atom, C １ ~C ６ represents alkoxy or cyano; R ６０ is a hydrogen atom or C １ ~C ６ represents alkyl, R ６１ is a hydrogen atom, C １ ~C ６ Alkyl or halo(C １ ~C ６ ) alkyl, R １ represents a hydrogen atom, a halogen atom, or C １ ~C ６ Alkyl, halo (C １ ~C ６) alkyl, C １ ~C ６ Alkoxy, hydroxy, C １ ~C ６ Alkylthio, C １ ~C ６ Alkylsulfinyl, C １ ~C ６ Alkyl sulfonyl, halo(C １ ~C ６ ) alkylthio, halo(C １ ~C ６ ) alkylsulfinyl, halo(C １ ~C ６ ) alkylsulfonyl, —N(R １ｄ ) R １ｅ , cyano or nitro; R １ａ represents a hydrogen atom, a halogen atom, or C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl, C １ ~C ６ Alkoxy, hydroxy, -N(R １ｄ ) R １ｅ , cyano or nitro; R １ｂ represents a hydrogen atom, a halogen atom, or C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl, C １ ~C ６ Alkoxy, hydroxy, -N(R １ｄ ) R １ｅ , cyano or nitro; R １ｃ represents a hydrogen atom, a halogen atom, or C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl, C １ ~C ６ Alkoxy, hydroxy, -N(R １ｄ ) R １ｅ , cyano or nitro; R １ｄ is a hydrogen atom or C １ ~C ６ represents alkyl, R １ｅ is a hydrogen atom or C １ ~C６ represents alkyl, R ２ is a hydrogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl, C ２ ~C ６ Alkenyl, C ２ ~C ６ Alkynyl, C ３ ~C ６ cycloalkyl, —C(O)R ４ , -C(O)OR ５ or R ６７ (C １ ~C ６ ) alkyl, R ６７ is C １ ~C ６ Alkoxy, C １ ~C ６ Alkylthio, C １ ~C ６ Alkylsulfinyl, C １ ~C ６ alkylsulfonyl, cyano, or V-1 to V-82; V １ is a halogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl, C １ ~C ６ Alkoxy, C １ ~C ６ Alkylthio, C １ ~C ６ Alkylsulfinyl, C １ ~C ６ represents alkylsulfonyl, cyano or nitro; V １ In the above relationship, when t2 represents an integer of 2, t3 represents an integer of 2 or 3, t4 represents an integer of 2, 3 or 4, and t5 represents an integer of 2, 3, 4 or 5, each of V １ may be the same as or different from each other, V ３ is a hydrogen atom, C １ ~C ６ Alkyl or halo(C １ ~C６ ) alkyl, R ４ is C １ ~C ６ Alkyl, C ２ ~C ６ Alkenyl, C ２ ~C ６ Alkynyl, C １ ~C ６ Alkylcarbonyl, C １ ~C ６ Alkoxycarbonyl, C １ ~C ６ Alkylamino, di(C １ ~C ６ ) alkylamino, R ６ (C １ ~C ６ ) alkyl or V-1 to V-82, R ５ is C １ ~C ６ Alkyl, C ２ ~C ６ Alkenyl, C ２ ~C ６ Alkynyl, R ９ (C １ ~C ６ ) alkyl, V-1 to V-63, V-65 to V-70, or V-72 to V-80; R ６ is a halogen atom, C １ ~C ６ represents alkoxy, cyano, nitro, or V-1 to V-82; R ９ is a halogen atom, C １ ~C ６ (ii) when Q is Q-B, Q-B is C １ ~C ６ Alkyl, R １７ (C １ ~C ６ ) alkyl, —N(R １８ ) R １９ , -OR ６２ or Q-1 to Q-82; R １７ is a halogen atom, C １~C ６ represents alkoxy or E-1 to E-83; R １８ is a hydrogen atom, C １ ~C ６ Alkyl or C ２ ~C ６ represents alkenyloxycarbonyl, R １９ are E-1 to E-63, E-65 to E-70, E-72 to E-80, C １ ~C ６ Alkyl, C １ ~C ６ Alkylcarbonyl, C １ ~C ６ Alkoxycarbonyl, C １ ~C ６ Alkylsulfonyl or R ２０ (C １ ~C ６ ) alkyl, R ２０ represents E-1 to E-83, and R ６２ is a hydrogen atom or C １ ~C ６ represents alkyl; Z １ is a halogen atom, C １ ~C ６ Alkyl, C ２ ~C ６ Alkenyl, C ２ ~C ６ Alkynyl, halo(C １ ~C ６ ) alkyl, halo (C ２ ~C ６ ) alkenyl, halo(C ２ ~C ６ ) alkynyl, C １ ~C ６ Alkoxy, halo (C １ ~C ６ ) alkoxy, C １ ~C ６ Alkenyloxy, halo(C ２ ~C ６ ) alkenyloxy, C １ ~C ６ Alkynyloxy, halo(C ２ ~C ６ ) alkynyloxy, hydroxy, C１ ~C ６ Alkylcarbonyloxy, C １ ~C ６ Alkoxycarbonyloxy, C １ ~C ６ Alkyl sulfonyloxy, halo(C １ ~C ６ ) alkylsulfonyloxy, —OC(O)N(R ２６ ) R ２７ , C １ ~C ６ Alkylthio, C １ ~C ６ Alkylsulfinyl, C １ ~C ６ Alkyl sulfonyl, halo(C １ ~C ６ ) alkylthio, halo(C １ ~C ６ ) alkylsulfinyl, halo(C １ ~C ６ ) alkylsulfonyl, C ２ ~C ６ Alkenylthio, C ２ ~C ６ Alkenylsulfinyl, C ２ ~C ６ Alkenylsulfonyl, halo(C ２ ~C ６ ) alkenylthio, halo(C ２ ~C ６ ) alkenylsulfinyl, halo(C ２ ~C ６ ) alkenylsulfonyl, C ２ ~C ６ Alkynylthio, C ２ ~C ６ Alkynylsulfinyl, C ２ ~C ６ Alkynylsulfonyl, halo(C ２ ~C ６ ) alkynylthio, halo(C ２ ~C ６ ) alkynylsulfinyl, halo(C ２ ~C ６ ) alkynylsulfonyl, —SO ３ H, -S(O) ２ N (R ２８ ) R２９ , -SC≡N, -S(O)(=NR ３０ ) R ３１ , -SF ５ , -N(R ３２ ) R ３３ , -N=S(O)(R ５４ ) R ５５ , formyl, carboxy, C １ ~C ６ Alkylcarbonyl, halo(C １ ~C ６ ) alkylcarbonyl, C １ ~C ６ Alkoxycarbonyl, halo(C １ ~C ６ ) alkoxycarbonyl, —C(O)N(R ３５ ) R ３６ , -C(=NOR １２ ) R １３ , Tori (C １ ~C ６ ) alkylsilyl, R ７ (C １ ~C ６ ) alkyl, R １６ (C １ ~C ６ ) alkoxy, C ３ ~C ６ Cycloalkyl, R ５８ (C ３ ~C ６ ) cycloalkyl, cyano, nitro, E-1 to E-56, E-61 to E-83, -O-(E-1) to -O-(E-63), -O-(E-65) to -O-(E-70), -O-(E-72) to -O-(E-80), -S-(E-1) to -S-(E-63), -S-(E-65) to -S-(E-70), -S-(E-72) to -S-(E-80), -S(O)-(E-1) to -S(O)-(E-83), -S(O) ２ -(E-1)~-S(O) ２ -(E-83), -C(O)-(E-1) to -C(O)-(E-83), -N=N-(E-1) to -N=N-(E-63), -N=N-(E-65) to -N=N-(E-70), or -N=N-(E-72) to -N=N-(E-80), Z １In the above relationship, when t2 represents an integer of 2, t3 represents an integer of 2 or 3, t4 represents an integer of 2, 3 or 4, and t5 represents an integer of 2, 3, 4 or 5, each of Z １ may be the same as or different from each other, １ is a halogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl, C １ ~C ６ Alkoxy, C １ ~C ６ Alkylthio, halo(C １ ~C ６ ) alkylthio, C １ ~C ６ Alkylsulfinyl, C １ ~C ６ represents alkylsulfonyl or cyano; １ In the above relationship, when t2 represents an integer of 2, t3 represents an integer of 2 or 3, t4 represents an integer of 2, 3 or 4, and t5 represents an integer of 2, 3, 4 or 5, each E １ may be the same as or different from each other, ３ is a hydrogen atom, C １ ~C ６ Alkyl or halo(C １ ~C ６ ) alkyl, R ７ is C １ ~C ６ Alkoxy (C １ ~C ６ ) alkoxy, cyano, C １ ~C ６ Alkoxy, C １ ~C ６ Alkylcarbonyloxy, carboxy, C １ ~C ６ Alkylcarbonyl, C １ ~C ６ Alkoxycarbonyl, —C(O)N(R ３７ ) R ３８ , -N(R ３９ ) R ４０ , C １ ~C ６Alkylthio, C １ ~C ６ alkylsulfonyl or E-1 to E-83, １６ is C １ ~C ６ Alkylthio, C １ ~C ６ Alkylsulfinyl, C １ ~C ６ Alkylsulfonyl, —C(O)N(R ４１ ) R ４２ , C １ ~C ６ Alkoxy, halo (C １ ~C ６ ) alkoxy, C １ ~C ６ Alkoxy (C １ ~C ６ ) alkoxy, E-1 to E-83, or —C(O)—(E-1) to —C(O)—(E-83), R １２ is a hydrogen atom, C １ ~C ６ Alkyl or halo(C １ ~C ６ ) alkyl, R １３ is a hydrogen atom, C １ ~C ６ Alkyl or halo(C １ ~C ６ ) alkyl; Z ３ is a hydrogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl, C １ ~C ６ Alkoxy (C １ ~C ６ ) alkyl, C １ ~C ６ Alkylcarbonyl, halo(C １ ~C ６ ) alkylcarbonyl, C １ ~C ６ Alkoxycarbonyl or halo(C １ ~C ６ ) alkoxycarbonyl; R ２６ is a hydrogen atom or C １ ~C ６represents alkyl, R ２７ is a hydrogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl or C ３ ~C ６ represents cycloalkyl, R ２８ is a hydrogen atom or C １ ~C ６ represents alkyl, R ２９ is a hydrogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl, C ３ ~C ６ Cycloalkyl, C １ ~C ６ Alkylcarbonyl, halo(C １ ~C ６ ) alkylcarbonyl or C １ ~C ６ represents an alkoxycarbonyl; R ３０ is a hydrogen atom, C １ ~C ６ Alkyl or halo(C １ ~C ６ ) alkyl, R ３１ is C １ ~C ６ Alkyl or halo(C １ ~C ６ ) alkyl, R ３２ is a hydrogen atom or C １ ~C ６ represents alkyl, R ３３ is a hydrogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl, C １ ~C ６ Alkylcarbonyl, halo(C １ ~C ６ ) alkylcarbonyl, C １ ~C ６ Alkoxycarbonyl, halo(C １ ~C ６ ) alkoxycarbonyl, C １ ~C６ Alkylaminocarbonyl, di(C １ ~C ６ ) alkylaminocarbonyl, —C(O)NHC(O)OR ３４ , -C(S)NHC(O)OR ３４ or C １ ~C ６ represents alkylsulfonyl, R ３４ is C １ ~C ６ represents alkyl, R ３５ is a hydrogen atom or C １ ~C ６ represents alkyl, R ３６ is a hydrogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl or C ３ ~C ６ represents cycloalkyl, R ３７ is a hydrogen atom or C １ ~C ６ represents alkyl, R ３８ is a hydrogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl or C ３ ~C ６ represents cycloalkyl, R ３９ is a hydrogen atom, C １ ~C ６ Alkyl or halo(C １ ~C ６ ) alkyl, R ４０ is a hydrogen atom, C １ ~C ６ Alkyl, C １ ~C ６ Alkylcarbonyl or C １ ~C ６ represents an alkoxycarbonyl; R ４１ is a hydrogen atom or C １ ~C ６ represents alkyl, R ４２ is a hydrogen atom, C １ ~C ６ Alkyl, halo (C １ ~C６ ) alkyl or C ３ ~C ６ represents cycloalkyl, R ５４ is C １ ~C ６ represents alkyl, R ５５ is C １ ~C ６ represents alkyl, R ５８ is a halogen atom, C １ ~C ６ alkoxy or cyano, J represents J-1′ or J-2′, A １ is a nitrogen atom or CR １ｃ G represents -N(R ２１ ) R ２２ , -C(=NOR ６７ ) R ６８ , R ６９ (C １ ~C ６ ) alkyl or G-1′ to G-160′, R ２１ is a hydrogen atom, C １ ~C ６ Alkyl or halo(C １ ~C ６ ) alkyl, R ２２ is a hydrogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl, C ２ ~C ６ Alkenyl, halo(C ２ ~C ６ ) alkenyl, C ２ ~C ６ Alkynyl, halo(C ２ ~C ６ ) alkynyl, R ２３ (C １ ~C ６ ) alkyl or M-1 to M-82, R ２３ is C １ ~C６ Alkoxy, C １ ~C ６ Alkylcarbonyl, C １ ~C ６ Alkoxycarbonyl, hydroxy, cyano, C １ ~C ６ Alkylamino, di(C １ ~C ６ ) alkylamino, C １ ~C ６ Alkylcarbonylamino, C １ ~C ６ represents alkoxycarbonylamino or M-1 to M-82, ６７ is a hydrogen atom, C １ ~C ６ Alkyl or halo(C １ ~C ６ ) alkyl, R ６８ is a hydrogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl or M-1 to M-82, R ６９ M-1 to M-82, -N(R ７０ ) R ７１ , -C(=O)N(R ７２ ) R ７３ or -C(=NOR ７４ ) R ７５ represents R ７０ is a hydrogen atom or C １ ~C ６ represents alkyl, R ７１ is -C(=O)R ７６ represents R ７６ is C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl or M-1 to M-82, R ７２ is a hydrogen atom or C １ ~C ６ represents alkyl, R ７３ represents M-1 to M-82, and R ７４ is a hydrogen atom or C １ ~C ６ represents alkyl, R ７５is a hydrogen atom, C １ ~C ６ Alkyl or C ３ ~C ６ represents cycloalkyl; Z ２ is a halogen atom, C １ ~C ６ Alkyl, C ２ ~C ６ Alkenyl, C ２ ~C ６ Alkynyl, halo(C １ ~C ６ ) alkyl, halo (C ２ ~C ６ ) alkenyl, halo(C ２ ~C ６ ) alkynyl, C １ ~C ６ Alkoxy, halo (C １ ~C ６ ) alkoxy, C ２ ~C ６ Alkenyloxy, halo(C ２ ~C ６ ) alkenyloxy, C ２ ~C ６ Alkynyloxy, halo(C ２ ~C ６ ) alkynyloxy, hydroxy, C １ ~C ６ Alkylcarbonyloxy, C １ ~C ６ Alkoxycarbonyloxy, C １ ~C ６ Alkyl sulfonyloxy, halo(C １ ~C ６ ) alkylsulfonyloxy, —OC(O)N(R ６０ ) R ６１ , C １ ~C ６ Alkylthio, C １ ~C ６ Alkylsulfinyl, C １ ~C ６ Alkyl sulfonyl, halo(C １ ~C ６ ) alkylthio, halo(C １ ~C ６ ) alkylsulfinyl, halo(C １ ~C６ ) alkylsulfonyl, C ２ ~C ６ Alkenylthio, C ２ ~C ６ Alkenylsulfinyl, C ２ ~C ６ Alkenylsulfonyl, halo(C ２ ~C ６ ) alkenylthio, halo(C ２ ~C ６ ) alkenylsulfinyl, halo(C ２ ~C ６ ) alkenylsulfonyl, C ２ ~C ６ Alkynylthio, C ２ ~C ６ Alkynylsulfinyl, C ２ ~C ６ Alkynylsulfonyl, halo(C ２ ~C ６ ) alkynylthio, halo(C ２ ~C ６ ) alkynylsulfinyl, halo(C ２ ~C ６ ) alkynylsulfonyl, —SO ３ H, -S(O) ２ N (R ４８ ) R ４９ , -SC≡N, -S(O)(=NR ５２ ) R ５３ , -SF ５ , -N(R ４４ ) R ４５ , -N=S(O)(R ５６ ) R ５７ , formyl, carboxy, C １ ~C ６ Alkylcarbonyl, halo(C １ ~C ６ ) alkylcarbonyl, C １ ~C ６ Alkoxycarbonyl, halo(C １ ~C ６ ) alkoxycarbonyl, —C(O)N(R ４６ ) R ４７ , -C(=NOR １４ ) R １５ , Tori (C １ ~C ６) alkylsilyl, R ２４ (C １ ~C ６ ) alkyl, R ２５ (C １ ~C ６ ) alkoxy, C ３ ~C ６ Cycloalkyl, R ５９ (C ３ ~C ６ ) represents cycloalkyl, cyano, nitro, M-1 to M-56, M-61 to M-82, —O-(M-1) to —O-(M-63), —O-(M-65) to —O-(M-70), or —O-(M-72) to —O-(M-80); Z ２ In the above relationship, when t2 represents an integer of 2, t3 represents an integer of 2 or 3, t4 represents an integer of 2, 3 or 4, and t5 represents an integer of 2, 3, 4 or 5, each of Z ２ may be the same as or different from each other; or t4 represents an integer of 2, and two Z ２ When two Z ２ together form oxo, -CH ２ CH ２ -, -OCH ２ CH ２ O-, -OCH ２ CH ２ CH ２ O-, = NOR ４３ , =NN(R ６３ ) R ６４ or =NN=C(R ６５ ) R ６６ represents R ４３ is a hydrogen atom or C １ ~C ６ represents alkyl, R ２４ is C １ ~C ６ Alkoxy, hydroxy or -N(R ５０ ) R ５１ represents R ２５ is C １ ~C ６ represents alkoxy or M-1 to M-82, １ is a halogen atom, C １ ~C６ Alkyl, halo (C １ ~C ６ ) alkyl, C １ ~C ６ Alkoxy, C １ ~C ６ Alkylthio, halo(C １ ~C ６ ) alkylthio, C １ ~C ６ Alkylsulfinyl, C １ ~C ６ represents alkylsulfonyl or cyano; M １ In the above relationship, when t2 represents an integer of 2, t3 represents an integer of 2 or 3, t4 represents an integer of 2, 3 or 4, and t5 represents an integer of 2, 3, 4 or 5, each of M １ may be the same as or different from each other, M ３ is a hydrogen atom, C １ ~C ６ Alkyl or halo(C １ ~C ６ ) alkyl, R １４ is a hydrogen atom, C １ ~C ６ Alkyl or halo(C １ ~C ６ ) alkyl, R １５ is a hydrogen atom, C １ ~C ６ Alkyl or halo(C １ ~C ６ ) alkyl; Z ４ is a hydrogen atom, C １ ~C ６ Alkyl, C １ ~C ６ Alkylcarbonyl, C １ ~C ６ Alkoxycarbonyl, C １ ~C ６ Alkoxy (C １ ~C ６ ) alkyl or C １ ~C ６ represents alkylsulfonyl, R ４４ is a hydrogen atom, C １ ~C ６ Alkyl or halo(C１ ~C ６ ) alkyl, R ４５ is a hydrogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl, C １ ~C ６ Alkylcarbonyl, halo(C １ ~C ６ ) alkylcarbonyl, C １ ~C ６ Alkoxycarbonyl, halo(C １ ~C ６ ) alkoxycarbonyl, C １ ~C ６ Alkyl sulfonyl or halo(C １ ~C ６ ) represents alkylsulfonyl, R ４６ is a hydrogen atom or C １ ~C ６ represents alkyl, R ４７ is a hydrogen atom, C １ ~C ６ Alkyl or halo(C １ ~C ６ ) alkyl, R ４８ is a hydrogen atom, C １ ~C ６ Alkyl or halo(C １ ~C ６ ) alkyl, R ４９ is a hydrogen atom, C １ ~C ６ Alkyl or halo(C １ ~C ６ ) alkyl, R ５０ is a hydrogen atom or C １ ~C ６ represents alkyl, R ５１ is a hydrogen atom, C １ ~C ６ Alkyl, C １ ~C ６ Alkylcarbonyl, halo(C １ ~C ６ ) alkylcarbonyl, C １ ~C ６ Alkoxycarbonyl, halo(C １ ~C６ ) alkoxycarbonyl, C １ ~C ６ Alkyl sulfonyl or halo(C １ ~C ６ ) represents alkylsulfonyl, R ５２ is a hydrogen atom or C １ ~C ６ represents alkyl, R ５３ is C １ ~C ６ represents alkyl, R ５６ is C １ ~C ６ represents alkyl, R ５７ is C １ ~C ６ represents alkyl, R ５９ is a halogen atom, C １ ~C ６ represents alkoxy or cyano; R ６０ is a hydrogen atom or C １ ~C ６ represents alkyl, R ６１ is a hydrogen atom, C １ ~C ６ Alkyl or halo(C １ ~C ６ ) alkyl, R ６３ is a hydrogen atom or C １ ~C ６ represents alkyl, R ６４ is a hydrogen atom, C １ ~C ６ Alkyl, C １ ~C ６ Alkylcarbonyl, halo(C １ ~C ６ ) alkylcarbonyl, C １ ~C ６ Alkoxycarbonyl, halo(C １ ~C ６ ) alkoxycarbonyl, C １ ~C ６ Alkyl sulfonyl or halo(C １ ~C ６ ) represents alkylsulfonyl, R ６５ is a hydrogen atom or C １ ~C ６ represents alkyl, R６６ is C １ ~C ６ represents alkyl, R １ represents a hydrogen atom, a halogen atom, or C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl, C １ ~C ６ Alkoxy, hydroxy, C １ ~C ６ Alkylthio, C １ ~C ６ Alkylsulfinyl, C １ ~C ６ Alkyl sulfonyl, halo(C １ ~C ６ ) alkylthio, halo(C １ ~C ６ ) alkylsulfinyl, halo(C １ ~C ６ ) alkylsulfonyl, —N(R １ｄ ) R １ｅ , cyano or nitro; R １ａ represents a hydrogen atom, a halogen atom, or C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl, C １ ~C ６ Alkoxy, hydroxy, -N(R １ｄ ) R １ｅ , cyano or nitro; R １ｂ represents a hydrogen atom, a halogen atom, or C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl, C １ ~C ６ Alkoxy, hydroxy, -N(R １ｄ ) R １ｅ , cyano or nitro; R １ｃ represents a hydrogen atom, a halogen atom, or C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl, C １ ~C ６Alkoxy, hydroxy, -N(R １ｄ ) R １ｅ , cyano or nitro; R １ｄ is a hydrogen atom or C １ ~C ６ represents alkyl, R １ｅ is a hydrogen atom or C １ ~C ６ represents alkyl, R ２ is a hydrogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl, C ２ ~C ６ Alkenyl, C ２ ~C ６ Alkynyl, C ３ ~C ６ cycloalkyl, —C(O)R ４ , -C(O)OR ５ , or R ６７ (C １ ~C ６ ) alkyl, R ６７ is C １ ~C ６ Alkoxy, C １ ~C ６ Alkylthio, C １ ~C ６ Alkylsulfinyl, C １ ~C ６ alkylsulfonyl, cyano, or V-1 to V-82; V １ is a halogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl, C １ ~C ６ Alkoxy, C １ ~C ６ Alkylthio, C １ ~C ６ Alkylsulfinyl, C １ ~C ６ represents alkylsulfonyl, cyano or nitro; V １In the above relationship, when t2 represents an integer of 2, t3 represents an integer of 2 or 3, t4 represents an integer of 2, 3 or 4, and t5 represents an integer of 2, 3, 4 or 5, each of V １ may be the same as or different from each other, V ３ is a hydrogen atom, C １ ~C ６ Alkyl or halo(C １ ~C ６ ) alkyl, R ４ is C １ ~C ６ Alkyl, C ２ ~C ６ Alkenyl, C ２ ~C ６ Alkynyl, C １ ~C ６ Alkylcarbonyl, C １ ~C ６ Alkoxycarbonyl, C １ ~C ６ Alkylamino, di(C １ ~C ６ ) alkylamino, R ６ (C １ ~C ６ ) alkyl or V-1 to V-82, R ５ is C １ ~C ６ Alkyl, C ２ ~C ６ Alkenyl, C ２ ~C ６ Alkynyl, R ９ (C １ ~C ６ ) alkyl, V-1 to V-63, V-65 to V-70, or V-72 to V-80; R ６ is a halogen atom, C １ ~C ６ represents alkoxy, cyano, nitro, or V-1 to V-82; R ９ is a halogen atom, C １ ~C ６ (iii) when Q is Q-C, Q-C is C １ ~C６ Alkyl, R １７ (C １ ~C ６ ) alkyl, —N(R １８ ) R １９ , -OR ６２ or Q-1 to Q-82; R １７ is a halogen atom, C １ ~C ６ represents alkoxy or E-1 to E-83; R １８ is a hydrogen atom, C １ ~C ６ Alkyl or C ２ ~C ６ represents alkenyloxycarbonyl, R １９ are E-1 to E-63, E-65 to E-70, E-72 to E-80, C １ ~C ６ Alkyl, C １ ~C ６ Alkylcarbonyl, C １ ~C ６ Alkoxycarbonyl, C １ ~C ６ Alkylsulfonyl or R ２０ (C １ ~C ６ ) alkyl, R ２０ represents E-1 to E-83, and R ６２ is a hydrogen atom or C １ ~C ６ represents alkyl; Z １ is a halogen atom, C １ ~C ６ Alkyl, C ２ ~C ６ Alkenyl, C ２ ~C ６ Alkynyl, halo(C １ ~C ６ ) alkyl, halo (C ２ ~C ６ ) alkenyl, halo(C ２ ~C ６ ) alkynyl, C １ ~C ６ Alkoxy, halo (C１ ~C ６ ) alkoxy, C ２ ~C ６ Alkenyloxy, halo(C ２ ~C ６ ) alkenyloxy, C ２ ~C ６ Alkynyloxy, halo(C ２ ~C ６ ) alkynyloxy, hydroxy, C １ ~C ６ Alkylcarbonyloxy, C １ ~C ６ Alkoxycarbonyloxy, C １ ~C ６ Alkyl sulfonyloxy, halo(C １ ~C ６ ) alkylsulfonyloxy, —OC(O)N(R ２６ ) R ２７ , C １ ~C ６ Alkylthio, C １ ~C ６ Alkylsulfinyl, C １ ~C ６ Alkyl sulfonyl, halo(C １ ~C ６ ) alkylthio, halo(C １ ~C ６ ) alkylsulfinyl, halo(C １ ~C ６ ) alkylsulfonyl, C ２ ~C ６ Alkenylthio, C ２ ~C ６ Alkenylsulfinyl, C ２ ~C ６ Alkenylsulfonyl, halo(C ２ ~C ６ ) alkenylthio, halo(C ２ ~C ６ ) alkenylsulfinyl, halo(C ２ ~C ６ ) alkenylsulfonyl, C ２ ~C ６ Alkynylthio, C ２ ~C ６ Alkynylsulfinyl, C ２ ~C６ Alkynylsulfonyl, halo(C ２ ~C ６ ) alkynylthio, halo(C ２ ~C ６ ) alkynylsulfinyl, halo(C ２ ~C ６ ) alkynylsulfonyl, —SO ３ H, -S(O) ２ N (R ２８ ) R ２９ , -SC≡N, -S(O)(=NR ３０ ) R ３１ , -SF ５ , -N(R ３２ ) R ３３ , -N=S(O)(R ５４ ) R ５５ , formyl, carboxy, C １ ~C ６ Alkylcarbonyl, halo(C １ ~C ６ ) alkylcarbonyl, C １ ~C ６ Alkoxycarbonyl, halo(C １ ~C ６ ) alkoxycarbonyl, —C(O)N(R ３５ ) R ３６ , -C(=NOR １２ ) R １３ , Tori (C １ ~C ６ ) alkylsilyl, R ７ (C １ ~C ６ ) alkyl, R １６ (C １ ~C ６ ) alkoxy, C ３ ~C ６ Cycloalkyl, R ５８ (C ３ ~C ６) cycloalkyl, cyano, nitro, E-1 to E-56, E-61 to E-83, -O-(E-1) to -O-(E-63), -O-(E-65) to -O-(E-70), -O-(E-72) to -O-(E-80), -S-(E-1) to -S-(E-63), -S-(E-65) to -S-(E-70), -S-(E-72) to -S-(E-80), -S(O)-(E-1) to -S(O)-(E-83), -S(O) ２ -(E-1)~-S(O) ２ -(E-83), -C(O)-(E-1) to -C(O)-(E-83), -N=N-(E-1) to -N=N-(E-63), -N=N-(E-65) to -N=N-(E-70), or -N=N-(E-72) to -N=N-(E-80), Z １ In the above relationship, when t2 represents an integer of 2, t3 represents an integer of 2 or 3, t4 represents an integer of 2, 3 or 4, and t5 represents an integer of 2, 3, 4 or 5, each of Z １ may be the same as or different from each other, １ is a halogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl, C １ ~C ６ Alkoxy, C １ ~C ６ Alkylthio, halo(C １ ~C ６ ) alkylthio, C １ ~C ６ Alkylsulfinyl, C １ ~C ６ represents alkylsulfonyl or cyano; １ In the above relationship, when t2 represents an integer of 2, t3 represents an integer of 2 or 3, t4 represents an integer of 2, 3 or 4, and t5 represents an integer of 2, 3, 4 or 5, each E １ may be the same as or different from each other, ３ is a hydrogen atom, C １ ~C ６ Alkyl or halo(C １ ~C ６ ) alkyl, R ７is C １ ~C ６ Alkoxy (C １ ~C ６ ) alkoxy, cyano, C １ ~C ６ Alkoxy, C １ ~C ６ Alkylcarbonyloxy, carboxy, C １ ~C ６ Alkylcarbonyl, C １ ~C ６ Alkoxycarbonyl, —C(O)N(R ３７ ) R ３８ , -N(R ３９ ) R ４０ , C １ ~C ６ Alkylthio, C １ ~C ６ alkylsulfonyl or E-1 to E-83, １６ is C １ ~C ６ Alkylthio, C １ ~C ６ Alkylsulfinyl, C １ ~C ６ Alkylsulfonyl, —C(O)N(R ４１ ) R ４２ , C １ ~C ６ Alkoxy, halo (C １ ~C ６ ) alkoxy, C １ ~C ６ Alkoxy (C １ ~C ６ ) alkoxy, E-1 to E-83, or —C(O)—(E-1) to —C(O)—(E-83), R １２ is a hydrogen atom, C １ ~C ６ Alkyl or halo(C １ ~C ６ ) alkyl, R １３ is a hydrogen atom, C １ ~C ６ Alkyl or halo(C １ ~C ６ ) alkyl; Z ３ is a hydrogen atom, C １ ~C ６Alkyl, halo (C １ ~C ６ ) alkyl, C １ ~C ６ Alkoxy (C １ ~C ６ ) alkyl, C １ ~C ６ Alkylcarbonyl, halo(C １ ~C ６ ) alkylcarbonyl, C １ ~C ６ Alkoxycarbonyl or halo(C １ ~C ６ ) alkoxycarbonyl; R ２６ is a hydrogen atom or C １ ~C ６ represents alkyl, R ２７ is a hydrogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl or C ３ ~C ６ represents cycloalkyl, R ２８ is a hydrogen atom or C １ ~C ６ represents alkyl, R ２９ is a hydrogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl, C ３ ~C ６ Cycloalkyl, C １ ~C ６ Alkylcarbonyl, halo(C １ ~C ６ ) alkylcarbonyl or C １ ~C ６ represents an alkoxycarbonyl; R ３０ is a hydrogen atom, C １ ~C ６ Alkyl or halo(C １ ~C ６ ) alkyl, R ３１ is C １ ~C ６ Alkyl or halo(C １ ~C ６ ) alkyl, R３２ is a hydrogen atom or C １ ~C ６ represents alkyl, R ３３ is a hydrogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl, C １ ~C ６ Alkylcarbonyl, halo(C １ ~C ６ ) alkylcarbonyl, C １ ~C ６ Alkoxycarbonyl, halo(C １ ~C ６ ) alkoxycarbonyl, C １ ~C ６ Alkylaminocarbonyl, di(C １ ~C ６ ) alkylaminocarbonyl, —C(O)NHC(O)OR ３４ , -C(S)NHC(O)OR ３４ or C １ ~C ６ represents alkylsulfonyl, R ３４ is C １ ~C ６ represents alkyl, R ３５ is a hydrogen atom or C １ ~C ６ represents alkyl, R ３６ is a hydrogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl or C ３ ~C ６ represents cycloalkyl, R ３７ is a hydrogen atom or C １ ~C ６ represents alkyl, R ３８ is a hydrogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl or C ３ ~C ６ represents cycloalkyl, R ３９ is a hydrogen atom, C １ ~C ６Alkyl or halo(C １ ~C ６ ) alkyl, R ４０ is a hydrogen atom, C １ ~C ６ Alkyl, C １ ~C ６ Alkylcarbonyl or C １ ~C ６ represents an alkoxycarbonyl; R ４１ is a hydrogen atom or C １ ~C ６ represents alkyl, R ４２ is a hydrogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl or C ３ ~C ６ represents cycloalkyl, R ５４ is C １ ~C ６ represents alkyl, R ５５ is C １ ~C ６ represents alkyl, R ５８ is a halogen atom, C １ ~C ６ alkoxy or cyano, J represents J-1 to J-52, Z ５ is a hydrogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl, C １ ~C ６ Alkoxy (C １ ~C ６ ) alkyl, C １ ~C ６ Alkylcarbonyl, halo(C １ ~C ６ ) alkylcarbonyl, C １ ~C ６ Alkoxycarbonyl, halo(C １ ~C ６ ) alkoxycarbonyl, C １ ~C ６ Alkyl sulfonyl or halo(C １ ~C ６) represents alkylsulfonyl, R １ represents a hydrogen atom, a halogen atom, or C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl, C １ ~C ６ Alkoxy, hydroxy, C １ ~C ６ Alkylthio, C １ ~C ６ Alkylsulfinyl, C １ ~C ６ Alkyl sulfonyl, halo(C １ ~C ６ ) alkylthio, halo(C １ ~C ６ ) alkylsulfinyl, halo(C １ ~C ６ ) alkylsulfonyl, —N(R １ｄ ) R １ｅ , cyano or nitro; R １ａ represents a hydrogen atom, a halogen atom, or C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl, C １ ~C ６ Alkoxy, hydroxy, -N(R １ｄ ) R １ｅ , cyano or nitro; R １ｂ represents a hydrogen atom, a halogen atom, or C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl, C １ ~C ６ Alkoxy, hydroxy, -N(R １ｄ ) R １ｅ , cyano or nitro; R １ｃ represents a hydrogen atom, a halogen atom, or C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl, C １ ~C ６ Alkoxy, hydroxy, -N(R １ｄ ) R １ｅ, cyano or nitro; R １ｄ is a hydrogen atom or C １ ~C ６ represents alkyl, R １ｅ is a hydrogen atom or C １ ~C ６ G represents an alkyl group; ２１ ) R ２２ , -C(=NOR ６７ ) R ６８ , R ６９ (C １ ~C ６ ) alkyl or G-1′ to G-160′, R ２１ is a hydrogen atom, C １ ~C ６ Alkyl or halo(C １ ~C ６ ) alkyl, R ２２ is a hydrogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl, C ２ ~C ６ Alkenyl, halo(C ２ ~C ６ ) alkenyl, C ２ ~C ６ Alkynyl, halo(C ２ ~C ６ ) alkynyl, R ２３ (C １ ~C ６ ) alkyl or M-1 to M-82, R ２３ is C １ ~C ６ Alkoxy, C １ ~C ６ Alkylcarbonyl, C １ ~C ６ Alkoxycarbonyl, hydroxy, cyano, C １ ~C ６ Alkylamino, di(C １ ~C ６) alkylamino, C １ ~C ６ Alkylcarbonylamino, C １ ~C ６ represents alkoxycarbonylamino or M-1 to M-82, ６７ is a hydrogen atom, C １ ~C ６ Alkyl or halo(C １ ~C ６ ) alkyl, R ６８ is a hydrogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl or M-1 to M-82, R ６９ M-1 to M-82, -N(R ７０ ) R ７１ , -C(=O)N(R ７２ ) R ７３ or -C(=NOR ７４ ) R ７５ represents R ７０ is a hydrogen atom or C １ ~C ６ represents alkyl, R ７１ is -C(=O)R ７６ represents R ７６ is C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl or M-1 to M-82, R ７２ is a hydrogen atom or C １ ~C ６ represents alkyl, R ７３ represents M-1 to M-82, and R ７４ is a hydrogen atom or C １ ~C ６ represents alkyl, R ７５ is a hydrogen atom, C １ ~C ６ Alkyl or C ３ ~C ６ represents cycloalkyl; Z ４ is a hydrogen atom, C １ ~C ６ Alkyl, C １ ~C ６ Alkoxy (C１ ~C ６ ) alkyl, C １ ~C ６ Alkylcarbonyl, C １ ~C ６ Alkoxycarbonyl or C １ ~C ６ represents alkylsulfonyl; Z ２ is a halogen atom, C １ ~C ６ Alkyl, C ２ ~C ６ Alkenyl, C ２ ~C ６ Alkynyl, halo(C １ ~C ６ ) alkyl, halo (C ２ ~C ６ ) alkenyl, halo(C ２ ~C ６ ) alkynyl, C １ ~C ６ Alkoxy, halo (C １ ~C ６ ) alkoxy, C ２ ~C ６ Alkenyloxy, halo(C ２ ~C ６ ) alkenyloxy, C ２ ~C ６ Alkynyloxy, halo(C ２ ~C ６ ) alkynyloxy, hydroxy, C １ ~C ６ Alkylcarbonyloxy, C １ ~C ６ Alkoxycarbonyloxy, C １ ~C ６ Alkyl sulfonyloxy, halo(C １ ~C ６ ) alkylsulfonyloxy, —OC(O)N(R ６０ ) R ６１ , C １ ~C ６ Alkylthio, C １ ~C ６ Alkylsulfinyl, C １ ~C ６ Alkyl sulfonyl, halo(C １ ~C ６) alkylthio, halo(C １ ~C ６ ) alkylsulfinyl, halo(C １ ~C ６ ) alkylsulfonyl, C ２ ~C ６ Alkenylthio, C ２ ~C ６ Alkenylsulfinyl, C ２ ~C ６ Alkenylsulfonyl, halo(C ２ ~C ６ ) alkenylthio, halo(C ２ ~C ６ ) alkenylsulfinyl, halo(C ２ ~C ６ ) alkenylsulfonyl, C ２ ~C ６ Alkynylthio, C ２ ~C ６ Alkynylsulfinyl, C ２ ~C ６ Alkynylsulfonyl, halo(C ２ ~C ６ ) alkynylthio, halo(C ２ ~C ６ ) alkynylsulfinyl, halo(C ２ ~C ６ ) alkynylsulfonyl, —SO ３ H, -S(O) ２ N (R ４８ ) R ４９ , -SC≡N, -S(O)(=NR ５２ ) R ５３ , -SF ５ , -N(R ４４ ) R ４５ , -N=S(O)(R ５６ ) R ５７ , formyl, carboxy, C １ ~C ６ Alkylcarbonyl, halo(C １ ~C ６ ) alkylcarbonyl, C １ ~C ６ Alkoxycarbonyl, halo(C １ ~C ６ ) alkoxycarbonyl, —C(O)N(R ４６ ) R４７ , -C(=NOR １４ ) R １５ , Tori (C １ ~C ６ ) alkylsilyl, R ２４ (C １ ~C ６ ) alkyl, R ２５ (C １ ~C ６ ) alkoxy, C ３ ~C ６ Cycloalkyl, R ５９ (C ３ ~C ６ ) cycloalkyl, cyano, nitro, M-1 to M-56, M-61 to M-82, —O-(M-1) to —O-(M-63), —O-(M-65) to —O-(M-70), or —O-(M-72) to —O-(M-80), n represents an integer of 0, 1, or 2, Z ２ In the above relationship, when t2 represents an integer of 2, t3 represents an integer of 2 or 3, t4 represents an integer of 2, 3 or 4, and t5 represents an integer of 2, 3, 4 or 5, each of Z ２ may be the same as or different from each other; or t4 represents an integer of 2, and two Z ２ When two Z ２ together form oxo, -CH ２ CH ２ -, -OCH ２ CH ２ O-, -OCH ２ CH ２ CH ２ O-, = NOR ４３ , =NN(R ６３ ) R ６４ or =NN=C(R ６５ ) R ６６ represents R ４３ is a hydrogen atom or C １ ~C ６ represents alkyl, R ２４ is C １ ~C ６ Alkoxy, hydroxy or -N(R ５０ ) R ５１ represents R２５ is C １ ~C ６ represents alkoxy or M-1 to M-82, １ is a halogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl, C １ ~C ６ Alkoxy, C １ ~C ６ Alkylthio, halo(C １ ~C ６ ) alkylthio, C １ ~C ６ Alkylsulfinyl, C １ ~C ６ represents alkylsulfonyl or cyano; M １ In the above relationship, when t2 represents an integer of 2, t3 represents an integer of 2 or 3, t4 represents an integer of 2, 3 or 4, and t5 represents an integer of 2, 3, 4 or 5, each of M １ may be the same as or different from each other, M ３ is a hydrogen atom, C １ ~C ６ Alkyl or halo(C １ ~C ６ ) alkyl, R １４ is a hydrogen atom, C １ ~C ６ Alkyl or halo(C １ ~C ６ ) alkyl, R １５ is a hydrogen atom, C １ ~C ６ Alkyl or halo(C １ ~C ６ ) alkyl, R ４４ is a hydrogen atom, C １ ~C ６ Alkyl or halo(C １ ~C ６ ) alkyl, R ４５ is a hydrogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl, C １ ~C６ Alkylcarbonyl, halo(C １ ~C ６ ) alkylcarbonyl, C １ ~C ６ Alkoxycarbonyl, halo(C １ ~C ６ ) alkoxycarbonyl, C １ ~C ６ Alkyl sulfonyl or halo(C １ ~C ６ ) represents alkylsulfonyl, R ４６ is a hydrogen atom or C １ ~C ６ represents alkyl, R ４７ is a hydrogen atom, C １ ~C ６ Alkyl or halo(C １ ~C ６ ) alkyl, R ４８ is a hydrogen atom, C １ ~C ６ Alkyl or halo(C １ ~C ６ ) alkyl, R ４９ is a hydrogen atom, C １ ~C ６ Alkyl or halo(C １ ~C ６ ) alkyl, R ５０ is a hydrogen atom or C １ ~C ６ represents alkyl, R ５１ is a hydrogen atom, C １ ~C ６ Alkyl, C １ ~C ６ Alkylcarbonyl, halo(C １ ~C ６ ) alkylcarbonyl, C １ ~C ６ Alkoxycarbonyl, halo(C １ ~C ６ ) alkoxycarbonyl, C １ ~C ６ Alkyl sulfonyl or halo(C １ ~C ６ ) represents alkylsulfonyl, R ５２ is a hydrogen atom or C １~C ６ represents alkyl, R ５３ is C １ ~C ６ represents alkyl, R ５６ is C １ ~C ６ represents alkyl, R ５７ is C １ ~C ６ represents alkyl, R ５９ is a halogen atom, C １ ~C ６ represents alkoxy or cyano; R ６０ is a hydrogen atom or C １ ~C ６ represents alkyl, R ６１ is a hydrogen atom, C １ ~C ６ Alkyl or halo(C １ ~C ６ ) alkyl, R ６３ is a hydrogen atom or C １ ~C ６ represents alkyl, R ６４ is a hydrogen atom, C １ ~C ６ Alkyl, C １ ~C ６ Alkylcarbonyl, halo(C １ ~C ６ ) alkylcarbonyl, C １ ~C ６ Alkoxycarbonyl, halo(C １ ~C ６ ) alkoxycarbonyl, C １ ~C ６ Alkyl sulfonyl or halo(C １ ~C ６ ) represents alkylsulfonyl, R ６５ is a hydrogen atom or C １ ~C ６ represents alkyl, R ６６ is C １ ~C ６ represents alkyl, R ２ is a hydrogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl, C２ ~C ６ Alkenyl, C ２ ~C ６ Alkynyl, C ３ ~C ６ cycloalkyl, —C(O)R ４ , -C(O)OR ５ or R ６７ (C １ ~C ６ ) alkyl, R ６７ is C １ ~C ６ Alkoxy, C １ ~C ６ Alkylthio, C １ ~C ６ Alkylsulfinyl, C １ ~C ６ alkylsulfonyl, cyano, or V-1 to V-82; V １ is a halogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl, C １ ~C ６ Alkoxy, C １ ~C ６ Alkylthio, C １ ~C ６ Alkylsulfinyl, C １ ~C ６ represents alkylsulfonyl, cyano or nitro; V １ In the above relationship, when t2 represents an integer of 2, t3 represents an integer of 2 or 3, t4 represents an integer of 2, 3 or 4, and t5 represents an integer of 2, 3, 4 or 5, each of V １ may be the same as or different from each other, V ３ is a hydrogen atom, C １ ~C ６ Alkyl or halo(C １ ~C ６ ) alkyl, R ４ is C １ ~C ６ Alkyl, C ２ ~C ６ Alkenyl, C２ ~C ６ Alkynyl, C １ ~C ６ Alkylcarbonyl, C １ ~C ６ Alkoxycarbonyl, C １ ~C ６ Alkylamino, di(C １ ~C ６ ) alkylamino, R ６ (C １ ~C ６ ) alkyl or V-1 to V-82, R ５ is C １ ~C ６ Alkyl, C ２ ~C ６ Alkenyl, C ２ ~C ６ Alkynyl, R ９ (C １ ~C ６ ) alkyl, V-1 to V-63, V-65 to V-70, or V-72 to V-80; R ６ is a halogen atom, C １ ~C ６ represents alkoxy, cyano, nitro, or V-1 to V-82; R ９ is a halogen atom, C １ ~C ６ alkoxy, cyano, nitro, or V-1 to V-82; when Q is Q-A, Q-B, or Q-C, R ３ is a hydrogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl, C ２ ~C ６ Alkenyl, C ２ ~C ６ Alkynyl, C ３ ~C ６ Cycloalkyl or C １ ~C ６an aryltetrahydropyridine compound or a salt thereof, wherein: X represents an oxygen atom or a sulfur atom, Y represents an oxygen atom or a sulfur atom, t1 represents an integer of 0 or 1, t2 represents an integer of 0, 1 or 2, t3 represents an integer of 0, 1, 2 or 3, t4 represents an integer of 0, 1, 2, 3 or 4, t5 represents an integer of 0, 1, 2, 3, 4 or 5, d1 represents an integer of 0 or 1, d2 represents an integer of 0, 1 or 2, d3 represents an integer of 0, 1, 2 or 3, d4 represents an integer of 0, 1, 2, 3 or 4, and d5 represents an integer of 0, 1, 2, 3, 4 or 5.

[0007] The compounds of the present invention represented by formula (1) exhibit excellent insecticidal and acaricidal activity against many agricultural pests, spider mites, and internal or external parasites of mammals or birds. Therefore, the present invention can provide novel aryltetrahydropyridine compounds or salts thereof that are useful as pest control agents, particularly as insecticides.

[0008] In the compound according to the present invention represented by formula (1) (hereinafter also referred to as "the compound of the present invention"), tautomers represented by the following formulas are considered to exist, and the compound of the present invention represented by formula (1) includes all tautomers or a mixture of tautomers containing all tautomers in any ratio.

[0009] The compound of the present invention may exist as E- and Z-geometric isomers depending on the types of substituents, and the compound of the present invention includes a mixture containing these E-, Z-, or E- and Z-isomers in any ratio.

[0010] Furthermore, the compound of the present invention may have optically active forms due to the presence of one or more asymmetric carbon atoms or asymmetric sulfur atoms, and the compound of the present invention includes all optically active forms and racemic forms.

[0011] Furthermore, the compound of the present invention may have tautomers depending on the type of substituent, and the compound of the present invention includes all tautomers or a mixture of tautomers containing all tautomers in any ratio.

[0012] Furthermore, the compound of the present invention may exist as one or more rotational isomers due to restricted bond rotation caused by steric hindrance between substituents, and the compound of the present invention encompasses all rotational isomers or a mixture of diastereomers containing all rotational isomers in any ratio.

[0013] Among the compounds of the present invention, those which can be converted into salts by a conventional method include salts of hydrohalic acids such as hydrofluoric acid, hydrochloric acid, hydrobromic acid, and hydroiodic acid; salts of inorganic acids such as nitric acid, sulfuric acid, phosphoric acid, chloric acid, and perchloric acid; salts of sulfonic acids such as methanesulfonic acid, ethanesulfonic acid, trifluoromethanesulfonic acid, benzenesulfonic acid, and p-toluenesulfonic acid; salts of carboxylic acids such as formic acid, acetic acid, propionic acid, trifluoroacetic acid, fumaric acid, tartaric acid, oxalic acid, maleic acid, malic acid, succinic acid, benzoic acid, mandelic acid, ascorbic acid, lactic acid, gluconic acid, and citric acid; salts of amino acids such as glutamic acid and aspartic acid; salts of alkali metals such as lithium, sodium, and potassium; salts of alkaline earth metals such as calcium, barium, and magnesium; aluminum salts; and quaternary ammonium salts such as tetramethylammonium salt, tetrabutylammonium salt, and benzyltrimethylammonium salt.

[0014] Next, specific examples of the substituents shown in this specification are shown below, where n- means normal, i- means iso, s- means secondary, and tert- means tertiary.

[0015] As used herein, the term "halogen atom" includes a fluorine atom, a chlorine atom, a bromine atom, and an iodine atom. The term "halo" also refers to these halogen atoms.

[0016] In this specification, "C ａ ~C ｂ The term "alkyl" refers to a linear or branched hydrocarbon group having a to b carbon atoms, and specific examples thereof include methyl, ethyl, n-propyl, i-propyl, n-butyl, i-butyl, s-butyl, tert-butyl, n-pentyl, 1,1-dimethylpropyl, and n-hexyl, each of which is selected within the range of the number of carbon atoms specified.

[0017] As used herein, "halo(C ａ ~C ｂ The expression "alkyl" refers to a linear or branched hydrocarbon group having a to b carbon atoms in which hydrogen atoms bonded to the carbon atoms are optionally substituted with halogen atoms, and in this case, when the alkyl group is substituted with two or more halogen atoms, the halogen atoms may be the same or different from one another. Examples of the alkyl group include fluoromethyl, chloromethyl, bromomethyl, iodomethyl, difluoromethyl, dichloromethyl, trifluoromethyl, chlorodifluoromethyl, trichloromethyl, bromodifluoromethyl, 1-fluoroethyl, 2-fluoroethyl, 2-chloroethyl, 2-bromoethyl, 2,2-difluoroethyl, 2,2,2-trifluoroethyl, 2-chloro-2,2-difluoroethyl, 2,2,2-trichloroethyl, 2-bromo-2,2-difluoroethyl, 1,1,2,2-tetrafluoroethyl, 2-chloro-1,1,2-trifluoroethyl, 2-chloro-1,1,2,2-tetrafluoroethyl, pentafluoroethyl, 2,2-difluoro Specific examples include propyl, 3,3,3-trifluoropropyl, 3-bromo-3,3-difluoropropyl, 2,2,3,3-tetrafluoropropyl, 2,2,3,3,3-pentafluoropropyl, 1,1,2,3,3,3-hexafluoropropyl, heptafluoropropyl, 2,2,2-trifluoro-1-(methyl)ethyl, 2,2,2-trifluoro-1-(trifluoromethyl)ethyl, 1,2,2,2-tetrafluoro-1-(trifluoromethyl)ethyl, 2,2,3,4,4,4-hexafluorobutyl, 2,2,3,3,4,4,4-heptafluorobutyl, nonafluorobutyl, and the like, and the number of carbon atoms is selected within the range specified for each.

[0018] In this specification, "C ａ ~C ｂThe term "alkenyl" refers to a linear or branched unsaturated hydrocarbon group containing a to b carbon atoms and having one or more double bonds in the molecule, and specific examples thereof include vinyl, 1-propenyl, 2-propenyl, 1-methylethenyl, 2-butenyl, 2-methyl-2-propenyl, 3-methyl-2-butenyl, and 1,1-dimethyl-2-propenyl, and each of these groups is selected within the range of the number of carbon atoms specified.

[0019] In this specification, "C ａ ~C ｂ The term "alkynyl" refers to a linear or branched unsaturated hydrocarbon group containing a to b carbon atoms and having one or more triple bonds in the molecule, and specific examples thereof include ethynyl, propargyl, 2-butynyl, 3-butynyl, 1-pentynyl, and 1-hexynyl, each selected from within the range of the number of carbon atoms specified.

[0020] As used herein, "halo(C ａ ~C ｂ The expression ")alkenyl" refers to a linear or branched unsaturated hydrocarbon group having a to b carbon atoms and one or more double bonds in the molecule, in which hydrogen atoms bonded to carbon atoms are optionally substituted with halogen atoms. In this case, when substituted with two or more halogen atoms, the halogen atoms may be the same or different. Specific examples include 2,2-dichlorovinyl, 2-fluoro-2-propenyl, 2-chloro-2-propenyl, 3-chloro-2-propenyl, 2-bromo-2-propenyl, 3,3-difluoro-2-propenyl, 2,3-dichloro-2-propenyl, 3,3-dichloro-2-propenyl, 2,3,3-trifluoro-2-propenyl, 2,3,3-trichloro-2-propenyl, 1-(trifluoromethyl)ethenyl, 4,4-difluoro-3-butenyl, 3,4,4-trifluoro-3-butenyl, and 3-chloro-4,4,4-trifluoro-2-butenyl, and the like, each of which is selected within the range of the number of carbon atoms specified for each.

[0021] As used herein, "halo(C ａ ~C ｂThe term "alkynyl" refers to a linear or branched unsaturated hydrocarbon group having a to b carbon atoms, in which hydrogen atoms bonded to carbon atoms are optionally substituted with halogen atoms, and which has one or more triple bonds in the molecule. In this case, when substituted with two or more halogen atoms, the halogen atoms may be the same or different. Specific examples include 2-chloroethynyl, 2-bromoethynyl, 2-iodoethynyl, 3-chloro-2-propynyl, 3-bromo-2-propynyl, and 3-iodo-2-propynyl, and each group may be selected within the range of the number of carbon atoms specified.

[0022] In this specification, "C ａ ~C ｂ The term "alkoxy" represents an alkyl-O- group having a to b carbon atoms as defined above, and specific examples thereof include methoxy, ethoxy, n-propyloxy, i-propyloxy, n-butyloxy, i-butyloxy, s-butyloxy, tert-butyloxy, and 2-ethylhexyloxy, and each group is selected within the range of the number of carbon atoms specified.

[0023] As used herein, "halo(C ａ ~C ｂ The notation of ")alkoxy" represents haloalkyl-O- as defined above having a to b carbon atoms, and specific examples thereof include difluoromethoxy, trifluoromethoxy, chlorodifluoromethoxy, bromodifluoromethoxy, 2-fluoroethoxy, 2-chloroethoxy, 2,2,2-trifluoroethoxy, 1,1,2,2-tetrafluoroethoxy, 2-chloro-1,1,2-trifluoroethoxy, and 1,1,2,3,3,3-hexafluoropropyloxy, and the like, each selected within the range of the specified number of carbon atoms.

[0024] In this specification, "C ａ ~C ｂ Alkoxy (C ｄ ~C ｅ The notation "alkyl" refers to any C alkyl group having the above meaning. ａ ~C ｂThe alkyl group has d to e carbon atoms and is selected from the range of the number of carbon atoms specified for each group, and is selected from the range of the number of carbon atoms specified for each group.

[0025] In this specification, "C ａ ~C ｂ Alkoxy (C ｄ ~C ｅ The notation "alkoxy" refers to any C-alkoxy group having the above-mentioned meaning. ａ ~C ｂ The alkoxy group represents an alkoxy group having d to e carbon atoms in which a hydrogen atom bonded to a carbon atom is optionally substituted, and specific examples thereof include methoxyethoxy and ethoxyethoxy, each selected from within the range of the number of carbon atoms specified.

[0026] In this specification, "C ａ ~C ｂ The term "alkenyloxy" represents an alkenyl-O- group having a to b carbon atoms as defined above, and specific examples thereof include 2-propenyloxy, 2-butenyloxy, 2-methyl-2-propenyloxy, and 3-methyl-2-butenyloxy, each selected from the range of the number of carbon atoms specified.

[0027] As used herein, "halo(C ａ ~C ｂ The notation of "haloalkenyloxy" represents a haloalkenyl-O- group having a to b carbon atoms as defined above, and specific examples thereof include 3,3-difluoroallyloxy and 3,3-dichloroallyloxy, and the number of carbon atoms is selected within the range specified for each group.

[0028] In this specification, "C ａ ~C ｂThe term "alkynyloxy" represents an alkynyl-O- group having a to b carbon atoms as defined above, and specific examples thereof include ethynyloxy, propargyloxy, 2-butynyloxy, 1-pentynyloxy, and 1-hexynyloxy, each selected from the range of the number of carbon atoms specified.

[0029] As used herein, "halo(C ａ ~C ｂ The notation of ")alkynyloxy" represents a haloalkynyl-O- group having the above-mentioned meaning and containing a to b carbon atoms, and specific examples thereof include 3-chloro-2-propynyloxy, 3-bromo-2-propynyloxy, and 3-iodo-2-propynyloxy, and the like, each selected within the range of the number of carbon atoms specified.

[0030] In this specification, "C ａ ~C ｂ The term "alkylcarbonyloxy" refers to an alkyl-C(O)-O- group having a to b carbon atoms as defined above. Specific examples include acetyloxy, propionyloxy, butyryloxy, isobutyryloxy, etc., and each group is selected within the range of the number of carbon atoms specified.

[0031] In this specification, "C ａ ~C ｂ The term "alkoxycarbonyloxy" represents an alkoxy-C(O)-O- group having a to b carbon atoms as defined above, and specific examples thereof include methoxycarbonyloxy, ethoxycarbonyloxy, i-butyloxycarbonyloxy, and tert-butyloxycarbonyloxy, and the like are selected within the range of the number of carbon atoms specified for each group.

[0032] In this specification, "C ａ ~C ｂ The term "alkylthio" represents an alkyl-S- group having a to b carbon atoms as defined above, and specific examples thereof include methylthio, ethylthio, n-propylthio, i-propylthio, n-butylthio, i-butylthio, s-butylthio, and tert-butylthio, each of which is selected within the range of the number of carbon atoms specified.

[0033] In this specification, "C ａ ~C ｂ The term "alkylsulfinyl" represents an alkyl-S(O)- group having a to b carbon atoms as defined above, and specific examples thereof include methylsulfinyl, ethylsulfinyl, n-propylsulfinyl, i-propylsulfinyl, n-butylsulfinyl, i-butylsulfinyl, s-butylsulfinyl, and tert-butylsulfinyl, and is selected within the range of the number of carbon atoms specified for each group.

[0034] In this specification, "C ａ ~C ｂ The expression "alkylsulfonyl" means alkyl-S(O) having the above meaning and containing a to b carbon atoms. ２ - group, and specific examples include methylsulfonyl, ethylsulfonyl, n-propylsulfonyl, i-propylsulfonyl, n-butylsulfonyl, i-butylsulfonyl, s-butylsulfonyl, tert-butylsulfonyl, etc., and each is selected within the range of the number of carbon atoms specified.

[0035] As used herein, "halo(C ａ ~C ｂ The notation of "(trifluoromethyl)alkylthio" represents a haloalkyl-S- group having the above-mentioned meaning and containing a to b carbon atoms, and specific examples thereof include difluoromethylthio, trifluoromethylthio, chlorodifluoromethylthio, bromodifluoromethylthio, 2,2,2-trifluoroethylthio, 1,1,2,2-tetrafluoroethylthio, 2-chloro-1,1,2-trifluoroethylthio, pentafluoroethylthio, 1,1,2,3,3,3-hexafluoropropylthio, heptafluoropropylthio, 1,2,2,2-tetrafluoro-1-(trifluoromethyl)ethylthio, and nonafluorobutylthio, and the like are selected within the range of the number of carbon atoms specified for each group.

[0036] As used herein, "halo(C ａ ~C ｂThe notation of "(1-(trifluoromethyl)alkylsulfinyl)" represents a haloalkyl-S(O)- group having the above-mentioned meaning and containing a to b carbon atoms, and specific examples thereof include difluoromethylsulfinyl, trifluoromethylsulfinyl, chlorodifluoromethylsulfinyl, bromodifluoromethylsulfinyl, 2,2,2-trifluoroethylsulfinyl, 1,2,2,2-tetrafluoro-1-(trifluoromethyl)ethylsulfinyl, nonafluorobutylsulfinyl, and the like, and is selected within the range of the number of carbon atoms specified for each group.

[0037] As used herein, "halo(C ａ ~C ｂ The expression "alkylsulfonyl" refers to the haloalkyl-SO 3 group having the above-mentioned meaning and containing a to b carbon atoms. ２ - group, and specific examples include difluoromethylsulfonyl, trifluoromethylsulfonyl, chlorodifluoromethylsulfonyl, bromodifluoromethylsulfonyl, 2,2,2-trifluoroethylsulfonyl, 1,1,2,2-tetrafluoroethylsulfonyl, 2-chloro-1,1,2-trifluoroethylsulfonyl, and the like, and each is selected within the range of the number of carbon atoms specified.

[0038] In this specification, "C ａ ~C ｂ The term "alkenylthio" represents an alkenyl-S- group having a to b carbon atoms as defined above, and specific examples thereof include 2-propenylthio, 2-butenylthio, 2-methyl-2-propenylthio, and 3-methyl-2-butenylthio, each selected from the range of the number of carbon atoms specified.

[0039] In this specification, "C ａ ~C ｂ The term "alkenylsulfinyl" represents an alkenyl-S(O)- group having a to b carbon atoms as defined above, and specific examples thereof include 2-propenylsulfinyl, 2-butenylsulfinyl, 2-methyl-2-propenylsulfinyl, and 3-methyl-2-butenylsulfinyl, each selected from the range of the number of carbon atoms specified.

[0040] In this specification, "C ａ ~C ｂ The expression "alkenylsulfonyl" means the alkenyl-SO 3 having the above-mentioned meaning and containing a to b carbon atoms. ２ - group, and specific examples include 2-propenylsulfonyl, 2-butenylsulfonyl, 2-methyl-2-propenylsulfonyl, 3-methyl-2-butenylsulfonyl, etc., and each group is selected within the range of the number of carbon atoms specified.

[0041] As used herein, "halo(C ａ ~C ｂ The notation of ")alkenylthio" represents a haloalkenyl-S- group having the above-mentioned meaning and containing a to b carbon atoms, and specific examples thereof include 2-fluoro-2-propenylthio, 2-chloro-2-propenylthio, 3,3-difluoro-2-propenylthio, 3,3-dichloro-2-propenylthio, 2,3,3-trifluoro-2-propenylthio, 4,4-difluoro-3-butenylthio, and 3,4,4-trifluoro-3-butenylthio, and the like, each selected within the range of the specified number of carbon atoms.

[0042] As used herein, "halo(C ａ ~C ｂ The notation of "haloalkenylsulfinyl" represents a haloalkenyl-S(O)- group having a to b carbon atoms as defined above, and specific examples thereof include 2-fluoro-2-propenylsulfinyl, 2-chloro-2-propenylsulfinyl, 3,3-difluoro-2-propenylsulfinyl, 3,3-dichloro-2-propenylsulfinyl, 4,4-difluoro-3-butenylsulfinyl, and 3,4,4-trifluoro-3-butenylsulfinyl, and the like, each selected within the range of the specified number of carbon atoms.

[0043] As used herein, "halo(C ａ ~C ｂ The notation "haloalkenylsulfonyl" means the haloalkenyl-SO 3 having the above-mentioned meaning and containing a to b carbon atoms. ２- group, and specific examples include 2-fluoro-2-propenylsulfonyl, 2-chloro-2-propenylsulfonyl, 3,3-difluoro-2-propenylsulfonyl, 3,3-dichloro-2-propenylsulfonyl, 4,4-difluoro-3-butenylsulfonyl, and 3,4,4-trifluoro-3-butenylsulfonyl, and the number of carbon atoms is selected within the range specified for each group.

[0044] In this specification, "C ａ ~C ｂ The term "alkynylthio" represents an alkynyl-S- group having a to b carbon atoms as defined above, and specific examples thereof include propynylthio, butynylthio, pentynylthio, and hexynylthio, each selected from the range of the number of carbon atoms specified.

[0045] In this specification, "C ａ ~C ｂ The term "alkynylsulfinyl" represents an alkynyl-S(O)- group having a to b carbon atoms as defined above, and specific examples thereof include 2-propynylsulfinyl and 2-butynylsulfinyl, each selected from within the range of the number of carbon atoms specified.

[0046] In this specification, "C ａ ~C ｂ The expression "alkynylsulfonyl" means an alkynyl-SO 3 group having the above-mentioned meaning and containing a to b carbon atoms. ２ Specific examples include 2-propynylsulfonyl and 2-butynylsulfonyl, and each is selected within the range of the number of carbon atoms specified.

[0047] As used herein, "halo(C ａ ~C ｂ The notation of ")alkynylthio" represents a haloalkynyl-S- group having the above-mentioned meaning and containing a to b carbon atoms, and specific examples thereof include 3-chloro-2-propynylthio, 3-bromo-2-propynylthio, and 3-iodo-2-propynylthio, and the like, each selected from the range of the specified number of carbon atoms.

[0048] As used herein, "halo(C ａ ~Cｂ The notation of "haloalkynylsulfinyl" represents a haloalkynyl-S(O)- group having the above-mentioned meaning and containing a to b carbon atoms, and specific examples thereof include 3-chloro-2-propynylsulfinyl, 3-bromo-2-propynylsulfinyl, and 3-iodo-2-propynylsulfinyl, and the like, each selected from within the range of the specified number of carbon atoms.

[0049] As used herein, "halo(C ａ ~C ｂ The notation "alkynylsulfonyl" means haloalkynyl-SO 3 having the above-mentioned meaning and containing a to b carbon atoms. ２ Specific examples include 3-chloro-2-propynylsulfonyl, 3-bromo-2-propynylsulfonyl, 3-iodo-2-propynylsulfonyl, and the like, and each is selected within the range of the number of carbon atoms specified.

[0050] In this specification, "C ａ ~C ｂ The term "alkylsulfonyloxy" represents an alkylsulfonyl-O- group having a to b carbon atoms as defined above, and specific examples thereof include methylsulfonyloxy, ethylsulfonyloxy, n-propylsulfonyloxy, and i-propylsulfonyloxy, and the like are selected within the range of the number of carbon atoms specified for each group.

[0051] As used herein, "halo(C ａ ~C ｂ The notation of "haloalkylsulfonyloxy" represents a haloalkylsulfonyl-O- group having the above-mentioned meaning and containing a to b carbon atoms, and specific examples thereof include difluoromethylsulfonyloxy, trifluoromethylsulfonyloxy, chlorodifluoromethylsulfonyloxy, bromodifluoromethylsulfonyloxy, and the like, and each group is selected within the range of the number of carbon atoms specified.

[0052] In this specification, "C ａ ~C ｂThe term "alkylamino" refers to an amino group in which one of the hydrogen atoms is substituted with alkyl having a to b carbon atoms as defined above, and specific examples thereof include methylamino, ethylamino, n-propylamino, i-propylamino, n-butylamino, i-butylamino, and tert-butylamino, each selected within the range of the number of carbon atoms specified.

[0053] In this specification, "di(C ａ ~C ｂ The expression "alkylamino" refers to an amino group in which both hydrogen atoms are substituted with alkyl as defined above, which may be the same or different and have a to b carbon atoms. Specific examples include dimethylamino, ethyl(methyl)amino, diethylamino, n-propyl(methyl)amino, i-propyl(methyl)amino, di(n-propyl)amino, di(n-butyl)amino, etc., and the number of carbon atoms is selected within the range specified for each group.

[0054] In this specification, "C ａ ~C ｂ The term "alkylcarbonyl" represents an alkyl-C(O)- group having a to b carbon atoms as defined above, and specific examples thereof include acetyl, propionyl, butyryl, isobutyryl, valeryl, isovaleryl, 2-methylbutanoyl, pivaloyl, hexanoyl, and heptanoyl, each of which is selected within the range of the number of carbon atoms specified.

[0055] In this specification, "C ａ ~C ｂ The term "alkoxycarbonyl" represents an alkyl-O-C(O)- group having a to b carbon atoms as defined above, and specific examples thereof include methoxycarbonyl, ethoxycarbonyl, n-propyloxycarbonyl, i-propyloxycarbonyl, n-butoxycarbonyl, i-butoxycarbonyl, s-butoxycarbonyl, tert-butoxycarbonyl, and 2-ethylhexyloxycarbonyl, and the number of carbon atoms is selected within the range specified for each group.

[0056] As used herein, "halo(C ａ ~Cｂ The notation of "haloalkylcarbonyl" represents a haloalkyl-C(O)- group having a to b carbon atoms as defined above, and specific examples thereof include fluoroacetyl, chloroacetyl, difluoroacetyl, dichloroacetyl, trifluoroacetyl, chlorodifluoroacetyl, bromodifluoroacetyl, trichloroacetyl, pentafluoropropionyl, heptafluorobutanoyl, and 3-chloro-2,2-dimethylpropanoyl, and the like are selected within the range of the number of carbon atoms specified for each group.

[0057] In this specification, "C ａ ~C ｂ The term "alkylcarbonylamino" refers to an amino group in which one of the hydrogen atoms is substituted with the above-mentioned alkylcarbonyl having a to b carbon atoms, and specific examples thereof include methylcarbonylamino and ethylcarbonylamino, each selected within the range of the number of carbon atoms specified.

[0058] As used herein, "halo(C ａ ~C ｂ The notation of ")alkoxycarbonyl" represents a haloalkyl-O-C(O)- group having the above-mentioned meaning and containing a to b carbon atoms, and specific examples thereof include chloromethoxycarbonyl, 2-chloroethoxycarbonyl, 2,2-difluoroethoxycarbonyl, 2,2,2-trifluoroethoxycarbonyl, and 2,2,2-trichloroethoxycarbonyl, and the like are selected within the range of the number of carbon atoms specified for each group.

[0059] In this specification, "C ａ ~C ｂ The term "alkenyloxycarbonyl" represents an alkenyl-O-C(O)- group having a to b carbon atoms as defined above, and specific examples thereof include 2-propenyloxycarbonyl, 2-butenyloxycarbonyl, 2-methyl-2-propenyloxycarbonyl, and 3-methyl-2-butenyloxycarbonyl, and each group is selected within the range of the number of carbon atoms specified.

[0060] In this specification, "C ａ ~C ｂThe term "alkoxycarbonylamino" refers to an amino group in which one of the hydrogen atoms is substituted with the above-mentioned alkoxycarbonyl having a to b carbon atoms, and specific examples thereof include methoxycarbonylamino and ethoxycarbonylamino, each selected within the range of the number of carbon atoms specified.

[0061] In this specification, "C ａ ~C ｂ The term "alkylaminocarbonyl" represents a carbamoyl group in which one of the hydrogen atoms is substituted with alkyl having a to b carbon atoms as defined above, and specific examples thereof include methylcarbamoyl, ethylcarbamoyl, n-propylcarbamoyl, i-propylcarbamoyl, n-butylcarbamoyl, i-butylcarbamoyl, s-butylcarbamoyl, and tert-butylcarbamoyl, each selected from the range of the number of carbon atoms specified.

[0062] In this specification, "C ａ ~C ｂ The expression "alkylaminocarbonylamino" represents an amino group in which one of the hydrogen atoms is substituted with the above-mentioned alkylaminocarbonyl having a to b carbon atoms, and specific examples thereof include methylaminocarbonylamino and ethylaminocarbonylamino, each selected within the range of the specified number of carbon atoms.

[0063] In this specification, "di(C ａ ~C ｂ The expression "(a) alkylaminocarbonyl" represents a carbamoyl group in which both hydrogen atoms are substituted with alkyl as defined above, each of which may be the same or different and has a to b carbon atoms. Specific examples include N,N-dimethylcarbamoyl, N-ethyl-N-methylcarbamoyl, N,N-diethylcarbamoyl, N,N-di(n-propyl)carbamoyl, and N,N-di(n-butyl)carbamoyl, and are selected within the range of the number of carbon atoms specified for each group.

[0064] In this specification, "C ａ ~C ｂThe term "cycloalkyl" refers to a cyclic saturated hydrocarbon group containing a to b carbon atoms, which can form a single ring or multiple ring structures having 3 to 6 members. Each ring may be optionally substituted with alkyl within the specified range of carbon atoms. Specific examples include cyclopropyl, 1-methylcyclopropyl, 2-methylcyclopropyl, 2,2-dimethylcyclopropyl, cyclobutyl, cyclopentyl, and cyclohexyl, each of which is selected within the specified range of carbon atoms.

[0065] As used herein, "tri(C ａ ~C ｂ The expression "(a) alkylsilyl" represents a silyl group substituted with alkyl as defined above, each of which may be the same or different and has a to b carbon atoms. Specific examples include trimethylsilyl, triethylsilyl, tri(n-propyl)silyl, ethyldimethylsilyl, n-propyldimethylsilyl, n-butyldimethylsilyl, i-butyldimethylsilyl, tert-butyldimethylsilyl, etc., and each is selected within the range of the number of carbon atoms specified.

[0066] In this specification, "R ６ (C ａ ~C ｂ The notation "alkyl" means that any hydrogen atom attached to a carbon atom is substituted with one or more substituents R ６ represents an alkyl group having the above-mentioned meaning and having a to b carbon atoms, which is partially or completely substituted with the following, and the number of carbon atoms is selected within the range specified for each group. ６ When two or more groups are present, the substituent R ６ may be the same or different from each other.

[0067] In this specification, "R ７ (C ａ ~C ｂ The notation "alkyl" means that any hydrogen atom attached to a carbon atom is substituted with one or more substituents R ７ represents an alkyl group having the above-mentioned meaning and having a to b carbon atoms, which is partially or completely substituted with the following, and the number of carbon atoms is selected within the range specified for each group.７ When two or more groups are present, the substituent R ７ may be the same or different from each other.

[0068] In this specification, "R ９ (C ａ ~C ｂ The notation "alkyl" means that any hydrogen atom attached to a carbon atom is substituted with one or more substituents R ９ represents an alkyl group having the above-mentioned meaning and having a to b carbon atoms, which is partially or completely substituted with the following, and the number of carbon atoms is selected within the range specified for each group. ９ When two or more groups are present, the substituent R ９ may be the same or different from each other.

[0069] In this specification, "R １７ (C ａ ~C ｂ The notation "alkyl" means that any hydrogen atom attached to a carbon atom is substituted with one or more substituents R １７ represents an alkyl group having the above-mentioned meaning and having a to b carbon atoms, which is partially or completely substituted with the following, and the number of carbon atoms is selected within the range specified for each group. １７ When two or more groups are present, the substituent R １７ may be the same or different from each other.

[0070] In this specification, "R ２０ (C ａ ~C ｂ The notation "alkyl" means that any hydrogen atom attached to a carbon atom is substituted with one or more substituents R ２０ represents an alkyl group having the above-mentioned meaning and having a to b carbon atoms, which is partially or completely substituted with the following, and the number of carbon atoms is selected within the range specified for each group. ２０ When two or more groups are present, the substituent R ２０ may be the same or different from each other.

[0071] In this specification, "R ２３ (C ａ ~C ｂThe notation "alkyl" means that any hydrogen atom attached to a carbon atom is substituted with one or more substituents R ２３ represents an alkyl group having the above-mentioned meaning and having a to b carbon atoms, which is partially or completely substituted with the following, and the number of carbon atoms is selected within the range specified for each group. ２３ When two or more groups are present, the substituent R ２３ may be the same or different from each other.

[0072] In this specification, "R ２４ (C ａ ~C ｂ The notation "alkyl" means that any hydrogen atom attached to a carbon atom is substituted with one or more substituents R ２４ represents an alkyl group having the above-mentioned meaning and having a to b carbon atoms, which is partially or completely substituted with the following, and the number of carbon atoms is selected within the range specified for each group. ２４ When two or more groups are present, the substituent R ２４ may be the same or different from each other.

[0073] In this specification, "R ６７ (C ａ ~C ｂ The notation "alkyl" means that any hydrogen atom attached to a carbon atom is substituted with one or more substituents R ６７ represents an alkyl group having the above-mentioned meaning and having a to b carbon atoms, which is partially or completely substituted with the following, and the number of carbon atoms is selected within the range specified for each group. ６７ When two or more groups are present, the substituent R ６７ may be the same or different from each other.

[0074] In this specification, "R ６９ (C ａ ~C ｂ The notation "alkyl" means that any hydrogen atom attached to a carbon atom is substituted with one or more substituents R ６９ represents an alkyl group having the above-mentioned meaning and having a to b carbon atoms, which is partially or completely substituted with the following, and the number of carbon atoms is selected within the range specified for each group. ６９ When two or more groups are present, the substituent R ６９may be the same or different from each other.

[0075] In this specification, "R １６ (C ａ ~C ｂ The notation "alkoxy" means that any hydrogen atom attached to a carbon atom is substituted with one or more substituents R １６ The alkoxy group has the above-mentioned meaning and has a to b carbon atoms, which are partially or completely substituted with the following, and the number of carbon atoms is selected within the range specified for each group. １６ When two or more groups are present, the substituent R １６ may be the same or different from each other.

[0076] In this specification, "R ２５ (C ａ ~C ｂ The notation "alkoxy" means that any hydrogen atom attached to a carbon atom is substituted with one or more substituents R ２５ The alkoxy group has the above-mentioned meaning and has a to b carbon atoms, which are partially or completely substituted with the following, and the number of carbon atoms is selected within the range specified for each group. ２５ When two or more groups are present, the substituent R ２５ may be the same or different from each other.

[0077] In this specification, "R ５８ (C ａ ~C ｂ The notation "cycloalkyl" means that any hydrogen atom attached to a carbon atom is substituted with one or more substituents R ５８ represents a cycloalkyl group having the above-mentioned meaning and having a to b carbon atoms, which is partially or completely substituted with the following, and the number of carbon atoms is selected within the range specified for each group. ５８ When two or more groups are present, the substituent R ５８ may be the same or different from each other.

[0078] In this specification, "R ５９ (C ａ ~C ｂ The notation "cycloalkyl" means that any hydrogen atom attached to a carbon atom is substituted with one or more substituents R ５９represents a cycloalkyl group having the above-mentioned meaning and having a to b carbon atoms, which is partially or completely substituted with the following, and the number of carbon atoms is selected within the range specified for each group. ５９ When two or more groups are present, the substituent R ５９ may be the same or different from each other.

[0079] In the present specification, "t4 represents an integer of 2, and two Z ２ When two Z ２ The notation "together represent oxo" represents a ═O group, for example, Z of G-2′. ２ Specific examples of the structure in which these groups are taken together to form oxo include the following Gb-1′, Gb-2′, and Gb-3′, and Z of G-3′ ２ Specific examples of the structure where represents oxo include the following Gb-4' and Gb-5'.

[0080] In the present specification, "t4 represents an integer of 2, and two Z ２ When two Z ２ Let's get together -CH ２ CH ２ The notation "-" represents, for example, Z of G-2'. ２ Together -CH ２ CH ２ Specific examples of the structure representing - include Gb-6', Gb-7', Gb-8' and the like shown below. Z of G-3' ２ Ga-CH ２ CH ２ Specific examples of the structure representing - include the following Gb-9' and Gb-10'.

[0081] In the present specification, "t4 represents an integer of 2, and two Z ２ When two Z ２ Let's get together -OCH ２ CH ２ The notation "represents O-" refers to, for example, Z of G-2'. ２ Together -OCH ２ CH ２Specific examples of the structure representing O- include Gb-11', Gb-12', Gb-13' and the like shown below. Z of G-3' ２ Ga-OCH ２ CH ２ Specific examples of the structure representing O- include the following Gb-14' and Gb-15'.

[0082] In the present specification, "t4 represents an integer of 2, and two Z ２ When two Z ２ Let's get together -OCH ２ CH ２ CH ２ The notation "represents O-" refers to, for example, Z of G-2'. ２ Together -OCH ２ CH ２ CH ２ Specific examples of the structure representing O- include Gb-16', Gb-17', Gb-18' and the like shown below. Z of G-3' ２ Ga-OCH ２ CH ２ CH ２ Specific examples of the structure representing O- include the following Gb-19' and Gb-20'.

[0083] In the present specification, "t4 represents an integer of 2, and two Z ２ When two Z ２ Let's get together = NOR ４３ The notation "represents" refers to, for example, Z of G-2'. ２ Together = NOR ４３ Specific examples of the structure represented by the formula (I) include Gb-21′, Gb-22′, and Gb-23′ shown below, and Z of G-3′ is ２ Ga = NOR ４３ Specific examples of the structure include the following Gb-24' and Gb-25'.

[0084] In the present specification, "t4 represents an integer of 2, and two Z ２ When two Z ２ together = NN(R ６３) R ６４ The notation "represents" refers to, for example, Z of G-2'. ２ together = NN(R ６３ ) R ６４ Specific examples of the structure represented by the formula (I) include Gb-26′, Gb-27′, Gb-28′, etc., and Z of G-3′ is ２ = NN(R ６３ ) R ６４ Specific examples of the structure include Gb-29' and Gb-30' shown below.

[0085] In the present specification, "t4 represents an integer of 2, and two Z ２ When two Z ２ together = NN = C(R ６５ ) R ６６ The notation "represents" refers to, for example, Z of G-2'. ２ together = NN = C(R ６５ ) R ６６ Specific examples of the structure represented by the formula (I) include Gb-31′, Gb-32′, and Gb-33′ shown below, and Z of G-3′ is ２ = NN = C (R ６５ ) R ６６ Specific examples of the structure include Gb-34' and Gb-35' shown below.

[0086] In the present specification, the expression "t1 represents an integer of 0 or 1" includes, for example, Q-13, Q-23, Q-24, Q-28, Q-29, Q-34, Q-35, Q-36, Q-48, Q-49, Q-50, Q-51, Q-52, Q-53, Q-54, Q-55, E-13, E-23, E-24, E-28, E-29, E-34, E-35, E-36, E-48, E-49, E-50, E-51, E-52, E-53, E-54, E-55, M-13, M-23, M- In the formulas of M-24, M-28, M-29, M-34, M-35, M-36, M-48, M-49, M-50, M-51, M-52, M-53, M-54, M-55, G-29, G-30, G-31, G-36, G-37, G-38, G-44, G-45, G-46, G-49, G-50, G-51, G-60, G-61, G-62, G-63, G-64 and G-65, each t1 may be the same as or different from each other and represents an integer of 0 or 1.

[0087] In the present specification, the expression "t2 represents an integer of 0, 1, or 2" includes, for example, Q-9, Q-10, Q-11, Q-12, Q-16, Q-17, Q-18, Q-20, Q-21, Q-22, Q-26, Q-27, Q-31, Q-32, Q-33, Q-41, Q-42, Q-43, Q-44, Q-45, Q-46, Q-47, E-9, E-10, E-11, E-12, E-16, E-17, E-18, E-20, E-21, E-22, E-26, E-2 7, E-31, E-32, E-33, E-41, E-42, E-43, E-44, E-45, E-46, E-47, M-9, M-10, M-11, M- 12, M-16, M-17, M-18, M-20, M-21, M-22, M-26, M-27, M-31, M-32, M-33, M-41, M-42 , M-43, M-44, M-45, M-46, M-47, G-6, G-8, G-10, G-14, G-15, G-16, G-21, G-22, G-23 , G-24, G-25, G-26, G-27, G-28, G-33, G-34, G-35, G-40, G-41, G-42, G-43, G-48, G-56, G-57, G-58 and G-59, each t2 may be the same as or different from each other and represents an integer of 0, 1 or 2.

[0088] In the present specification, the expression "t3 represents an integer of 0, 1, 2 or 3" means, for example, Q-4, Q-5, Q-6, Q-7, Q-8, Q-15, Q-19, Q-25, Q-30, Q-38, Q-39, Q-40, E-4, E-5, E-6, E-7, E-8, E-15, E-19, E-25, E-30, E-38, E-39, E-40, M-4, M-5, M-6, M-7, In M-8, M-15, M-19, M-25, M-30, M-38, M-39, M-40, G-4, G-5, G-9, G-11, G-12, G-13, G-17, G-18, G-19, G-20, G-32, G-47, G-54, G-55 and G-29′, each t3 may be the same as or different from each other and represents an integer of 0, 1, 2 or 3.

[0089] In the present specification, the expression "t4 represents an integer of 0, 1, 2, 3, or 4" means, for example, Q-2, Q-3, Q-14, Q-57, Q-58, Q-59, Q-60, Q-61, Q-62, Q-63, Q-64, Q-65, Q-66, Q-67, Q-68, Q-69, Q-70, Q-71, Q-72, Q-73, Q-74, Q-75, Q-76, Q-77, Q-78, Q-79, Q-80, Q-81, Q-82, E-2, E-3, E-14, E-57, E-58, E-59, E-60, E-61, E-62, E-63, E-64, E-65, E-66, E-67 , E-68, E-69, E-70, E-71, E-72, E-73, E-74, E-75, E-76, E-77, E-78, E-79, E -80, E-81, E-82, E-83, M-2, M-3, M-14, M-57, M-58, M-59, M-60, M-61, M-62, M-63, M-64, M-65, M-66, M-67, M-68, M-69, M-70, M-71, M-72, M-73, M-74, M- 75, M-76, M-77, M-78, M-79, M-80, M-81, M-82, G-1, G-3, G-7, G-53, G-1', G-2 ', G-3', G-4', G-5', G-6', G-7', G-8', G-9', G-10', G-11', G-12', G-13', G -14', G-15', G-16', G-17', G-18', G-19', G-20', G-21', G-22', G-23', G-2 4', G-25', G-26', G-27', G-28', G-30', G-31', G-32', G-33', G-34', G-35' , G-36', G-37', G-38', G-39', G-40', G-41', G-42', G-43', G-44', G-45', G- 46', G-47', G-48', G-49', G-50', G-51', G-52', G-53', G-54', G-55', G-56 ', G-57', G-58', G-59', G-60', G-61', G-62', G-63', G-64', G-65', G-66', G -67', G-68', G-69', G-70', G-71', G-72', G-73', G-74', G-75', G-76', G-7 7', G-78', G-79', G-80', G-81', G-82', G-83', G-84', G-85', G-86', G-87',G-88', G-89', G-90', G-91', G-92', G-93', G-94', G-95', G-96', G-97', G-98', G-9 9', G-100', G-101', G-102', G-103', G-104', G-105', G-106', G-107', G-108', G-1 09', G-110', G-111', G-112', G-113', G-114', G-115', G-116', G-117', G-118', G- 119', G-120', G-121', G-122', G-123', G-124', G-125', G-126', G-127', G-128', G -129', G-130', G-131', G-132', G-133', G-134', G-135', G-136', G-137', G-138', G-139', G-140', G-141', G-142', G-143', G-144', G-145', G-146', G-147', G-148' In G-149', G-150', G-151', G-152', G-153', G-154', G-155', G-156', G-157', G-158', G-159' and G-160', each t4 may be the same as or different from each other and represents an integer of 0, 1, 2, 3 or 4.

[0090] In the present specification, the expression "t5 represents an integer of 0, 1, 2, 3, 4, or 5" means that, for example, in Q-1, E-1, M-1, and G-2, each t5 may be the same as or different from each other and represents an integer of 0, 1, 2, 3, 4, or 5.

[0091] In the present specification, the expression "n represents an integer of 0, 1 or 2" includes, for example, Q-62, Q-69, Q-70, Q-78, Q-79, Q-80, Q-82, E-62, E-69, E-70, E-78, E-79, E-80, E-82, M-62, M-69, M-70, M-78, M-79, M-80, M-82, V-62, V-69, V-70, V-78, V-79, V-80, V-82, G-4', G-18', G-31', G-34', G-40', G-41' , G-42', G-44', G-45', G-46', G-47', G-50', G-51', G-60', G-61', G-62', G-67', G-6 8', G-69', G-71', G-72', G-73', G-74', G-76', G-78', G-81', G-82', G-87', G-88', G-89', G-90', G-95', G-96', G-97', G-98', G-101', G-102', G-113', G-118', G-120' , G-123', G-135', G-136', G-137', G-139', G-140', G-141', G-142', G-143', G-144', G-153', G-154' and G-155', each n may be the same as or different from each other and represents an integer of 0, 1 or 2.

[0092] The notation "-O-(E-1)" in this specification represents an (E-1)-O- group including the above-mentioned E-1. For example, a specific example of a structure representing "-O-(E-1)" is OE-1 below. Similarly, a specific example of a structure representing "-O-(E-2)" is OE-2 below, and a specific example of a structure representing "-O-(E-3)" is OE-3 below. The same applies to "-O-(E-4)" to "-O-(E-83)".

[0093] The notation "-S-(E-1)" in this specification represents an (E-1)-S- group including the above-mentioned E-1. For example, a specific example of a structure representing "-S-(E-1)" is SE-1 below. Similarly, a specific example of a structure representing "-S-(E-2)" is SE-2 below. A specific example of a structure representing "-S-(E-3)" is SE-3 below. The same applies to "-S-(E-4)" to "-S-(E-83)".

[0094] The notation "-S(O)-(E-1)" in this specification represents an (E-1)-S(O)- group including the above-mentioned E-1. For example, a specific example of a structure representing "-S(O)-(E-1)" is SOE-1 below. Similarly, a specific example of a structure representing "-S(O)-(E-2)" is SOE-2 below, and a specific example of a structure representing "-S(O)-(E-3)" is SOE-3 below. The same applies to "-S(O)-(E-4)" to "-S(O)-(E-83)".

[0095]

[0096] In this specification, "-S(O) ２ The notation "-(E-1)" includes the above E-1, (E-1)-S(O) ２ - group, for example, "-S(O) ２ A specific example of the structure representing "-S(O) ２ A specific example of the structure representing "-S(O) ２ A specific example of the structure representing "-S(O) ２ -(E-4)" ~ "-S(O) ２ The same applies to "-(E-83)".

[0097] The notation "-C(O)-(E-1)" in this specification represents an (E-1)-C(O)- group including the above-mentioned E-1. For example, a specific example of a structure representing "-C(O)-(E-1)" is COE-1 below. Similarly, a specific example of a structure representing "-C(O)-(E-2)" is COE-2 below, and a specific example of a structure representing "-C(O)-(E-3)" is COE-3 below. The same applies to "-C(O)-(E-4)" to "-C(O)-(E-83)".

[0098] The notation "-N=N-(E-1)" in this specification represents an (E-1)-N=N- group including the above-mentioned E-1. For example, a specific example of a structure representing "-N=N-(E-1)" is the following NNE-1. Similarly, a specific example of a structure representing "-N=N-(E-2)" is the following NNE-2, and a specific example of a structure representing "-N=N-(E-3)" is the following NNE-3. The same applies to "-N=N-(E-4)" to "-N=N-(E-83)".

[0099] The notation "-O-(M-1)" in this specification represents a (M-1)-O- group including the above-mentioned M-1. For example, a specific example of a structure representing "-O-(M-1)" is OM-1 below. Similarly, a specific example of a structure representing "-O-(M-2)" is OM-2 below. A specific example of a structure representing "-O-(M-3)" is OM-3 below. The same applies to "-O-(M-4)" to "-O-(M-82)".

[0100] Next, a method for producing the compound of the present invention represented by formula (1) is described below. The compound of the present invention can be produced, for example, by the following method. Note that the following description is merely illustrative, and the compound of the present invention represented by formula (1) may also be produced by other methods. Hereinafter, "the compound of the present invention represented by formula (1)" will also be described as "compound of the present invention (1)," and "compound of formula (2)" will also be described as "compound of the present invention (2)." Other compounds will also be described similarly. Note that, among compounds of the present invention (1), a compound in which Q is Q-A will also be described as compound of the present invention (1-A), a compound in which Q is Q-B will also be described as compound of the present invention (1-B), and a compound in which Q is Q-C will also be described as compound of the present invention (1-C).

[0101] [Production Method 1-A] Among the compounds of the present invention (1-A), those in which J is J-1, J-2, J-3, J-4, J-5, J-6, J-7, J-8, J-9, J-10, J-11, J-12, J-13, J-17, J-18, J-19, J-20, J-22, J-23, J-24, J-25, J-26, J-27, J-28, J-29, J-30, J- 31, J-32, J-33, J-34, J-35, J-36, J-37, J-38, J-39, J-40, J-41, J-42, J-43, J-44, J-45, J-46, J-50, J-51 or J-52, and G represents G-1, G-2, G-3, G-4, G-5, G-6, G-7, G-8, G-9, G-10, G-11, G-12, G-13, G-14, G-15, G-16, G-17, G-18, G-19, G-20, G-21, G-22, G-23, G-24, G-25, G-26, G-27, G-28, G-29, G-30, G-31, G-32, G-33, G-34, G-35, G-36, G-37, G-38, G Compound (1a) representing G-39, G-40, G-41, G-42, G-43, G-44, G-45, G-46, G-47, G-48, G-49, G-50, G-51, G-52, G-62, G-63, G-64 or G-65 can be produced by reacting compound (2-A) with compound (3-A). (In the formula, Ja is Ja-1, Ja-2, Ja-3, Ja-4, Ja-5, Ja-6, Ja-7, Ja-8, Ja-9, Ja-10, Ja-11, Ja- 12, Ja-13, Ja-17, Ja-18, Ja-19, Ja-20, Ja-22, Ja-23, Ja-24, Ja-25, Ja-26, Ja-27 , Ja-28, Ja-29, Ja-30, Ja-31, Ja-32, Ja-33, Ja-34, Ja-35, Ja-36, Ja-37, Ja-38, J Represents a-39, Ja-40, Ja-41, Ja-42, Ja-43, Ja-44, Ja-45, Ja-46, Ja-50, Ja-51 or Ja-52, Jb is J-1, J-2, J-3, J-4, J-5, J-6, J-7, J-8, J-9, J-10, J-11, J-12, J-13, J-1 7, J-18, J-19, J-20, J-22, J-23, J-24, J-25, J-26, J-27, J-28, J-29, J-30, J- 31, J-32, J-33, J-34, J-35, J-36, J-37, J-38, J-39, J-40, J-41, J-42, J-43, J-44, J-45, J-46, J-50, J-51 or J-52, and Gf represents G-1, G-2, G-3, G-4, G-5, G-6, G-7 , G-8, G-9, G-10, G-11, G-12, G-13, G-14, G-15, G-16, G-17, G-18, G-19, G-20 , G-21, G-22, G-23, G-24, G-25, G-26, G-27, G-28, G-29, G-30, G-31, G-32, G-3 Q, X, Y, R represent G-3, G-4, G-5, G-6, G-7, G-8, G-9, G-10, G-11, G-12, G-13, G-14, G-15, G-16, G-17, G-18, G-19, G-20, G-21, G-22, G-23, G-24, G-25, G-26, G-27, G-28, G-29, G-30, G-31, G-32, G-33, G-34, G-35, G-36, G-37, G-38, G-39, G-40, G-41, G-42, G-43, G-44, G-45, G-46, G-47, G-48, G-49, G-50, G-51, G-52, G-62, G-63, G-64, or G-65; １ , R １ａ , R １ｂ , R １ｃ , R ２ , R ３ and Z ５ represents the same meaning as above, Ga represents a halogen atom or the like, and Gb represents B(OH) ２ represents a leaving group such as

[0102] The compound (1a) of the present invention can be produced by reacting the compound (2-A) with the compound (3-A) in a solvent or without a solvent.

[0103] When a solvent is used, any solvent may be used as long as it is inert to the reaction, and examples thereof include water, alcohol solvents such as methanol, ethanol, etc.; ether solvents such as diethyl ether, tetrahydrofuran, 1,4-dioxane, 1,2-dimethoxyethane, etc.; aromatic hydrocarbon solvents such as benzene, xylene, toluene, etc.; aliphatic hydrocarbon solvents such as pentane, hexane, cyclohexane, etc.; halogenated hydrocarbon solvents such as dichloromethane, chloroform, 1,2-dichloroethane, etc.; nitrile solvents such as acetonitrile, propionitrile, etc.; amide solvents such as N,N-dimethylformamide, N,N-dimethylacetamide, N-methylpyrrolidone, N,N'-dimethylimidazolidinone, etc.; dimethyl sulfoxide, and mixed solvents thereof.

[0104] The reaction can also be carried out using a base. Examples of bases that can be used include organic bases such as pyridine, 2,6-lutidine, 4-dimethylaminopyridine, triethylamine, diisopropylethylamine, tributylamine, N,N-dimethylaniline, 1,4-diazabicyclo[2.2.2]octane (DABCO), 1,8-diazabicyclo[5.4.0]-7-undecene (DBU), and 1,5-diazabicyclo[4.3.0]-5-nonene (DBN); inorganic bases such as sodium hydroxide, potassium hydroxide, sodium hydride, sodium bicarbonate, potassium carbonate, cesium carbonate, and potassium phosphate; and metal alkoxides such as sodium methoxide, sodium ethoxide, and potassium tert-butoxide. The amount (equivalent) of the base used can be 0.1 to 100 equivalents per equivalent of compound (2-A).

[0105] The reaction can be carried out in the presence of a palladium catalyst. Examples of the palladium catalyst include [1,1'-bis(diphenylphosphino)ferrocene]palladium(divalent) dichloride dichloromethane adduct. The amount of the palladium catalyst used can be 0.005 to 20 equivalents per equivalent of compound (2-A).

[0106] The reaction can be carried out in the presence of a ligand. Examples of the ligand include 1,1'-bis(diphenylphosphino)ferrocene. The amount of the ligand used can be 0.005 to 20 equivalents per equivalent of compound (2-A).

[0107] The reaction temperature can be set at any temperature between −78° C. and the reflux temperature of the reaction mixture, and the reaction time varies depending on the concentration of the reactant and the reaction temperature, but can usually be set at any time within the range of 5 minutes to 100 hours.

[0108] Compound (2-A) can be produced according to a known method known in the literature, for example, the method described in WO 2021 / 261562.

[0109] Some of the compounds (3-A) are known compounds, some of which are commercially available, and others can be prepared according to the synthetic methods of known compounds.

[0110] [Production Method 2-A] The compound (1-A) of the present invention can be produced by reacting the compound (4-A) with the compound (5-A). (In the formula, J, Q, X, Y, R ２ and R ３ has the same meaning as above, and Qa is C １ ~C ６ represents alkoxy.)

[0111] The compound (1-A) of the present invention can be produced by reacting the compound (4-A) with the compound (5-A) in a solvent or without a solvent.

[0112] When a solvent is used, the solvent to be used may be any solvent inert to the reaction, and examples thereof include the solvents exemplified in Production Method 1-A.

[0113] The reaction can also be carried out using a base. Examples of bases that can be used include the bases exemplified in Production Method 1-A. The amount (equivalent) of the base used can be 0.1 to 100 equivalents per equivalent of compound (4-A).

[0114] The reaction temperature can be set at any temperature between −78° C. and the reflux temperature of the reaction mixture, and the reaction time varies depending on the concentration of the reactant and the reaction temperature, but can usually be set at any time within the range of 5 minutes to 100 hours.

[0115] The compound (4-A) used in the production method 2-A can be produced according to reaction scheme 3-A.

[0116] Some of the compounds (5-A) are known compounds, some of which are commercially available, and others can be prepared according to the synthetic methods of known compounds.

[0117] [Production Method 3-A] In the compound (1-A) of the present invention, J represents J-10, G represents G-1, G-2, G-3, G-4, G-5, G-6, G-7, G-8, G-9, G-10, G-11, G-12, G-13, G-14, G-15, G-16, G-17, G-18, G-19, G-20, G-21, G-22, G-23, G-24, G-25, G-26, G-27, G-28, G-29, G-30, G Compound (1b) representing G-31, G-32, G-33, G-34, G-35, G-36, G-37, G-38, G-39, G-40, G-41, G-42, G-43, G-44, G-45, G-46, G-47, G-48, G-49, G-50, G-51, G-52, G-62, G-63, G-64 or G-65 can be produced by reacting compound (6-A). (In the formula, Q, Gf, X, Y, R ２ and R ３ represents the same meaning as above.)

[0118] The compound (1b) of the present invention can be produced by reacting the compound (6-A) in a solvent or without a solvent.

[0119] When a solvent is used, the solvent to be used may be any solvent inert to the reaction, and examples thereof include the solvents exemplified in Production Method 1-A.

[0120] The reaction can also be carried out using a base. Examples of bases that can be used include the bases exemplified in Production Method 1-A. The amount (equivalent) of the base used can be 0.1 to 100 equivalents per equivalent of compound (6-A).

[0121] The reaction temperature can be set at any temperature between −78° C. and the reflux temperature of the reaction mixture, and the reaction time varies depending on the concentration of the reactant and the reaction temperature, but can usually be set at any time within the range of 5 minutes to 100 hours.

[0122] The compound (6-A) used in the production method 3-A can be produced according to reaction scheme 1-A.

[0123] [Production Method 4-A] In the compound (1-A) of the present invention, J represents J-1, G represents G-1, G-2, G-3, G-4, G-5, G-6, G-7, G-8, G-9, G-10, G-11, G-12, G-13, G-14, G-15, G-16, G-17, G-18, G-19, G-20, G-21, G-22, G-23, G-24, G-25, G-26, G-27, G-28, G-29, G-30, G- Compound (1c) representing G-31, G-32, G-33, G-34, G-35, G-36, G-37, G-38, G-39, G-40, G-41, G-42, G-43, G-44, G-45, G-46, G-47, G-48, G-49, G-50, G-51, G-52, G-62, G-63, G-64 or G-65 can be produced by reacting compound (14-A). (In the formula, Q, Gf, X, Y, R ２ and R ３ represents the same meaning as above.)

[0124] The compound (1c) of the present invention can be produced by reacting the compound (14-A) in a solvent or without a solvent.

[0125] When a solvent is used, the solvent to be used may be any solvent inert to the reaction, and examples thereof include the solvents exemplified in Production Method 1-A.

[0126] The reaction can also be carried out using a base. Examples of bases that can be used include the bases exemplified in Production Method 1-A. The amount (equivalent) of the base used can be 0.1 to 100 equivalents per equivalent of compound (14-A).

[0127] The reaction can also be carried out using an acid halide. Examples of acid halides that can be used include acetyl chloride, benzoyl chloride, methanesulfonyl chloride, and p-toluenesulfonyl chloride. The amount (equivalent) of the acid halide used can be 0.1 to 100 equivalents per equivalent of compound (14-A).

[0128] The reaction can also be carried out using an acid anhydride. Examples of acid anhydrides that can be used include acetic anhydride, benzoic anhydride, methanesulfonic anhydride, and p-toluenesulfonic anhydride. The amount (equivalent) of the acid anhydride used is 0.1 to 100 equivalents per equivalent of compound (14-A).

[0129] The reaction can also be carried out using an acid. Examples of acids that can be used include hydrogen chloride, sulfuric acid, acetic acid, trifluoroacetic acid, benzoic acid, methanesulfonic acid, and p-toluenesulfonic acid. The amount (equivalent) of the acid used is 0.1 to 100 equivalents per equivalent of compound (14-A).

[0130] The reaction temperature can be set at any temperature between −78° C. and the reflux temperature of the reaction mixture, and the reaction time varies depending on the concentration of the reactant and the reaction temperature, but can usually be set at any time within the range of 5 minutes to 100 hours.

[0131] The compound (14-A) used in the production method 4-A can be produced according to reaction scheme 2-A.

[0132] [Reaction Scheme 1-A] (In the formula, Q, Gf, X, Y, R ２ and R ３ has the same meaning as above, and J ｃ is C １ ~C ６ represents alkyl.)

[0133] [Production Step 1] Compound (11-A) can be produced by reacting compound (12-A) with compound (5-A) according to a known method known in the literature, for example, the method described in WO 2016 / 118611.

[0134] Some of the compounds (12-A) are known compounds, and some are commercially available. Others can be prepared by known methods described in the literature, for example, the method described in The Journal of Organic Chemistry, 2004, Vol. 69, pp. 130-141.

[0135] [Production Step 2] Compound (10-A) can be produced by reacting compound (11-A) according to a known method known in the literature, for example, the method described in The Journal of Organic Chemistry, 2006, Vol. 24, pages 9045-9050.

[0136] [Production Step 3] Compound (9-A) can be produced by reacting compound (10-A) according to a known method known in the literature, for example, the method described in Asian Journal of Chemistry, Vol. 26, pages 6275-6278, 2014.

[0137] [Production Step 4] Compound (9-A) can be reacted in accordance with a known method known in the literature, for example, the method described in Asian Journal of Chemistry, Vol. 26, pages 6275-6278, 2014, to produce compound (8-A).

[0138] [Production Step 5] Compound (7-A) can be produced by reacting compound (8-A) according to a known method known in the literature, for example, the method described in Bioorganic & Medicinal Chemistry, 2018, Vol. 26, pages 1713-1726.

[0139] [Production Step 6] Compound (6-A) can be produced by reacting compound (7-A) with compound (13-A) according to a known method known in the literature, for example, the method described in Synthetic Communications, 2006, Vol. 36, pages 729-741.

[0140] Some of the compounds (13-A) are known compounds, and some are commercially available.

[0141] [Reaction Scheme 2-A] (In the formula, Q, Gf, X, Y, R ２ and R ３ represents the same meaning as above.)

[0142] [Production Step 1] Compound (14-A) can be produced by reacting compound (10-A) with compound (15-A) according to a known method known in the literature, for example, the method described in Tetrahedron Letters, 2010, Vol. 51, pages 4801-4805.

[0143] Some of the compounds (15-A) are known compounds, and some are commercially available.

[0144] [Reaction Scheme 3-A] (Wherein J, X, Y and R ２ has the same meaning as above, and Qa is C １ ~C ６ Xa represents a halogen atom or a leaving group such as OH; Xb represents C １ ~C ６ represents alkoxy.)

[0145] [Production Step 1] Compound (16-A) can be produced by reacting compound (17-A) with compound (18-A) according to a known method known in the literature, for example, the method described in Bioorganic & Medicinal Chemistry Letters, 2008, Vol. 18, pages 1840-1844.

[0146] Some of the compounds (17-A) are known compounds, and some are commercially available. Others can be prepared by known methods described in the literature, for example, in accordance with the method described in U.S. Patent Application Publication No. 2003 / 0045555.

[0147] Some of the compounds (18-A) are known compounds, and some are commercially available.

[0148] [Production Step 2] Compound (4-A) can be produced by reacting compound (16-A) according to a known method known in the literature, for example, the method described in Bioorganic & Medicinal Chemistry Letters, 2008, Vol. 18, pages 1840-1844.

[0149] In the reactions of Production Methods 1-A to 4-A and Reaction Schemes 1-A to 3-A, the reaction mixture after completion of the reaction can be subjected to a conventional post-treatment such as direct concentration, dissolving in an organic solvent and washing with water followed by concentration, or pouring into ice water and extracting with an organic solvent followed by concentration, to obtain the target compound of the present invention. Furthermore, when purification becomes necessary, the compound can be separated and purified by any purification method such as recrystallization, column chromatography, thin-layer chromatography, or liquid chromatography fractionation.

[0150] Examples of the compound (1-A) of the present invention that can be produced by these methods include the compounds shown in Tables 1-A to 2-A.

[0151] In the table, Q-1, Q-2, Q-3, Q-4, Q-9, Q-12a and Q-14 represent the following structures.

[0152] In addition, the descriptions G-1 and G-3 in the table represent the following structures, respectively.

[0153] The numbers in the structural formulas above indicate the substituents (Z １ ) ｔ２ , (Z １ ) ｔ３ , (Z １ ) ｔ４ , (Z １ ) ｔ５ or (Z ２ ) ｔ４ For example, in the table, "Q-3(4-F)" represents "5-fluoropyridin-2-yl", and "Q-3" represents unsubstituted Q-3, i.e., "pyridin-2-yl".

[0154] [Table 1-A] ―――――――――――――――― Q G ―――――――――――――― Q-1(4-F) G-1(4-F) Q-1(2-F,4-F) G-1(4-F) Q-1(3-F,4-F) G-1(4-F) Q-2(4-F) G-1(4-F) Q-2(4-Cl) G-1(4-F) Q-3 G-1(4-F) Q-3(3-F) G-1(4-F) Q-3(3-Cl) G-1(4-F) Q-3(3-Br) G-1(4-F) Q-3(3-CH ３ ) G-1(4-F) Q-3(3-OCH ３ ) G-1(4-F) Q-3(4-F) G-1(4-F) Q-3(4-Cl) G-1(4-F) Q-3(4-Br) G-1(4-F) Q-3(4-CN) G-1(4-F) Q-4 G-1(4-F) Q-4(4-Cl) G-1(4-F) Q-4(4-CH ３) G-1(4-F) Q-9 G-1(4-F) Q-12a G-1(4-F) Q-14(3-F) G-1(4-F) Q-1(4-F) G-3(3-F) Q-1(2-F,4-F) G-3(3-F) Q-1(3-F,4-F) G-3(3-F) Q-2(4-F) G-3(3-F) Q-2(4-Cl) G-3(3-F) Q-3 G-3(3-F) Q-3(3-F) G-3(3-F) Q-3(3-Cl) G-3(3-F) Q-3(3-Br) G-3(3-F) Q-3(3-CH ３ ) G-3(3-F) Q-3(3-OCH ３ ) G-3(3-F) Q-3(4-F) G-3(3-F) Q-3(4-Cl) G-3(3-F) Q-3(4-Br) G-3(3-F) Q-3(4-CN) G-3(3-F) Q-4 G-3(3-F) Q-4(4-Cl) G-3(3-F) Q-4(4-CH ３ ) G-3(3-F) Q-9 G-3(3-F) Q-12a G-3(3-F) Q-14(3-F) G-3(3-F) Q-1(4-F) G-3(3-Cl) Q-1(2-F,4-F) G-3(3-Cl) Q-1(3-F,4-F) G-3(3-Cl) Q-2(4-F) G-3(3-Cl) Q-2(4-Cl) G-3(3-Cl) Q-3 G-3(3-Cl) Q-3(3-F) G-3(3-Cl) Q-3(3-Cl) G-3(3-Cl) Q-3(3-Br) G-3(3-Cl) Q-3(3-CH ３ ) G-3(3-Cl) Q-3(3-OCH ３) G-3(3-Cl) Q-3(4-F) G-3(3-Cl) Q-3(4-Cl) G-3(3-Cl) Q-3(4-Br) G-3(3-Cl) Q-3(4-CN) G-3(3-Cl) Q-4 G-3(3-Cl) Q-4(4-Cl) G-3(3-Cl) Q-4(4-CH ３ ) G-3(3-Cl) Q-9 G-3(3-Cl) Q-12a G-3(3-Cl) Q-14(3-F) G-3(3-Cl) Q-1(4-F) G-3(3-CF ３ ) Q-1(2-F,4-F) G-3(3-CF ３ ) Q-1(3-F,4-F) G-3(3-CF ３ ) Q-2(4-F) G-3(3-CF ３ ) Q-2(4-Cl) G-3(3-CF ３ ) Q-3 G-3(3-CF ３ ) Q-3(3-F) G-3(3-CF ３ ) Q-3(3-Cl) G-3(3-CF ３ ) Q-3(3-Br) G-3(3-CF ３ ) Q-3(3-CH ３ ) G-3(3-CF ３ ) Q-3(3-OCH ３ ) G-3(3-CF ３ ) Q-3(4-F) G-3(3-CF ３ ) Q-3(4-Cl) G-3(3-CF ３ ) Q-3(4-Br) G-3(3-CF ３ ) Q-3(4-CN) G-3(3-CF ３ ) Q-4 G-3(3-CF ３ ) Q-4(4-Cl) G-3(3-CF ３ ) Q-4(4-CH ３) G-3(3-CF ３ ) Q-9 G-3(3-CF ３ ) Q-12a G-3(3-CF ３ ) Q-14(3-F) G-3(3-CF ３ ) Q-1(4-F) G-3(3-CH ３ ) Q-1(2-F,4-F) G-3(3-CH ３ ) Q-1(3-F,4-F) G-3(3-CH ３ ) Q-2(4-F) G-3(3-CH ３ ) Q-2(4-Cl) G-3(3-CH ３ ) Q-3 G-3(3-CH ３ ) Q-3(3-F) G-3(3-CH ３ ) Q-3(3-Cl) G-3(3-CH ３ ) Q-3(3-Br) G-3(3-CH ３ ) Q-3(3-CH ３ ) G-3(3-CH ３ ) Q-3(3-OCH ３ ) G-3(3-CH ３ ) Q-3(4-F) G-3(3-CH ３ ) Q-3(4-Cl) G-3(3-CH ３ ) Q-3(4-Br) G-3(3-CH ３ ) Q-3(4-CN) G-3(3-CH ３ ) Q-4 G-3(3-CH ３ ) Q-4(4-Cl) G-3(3-CH ３ ) Q-4(4-CH ３ ) G-3(3-CH ３ ) Q-9 G-3(3-CH ３ ) Q-12a G-3(3-CH ３ ) Q-14(3-F) G-3(3-CH ３) Q-1(4-F) G-3(3-CN) Q-1(2-F,4-F) G-3(3-CN) Q-1(3-F,4-F) G-3(3-CN) Q-2(4-F) G-3(3-CN) Q-2(4-Cl) G-3(3-CN) Q-3 G-3(3-CN) Q-3(3-F) G-3(3-CN) Q-3(3-Cl) G-3(3-CN) Q-3(3-Br) G-3(3-CN) Q-3(3-CH ３ ) G-3(3-CN) Q-3(3-OCH ３ ) G-3(3-CN) Q-3(4-F) G-3(3-CN) Q-3(4-Cl) G-3(3-CN) Q-3(4-Br) G-3(3-CN) Q-3(4-CN) G-3(3-CN) Q-4 G-3(3-CN) Q-4(4-Cl) G-3(3-CN) Q-4(4-CH ３ ) G-3(3-CN) Q-9 G-3(3-CN) Q-12a G-3(3-CN) Q-14(3-F) G-3(3-CN) ――――――――――――――――

[0155] [Table 2-A] ――――――――――――――――― Q G ――――――――――――――――― Q-1(4-F) G-1(4-F) Q-1(2-F,4-F) G-1(4-F) Q-1(3-F,4-F) G-1(4-F) Q-2(4-F) G-1(4-F) Q-2(4-Cl) G-1(4-F) Q-3 G-1(4-F) Q-3(3-F) G-1(4-F) Q-3(3-Cl) G-1(4-F) Q-3(3-Br) G-1(4-F) Q-3(3-CH ３ ) G-1(4-F) Q-3(3-OCH ３) G-1(4-F) Q-3(4-F) G-1(4-F) Q-3(4-Cl) G-1(4-F) Q-3(4-Br) G-1(4-F) Q-3(4-CN) G-1(4-F) Q-4 G-1(4-F) Q-4(4-Cl) G-1(4-F) Q-4(4-CH ３ ) G-1(4-F) Q-9 G-1(4-F) Q-12a G-1(4-F) Q-14(3-F) G-1(4-F) Q-1(4-F) G-3(3-F) Q-1(2-F,4-F) G-3(3-F) Q-1(3-F,4-F) G-3(3-F) Q-2(4-F) G-3(3-F) Q-2(4-Cl) G-3(3-F) Q-3 G-3(3-F) Q-3(3-F) G-3(3-F) Q-3(3-Cl) G-3(3-F) Q-3(3-Br) G-3(3-F) Q-3(3-CH ３ ) G-3(3-F) Q-3(3-OCH ３ ) G-3(3-F) Q-3(4-F) G-3(3-F) Q-3(4-Cl) G-3(3-F) Q-3(4-Br) G-3(3-F) Q-3(4-CN) G-3(3-F) Q-4 G-3(3-F) Q-4(4-Cl) G-3(3-F) Q-4(4-CH ３) G-3(3-F) Q-9 G-3(3-F) Q-12a G-3(3-F) Q-14(3-F) G-3(3-F) Q-1(4-F) G-3(3-Cl) Q-1(2-F,4-F) G-3(3-Cl) Q-1(3-F,4-F) G-3(3-Cl) Q-2(4-F) G-3(3-Cl) Q-2(4-Cl) G-3(3-Cl) Q-3 G-3(3-Cl) Q-3(3-F) G-3(3-Cl) Q-3(3-Cl) G-3(3-Cl) Q-3(3-Br) G-3(3-Cl) Q-3(3-CH ３ ) G-3(3-Cl) Q-3(3-OCH ３ ) G-3(3-Cl) Q-3(4-F) G-3(3-Cl) Q-3(4-Cl) G-3(3-Cl) Q-3(4-Br) G-3(3-Cl) Q-3(4-CN) G-3(3-Cl) Q-4 G-3(3-Cl) Q-4(4-Cl) G-3(3-Cl) Q-4(4-CH ３ ) G-3(3-Cl) Q-9 G-3(3-Cl) Q-12a G-3(3-Cl) Q-14(3-F) G-3(3-Cl) Q-1(4-F) G-3(3-CF ３ ) Q-1(2-F,4-F) G-3(3-CF ３ ) Q-1(3-F,4-F) G-3(3-CF ３ ) Q-2(4-F) G-3(3-CF ３ ) Q-2(4-Cl) G-3(3-CF ３ ) Q-3 G-3(3-CF ３ ) Q-3(3-F) G-3(3-CF ３) Q-3(3-Cl) G-3(3-CF ３ ) Q-3(3-Br) G-3(3-CF ３ ) Q-3(3-CH ３ ) G-3(3-CF ３ ) Q-3(3-OCH ３ ) G-3(3-CF ３ ) Q-3(4-F) G-3(3-CF ３ ) Q-3(4-Cl) G-3(3-CF ３ ) Q-3(4-Br) G-3(3-CF ３ ) Q-3(4-CN) G-3(3-CF ３ ) Q-4 G-3(3-CF ３ ) Q-4(4-Cl) G-3(3-CF ３ ) Q-4(4-CH ３ ) G-3(3-CF ３ ) Q-9 G-3(3-CF ３ ) Q-12a G-3(3-CF ３ ) Q-14(3-F) G-3(3-CF ３ ) Q-1(4-F) G-3(3-CH ３ ) Q-1(2-F,4-F) G-3(3-CH ３ ) Q-1(3-F,4-F) G-3(3-CH ３ ) Q-2(4-F) G-3(3-CH ３ ) Q-2(4-Cl) G-3(3-CH ３ ) Q-3 G-3(3-CH ３ ) Q-3(3-F) G-3(3-CH ３ ) Q-3(3-Cl) G-3(3-CH ３ ) Q-3(3-Br) G-3(3-CH ３ ) Q-3(3-CH ３ ) G-3(3-CH３ ) Q-3(3-OCH ３ ) G-3(3-CH ３ ) Q-3(4-F) G-3(3-CH ３ ) Q-3(4-Cl) G-3(3-CH ３ ) Q-3(4-Br) G-3(3-CH ３ ) Q-3(4-CN) G-3(3-CH ３ ) Q-4 G-3(3-CH ３ ) Q-4(4-Cl) G-3(3-CH ３ ) Q-4(4-CH ３ ) G-3(3-CH ３ ) Q-9 G-3(3-CH ３ ) Q-12a G-3(3-CH ３ ) Q-14(3-F) G-3(3-CH ３ ) Q-1(4-F) G-3(3-CN) Q-1(2-F,4-F) G-3(3-CN) Q-1(3-F,4-F) G-3(3-CN) Q-2(4-F) G-3(3-CN) Q-2(4-Cl) G-3(3-CN) Q-3 G-3(3-CN) Q-3(3-F) G-3(3-CN) Q-3(3-Cl) G-3(3-CN) Q-3(3-Br) G-3(3-CN) Q-3(3-CH ３ ) G-3(3-CN) Q-3(3-OCH ３ ) G-3(3-CN) Q-3(4-F) G-3(3-CN) Q-3(4-Cl) G-3(3-CN) Q-3(4-Br) G-3(3-CN) Q-3(4-CN) G-3(3-CN) Q-4 G-3(3-CN) Q-4(4-Cl) G-3(3-CN) Q-4(4-CH ３) G-3(3-CN) Q-9 G-3(3-CN) Q-12a G-3(3-CN) Q-14(3-F) G-3(3-CN) Q-1(4-F) G-3(3-SCH ３ ) Q-1(2-F,4-F) G-3(3-SCH ３ ) Q-1(3-F,4-F) G-3(3-SCH ３ ) Q-2(4-F) G-3(3-SCH ３ ) Q-2(4-Cl) G-3(3-SCH ３ ) Q-3 G-3(3-SCH ３ ) Q-3(3-F) G-3(3-SCH ３ ) Q-3(3-Cl) G-3(3-SCH ３ ) Q-3(3-Br) G-3(3-SCH ３ ) Q-3(3-CH ３ ) G-3(3-SCH ３ ) Q-3(3-OCH ３ ) G-3(3-SCH ３ ) Q-3(4-F) G-3(3-SCH ３ ) Q-3(4-Cl) G-3(3-SCH ３ ) Q-3(4-Br) G-3(3-SCH ３ ) Q-3(4-CN) G-3(3-SCH ３ ) Q-4 G-3(3-SCH ３ ) Q-4(4-Cl) G-3(3-SCH ３ ) Q-4(4-CH ３ ) G-3(3-SCH ３ ) Q-9 G-3(3-SCH ３ ) Q-12a G-3(3-SCH ３ ) Q-14(3-F) G-3(3-SCH ３) Q-1(4-F) G-3(3-S(O)CH ３ ) Q-1(2-F,4-F) G-3(3-S(O)CH ３ ) Q-1(3-F,4-F) G-3(3-S(O)CH ３ ) Q-2(4-F) G-3(3-S(O)CH ３ ) Q-2(4-Cl) G-3(3-S(O)CH ３ ) Q-3 G-3(3-S(O)CH ３ ) Q-3(3-F) G-3(3-S(O)CH ３ ) Q-3(3-Cl) G-3(3-S(O)CH ３ ) Q-3(3-Br) G-3(3-S(O)CH ３ ) Q-3(3-CH ３ ) G-3(3-S(O)CH ３ ) Q-3(3-OCH ３ ) G-3(3-S(O)CH ３ ) Q-3(4-F) G-3(3-S(O)CH ３ ) Q-3(4-Cl) G-3(3-S(O)CH ３ ) Q-3(4-Br) G-3(3-S(O)CH ３ ) Q-3(4-CN) G-3(3-S(O)CH ３ ) Q-4 G-3(3-S(O)CH ３ ) Q-4(4-Cl) G-3(3-S(O)CH ３ ) Q-4(4-CH ３ ) G-3(3-S(O)CH ３ ) Q-9 G-3(3-S(O)CH ３ ) Q-12a G-3(3-S(O)CH ３ ) Q-14(3-F) G-3(3-S(O)CH ３ ) Q-1(4-F) G-3(3-S(O) ２CH ３ ) Q-1(2-F,4-F) G-3(3-S(O) ２ CH ３ ) Q-1(3-F,4-F) G-3(3-S(O) ２ CH ３ ) Q-2(4-F) G-3(3-S(O) ２ CH ３ ) Q-2(4-Cl) G-3(3-S(O) ２ CH ３ ) Q-3 G-3(3-S(O) ２ CH ３ ) Q-3(3-F) G-3(3-S(O) ２ CH ３ ) Q-3(3-Cl) G-3(3-S(O) ２ CH ３ ) Q-3(3-Br) G-3(3-S(O) ２ CH ３ ) Q-3(3-CH ３ ) G-3(3-S(O) ２ CH ３ ) Q-3(3-OCH ３ ) G-3(3-S(O) ２ CH ３ ) Q-3(4-F) G-3(3-S(O) ２ CH ３ ) Q-3(4-Cl) G-3(3-S(O) ２ CH ３ ) Q-3(4-Br) G-3(3-S(O) ２ CH ３ ) Q-3(4-CN) G-3(3-S(O) ２ CH ３ ) Q-4 G-3(3-S(O) ２ CH ３ ) Q-4(4-Cl) G-3(3-S(O) ２ CH ３ ) Q-4(4-CH ３ ) G-3(3-S(O)２ CH ３ ) Q-9 G-3(3-S(O) ２ CH ３ ) Q-12a G-3(3-S(O) ２ CH ３ ) Q-14(3-F) G-3(3-S(O) ２ CH ３ ) ―――――――――――――――――

[0156] [Production Method 1-B] The compound (1-B) of the present invention can be produced by reacting the compound (2-B) with the compound (3-B). (In the formula, J, Q, X, Y, R ２ and R ３ has the same meaning as above, and Qa is C １ ~C ６ represents alkoxy.)

[0157] The compound (1-B) of the present invention can be produced by reacting the compound (2-B) with the compound (3-B) in a solvent or without a solvent.

[0158] When a solvent is used, any solvent may be used as long as it is inert to the reaction, and examples thereof include water, alcohol solvents such as methanol, ethanol, etc.; ether solvents such as diethyl ether, tetrahydrofuran, 1,4-dioxane, 1,2-dimethoxyethane, etc.; aromatic hydrocarbon solvents such as benzene, xylene, toluene, etc.; aliphatic hydrocarbon solvents such as pentane, hexane, cyclohexane, etc.; halogenated hydrocarbon solvents such as dichloromethane, chloroform, 1,2-dichloroethane, etc.; nitrile solvents such as acetonitrile, propionitrile, etc.; amide solvents such as N,N-dimethylformamide, N,N-dimethylacetamide, N-methylpyrrolidone, N,N'-dimethylimidazolidinone, etc.; dimethyl sulfoxide, and mixed solvents thereof.

[0159] The reaction can also be carried out using a base. Examples of bases that can be used include organic bases such as pyridine, 2,6-lutidine, 4-dimethylaminopyridine, triethylamine, diisopropylethylamine, tributylamine, N,N-dimethylaniline, 1,4-diazabicyclo[2.2.2]octane (DABCO), 1,8-diazabicyclo[5.4.0]-7-undecene (DBU), and 1,5-diazabicyclo[4.3.0]-5-nonene (DBN); inorganic bases such as sodium hydroxide, potassium hydroxide, sodium hydride, sodium bicarbonate, potassium carbonate, cesium carbonate, and potassium phosphate; and metal alkoxides such as sodium methoxide, sodium ethoxide, and potassium tert-butoxide. The amount (equivalent) of the base used can be 0.1 to 100 equivalents per equivalent of compound (2-B).

[0160] The reaction temperature can be set at any temperature between −78° C. and the reflux temperature of the reaction mixture, and the reaction time varies depending on the concentration of the reactant and the reaction temperature, but can usually be set at any time within the range of 5 minutes to 100 hours.

[0161] Compound (2-B) can be produced according to a known method known in the literature, for example, the method described in WO 2021 / 261562.

[0162] Some of the compounds (3-B) are known compounds, some of which are commercially available, and others can be prepared according to the synthetic methods of known compounds.

[0163] [Production Method 2-B] Among the compounds (1-B) of the present invention, compound (1d) in which J represents J-2′ can be produced by reacting compound (4-B) with compound (5-B). (In the formula, Q, G, X, Y, R ２ and R ３ represents the same meaning as above.)

[0164] Compound (1d) can be produced by reacting compound (4-B) with compound (5-B) in a solvent or without a solvent.

[0165] When a solvent is used, the solvent to be used may be any solvent inert to the reaction, and examples thereof include the solvents exemplified in Production Method 1-B.

[0166] The reaction can also be carried out using a base. Examples of bases that can be used include the bases exemplified in Production Method 1-B. The amount (equivalent) of the base used can be 0.1 to 100 equivalents per equivalent of compound (4-B).

[0167] The reaction can also be carried out using a dehydration condensation agent. Examples of dehydration condensation agents that can be used include 1H-benzotriazol-1-yloxytris(dimethylamino)phosphonium hexafluorophosphate, N,N'-dicyclohexylcarbodiimide, 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride, and 1-[bis(dimethylamino)methylene]-1H-1,2,3-triazolo[4,5-b]pyridinium 3-oxide hexafluorophosphate. The amount (equivalent) of the dehydration condensation agent used can be 0.1 to 100 equivalents per equivalent of compound (4-B).

[0168] The reaction can also be carried out in the presence of an additive. Examples of the additive that can be used include 1-hydroxybenzotriazole, 1-hydroxy-7-azabenzotriazole, and 4-(dimethylamino)pyridine. The amount (equivalent) of the additive used can be 0.005 to 100 equivalents per equivalent of compound (4-B).

[0169] The reaction temperature can be set at any temperature between −78° C. and the reflux temperature of the reaction mixture, and the reaction time varies depending on the concentration of the reactant and the reaction temperature, but can usually be set at any time within the range of 5 minutes to 100 hours.

[0170] Some of the compounds (5-B) are known compounds, and some are commercially available. Others can be prepared according to the synthetic methods of known compounds. Compound (4-B) used in Preparation Method 2-B can be prepared according to the following Reaction Scheme 1-B.

[0171] [Reaction Scheme 1-B] (In the formula, Q, X, Y, R ２ and R ３ has the same meaning as above, and Jb is C １ ~C ６ represents alkyl.)

[0172] [Production Step 1] Compound (7-B) can be reacted with compound (8-B) in accordance with a known method disclosed in the literature, for example, the method described in WO 2016 / 118611, to produce compound (6-B).

[0173] Some of the compounds (7-B) are known compounds, and some are commercially available. Others can be prepared by known methods described in the literature, for example, the method described in The Journal of Organic Chemistry, 2004, Vol. 69, pp. 130-141.

[0174] [Production Step 2] Compound (4-B) can be produced by reacting compound (6-B) according to a known method known in the literature, for example, the method described in The Journal of Organic Chemistry, 2006, Vol. 24, pages 9045-9050.

[0175] In the reactions of Production Methods 1-B to 2-B and Reaction Scheme 1-B, the reaction mixture after completion of the reaction can be subjected to a conventional post-treatment such as direct concentration, dissolving in an organic solvent and washing with water followed by concentration, or pouring into ice water and extracting with an organic solvent followed by concentration, to obtain the target compound of the present invention. Furthermore, when purification becomes necessary, the compound can be separated and purified by any purification method such as recrystallization, column chromatography, thin-layer chromatography, or liquid chromatography fractionation.

[0176] Compound 1-B of the present invention and intermediates for its preparation that can be produced by these methods include, for example, the compounds shown in Tables 1-B to 4-B.

[0177] In the table, Q-1, Q-2, Q-3, Q-4, Q-6, Q-9, Q-12a and Q-14 represent the following structures.

[0178] In addition, the descriptions G-1a' and G-9a' in the table represent the following structures.

[0179] The numbers in the structural formulas above indicate the substituents (Z １ ) ｔ２ , (Z １ ) ｔ３ , (Z １ ) ｔ４ , (Z １ ) ｔ５ or (Z ２ ) ｔ４ For example, in the table, "Q-1(4-F)" represents "4-fluorophenyl", "G-1a'" represents unsubstituted "G-1a'", i.e., "morpholin-4-yl", and "G-1a'(3-CH ３ , 3-CH ３ )" represents "2,2-dimethylmorpholin-4-yl", and "Q-1" represents unsubstituted "Q-1", that is, "phenyl".

[0180] [Table 1-B] ―――――――――――――――― R 1 QG ―――――――――――――――― Cl Q-1 G-1a' CF3 Q-1 G-1a' ――――――――――――――――

[0181] [Table 2-B] ―――――――――――――――― R 1 QG ―――――――――――――――― Cl Q-1 G-1a' CF3 Q-1 G-1a' ――――――――――――――――

[0182] [Table 3-B] ――――――――――――――――――― Q G ――――――――――――――――――― Q-1 G-1a’ Q-1(4-F) G-1a’ Q-1(4-CN) G-1a’ Q-1(2-F,4-F) G-1a’ Q-1(3-F,4-F) G-1a’ Q-2(4-F) G-1a’ Q-2(4-Cl) G-1a’ Q-3 G-1a’ Q-3(3-F) G-1a’ Q-3(3-Cl) G-1a’ Q-3(3-Br) G-1a’ Q-3(3-CH3) G-1a’ Q-3(3-OCH3) G-1a’ Q-3(4-F) G-1a’ Q-3(4-Cl) G-1a’ Q-3(4-F,6-F) G-1a’ Q-4 G-1a’ Q-4(4-Cl) G-1a’ Q-4(4-Br) G-1a’ Q-6 G-1a’ Q-6(4-Cl) G-1a’ Q-9 G-1a’ Q-12a G-1a’ Q-14(3-F) G-1a’ Q-14(3-Cl) G-1a’ Q-1(4-F) G-1a’(3-CH3,3-CH3) Q-1(4-CN) G-1a’(3-CH3,3-CH3) Q-1(2-F,4-F) G-1a’(3-CH3,3-CH3) Q-1(3-F,4-F) G-1a’(3-CH3,3-CH3) Q-2(4-F) G-1a’(3-CH3,3-CH3) Q-2(4-Cl) G-1a’(3-CH3,3-CH3) Q-3 G-1a’(3-CH3,3-CH3) Q-3(3-F) G-1a’(3-CH3,3-CH3) Q-3(3-Cl) G-1a’(3-CH3,3-CH3) Q-3(3-Br) G-1a’(3-CH3,3-CH3) Q-3(3-CH3) G-1a’(3-CH3,3-CH3) Q-3(3-OCH3) G-1a’(3-CH3,3-CH3) Q-3(4-F) G-1a’(3-CH3,3-CH3) Q-3(4-F,6-F) G-1a’(3-CH3,3-CH3) Q-4 G-1a’(3-CH3,3-CH3) Q-4(4-Cl) G-1a’(3-CH3,3-CH3) Q-4(4-Br) G-1a’(3-CH3,3-CH3) Q-6(4-Cl) G-1a’(3-CH3,3-CH3) Q-9 G-1a’(3-CH3,3-CH3) Q-12a G-1a’(3-CH3,3-CH3) Q-14(3-F) G-1a’(3-CH3,3-CH3) Q-14(3-Cl) G-1a’(3-CH3,3-CH3) Q-1(4-F) G-9a’ Q-1(4-CN) G-9a’ Q-1(2-F,4-F) G-9a’ Q-1(3-F,4-F) G-9a’ Q-2(4-F) G-9a’ Q-2(4-Cl) G-9a’ Q-3 G-9a’ Q-3(3-F) G-9a’ Q-3(3-Cl) G-9a’ Q-3(3-Br) G-9a’ Q-3(3-CH3) G-9a’ Q-3(3-OCH3) G-9a’ Q-3(4-F) G-9a’ Q-3(4-F,6-F) G-9a' Q-4 G-9a' Q-4(4-Cl) G-9a' Q-4(4-Br) G-9a' Q-6(4-Cl) G-9a' Q-9 G-9a' Q-12a G-9a' Q-14(3-F) G-9a' Q-14(3-Cl) G-9a' ――――――――――――――――――――,

[0183] [Table 4-B] ―――――――――――――――― R 1 G ―――――――――――――――― CH3 G-1a' Cl G-1a' CF3 G-1a' CHF2 G-1a' OCH3 G-1a' SCH3 G-1a' CN G-1a' CH3 Br Cl Br CF3 Br CHF2 Br OCH3 Br SCH3 Br CN Br ――――――――――――――――

[0184] [Production Method 1-C] The compound (1-C) of the present invention can be produced by reacting the compound (2-C) with the compound (3-C). (In the formula, J, Q, X, Y, R ２ and R ３ has the same meaning as above, and Qa is C １ ~C ６ represents alkoxy.)

[0185] The compound (1-C) of the present invention can be produced by reacting the compound (2-C) with the compound (3-C) in a solvent or without a solvent.

[0186] When a solvent is used, any solvent may be used as long as it is inert to the reaction, and examples thereof include water, alcohol solvents such as methanol, ethanol, etc.; ether solvents such as diethyl ether, tetrahydrofuran, 1,4-dioxane, 1,2-dimethoxyethane, etc.; aromatic hydrocarbon solvents such as benzene, xylene, toluene, etc.; aliphatic hydrocarbon solvents such as pentane, hexane, cyclohexane, etc.; halogenated hydrocarbon solvents such as dichloromethane, chloroform, 1,2-dichloroethane, etc.; nitrile solvents such as acetonitrile, propionitrile, etc.; amide solvents such as N,N-dimethylformamide, N,N-dimethylacetamide, N-methylpyrrolidone, N,N'-dimethylimidazolidinone, etc.; dimethyl sulfoxide, and mixed solvents thereof.

[0187] The reaction can also be carried out using a base. Examples of bases that can be used include organic bases such as pyridine, 2,6-lutidine, 4-dimethylaminopyridine, triethylamine, diisopropylethylamine, tributylamine, N,N-dimethylaniline, 1,4-diazabicyclo[2.2.2]octane (DABCO), 1,8-diazabicyclo[5.4.0]-7-undecene (DBU), and 1,5-diazabicyclo[4.3.0]-5-nonene (DBN); inorganic bases such as sodium hydroxide, potassium hydroxide, sodium hydride, sodium bicarbonate, potassium carbonate, cesium carbonate, and potassium phosphate; and metal alkoxides such as sodium methoxide, sodium ethoxide, and potassium tert-butoxide. The amount (equivalent) of the base used can be 0.1 to 100 equivalents per equivalent of compound (2-C).

[0188] The reaction temperature can be set at any temperature between −78° C. and the reflux temperature of the reaction mixture, and the reaction time varies depending on the concentration of the reactant and the reaction temperature, but can usually be set at any time within the range of 5 minutes to 100 hours.

[0189] Some of the compounds (3-C) are known compounds, some of which are commercially available, and others can be prepared according to the synthetic methods of known compounds.

[0190] [Production Method 2-C] Among the compounds of the present invention (1-C), J is J-1, J-2, J-3, J-4, J-5, J-6, J-7, J-8, J-9, J-10, J-11, J-12, J-13, J-17, J-18, J-19, J-20, J-22, J-23, J-24, J-25, J-26, J-27, J-28, J-29, J-30, J-31 , J-32, J-33, J-34, J-35, J-36, J-37, J-38, J-39, J-40, J-41, J-42, J-43, J-44, J-45, J-46, J-50, J-51 or J-52 can be produced by reacting compound (4-C) with compound (5-C). (In the formula, Ja is Ja-1, Ja-2, Ja-3, Ja-4, Ja-5, Ja-6, Ja-7, Ja-8, Ja-9, Ja-10, Ja-11, Ja- 12, Ja-13, Ja-17, Ja-18, Ja-19, Ja-20, Ja-22, Ja-23, Ja-24, Ja-25, Ja-26, Ja-27 , Ja-28, Ja-29, Ja-30, Ja-31, Ja-32, Ja-33, Ja-34, Ja-35, Ja-36, Ja-37, Ja-38, J Represents a-39, Ja-40, Ja-41, Ja-42, Ja-43, Ja-44, Ja-45, Ja-46, Ja-50, Ja-51 or Ja-52, J, Q, G, X, Y, R １ , R １ａ , R １ｂ , R １ｃ , Z ５ , R ２ and R ３ represents the same meaning as above, Ga represents a halogen atom or the like, and Gb represents B(OH) ２ represents a leaving group such as or a hydrogen atom.)

[0191] The compound (1f) of the present invention can be produced by reacting the compound (4-C) with the compound (5-C) in a solvent or without a solvent.

[0192] When a solvent is used, any solvent may be used as long as it is inert to the reaction, and examples thereof include the solvents exemplified in Production Method 1-C.

[0193] The reaction can also be carried out using a base. Examples of bases that can be used include the bases exemplified in Production Method 1-C. The amount (equivalent) of the base used can be 0.1 to 100 equivalents per equivalent of compound (4-C).

[0194] The reaction can be carried out in the presence of a palladium catalyst. Examples of the palladium catalyst include [1,1'-bis(diphenylphosphino)ferrocene]palladium(divalent) dichloride dichloromethane adduct. The amount of the palladium catalyst used can be 0.005 to 20 equivalents per equivalent of compound (4-C).

[0195] The reaction can be carried out in the presence of a ligand. Examples of the ligand include 1,1'-bis(diphenylphosphino)ferrocene. The amount of the ligand used can be 0.005 to 20 equivalents per equivalent of compound (4-C).

[0196] The reaction temperature can be set at any temperature between −78° C. and the reflux temperature of the reaction mixture, and the reaction time varies depending on the concentration of the reactant and the reaction temperature, but can usually be set at any time within the range of 5 minutes to 100 hours.

[0197] Compound (4-C) can be produced according to a known method known in the literature, for example, the method described in WO 2021 / 261562.

[0198] Some of the compounds (5-C) are known compounds, some of which are commercially available, and others can be prepared according to the synthetic methods of known compounds.

[0199] [Production Method 3-C] Among the compounds (1-C) of the present invention, compound (1e) in which J represents J-1 and G represents G-1', G-2', G-3', G-4', G-6', G-8', G-12', G-14', G-20', G-21', G-22', G-23', G-48', G-49', G-50', G-51', G-52', G-53', G-79', G-80', G-81', G-82', G-103', G-104', G-108', G-109', G-110', G-126' or G-130' can be produced by reacting compound (6-C) with compound (7-C). (In the formula, Gc represents G-1′, G-2′, G-3′, G-4′, G-6′, G-8′, G-12′, G-14′, G-20′, G-21′, G-22′, G-23′, G-48′, G-49′, G-50′, G-51′, G-52′, G-53′, G-79′, G-80′, G-81′, G-82′, G-103′, G-104′, G-108′, G-109′, G-110′, G-126′, or G-130′; and Q, G, X, Y, and R ２ and R ３ represents the same meaning as above.)

[0200] Compound (1e) can be produced by reacting compound (6-C) with compound (7-C) in a solvent or without a solvent.

[0201] When a solvent is used, any solvent may be used as long as it is inert to the reaction, and examples thereof include the solvents exemplified in Production Method 1-C.

[0202] The reaction can also be carried out using a base. Examples of bases that can be used include the bases exemplified in Production Method 1-C. The amount (equivalent) of the base used can be 0.1 to 100 equivalents per equivalent of compound (6-C).

[0203] The reaction can also be carried out using a dehydration condensation agent. Examples of dehydration condensation agents that can be used include 1H-benzotriazol-1-yloxytris(dimethylamino)phosphonium hexafluorophosphate, 1H-benzotriazol-1-yloxytripyrrolidinophosphonium hexafluorophosphate, N,N'-dicyclohexylcarbodiimide, 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride, and 1-[bis(dimethylamino)methylene]-1H-1,2,3-triazolo[4,5-b]pyridinium 3-oxide hexafluorophosphate. The amount (equivalent) of the dehydration condensation agent used can be 0.1 to 100 equivalents per equivalent of compound (6-C).

[0204] The reaction can also be carried out in the presence of an additive. Examples of the additive that can be used include 1-hydroxybenzotriazole, 1-hydroxy-7-azabenzotriazole, and 4-(dimethylamino)pyridine. The amount (equivalent) of the additive used can be 0.005 to 100 equivalents relative to 1 equivalent of compound (6-C).

[0205] The reaction temperature can be set at any temperature between −78° C. and the reflux temperature of the reaction mixture, and the reaction time varies depending on the concentration of the reactant and the reaction temperature, but can usually be set at any time within the range of 5 minutes to 100 hours.

[0206] Some of the compounds (7-C) are known compounds, and some are commercially available. Others can be prepared according to the synthetic methods of known compounds. Compound (6-C) used in Production Method 3-C can be prepared according to Reaction Scheme 1-C.

[0207] [Reaction Scheme 1-C] (In the formula, Q, X, Y, R ２ and R ３ has the same meaning as above, and Gd is C １ ~C ６ represents alkoxy.)

[0208] [Production Step 1] Compound (9-C) can be produced by reacting compound (8-C) according to a known method known in the literature, for example, the method described in Bioorganic & Medicinal Chemistry Letters, 2012, Vol. 22, pages 4133-4138.

[0209] Some of the compounds (8-C) are known compounds and can be prepared according to known methods described in the literature, for example, the method described in WO 2024 / 048778.

[0210] [Production Step 2] Compound (9-C) can be reacted in accordance with a known method known in the literature, for example, the method described in Bioorganic & Medicinal Chemistry Letters, 2012, Vol. 22, pages 4133-4138, to produce compound (10-C).

[0211] [Production Step 3] Compound (6-C) can be produced by reacting compound (10-C) according to a known method known in the literature, for example, the method described in Bioorganic & Medicinal Chemistry Letters, 2012, Vol. 22, pages 4133-4138.

[0212] The compound (2-C) used in the production method 1-C can be produced according to reaction scheme 2-C.

[0213] [Reaction Scheme 2-C] (Wherein J, X, Y, Qa and R ２ represents the same meaning as above, Xa represents a halogen atom or a leaving group such as OH, and Xb represents C １ ~C ６ represents alkoxy.)

[0214] [Production Step 1] Compound (11-C) can be produced by reacting compound (12-C) with compound (13-C) according to a known method known in the literature, for example, the method described in Bioorganic & Medicinal Chemistry Letters, 2008, Vol. 18, pages 1840-1844.

[0215] Some of the compounds (12-C) are known compounds, and some are commercially available. Others can be prepared by known methods described in the literature, for example, in accordance with the method described in U.S. Patent Application Publication No. 2003 / 0045555.

[0216] Some of the compounds (13-C) are known compounds, and some are commercially available.

[0217] [Production Step 2] Compound (2-C) can be produced by reacting compound (11-C) according to a known method known in the literature, for example, the method described in Bioorganic & Medicinal Chemistry Letters, 2008, Vol. 18, pages 1840-1844.

[0218] In the reactions of Production Methods 1-C to 3-C and Reaction Schemes 1-C to 2-C, the reaction mixture after completion of the reaction can be subjected to a conventional post-treatment such as direct concentration, dissolving in an organic solvent and washing with water followed by concentration, or pouring into ice water and extracting with an organic solvent followed by concentration, to obtain the target compound of the present invention. Furthermore, when purification becomes necessary, the compound can be separated and purified by any purification method such as recrystallization, column chromatography, thin-layer chromatography, or liquid chromatography fractionation.

[0219] The pest control agent in the present invention means a pest control agent that targets harmful arthropods in the fields of agriculture and horticulture or livestock and sanitation (endoparasites and ectoparasites of mammals or birds as livestock or pets, and sanitary pests and nuisance pests for household and commercial use).

[0220] Furthermore, the agricultural chemicals in the present invention refer to insecticides, acaricides, nematicides, herbicides, fungicides, and the like in the agricultural and horticultural fields.

[0221] In this specification, "sanitary pests" refers to harmful invertebrates that bite target animals, causing allergic symptoms such as severe pain, swelling, and itching, and in some cases, causing fatal anaphylactic shock, or that transmit serious diseases through blood-sucking, sometimes even leading to death; invertebrates that sometimes contaminate food with pathogens such as viruses, bacteria, and parasites through contact with food; invertebrates whose living organisms, carcasses, molted skins, and feces act as allergens, causing allergic diseases such as bronchial asthma, rhinitis, conjunctivitis, and atopic dermatitis; invertebrates that cause economic damage by eating food, clothing, and housing; and invertebrates that do not directly harm humans but cause discomfort by invading and invading their living environments. More specifically, these include ants that bite with their mandibles, hornets that sting with their poisonous stingers, mosquitoes and assassin bugs that suck blood through the skin, and termites that are omnivorous and damage buildings such as houses.

[0222] In this specification, the term "nuisance pests" refers to pests that do not directly harm humans in their living environment, but that cause discomfort and psychological harm due to their appearance or shape.

[0223] Specific examples of insects, mites, crustaceans, mollusks, nematodes, ectoparasites, and endoparasites that can be controlled using the compound (1) of the present invention include, but are not limited to, the following organisms:

[0224] Pests include the following from the order Lepidoptera: Allium leafminer (Acrolepiopsis sapporensis), Yam leafminer (Acrolepiopsis suzukiella), Smaller tea tortrix (Adoxophyes honmai), Summer fruit tortrix (Adoxophyes orana fasciata), Fruit-piercing moth (Adris tyrannus), Sweet potato leafworm (Aedia leucomelas), Black cutworm (Agrotis ipsilon), Turnip moth (Agrotis segetum), Cotton leafworm (Alabama argillacea), Asiatic leafroller (Archips breviplicanus), and Apple tortrix (Agrotis segetum). tortrix (Archips fuscocupreanus), Oriental tussock moth (Artaxa subflava), Bamboo zygaenid (Artona martini), Japanese giant looper (Ascotis selenaria), Asiatic common looper (Autographa nigrisigna), Pear leaf miner (Bucculatrix pyrivorella), Tea leafroller (Caloptilia theivora), Peach fruit moth (Carposina sasakii), Rice stem borer (Chilo suppressalis), Rice leafroller (Cnaphalocrocis medinalis), Yellow peach moth (Conogethespunctiferalis), Carpenter moth (Cossus insularis), Three-spotted plusia moth (Ctenoplusia agnata), Codling moth (Cydia pomonella), Pine moth (Dendrolimus spectabilis), Japanese hemlock caterpillar (Dendrolimus superans), Cucumber moth (Diaphania indica), Sugarcane borer (Diatraea saccharalis), Scarlet corn moth (Eilema fuscodorsalis), Scarlet corn moth (Eilema laevis), Lesser corn stalk borer (Elasmopalpus lignosellus), Grape berry moth (Endopiza viteana), Limabean pod borer (Etiella zinckenella), Japanese tussock moth (Euproctis piperita), Tea tussock moth (Euproctis pseudoconspersa), Japanese bamboo lappet moth (Euthrix albomaculata), Reed moth (Euthrix potatoria), Oriental lappet moth (Gastropacha orientalis), Mulberry pyralid (Glyphodes pyloalis), Plum fruit moth (Grapholita dimorpha), Pear fruit moth (Grapholita molesta), Sweet potato leaffolder (Helcystogramma triannulella), CottonBollworm (Helicoverpa armigera), Oriental tobacco budworm (Helicoverpa assulta), Corn earworm (Helicoverpa zea), Tobacco budworm (Heliothis virescens), Cabbage webworm (Hellula undalis), Oriental tea tortrix (Homona magnanima), Fall webworm moth (Hyphantria cunea), Pearlleaf worm (Illiberis pruni), Prunus bud moth (Illiberis rotundata), Oak moth (Quercus lasiocampid) (Kunugia undans), Mountain moth (Quercus lasiocampid) (Kunugia yamadai), Soybean pod borer (Leguminivora glycinivorella), Mulberry tiger moth (Lemyra imparilis), Gypsy moth (Lymantria dispar), Peach leafminer (Lyonetia clerkella), Silver leafminer (Lyonetia prunifoliella malinella), Cabbage armyworm (Mamestra brassicae), Tomato hornworm (Manduca quinquemaculata), Tobacco hornworm (Manduca sexta), Soybean podworm (Matsumuraeses phaseoli), Oriental moth (Monema flavescens), Rice green caterpillar (Narangaaenescens), White-spotted tussock moth (Orgyia thyellina), Asian corn borer (Ostrinia furnacalis), European corn borer (Ostrinia nubilalis), Adzuki bean borer (Ostrinia scapulalis), Dark fruit-tree tortrix (Pandemis heparana), Bluegrass webworm (Parapediasia teterrella), Green cochlid (Parasa consocia), Broad-headed oak moth (Parasa lepida), Chinese cochlid (Parasa sinica), Straight swift (Parnara guttata), Pink bollworm Bollworm (Pectinophora gossypiella), Citrus leafminer (Phyllocnistis citrella), Apple leafminer (Phyllonorycter ringoniella), Large white (Pieris brassicae), Cabbage white butterfly (Pieris rapae crucivora), Diamondback moth (Plutella xylostella), Oriental armyworm (Pseudaletia separata), Soybean looper (Pseudoplusia includens), Swan moth (Sphrageidus similis), Lawn grass cutworm (Spodoptera depravata), Southern armyworm (Spodoptera eridania), Beet armyworm (Spodopteraexigua), Fall armyworm (Spodoptera frugiperda), Cotton leafworm (Spodoptera littoralis), Common cutworm (Spodoptera litura), Persimmon fruit moth (Stathmopoda masinissa), Peach tree borer (Synanthedon exitiosa), Cherry tree borer (Synanthedon hector), Red-necked long-eared moth (Toleria romanovi), Cabbage looper (Trichoplusia ni), etc. Coleoptera: Common bean weevil (Acanthoscelides obtectus), Cupreous chafer (Anomala cuprea), Soybean beetle beetle (Anomala rufocuprea), Asian long-horn beetle (Anoplophora glabripennis), White-spotted longicorn beetle (Anoplophora malasiaca), Boll weevil (Anthonomus grandis), Cucurbit leaf beetle (Aulacophora femoralis), Adzuki bean beetle (Callosobruchus chinensis), Flea beetle (Chaetocnema concinna), Sweet potato weevil (Cylas formicarius), Leaf beetle (Demotina fasciculata), Northern corn rootworm (Diabroticabarberi), Southern corn rootworm (Diabrotica undecimpunctata), Western corn rootworm (Diabrotica virgifera), Rice plant weevil (Echinocnemus squameus), Mexican bean beetle (Epilachna varivestis), Large 28-spotted ladybird (Epilachna vigintioctomaculata), 28-spotted ladybird (Epilachna vigintioctopunctata), Epuraea domina, West Indian sweet potato weevil (Euscepes postfasciatus), Citrus flower chafer (Gametis jucunda), White-fringed beetle (Graphognatus leucoloma), Yellowish elongate chafer (Heptophylla picea), Alfalfa weevil (Hypera postica), Tobacco beetle (Lasioderma serricorne), Colorado potato beetle (Leptinotarsa ​​decemlineata), Rice water weevil (Lissohoptrus oryzophilus), Sweetpotato wireworm (Melanotus fortnumi), Sugarcane wireworm (Melanotus tamsuyensis), Pollen beetle (Meligethes aeneus), Japanese pine sawyerPine sawyer (Monochamus alternatus), Black vine weevil (Otiorhynchus sulcatus), Rice leaf beetle (Oulema oryzae), Rove beetle (Paederus fuscipes), Mustard leaf beetle (Phaedon cochleariae), Striped flea beetle (Phyllotreta striolata), Japanese beetle (Popillia japonica), Yellow-spotted longicorn beetle (Psacothea hilaris), Solanum flea beetle (Psylliodes angusticollis), Peach curculio (Rhynchites heros), Granary weevil (Sitophilus granarius), Maize weevil (Sitophilus zeamais), Hunting billbug (Sphenophorus venatus vestitus), Yellow mealworm (Tenebrio molitor), Red flour beetle (Tribolium castaneum), Grape borer (Xylotrechus pyrrhoderus), etc. Hymenoptera: Chestnut sawfly (Apethymus kuri), Large rose sawfly (Arge pagana), Cabbage sawfly (Athalia infumata), Turnip sawfly (Athalia rosae), Japanese carpenter Ant (Camponotus japonicus), chestnut gall waspWasp (Dryocosmus kuriphilus), Army ant (Eciton burchellii, E. schmitti), Argentine ant (Linepithema humile), Pharaoh ant (Monomorium pharaonis), Bulldog ant (Myrmecia spp.), European pine sawfly (Neodiprion sertifer), Fire ant (Solenopsis spp.), Asian giant hornet (Vespa mandarinia), Japanese yellow hornet (Vespa simillima), etc. Diptera: Yellow fever mosquito (Aedes aegypti), Asian tiger mosquito (Aedes albopictus), Aedes species (Aedes spp.), Aedes taeniorhynchus, Rice leaf miner (Agromyza oryzae), Mexican fruit fly (Anastrepha ludens), African malaria mosquito (Anopheles gambiae), African malaria mosquito (Anopheles hyrcanus sinensis), Anopheles koreicus, Anopheles lesteri, Anopheles maculipennis, Anopheles spp., Soybean pod gall midge (Asphondylia yushimai), Atylotus spp., Melon fly (Bactroceracucurbitae), Oriental fruit fly (Bactrocera dorsalis), Queensland fruit fly (Bactrocera tryoni), Japanese orange fly (Bactrocera tsuneonis), Boophthora erythrocephala, Braula coeca, Braula spp., Calliphora erythrocephala, Calliphora lata, Calliphora spp., Bottle fly (Calliphora vicina), Mediterranean fruit fly (Ceratitis capitata), Pea leaf miner (Chromatomyia horticola), Old World screw-worm fly (Chrysomya bezziana), Blow fly (Chrysomya chloropyga), Oriental latrine fly (Chrysomya megacephala), Chrysomya spp., Splayed deerfly (Chrysops caecutiens), Chrysops relictus, Chrysops spp., Deer fly (Chrysops suavis), Chrysozona pluvialis, New World screw-worm fly (Cochliomyia hominivorax), House mosquito (Culex pipiens molestus), House mosquito (Culex pipiens pallens), Culex quinquefasciatusquinquefasciatus), Culex tarsalis, Culex tritaeniorhynchus, Culex spp., Biting midge (Culicoides arakawae), Culicoides spp., Bot flies (Cuterebra spp.), Onion fly (Delia antiqua), Seed corn maggot (Delia platura), Human botfly (Dermatobia hominis), Japanese fruit fly (Drosophila suzukii), Eusimulium spp., Lesser house fly (Fannia canicularis), Fannia spp. spp.), Horse nose bot fly (Gasterophilus haemorrhoidalis), Gasterophilus inermis, Horse bot fly (Gasterophilus intestinalis), Throat bot fly (Gasterophilus nasalis), Gasterophilus nigricornis, Gasterophilus pecorum, Gasterophilus spp., Tsetse fly (Glossina morsitans, G. palpalis), Glossina spp., Horn fly (Haematobia irritans), Haematobia irritans exigua, Haematobia spp. spp.), Haematobia stimulans, Haematopota italicaitalic), Common horse fly (Haematopota pluvialis), Haematopota spp., Forest fly (Hippobosca equina), Hippobosca spp., Hippobosca variegate, Hybomitra ciurea, Hybomitra spp., Smaller rice leaf miner (Hydrellia griseola), Hydrotaea albipuncta, Sheep headfly (Hydrotaea irritans), Hydrotaea spp., Warble fly (Hypoderma bovis), Common cow fly Cattle grub (Hypoderma lineatum), Hypoderma spp., Black gnat (Leptoconops nipponensis), Lipoptena capreoli, Lipoptena cervi, Lipoptena spp., Cabbage leafminer (Liriomyza brassicae), Tomato leafminer (Liriomyza bryoniae), Stone leek leafminer (Liriomyza chinensis), Pea leafminer (Liriomyza huidobrensis), Tomato leafminer (Liriomyza sativae), Serpentine leafminer (Liriomyza trifolii), Australian sheep blowfly (Lucilia cuprina), Green bottle fly (Luciliaillustris), Common green bottle fly (Lucilia sericata), Lucilia spp., Lutzomyia spp., Hessian fly (Mayetiola destructor), Sheep ked (Melophagus ovinus), Melophagus spp., Sweat fly (Morellia simplex), Morellia spp., Face fly (Musca autumnalis), Housefly (Musca domestica), Musca spp., Australian bush fly (Musca vetustissima), Odagmia ornate, Odagmia spp., Sheep nasal Bot fly (Oestrus ovis), Oestrus spp., Beet leaf miner (Pegomya cunicularia), Philipomyia spp., Phlebotomus longipalpis, Phlebotomus papatasi, Sandfly (Phlebotomus spp.), Black blow fly (Phormia regina), Yellow-legged fly (Prosimulium yezoensis), Northern blowfly (Protophormia terraenovae), Przhevalskiana silenus, Apple maggot (Rhagoletis pomonella), Rhinoestrus spp., Flesh fly fly (Sarcophaga carnaria), flesh fly (Sarcophagaperegrina), Sarcophaga spp., Black fly (Simulium ochraceum), Simulium reptans, Simulium spp., Orange wheat blossom midge (Sitodiplosis mosellana), Stable fly (Stomoxys calcitrans), Stomoxys spp., Tabanus atratus, Tabanus bromius, Greenhead horse fly (Tabanus nigrovittatus), Tabanus spodopterus, Tabanus spp., Tabanus sudeticus, Horse fly (Tabanus trigonus), Moth fly (Telmatoscopus albipunctatus), Tipula paludosa, Tipula spp., Wilhelmia equine, Wilhelmia spp., Wohlfahrtia spp., etc. Hemiptera: green stink bug (Acrosternum hilare), pea aphid (Acyrthosiphon pisum), Camellia spiny whitefly (Aleurocanthus camelliae), orange spiny whitefly (Aleurocanthus spiniferus), Indian cotton leafhopper (Amrasca devastans), California red scale (Aonidiella aurantii), Cowpea aphidAphid (Aphis craccivora), Black bean aphid (Aphis fabae), Soybean aphid (Aphis glycines), Cotton aphid (Aphis gossypii), Green apple aphid (Aphis pomi), Spiraea aphid (Aphis spiraecola), Pale greenplant bug (Apolygus spinolae), Grape leafhopper (Arboridia apicalis), Foxglove aphid (Aulacorthum solani), Beardsley leafhopper (Balclutha saltuella), Silverleaf whitefly (Bemisia argentifolii), Sweetpotato Whitefly (Bemisia tabaci), True chinch bug (Blissus leucopterus), Leafcurl plum aphid (Brachycaudus helichrysi), Cabbage aphid (Brevicoryne brassicae), Oriental chinch bug (Cavelerius saccharivorus), Indian wax scale (Ceroplastes ceriferus), Red wax scale (Ceroplastes rubens), Walnut aphid (Chromaphis juglandicola), Bed bug (Cimex lectularius), Rice stink bug (Cletus punctiger), Citricola scale (Coccuspseudomagnoliarum), San jose scale (Comstockaspis perniciosa), Citrus whitefly (Dialeurodes citri), Asian citrus psyllid (Diaphorina citri), stinkbag (Dichelops furcatus), Russian wheat aphid (Diuraphis noxia), Sloe bug (Dolycoris baccarum), Giant margarodid scale (Drosicha corpulenta), Rosy apple aphid (Dysaphis plantaginea), Red cotton bug (Dysdercus cingulatus), Potato leafhopper (Empoasca fabae), persimmon leafhopper Empoasca nipponica (Empoasca nipponica), tea green leafhopper Empoasca onukii, bean's smaller green leafhopper Empoasca sakaii, grape leafhopper Epiacanthus stramineus, woolly apple aphid Eriosoma lanigerum, cabbage bug Eurydema rugosa, brown stink bug Euschistus servus, white-spotted spined bug Eysarcoris aeneus, large spiny white-spotted bug Eysarcoris lewisi (Eysarcoris lewisi), White-spotted stink bug (Eysarcoris ventralis), Tea leaf scaleScale (Fiorinia theae), Shield bug (Glaucias subpunctatus), Island fleahopper (Halticus insularis), Brown marmorated stink bug (Halyomorpha halys), Mealy plum aphid (Hyalopterus pruni), Cottony cushion scale (Icerya purchasi), Small brown planthopper (Laodelphax striatellus), Rice bug (Leptocorisa chinensis), Turnip aphid (Lipaphis erysimi), Western tarnished plant bug (Lygus hesperus), Tarnished plant bug (Lygus lineolaris), Potato aphid (Macrosiphum euphorbiae), Aster leafhopper (Macrosteles fascifrons), Grape leafhopper (Macrosteles striifrons), Sugarcane spittlebug (Mahanarva fimbriolata), Black-margined aphid (Monellia caryella), Green peach aphid (Myzus persicae), Lettuce aphid (Nasonovia ribisnigri), Onion aphid (Neotoxoptera formosana), Green rice leafhopper (Nephotettix cincticeps), Eastern green stink bug (Nezaraantennata), Southern green stink bug (Nezara viridula), Brown rice planthopper (Nilaparvata lugens), Squash bug (Paradasynus spinosus), Cotton mealy bug (Phenacoccus solani), Red-banded stink bug (Piezodorus guildinii), Red-banded shield bug (Piezodorus hybneri), Citrus mealybug (Planococcus citri), Japanese mealybug (Planococcus kraunhiae), Brown-winged green bug (Plautia crossota), Peony scale (Pseudaonidia paeoniae), Cotton fleahopper (Pseudatomoscelis seriatus), Mulberry scale (Pseudaulacaspis pentagona), White peach scale (Pseudaulacaspis prunicola), Comstock mealybug (Pseudococcus comstocki), Grape mealybug (Pseudococcus maritimus), Pear psylla (Psylla pyrisuga), Blood-sucking bug (Rhodnius prolixus), Bird cherry-oat aphid (Rhopalosiphum padi), Rice root aphid (Rhopalosiphum rufiabdominalis), Rhopalid bug (Rhopalusmaculatus), Bean bug (Riptortus clavatus), Greenbug (Schizaphis graminum), Japanese black rice bug (Scotinophora lurida), Corn leaf aphid (Sitobion akebiae), English grain aphid (Sitobion avenae), White-backed rice planthopper (Sogatella furcifera), Rice stink bug (Stenodema sibiricum), Sorghum plant bug (Stenotus rubrovittatus), Azalea lace bug (Stephanitis pyrioides), Seed bug (Togo hemipterus), Black citrus aphid (Toxoptera aurantii), Brown citrus aphid (Toxoptera citricida), Greenhouse whitefly (Trialeurodes vaporariorum), Mexican kissing bug (Triatoma dimidiata), Brazilian kissing bug (Triatoma infestans), Rice leaf bug (Trigonotylus caelestialium), Citrus snow scale (Unaspis citri), Euonymus scale (Unaspis euonymi), Arrowhead scale (Unaspis yanonensis), Grape phylloxera (Viteus vitifolii), etc., Thysanoptera; Flower thripsOrthoptera: Australian plague locust (Chortoicetes terminifera), Oriental mole cricket (Gryllotalpa orientalis), Migratory locust (Migratory locust), etc. Locust (Locusta migratoria), Lesser paddy grasshopper (Oxya japonica), Rice grasshopper (Oxya yezoensis), Desert locust (Schistocerca gregaria), Emma field cricket (Teleogryllus emma), etc. Order Blattola: German cockroach (Blattella germanica), Formosan subterranean termite (Coptotermes formosanus), Daikoku dry-wood termite (Cryptotermes domesticus), Western dry-wood termite (Incisitermes minor), Black-winged subterranean termite (Odontotermesformosanus), American cockroach (Periplaneta americana), Smoky-brown cockroach (Periplaneta fuliginosa), Japanese cockroach (Periplaneta japonica), Japanese subterranean termite (Reticulitermes speratus), etc., Isoptera: Coptotermes formosanus (Coptotermes formosanus), Reticulitermes speratus (Reticulitermes speratus), Odontotermes formosanus (Odontotermes formosanus), etc., Acari: Cyclamen mite (Phytonemus pallidus), Broad mite (Polyphagotarsonemus latus), Tarsonemus bilobatus (Tarsonemus bilobatus), Chinese cabbage mite (Penthaleus erythrocephalus), Winter grain mite (Penthaleus major), Rice spider mite (Oligonychus shinkajii), Citrus red mite (Panonychus citri), Mulberry giant spider mite (Panonychus mori), European red mite (Panonychus ulmi), Kanzawa spider mite (Tetranychus kanzawai), Two-spotted spider mite (Tetranychus urticae), Tea long-spotted rust mite (Acaphylla theavagrans), Tulip rust mite (DryBulb mite (Aceria tulipae), Tomato erineum mite (Aculops lycopersici), Pink citrus rust mite (Aculops pelekassi), Apple rust mite (Aculus schlechtendali), Pear rust mite (Eriophyes chibaensis), Citrus rust mite (Phyllocoptruta oleivora), Bulb mite (Rhizoglyphus robini), Mold mite (Tyrophagus putrescentiae), Spinach mite (Tyrophagus similis), Acarapis spp., Honey bee tracheal mite (Acarapis woodi), and Acarus spp. spp.), Lone star tick (Amblyomma americanum), Cayenne tick (Amblyomma cajennense), South African bont tick (Amblyomma hebraeum), Gulf coast tick (Amblyomma maculatum), Amblyomma spp., Tropical bont tick (Amblyomma variegatum), Fowl tick (Argas persicus), Pigeon tick (Argas reflexus), Argas spp., Blue cattle tick (Boophilus annulatus), Boophilus calceratus, African blue tick (Boophilusdecoloratus), Tropical cattle tick (Boophilus microplus), Boophilus spp., Caloglyphus spp., Chelacaropsis moorei, Cat tick (Cheyletiella blakei), Rabbit fur mite (Cheyletiella parasitovorax), Cheyletiella spp., Dog tick (Cheyletiella yasguri), Cheyletus eruditus, Stag beetle tick (Cheyletus malaccensis), Chorioptic mange mite (Chorioptes bovis), Chorioptes spp., Cytodites spp., and Demodex follicle Demodex mite (Demodex bovis), Demodex caballi, Dog follicle mite (Demodex canis), Demodex caprae, Cat follicle mite (Demodex cati), Demodex equi, Face mite (Demodex folliculorum), Demodex ovis, Demodex spp., Sarcoptes suis mite (Demodex suis), Winter tick (Dermacentor albipictus), Rocky Mountain wood tick (Dermacentor andersoni), Ornate sheep tick (Dermacentor marginatus), Meadow tick (Dermacentor pictus), Ornate dog ticktick (Dermacentor reticulatus), Dermacentor spp., American dog tick (Dermacentor variabilis), Poultry red mite (Dermanyssus gallinae), Dermacentor spp., American house dust mite (Dermatophagoides farina), House dust mite (Dermatophagoides pteronyssinus), Asian chigger (Eutrombicula wichmanni), Storage mite (Glycyphagus destructor), House itch mite (Glycyphagus domesticus), Haemaphysalis cinnabarina, Common rodent tick (Haemaphysalis concinna), Yellow dog tick tick (Haemaphysalis leachi), Bush tick (Haemaphysalis longicornis), Haemaphysalis otophila, Red sheep tick (Haemaphysalis punctate), Haemophysalis spp., House mite (Haplochthonius simplex), Trombiculid mite (Helenicula miyagawai), Tortoise tick (Hyalomma aegyptium), Hyalomma anatolicum, Bont-legged tick (Hyalomma marginatum), Hyalomma mauritanicus, Hyalomma spp.spp.), Small smooth bont-legged tick (Hyalomma transiens), Hypodectes spp., Dog tick (Ixodes canisuga), Hedgehog tick (Ixodes hexagonus), Australian paralysis tick (Ixodes holocyclus), Western black-legged tick (Ixodes pilosus), Castor bean tick (Ixodes ricinus), Karoo paralysis tick (Ixodes rubicundus), Deer tick (Ixodes scapularis), Ixodes spp., Knemidocoptes spp., Laminosioptes spp.), Leptotrombidium akamushi, Leptotrombidium pallida, Leptotrombidium scutellare, Listrophorus spp., Megninia cubitalis, Myobia spp., Neoschoengastia xerothermobia, Neotrombicula autumnalis, Neotrombicula desaleri, Notoedres cati, Notoedres spp., Ornithocheyletia spp., Soft tick tick (Ornithodorus moubata), Ornithodorus species (Ornithodorusspp.), Tropical fowl mite (Ornithonyssus bursa), Ornithonyssus spp., Northern fowl mite (Ornithonyssus sylviarum), Spinose ear tick (Otobius megnini), Otobius spp., Dog ear mite (Otodectes cynotis), Otodectes spp., Canine nasal mite (Pneumonyssoides caninum), Pneumonyssoides mange, Pneumonyssus spp., Pneumonyssus spp., Psorergates spp.), Psoroptic mite (Psoroptes communis), Rabbit ear mite (Psoroptes cuniculi), Psoroptes equi, Sheep scab mite (Psoroptes ovis), Psoroptes ovis, Psoroptes spp., Feather mite (Pterolichus obtusus), Pterolichus spp., Raillietia spp., Brown ear tick (Rhipicephalus appendiculatus), Brown ear tick (Rhipicephalus bursa), Rhipicephalus capensis, Asian blue tick tick (Rhipicephalus evertsi), Kennel tick (Rhipicephalussanguineus), Rhipicephalus spp., Rhipicephalus turanicus, Rhipicephalus zambeziensis, Sarcoptes bovis, Sarcoptes equi, Sarcoptes ovis, Sarcoptes rupicaprae (=S. caprae), Itch mite (Sarcoptes scabiei), Sarcoptes spp., Sarcoptes suis, Itch mite (Sarcoptis canis), Sternostoma spp., Trombicula spp. spp.), Cheese mite (Tyrophagus putrescentiae), Tyrophagus spp., Varroa mite (Varroa jacobsoni), Varroa spp., etc. Order Anoplura: Short-nosed cattle louse (Haematopinus eurysternus), Tail switch louse (Haematopinus quadripertusus), Pig louse (Haematopinus spp.), Large pig louse (Haematopinus suis), Buffalo louse (Haematopinus tuberculatus), Rabbit louse (Haemodipsus ventricosus), Dog sucking louse (Linognathus setosus), Linognathus spp., Long-nosed cattle louse (Linognathus vituri), Head louse (Pediculushumanus), Pediculus spp., Mouse louse (Polyplax serratus), Crab louse (Pthirus pubis), Pthirus spp., Little blue cattle louse (Solenopotes capillatus), Solenopotes spp., etc.; Mallophaga: Goat biting louse (Bovicola caprae), Bovicola limbata, Sheep body louse (Bovicola ovis), Bovicola spp., Chicken head louse (Cuclotogaster heterographa), Cattle chewing louse (Damalinia bovis), Felicola spp., Cat louse (Felicola subrostrata), Brown chicken louse (Goniodes dissmilis), Fluff louse (Goniodes gallinae), Large hen louse (Goniodes gigas), Lepikentron ovis, Lepikentron spp., Wing louse (Lipeurus caponis), Body louse (Menacanthus cornutus), Small body louse (Menacanthus pallidulus), Menacanthus spp., Chicken body louse (Menacanthus stramineus), Chicken shaft louse (Menopon gallinae), Menopon spp., Dog biting louselouse (Trichodectes canis), flea species (Trichodectes spp.), Werneckiella equi, Werneckiella spp., etc. Siphonaptera: chicken flea (Ceratophyllus gallinae), dog flea (Ctenocephalides canis), cat flea (Ctenocephalides felis), sticktight flea (Echidnophaga gallinacean), human flea (Pulex irritans), chigoe flea (Tunga penetrans), oriental rat flea (Xenopsylla cheopis), etc. Other parasites include Monogenea: Benedenia epinephrii, epinepheli, Benedenia hoshinai, Benedenia sekii, Benedenia seriolae, Bivagina tai, Sea louse (Caligus curtus), Caligus elongates, Caligus labaracis, Caligus longipedis, Caligus orientalis, Caligus teres, Dactylogyrus spp., Gyrodactylus spp., Heteraxine heterocerca, Heterobothrium okamotoi okamotoi), Lamellodiscus spp., copepods (Lepeophtheirus cuneifer), Lepeophtheirus hypoglossihippoglossi, Lepeophtheirus pectoralis, salmon louse (Lepeophtheirus salmonis), Microcotyle sebastis, Microcotyle sebastisci, Neobenedenia, Neobenedenia congeri, Neobenedenia girellae, Neoheterobothrium hirame, Polystoma spp., Pseudocaligus fugu, Zeuxapta japonica, etc., Cestoda; Andyra spp. spp.), Anoplocephala spp., Avitellina spp., Bertiella spp., Bothridium spp., Cittotaenia spp., Davainea spp., Diorchis spp., Manson's tapeworm (Diphyllobothrium erinacei), fish tapeworm (Diphyllobothrium latum), Diphyllobothrium spp., Diphyllogonoporus spp., Diplopylidium spp., dog tapeworm (Dipylidium caninum), Dipylidium spp., dog tapeworm (Dipylidium granulosus) tapeworm (Echinococcus granulosus), fox tapeworm (Echinococcus multilocularis), Echinococcus spp., Echinocotyle spp.spp.), Echinolepsis spp., Hydatigera spp., Hymenolepis diminuta, Hymenolepis spp., Joyeuxiella spp., Ligura spp., Mesocestoides spp., Moniezia benedeni, Moniezia spp., Paranoplocephala spp., Raillietina spp., Schistocephalus spp., Spirometra spp., Stilesia spp., beef tapeworm (Taenia spp.) saginata), pork tapeworm (Taenia solium), Taenia spp., cat tapeworm (Taenia taeniaeformis), Thysaniezia spp., Thysanosomsa spp., etc. Trematoda; Austrobilharzia spp., Brachylaema spp., Calicophoron spp., Catatropis spp., chinese river fluke (Clonorchis sinensis), Clonorchis spp. spp.), Collyriclum spp., Cotylophoron spp., Cyclocoelum spp. spp.), Dicrocoelium spp., Diplostomum spp., Echinochasmus spp., Echinoparyphium spp., Echinostoma spp., the small pancreatic fluke Eurytrema coelomaticumcoelomaticum), pancreas fluke (Eurytrema pancreaticum), Eurytrema spp., liver fluke (Fasciola gigantica), sheep liver fluke (Fasciola hepatica), Fasciola spp., Fasciolides spp., large intestinal fluke (Fasciolopsis bruski), Fasciolopsis spp., Fischoederius spp., Gastrothylacus spp., Gigantobilharzia spp., Gigantocotyle spp., Heterophyes spp. spp.), Hypoderaeum spp., Leucochloridium spp., Metagonimus spp., Metorchis spp., Nanophyetus spp., Notocotylus spp., Opisthorchis spp., Ornithobilharzia spp., Paragonimus spp., Oriental lung fluke (Paragonimus westermani), Paramphistomum spp., Plagiorchis spp., Posthodiplostomum spp. spp.), Prosthogonimus spp., Schistosoma haematobium, Schistosoma japonicum, Schistosoma mansoni, Schistosoma spp.spp.), Trichobilharzia spp., Troglotrema spp., Typhlocoelum spp., etc., Nematoda: Aelurostrongylus spp., Amidostomum spp., Ancylostoma spp., Angiostrongylus spp., Anisakis spp., Ascaridia galli, Ascaridia spp., Ascaris spp., Ascaris suum, Aspiculuris spp., Brugia spp., Bunostomum spp. spp.), Capillaria spp., Chabertia spp., Cooperia oncophora (intestinal worm), Cooperia spp., Crenosoma spp., Cyathostoma spp., Cyclocercus spp., Cylicostephanus spp., Cylindropharynx spp., Cystocaulus spp., Dictyocaulus spp., Dirofilaria immitis (heartworm), Dirofilaria spp., Dracunculus spp. spp.), Draschia spp., Elaphostrongylus spp., Enoplida spp., Enterobius spp., Filaroides spp., Filicollis spp., Globocephalus spp., Gnathostoma spp.spp.), Gongylonema spp., Gyalocephalus spp., Habronema spp., Barber's pole worm (Haemonchus contortus), Haemonchus spp., Heterakis spp., Hyostrongylus spp., Litomosoides spp., Loa spp., Macracanthorhynchus spp., Marshallagia spp., Metastrongylus spp., Micronema spp., Moniliformis spp., Muellerius spp. spp.), Nematodirus spp., Neostrongylus spp., Obeliscoides spp., Oeophagostomum dentatum, Oesophagodontus spp., Oesophagostomum radiatum, Oesophagostomum spp., Ollulanus spp., Onchocerca gibsoni, Onchocerca spp., Brown stomach worm, Ostertagia ostertagi, Ostertagia spp., Oxyuris spp., Parabronema spp. spp.), Paraclenosoma spp., Parafilaria spp., Parafilaroides spp., Parascaris spp., Parelaphostrongylus spp.spp.), Passalurus spp., Physaloptera spp., Pneumostrongylus spp., Poteriostomum spp., Prostenorchis spp., Protostrongylus spp., Setaria spp., Spicocaulus spp., Stephanofilaria spp., Stephanurus spp., Strongyloides spp., Strongylus spp., Syngamus spp., Syphacia spp., Thelazia spp. spp.), Toxascaris spp., Toxocara spp., Trichinella spp., Trichomosoides spp., Trichonema spp., Colubriformis ruminant nematode, Trichostrongylus spp., Trichuris spp., Triodontophorus spp., Uncinaria spp., Wuchereria spp., etc. Protozoa: Babesia spp., Eimeria acervulina, Eimeria bovis, etc. bovis), Eimeria brunette, Eimeria maxima, Eimeria necatrix, Eimeria ovinoidalis, Eimeria spp., Eimeria tenellatenella), Entamoeba histolytica, Giardia spp., Histomanas spp., Plasmodium spp., Theileria spp., Toxoplasma spp., Trichomonadidae spp., Trypanosomsa cruzi, and the like.

[0225] Furthermore, the compound (1) of the present invention is also effective against pests that have developed resistance to existing insecticides such as organophosphorus compounds, carbamate compounds, and pyrethroid compounds.

[0226] That is, the compound (1) of the present invention can effectively control pests belonging to the order Collembola, Dictyoptera (Bockroaches), Orthoptera (Orthoptera), Termitida, Thysanoptera (Thysanoptera), Hemiptera (Hemiptera and Cicadellida), Lepidoptera (Lepidoptera), Coleoptera (Coleoptera), Hymenoptera (Hymenoptera), Diptera (Flea Bugs), and Phthiraptera, as well as crustaceans such as Lepidoptera, Cynodontida, and Cyclopida, as well as mites, gastropods, cestodes, trematodes, nematodes, and protozoa, even at a low concentration.

[0227] On the other hand, the compound (1) of the present invention has an extremely useful feature of having almost no adverse effect on mammals, fish, crustaceans, and beneficial insects (useful insects such as honeybees and bumblebees, and natural enemies such as aster wasps, oil wasps, parasitic flies, orthoptera, and phytoseiid mites).

[0228] When using compound (1) of the present invention, it is usually mixed with a suitable solid or liquid carrier, and optionally, surfactants, penetrants, spreaders, thickeners, antifreeze agents, binders, anticaking agents, disintegrants, antifoaming agents, preservatives, antidegradants, etc. may be added to prepare a formulation of any dosage form, such as a soluble concentrate, emulsifiable concentrate, wettable powder, water-soluble powder, water-dispersible granules, water-soluble granules, suspension concentrate, concentrated emulsion, suspoemulsion, microemulsion, dustable powder, granules, tablets, emulsifiable gel, etc. From the viewpoint of labor saving and improved safety, the formulation of any of the above dosage forms may also be enclosed in a water-soluble package, such as a water-soluble capsule or a water-soluble film bag, for practical use.

[0229] Examples of solid carriers include natural minerals such as quartz, calcite, sepiolite, dolomite, chalk, kaolinite, pyrophyllite, sericite, halloysite, metahalloysite, kibushi clay, gairome clay, pottery stone, allophane, shirasu, kira, talc, bentonite, activated clay, acid clay, pumice, attapulgite, zeolite, and diatomaceous earth; calcined products of natural minerals such as calcined clay, perlite, shirasu balloon, vermiculite, attapulgus clay, and calcined diatomaceous earth; magnesium carbonate, calcium carbonate, sodium carbonate, and carbonate Examples of suitable inorganic salts include sodium hydrogen carbonate, ammonium sulfate, sodium sulfate, magnesium sulfate, diammonium hydrogen phosphate, ammonium dihydrogen phosphate, and potassium chloride; sugars such as glucose, fructose, sucrose, and lactose; polysaccharides such as starch, powdered cellulose, and dextrin; organic substances such as urea, urea derivatives, benzoic acid, and salts of benzoic acid; plants such as wood flour, cork powder, corn cobs, walnut shells, and tobacco stalks; fly ash, white carbon (e.g., hydrated synthetic silica, anhydrous synthetic silica, hydrated synthetic silicate, etc.), and fertilizers.

[0230] Examples of the liquid carrier include xylene, alkyl (C ９ or C １０ etc.) benzene, phenylxylylethane, alkyl (C １ or C ３aliphatic hydrocarbons such as machine oil, normal paraffin, isoparaffin, naphthene; mixtures of aromatic and aliphatic hydrocarbons such as kerosene; alcohols such as ethanol, isopropyl alcohol, cyclohexanol, phenoxyethanol, benzyl alcohol; polyhydric alcohols such as ethylene glycol, propylene glycol, diethylene glycol, hexylene glycol, polyethylene glycol, polypropylene glycol; propyl cellosolve, butyl cellosolve, phenyl cellosolve, propylene glycol monomethyl ether, propylene glycol ethers such as cholesteryl ether, propylene glycol monopropyl ether, propylene glycol monobutyl ether, and propylene glycol monophenyl ether; ketones such as acetophenone, cyclohexanone, and γ-butyrolactone; esters such as fatty acid methyl esters, dialkyl succinate esters, dialkyl glutamate esters, dialkyl adipate esters, and dialkyl phthalate esters; acid amides such as N-alkyl (C1, C8, or C12, etc.) pyrrolidone; oils and fats such as soybean oil, linseed oil, rapeseed oil, palm oil, cottonseed oil, and castor oil; dimethyl sulfoxide, water, and the like.

[0231] These solid carriers and liquid carriers may be used alone or in combination of two or more.

[0232] Examples of surfactants include nonionic surfactants such as polyoxyethylene alkyl ethers, polyoxyethylene alkyl (mono- or di-)phenyl ethers, polyoxyethylene (mono-, di-, or tri-)styrylphenyl ethers, polyoxyethylene polyoxypropylene block copolymers, polyoxyethylene fatty acid (mono- or di-)esters, sorbitan fatty acid esters, polyoxyethylene sorbitan fatty acid esters, castor oil ethylene oxide adducts, acetylene glycol, acetylene alcohol, ethylene oxide adducts of acetylene glycol, ethylene oxide adducts of acetylene alcohol, and alkyl glycosides; alkyl sulfate ester salts, alkylbenzene sulfonates, lignin sulfonates, alkyl sulfosuccinates, naphthalene anionic surfactants such as alkyl phenyl ether sulfonates, alkyl naphthalene sulfonates, salts of formalin condensates of naphthalene sulfonic acid, salts of formalin condensates of alkyl naphthalene sulfonic acid, polyoxyethylene alkyl ether sulfates or phosphate ester salts, polyoxyethylene (mono- or di-) alkyl phenyl ether sulfates or phosphate ester salts, polyoxyethylene (mono-, di-, or tri-) styryl phenyl ether sulfates or phosphate ester salts, polycarboxylates (for example, polyacrylates, polymaleates, copolymers of maleic acid and olefins, etc.), and polystyrene sulfonates; cationic surfactants such as alkylamine salts and alkyl quaternary ammonium salts; amphoteric surfactants such as amino acid type and betaine type; silicone-based surfactants; and fluorine-based surfactants.

[0233] The content of these surfactants is not particularly limited, but is generally preferably in the range of 0.05 to 20 parts by mass per 100 parts by mass of the formulation of the present invention. These surfactants may be used alone or in combination of two or more.

[0234] The dosage of the compound of the present invention varies depending on the application site, application time, application method, cultivated crop, etc., but usually, an amount of the active ingredient of about 0.005 to 50 kg per hectare (ha) is appropriate.

[0235] On the other hand, when the compound of the present invention is used to control internal or external parasites in mammals and birds as livestock and pets, an effective amount of the compound of the present invention can be administered together with formulation additives by oral administration; parenteral administration such as injection (intramuscular, subcutaneous, intravenous, intraperitoneal, etc.); transdermal administration such as immersion, spraying, bathing, washing, pouring-on, spotting-on, dusting, etc.; nasal administration; etc. The compound of the present invention can also be administered by a molded product using a strip, plate, band, collar, ear mark, limb band, marking device, etc.

[0236] For administration, the compound (1) of the present invention can be prepared in any dosage form suitable for the administration route.

[0237] When compound (1) of the present invention is used to eliminate external or internal parasites, the preferred dosage of compound (1) of the present invention as the active ingredient depends on the type of target parasite to be controlled, the species of target animal to be administered, the method of administration, etc., but is usually 0.01 to 100 mg / kg, preferably 0.01 to 50 mg / kg, of the body weight of the target animal to be administered. In particular, the dosage for dogs may vary depending on the type or age of the target dog or the ectoparasite to be controlled, but is usually 1 to 5000 mg / kg, preferably 1 to 100 mg / kg, of the live body weight of the target dog.

[0238] When administering the compound (1) of the present invention to eliminate external or internal parasites, the administration interval depends on the type of target parasite to be controlled, the species of target animal to be administered, the administration method, etc., but can usually be set arbitrarily in the range of once every day to once every year, preferably once every week to once every six months, more preferably every day (24 hours), every month, once every month, once every two months, once every three months, or once every six months.

[0239] Furthermore, when compound (1) of the present invention is used to control ectoparasites in dogs, the timing of administration of the compound of the present invention to dogs can be, for example, 30 minutes before the start of feeding or 120 minutes after the end of feeding. Here, 30 minutes before the start of feeding and 120 minutes after the end of feeding are based on the act of eating food given to the dog for the purpose of nutritional intake. For example, if a dog's feeding time is 20 minutes, the specified time is based on the act of eating, and is a total of 170 minutes from 30 minutes before the start of feeding to 120 minutes after the end of feeding. This also includes cases where feeding is temporarily interrupted during feeding and then resumed after oral administration of the compound of the present invention. In this specification, "feeding" refers to the act of an animal eating food.

[0240] Generally, the number of times a dog is fed per day varies depending on the breed, age, and habits of the dog, but is usually 3 to 4 times a day for dogs under six months old, 2 to 3 times a day for dogs between six months and one year old, 2 to 3 times a day for adult dogs about 1 to 5 years old, and 2 to 3 times a day for dogs 6 years old or older. In the present invention, "feeding" means the act of eating for the purpose of taking in nutrients, and does not include the act of feeding food or the like for the purpose of so-called dog discipline or training.

[0241] The dosage forms that may be prepared include solid preparations such as powders, granules, wettable powders, pellets, tablets, boli, capsules, and molded products containing the active compound; liquid preparations such as injectable solutions, oral solutions, and solutions for application on the skin or into body cavities; solution preparations such as pour-on preparations, spot-on preparations, flowable preparations, and emulsions; and semi-solid preparations such as ointments and gels.

[0242] Examples of dosage forms for oral administration of compound (1) of the present invention include solid preparations such as tablets, chewables, capsules, pills, boluses, granules, and powders; semisolid preparations such as pastes and gels; and liquid preparations such as drinks.

[0243] Furthermore, examples of dosage forms for transdermal administration include solid preparations such as powders; semi-solid preparations such as creams, ointments, pastes, and gels; and liquid preparations such as sprays, aerosols, solutions and emulsions, suspensions, and lotions.

[0244] Furthermore, dosage forms for administration by injection include, for example, liquid preparations such as solutions and emulsions and suspensions, and dosage forms for administration via the nose include, for example, liquid preparations such as aerosols.

[0245] Furthermore, examples of the formulation for spraying in animal rearing environments such as livestock barns include solid preparations such as wettable powders, dusts, and granules; and liquid preparations such as emulsions and suspension concentrates.

[0246] However, the formulations used in the parasite control agent of the present invention are not limited to these dosage forms.

[0247] The solid preparation can be administered orally as it is, or diluted with water and used by transdermal administration or by spraying in the animal rearing environment such as a livestock barn.

[0248] A solid preparation for oral administration can be prepared by mixing the compound (1) of the present invention or a salt thereof with one or more excipients and binders suitable for oral administration, and further, if necessary, physiologically acceptable additives such as lubricants, disintegrants, dyes, pigments, etc., and molding the mixture into a desired shape.

[0249] Examples of excipients and binders include sugars or sugar derivatives such as lactose, sucrose, mannitol, and sorbitol; starches such as corn starch, wheat starch, rice starch, and potato starch; celluloses or cellulose derivatives such as methyl cellulose, carboxymethyl cellulose, hydroxyethyl cellulose, hydroxypropyl cellulose, and hydroxypropylmethyl cellulose; proteins or protein derivatives such as zein and gelatin; and synthetic polymer compounds such as honey, gum arabic paste, polyvinyl alcohol, and polyvinylpyrrolidone.

[0250] Examples of lubricants include magnesium stearate, and examples of disintegrants include cellulose, agar, alginic acid, cross-linked polyvinylpyrrolidinone, carbonates, and the like.

[0251] Furthermore, among solid preparations used for oral administration, particularly in the case of solid preparations such as chewable preparations, additives are also used to impart a taste, texture, and flavor preferred by the animal to which the preparation is administered, but the carriers and additives used in solid preparations of parasite control compositions are not limited to these.

[0252] The liquid preparation can be administered transdermally or by injection as is, or can be mixed with feed and administered orally, diluted with water and administered orally or transdermally, or sprayed in the animal rearing environment such as a livestock barn.

[0253] Injectable solutions can be administered intravenously, intramuscularly, or subcutaneously. Injectable solutions can be prepared by dissolving the active compound in a suitable solvent and adding, if necessary, additives such as solubilizers, acids, bases, buffer salts, antioxidants, and protective agents.

[0254] Suitable solvents include water, ethanol, butanol, benzyl alcohol, glycerin, propylene glycol, polyethylene glycol, N-methylpyrrolidone, and mixtures thereof, physiologically acceptable vegetable oils, synthetic oils suitable for injection, and the like.

[0255] Examples of the solubilizing agent include polyvinylpyrrolidone, polyoxyethylated castor oil, and polyoxyethylated sorbitan ester.

[0256] Examples of the protecting agent include benzyl alcohol, trichlorobutanol, p-hydroxybenzoic acid ester, and n-butanol.

[0257] Oral liquid preparations can be administered directly or after dilution, and can be prepared in the same manner as injectable liquid preparations.

[0258] Flowables, emulsions, etc. can be administered directly or diluted, transdermally, or by environmental treatment.

[0259] Solutions for use on the skin can be administered by dropping, spreading, rubbing, spraying, sprinkling, or by application by immersion (dipping, bathing, or washing). These solutions can be prepared in the same way as solutions for injection.

[0260] Pour-on and spot-on preparations are applied or sprayed onto a limited area of ​​the skin, allowing the active compound to penetrate the skin and act systemically.

[0261] Drops and drops can be prepared by dissolving, suspending, or emulsifying the active ingredient in a suitable skin-compatible solvent or solvent mixture, and, if necessary, adding auxiliary agents such as surfactants, colorants, absorption promoters, antioxidants, light stabilizers, adhesives, etc.

[0262] Suitable solvents include water, alkanols, glycols, polyethylene glycol, polypropylene glycol, glycerin, benzyl alcohol, phenylethanol, phenoxyethanol, ethyl acetate, butyl acetate, benzyl benzoate, dipropylene glycol monomethyl ether, diethylene glycol monobutyl ether, acetone, methyl ethyl ketone, aromatic and / or aliphatic hydrocarbons, vegetable or synthetic oils, DMF (N,N-dimethylformamide), liquid paraffin, light liquid paraffin, silicone, dimethylacetamide, N-methylpyrrolidone, or 2,2-dimethyl-4-oxy-methylene-1,3-dioxolane.

[0263] Absorption promoters include DMSO (dimethyl sulfoxide), isopropyl myristate, dipropylene glycol pelargonate, silicone oil, aliphatic esters, triglycerides, fatty alcohols, and the like.

[0264] Antioxidants include sulfites, metabisulfites, ascorbic acid, butylhydroxytoluene, butylhydroxyanisole, tocopherol, and the like.

[0265] Emulsifiable concentrates can be administered orally, transdermally, or by injection. Emulsifiable concentrates can be prepared by dissolving the active ingredient in a hydrophobic or hydrophilic phase, and homogenizing the solution with a solvent for another phase using an appropriate emulsifier, and, if necessary, with auxiliary agents such as colorants, absorption promoters, protectants, antioxidants, light-blocking agents, and thickeners.

[0266] Examples of the hydrophobic phase (oil) include paraffin oil, silicone oil, sesame oil, almond oil, castor oil, synthetic triglycerides, ethyl stearate, di-n-butyl adipate, hexyl laurate, dipropylene glycol pelargonate, esters of branched short-chain fatty acids with saturated fatty acids having a chain length of C16 to C18, isopropyl myristate, isopropyl palmitate, caprylic / capric acid esters of saturated fatty alcohols having a chain length of C12 to C18, isopropyl stearate, oleyl oleate, decyl oleate, ethyl oleate, ethyl lactate, waxy fatty acid esters, dibutyl phthalate, diisopropyl adipate, isotridecyl alcohol, 2-octyldodecanol, cetylstearyl alcohol, and oleyl alcohol.

[0267] The hydrophilic phase includes water, propylene glycol, glycerin, sorbitol, and the like.

[0268] Examples of the emulsifier include nonionic surfactants such as polyoxyethylated castor oil, polyoxyethylated sorbitan monoolefinate, sorbitan monostearate, glycerin monostearate, polyoxyethyl stearate, and alkylphenol polyglycol ether; amphoteric surfactants such as disodium N-lauryl-β-iminodipropionate and lecithin; anionic surfactants such as sodium lauryl sulfate, fatty alcohol sulfate esters, and monoethanolamine salts of mono / dialkyl polyglycol orthophosphate esters; and cationic surfactants such as cetyltrimethylammonium chloride.

[0269] Other adjuvants include carboxymethylcellulose, methylcellulose, polyacrylates, alginates, gelatin, gum arabic, polyvinylpyrrolidone, polyvinyl alcohol, methyl vinyl ether, copolymers of maleic anhydride, polyethylene glycol, waxes, colloidal silica, and the like.

[0270] Semisolid preparations can be administered by painting or spreading on the skin or by introducing into body cavities. Gels can be prepared by adding to the solutions prepared as above for injectable solutions sufficient thickener to produce a clear material with an ointment-like consistency.

[0271] Next, formulation examples using the compound (1) of the present invention will be shown. However, the formulation examples of formulations containing the compound (1) of the present invention are not limited to these. In the following formulation examples, "parts" means parts by mass.

[0272] [Wettable powder] Compound (1) of the present invention 0.1-80 parts Solid carrier 5-98.9 parts Surfactant 1-10 parts Others 0-5 parts As the others, for example, an anti-caking agent, an anti-decomposition agent and the like can be mentioned.

[0273] [Emulsifiable concentrate] Compound (1) of the present invention 0.1-30 parts Liquid carrier 45-95 parts Surfactant 4.9-15 parts Others 0-10 parts As the other ingredients, for example, a spreading agent, a decomposition inhibitor and the like can be mentioned.

[0274] [Suspension Agent] Compound (1) of the present invention 0.1 to 70 parts Liquid carrier 15 to 98.89 parts Surfactant 1 to 12 parts Others 0.01 to 30 parts As the other agents, for example, an antifreeze agent, a thickener, etc. may be mentioned.

[0275] [Water Dispersible Granule] Compound (1) of the present invention 0.1-90 parts Solid carrier 0-98.9 parts Surfactant 1-20 parts Others 0-10 parts As the others, for example, a binder, a decomposition inhibitor and the like can be mentioned.

[0276] [Liquid Formulation] Compound (1) of the present invention 0.01-70 parts Liquid carrier 20-99.99 parts Others 0-10 parts As the other ingredients, for example, an antifreeze agent, a spreading agent, etc. may be mentioned.

[0277] [Granules] Compound (1) of the present invention 0.01-80 parts Solid carrier 10-99.99 parts Others 0-10 parts As the other ingredients, for example, a binder, a decomposition inhibitor and the like can be mentioned.

[0278] [Dust] Compound (1) of the present invention 0.01-30 parts Solid carrier 65-99.99 parts Others 0-5 parts As the other ingredients, for example, anti-drift agents, anti-decomposition agents and the like can be mentioned.

[0279] Next, formulation examples containing the compound (1) of the present invention as an active ingredient will be shown more specifically, but the present invention is not limited to these. Note that the compound No. 1-001 of the present invention shown below means any of the compound No. 1A-001 of the present invention, the compound No. 1B-001 of the present invention, and the compound No. 1C-001 of the present invention. The compound No. 1A-001 of the present invention means N-(5-fluoropyridin-2-yl)-6-(5-(2-fluoropyridin-4-yl)-1,3,4-oxadiazol-2-yl)-4-hydroxy-2-oxo-1,2,5,6-tetrahydropyridine-3-carboxamide described in Synthesis Example 2-A described later, and the compound No. Inventive Compound No. 1B-001 means N-(5-fluoropyridin-2-yl)-4-hydroxy-6-(3-morpholino-1,2,4-oxadiazol-5-yl)-2-oxo-1,2,5,6-tetrahydropyridine-3-carboxamide, which is described in Synthesis Example 1-B, which will be described later, and Inventive Compound No. 1C-001 means N-(5-fluoropyridin-2-yl)-4-hydroxy-6-(5-morpholino-1,3,4-oxadiazol-2-yl)-2-oxo-1,2,5,6-tetrahydropyridine-3-carboxamide, which is described in Synthesis Example 1-C, which will be described later.

[0280] [Formulation Example 1] Wettable powder Compound No. 1-001 of the present invention 20 parts Pyrophyllite 74 parts Sorpol 5039 4 parts (trade name of Toho Chemical Industry Co., Ltd., a mixture of a nonionic surfactant and an anionic surfactant) Carplex #80D 2 parts (trade name of Shionogi & Co., Ltd., synthetic hydrous silica) The above ingredients are uniformly mixed and pulverized to prepare a wettable powder.

[0281] [Formulation Example 2] Emulsifiable concentrate Compound No. 1-001 of the present invention 5 parts Xylene 75 parts N-methylpyrrolidone 15 parts Sorpol 2680 5 parts (trade name of Toho Chemical Industry Co., Ltd., a mixture of a nonionic surfactant and an anionic surfactant) The above ingredients are mixed uniformly to prepare an emulsion.

[0282] Formulation Example 3 Suspension agent Compound No. 1-001 of the present invention 25 parts Agrisol S-710 10 parts (trade name of Kao Corporation, nonionic surfactant) Lunox 1000C 0.5 parts (trade name of Toho Chemical Industry Co., Ltd., anionic surfactant) Xanthan gum 0.2 parts Water 64.3 parts The above ingredients are uniformly mixed and then wet-pulverized to obtain a suspension agent.

[0283] Formulation Example 4: Water Dispersible Granule Compound of the present invention No. 1-001 75 parts Hitenol NE-15 5 parts (trade name, Dai-ichi Kogyo Seiyaku Co., Ltd., anionic surfactant) Vanilex N 10 parts (trade name, Nippon Paper Industries Co., Ltd., anionic surfactant) Carplex #80D 10 parts (trade name, synthetic hydrous silica, Shionogi & Co., Ltd.) The above ingredients are uniformly mixed and pulverized, and then a small amount of water is added and the mixture is stirred and mixed, granulated in an extrusion granulator, and dried to give a water dispersible granule.

[0284] Formulation Example 5 Granules Compound of the present invention No. 1-001 5 parts Bentonite 50 parts Talc 45 parts After the above ingredients are uniformly mixed and pulverized, a small amount of water is added and the mixture is stirred and mixed, granulated in an extrusion granulator, and dried to give granules.

[0285] Formulation Example 6: Dust Compound of the present invention No. 1-001 3 parts Carplex #80D 0.5 parts (Shionogi & Co., Ltd. trade name, synthetic hydrous silica) Kaolinite 95 parts Diisopropyl phosphate 1.5 parts The above ingredients are uniformly mixed and pulverized to prepare a dust. When used, the above formulation is diluted 1 to 10,000 times with water, or sprayed directly without dilution.

[0286] Formulation Example 7 Wettable Powder Preparation Compound No. 1-001 of the present invention 25 parts Sodium diisobutylnaphthalenesulfonate 1 part Calcium n-dodecylbenzenesulfonate 10 parts Alkylaryl polyglycol ether 12 parts Sodium salt of naphthalenesulfonic acid formalin condensate 3 parts Emulsion-type silicone 1 part Silicon dioxide 3 parts Kaolin 45 parts

[0287] Formulation Example 8: Water-soluble thickener preparation Compound No. 1-001 of the present invention 20 parts Polyoxyethylene lauryl ether 3 parts Sodium dioctyl sulfosuccinate 3.5 parts Dimethyl sulfoxide 37 parts 2-propanol 36.5 parts

[0288] Formulation Example 9: Spray liquid Compound of the present invention No. 1-001 2 parts Dimethyl sulfoxide 10 parts 2-propanol 35 parts Acetone 53 parts

[0289] Formulation Example 10: Liquid preparation for transdermal administration Compound No. 1-001 of the present invention 5 parts Hexylene glycol 50 parts 2-propanol 45 parts

[0290] Formulation Example 11: Liquid preparation for transdermal administration Compound No. 1-001 of the present invention 5 parts Propylene glycol monomethyl ether 50 parts Dipropylene glycol 45 parts

[0291] Formulation Example 12: Liquid preparation for transdermal administration (dropping) Compound of the present invention No. 1-001 2 parts Light liquid paraffin 98 parts

[0292] Formulation Example 13: Liquid preparation for transdermal administration (dropping): Compound No. 1-001 of the present invention 2 parts, Light liquid paraffin 58 parts, Olive oil 30 parts, O.D.O 9 parts (product name of Nisshin Oillio Group, medium-chain fatty acid oil), Shin-Etsu Silicone 1 part

[0293] Furthermore, when the compound (1) of the present invention is used as an agricultural chemical or an animal drug, it may be mixed with other chemicals at the time of formulation or application, if necessary. By applying the mixed chemicals, costs can be reduced by reducing the amount of chemicals applied, and the control spectrum can be expanded and a higher pest control effect can be achieved by the synergistic action of the mixed chemicals. In this case, it is also possible to combine the compound (1) with multiple known chemicals at the same time.

[0294] For example, types of pesticides to be mixed with compound (1) of the present invention include compounds described in The Pesticide Manual, 18th Edition, 2018 and The Pesticide Manual, 19th Edition, 2021. Specific examples of the common names of antiparasitic drugs and antibiotics to be mixed and used as veterinary drugs are as follows, but are not necessarily limited to these.

[0295] Insecticides: abamectin, acephate, acequinocyl, acetamiprid, acrinathrin, acinonapyr, afidopyropen, afoxolaner, alanycarb, aldicarb, allethrin, alpha-cypermethrin, alpha-endosulfan, amidoflumet, amitraz, azamethiphos, azinphos-ethyl, azinphos-methyl, azocyclotin, Bacillus thuringiensis thuringiensis), bendiocarb, benfluthrin, benfuracarb, bensultap, bentioflumin, benzoximate, benzpyrimoxan, beta-cyfluthrin, beta-cypermethrin, bifenazate, bifenthrin, bioallergy Bioallethrin, bioresmethrin, bistrifluron, bisulfuron, broflanilide, bromopropylate, buprofezin, butocarboxim, carbaryl, carbofuran, carbosulfan, cartap, chinomethionate,Chlorantraniliprole, chlorethoxyfos, chlorfenapyr, chlorfenvinphos, chlorfluazuron, chlormephos, chlorobenzilate, chloroprallethrin, chlorpyrifos, chlorpyrifos-methyl, chromafenozide, clofentezine, clothianidin, cyanophos, cyantraniliprole, cybenzoxasulfyl, cyclaniliprole, cycloprothrin, cyenopyrafen, cyetopyrafen tpyrafen), cyflumetofen, cyfluthrin, cyhalodiamide, cyhalothrin, cyhexatin, cypermethrin, cyphenothrin, cyproflanilide, cyromazine, deltamethrin, diacloden, diafenthiuron (diafenthiuron), diazinon (diazinon), dichlorvos (dichlorvos), dichloromezotiaz (dicloromezotiaz), dicofol (dicofol), dienochlor (dienochlor), diflovidadin (diflovidazin), diflubenzuron (diflubenzuron), dimefluthrin (dimefluthrin), dimethoate (dimethoate), dimethylvinphos (dimethylvinphos), jinpropyridaz (dimpropyridaz),Dinotefuran, diofenolan, disulfoton, DNOC, d-T-80-phthalthrin, emamectin benzoate, empenthrin, endosulfan, EPN, epsilon-metofluthrin, epsilon-momfluorothrin, esfenvalerate, ethifencarb, ethiprole, etofenprox, etoxazole, etrimfos, Febantel, fenazaquin, fenbutatin oxide oxide), fenitrothion, fenmezoditiaz, fenobucarb, fenothiocarb, fenoxycarb, fenpropathrin, fenpyroximate, fenthion, fenvalerate, fipronil, flometoquin, flonicamid, fluacrylamide, Pyrim (fluacrypyrim), fluazuron (fluazuron), flubendiamide (flubendiamide), fluchlordiniliprole (fluchlordiniliprole), flucycloxuron (flucycloxuron), flucythrinate (flucythrinate), flufenerim (flufenerim), flufenoxuron (flufenoxuron), flufenprox (flufenprox), flufiprole (flufiprole), fluhexafon (fluhexafon), flumethrin (flumethrin),Flumetnicam (flumetnicam), flupentiofenox (flupentiofenox), flupyradifurone (flupyradifurone), flupirimin (flupyrimin), flupyroxystrobin (flupyroxystrobin), flupiroxystrobin (flupyroxystrobin), fluralaner (fluralaner), fluvalinate (fluvalinate), fluxametamide (fluxametamide), fonophos (fonophos), formethicone Formetanate, formothion, furathiocarb, gamma-cyhalothrin, halfenprox, halofenozide, heptafluthrin, hexaflumuron, hexythiazox, hydramethylnon, imidacloprid id), imiprothrin, indazapyroxamet, indoxacarb, indoxacarb-MP, isocycloseram, isofenphos, isoflualanam, isoprocarb, isoxathion, kappa-bifenthrin, kappa-tefluthrin kappa-tefluthrin, lambda-cyhalothrin, ledprona, lepimectin, lufenuron, malathion, meperfluthrin, metaflumizone, metalcarb, metaldehyde, methacrifos, methamidophos,Methidathion, methomyl, methoprene, methoxychlor, methoxyfenozide, methyl bromide bromide, metofluthrin, milbemectin, momfluorothrin, monocrotophos, muscalure, nicofluprole, nitenpyram, novaluron, noviflumuron, omethoate, oxazosulfyl, oxydemeton-methyl, oxydeprofos, parathion, parathion-methyl, pentachlorophenol, permethrin, phenothrin, phenthoate, phorate orate), phosalone, phosmet, phosphamidon, phoxim, pioxaniliprole, piperflanilide, pirimicarb, pirimiphos-methyl, praziquantel, profenofos, profluthrin, propaphos, propargite, prothiofos, protrifenbut, pyflubumide, pymetrozine, pyraclofos, pyrafluprole, pyrethrins, pyridaben,Pyridalyl, pyrifluquinazon, pyrimidifen, pyriprole, pyriproxyfen, resmethrin, rotenone, silafluofen, spidoxamat, spinetoram, spinosad, spirobudifen, spirodiclofen spirodiclofen, spiromesifen, spiropidione, spirotetramat, spiromesifen, sulfiflumin, sulfotep, sulfoxaflor, sulprofos, tau-fluvalinate, tebufenozide, tebufenpyrad npyrad), teflubenzuron (teflubenzuron), tefluthrin (tefluthrin), terbufos (terbufos), tetrachlorantraniliprole (tetrachlorantraniliprole), tetrachlorvinphos (tetrachlorvinphos), tetramethrin (tetramethrin), tetramethylfluthrin (tetramethylfluthrin), tetraniliprole (tetraniliprole), thiacloprid (thiacloprid), thiamethoxam (thiamethoxam), thiocyclam (thiocyclam), thiodicarb (thiodicarb), thiofanox (thiofanox), thiometon (thiometon), thiapyrachlor (tiapyrachlor), thioantraniliprole (tiorantraniliprole), tolfenpyrad (tolfenpyrad), tralomethrin (tralomethrin), transfluthrin (transfluthrin), triazamate (triazamate), triazuron (triazuron),Trichlorfon, triflumezopyrim, triflumuron, tyclopyrazoflor, vamidothion, vadescana, and zeta-cypermethrin, etc.

[0296] Fungicides: acibenzolar-S-methyl, acypetacs, aldimorph, allyl alcohol, ametoctradin, aminopyrifen, amisulbrom, amobam, ampropylfos, anilazine, azaconazole, azithiram, azoxystrobin, barium polysulfide polysulfide), benalaxyl, benalaxyl-M, benodanil, benomyl, benquinox, bentaluron, benthiavalicarb-isopropyl, benthiazole, benzamacril, benzamorph, benzovindiflupyr, binapacryl, biphenyl, bitertanol, bixafen, blasticidin-S, Bordeaux mixture mixture), boscalid (boscalid), bromuconazole (bromuconazole), bupirimate (bupirimate), buthiobate (buthiobate), butylamine (butylamine), lime sulfur mixture (calcium polysulfide), captafol (captafol), captan (captan), carbamorph (carbamorph), carbendazim (carbendazim), carboxin (carboxin), carpropamid (carpropamid), carvone (carvone), cheshunt mixture (cheshunt mixture), chinomethionate (chinomethionat),Chlobenthiazone, chloraniformethane, chloranil, chlorfenazole, chloroneb, chloroinconazide, chloropicrin, chlorothalonil, chlorquinox, chlozolinate, climbazole, copper acetate, copper carbonate, basic, copper hydroxide, copper naphthenate, copper oleate, copper oxychloride, copper sulfate, copper sulfate, basic, copper zinc chromate chromate), coumoxystrobin, cresol, cufraneb, cuprobam, cyazofamid, cyclafuramid, cycloheximide, cyflufenamid, cymoxanil, cypendazole, cyproconazole, cyprodinil, cyprofuram, dazomet, debacarb, decafentin, dehydroacetate acid), dichlobentiazox, dichlofluanid, diclone, dichlorophen, dichlozoline, diclobutrazol,Diclocymet (diclocymet), diclomezine (diclomezine), dicloran (dicloran), diethofencarb (diethofencarb), difenoconazole (difenoconazole), diflumetorim (diflumetorim), dimethirimol (dimethirimol), dimethomorph (dimethomorph), dimoxystrobin (dimoxystrobin), diniconazole (diniconazole), diniconazole-M (diniconazole-M), dinobut Dinobuton, dinocap, dinocap-4, dinocap-6, dinocton, dinosulfon, dinoterbone, diphenylamine, dipymetitrone, dipyrithione, disulfiram, ditalimfos, dithianon, DENON DNOC, dodemorph, dodine, drazoxolon, edifenphos, enestrobin, enoxastrobin, epoxiconazole, ethaboxam, etaconazole, etem, ethirimol, ethoxyquin, etridiazole azole), famoxadone, fenamidone, fenaminosulf, phenaminestrobin, fenapanil, fenarimol, fenbuconazole, feneptamidoquine, fenfuram, fenhexamid, fenitropan,Fenopyramid, fenoxanil, fenpiclonil, fenpicoxamid, fenpropidin, fenpropimorph, fenpyrazamine, fentin, ferbam, ferimzone, florylpicoxamid, fluazinam azinam), flubeneteram (flubeneteram), fludioxonil (fludioxonil), flufenoxadiazam (flufenoxadiazam), flufenoxystrobin (flufenoxystrobin), fluindapyr (fluindapyr), flumethylsulforim (flumetylsulforim), flumetover (flumetover), flumorph (flumorph), fluopicolide (fluopicolide), fluopimomide (fluopimomide), Fluopyram (fluopyram), fluorimide (fluoroimide), fluotrimazole (fluotrimazole), fluoxapiprolin (fluoxapiprolin), fluoxastrobin (fluoxastrobin), fluoxytioconazole (fluoxytioconazole), fluquinconazole (fluquinconazole), flusilazole (flusilazole), flusulfamide (flusulfamide), flutolanil (flutolanil), flutianil (flutianil), flutriafol (flutriafol), fluxapyroxad (fluxapyroxad), folpet (folpet), fosetyl - aluminum (fosetyl-aluminium), fthalide (fthalide), fuberidazole (fuberidazole), furalaxyl (furalaxyl), furametpyr (furametpyr), furcarbanil (furcarbanil), fluconazole (furconazole), fluconazole - cis (furconazole-cis),Flumecyclox, furophanate, galquin, glyodin, griseofulvin, guazatine, halacrinate, hexachlorobenzene, hexaconazole, hexylthiofos, oxyquinoline sulfate (8-hydroxyquinoline sulfate), sulfate), hymexazol, imazalil, imibenconazole, iminoctadine-albesilate, iminoctadine-triacetate, inpyrfluxam, iodocarb, ipconazole, ipfentrifluconazole, ipflufenoquin, iprobenfos, iprodione, iprovalicarb, isofetamide, isofetamide, isofleucipram, Sotianil (isotianil), isoprothiolane (isoprothiolane), isopyrazam (isopyrazam), isovaledione (isovaledione), kasugamycin (kasugamycin), kresoxim-methyl (kresoxim-methyl), laminarin (laminarin), mancopper (mancopper), mancozeb (mancozeb), mandestrobin (mandestrobin), mandipropamid (mandipropamid), maneb (maneb), mebenil (mebenil), mecarbinzid (mecarbinzid), mefentrifluconazole (mefentrifluconazole), mepanipyrim (mepanipyrim), mepronil (mepronil), meptyldinocap (meptyldinocap),Metalaxyl, metalaxyl-M, metam, metarylpicoxamid, metazoxolone, metconazole, methasulfocarb, metofuroxam, methyltetraprole, metiram, metominostrobin, metrafenone, metsulfovax, milneb, myclobutanil, myclozolin, nabam, naftifine, natamycin, organic nickel (nickel bis (dimethyldithiocarbamate), nitrostyrene, nitrothal-isopropyl, nuarimol, octhilinone, ofurace, orysastrobin, oxadixyl, oxathiapiprolin, oxyquinoline copper, oxpoconazole fumarate fumarate), oxycarboxin, pefurazoate, penconazole, pencycuron, penflufen, pentachlorophenol, penthiopyrad, orthophenylphenol (2-phenylphenol), phosdiphen, phthalide, picarbutrazox, picoxystrobin, piperalin, polycarbamate, polyoxins,Polyoxin-D, potassium azide, potassium hydrogen carbonate, probenazole, prochloraz, procymidone, propamocarb hydrochloride hydrochloride), propiconazole, propineb, proquinazid, prothiocarb, pyrazophos, pyribencarb, pyrifenox, pyrimethanil, pyriminostrobin, pyroquilon, prothiocarb, prothioconazole, pydiflumetofen, pyracarbolid, pyraclostrobin, pyrametostrobin, pyraoxystrobin, pyrapropion e), pyraziflumid, pyridaclomethyl, pyridinitril, pyriophenone, pyrisoxazole, pyroxychlor, pyroxyfur, quinacetol-sulfate, quinazamid, quinconazole, quinoxyfen, quinofumelin, quintozene, rabenzazole, salicylanilide, seboctylamine, sedaxane, silthiofam, simeconazole,Sodium hydrogen carbonate, sodium hypochlorite, spiroxamine, sulfur, tebuconazole, tebufloquin, tefloctalam, tecnazene, tecoram, tetraconazole, thiabendazole, thiadifluor, thicyofen, thifluzamide, thiochlorfenphim, thiophanate e), thiophanate-methyl, thiuram, tiadinil, tioximid, tolclofos-methyl, tolprocarb, tolylfluanid, triadimefon, triadimenol, triamiphos, triarimol, triazbutil, triazoxide, tributyltin oxide oxide), trichlamide, triclopyricarb, tricyclazole, tridemorph, trifloxystrobin, triflumizole, triforine, triticonazole, validamycin, valifenalate, vinclozolin, zalilamid, zinc naphthenate, zinc sulfate, zineb, ziram,Zoxamide, shiitake mycelium extract, shiitake fruiting body extract, etc.

[0297] Nematicides: aldoxycarb, benclothiaz, cadusafos, cyclobutrifluram, DBCP, diclofenthion, DSP, ethoprophos, fenamiphos, fensulfothion, fluazaindolizine , fluensulfone, fosthiazate, fosthietan, galquin, imicyafos, isamidofos, isazofos, oxamyl, sulfoxamyl, thionazin, tioxazafen and trifluenfuronate and the like. Antiparasitic drugs: abamectin, albendazole-sulphoxide, amidantel, amoscanate, amprolium, bephenium, bromoxanide, brotianide, bunamidine, butamisole, chlorotetracycline, clindamycin, clioxanide, clonazepam, crufomate, cyclobendazole, deacylated amidantel amidantel), derquantel, diamfenetide, diclazuril, disophenol, doxycycline, emamectin,Emetine, enrofloxacin, erythromycin, flumetnicam, halofiginon, haloxon, hetolin, hexachlorophene, hycanthone, hydroxyzine, latidectin, lepimectin, letrazuril razuril), lucanthone, meniclofolan, milbemectin, miracil, mirasan, monensin, morantel, naphthalofos, narasin, nemadectin, netobimin, niclofolan, nifurtimox, niridazol Niridazole, nitroscanate, nitroxynil, oltipraz, omphalotin, oxamniquine, oxantel, oxyfendazole, oxytetracycline, paraherquamide, parbendazole, paromomycin, piperazine, ponazuril, pradofloxacin, pyrantel, pyrimethamine, resorantel, rolitetracycline, salinomycin, sulfaclozin, sulfaquinoxaline, tetracycline,Tetramisole, thiophanate, toltrazuril, tribendimidine, tribromsalan, trichlorfon, trimethoprim, esfenvalerate, fenpropathrin, fenvalerate, alphacypermethrin thrin, bifenthrin, cypermethrin, deltamethrin, etofenprox, lambda-cyhalothrin, permethrin, tefluthrin, zeta-cypermethrin, acetamiprid, clothianidin, dinotefuran Tefuran), imidacloprid, nitenpyram, thiamethoxam, chromafenozide, fenoxycarb, lufenuron, methoprene, pyriproxyfen, triflumuron, chlorpyrifos, chlorpyrifos-methyl, diazinon, dichlorvos, fenitrothion, fenthion, malathion, pirimiphos-methyl, tetrachlorvinphos, ethiprole, fipronil, propoxur, carbaryl, bendiocarb,Methoxadiazone, fenocarb, carbofuran, afoxolaner, fluralaner, fluxametamide, sarolaner, lotilaner, tigolaner, esafoxolaner, modoflaner, umifoxolaner, mivorilaner, avermectin, ivermectin, doramectin, eprinomectin, madeuramycin, milbemycin, milbemycin oxime oxime), moxidectin, selamectin, indoxacarb, amitraz, bistrifluron, spinosad, albendazole, atovaquone, bithionol, cambendazole, carnidazole, chloroquine, clazuril, clorsulon, closantel, coumaphos, dichlorophen, diethylcarbamazine, diminazene, dinitolmide, dithiazanine iodide iodide), emodepside, epsiprantel, febantel, fenbendazole, flubendazole, glycalpyramide, imidocarb,Levamisole, mebendazole, mefloquine hydrochloride, melarsomine dihydrochloride, metronidazole, methylidine, monepantel, morantel tartrate, niclosamide, oxantel pamoate, oxantel tartrate, oxibendazole, oxyclozanide, piperazine adipate, piperazine citrate, piperazine phosphate, praziquantel, pyrantel pamoate, rafoxanide, tetramisole hydrochloride hydrochloride), thiabendazole, and triclabendazole, etc.

[0298] Antibiotics: amoxicillin, ampicillin, cefapirin, cefazolin sodium, cefquinome, ceftiofur, penicillin, chlortetracycline, oxytetracycline, danofloxacin, difloxacin, oxolinic acid acid), enrofloxacin, florfenicol, lincomycin, lomefloxacin, marbofloxacin, miloxacin, mirosamycin, norfloxacin, ofloxacin, orbifloxacin, valnemulin, thiamphenicol, tiamulin fumarate, tilmicosin phosphate, tylosin acetate isovalerate, tylosin phosphate, tulathromycin, ketoconazole, miconazole nitrate nitrate and clavulanic acid, etc.

[0299] The compound (1) of the present invention has excellent insecticidal and acaricidal activity against many agricultural pests, spider mites, and internal or external parasites of mammals or birds, and also exhibits sufficient control effect against pests that have acquired resistance to existing insecticides. Furthermore, it has almost no adverse effect on mammals, fish, and beneficial insects, has low residual properties, and is environmentally friendly. Therefore, the present invention can provide a useful novel pest control agent.

[0300] In light of the above, embodiments of the present invention relate to the following [1] to

[132] . [1] Formula (1): wherein Q is Q-A, Q-B or Q-C, and (i) when Q is Q-A, Q-A is C １ ~C ６ Alkyl, R １７ (C １ ~C ６ ) alkyl, —N(R １８ ) R １９ , -OR ６２ or Q-1 to Q-82; R １７ is a halogen atom, C １ ~C ６ represents alkoxy or E-1 to E-83; R １８ is a hydrogen atom, C １ ~C ６ Alkyl or C ２ ~C ６ represents alkenyloxycarbonyl, R １９ are E-1 to E-63, E-65 to E-70, E-72 to E-80, C １ ~C ６ Alkyl, C １ ~C ６ Alkylcarbonyl, C １ ~C ６ Alkoxycarbonyl, C １ ~C ６ Alkylsulfonyl or R ２０ (C １ ~C ６ ) alkyl, R ２０ represents E-1 to E-83, and R ６２ is a hydrogen atom or C １ ~C ６ represents alkyl; Z １ is a halogen atom, C １ ~C ６ Alkyl, C ２ ~C ６ Alkenyl, C ２ ~C ６ Alkynyl, halo(C １ ~C ６) alkyl, halo (C ２ ~C ６ ) alkenyl, halo(C ２ ~C ６ ) alkynyl, C １ ~C ６ Alkoxy, halo (C １ ~C ６ ) alkoxy, C ２ ~C ６ Alkenyloxy, halo(C ２ ~C ６ ) alkenyloxy, C ２ ~C ６ Alkynyloxy, halo(C ２ ~C ６ ) alkynyloxy, hydroxy, C １ ~C ６ Alkylcarbonyloxy, C １ ~C ６ Alkoxycarbonyloxy, C １ ~C ６ Alkyl sulfonyloxy, halo(C １ ~C ６ ) alkylsulfonyloxy, —OC(O)N(R ２６ ) R ２７ , C １ ~C ６ Alkylthio, C １ ~C ６ Alkylsulfinyl, C １ ~C ６ Alkyl sulfonyl, halo(C １ ~C ６ ) alkylthio, halo(C １ ~C ６ ) alkylsulfinyl, halo(C １ ~C ６ ) alkylsulfonyl, C ２ ~C ６ Alkenylthio, C ２ ~C ６ Alkenylsulfinyl, C ２ ~C ６ Alkenylsulfonyl, halo(C ２ ~C ６ ) alkenylthio, halo(C ２ ~C ６ ) alkenylsulfinyl, halo(C ２ ~C６ ) alkenylsulfonyl, C ２ ~C ６ Alkynylthio, C ２ ~C ６ Alkynylsulfinyl, C ２ ~C ６ Alkynylsulfonyl, halo(C ２ ~C ６ ) alkynylthio, halo(C ２ ~C ６ ) alkynylsulfinyl, halo(C ２ ~C ６ ) alkynylsulfonyl, —SO ３ H, -S(O) ２ N (R ２８ ) R ２９ , -SC≡N, -S(O)(=NR ３０ ) R ３１ , -SF ５ , -N(R ３２ ) R ３３ , -N=S(O)(R ５４ ) R ５５ , formyl, carboxy, C １ ~C ６ Alkylcarbonyl, halo(C １ ~C ６ ) alkylcarbonyl, C １ ~C ６ Alkoxycarbonyl, halo(C １ ~C ６ ) alkoxycarbonyl, —C(O)N(R ３５ ) R ３６ , -C(=NOR １２ ) R １３ , Tori (C １ ~C ６ ) alkylsilyl, R ７ (C １ ~C ６ ) alkyl, R １６ (C １ ~C ６ ) alkoxy, C ３ ~C ６ Cycloalkyl, R ５８ (C ３ ~C ６) cycloalkyl, cyano, nitro, E-1 to E-56, E-61 to E-83, -O-(E-1) to -O-(E-63), -O-(E-65) to -O-(E-70), -O-(E-72) to -O-(E-80), -S-(E-1) to -S-(E-63), -S-(E-65) to -S-(E-70), -S-(E-72) to -S-(E-80), -S(O)-(E-1) to -S(O)-(E-83), -S(O) ２ -(E-1)~-S(O) ２ -(E-83), -C(O)-(E-1) to -C(O)-(E-83), -N=N-(E-1) to -N=N-(E-63), -N=N-(E-65) to -N=N-(E-70), or -N=N-(E-72) to -N=N-(E-80), Z １ In the above relationship, when t2 represents an integer of 2, t3 represents an integer of 2 or 3, t4 represents an integer of 2, 3 or 4, and t5 represents an integer of 2, 3, 4 or 5, each of Z １ may be the same as or different from each other, １ is a halogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl, C １ ~C ６ Alkoxy, C １ ~C ６ Alkylthio, halo(C １ ~C ６ ) alkylthio, C １ ~C ６ Alkylsulfinyl, C １ ~C ６ represents alkylsulfonyl or cyano; １ In the above relationship, when t2 represents an integer of 2, t3 represents an integer of 2 or 3, t4 represents an integer of 2, 3 or 4, and t5 represents an integer of 2, 3, 4 or 5, each E １ may be the same as or different from each other, ３ is a hydrogen atom, C １ ~C ６ Alkyl or halo(C １ ~C ６ ) alkyl, R ７is C １ ~C ６ Alkoxy (C １ ~C ６ ) alkoxy, cyano, C １ ~C ６ Alkoxy, C １ ~C ６ Alkylcarbonyloxy, carboxy, C １ ~C ６ Alkylcarbonyl, C １ ~C ６ Alkoxycarbonyl, —C(O)N(R ３７ ) R ３８ , -N(R ３９ ) R ４０ , C １ ~C ６ Alkylthio, C １ ~C ６ alkylsulfonyl or E-1 to E-83, １６ is C １ ~C ６ Alkylthio, C １ ~C ６ Alkylsulfinyl, C １ ~C ６ Alkylsulfonyl, —C(O)N(R ４１ ) R ４２ , C １ ~C ６ Alkoxy, halo (C １ ~C ６ ) alkoxy, C １ ~C ６ Alkoxy (C １ ~C ６ ) alkoxy, E-1 to E-83, or —C(O)—(E-1) to —C(O)—(E-83), R １２ is a hydrogen atom, C １ ~C ６ Alkyl or halo(C １ ~C ６ ) alkyl, R １３ is a hydrogen atom, C １ ~C ６ Alkyl or halo(C １ ~C ６ ) alkyl; Z ３ is a hydrogen atom, C １ ~C ６Alkyl, halo (C １ ~C ６ ) alkyl, C １ ~C ６ Alkoxy (C １ ~C ６ ) alkyl, C １ ~C ６ Alkylcarbonyl, halo(C １ ~C ６ ) alkylcarbonyl, C １ ~C ６ Alkoxycarbonyl or halo(C １ ~C ６ ) alkoxycarbonyl; R ２６ is a hydrogen atom or C １ ~C ６ represents alkyl, R ２７ is a hydrogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl or C ３ ~C ６ represents cycloalkyl, R ２８ is a hydrogen atom or C １ ~C ６ represents alkyl, R ２９ is a hydrogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl, C ３ ~C ６ Cycloalkyl, C １ ~C ６ Alkylcarbonyl, halo(C １ ~C ６ ) alkylcarbonyl or C １ ~C ６ represents an alkoxycarbonyl; R ３０ is a hydrogen atom, C １ ~C ６ Alkyl or halo(C １ ~C ６ ) alkyl, R ３１ is C １ ~C ６ Alkyl or halo(C １ ~C ６ ) alkyl, R３２ is a hydrogen atom or C １ ~C ６ represents alkyl, R ３３ is a hydrogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl, C １ ~C ６ Alkylcarbonyl, halo(C １ ~C ６ ) alkylcarbonyl, C １ ~C ６ Alkoxycarbonyl, halo(C １ ~C ６ ) alkoxycarbonyl, C １ ~C ６ Alkylaminocarbonyl, di(C １ ~C ６ ) alkylaminocarbonyl, —C(O)NHC(O)OR ３４ , -C(S)NHC(O)OR ３４ or C １ ~C ６ represents alkylsulfonyl, R ３４ is C １ ~C ６ represents alkyl, R ３５ is a hydrogen atom or C １ ~C ６ represents alkyl, R ３６ is a hydrogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl or C ３ ~C ６ represents cycloalkyl, R ３７ is a hydrogen atom or C １ ~C ６ represents alkyl, R ３８ is a hydrogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl or C ３ ~C ６ represents cycloalkyl, R ３９ is a hydrogen atom, C １ ~C ６Alkyl or halo(C １ ~C ６ ) alkyl, R ４０ is a hydrogen atom, C １ ~C ６ Alkyl, C １ ~C ６ Alkylcarbonyl or C １ ~C ６ represents an alkoxycarbonyl; R ４１ is a hydrogen atom or C １ ~C ６ represents alkyl, R ４２ is a hydrogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl or C ３ ~C ６ represents cycloalkyl, R ５４ is C １ ~C ６ represents alkyl, R ５５ is C １ ~C ６ represents alkyl, R ５８ is a halogen atom, C １ ~C ６ alkoxy or cyano, J represents J-1 to J-52, Z ５ is a hydrogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl, C １ ~C ６ Alkoxy (C １ ~C ６ ) alkyl, C １ ~C ６ Alkylcarbonyl, halo(C １ ~C ６ ) alkylcarbonyl, C １ ~C ６ Alkoxycarbonyl, halo(C １ ~C ６ ) alkoxycarbonyl, C １ ~C ６ Alkyl sulfonyl or halo(C １ ~C ６) alkylsulfonyl; G represents G-1 to G-65; Z ２ is a halogen atom, C １ ~C ６ Alkyl, C ２ ~C ６ Alkenyl, C ２ ~C ６ Alkynyl, halo(C １ ~C ６ ) alkyl, halo (C ２ ~C ６ ) alkenyl, halo(C ２ ~C ６ ) alkynyl, C １ ~C ６ Alkoxy, halo (C １ ~C ６ ) alkoxy, C ２ ~C ６ Alkenyloxy, halo(C ２ ~C ６ ) alkenyloxy, C ２ ~C ６ Alkynyloxy, halo(C ２ ~C ６ ) alkynyloxy, hydroxy, C １ ~C ６ Alkylcarbonyloxy, C １ ~C ６ Alkoxycarbonyloxy, C １ ~C ６ Alkyl sulfonyloxy, halo(C １ ~C ６ ) alkylsulfonyloxy, —OC(O)N(R ６０ ) R ６１ , C １ ~C ６ Alkylthio, C １ ~C ６ Alkylsulfinyl, C １ ~C ６ Alkyl sulfonyl, halo(C １ ~C ６ ) alkylthio, halo(C １ ~C ６ ) alkylsulfinyl, halo(C １ ~C ６ ) alkylsulfonyl, C２ ~C ６ Alkenylthio, C ２ ~C ６ Alkenylsulfinyl, C ２ ~C ６ Alkenylsulfonyl, halo(C ２ ~C ６ ) alkenylthio, halo(C ２ ~C ６ ) alkenylsulfinyl, halo(C ２ ~C ６ ) alkenylsulfonyl, C ２ ~C ６ Alkynylthio, C ２ ~C ６ Alkynylsulfinyl, C ２ ~C ６ Alkynylsulfonyl, halo(C ２ ~C ６ ) alkynylthio, halo(C ２ ~C ６ ) alkynylsulfinyl, halo(C ２ ~C ６ ) alkynylsulfonyl, —SO ３ H, -S(O) ２ N (R ４８ ) R ４９ , -SC≡N, -S(O)(=NR ５２ ) R ５３ , -SF ５ , -N(R ４４ ) R ４５ , -N=S(O)(R ５６ ) R ５７ , formyl, carboxy, C １ ~C ６ Alkylcarbonyl, halo(C １ ~C ６ ) alkylcarbonyl, C １ ~C ６ Alkoxycarbonyl, halo(C １ ~C ６ ) alkoxycarbonyl, —C(O)N(R ４６ ) R ４７ , -C(=NOR １４ ) R １５ , Tori (C １ ~C ６ ) alkylsilyl, R ２４(C １ ~C ６ ) alkyl, R ２５ (C １ ~C ６ ) alkoxy, C ３ ~C ６ Cycloalkyl, R ５９ (C ３ ~C ６ ) represents cycloalkyl, cyano, nitro, M-1 to M-56, M-61 to M-82, —O-(M-1) to —O-(M-63), —O-(M-65) to —O-(M-70), or —O-(M-72) to —O-(M-80); Z ２ In the above relationship, when t2 represents an integer of 2, t3 represents an integer of 2 or 3, t4 represents an integer of 2, 3 or 4, and t5 represents an integer of 2, 3, 4 or 5, each of Z ２ may be the same as or different from each other, R ２４ is C １ ~C ６ Alkoxy, hydroxy or -N(R ５０ ) R ５１ represents R ２５ is C １ ~C ６ represents alkoxy or M-1 to M-82, １ is a halogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl, C １ ~C ６ Alkoxy, C １ ~C ６ Alkylthio, halo(C １ ~C ６ ) alkylthio, C １ ~C ６ Alkylsulfinyl, C １ ~C ６ represents alkylsulfonyl or cyano; M １ In the above relationship, when t2 represents an integer of 2, t3 represents an integer of 2 or 3, t4 represents an integer of 2, 3 or 4, and t5 represents an integer of 2, 3, 4 or 5, each of M１ may be the same as or different from each other, M ３ is a hydrogen atom, C １ ~C ６ Alkyl or halo(C １ ~C ６ ) alkyl, R １４ is a hydrogen atom, C １ ~C ６ Alkyl or halo(C １ ~C ６ ) alkyl, R １５ is a hydrogen atom, C １ ~C ６ Alkyl or halo(C １ ~C ６ ) alkyl; Z ４ is a hydrogen atom, C １ ~C ６ Alkyl, C １ ~C ６ Alkylcarbonyl, C １ ~C ６ Alkoxycarbonyl, C １ ~C ６ Alkoxy (C １ ~C ６ ) alkyl or C １ ~C ６ represents alkylsulfonyl, R ４４ is a hydrogen atom, C １ ~C ６ Alkyl or halo(C １ ~C ６ ) alkyl, R ４５ is a hydrogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl, C １ ~C ６ Alkylcarbonyl, halo(C １ ~C ６ ) alkylcarbonyl, C １ ~C ６ Alkoxycarbonyl, halo(C １ ~C ６ ) alkoxycarbonyl, C １ ~C ６ Alkyl sulfonyl or halo(C １~C ６ ) represents alkylsulfonyl, R ４６ is a hydrogen atom or C １ ~C ６ represents alkyl, R ４７ is a hydrogen atom, C １ ~C ６ Alkyl or halo(C １ ~C ６ ) alkyl, R ４８ is a hydrogen atom, C １ ~C ６ Alkyl or halo(C １ ~C ６ ) alkyl, R ４９ is a hydrogen atom, C １ ~C ６ Alkyl or halo(C １ ~C ６ ) alkyl, R ５０ is a hydrogen atom or C １ ~C ６ represents alkyl, R ５１ is a hydrogen atom, C １ ~C ６ Alkyl, C １ ~C ６ Alkylcarbonyl, halo(C １ ~C ６ ) alkylcarbonyl, C １ ~C ６ Alkoxycarbonyl, halo(C １ ~C ６ ) alkoxycarbonyl, C １ ~C ６ Alkyl sulfonyl or halo(C １ ~C ６ ) represents alkylsulfonyl, R ５２ is a hydrogen atom or C １ ~C ６ represents alkyl, R ５３ is C １ ~C ６ represents alkyl, R ５６ is C １ ~C ６ represents alkyl, R ５７ is C １ ~C ６ represents alkyl, R ５９is a halogen atom, C １ ~C ６ represents alkoxy or cyano; R ６０ is a hydrogen atom or C １ ~C ６ represents alkyl, R ６１ is a hydrogen atom, C １ ~C ６ Alkyl or halo(C １ ~C ６ ) alkyl, R １ represents a hydrogen atom, a halogen atom, or C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl, C １ ~C ６ Alkoxy, hydroxy, C １ ~C ６ Alkylthio, C １ ~C ６ Alkylsulfinyl, C １ ~C ６ Alkyl sulfonyl, halo(C １ ~C ６ ) alkylthio, halo(C １ ~C ６ ) alkylsulfinyl, halo(C １ ~C ６ ) alkylsulfonyl, —N(R １ｄ ) R １ｅ , cyano or nitro; R １ａ represents a hydrogen atom, a halogen atom, or C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl, C １ ~C ６ Alkoxy, hydroxy, -N(R １ｄ ) R １ｅ , cyano or nitro; R １ｂ represents a hydrogen atom, a halogen atom, or C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl, C １ ~C ６ Alkoxy, hydroxy, -N(R １ｄ ) R１ｅ , cyano or nitro; R １ｃ represents a hydrogen atom, a halogen atom, or C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl, C １ ~C ６ Alkoxy, hydroxy, -N(R １ｄ ) R １ｅ , cyano or nitro; R １ｄ is a hydrogen atom or C １ ~C ６ represents alkyl, R １ｅ is a hydrogen atom or C １ ~C ６ represents alkyl, R ２ is a hydrogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl, C ２ ~C ６ Alkenyl, C ２ ~C ６ Alkynyl, C ３ ~C ６ cycloalkyl, —C(O)R ４ , -C(O)OR ５ or R ６７ (C １ ~C ６ ) alkyl, R ６７ is C １ ~C ６ Alkoxy, C １ ~C ６ Alkylthio, C １ ~C ６ Alkylsulfinyl, C １ ~C ６ alkylsulfonyl, cyano, or V-1 to V-82; V １ is a halogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl, C １ ~C ６ Alkoxy, C １ ~C６ Alkylthio, C １ ~C ６ Alkylsulfinyl, C １ ~C ６ represents alkylsulfonyl, cyano or nitro; V １ In the above relationship, when t2 represents an integer of 2, t3 represents an integer of 2 or 3, t4 represents an integer of 2, 3 or 4, and t5 represents an integer of 2, 3, 4 or 5, each of V １ may be the same as or different from each other, V ３ is a hydrogen atom, C １ ~C ６ Alkyl or halo(C １ ~C ６ ) alkyl, R ４ is C １ ~C ６ Alkyl, C ２ ~C ６ Alkenyl, C ２ ~C ６ Alkynyl, C １ ~C ６ Alkylcarbonyl, C １ ~C ６ Alkoxycarbonyl, C １ ~C ６ Alkylamino, di(C １ ~C ６ ) alkylamino, R ６ (C １ ~C ６ ) alkyl or V-1 to V-82, R ５ is C １ ~C ６ Alkyl, C ２ ~C ６ Alkenyl, C ２ ~C ６ Alkynyl, R ９ (C １ ~C ６ ) alkyl, V-1 to V-63, V-65 to V-70, or V-72 to V-80; R ６ is a halogen atom, C １ ~C ６ represents alkoxy, cyano, nitro, or V-1 to V-82; R ９is a halogen atom, C １ ~C ６ (ii) when Q is Q-B, Q-B is C １ ~C ６ Alkyl, R １７ (C １ ~C ６ ) alkyl, —N(R １８ ) R １９ , -OR ６２ or Q-1 to Q-82; R １７ is a halogen atom, C １ ~C ６ represents alkoxy or E-1 to E-83; R １８ is a hydrogen atom, C １ ~C ６ Alkyl or C ２ ~C ６ represents alkenyloxycarbonyl, R １９ are E-1 to E-63, E-65 to E-70, E-72 to E-80, C １ ~C ６ Alkyl, C １ ~C ６ Alkylcarbonyl, C １ ~C ６ Alkoxycarbonyl, C １ ~C ６ Alkylsulfonyl or R ２０ (C １ ~C ６ ) alkyl, R ２０ represents E-1 to E-83, and R ６２ is a hydrogen atom or C １ ~C ６ represents alkyl; Z １ is a halogen atom, C １ ~C ６ Alkyl, C ２ ~C ６ Alkenyl, C ２ ~C ６ Alkynyl, halo(C １ ~C ６) alkyl, halo (C ２ ~C ６ ) alkenyl, halo(C ２ ~C ６ ) alkynyl, C １ ~C ６ Alkoxy, halo (C １ ~C ６ ) alkoxy, C １ ~C ６ Alkenyloxy, halo(C ２ ~C ６ ) alkenyloxy, C １ ~C ６ Alkynyloxy, halo(C ２ ~C ６ ) alkynyloxy, hydroxy, C １ ~C ６ Alkylcarbonyloxy, C １ ~C ６ Alkoxycarbonyloxy, C １ ~C ６ Alkyl sulfonyloxy, halo(C １ ~C ６ ) alkylsulfonyloxy, —OC(O)N(R ２６ ) R ２７ , C １ ~C ６ Alkylthio, C １ ~C ６ Alkylsulfinyl, C １ ~C ６ Alkyl sulfonyl, halo(C １ ~C ６ ) alkylthio, halo(C １ ~C ６ ) alkylsulfinyl, halo(C １ ~C ６ ) alkylsulfonyl, C ２ ~C ６ Alkenylthio, C ２ ~C ６ Alkenylsulfinyl, C ２ ~C ６ Alkenylsulfonyl, halo(C ２ ~C ６ ) alkenylthio, halo(C ２ ~C ６ ) alkenylsulfinyl, halo(C ２ ~C６ ) alkenylsulfonyl, C ２ ~C ６ Alkynylthio, C ２ ~C ６ Alkynylsulfinyl, C ２ ~C ６ Alkynylsulfonyl, halo(C ２ ~C ６ ) alkynylthio, halo(C ２ ~C ６ ) alkynylsulfinyl, halo(C ２ ~C ６ ) alkynylsulfonyl, —SO ３ H, -S(O) ２ N (R ２８ ) R ２９ , -SC≡N, -S(O)(=NR ３０ ) R ３１ , -SF ５ , -N(R ３２ ) R ３３ , -N=S(O)(R ５４ ) R ５５ , formyl, carboxy, C １ ~C ６ Alkylcarbonyl, halo(C １ ~C ６ ) alkylcarbonyl, C １ ~C ６ Alkoxycarbonyl, halo(C １ ~C ６ ) alkoxycarbonyl, —C(O)N(R ３５ ) R ３６ , -C(=NOR １２ ) R １３ , Tori (C １ ~C ６ ) alkylsilyl, R ７ (C １ ~C ６ ) alkyl, R １６ (C １ ~C ６ ) alkoxy, C ３ ~C ６ Cycloalkyl, R ５８ (C ３ ~C ６) cycloalkyl, cyano, nitro, E-1 to E-56, E-61 to E-83, -O-(E-1) to -O-(E-63), -O-(E-65) to -O-(E-70), -O-(E-72) to -O-(E-80), -S-(E-1) to -S-(E-63), -S-(E-65) to -S-(E-70), -S-(E-72) to -S-(E-80), -S(O)-(E-1) to -S(O)-(E-83), -S(O) ２ -(E-1)~-S(O) ２ -(E-83), -C(O)-(E-1) to -C(O)-(E-83), -N=N-(E-1) to -N=N-(E-63), -N=N-(E-65) to -N=N-(E-70), or -N=N-(E-72) to -N=N-(E-80), Z １ In the above relationship, when t2 represents an integer of 2, t3 represents an integer of 2 or 3, t4 represents an integer of 2, 3 or 4, and t5 represents an integer of 2, 3, 4 or 5, each of Z １ may be the same as or different from each other, １ is a halogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl, C １ ~C ６ Alkoxy, C １ ~C ６ Alkylthio, halo(C １ ~C ６ ) alkylthio, C １ ~C ６ Alkylsulfinyl, C １ ~C ６ represents alkylsulfonyl or cyano; １ In the above relationship, when t2 represents an integer of 2, t3 represents an integer of 2 or 3, t4 represents an integer of 2, 3 or 4, and t5 represents an integer of 2, 3, 4 or 5, each E １ may be the same as or different from each other, ３ is a hydrogen atom, C １ ~C ６ Alkyl or halo(C １ ~C ６ ) alkyl, R ７is C １ ~C ６ Alkoxy (C １ ~C ６ ) alkoxy, cyano, C １ ~C ６ Alkoxy, C １ ~C ６ Alkylcarbonyloxy, carboxy, C １ ~C ６ Alkylcarbonyl, C １ ~C ６ Alkoxycarbonyl, —C(O)N(R ３７ ) R ３８ , -N(R ３９ ) R ４０ , C １ ~C ６ Alkylthio, C １ ~C ６ alkylsulfonyl or E-1 to E-83, １６ is C １ ~C ６ Alkylthio, C １ ~C ６ Alkylsulfinyl, C １ ~C ６ Alkylsulfonyl, —C(O)N(R ４１ ) R ４２ , C １ ~C ６ Alkoxy, halo (C １ ~C ６ ) alkoxy, C １ ~C ６ Alkoxy (C １ ~C ６ ) alkoxy, E-1 to E-83, or —C(O)—(E-1) to —C(O)—(E-83), R １２ is a hydrogen atom, C １ ~C ６ Alkyl or halo(C １ ~C ６ ) alkyl, R １３ is a hydrogen atom, C １ ~C ６ Alkyl or halo(C １ ~C ６ ) alkyl; Z ３ is a hydrogen atom, C １ ~C ６Alkyl, halo (C １ ~C ６ ) alkyl, C １ ~C ６ Alkoxy (C １ ~C ６ ) alkyl, C １ ~C ６ Alkylcarbonyl, halo(C １ ~C ６ ) alkylcarbonyl, C １ ~C ６ Alkoxycarbonyl or halo(C １ ~C ６ ) alkoxycarbonyl; R ２６ is a hydrogen atom or C １ ~C ６ represents alkyl, R ２７ is a hydrogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl or C ３ ~C ６ represents cycloalkyl, R ２８ is a hydrogen atom or C １ ~C ６ represents alkyl, R ２９ is a hydrogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl, C ３ ~C ６ Cycloalkyl, C １ ~C ６ Alkylcarbonyl, halo(C １ ~C ６ ) alkylcarbonyl or C １ ~C ６ represents an alkoxycarbonyl; R ３０ is a hydrogen atom, C １ ~C ６ Alkyl or halo(C １ ~C ６ ) alkyl, R ３１ is C １ ~C ６ Alkyl or halo(C １ ~C ６ ) alkyl, R３２ is a hydrogen atom or C １ ~C ６ represents alkyl, R ３３ is a hydrogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl, C １ ~C ６ Alkylcarbonyl, halo(C １ ~C ６ ) alkylcarbonyl, C １ ~C ６ Alkoxycarbonyl, halo(C １ ~C ６ ) alkoxycarbonyl, C １ ~C ６ Alkylaminocarbonyl, di(C １ ~C ６ ) alkylaminocarbonyl, —C(O)NHC(O)OR ３４ , -C(S)NHC(O)OR ３４ or C １ ~C ６ represents alkylsulfonyl, R ３４ is C １ ~C ６ represents alkyl, R ３５ is a hydrogen atom or C １ ~C ６ represents alkyl, R ３６ is a hydrogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl or C ３ ~C ６ represents cycloalkyl, R ３７ is a hydrogen atom or C １ ~C ６ represents alkyl, R ３８ is a hydrogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl or C ３ ~C ６ represents cycloalkyl, R ３９ is a hydrogen atom, C １ ~C ６Alkyl or halo(C １ ~C ６ ) alkyl, R ４０ is a hydrogen atom, C １ ~C ６ Alkyl, C １ ~C ６ Alkylcarbonyl or C １ ~C ６ represents an alkoxycarbonyl; R ４１ is a hydrogen atom or C １ ~C ６ represents alkyl, R ４２ is a hydrogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl or C ３ ~C ６ represents cycloalkyl, R ５４ is C １ ~C ６ represents alkyl, R ５５ is C １ ~C ６ represents alkyl, R ５８ is a halogen atom, C １ ~C ６ alkoxy or cyano, J represents J-1′ or J-2′, A １ is a nitrogen atom or CR １ｃ G represents -N(R ２１ ) R ２２ , -C(=NOR ６７ ) R ６８ , R ６９ (C １ ~C ６ ) alkyl or G-1′ to G-160′, R ２１ is a hydrogen atom, C １ ~C ６ Alkyl or halo(C １ ~C ６ ) alkyl, R ２２ is a hydrogen atom, C １ ~C ６Alkyl, halo (C １ ~C ６ ) alkyl, C ２ ~C ６ Alkenyl, halo(C ２ ~C ６ ) alkenyl, C ２ ~C ６ Alkynyl, halo(C ２ ~C ６ ) alkynyl, R ２３ (C １ ~C ６ ) alkyl or M-1 to M-82, R ２３ is C １ ~C ６ Alkoxy, C １ ~C ６ Alkylcarbonyl, C １ ~C ６ Alkoxycarbonyl, hydroxy, cyano, C １ ~C ６ Alkylamino, di(C １ ~C ６ ) alkylamino, C １ ~C ６ Alkylcarbonylamino, C １ ~C ６ represents alkoxycarbonylamino or M-1 to M-82, ６７ is a hydrogen atom, C １ ~C ６ Alkyl or halo(C １ ~C ６ ) alkyl, R ６８ is a hydrogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl or M-1 to M-82, R ６９ M-1 to M-82, -N(R ７０ ) R ７１ , -C(=O)N(R ７２ ) R ７３ or -C(=NOR ７４ ) R ７５ represents R ７０ is a hydrogen atom or C １ ~C ６represents alkyl, R ７１ is -C(=O)R ７６ represents R ７６ is C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl or M-1 to M-82, R ７２ is a hydrogen atom or C １ ~C ６ represents alkyl, R ７３ represents M-1 to M-82, and R ７４ is a hydrogen atom or C １ ~C ６ represents alkyl, R ７５ is a hydrogen atom, C １ ~C ６ Alkyl or C ３ ~C ６ represents cycloalkyl; Z ２ is a halogen atom, C １ ~C ６ Alkyl, C ２ ~C ６ Alkenyl, C ２ ~C ６ Alkynyl, halo(C １ ~C ６ ) alkyl, halo (C ２ ~C ６ ) alkenyl, halo(C ２ ~C ６ ) alkynyl, C １ ~C ６ Alkoxy, halo (C １ ~C ６ ) alkoxy, C ２ ~C ６ Alkenyloxy, halo(C ２ ~C ６ ) alkenyloxy, C ２ ~C ６ Alkynyloxy, halo(C ２ ~C ６ ) alkynyloxy, hydroxy, C １ ~C ６ Alkylcarbonyloxy, C １ ~C ６ Alkoxycarbonyloxy, C １ ~C ６Alkyl sulfonyloxy, halo(C １ ~C ６ ) alkylsulfonyloxy, —OC(O)N(R ６０ ) R ６１ , C １ ~C ６ Alkylthio, C １ ~C ６ Alkylsulfinyl, C １ ~C ６ Alkyl sulfonyl, halo(C １ ~C ６ ) alkylthio, halo(C １ ~C ６ ) alkylsulfinyl, halo(C １ ~C ６ ) alkylsulfonyl, C ２ ~C ６ Alkenylthio, C ２ ~C ６ Alkenylsulfinyl, C ２ ~C ６ Alkenylsulfonyl, halo(C ２ ~C ６ ) alkenylthio, halo(C ２ ~C ６ ) alkenylsulfinyl, halo(C ２ ~C ６ ) alkenylsulfonyl, C ２ ~C ６ Alkynylthio, C ２ ~C ６ Alkynylsulfinyl, C ２ ~C ６ Alkynylsulfonyl, halo(C ２ ~C ６ ) alkynylthio, halo(C ２ ~C ６ ) alkynylsulfinyl, halo(C ２ ~C ６ ) alkynylsulfonyl, —SO ３ H, -S(O) ２ N (R ４８ ) R ４９ , -SC≡N, -S(O)(=NR ５２ ) R ５３ , -SF ５ , -N(R ４４ ) R ４５, -N=S(O)(R ５６ ) R ５７ , formyl, carboxy, C １ ~C ６ Alkylcarbonyl, halo(C １ ~C ６ ) alkylcarbonyl, C １ ~C ６ Alkoxycarbonyl, halo(C １ ~C ６ ) alkoxycarbonyl, —C(O)N(R ４６ ) R ４７ , -C(=NOR １４ ) R １５ , Tori (C １ ~C ６ ) alkylsilyl, R ２４ (C １ ~C ６ ) alkyl, R ２５ (C １ ~C ６ ) alkoxy, C ３ ~C ６ Cycloalkyl, R ５９ (C ３ ~C ６ ) represents cycloalkyl, cyano, nitro, M-1 to M-56, M-61 to M-82, —O-(M-1) to —O-(M-63), —O-(M-65) to —O-(M-70), or —O-(M-72) to —O-(M-80); Z ２ In the above relationship, when t2 represents an integer of 2, t3 represents an integer of 2 or 3, t4 represents an integer of 2, 3 or 4, and t5 represents an integer of 2, 3, 4 or 5, each of Z ２ may be the same as or different from each other; or t4 represents an integer of 2, and two Z ２ When two Z ２ together form oxo, -CH ２ CH ２ -, -OCH ２ CH ２ O-, -OCH ２ CH ２ CH ２ O-, = NOR ４３ , =NN(R ６３ ) R６４ or =NN=C(R ６５ ) R ６６ represents R ４３ is a hydrogen atom or C １ ~C ６ represents alkyl, R ２４ is C １ ~C ６ Alkoxy, hydroxy or -N(R ５０ ) R ５１ represents R ２５ is C １ ~C ６ represents alkoxy or M-1 to M-82, １ is a halogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl, C １ ~C ６ Alkoxy, C １ ~C ６ Alkylthio, halo(C １ ~C ６ ) alkylthio, C １ ~C ６ Alkylsulfinyl, C １ ~C ６ represents alkylsulfonyl or cyano; M １ In the above relationship, when t2 represents an integer of 2, t3 represents an integer of 2 or 3, t4 represents an integer of 2, 3 or 4, and t5 represents an integer of 2, 3, 4 or 5, each of M １ may be the same as or different from each other, M ３ is a hydrogen atom, C １ ~C ６ Alkyl or halo(C １ ~C ６ ) alkyl, R １４ is a hydrogen atom, C １ ~C ６ Alkyl or halo(C １ ~C ６ ) alkyl, R １５ is a hydrogen atom, C １ ~C ６ Alkyl or halo(C １ ~C ６ ) alkyl; Z４ is a hydrogen atom, C １ ~C ６ Alkyl, C １ ~C ６ Alkylcarbonyl, C １ ~C ６ Alkoxycarbonyl, C １ ~C ６ Alkoxy (C １ ~C ６ ) alkyl or C １ ~C ６ represents alkylsulfonyl, R ４４ is a hydrogen atom, C １ ~C ６ Alkyl or halo(C １ ~C ６ ) alkyl, R ４５ is a hydrogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl, C １ ~C ６ Alkylcarbonyl, halo(C １ ~C ６ ) alkylcarbonyl, C １ ~C ６ Alkoxycarbonyl, halo(C １ ~C ６ ) alkoxycarbonyl, C １ ~C ６ Alkyl sulfonyl or halo(C １ ~C ６ ) represents alkylsulfonyl, R ４６ is a hydrogen atom or C １ ~C ６ represents alkyl, R ４７ is a hydrogen atom, C １ ~C ６ Alkyl or halo(C １ ~C ６ ) alkyl, R ４８ is a hydrogen atom, C １ ~C ６ Alkyl or halo(C １ ~C ６ ) alkyl, R ４９ is a hydrogen atom, C １ ~C ６Alkyl or halo(C １ ~C ６ ) alkyl, R ５０ is a hydrogen atom or C １ ~C ６ represents alkyl, R ５１ is a hydrogen atom, C １ ~C ６ Alkyl, C １ ~C ６ Alkylcarbonyl, halo(C １ ~C ６ ) alkylcarbonyl, C １ ~C ６ Alkoxycarbonyl, halo(C １ ~C ６ ) alkoxycarbonyl, C １ ~C ６ Alkyl sulfonyl or halo(C １ ~C ６ ) represents alkylsulfonyl, R ５２ is a hydrogen atom or C １ ~C ６ represents alkyl, R ５３ is C １ ~C ６ represents alkyl, R ５６ is C １ ~C ６ represents alkyl, R ５７ is C １ ~C ６ represents alkyl, R ５９ is a halogen atom, C １ ~C ６ represents alkoxy or cyano; R ６０ is a hydrogen atom or C １ ~C ６ represents alkyl, R ６１ is a hydrogen atom, C １ ~C ６ Alkyl or halo(C １ ~C ６ ) alkyl, R ６３ is a hydrogen atom or C １ ~C ６ represents alkyl, R ６４ is a hydrogen atom, C １ ~C ６ Alkyl, C １~C ６ Alkylcarbonyl, halo(C １ ~C ６ ) alkylcarbonyl, C １ ~C ６ Alkoxycarbonyl, halo(C １ ~C ６ ) alkoxycarbonyl, C １ ~C ６ Alkyl sulfonyl or halo(C １ ~C ６ ) represents alkylsulfonyl, R ６５ is a hydrogen atom or C １ ~C ６ represents alkyl, R ６６ is C １ ~C ６ represents alkyl, R １ represents a hydrogen atom, a halogen atom, or C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl, C １ ~C ６ Alkoxy, hydroxy, C １ ~C ６ Alkylthio, C １ ~C ６ Alkylsulfinyl, C １ ~C ６ Alkyl sulfonyl, halo(C １ ~C ６ ) alkylthio, halo(C １ ~C ６ ) alkylsulfinyl, halo(C １ ~C ６ ) alkylsulfonyl, —N(R １ｄ ) R １ｅ , cyano or nitro; R １ａ represents a hydrogen atom, a halogen atom, or C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl, C １ ~C ６ Alkoxy, hydroxy, -N(R １ｄ ) R １ｅ , cyano or nitro; R １ｂrepresents a hydrogen atom, a halogen atom, or C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl, C １ ~C ６ Alkoxy, hydroxy, -N(R １ｄ ) R １ｅ , cyano or nitro; R １ｃ represents a hydrogen atom, a halogen atom, or C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl, C １ ~C ６ Alkoxy, hydroxy, -N(R １ｄ ) R １ｅ , cyano or nitro; R １ｄ is a hydrogen atom or C １ ~C ６ represents alkyl, R １ｅ is a hydrogen atom or C １ ~C ６ represents alkyl, R ２ is a hydrogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl, C ２ ~C ６ Alkenyl, C ２ ~C ６ Alkynyl, C ３ ~C ６ cycloalkyl, —C(O)R ４ , -C(O)OR ５ , or R ６７ (C １ ~C ６ ) alkyl, R ６７ is C １ ~C ６ Alkoxy, C １ ~C ６ Alkylthio, C １ ~C ６ Alkylsulfinyl, C １ ~C ６ alkylsulfonyl, cyano, or V-1 to V-82; V１ is a halogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl, C １ ~C ６ Alkoxy, C １ ~C ６ Alkylthio, C １ ~C ６ Alkylsulfinyl, C １ ~C ６ represents alkylsulfonyl, cyano or nitro; V １ In the above relationship, when t2 represents an integer of 2, t3 represents an integer of 2 or 3, t4 represents an integer of 2, 3 or 4, and t5 represents an integer of 2, 3, 4 or 5, each of V １ may be the same as or different from each other, V ３ is a hydrogen atom, C １ ~C ６ Alkyl or halo(C １ ~C ６ ) alkyl, R ４ is C １ ~C ６ Alkyl, C ２ ~C ６ Alkenyl, C ２ ~C ６ Alkynyl, C １ ~C ６ Alkylcarbonyl, C １ ~C ６ Alkoxycarbonyl, C １ ~C ６ Alkylamino, di(C １ ~C ６ ) alkylamino, R ６ (C １ ~C ６ ) alkyl or V-1 to V-82, R ５ is C １ ~C ６ Alkyl, C ２ ~C ６ Alkenyl, C ２ ~C ６ Alkynyl, R ９ (C １ ~C ６) alkyl, V-1 to V-63, V-65 to V-70, or V-72 to V-80; R ６ is a halogen atom, C １ ~C ６ represents alkoxy, cyano, nitro, or V-1 to V-82; R ９ is a halogen atom, C １ ~C ６ (iii) when Q is Q-C, Q-C is C １ ~C ６ Alkyl, R １７ (C １ ~C ６ ) alkyl, —N(R １８ ) R １９ , -OR ６２ or Q-1 to Q-82; R １７ is a halogen atom, C １ ~C ６ represents alkoxy or E-1 to E-83; R １８ is a hydrogen atom, C １ ~C ６ Alkyl or C ２ ~C ６ represents alkenyloxycarbonyl, R １９ are E-1 to E-63, E-65 to E-70, E-72 to E-80, C １ ~C ６ Alkyl, C １ ~C ６ Alkylcarbonyl, C １ ~C ６ Alkoxycarbonyl, C １ ~C ６ Alkylsulfonyl or R ２０ (C １ ~C ６ ) alkyl, R ２０ represents E-1 to E-83, and R ６２ is a hydrogen atom or C １ ~C ６ represents alkyl; Z １is a halogen atom, C １ ~C ６ Alkyl, C ２ ~C ６ Alkenyl, C ２ ~C ６ Alkynyl, halo(C １ ~C ６ ) alkyl, halo (C ２ ~C ６ ) alkenyl, halo(C ２ ~C ６ ) alkynyl, C １ ~C ６ Alkoxy, halo (C １ ~C ６ ) alkoxy, C ２ ~C ６ Alkenyloxy, halo(C ２ ~C ６ ) alkenyloxy, C ２ ~C ６ Alkynyloxy, halo(C ２ ~C ６ ) alkynyloxy, hydroxy, C １ ~C ６ Alkylcarbonyloxy, C １ ~C ６ Alkoxycarbonyloxy, C １ ~C ６ Alkyl sulfonyloxy, halo(C １ ~C ６ ) alkylsulfonyloxy, —OC(O)N(R ２６ ) R ２７ , C １ ~C ６ Alkylthio, C １ ~C ６ Alkylsulfinyl, C １ ~C ６ Alkyl sulfonyl, halo(C １ ~C ６ ) alkylthio, halo(C １ ~C ６ ) alkylsulfinyl, halo(C １ ~C ６ ) alkylsulfonyl, C ２ ~C ６ Alkenylthio, C ２ ~C ６ Alkenylsulfinyl, C２ ~C ６ Alkenylsulfonyl, halo(C ２ ~C ６ ) alkenylthio, halo(C ２ ~C ６ ) alkenylsulfinyl, halo(C ２ ~C ６ ) alkenylsulfonyl, C ２ ~C ６ Alkynylthio, C ２ ~C ６ Alkynylsulfinyl, C ２ ~C ６ Alkynylsulfonyl, halo(C ２ ~C ６ ) alkynylthio, halo(C ２ ~C ６ ) alkynylsulfinyl, halo(C ２ ~C ６ ) alkynylsulfonyl, —SO ３ H, -S(O) ２ N (R ２８ ) R ２９ , -SC≡N, -S(O)(=NR ３０ ) R ３１ , -SF ５ , -N(R ３２ ) R ３３ , -N=S(O)(R ５４ ) R ５５ , formyl, carboxy, C １ ~C ６ Alkylcarbonyl, halo(C １ ~C ６ ) alkylcarbonyl, C １ ~C ６ Alkoxycarbonyl, halo(C １ ~C ６ ) alkoxycarbonyl, —C(O)N(R ３５ ) R ３６ , -C(=NOR １２ ) R １３ , Tori (C １ ~C ６ ) alkylsilyl, R ７ (C １ ~C ６ ) alkyl, R １６ (C １ ~C６ ) alkoxy, C ３ ~C ６ Cycloalkyl, R ５８ (C ３ ~C ６ ) cycloalkyl, cyano, nitro, E-1 to E-56, E-61 to E-83, -O-(E-1) to -O-(E-63), -O-(E-65) to -O-(E-70), -O-(E-72) to -O-(E-80), -S-(E-1) to -S-(E-63), -S-(E-65) to -S-(E-70), -S-(E-72) to -S-(E-80), -S(O)-(E-1) to -S(O)-(E-83), -S(O) ２ -(E-1)~-S(O) ２ -(E-83), -C(O)-(E-1) to -C(O)-(E-83), -N=N-(E-1) to -N=N-(E-63), -N=N-(E-65) to -N=N-(E-70), or -N=N-(E-72) to -N=N-(E-80), Z １ In the above relationship, when t2 represents an integer of 2, t3 represents an integer of 2 or 3, t4 represents an integer of 2, 3 or 4, and t5 represents an integer of 2, 3, 4 or 5, each of Z １ may be the same as or different from each other, １ is a halogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl, C １ ~C ６ Alkoxy, C １ ~C ６ Alkylthio, halo(C １ ~C ６ ) alkylthio, C １ ~C ６ Alkylsulfinyl, C １ ~C ６ represents alkylsulfonyl or cyano; １ In the above relationship, when t2 represents an integer of 2, t3 represents an integer of 2 or 3, t4 represents an integer of 2, 3 or 4, and t5 represents an integer of 2, 3, 4 or 5, each E １ may be the same as or different from each other,３ is a hydrogen atom, C １ ~C ６ Alkyl or halo(C １ ~C ６ ) alkyl, R ７ is C １ ~C ６ Alkoxy (C １ ~C ６ ) alkoxy, cyano, C １ ~C ６ Alkoxy, C １ ~C ６ Alkylcarbonyloxy, carboxy, C １ ~C ６ Alkylcarbonyl, C １ ~C ６ Alkoxycarbonyl, —C(O)N(R ３７ ) R ３８ , -N(R ３９ ) R ４０ , C １ ~C ６ Alkylthio, C １ ~C ６ alkylsulfonyl or E-1 to E-83, １６ is C １ ~C ６ Alkylthio, C １ ~C ６ Alkylsulfinyl, C １ ~C ６ Alkylsulfonyl, —C(O)N(R ４１ ) R ４２ , C １ ~C ６ Alkoxy, halo (C １ ~C ６ ) alkoxy, C １ ~C ６ Alkoxy (C １ ~C ６ ) alkoxy, E-1 to E-83, or —C(O)—(E-1) to —C(O)—(E-83), R １２ is a hydrogen atom, C １ ~C ６ Alkyl or halo(C １ ~C ６ ) alkyl, R １３ is a hydrogen atom, C １ ~C６ Alkyl or halo(C １ ~C ６ ) alkyl; Z ３ is a hydrogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl, C １ ~C ６ Alkoxy (C １ ~C ６ ) alkyl, C １ ~C ６ Alkylcarbonyl, halo(C １ ~C ６ ) alkylcarbonyl, C １ ~C ６ Alkoxycarbonyl or halo(C １ ~C ６ ) alkoxycarbonyl; R ２６ is a hydrogen atom or C １ ~C ６ represents alkyl, R ２７ is a hydrogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl or C ３ ~C ６ represents cycloalkyl, R ２８ is a hydrogen atom or C １ ~C ６ represents alkyl, R ２９ is a hydrogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl, C ３ ~C ６ Cycloalkyl, C １ ~C ６ Alkylcarbonyl, halo(C １ ~C ６ ) alkylcarbonyl or C １ ~C ６ represents an alkoxycarbonyl; R ３０ is a hydrogen atom, C １ ~C ６ Alkyl or halo(C １ ~C ６) alkyl, R ３１ is C １ ~C ６ Alkyl or halo(C １ ~C ６ ) alkyl, R ３２ is a hydrogen atom or C １ ~C ６ represents alkyl, R ３３ is a hydrogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl, C １ ~C ６ Alkylcarbonyl, halo(C １ ~C ６ ) alkylcarbonyl, C １ ~C ６ Alkoxycarbonyl, halo(C １ ~C ６ ) alkoxycarbonyl, C １ ~C ６ Alkylaminocarbonyl, di(C １ ~C ６ ) alkylaminocarbonyl, —C(O)NHC(O)OR ３４ , -C(S)NHC(O)OR ３４ or C １ ~C ６ represents alkylsulfonyl, R ３４ is C １ ~C ６ represents alkyl, R ３５ is a hydrogen atom or C １ ~C ６ represents alkyl, R ３６ is a hydrogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl or C ３ ~C ６ represents cycloalkyl, R ３７ is a hydrogen atom or C １ ~C ６ represents alkyl, R ３８ is a hydrogen atom, C １ ~C ６ Alkyl, halo (C １ ~C６ ) alkyl or C ３ ~C ６ represents cycloalkyl, R ３９ is a hydrogen atom, C １ ~C ６ Alkyl or halo(C １ ~C ６ ) alkyl, R ４０ is a hydrogen atom, C １ ~C ６ Alkyl, C １ ~C ６ Alkylcarbonyl or C １ ~C ６ represents an alkoxycarbonyl; R ４１ is a hydrogen atom or C １ ~C ６ represents alkyl, R ４２ is a hydrogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl or C ３ ~C ６ represents cycloalkyl, R ５４ is C １ ~C ６ represents alkyl, R ５５ is C １ ~C ６ represents alkyl, R ５８ is a halogen atom, C １ ~C ６ alkoxy or cyano, J represents J-1 to J-52, Z ５ is a hydrogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl, C １ ~C ６ Alkoxy (C １ ~C ６ ) alkyl, C １ ~C ６ Alkylcarbonyl, halo(C １ ~C ６ ) alkylcarbonyl, C １ ~C ６ Alkoxycarbonyl, halo(C１ ~C ６ ) alkoxycarbonyl, C １ ~C ６ Alkyl sulfonyl or halo(C １ ~C ６ ) represents alkylsulfonyl, R １ represents a hydrogen atom, a halogen atom, or C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl, C １ ~C ６ Alkoxy, hydroxy, C １ ~C ６ Alkylthio, C １ ~C ６ Alkylsulfinyl, C １ ~C ６ Alkyl sulfonyl, halo(C １ ~C ６ ) alkylthio, halo(C １ ~C ６ ) alkylsulfinyl, halo(C １ ~C ６ ) alkylsulfonyl, —N(R １ｄ ) R １ｅ , cyano or nitro; R １ａ represents a hydrogen atom, a halogen atom, or C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl, C １ ~C ６ Alkoxy, hydroxy, -N(R １ｄ ) R １ｅ , cyano or nitro; R １ｂ represents a hydrogen atom, a halogen atom, or C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl, C １ ~C ６ Alkoxy, hydroxy, -N(R １ｄ ) R １ｅ , cyano or nitro; R １ｃ represents a hydrogen atom, a halogen atom, or C １ ~C ６ Alkyl, halo (C１ ~C ６ ) alkyl, C １ ~C ６ Alkoxy, hydroxy, -N(R １ｄ ) R １ｅ , cyano or nitro; R １ｄ is a hydrogen atom or C １ ~C ６ represents alkyl, R １ｅ is a hydrogen atom or C １ ~C ６ G represents an alkyl group; ２１ ) R ２２ , -C(=NOR ６７ ) R ６８ , R ６９ (C １ ~C ６ ) alkyl or G-1′ to G-160′, R ２１ is a hydrogen atom, C １ ~C ６ Alkyl or halo(C １ ~C ６ ) alkyl, R ２２ is a hydrogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl, C ２ ~C ６ Alkenyl, halo(C ２ ~C ６ ) alkenyl, C ２ ~C ６ Alkynyl, halo(C ２ ~C ６ ) alkynyl, R ２３ (C １ ~C ６ ) alkyl or M-1 to M-82, R ２３ is C １ ~C ６ Alkoxy, C １ ~C ６ Alkylcarbonyl, C １ ~C６ Alkoxycarbonyl, hydroxy, cyano, C １ ~C ６ Alkylamino, di(C １ ~C ６ ) alkylamino, C １ ~C ６ Alkylcarbonylamino, C １ ~C ６ represents alkoxycarbonylamino or M-1 to M-82, ６７ is a hydrogen atom, C １ ~C ６ Alkyl or halo(C １ ~C ６ ) alkyl, R ６８ is a hydrogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl or M-1 to M-82, R ６９ M-1 to M-82, -N(R ７０ ) R ７１ , -C(=O)N(R ７２ ) R ７３ or -C(=NOR ７４ ) R ７５ represents R ７０ is a hydrogen atom or C １ ~C ６ represents alkyl, R ７１ is -C(=O)R ７６ represents R ７６ is C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl or M-1 to M-82, R ７２ is a hydrogen atom or C １ ~C ６ represents alkyl, R ７３ represents M-1 to M-82, and R ７４ is a hydrogen atom or C １ ~C ６ represents alkyl, R ７５ is a hydrogen atom, C １ ~C ６ Alkyl or C ３ ~C ６represents cycloalkyl; Z ４ is a hydrogen atom, C １ ~C ６ Alkyl, C １ ~C ６ Alkoxy (C １ ~C ６ ) alkyl, C １ ~C ６ Alkylcarbonyl, C １ ~C ６ Alkoxycarbonyl or C １ ~C ６ represents alkylsulfonyl; Z ２ is a halogen atom, C １ ~C ６ Alkyl, C ２ ~C ６ Alkenyl, C ２ ~C ６ Alkynyl, halo(C １ ~C ６ ) alkyl, halo (C ２ ~C ６ ) alkenyl, halo(C ２ ~C ６ ) alkynyl, C １ ~C ６ Alkoxy, halo (C １ ~C ６ ) alkoxy, C ２ ~C ６ Alkenyloxy, halo(C ２ ~C ６ ) alkenyloxy, C ２ ~C ６ Alkynyloxy, halo(C ２ ~C ６ ) alkynyloxy, hydroxy, C １ ~C ６ Alkylcarbonyloxy, C １ ~C ６ Alkoxycarbonyloxy, C １ ~C ６ Alkyl sulfonyloxy, halo(C １ ~C ６ ) alkylsulfonyloxy, —OC(O)N(R ６０ ) R ６１ , C １ ~C ６ Alkylthio, C１ ~C ６ Alkylsulfinyl, C １ ~C ６ Alkyl sulfonyl, halo(C １ ~C ６ ) alkylthio, halo(C １ ~C ６ ) alkylsulfinyl, halo(C １ ~C ６ ) alkylsulfonyl, C ２ ~C ６ Alkenylthio, C ２ ~C ６ Alkenylsulfinyl, C ２ ~C ６ Alkenylsulfonyl, halo(C ２ ~C ６ ) alkenylthio, halo(C ２ ~C ６ ) alkenylsulfinyl, halo(C ２ ~C ６ ) alkenylsulfonyl, C ２ ~C ６ Alkynylthio, C ２ ~C ６ Alkynylsulfinyl, C ２ ~C ６ Alkynylsulfonyl, halo(C ２ ~C ６ ) alkynylthio, halo(C ２ ~C ６ ) alkynylsulfinyl, halo(C ２ ~C ６ ) alkynylsulfonyl, —SO ３ H, -S(O) ２ N (R ４８ ) R ４９ , -SC≡N, -S(O)(=NR ５２ ) R ５３ , -SF ５ , -N(R ４４ ) R ４５ , -N=S(O)(R ５６ ) R ５７ , formyl, carboxy, C １ ~C ６ Alkylcarbonyl, halo(C １ ~C ６ ) alkylcarbonyl, C１ ~C ６ Alkoxycarbonyl, halo(C １ ~C ６ ) alkoxycarbonyl, —C(O)N(R ４６ ) R ４７ , -C(=NOR １４ ) R １５ , Tori (C １ ~C ６ ) alkylsilyl, R ２４ (C １ ~C ６ ) alkyl, R ２５ (C １ ~C ６ ) alkoxy, C ３ ~C ６ Cycloalkyl, R ５９ (C ３ ~C ６ ) cycloalkyl, cyano, nitro, M-1 to M-56, M-61 to M-82, —O-(M-1) to —O-(M-63), —O-(M-65) to —O-(M-70), or —O-(M-72) to —O-(M-80), n represents an integer of 0, 1, or 2, Z ２ In the above relationship, when t2 represents an integer of 2, t3 represents an integer of 2 or 3, t4 represents an integer of 2, 3 or 4, and t5 represents an integer of 2, 3, 4 or 5, each of Z ２ may be the same as or different from each other; or t4 represents an integer of 2, and two Z ２ When two Z ２ together form oxo, -CH ２ CH ２ -, -OCH ２ CH ２ O-, -OCH ２ CH ２ CH ２ O-, = NOR ４３ , =NN(R ６３ ) R ６４ or =NN=C(R ６５ ) R ６６ represents R ４３ is a hydrogen atom or C １ ~C ６ represents alkyl, R２４ is C １ ~C ６ Alkoxy, hydroxy or -N(R ５０ ) R ５１ represents R ２５ is C １ ~C ６ represents alkoxy or M-1 to M-82, １ is a halogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl, C １ ~C ６ Alkoxy, C １ ~C ６ Alkylthio, halo(C １ ~C ６ ) alkylthio, C １ ~C ６ Alkylsulfinyl, C １ ~C ６ represents alkylsulfonyl or cyano; M １ In the above relationship, when t2 represents an integer of 2, t3 represents an integer of 2 or 3, t4 represents an integer of 2, 3 or 4, and t5 represents an integer of 2, 3, 4 or 5, each of M １ may be the same as or different from each other, M ３ is a hydrogen atom, C １ ~C ６ Alkyl or halo(C １ ~C ６ ) alkyl, R １４ is a hydrogen atom, C １ ~C ６ Alkyl or halo(C １ ~C ６ ) alkyl, R １５ is a hydrogen atom, C １ ~C ６ Alkyl or halo(C １ ~C ６ ) alkyl, R ４４ is a hydrogen atom, C １ ~C ６ Alkyl or halo(C １ ~C ６ ) alkyl, R ４５is a hydrogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl, C １ ~C ６ Alkylcarbonyl, halo(C １ ~C ６ ) alkylcarbonyl, C １ ~C ６ Alkoxycarbonyl, halo(C １ ~C ６ ) alkoxycarbonyl, C １ ~C ６ Alkyl sulfonyl or halo(C １ ~C ６ ) represents alkylsulfonyl, R ４６ is a hydrogen atom or C １ ~C ６ represents alkyl, R ４７ is a hydrogen atom, C １ ~C ６ Alkyl or halo(C １ ~C ６ ) alkyl, R ４８ is a hydrogen atom, C １ ~C ６ Alkyl or halo(C １ ~C ６ ) alkyl, R ４９ is a hydrogen atom, C １ ~C ６ Alkyl or halo(C １ ~C ６ ) alkyl, R ５０ is a hydrogen atom or C １ ~C ６ represents alkyl, R ５１ is a hydrogen atom, C １ ~C ６ Alkyl, C １ ~C ６ Alkylcarbonyl, halo(C １ ~C ６ ) alkylcarbonyl, C １ ~C ６ Alkoxycarbonyl, halo(C １ ~C ６ ) alkoxycarbonyl, C １ ~C ６Alkyl sulfonyl or halo(C １ ~C ６ ) represents alkylsulfonyl, R ５２ is a hydrogen atom or C １ ~C ６ represents alkyl, R ５３ is C １ ~C ６ represents alkyl, R ５６ is C １ ~C ６ represents alkyl, R ５７ is C １ ~C ６ represents alkyl, R ５９ is a halogen atom, C １ ~C ６ represents alkoxy or cyano; R ６０ is a hydrogen atom or C １ ~C ６ represents alkyl, R ６１ is a hydrogen atom, C １ ~C ６ Alkyl or halo(C １ ~C ６ ) alkyl, R ６３ is a hydrogen atom or C １ ~C ６ represents alkyl, R ６４ is a hydrogen atom, C １ ~C ６ Alkyl, C １ ~C ６ Alkylcarbonyl, halo(C １ ~C ６ ) alkylcarbonyl, C １ ~C ６ Alkoxycarbonyl, halo(C １ ~C ６ ) alkoxycarbonyl, C １ ~C ６ Alkyl sulfonyl or halo(C １ ~C ６ ) represents alkylsulfonyl, R ６５ is a hydrogen atom or C １ ~C ６ represents alkyl, R ６６ is C １ ~C ６ represents alkyl, R２ is a hydrogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl, C ２ ~C ６ Alkenyl, C ２ ~C ６ Alkynyl, C ３ ~C ６ cycloalkyl, —C(O)R ４ , -C(O)OR ５ or R ６７ (C １ ~C ６ ) alkyl, R ６７ is C １ ~C ６ Alkoxy, C １ ~C ６ Alkylthio, C １ ~C ６ Alkylsulfinyl, C １ ~C ６ alkylsulfonyl, cyano, or V-1 to V-82; V １ is a halogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl, C １ ~C ６ Alkoxy, C １ ~C ６ Alkylthio, C １ ~C ６ Alkylsulfinyl, C １ ~C ６ represents alkylsulfonyl, cyano or nitro; V １ In the above relationship, when t2 represents an integer of 2, t3 represents an integer of 2 or 3, t4 represents an integer of 2, 3 or 4, and t5 represents an integer of 2, 3, 4 or 5, each of V １ may be the same as or different from each other, V ３ is a hydrogen atom, C １ ~C ６ Alkyl or halo(C １ ~C ６) alkyl, R ４ is C １ ~C ６ Alkyl, C ２ ~C ６ Alkenyl, C ２ ~C ６ Alkynyl, C １ ~C ６ Alkylcarbonyl, C １ ~C ６ Alkoxycarbonyl, C １ ~C ６ Alkylamino, di(C １ ~C ６ ) alkylamino, R ６ (C １ ~C ６ ) alkyl or V-1 to V-82, R ５ is C １ ~C ６ Alkyl, C ２ ~C ６ Alkenyl, C ２ ~C ６ Alkynyl, R ９ (C １ ~C ６ ) alkyl, V-1 to V-63, V-65 to V-70, or V-72 to V-80; R ６ is a halogen atom, C １ ~C ６ represents alkoxy, cyano, nitro, or V-1 to V-82; R ９ is a halogen atom, C １ ~C ６ alkoxy, cyano, nitro, or V-1 to V-82; when Q is Q-A, Q-B, or Q-C, R ３ is a hydrogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl, C ２ ~C ６ Alkenyl, C ２ ~C ６ Alkynyl, C ３ ~C ６ Cycloalkyl or C １ ~C ６an aryltetrahydropyridine compound or a salt thereof, wherein: X represents an oxygen atom or a sulfur atom, Y represents an oxygen atom or a sulfur atom, t1 represents an integer of 0 or 1, t2 represents an integer of 0, 1 or 2, t3 represents an integer of 0, 1, 2 or 3, t4 represents an integer of 0, 1, 2, 3 or 4, t5 represents an integer of 0, 1, 2, 3, 4 or 5, d1 represents an integer of 0 or 1, d2 represents an integer of 0, 1 or 2, d3 represents an integer of 0, 1, 2 or 3, d4 represents an integer of 0, 1, 2, 3 or 4, and d5 represents an integer of 0, 1, 2, 3, 4 or 5. [2] Q is QA, QB, or QC, and (i) if Q is QA, then QA is C １ ~C ６ Alkyl, R １７ (C １ ~C ６ ) alkyl, —N(R １８ ) R １９ , Q-1, Q-2, Q-3, Q-4, Q-5, Q-6, Q-8, Q-9, Q-10, Q-12, Q-13, Q-14, Q-15, Q-19, Q-20, Q-21, Q-22, Q-23, Q-24, Q-25, Q-26, Q-28, Q-29, Q-31, Q-34, Q-35, Q-37, Q-38, Q-39, Q-40, Q-42, Q-44, Q-45, Q-46, Q-47, Q-49, Q-50, Q-51, Q-52, Q-53, Q-55, Q-56, Q-59 or Q-60; J represents J-1 to J-27; G represents G-1, G-2, G-3, G-4, G-5, G-7, G-8, G-9, G-11, G-12, G-13, G-14, G-15, G-16, G-17, G-18, G-19, G-20, G-25, G-26, G-28, G-29, G-33, G-35, G-36, G-37, G-40, G-41, G-42, G-44 or G-46; １７ is a halogen atom, C １ ~C ６ alkoxy, E-1 or E-60; R １８ is C １ ~C ６ Alkyl or C ２ ~C６ represents alkenyloxycarbonyl, R １９ is E-1, C １ ~C ６ Alkoxycarbonyl or R ２０ (C １ ~C ６ ) alkyl, R ２０ represents E-1, and Z １ is a halogen atom, C １ ~C ６ Alkyl, C ２ ~C ６ Alkenyl, C ２ ~C ６ Alkynyl, halo(C １ ~C ６ ) alkyl, C １ ~C ６ Alkoxy, halo (C １ ~C ６ ) alkoxy, C ２ ~C ６ Alkenyloxy, C ２ ~C ６ Alkynyloxy, hydroxy, C １ ~C ６ Alkylcarbonyloxy, —OC(O)N(R ２６ ) R ２７ , C １ ~C ６ Alkylthio, C １ ~C ６ Alkyl sulfonyl, halo(C １ ~C ６ ) alkylthio, halo(C １ ~C ６ ) alkylsulfonyl, —S(O) ２ N (R ２８ ) R ２９ , -SC≡N, -S(O)(=NR ３０ ) R ３１ , -SF ５ , -N(R ３２ ) R ３３ , carboxy, C １ ~C ６ Alkylcarbonyl, halo(C １ ~C ６ ) alkylcarbonyl, C １ ~C ６Alkoxycarbonyl, —C(O)N(R ３５ ) R ３６ , R ７ (C １ ~C ６ ) alkyl, R １６ (C １ ~C ６ ) alkoxy, C ３ ~C ６ Cycloalkyl, cyano, nitro, E-1, E-50, —O-(E-1), —O-(E-2), —O-(E-3), —O-(E-12), —O-(E-14), —S-(E-1), —S(O) ２ -(E-1), -C(O)-(E-1), -C(O)-(E-64), -C(O)-(E-71), -C(O)-(E-81), -C(O)-(E-82), -C(O)-(E-83) or -N=N-(E-1), Z １ In the above relationship, when t2 represents an integer of 2, t3 represents an integer of 2 or 3, t4 represents an integer of 2, 3 or 4, and t5 represents an integer of 2, 3, 4 or 5, each of Z １ may be the same as or different from each other, １ is a halogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl, C １ ~C ６ Alkoxy, C １ ~C ６ represents alkylthio or cyano; １ In the above relationship, when t2 represents an integer of 2, t3 represents an integer of 2 or 3, t4 represents an integer of 2, 3 or 4, and t5 represents an integer of 2, 3, 4 or 5, each E １ may be the same as or different from each other, ３ is C １ ~C ６ represents alkyl, R ７ is C １ ~C ６ Alkoxy (C １ ~C ６ ) alkoxy, cyano, C １ ~C ６Alkoxy, carboxy, —C(O)N(R ３７ ) R ３８ , -N(R ３９ ) R ４０ , C １ ~C ６ alkylsulfonyl or E-1, R １６ is C １ ~C ６ Alkylsulfonyl, —C(O)N(R ４１ ) R ４２ , C １ ~C ６ Alkoxy, C １ ~C ６ Alkoxy (C １ ~C ６ ) alkoxy, E-1 or —C(O)—(E-81), R ２ is a hydrogen atom, C １ ~C ６ Alkyl, —C(O)R ４ or -C(O)OR ５ represents R ４ is C １ ~C ６ alkyl, V-1 or V-19; R ５ is C １ ~C ６ represents alkyl; Z ３ is C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl or C １ ~C ６ Alkoxy (C １ ~C ６ ) alkyl, R ２６ is C １ ~C ６ represents alkyl, R ２７ is C １ ~C ６ represents alkyl, R ２９ is a hydrogen atom, C １ ~C ６ Alkyl or C １ ~C ６ represents alkylcarbonyl, R ３０ is C １ ~C ６represents alkyl, R ３１ is C １ ~C ６ represents alkyl, R ３３ is C １ ~C ６ Alkyl, C １ ~C ６ Alkylcarbonyl, C １ ~C ６ Alkoxycarbonyl, C １ ~C ６ Alkylaminocarbonyl, —C(S)NHC(O)OR ３４ or C １ ~C ６ represents alkylsulfonyl, R ３６ is a hydrogen atom or C １ ~C ６ represents alkyl, R ３８ is a hydrogen atom or C １ ~C ６ represents alkyl, R ３９ is a hydrogen atom or C １ ~C ６ represents alkyl, R ４０ is C １ ~C ６ Alkyl or C １ ~C ６ represents an alkoxycarbonyl; R ４１ is C １ ~C ６ represents alkyl, R ４２ is C １ ~C ６ represents alkyl; Z ５ is C １ ~C ６ represents alkyl, R １ represents a hydrogen atom, a halogen atom, or C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl, C １ ~C ６ Alkoxy, hydroxy, C １ ~C ６ Alkylthio or C １ ~C ６ represents alkylsulfinyl, R １ａrepresents a hydrogen atom, R １ｂ represents a hydrogen atom, R １ｃ represents a hydrogen atom, a halogen atom, or a halo(C １ ~C ６ ) alkyl; Z ２ is a halogen atom, C １ ~C ６ Alkyl, C ２ ~C ６ Alkenyl, halo(C １ ~C ６ ) alkyl, C １ ~C ６ Alkoxy, halo (C １ ~C ６ ) alkoxy, hydroxy, C １ ~C ６ Alkylcarbonyloxy, C １ ~C ６ Alkylthio, C １ ~C ６ Alkylsulfinyl, C １ ~C ６ Alkyl sulfonyl, halo(C １ ~C ６ ) alkylthio, —S(O) ２ N (R ４８ ) R ４９ , -N(R ４４ ) R ４５ , carboxy, C １ ~C ６ Alkylcarbonyl, C １ ~C ６ Alkoxycarbonyl, —C(O)N(R ４６ ) R ４７ , -C(=NOR １４ ) R １５ , Tori (C １ ~C ６ ) alkylsilyl, R ２４ (C １ ~C ６ ) alkyl, R ２５ (C １ ~C ６ ) alkoxy, C ３ ~C ６ represents cycloalkyl, cyano, nitro, M-1 or —O-(M-1); Z ２In the above relationship, when t2 represents an integer of 2, t3 represents an integer of 2 or 3, t4 represents an integer of 2, 3 or 4, and t5 represents an integer of 2, 3, 4 or 5, each of Z ２ may be the same as or different from each other, R ２５ is C １ ~C ６ represents alkoxy or M-1, １ is a halogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl or C １ ~C ６ represents alkoxy; M １ In the above relationship, when t2 represents an integer of 2, t3 represents an integer of 2 or 3, t4 represents an integer of 2, 3 or 4, and t5 represents an integer of 2, 3, 4 or 5, each of M １ may be the same as or different from each other, R １４ is C １ ~C ６ represents alkyl, R １５ is C １ ~C ６ represents alkyl, R ４４ is a hydrogen atom or C １ ~C ６ represents alkyl, R ４５ is C １ ~C ６ Alkyl, C １ ~C ６ Alkylcarbonyl or C １ ~C ６ represents an alkoxycarbonyl; R ４８ is a hydrogen atom or C １ ~C ６ represents alkyl, R ４９ is a hydrogen atom or C １ ~C ６ represents alkyl, R ５１ is C １ ~C ６ Alkyl or C １ ~C ６ (ii) when Q is Q-B, Q-B is C １~C ６ Alkyl, R １７ (C １ ~C ６ ) alkyl, —N(R １８ ) R １９ , Q-1, Q-2, Q-3, Q-4, Q-5, Q-6, Q-8, Q-9, Q-10, Q-12, Q-13, Q-14, Q-15, Q-19, Q-20, Q-21, Q-22, Q-23, Q-24, Q-25, Q-26, Q-28, Q-29, Q-31, Q-34, Q-35, Q-37, Q-38, Q-39, Q-40, Q-42, Q-44, Q-45, Q-46, Q-47, Q-49, Q-50, Q-51, Q-52, Q-53, Q-55, Q-56, Q-59 or Q-60; J represents J-1' or J-2'; １ is a nitrogen atom or CR １ｃ G represents -N(R ２１ ) R ２２ , -C(=NOR ６７ ) R ６８ , R ６９ (C １ ~C ６ ) alkyl, G-1′ to G-28′, G-40′, G-68′, G-69′, G-157′ or G-159′, R １７ is a halogen atom, C １ ~C ６ alkoxy, E-1 or E-60; R １８ is C １ ~C ６ Alkyl or C ２ ~C ６ represents alkenyloxycarbonyl, R １９ is E-1, C １ ~C ６ Alkoxycarbonyl or R ２０ (C １ ~C ６ ) alkyl, R ２０ represents E-1, and Z １ is a halogen atom, C １ ~C ６ Alkyl, C ２ ~C ６ Alkenyl, C ２ ~C６ Alkynyl, halo(C １ ~C ６ ) alkyl, C １ ~C ６ Alkoxy, halo (C １ ~C ６ ) alkoxy, C ２ ~C ６ Alkenyloxy, C ２ ~C ６ Alkynyloxy, hydroxy, C １ ~C ６ Alkylcarbonyloxy, —OC(O)N(R ２６ ) R ２７ , C １ ~C ６ Alkylthio, C １ ~C ６ Alkyl sulfonyl, halo(C １ ~C ６ ) alkylthio, halo(C １ ~C ６ ) alkylsulfonyl, —S(O) ２ N (R ２８ ) R ２９ , -SC≡N, -S(O)(=NR ３０ ) R ３１ , -SF ５ , -N(R ３２ ) R ３３ , carboxy, C １ ~C ６ Alkylcarbonyl, halo(C １ ~C ６ ) alkylcarbonyl, C １ ~C ６ Alkoxycarbonyl, —C(O)N(R ３５ ) R ３６ , R ７ (C １ ~C ６ ) alkyl, R １６ (C １ ~C ６ ) alkoxy, C ３ ~C ６ Cycloalkyl, cyano, nitro, E-1, E-50, —O-(E-1), —O-(E-2), —O-(E-3), —O-(E-12), —O-(E-14), —S-(E-1), —S(O) ２-(E-1), -C(O)-(E-1), -C(O)-(E-64), -C(O)-(E-71), -C(O)-(E-81), -C(O)-(E-82), -C(O)-(E-83) or -N=N-(E-1), Z １ In the above relationship, when t2 represents an integer of 2, t3 represents an integer of 2 or 3, t4 represents an integer of 2, 3 or 4, and t5 represents an integer of 2, 3, 4 or 5, each of Z １ may be the same as or different from each other, １ is a halogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl, C １ ~C ６ Alkoxy, C １ ~C ６ represents alkylthio or cyano; １ In the above relationship, when t2 represents an integer of 2, t3 represents an integer of 2 or 3, t4 represents an integer of 2, 3 or 4, and t5 represents an integer of 2, 3, 4 or 5, each E １ may be the same as or different from each other, ３ is C １ ~C ６ represents alkyl, R ７ is C １ ~C ６ Alkoxy (C １ ~C ６ ) alkoxy, cyano, C １ ~C ６ Alkoxy, carboxy, —C(O)N(R ３７ ) R ３８ , -N(R ３９ ) R ４０ , C １ ~C ６ alkylsulfonyl or E-1, R １６ is C １ ~C ６ Alkylsulfonyl, —C(O)N(R ４１ ) R ４２ , C １ ~C ６ Alkoxy, C １ ~C ６Alkoxy (C １ ~C ６ ) alkoxy, E-1 or —C(O)—(E-81), R ２ is a hydrogen atom, C １ ~C ６ Alkyl, —C(O)R ４ or -C(O)OR ５ represents R ４ is C １ ~C ６ alkyl, V-1 or V-19; R ５ is C １ ~C ６ represents alkyl; Z ３ is C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl or C １ ~C ６ Alkoxy (C １ ~C ６ ) alkyl, R ２６ is C １ ~C ６ represents alkyl, R ２７ is C １ ~C ６ represents alkyl, R ２９ is a hydrogen atom, C １ ~C ６ Alkyl or C １ ~C ６ represents alkylcarbonyl, R ３０ is C １ ~C ６ represents alkyl, R ３１ is C １ ~C ６ represents alkyl, R ３３ is C １ ~C ６ Alkyl, C １ ~C ６ Alkylcarbonyl, C １ ~C ６ Alkoxycarbonyl, C １ ~C ６ Alkylaminocarbonyl, —C(S)NHC(O)OR ３４ or C １ ~C ６represents alkylsulfonyl, R ３６ is a hydrogen atom or C １ ~C ６ represents alkyl, R ３８ is a hydrogen atom or C １ ~C ６ represents alkyl, R ３９ is a hydrogen atom or C １ ~C ６ represents alkyl, R ４０ is C １ ~C ６ Alkyl or C １ ~C ６ represents an alkoxycarbonyl; R ４１ is C １ ~C ６ represents alkyl, R ４２ is C １ ~C ６ represents alkyl, R １ represents a hydrogen atom, a halogen atom, or C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl, C １ ~C ６ Alkoxy, hydroxy, C １ ~C ６ Alkylthio or C １ ~C ６ represents alkylsulfinyl, R １ａ represents a hydrogen atom, R １ｂ represents a hydrogen atom, R １ｃ represents a hydrogen atom, a halogen atom, or a halo(C １ ~C ６ ) alkyl, R ２１ is a hydrogen atom or C １ ~C ６ represents alkyl, R ２２ is C １ ~C ６ Alkyl, C ２ ~C ６ Alkenyl, C ２ ~C ６ Alkynyl, R ２３ (C １ ~C ６) alkyl, M-57, M-60, M-61 or M-81; R ２３ is C １ ~C ６ Alkoxy, C １ ~C ６ Alkoxycarbonyl, hydroxy, cyano, C １ ~C ６ represents alkylamino or M-1, R ６７ is C １ ~C ６ represents alkyl, R ６８ is C １ ~C ６ represents alkyl or M-1, ６９ are M-1, M-2, M-14, -N(R ７０ ) R ７１ , -C(=O)N(R ７２ ) R ７３ or -C(=NOR ７４ ) R ７５ represents R ７０ represents a hydrogen atom, R ７６ is C １ ~C ６ represents alkyl or M-1, ７２ represents a hydrogen atom, R ７３ represents M-1, and R ７４ is C １ ~C ６ represents alkyl, R ７５ is C ３ ~C ６ represents cycloalkyl; Z ２ is a halogen atom, C １ ~C ６ Alkyl, C ２ ~C ６ Alkenyl, halo(C １ ~C ６ ) alkyl, C １ ~C ６ Alkoxy, halo (C １ ~C ６ ) alkoxy, hydroxy, C １ ~C ６ Alkylcarbonyloxy, C １ ~C ６ Alkylthio, C １ ~C６ Alkylsulfinyl, C １ ~C ６ Alkyl sulfonyl, halo(C １ ~C ６ ) alkylthio, —S(O) ２ N (R ４８ ) R ４９ , -N(R ４４ ) R ４５ , carboxy, C １ ~C ６ Alkylcarbonyl, C １ ~C ６ Alkoxycarbonyl, —C(O)N(R ４６ ) R ４７ , -C(=NOR １４ ) R １５ , Tori (C １ ~C ６ ) alkylsilyl, R ２４ (C １ ~C ６ ) alkyl, R ２５ (C １ ~C ６ ) alkoxy, C ３ ~C ６ represents cycloalkyl, cyano, nitro, M-1 or —O-(M-1); Z ２ In the above relationship, when t2 represents an integer of 2, t3 represents an integer of 2 or 3, t4 represents an integer of 2, 3 or 4, and t5 represents an integer of 2, 3, 4 or 5, each of Z ２ may be the same as or different from each other; or t4 represents an integer of 2, and two Z ２ When two Z ２ together form oxo, -CH ２ CH ２ -, -OCH ２ CH ２ O- or =NOR ４３ represents R ２５ is C １ ~C ６ represents alkoxy or M-1, １ is a halogen atom, C １ ~C ６ Alkyl, halo (C １~C ６ ) alkyl or C １ ~C ６ represents alkoxy; M １ In the above relationship, when t2 represents an integer of 2, t3 represents an integer of 2 or 3, t4 represents an integer of 2, 3 or 4, and t5 represents an integer of 2, 3, 4 or 5, each of M １ may be the same as or different from each other, R １４ is C １ ~C ６ represents alkyl, R １５ is C １ ~C ６ represents alkyl, R ４４ is a hydrogen atom or C １ ~C ６ represents alkyl, R ４５ is C １ ~C ６ Alkyl, C １ ~C ６ Alkylcarbonyl or C １ ~C ６ represents an alkoxycarbonyl; R ４８ is a hydrogen atom or C １ ~C ６ represents alkyl, R ４９ is a hydrogen atom or C １ ~C ６ represents alkyl, R ５１ is C １ ~C ６ Alkyl or C １ ~C ６ (iii) when Q is Q-C, Q-C is C １ ~C ６ Alkyl, R １７ (C １ ~C ６ ) alkyl, —N(R １８ ) R １９, Q-1, Q-2, Q-3, Q-4, Q-5, Q-6, Q-8, Q-9, Q-10, Q-12, Q-13, Q-14, Q-15, Q-19, Q-20, Q-21, Q-22, Q-23, Q-24, Q-25, Q-26, Q-28, Q-29, Q-31, Q-34, Q-35, Q-37, Q-38, Q-39, Q-40, Q-42, Q-44, Q-45, Q-46, Q-47, Q-49, Q-50, Q-51, Q-52, Q-53, Q-55, Q-56, Q-59 or Q-60; J represents J-1 to J-27; G is -N(R ２１ ) R ２２ , -C(=NOR ６７ ) R ６８ , R ６９ (C １ ~C ６ ) alkyl, G-1′ to G-28′, G-40′, G-68′, G-69′, G-157′ or G-159′, R １７ is a halogen atom, C １ ~C ６ alkoxy, E-1 or E-60; R １８ is C １ ~C ６ Alkyl or C ２ ~C ６ represents alkenyloxycarbonyl, R １９ is E-1, C １ ~C ６ Alkoxycarbonyl or R ２０ (C １ ~C ６ ) alkyl, R ２０ represents E-1, and Z １ is a halogen atom, C １ ~C ６ Alkyl, C ２ ~C ６ Alkenyl, C ２ ~C ６ Alkynyl, halo(C １ ~C ６ ) alkyl, C １ ~C ６ Alkoxy, halo (C １ ~C ６ ) alkoxy, C ２ ~C ６Alkenyloxy, C ２ ~C ６ Alkynyloxy, hydroxy, C １ ~C ６ Alkylcarbonyloxy, —OC(O)N(R ２６ ) R ２７ , C １ ~C ６ Alkylthio, C １ ~C ６ Alkyl sulfonyl, halo(C １ ~C ６ ) alkylthio, halo(C １ ~C ６ ) alkylsulfonyl, —S(O) ２ N (R ２８ ) R ２９ , -SC≡N, -S(O)(=NR ３０ ) R ３１ , -SF ５ , -N(R ３２ ) R ３３ , carboxy, C １ ~C ６ Alkylcarbonyl, halo(C １ ~C ６ ) alkylcarbonyl, C １ ~C ６ Alkoxycarbonyl, —C(O)N(R ３５ ) R ３６ , R ７ (C １ ~C ６ ) alkyl, R １６ (C １ ~C ６ ) alkoxy, C ３ ~C ６ Cycloalkyl, cyano, nitro, E-1, E-50, —O-(E-1), —O-(E-2), —O-(E-3), —O-(E-12), —O-(E-14), —S-(E-1), —S(O) ２ -(E-1), -C(O)-(E-1), -C(O)-(E-64), -C(O)-(E-71), -C(O)-(E-81), -C(O)-(E-82), -C(O)-(E-83) or -N=N-(E-1), Z １In the above relationship, when t2 represents an integer of 2, t3 represents an integer of 2 or 3, t4 represents an integer of 2, 3 or 4, and t5 represents an integer of 2, 3, 4 or 5, each of Z １ may be the same as or different from each other, １ is a halogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl, C １ ~C ６ Alkoxy, C １ ~C ６ represents alkylthio or cyano; １ In the above relationship, when t2 represents an integer of 2, t3 represents an integer of 2 or 3, t4 represents an integer of 2, 3 or 4, and t5 represents an integer of 2, 3, 4 or 5, each E １ may be the same as or different from each other, ３ is C １ ~C ６ represents alkyl, R ７ is C １ ~C ６ Alkoxy (C １ ~C ６ ) alkoxy, cyano, C １ ~C ６ Alkoxy, carboxy, —C(O)N(R ３７ ) R ３８ , -N(R ３９ ) R ４０ , C １ ~C ６ alkylsulfonyl or E-1, R １６ is C １ ~C ６ Alkylsulfonyl, —C(O)N(R ４１ ) R ４２ , C １ ~C ６ Alkoxy, C １ ~C ６ Alkoxy (C １ ~C ６ ) alkoxy, E-1 or —C(O)—(E-81), R ２ is a hydrogen atom, C １ ~C ６Alkyl, —C(O)R ４ or -C(O)OR ５ represents R ４ is C １ ~C ６ alkyl, V-1 or V-19; R ５ is C １ ~C ６ represents alkyl; Z ３ is C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl or C １ ~C ６ Alkoxy (C １ ~C ６ ) alkyl, R ２６ is C １ ~C ６ represents alkyl, R ２７ is C １ ~C ６ represents alkyl, R ２９ is a hydrogen atom, C １ ~C ６ Alkyl or C １ ~C ６ represents alkylcarbonyl, R ３０ is C １ ~C ６ represents alkyl, R ３１ is C １ ~C ６ represents alkyl, R ３３ is C １ ~C ６ Alkyl, C １ ~C ６ Alkylcarbonyl, C １ ~C ６ Alkoxycarbonyl, C １ ~C ６ Alkylaminocarbonyl, —C(S)NHC(O)OR ３４ or C １ ~C ６ represents alkylsulfonyl, R ３６ is a hydrogen atom or C １ ~C ６ represents alkyl, R ３８ is a hydrogen atom or C １ ~C６ represents alkyl, R ３９ is a hydrogen atom or C １ ~C ６ represents alkyl, R ４０ is C １ ~C ６ Alkyl or C １ ~C ６ represents an alkoxycarbonyl; R ４１ is C １ ~C ６ represents alkyl, R ４２ is C １ ~C ６ represents alkyl; Z ５ is C １ ~C ６ represents alkyl, R １ represents a hydrogen atom, a halogen atom, or C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl, C １ ~C ６ Alkoxy, hydroxy, C １ ~C ６ Alkylthio or C １ ~C ６ represents alkylsulfinyl, R １ａ represents a hydrogen atom, R １ｂ represents a hydrogen atom, R １ｃ represents a hydrogen atom, a halogen atom, or a halo(C １ ~C ６ ) alkyl, R ２１ is a hydrogen atom or C １ ~C ６ represents alkyl, R ２２ is C １ ~C ６ Alkyl, C ２ ~C ６ Alkenyl, C ２ ~C ６ Alkynyl, R ２３ (C １ ~C ６ ) alkyl, M-57, M-60, M-61 or M-81; R ２３ is C １ ~C ６Alkoxy, C １ ~C ６ Alkoxycarbonyl, hydroxy, cyano, C １ ~C ６ represents alkylamino or M-1, R ６７ is C １ ~C ６ represents alkyl, R ６８ is C １ ~C ６ represents alkyl or M-1, ６９ are M-1, M-2, M-14, -N(R ７０ ) R ７１ , -C(=O)N(R ７２ ) R ７３ or -C(=NOR ７４ ) R ７５ represents R ７０ represents a hydrogen atom, R ７６ is C １ ~C ６ represents alkyl or M-1, ７２ represents a hydrogen atom, R ７３ represents M-1, and R ７４ is C １ ~C ６ represents alkyl, R ７５ is C ３ ~C ６ represents cycloalkyl; Z ２ is a halogen atom, C １ ~C ６ Alkyl, C ２ ~C ６ Alkenyl, halo(C １ ~C ６ ) alkyl, C １ ~C ６ Alkoxy, halo (C １ ~C ６ ) alkoxy, hydroxy, C １ ~C ６ Alkylcarbonyloxy, C １ ~C ６ Alkylthio, C １ ~C ６ Alkylsulfinyl, C １ ~C ６ Alkyl sulfonyl, halo(C １ ~C６ ) alkylthio, —S(O) ２ N (R ４８ ) R ４９ , -N(R ４４ ) R ４５ , carboxy, C １ ~C ６ Alkylcarbonyl, C １ ~C ６ Alkoxycarbonyl, —C(O)N(R ４６ ) R ４７ , -C(=NOR １４ ) R １５ , Tori (C １ ~C ６ ) alkylsilyl, R ２４ (C １ ~C ６ ) alkyl, R ２５ (C １ ~C ６ ) alkoxy, C ３ ~C ６ represents cycloalkyl, cyano, nitro, M-1 or —O-(M-1); Z ２ In the above relationship, when t2 represents an integer of 2, t3 represents an integer of 2 or 3, t4 represents an integer of 2, 3 or 4, and t5 represents an integer of 2, 3, 4 or 5, each of Z ２ may be the same as or different from each other; or t4 represents an integer of 2, and two Z ２ When two Z ２ together form oxo, -CH ２ CH ２ -, -OCH ２ CH ２ O- or =NOR ４３ represents R ２５ is C １ ~C ６ represents alkoxy or M-1, １ is a halogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl or C １ ~C ６ represents alkoxy; M １In the above relationship, when t2 represents an integer of 2, t3 represents an integer of 2 or 3, t4 represents an integer of 2, 3 or 4, and t5 represents an integer of 2, 3, 4 or 5, each of M １ may be the same as or different from each other, R １４ is C １ ~C ６ represents alkyl, R １５ is C １ ~C ６ represents alkyl, R ４４ is a hydrogen atom or C １ ~C ６ represents alkyl, R ４５ is C １ ~C ６ Alkyl, C １ ~C ６ Alkylcarbonyl or C １ ~C ６ represents an alkoxycarbonyl; R ４８ is a hydrogen atom or C １ ~C ６ represents alkyl, R ４９ is a hydrogen atom or C １ ~C ６ represents alkyl, R ５１ is C １ ~C ６ Alkyl or C １ ~C ６ When Q is Q-A, Q-B, or Q-C, R ３ represents a hydrogen atom, and Y represents an oxygen atom, or a salt thereof. [3] Q is Q-A, Q-B or Q-C, (i) when Q is Q-A, Q-A represents Q-1, Q-2, Q-3, Q-4, Q-9, Q-12 or Q-14, J represents J-1 to J-27, G represents G-1, G-2, G-3, G-4, G-5, G-7, G-8, G-9, G-11, G-12, G-13, G-14, G-15, G-16, G-17, G-18, G-19, G-20, G-25, G-26, G-28, G-29, G-33, G-35, G-36, G-37, G-40, G-41, G-42, G-44 or G-46, Z１ is a halogen atom, C １ ~C ６ Alkyl, C １ ~C ６ represents alkoxy or cyano; Z １ In the above relationship, when t2 represents an integer of 2, t3 represents an integer of 2 or 3, t4 represents an integer of 2, 3 or 4, and t5 represents an integer of 2, 3, 4 or 5, each of Z １ may be the same as or different from each other, R ２ is a hydrogen atom or C １ ~C ６ represents alkyl; Z ３ is C １ ~C ６ represents alkyl, R １ is a hydrogen atom, halo (C １ ~C ６ ) alkyl, C １ ~C ６ represents alkoxy or hydroxy; R １ｃ represents a hydrogen atom; Z ４ is C １ ~C ６ represents alkyl, X represents an oxygen atom; (ii) when Q is Q-B, Q-B represents Q-1, Q-2, Q-3, Q-4, Q-5, Q-6, Q-8, Q-9, Q-10, Q-12, Q-14, Q-15, Q-19, Q-22, Q-23, Q-24, Q-25, Q-26, Q-28, Q-29, Q-34, Q-35, Q-37, Q-38, Q-40, Q-42, Q-44, Q-45, Q-46, Q-47, Q-49, Q-50, Q-51, Q-52, Q-55 or Q-56, G represents -N(R ２１ ) R ２２ , R ６９ (C １ ~C ６ ) alkyl, G-1′, G-2′, G-5′, G-6′, G-9′, G-10′, G-11′ or G-19′; Z １ is a halogen atom, C ２ ~C ６ Alkenyl, C ２ ~C ６ Alkynyl, halo(C １ ~C６ ) alkyl, C １ ~C ６ Alkoxy, halo (C １ ~C ６ ) alkoxy, C ２ ~C ６ Alkenyloxy, C ２ ~C ６ Alkynyloxy, hydroxy, C １ ~C ６ Alkylcarbonyloxy, —OC(O)N(R ２６ ) R ２７ , C １ ~C ６ Alkylthio, C １ ~C ６ Alkyl sulfonyl, halo(C １ ~C ６ ) alkylthio, halo(C １ ~C ６ ) alkylsulfonyl, —S(O) ２ N (R ２８ ) R ２９ , -SC≡N, -S(O)(=NR ３０ ) R ３１ , -N(R ３２ ) R ３３ , carboxy, C １ ~C ６ Alkylcarbonyl, halo(C １ ~C ６ ) alkylcarbonyl, C １ ~C ６ Alkoxycarbonyl, —C(O)N(R ３５ ) R ３６ , R ７ (C １ ~C ６ ) alkyl, R １６ (C １ ~C ６ ) alkoxy, C ３ ~C ６ Cycloalkyl, cyano, nitro, E-1, E-50, —O-(E-1), —O-(E-2), —O-(E-3), —O-(E-14), —S-(E-1), —S(O) ２-(E-1), -C(O)-(E-1), -C(O)-(E-64), -C(O)-(E-71), -C(O)-(E-81), -C(O)-(E-82), -C(O)-(E-83) or -N=N-(E-1), Z １ In the above relationship, when t2 represents an integer of 2, t3 represents an integer of 2 or 3, t4 represents an integer of 2, 3 or 4, and t5 represents an integer of 2, 3, 4 or 5, each of Z １ may be the same as or different from each other, R ２ is a hydrogen atom, -C(O)R ４ or -C(O)OR ５ represents R ２８ represents a hydrogen atom, R ２９ is a hydrogen atom or C １ ~C ６ represents alkylcarbonyl, R ３３ is C １ ~C ６ Alkyl, C １ ~C ６ Alkylcarbonyl, C １ ~C ６ Alkoxycarbonyl, C １ ~C ６ Alkylaminocarbonyl or —C(S)NHC(O)OR ３４ represents R １ｃ represents a hydrogen atom, R ２１ is C １ ~C ６ represents alkyl, R ２２ is C １ ~C ６ Alkyl or C ２ ~C ６ represents alkenyl; Z ２ is a halogen atom or C １ ~C ６ represents alkyl; Z ２ In the above relationship, when t2 represents an integer of 2, t3 represents an integer of 2 or 3, t4 represents an integer of 2, 3 or 4, and t5 represents an integer of 2, 3, 4 or 5, each of Z ２ may be the same as or different from each other; or t4 represents an integer of 2, and two Z ２When two Z ２ Let's get together -CH ２ CH ２ represents -, M １ represents a halogen atom; １ In the above relationship, when t2 represents an integer of 2, t3 represents an integer of 2 or 3, t4 represents an integer of 2, 3 or 4, and t5 represents an integer of 2, 3, 4 or 5, each of M １ may be the same as or different from each other; (iii) when Q is Q-C, Q-C is C １ ~C ６ Alkyl, R １７ (C １ ~C ６ ) alkyl, —N(R １８ ) R １９ , Q-1, Q-2, Q-3, Q-4, Q-5, Q-9, Q-12, Q-13, Q-14, Q-20, Q-21, Q-23, Q-29, Q-31, Q-39, Q-53, Q-59 or Q-60; J represents J-1, J-5, J-6, J-10, J-12, J-17, J-18, J-19 or J-24; G represents -N(R ２１ ) R ２２ , -C(=NOR ６７ ) R ６８ , G-1′ to G-9′, G-12′ to G-28′, G-40′, G-68′, G-69′, G-157′ or G-159′; Z １ is a halogen atom, C １ ~C ６ Alkyl, C １ ~C ６ Alkoxy, halo (C １ ~C ６ ) alkoxy, C １ ~C ６ Alkylthio, —S(O) ２ N (R ２８ ) R ２９ , -SF ５ , -N(R ３２ ) R ３３ , carboxy, C １ ~C ６ Alkoxycarbonyl, —C(O)N(R ３５ ) R３６ , R １６ (C １ ~C ６ ) alkoxy, C ３ ~C ６ represents cycloalkyl, cyano, E-1, —O-(E-1) or —O-(E-12); Z １ In the above relationship, when t2 represents an integer of 2, t3 represents an integer of 2 or 3, t4 represents an integer of 2, 3 or 4, and t5 represents an integer of 2, 3, 4 or 5, each of Z １ may be the same as or different from each other, １ is a halogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl or C １ ~C ６ represents alkoxy; １ In the above relationship, when t2 represents an integer of 2, t3 represents an integer of 2 or 3, t4 represents an integer of 2, 3 or 4, and t5 represents an integer of 2, 3, 4 or 5, each E １ may be the same as or different from each other, R １６ represents E-1, and R ２ represents a hydrogen atom or —C(O)OR ５ represents Z ３ is C １ ~C ６ represents alkyl, R ２８ is C １ ~C ６ represents alkyl, R ２９ is C １ ~C ６ represents alkyl, R ３２ represents a hydrogen atom, R ３３ is C １ ~C ６ Alkylcarbonyl or C １ ~C ６ represents alkylsulfonyl, R ３５ represents a hydrogen atom, R ３６ is C １ ~C ６ represents alkyl, R １represents a hydrogen atom or a halogen atom; ２２ is C １ ~C ６ Alkyl, C ２ ~C ６ Alkynyl, R ２３ (C １ ~C ６ ) alkyl, M-57, M-60, M-61 or M-81; Z ２ is a halogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl, C １ ~C ６ Alkoxy, C １ ~C ６ Alkylsulfonyl, C １ ~C ６ represents alkoxycarbonyl or cyano; Z ２ In the above relationship, when t2 represents an integer of 2, t3 represents an integer of 2 or 3, t4 represents an integer of 2, 3 or 4, and t5 represents an integer of 2, 3, 4 or 5, each of Z ２ may be the same as or different from each other; or t4 represents an integer of 2, and two Z ２ When two Z ２ together form oxo, -CH ２ CH ２ -, -OCH ２ CH ２ O- or =NOR ４３[4] The aryltetrahydropyridine compound or salt thereof according to the above [1] or [2], wherein Q is Q-A, Q-B, or Q-C, (i) when Q is Q-A, J represents J-1, J-5, J-6, J-8, J-10, J-14, J-15, J-17, J-18, J-19, J-21, J-22, J-23, J-24, J-25, J-26, or J-27, G represents G-1, G-3, G-4, G-5, G-7, G-9, G-11, G-12, G-13, G-14, G-15, G-16, G-17, G-18, G-19, G-20, G-25, G-26, G-28, G-29, G-35, G-36, G-37, G-40, G-41, G-42, G-44 or G-46; ２ is a halogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl, C １ ~C ６ Alkoxy, C １ ~C ６ Alkylthio, C １ ~C ６ Alkylsulfinyl, C １ ~C ６ Alkylsulfonyl, —N(R ４４ ) R ４５ , C １ ~C ６ Alkoxycarbonyl, C ３ ~C ６ represents cycloalkyl, cyano, nitro, M-1 or —O-(M-1); Z ２ In the above relationship, when t2 represents an integer of 2, t3 represents an integer of 2 or 3, t4 represents an integer of 2, 3 or 4, and t5 represents an integer of 2, 3, 4 or 5, each of Z ２ may be the same as or different from each other, R ４５ is C １ ~C ６ Alkyl or C １ ~C ６[5] The aryltetrahydropyridine compound or a salt thereof according to any one of [1] to [3], wherein Q is Q-A or Q-C, and (i) when Q is Q-A, Q-A is C １ ~C ６ Alkyl, R １７ (C １ ~C ６ ) alkyl, —N(R １８ ) R １９ , Q-1, Q-2, Q-3, Q-4, Q-5, Q-9, Q-12, Q-13, Q-14, Q-20, Q-21, Q-23, Q-29, Q-31, Q-39, Q-53, Q-59 or Q-60, J represents J-1 to J-27, Z １ is a halogen atom, C １ ~C ６ Alkyl, C １ ~C ６ Alkoxy, halo (C １ ~C ６ ) alkoxy, C １ ~C ６ Alkylthio, —S(O) ２ N (R ２８ ) R ２９ , -SF ５ , -N(R ３２ ) R ３３ , carboxy, C １ ~C ６ Alkoxycarbonyl, —C(O)N(R ３５ ) R ３６ , R １６ (C １ ~C ６ ) alkoxy, C ３ ~C ６ represents cycloalkyl, cyano, E-1, —O-(E-1) or —O-(E-12); Z １ In the above relationship, when t2 represents an integer of 2, t3 represents an integer of 2 or 3, t4 represents an integer of 2, 3 or 4, and t5 represents an integer of 2, 3, 4 or 5, each of Z １ may be the same as or different from each other, １ is a halogen atom, C １ ~C ６ Alkyl, halo (C１ ~C ６ ) alkyl or C １ ~C ６ represents alkoxy; １ In the above relationship, when t2 represents an integer of 2, t3 represents an integer of 2 or 3, t4 represents an integer of 2, 3 or 4, and t5 represents an integer of 2, 3, 4 or 5, each E １ may be the same as or different from each other, R １６ represents E-1, and R ２ is a hydrogen atom, C １ ~C ６ Alkyl or —C(O)OR ５ represents Z ３ is C １ ~C ６ represents alkyl, R ２８ is C １ ~C ６ represents alkyl, R ２９ is C １ ~C ６ represents alkyl, R ３２ represents a hydrogen atom, R ３３ is C １ ~C ６ Alkylcarbonyl or C １ ~C ６ represents alkylsulfonyl, R ３５ represents a hydrogen atom, R ３６ is C １ ~C ６ represents alkyl, R １ represents a hydrogen atom, a halogen atom, a halo (C １ ~C ６ ) alkyl, C １ ~C ６ (iii) when Q is Q-C, Q-C is C １ ~C ６ Alkyl, R １７ (C １ ~C ６ ) alkyl, —N(R １８ ) R １９, Q-1, Q-2, Q-3, Q-4, Q-5, Q-9, Q-12, Q-13, Q-14, Q-20, Q-21, Q-23, Q-29, Q-31, Q-39, Q-53, Q-59 or Q-60, J represents J-1 to J-27, G is -N(R ２１ ) R ２２ , -C(=NOR ６７ ) R ６８ , G-1′ to G-9′, G-12′ to G-28′, G-40′, G-68′, G-69′, G-157′ or G-159′; Z １ is a halogen atom, C １ ~C ６ Alkyl, C １ ~C ６ Alkoxy, halo (C １ ~C ６ ) alkoxy, C １ ~C ６ Alkylthio, —S(O) ２ N (R ２８ ) R ２９ , -SF ５ , -N(R ３２ ) R ３３ , carboxy, C １ ~C ６ Alkoxycarbonyl, —C(O)N(R ３５ ) R ３６ , R １６ (C １ ~C ６ ) alkoxy, C ３ ~C ６ represents cycloalkyl, cyano, E-1, —O-(E-1) or —O-(E-12); Z １ In the above relationship, when t2 represents an integer of 2, t3 represents an integer of 2 or 3, t4 represents an integer of 2, 3 or 4, and t5 represents an integer of 2, 3, 4 or 5, each of Z １ may be the same as or different from each other, １ is a halogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl or C １ ~C ６ represents alkoxy; １In the above relationship, when t2 represents an integer of 2, t3 represents an integer of 2 or 3, t4 represents an integer of 2, 3 or 4, and t5 represents an integer of 2, 3, 4 or 5, each E １ may be the same as or different from each other, R １６ represents E-1, and R ２ is a hydrogen atom, C １ ~C ６ Alkyl or —C(O)OR ５ represents Z ３ is C １ ~C ６ represents alkyl, R ２８ is C １ ~C ６ represents alkyl, R ２９ is C １ ~C ６ represents alkyl, R ３２ represents a hydrogen atom, R ３３ is C １ ~C ６ Alkylcarbonyl or C １ ~C ６ represents alkylsulfonyl, R ３５ represents a hydrogen atom, R ３６ is C １ ~C ６ represents alkyl, R ２２ is C １ ~C ６ Alkyl, C ２ ~C ６ Alkynyl, R ２３ (C １ ~C ６ ) alkyl, M-57, M-60, M-61 or M-81; R １ represents a hydrogen atom, a halogen atom, a halo (C １ ~C ６ ) alkyl, C １ ~C ６[6] The aryltetrahydropyridine compound or salt thereof according to the above [1] or [2], wherein Q is Q-A or Q-C, and X represents an oxygen atom. [6] Q is Q-A or Q-C, and (i) when Q is Q-A, J represents J-1, J-5, J-6, J-8, J-10, J-12, J-14, J-15, J-17, J-18, J-19, J-21, J-22, J-23, J-24, J-25, J-26, or J-27, G represents G-1, G-3, G-4, G-5, G-7, G-9, G-11, G-12, G-13, G-14, G-15, G-16, G-17, G-18, G-19, G-20, G-25, G-26, G-28, G-29, G-35, G-36, G-37, G-40, G-41, G-42, G-44 or G-46; Z ２ is a halogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl, C １ ~C ６ Alkoxy, C １ ~C ６ Alkylthio, C １ ~C ６ Alkylsulfinyl, C １ ~C ６ Alkylsulfonyl, —N(R ４４ ) R ４５ , C １ ~C ６ Alkoxycarbonyl, C ３ ~C ６ represents cycloalkyl, cyano, nitro, M-1 or —O-(M-1); Z ２ In the above relationship, when t2 represents an integer of 2, t3 represents an integer of 2 or 3, t4 represents an integer of 2, 3 or 4, and t5 represents an integer of 2, 3, 4 or 5, each of Z ２ may be the same as or different from each other, R ４５ is C １ ~C ６ Alkyl or C １ ~C ６(iii) when Q is Q-C, J represents J-1, J-5, J-6, J-8, J-10, J-12, J-14, J-15, J-17, J-18, J-19, J-21, J-22, J-23, J-24, J-25, J-26 or J-27, and Z ２ is a halogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl, C １ ~C ６ Alkoxy, C １ ~C ６ Alkylthio, C １ ~C ６ Alkylsulfinyl, C １ ~C ６ Alkylsulfonyl, —N(R ４４ ) R ４５ , C １ ~C ６ Alkoxycarbonyl, C ３ ~C ６ represents cycloalkyl, cyano, nitro, M-1 or —O-(M-1); Z ２ In the above relationship, when t2 represents an integer of 2, t3 represents an integer of 2 or 3, t4 represents an integer of 2, 3 or 4, and t5 represents an integer of 2, 3, 4 or 5, each of Z ２ may be the same as or different from each other; or t4 represents an integer of 2, and two Z ２ When two Z ２ together form oxo, -CH ２ CH ２ -, -OCH ２ CH ２ O- or =NOR ４３ represents R ４５ is C １ ~C ６ Alkyl or C １ ~C ６ [7] The aryltetrahydropyridine compound or a salt thereof according to the above [5], wherein Q is Q-B or Q-C, and (ii) when Q is Q-B, R ２is a hydrogen atom, -C(O)R ４ or -C(O)OR ５ represents Z ２ is a halogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl, C １ ~C ６ Alkoxy, C １ ~C ６ Alkylsulfonyl, C １ ~C ６ represents alkoxycarbonyl or cyano; Z ２ In the above relationship, when t2 represents an integer of 2, t3 represents an integer of 2 or 3, t4 represents an integer of 2, 3 or 4, and t5 represents an integer of 2, 3, 4 or 5, each of Z ２ may be the same as or different from each other; or t4 represents an integer of 2, and two Z ２ When two Z ２ together form oxo, -CH ２ CH ２ -, -OCH ２ CH ２ O- or =NOR ４３ (iii) when Q is Q-C, J represents J-1, J-5, J-6, J-10, J-12, J-17, J-18, J-19 or J-24, and R ２ is a hydrogen atom, -C(O)R ４ or -C(O)OR ５ represents Z ２ is a halogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl, C １ ~C ６ Alkoxy, C １ ~C ６ Alkylsulfonyl, C １ ~C ６ represents alkoxycarbonyl or cyano; Z ２In the above relationship, when t2 represents an integer of 2, t3 represents an integer of 2 or 3, t4 represents an integer of 2, 3 or 4, and t5 represents an integer of 2, 3, 4 or 5, each of Z ２ may be the same as or different from each other; or t4 represents an integer of 2, and two Z ２ When two Z ２ together form oxo, -CH ２ CH ２ -, -OCH ２ CH ２ O- or =NOR ４３ [8] The aryltetrahydropyridine compound or a salt thereof according to [1] or [2], wherein Q is Q-A, Q-B, or Q-C, and (i) when Q is Q-A, Q-A represents Q-1, Q-2, Q-3, Q-4, Q-6, Q-9, Q-10, Q-12, or Q-14, and Z １ is a halogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl, C １ ~C ６ represents alkoxy or cyano; Z １ In the above relationship, when t2 represents an integer of 2, t3 represents an integer of 2 or 3, t4 represents an integer of 2, 3 or 4, and t5 represents an integer of 2, 3, 4 or 5, each of Z １ may be the same as or different from each other, ３ is C １ ~C ６ J represents J-1, J-2, J-3, J-4, J-5, J-6, J-7, J-8, J-9, J-10, J-11, J-12, J-13, J-14, J-15, J-16, J-17, J-18, J-19, J-20, J-21, J-22, J-23, J-24, J-25 or J-26; Z ５ is C １ ~C ６ represents alkyl, R １ａ represents a hydrogen atom, R １ｂ represents a hydrogen atom, R １ｃrepresents a hydrogen atom, G represents G-1, G-2, G-3, G-5, G-7, G-14, G-19, G-25, G-26, G-35 or G-41, Z ２ is a halogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl, C １ ~C ６ Alkoxy, C １ ~C ６ Alkylthio, C １ ~C ６ Alkylsulfinyl, C １ ~C ６ Alkylsulfonyl, —N(R ４４ ) R ４５ , C １ ~C ６ Alkoxycarbonyl, C ３ ~C ６ represents cycloalkyl, cyano or nitro; Z ２ In the above relationship, when t2 represents an integer of 2, t3 represents an integer of 2 or 3, t4 represents an integer of 2, 3 or 4, and t5 represents an integer of 2, 3, 4 or 5, each of Z ２ may be the same as or different from each other, R ４４ is a hydrogen atom or C １ ~C ６ represents alkyl, R ４４ and R ４５ In the relationship, R ４４ When represents a hydrogen atom, R ４５ is C １ ~C ６ represents alkylcarbonyl, R ４４ is C １ ~C ６ When it represents alkyl, R ４５ is C １ ~C ６ represents alkyl; Z ４ is C １ ~C ６ represents alkyl, R １ represents a hydrogen atom, a halogen atom, a halo (C １ ~C ６ ) alkyl, C １ ~C６ represents alkyl or hydroxy; R ２ is a hydrogen atom, C １ ~C ６ Alkyl or —C(O)OR ５ represents R ５ is C １ ~C ６ (ii) when Q is Q-B, Q-B represents Q-1, Q-2, Q-3, Q-4, Q-5, Q-6, Q-8, Q-9, Q-12, Q-14 or Q-15; Z １ is a halogen atom, C １ ~C ６ Alkyl, C ２ ~C ６ Alkenyl, C ２ ~C ６ Alkynyl, halo(C １ ~C ６ ) alkyl, C １ ~C ６ Alkoxy, halo (C １ ~C ６ ) alkoxy, C １ ~C ６ Alkenyloxy, C １ ~C ６ Alkynyloxy, C １ ~C ６ Alkylthio, C １ ~C ６ Alkyl sulfonyl, halo(C １ ~C ６ ) alkylthio, —N(R ３２ ) R ３３ , C １ ~C ６ Alkylcarbonyl, C １ ~C ６ Alkoxycarbonyl, —C(O)N(R ３５ ) R ３６ , C ３ ~C ６ Cycloalkyl, R ７ (C １ ~C ６ ) alkyl, R １６ (C １ ~C ６ ) represents alkoxy, cyano or nitro; Z １In the above relationship, when t2 represents an integer of 2, t3 represents an integer of 2 or 3, t4 represents an integer of 2, 3 or 4, and t5 represents an integer of 2, 3, 4 or 5, each of Z １ may be the same as or different from each other, R ７ is C １ ~C ６ Alkoxy or C １ ~C ６ Alkoxy (C １ ~C ６ ) represents alkoxy, R １６ is C １ ~C ６ represents alkoxy, R ３２ is a hydrogen atom or C １ ~C ６ represents alkyl, R ３２ and R ３３ In the relationship, R ３２ When represents a hydrogen atom, R ３３ is C １ ~C ６ Alkylcarbonyl, C １ ~C ６ Alkoxycarbonyl or C １ ~C ６ represents alkylaminocarbonyl, R ３２ is C １ ~C ６ When it represents alkyl, R ３３ is C １ ~C ６ represents alkyl, R ３５ is C １ ~C ６ represents alkyl, R ３６ is C １ ~C ６ represents alkyl; Z ３ is C １ ~C ６ Alkyl or halo(C １ ~C ６ ) alkyl, J represents J-1′ or J-2′, A １ is a nitrogen atom or CR １ｃ represents R １ａ represents a hydrogen atom, R １ｂ represents a hydrogen atom, R１ｃ represents a hydrogen atom; G represents G-1′, G-2′, G-5′, G-6′, G-9′, G-10′ or G-11′; Z ２ is a halogen atom or C １ ~C ６ represents alkyl; Z ２ In the relationship, when t4 represents an integer of 2, 3 or 4, each Z ２ may be the same as or different from each other, R １ represents a hydrogen atom, a halogen atom, or a halo(C １ ~C ６ ) alkyl, R ２ is a hydrogen atom, C １ ~C ６ Alkyl, —C(O)R ４ or -C(O)OR ５ represents R ４ is C １ ~C ６ alkyl, V-1 or V-19; R ５ is C １ ~C ６ (iii) when Q is Q-C, Q-C represents Q-1, Q-2, Q-3, Q-4, Q-6, Q-9, Q-12 or Q-14; Z １ is a halogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl, C １ ~C ６ Alkoxy, —C(O)N(R ３５ ) R ３６ , -N(R ３２ ) R ３３ , cyano or nitro; Z １ In the above relationship, when t2 represents an integer of 2, t3 represents an integer of 2 or 3, t4 represents an integer of 2, 3 or 4, and t5 represents an integer of 2, 3, 4 or 5, each of Z １ may be the same as or different from each other, R ３５ represents a hydrogen atom, R ３６ is C １ ~C ６represents alkyl, R ３２ represents a hydrogen atom, R ３３ is C １ ~C ６ represents alkylcarbonyl; Z ３ is C １ ~C ６ alkyl, J represents J-1, J-5, J-6, J-10, J-17, J-18, J-19 or J-24, R １ represents a hydrogen atom or a halogen atom, G represents G-1′, G-2′, G-3′, G-4′, G-5′, G-6′, G-7′, G-8′, G-9′, G-12′, G-13′, G-14′, G-15′ or G-16′, R １ａ represents a hydrogen atom, R １ｂ represents a hydrogen atom, R １ｃ represents a hydrogen atom; Z ４ is a hydrogen atom, C １ ~C ６ Alkyl, C １ ~C ６ Alkoxy (C １ ~C ６ ) alkyl, C １ ~C ６ Alkylcarbonyl or C １ ~C ６ represents an alkoxycarbonyl; Z ２ is a halogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl, C １ ~C ６ represents alkoxy, cyano or nitro, n represents an integer of 0, 1 or 2, Z ２ In the relationship, when t4 represents an integer of 2, 3 or 4, each Z ２ may be the same as or different from each other; or t4 represents an integer of 2, and two Z ２ When two Z ２ together represent oxo, and R ２ is a hydrogen atom, C １ ~C ６Alkyl or —C(O)OR ５ represents R ５ is C １ ~C ６ When Q is Q-A, Q-B, or Q-C, R ３ represents a hydrogen atom, X represents an oxygen atom or a sulfur atom, Y represents an oxygen atom or a sulfur atom, t2 represents an integer of 0, 1 or 2, t3 represents an integer of 0, 1, 2 or 3, t4 represents an integer of 0, 1, 2, 3 or 4, t5 represents an integer of 0, 1, 2, 3, 4 or 5, d3 represents an integer of 0, and d5 represents an integer of 0. [9] The aryltetrahydropyridine compound or a salt thereof according to the above [1], wherein (i) Q is Q-A, Q-B or Q-C, and (i) when Q is Q-A, Q-A represents Q-1, Q-2, Q-3, Q-4, Q-9 or Q-12, and Z １ represents a halogen atom or cyano, J represents J-1, J-5, J-6, J-8, J-10, J-15, J-17, J-18, J-19, J-21, J-22, J-23, J-24, J-25 or J-26, G represents G-1, G-3, G-5, G-7, G-14, G-19, G-25, G-26, G-35 or G-41, Z ２ is a halogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl, C １ ~C ６ Alkoxy, C １ ~C ６ Alkylthio, C １ ~C ６ Alkylsulfonyl, —N(R ４４ ) R ４５ , C １ ~C ６ Alkoxycarbonyl, C ３ ~C ６ represents cycloalkyl, cyano or nitro; R １ is a hydrogen atom, halo (C １ ~C ６ ) alkyl or hydroxy; R ２ is a hydrogen atom or C１ ~C ６ (ii) when Q is Q-B, then R ２ is a hydrogen atom, -C(O)R ４ or -C(O)OR ５ (iii) when Q is Q-C, Q represents Q-1, Q-2, Q-3, Q-4, Q-9, Q-12 or Q-14, Z １ is a halogen atom, —C(O)N(R ３５ ) R ３６ , -N(R ３２ ) R ３３ or cyano; Z ２ is a halogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl or C １ ~C ６ represents alkoxy, R ２ represents a hydrogen atom or —C(O)OR ５

[10] The aryl tetrahydropyridine compound or salt thereof according to any one of the above [1] to [6] and [8] to [9], wherein Q is Q-A.

[11] The aryl tetrahydropyridine compound or salt thereof according to any one of the above [1] to [4] and [7] to [9], wherein Q is Q-B.

[12] The aryl tetrahydropyridine compound or salt thereof according to any one of the above [1] to [9], wherein Q is Q-C.

[13] G is -N(R ２１ ) R ２２

[14] The aryl tetrahydropyridine compound or salt thereof according to any one of the above [1] to [6], [8] to [9], wherein G is G-1, G-3 or G-7.

[15] The aryl tetrahydropyridine compound or salt thereof according to any one of the above [1] to [9], wherein G is G-1', G-2', G-5', G-6', G-9', G-13', G-19' or G-27'.

[16] Q is Q-A, Q-B or Q-C, (i) when Q is Q-A, J represents J-1, J-10, J-17 or J-19; (ii) when Q is Q-B, A １ represents a nitrogen atom; (iii) when Q is Q-C, J is J-1, J-10, J-17 or J-19. The aryltetrahydropyridine compound or a salt thereof according to any one of the above [1] to [4], [8] or [9].

[17] The aryltetrahydropyridine compound or a salt thereof according to any one of the above [1] to [4] and [8], wherein Q is Q-A, Q-B, or Q-C, (i) when Q is Q-A, Q-A represents Q-1, Q-2, Q-3, Q-4, Q-12, or Q-14; (ii) when Q is Q-B, Q-B represents Q-1, Q-2, Q-3, Q-4, Q-12, or Q-14; or (iii) when Q is Q-C, Q-C represents Q-1, Q-2, Q-3, Q-4, Q-12, or Q-14.

[18] Q is Q-A, (i) when Q is Q-A, Q-A represents Q-1, Q-2, Q-3, Q-4, Q-6, Q-9, Q-10, Q-12 or Q-14, Z １ is a halogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl, C １ ~C ６ represents alkoxy or cyano; Z １ In the above relationship, when t2 represents an integer of 2, t3 represents an integer of 2 or 3, t4 represents an integer of 2, 3 or 4, and t5 represents an integer of 2, 3, 4 or 5, each of Z １may be the same as or different from each other, ３ is C １ ~C ６ J represents J-1, J-2, J-3, J-4, J-5, J-6, J-7, J-8, J-9, J-10, J-11, J-12, J-13, J-14, J-15, J-16, J-17, J-18, J-19, J-20, J-21, J-22, J-23, J-24, J-25 or J-26; Z ５ is C １ ~C ６ represents alkyl, R １ａ represents a hydrogen atom, R １ｂ represents a hydrogen atom, R １ｃ represents a hydrogen atom, G represents G-1, G-2, G-3, G-5, G-7, G-14, G-19, G-25, G-26, G-35 or G-41, Z ２ is a halogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl, C １ ~C ６ Alkoxy, C １ ~C ６ Alkylthio, C １ ~C ６ Alkylsulfinyl, C １ ~C ６ Alkylsulfonyl, —N(R ４４ ) R ４５ , C １ ~C ６ Alkoxycarbonyl, C ３ ~C ６ represents cycloalkyl, cyano or nitro; Z ２ In the above relationship, when t2 represents an integer of 2, t3 represents an integer of 2 or 3, t4 represents an integer of 2, 3 or 4, and t5 represents an integer of 2, 3, 4 or 5, each of Z ２ may be the same as or different from each other, R ４４ is a hydrogen atom or C １ ~C ６ represents alkyl, R ４４ and R ４５In the relationship, R ４４ When represents a hydrogen atom, R ４５ is C １ ~C ６ represents alkylcarbonyl, R ４４ is C １ ~C ６ When it represents alkyl, R ４５ is C １ ~C ６ represents alkyl; Z ４ is C １ ~C ６ represents alkyl, R １ represents a hydrogen atom, a halogen atom, a halo (C １ ~C ６ ) alkyl, C １ ~C ６ represents alkyl or hydroxy; R ２ is a hydrogen atom, C １ ~C ６ Alkyl or —C(O)OR ５ represents R ５ is C １ ~C ６ represents alkyl, R ３ represents a hydrogen atom, X represents an oxygen atom or a sulfur atom, Y represents an oxygen atom or a sulfur atom, t2 represents an integer of 0, 1 or 2, t3 represents an integer of 0, 1, 2 or 3, t4 represents an integer of 0, 1, 2, 3 or 4, and t5 represents an integer of 0, 1, 2, 3, 4 or 5.

[19] The aryltetrahydropyridine compound or a salt thereof according to the above [1], wherein Q is Q-A, (i) when Q is Q-A, Q-A represents Q-1, Q-2, Q-3, Q-4, Q-9 or Q-12, and Z １ represents a halogen atom or cyano, J represents J-1, J-5, J-6, J-8, J-10, J-15, J-17, J-18, J-19, J-21, J-22, J-23, J-24, J-25 or J-26, G represents G-1, G-3, G-5, G-7, G-14, G-19, G-25, G-26, G-35 or G-41, Z ２ is a halogen atom, C １ ~C ６ Alkyl, halo (C １~C ６ ) alkyl, C １ ~C ６ Alkoxy, C １ ~C ６ Alkylthio, C １ ~C ６ Alkylsulfonyl, —N(R ４４ ) R ４５ , C １ ~C ６ Alkoxycarbonyl, C ３ ~C ６ represents cycloalkyl, cyano or nitro; R １ is a hydrogen atom, halo (C １ ~C ６ ) alkyl or hydroxy; R ２ is a hydrogen atom or C １ ~C ６

[20] The aryltetrahydropyridine compound or a salt thereof according to the above

[18] , wherein Q is Q-A, (i) when Q is Q-A, Q-A represents Q-1, Q-2, Q-3, Q-4, Q-6, Q-9, Q-10, Q-12 or Q-14, and Z １ is a halogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl, C １ ~C ６ represents alkoxy or cyano; Z ３ is C １ ~C ６ represents alkyl; Z ５ is C １ ~C ６ G represents G-1, G-2, G-3, G-5, G-7, G-14, G-19, G-25, G-26, G-35 or G-41; Z ２ is a halogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl, C １ ~C ６ Alkoxy, C １ ~C ６Alkylthio, C １ ~C ６ Alkylsulfinyl, C １ ~C ６ Alkylsulfonyl, —N(R ４４ ) R ４５ , C １ ~C ６ Alkoxycarbonyl, C １ ~C ６ Alkylcarbonylamino, C ３ ~C ６ represents cycloalkyl, cyano or nitro; Z ４ is C １ ~C ６ represents alkyl, R １ represents a hydrogen atom, a halogen atom, a halo (C １ ~C ６ ) alkyl, C １ ~C ６ represents alkyl or hydroxy; R ２ is a hydrogen atom, C １ ~C ６ Alkyl or —C(O)OR ５ represents R ３ represents a hydrogen atom, X represents an oxygen atom or a sulfur atom, Y represents an oxygen atom or a sulfur atom, t2 represents an integer of 0, 1 or 2, t3 represents an integer of 0, 1, 2 or 3, t4 represents an integer of 0, 1, 2, 3 or 4, and t5 represents an integer of 0, 1, 2, 3, 4 or 5.

[21] The aryltetrahydropyridine compound or a salt thereof according to the above

[18] , wherein Q is Q-A, and (i) when Q is Q-A, Q-A represents Q-1, Q-2, Q-3, Q-4, Q-9 or Q-12, and Z １ represents a halogen atom or cyano, J represents J-1, J-5, J-6, J-8, J-10, J-15, J-17, J-18, J-19, J-21, J-22, J-23, J-24, J-25 or J-26, G represents G-1, G-3, G-5, G-7, G-14, G-19, G-25, G-26, G-35 or G-41, Z ２ is a halogen atom, C １ ~C ６ Alkyl, halo (C １ ~C６ ) alkyl, C １ ~C ６ Alkoxy, C １ ~C ６ Alkylthio, C １ ~C ６ Alkylsulfonyl, —N(R ４４ ) R ４５ , C １ ~C ６ Alkoxycarbonyl, C １ ~C ６ Alkylcarbonylamino, C ３ ~C ６ represents cycloalkyl, cyano or nitro; R １ is a hydrogen atom, halo (C １ ~C ６ ) alkyl or hydroxy; R ２ is a hydrogen atom or C １ ~C ６

[22] The aryltetrahydropyridine compound or a salt thereof according to the above

[20] , wherein Q is Q-A, and (i) when Q is Q-A, Q-A represents Q-1, Q-2, Q-3, Q-4, Q-6, Q-9, Q-10, Q-12 or Q-14, and Z １ is a halogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl, C １ ~C ６ represents alkoxy or cyano; Z ３ is C １ ~C ６ J represents J-1, J-2, J-3, J-4, J-5, J-6, J-7, J-8, J-9, J-10, J-11, J-12, J-13, J-14, J-15, J-16, J-17, J-18, J-19, J-20, J-21, J-22 or J-23; Z ５ is C １ ~C ６ G represents G-1, G-2, G-3, G-5, G-7, G-14, G-26, G-35 or G-41; Z ２is a halogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl, C １ ~C ６ Alkylthio, C １ ~C ６ Alkylsulfinyl, C １ ~C ６ Alkylsulfonyl, C １ ~C ６ represents alkoxycarbonyl, cyano or nitro; Z ４ is C １ ~C ６ represents alkyl, R １ represents a hydrogen atom, a halogen atom, a halo (C １ ~C ６ ) alkyl or C １ ~C ６ represents alkyl, R ２ is a hydrogen atom, C １ ~C ６ Alkyl or —C(O)OR ５ represents R ３ represents a hydrogen atom, X represents an oxygen atom or a sulfur atom, Y represents an oxygen atom or a sulfur atom, t2 represents an integer of 0, 1 or 2, t3 represents an integer of 0, 1, 2 or 3, t4 represents an integer of 0, 1, 2, 3 or 4, and t5 represents an integer of 0, 1, 2, 3, 4 or 5.

[23] The aryltetrahydropyridine compound or a salt thereof according to the above

[18] , wherein Q is Q-A, and (i) when Q is Q-A, Q-A represents Q-1, Q-2, Q-3, Q-4, Q-9 or Q-12, and Z １ represents a halogen atom, J represents J-1, J-5, J-6, J-8, J-10, J-15, J-17, J-18, J-19, J-21, J-22 or J-23, G represents G-1, G-3, G-5, G-7, G-14, G-26, G-35 or G-41, Z ２ is a halogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl, C １ ~C６ represents alkoxycarbonyl, cyano or nitro; R １ is a hydrogen atom or halo (C １ ~C ６ ) alkyl, R ２ is a hydrogen atom or C １ ~C ６

[24] The aryltetrahydropyridine compound or a salt thereof according to the above

[22] , wherein Q is Q-A, and (i) when Q is Q-A, Q-A represents Q-1, Q-2, Q-3, Q-4, Q-6, Q-9, Q-10, Q-12 or Q-14, and Z １ is a halogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) represents alkyl or cyano; Z ３ is C １ ~C ６ J represents J-1, J-2, J-3, J-4, J-5, J-6, J-7, J-8, J-9, J-10, J-11, J-12, J-13, J-14, J-15, J-16, J-17, J-18, J-19, J-20, J-21, J-22 or J-23; Z ５ is C １ ~C ６ G represents G-1, G-2, G-3, G-5, G-7, G-14, G-26, G-35 or G-41; Z ２ is a halogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl, C １ ~C ６ represents alkoxycarbonyl, cyano or nitro; Z ４ is C １ ~C ６ represents alkyl, R ２ is a hydrogen atom, C １ ~C ６ Alkyl or —C(O)OR ５ represents R ３represents a hydrogen atom, X represents an oxygen atom or a sulfur atom, Y represents an oxygen atom or a sulfur atom, t2 represents an integer of 0, 1 or 2, t3 represents an integer of 0, 1, 2 or 3, t4 represents an integer of 0, 1, 2, 3 or 4, and t5 represents an integer of 0, 1, 2, 3, 4 or 5.

[25] The aryltetrahydropyridine compound or a salt thereof according to the above

[18] , wherein Q is Q-A, and (i) when Q is Q-A, Q-A represents Q-1, Q-2, Q-3, Q-4, Q-9 or Q-12, and Z １ represents a halogen atom, J represents J-1, J-5, J-6, J-8, J-10, J-15, J-17, J-18, J-19, J-21, J-22 or J-23, G represents G-1, G-3, G-5, G-7, G-14, G-26, G-35 or G-41, R ２ is a hydrogen atom or C １ ~C ６

[26] The aryltetrahydropyridine compound or salt thereof according to the above [1] to

[25] , wherein Q is Q-A, (i) when Q is Q-A, Q-A represents Q-1, Q-2, Q-3 or Q-4.

[27] The aryltetrahydropyridine compound or salt thereof according to any one of the above [1] to

[25] , wherein Q is Q-A, (i) when Q is Q-A, Q-A represents Q-1, Q-2 or Q-3.

[28] The aryltetrahydropyridine compound or salt thereof according to any one of the above [1] to

[25] , wherein Q is Q-A, (i) when Q is Q-A, Q-A represents Q-1.

[29] The aryltetrahydropyridine compound or salt thereof according to any one of the above [1] to

[25] , wherein Q is Q-A, (i) when Q is Q-A, Q-A represents Q-2 or Q-3.

[30] The aryltetrahydropyridine compound or salt thereof according to any one of the above [1] to

[25] , wherein Q is Q-A, (i) when Q is Q-A, Q-A represents Q-4.

[31] The aryltetrahydropyridine compound or salt thereof according to any one of the above [1] to

[25] , wherein Q is Q-A, (i) when Q is Q-A, Q-A represents Q-9, Q-10, Q-12 or Q-14.

[32] The aryltetrahydropyridine compound or salt thereof according to any one of the above [1] to

[25] , wherein Q is Q-A, (i) when Q is Q-A, Q-A represents Q-9 or Q-10.

[33] The aryltetrahydropyridine compound or salt thereof according to any one of the above [1] to

[25] , wherein Q is Q-A, (i) when Q is Q-A, Q-A represents Q-12 or Q-14.

[34] Q is Q-A, (i) when Q is Q-A, Z １ is a halogen atom or halo(C １ ~C ６

[35] The aryltetrahydropyridine compound or a salt thereof according to any one of the above [1] to

[33] , wherein Q is Q-A, and (i) when Q is Q-A, Z １

[36] The aryltetrahydropyridine compound or a salt thereof according to any one of the above [1] to

[33] , wherein Q is Q-A, and (i) when Q is Q-A, Z １ is Halo (C １ ~C ６

[37] The aryltetrahydropyridine compound or a salt thereof according to any one of the above [1] to

[33] , wherein Q is Q-A, and (i) when Q is Q-A, Z １ is C １ ~C ６ Alkyl, C １ ~C ６

[38] The aryltetrahydropyridine compound or a salt thereof according to any one of the above [1] to

[33] , wherein Q is Q-A, and (i) when Q is Q-A, Z １ is C １ ~C ６

[39] The aryltetrahydropyridine compound or a salt thereof according to any one of the above [1] to

[33] , wherein Q is Q-A, and (i) when Q is Q-A, Z １ is C １ ~C ６

[40] The aryltetrahydropyridine compound or a salt thereof according to any one of the above [1] to

[33] , wherein Q is Q-A, and (i) when Q is Q-A, Z １ is C １ ~C ６

[41] The aryltetrahydropyridine compound or a salt thereof according to any one of the above [1] to

[33] , wherein Q is Q-A, and (i) when Q is Q-A, J represents J-1, J-2, J-3, J-4, J-5, J-6, J-7, J-8, J-9, J-10, J-11, J-12, J-13, J-14, J-15, J-16, J-17, J-18, J-19, J-20, J-21, J-22, or J-23.

[42] The aryl tetrahydropyridine compound or salt thereof according to any one of the above [1] to

[40] , wherein Q is Q-A, (i) when Q is Q-A, J represents J-1, J-5, J-6, J-10, J-15, J-17, J-19, J-21, J-24 or J-27.

[43] The aryl tetrahydropyridine compound or salt thereof according to any one of the above [1] to

[40] , wherein Q is Q-A, (i) when Q is Q-A, J represents J-1, J-10 or J-19.

[44] The aryl tetrahydropyridine compound or salt thereof according to any one of the above [1] to

[40] , wherein Q is Q-A, (i) when Q is Q-A, J represents J-1.

[45] The aryl tetrahydropyridine compound or salt thereof according to any one of the above [1] to

[40] , wherein Q is Q-A, (i) when Q is Q-A, J represents J-10.

[46] The aryl tetrahydropyridine compound or salt thereof according to any one of the above [1] to

[40] , wherein Q is Q-A, (i) when Q is Q-A, J represents J-19.

[47] The aryl tetrahydropyridine compound or salt thereof according to any one of the above [1] to

[46] , wherein Q is Q-A, (i) when Q is Q-A, G represents G-1, G-2 or G-3.

[48] ​​The aryltetrahydropyridine compound or a salt thereof according to any one of the above [1] to

[46] , wherein Q is Q-A, and (i) when Q is Q-A, G represents G-2 or G-3.

[49] The aryl tetrahydropyridine compound or salt thereof according to any one of the above [1] to

[46] , wherein Q is Q-A, (i) when Q is Q-A, G represents G-2.

[50] The aryl tetrahydropyridine compound or salt thereof according to any one...

Claims

Formula (1): wherein Q is Q-A, Q-B or Q-C; (i) If Q is Q-A, then: Q-A is C １ ~C ６ Alkyl, R １７ (C １ ~C ６ ) alkyl, —N(R １８ ) R １９ , -OR ６２ or Q-1 to Q-82; R １７ is a halogen atom, C １ ~C ６ represents alkoxy or E-1 to E-83; R １８ is a hydrogen atom, C １ ~C ６ Alkyl or C ２ ~C ６ represents alkenyloxycarbonyl, R １９ are E-1 to E-63, E-65 to E-70, E-72 to E-80, C １ ~C ６ Alkyl, C １ ~C ６ Alkylcarbonyl, C １ ~C ６ Alkoxycarbonyl, C １ ~C ６ Alkylsulfonyl or R ２０ (C １ ~C ６ ) represents alkyl, R ２０ represents E-1 to E-83, R ６２ is a hydrogen atom or C １ ~C ６ represents alkyl, Z １ is a halogen atom, C １ ~C ６ Alkyl, C ２ ~C ６ Alkenyl, C ２ ~C ６ Alkynyl, halo(C １ ~C ６ ) alkyl, halo (C ２ ~C ６ ) alkenyl, halo(C ２ ~C ６ ) alkynyl, C １ ~C ６ Alkoxy, halo (C １ ~C ６ ) alkoxy, C ２ ~C ６ Alkenyloxy, halo(C ２ ~C ６ ) alkenyloxy, C ２ ~C ６ Alkynyloxy, halo(C ２ ~C ６ ) alkynyloxy, hydroxy, C １ ~C ６ Alkylcarbonyloxy, C １ ~C ６ Alkoxycarbonyloxy, C １ ~C ６ Alkyl sulfonyloxy, halo(C １ ~C ６ ) alkylsulfonyloxy, —OC(O)N(R ２６ ) R ２７ , C １ ~C ６ Alkylthio, C １ ~C ６ Alkylsulfinyl, C １ ~C ６ Alkyl sulfonyl, halo(C １ ~C ６ ) alkylthio, halo(C １ ~C ６ ) alkylsulfinyl, halo(C １ ~C ６ ) alkylsulfonyl, C ２ ~C ６ Alkenylthio, C ２ ~C ６ Alkenylsulfinyl, C ２ ~C ６ Alkenylsulfonyl, halo(C ２ ~C ６ ) alkenylthio, halo(C ２ ~C ６ ) alkenylsulfinyl, halo(C ２ ~C ６ ) alkenylsulfonyl, C ２ ~C ６ Alkynylthio, C ２ ~C ６ Alkynylsulfinyl, C ２ ~C ６ Alkynylsulfonyl, halo(C ２ ~C ６ ) alkynylthio, halo(C ２ ~C ６ ) alkynylsulfinyl, halo(C ２ ~C ６ ) alkynylsulfonyl, —SO ３ H, -S(O) ２ N (R ２８ ) R ２９ , -SC≡N, -S(O)(=NR ３０ ) R ３１ , -SF ５ , -N(R ３２ ) R ３３ , -N=S(O)(R ５４ ) R ５５ , formyl, carboxy, C １ ~C ６ Alkylcarbonyl, halo(C １ ~C ６ ) alkylcarbonyl, C １ ~C ６ Alkoxycarbonyl, halo(C １ ~C ６ ) alkoxycarbonyl, —C(O)N(R ３５ ) R ３６ , -C(=NOR １２ ) R １３ , Tori (C １ ~C ６ ) alkylsilyl, R ７ (C １ ~C ６ ) alkyl, R １６ (C １ ~C ６ ) alkoxy, C ３ ~C ６ Cycloalkyl, R ５８ (C ３ ~C ６ ) cycloalkyl, cyano, nitro, E-1 to E-56, E-61 to E-83, -O-(E-1) to -O-(E-63), -O-(E-65) to -O-(E-70), -O-(E-72) to -O-(E-80), -S-(E-1) to -S-(E-63), -S-(E-65) to -S-(E-70), -S-(E-72) to -S-(E-80), -S(O)-(E-1) to -S(O)-(E-83), -S(O) ２ -(E-1)~-S(O) ２ -(E-83), -C(O)-(E-1) to -C(O)-(E-83), -N=N-(E-1) to -N=N-(E-63), -N=N-(E-65) to -N=N-(E-70), or -N=N-(E-72) to -N=N-(E-80), Z １ In the above relationship, when t2 represents an integer of 2, t3 represents an integer of 2 or 3, t4 represents an integer of 2, 3 or 4, and t5 represents an integer of 2, 3, 4 or 5, each of Z １ may be the same as or different from each other, E １ is a halogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl, C １ ~C ６ Alkoxy, C １ ~C ６ Alkylthio, halo(C １ ~C ６ ) alkylthio, C １ ~C ６ Alkylsulfinyl, C １ ~C ６ represents alkylsulfonyl or cyano; E １ In the above relationship, when t2 represents an integer of 2, t3 represents an integer of 2 or 3, t4 represents an integer of 2, 3 or 4, and t5 represents an integer of 2, 3, 4 or 5, each E １ may be the same as or different from each other, E ３ is a hydrogen atom, C １ ~C ６ Alkyl or halo(C １ ~C ６ ) represents alkyl, R ７ is C １ ~C ６ Alkoxy (C １ ~C ６ ) alkoxy, cyano, C １ ~C ６ Alkoxy, C １ ~C ６ Alkylcarbonyloxy, carboxy, C １ ~C ６ Alkylcarbonyl, C １ ~C ６ Alkoxycarbonyl, —C(O)N(R ３７ ) R ３８ , -N(R ３９ ) R ４０ , C １ ~C ６ Alkylthio, C １ ~C ６ alkylsulfonyl or E-1 to E-83; R １６ is C １ ~C ６ Alkylthio, C １ ~C ６ Alkylsulfinyl, C １ ~C ６ Alkylsulfonyl, —C(O)N(R ４１ ) R ４２ , C １ ~C ６ Alkoxy, halo (C １ ~C ６ ) alkoxy, C １ ~C ６ Alkoxy (C １ ~C ６ ) alkoxy, E-1 to E-83, or —C(O)—(E-1) to —C(O)—(E-83), R １２ is a hydrogen atom, C １ ~C ６ Alkyl or halo(C １ ~C ６ ) represents alkyl, R １３ is a hydrogen atom, C １ ~C ６ Alkyl or halo(C １ ~C ６ ) represents alkyl, Z ３ is a hydrogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl, C １ ~C ６ Alkoxy (C １ ~C ６ ) alkyl, C １ ~C ６ Alkylcarbonyl, halo(C １ ~C ６ ) alkylcarbonyl, C １ ~C ６ Alkoxycarbonyl or halo(C １ ~C ６ ) represents alkoxycarbonyl; R ２６ is a hydrogen atom or C １ ~C ６ represents alkyl, R ２７ is a hydrogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl or C ３ ~C ６ represents cycloalkyl, R ２８ is a hydrogen atom or C １ ~C ６ represents alkyl, R ２９ is a hydrogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl, C ３ ~C ６ Cycloalkyl, C １ ~C ６ Alkylcarbonyl, halo(C １ ~C ６ ) alkylcarbonyl or C １ ~C ６ represents an alkoxycarbonyl; R ３０ is a hydrogen atom, C １ ~C ６ Alkyl or halo(C １ ~C ６ ) represents alkyl, R ３１ is C １ ~C ６ Alkyl or halo(C １ ~C ６ ) represents alkyl, R ３２ is a hydrogen atom or C １ ~C ６ represents alkyl, R ３３ is a hydrogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl, C １ ~C ６ Alkylcarbonyl, halo(C １ ~C ６ ) alkylcarbonyl, C １ ~C ６ Alkoxycarbonyl, halo(C １ ~C ６ ) alkoxycarbonyl, C １ ~C ６ Alkylaminocarbonyl, di(C １ ~C ６ ) alkylaminocarbonyl, —C(O)NHC(O)OR ３４ , -C(S)NHC(O)OR ３４ or C １ ~C ６ represents alkylsulfonyl, R ３４ is C １ ~C ６ represents alkyl, R ３５ is a hydrogen atom or C １ ~C ６ represents alkyl, R ３６ is a hydrogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl or C ３ ~C ６ represents cycloalkyl, R ３７ is a hydrogen atom or C １ ~C ６ represents alkyl, R ３８ is a hydrogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl or C ３ ~C ６ represents cycloalkyl, R ３９ is a hydrogen atom, C １ ~C ６ Alkyl or halo(C １ ~C ６ ) represents alkyl, R ４０ is a hydrogen atom, C １ ~C ６ Alkyl, C １ ~C ６ Alkylcarbonyl or C １ ~C ６ represents an alkoxycarbonyl; R ４１ is a hydrogen atom or C １ ~C ６ represents alkyl, R ４２ is a hydrogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl or C ３ ~C ６ represents cycloalkyl, R ５４ is C １ ~C ６ represents alkyl, R ５５ is C １ ~C ６ represents alkyl, R ５８ is a halogen atom, C １ ~C ６ represents alkoxy or cyano; J represents J-1 to J-52; Z ５ is a hydrogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl, C １ ~C ６ Alkoxy (C １ ~C ６ ) alkyl, C １ ~C ６ Alkylcarbonyl, halo(C １ ~C ６ ) alkylcarbonyl, C １ ~C ６ Alkoxycarbonyl, halo(C １ ~C ６ ) alkoxycarbonyl, C １ ~C ６ Alkyl sulfonyl or halo(C １ ~C ６ ) represents alkylsulfonyl, G represents G-1 to G-65; Z ２ is a halogen atom, C １ ~C ６ Alkyl, C ２ ~C ６ Alkenyl, C ２ ~C ６ Alkynyl, halo(C １ ~C ６ ) alkyl, halo (C ２ ~C ６ ) alkenyl, halo(C ２ ~C ６ ) alkynyl, C １ ~C ６ Alkoxy, halo (C １ ~C ６ ) alkoxy, C ２ ~C ６ Alkenyloxy, halo(C ２ ~C ６ ) alkenyloxy, C ２ ~C ６ Alkynyloxy, halo(C ２ ~C ６ ) alkynyloxy, hydroxy, C １ ~C ６ Alkylcarbonyloxy, C １ ~C ６ Alkoxycarbonyloxy, C １ ~C ６ Alkyl sulfonyloxy, halo(C １ ~C ６ ) alkylsulfonyloxy, —OC(O)N(R ６０ ) R ６１ , C １ ~C ６ Alkylthio, C １ ~C ６ Alkylsulfinyl, C １ ~C ６ Alkyl sulfonyl, halo(C １ ~C ６ ) alkylthio, halo(C １ ~C ６ ) alkylsulfinyl, halo(C １ ~C ６ ) alkylsulfonyl, C ２ ~C ６ Alkenylthio, C ２ ~C ６ Alkenylsulfinyl, C ２ ~C ６ Alkenylsulfonyl, halo(C ２ ~C ６ ) alkenylthio, halo(C ２ ~C ６ ) alkenylsulfinyl, halo(C ２ ~C ６ ) alkenylsulfonyl, C ２ ~C ６ Alkynylthio, C ２ ~C ６ Alkynylsulfinyl, C ２ ~C ６ Alkynylsulfonyl, halo(C ２ ~C ６ ) alkynylthio, halo(C ２ ~C ６ ) alkynylsulfinyl, halo(C ２ ~C ６ ) alkynylsulfonyl, —SO ３ H, -S(O) ２ N (R ４８ ) R ４９ , -SC≡N, -S(O)(=NR ５２ ) R ５３ , -SF ５ , -N(R ４４ ) R ４５ , -N=S(O)(R ５６ ) R ５７ , formyl, carboxy, C １ ~C ６ Alkylcarbonyl, halo(C １ ~C ６ ) alkylcarbonyl, C １ ~C ６ Alkoxycarbonyl, halo(C １ ~C ６ ) alkoxycarbonyl, —C(O)N(R ４６ ) R ４７ , -C(=NOR １４ ) R １５ , Tori (C １ ~C ６ ) alkylsilyl, R ２４ (C １ ~C ６ ) alkyl, R ２５ (C １ ~C ６ ) alkoxy, C ３ ~C ６ Cycloalkyl, R ５９ (C ３ ~C ６ ) cycloalkyl, cyano, nitro, M-1 to M-56, M-61 to M-82, —O-(M-1) to —O-(M-63), —O-(M-65) to —O-(M-70), or —O-(M-72) to —O-(M-80), Z ２ In the above relationship, when t2 represents an integer of 2, t3 represents an integer of 2 or 3, t4 represents an integer of 2, 3 or 4, and t5 represents an integer of 2, 3, 4 or 5, each of Z ２ may be the same as or different from each other, R ２４ is C １ ~C ６ Alkoxy, hydroxy or -N(R ５０ ) R ５１ represents R ２５ is C １ ~C ６ represents alkoxy or M-1 to M-82; M １ is a halogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl, C １ ~C ６ Alkoxy, C １ ~C ６ Alkylthio, halo(C １ ~C ６ ) alkylthio, C １ ~C ６ Alkylsulfinyl, C １ ~C ６ represents alkylsulfonyl or cyano; M １ In the above relationship, when t2 represents an integer of 2, t3 represents an integer of 2 or 3, t4 represents an integer of 2, 3 or 4, and t5 represents an integer of 2, 3, 4 or 5, each of M １ may be the same as or different from each other, M ３ is a hydrogen atom, C １ ~C ６ Alkyl or halo(C １ ~C ６ ) represents alkyl, R １４ is a hydrogen atom, C １ ~C ６ Alkyl or halo(C １ ~C ６ ) represents alkyl, R １５ is a hydrogen atom, C １ ~C ６ Alkyl or halo(C １ ~C ６ ) represents alkyl, Z ４ is a hydrogen atom, C １ ~C ６ Alkyl, C １ ~C ６ Alkylcarbonyl, C １ ~C ６ Alkoxycarbonyl, C １ ~C ６ Alkoxy (C １ ~C ６ ) alkyl or C １ ~C ６ represents alkylsulfonyl, R ４４ is a hydrogen atom, C １ ~C ６ Alkyl or halo(C １ ~C ６ ) represents alkyl, R ４５ is a hydrogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl, C １ ~C ６ Alkylcarbonyl, halo(C １ ~C ６ ) alkylcarbonyl, C １ ~C ６ Alkoxycarbonyl, halo(C １ ~C ６ ) alkoxycarbonyl, C １ ~C ６ Alkyl sulfonyl or halo(C １ ~C ６ ) represents alkylsulfonyl, R ４６ is a hydrogen atom or C １ ~C ６ represents alkyl, R ４７ is a hydrogen atom, C １ ~C ６ Alkyl or halo(C １ ~C ６ ) represents alkyl, R ４８ is a hydrogen atom, C １ ~C ６ Alkyl or halo(C １ ~C ６ ) represents alkyl, R ４９ is a hydrogen atom, C １ ~C ６ Alkyl or halo(C １ ~C ６ ) represents alkyl, R ５０ is a hydrogen atom or C １ ~C ６ represents alkyl, R ５１ is a hydrogen atom, C １ ~C ６ Alkyl, C １ ~C ６ Alkylcarbonyl, halo(C １ ~C ６ ) alkylcarbonyl, C １ ~C ６ Alkoxycarbonyl, halo(C １ ~C ６ ) alkoxycarbonyl, C １ ~C ６ Alkyl sulfonyl or halo(C １ ~C ６ ) represents alkylsulfonyl, R ５２ is a hydrogen atom or C １ ~C ６ represents alkyl, R ５３ is C １ ~C ６ represents alkyl, R ５６ is C １ ~C ６ represents alkyl, R ５７ is C １ ~C ６ represents alkyl, R ５９ is a halogen atom, C １ ~C ６ represents alkoxy or cyano; R ６０ is a hydrogen atom or C １ ~C ６ represents alkyl, R ６１ is a hydrogen atom, C １ ~C ６ Alkyl or halo(C １ ~C ６ ) represents alkyl, R １ represents a hydrogen atom, a halogen atom, or C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl, C １ ~C ６ Alkoxy, hydroxy, C １ ~C ６ Alkylthio, C １ ~C ６ Alkylsulfinyl, C １ ~C ６ Alkyl sulfonyl, halo(C １ ~C ６ ) alkylthio, halo(C １ ~C ６ ) alkylsulfinyl, halo(C １ ~C ６ ) alkylsulfonyl, —N(R １ｄ ) R １ｅ , cyano or nitro; R １ａ represents a hydrogen atom, a halogen atom, or C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl, C １ ~C ６ Alkoxy, hydroxy, -N(R １ｄ ) R １ｅ , cyano or nitro; R １ｂ represents a hydrogen atom, a halogen atom, or C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl, C １ ~C ６ Alkoxy, hydroxy, -N(R １ｄ ) R １ｅ , cyano or nitro; R １ｃ represents a hydrogen atom, a halogen atom, or C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl, C １ ~C ６ Alkoxy, hydroxy, -N(R １ｄ ) R １ｅ , cyano or nitro; R １ｄ is a hydrogen atom or C １ ~C ６ represents alkyl, R １ｅ is a hydrogen atom or C １ ~C ６ represents alkyl, R ２ is a hydrogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl, C ２ ~C ６ Alkenyl, C ２ ~C ６ Alkynyl, C ３ ~C ６ cycloalkyl, —C(O)R ４ , -C(O)OR ５ or R ６７ (C １ ~C ６ ) represents alkyl, R ６７ is C １ ~C ６ Alkoxy, C １ ~C ６ Alkylthio, C １ ~C ６ Alkylsulfinyl, C １ ~C ６ alkylsulfonyl, cyano, or V-1 to V-82; V １ is a halogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl, C １ ~C ６ Alkoxy, C １ ~C ６ Alkylthio, C １ ~C ６ Alkylsulfinyl, C １ ~C ６ represents alkylsulfonyl, cyano or nitro, V １ In the above relationship, when t2 represents an integer of 2, t3 represents an integer of 2 or 3, t4 represents an integer of 2, 3 or 4, and t5 represents an integer of 2, 3, 4 or 5, each of V １ may be the same as or different from each other, V ３ is a hydrogen atom, C １ ~C ６ Alkyl or halo(C １ ~C ６ ) represents alkyl, R ４ is C １ ~C ６ Alkyl, C ２ ~C ６ Alkenyl, C ２ ~C ６ Alkynyl, C １ ~C ６ Alkylcarbonyl, C １ ~C ６ Alkoxycarbonyl, C １ ~C ６ Alkylamino, di(C １ ~C ６ ) alkylamino, R ６ (C １ ~C ６ ) alkyl or V-1 to V-82; R ５ is C １ ~C ６ Alkyl, C ２ ~C ６ Alkenyl, C ２ ~C ６ Alkynyl, R ９ (C １ ~C ６ ) alkyl, V-1 to V-63, V-65 to V-70, or V-72 to V-80; R ６ is a halogen atom, C １ ~C ６ represents alkoxy, cyano, nitro, or V-1 to V-82; R ９ is a halogen atom, C １ ~C ６ represents alkoxy, cyano, nitro, or V-1 to V-82; n represents an integer of 0, 1 or 2; (ii) When Q is Q-B, Q-B is C １ ~C ６ Alkyl, R １７ (C １ ~C ６ ) alkyl, —N(R １８ ) R １９ , -OR ６２ or Q-1 to Q-82; R １７ is a halogen atom, C １ ~C ６ represents alkoxy or E-1 to E-83; R １８ is a hydrogen atom, C １ ~C ６ Alkyl or C ２ ~C ６ represents alkenyloxycarbonyl, R １９ are E-1 to E-63, E-65 to E-70, E-72 to E-80, C １ ~C ６ Alkyl, C １ ~C ６ Alkylcarbonyl, C １ ~C ６ Alkoxycarbonyl, C １ ~C ６ Alkylsulfonyl or R ２０ (C １ ~C ６ ) represents alkyl, R ２０ represents E-1 to E-83, R ６２ is a hydrogen atom or C １ ~C ６ represents alkyl, Z １ is a halogen atom, C １ ~C ６ Alkyl, C ２ ~C ６ Alkenyl, C ２ ~C ６ Alkynyl, halo(C １ ~C ６ ) alkyl, halo (C ２ ~C ６ ) alkenyl, halo(C ２ ~C ６ ) alkynyl, C １ ~C ６ Alkoxy, halo (C １ ~C ６ ) alkoxy, C １ ~C ６ Alkenyloxy, halo(C ２ ~C ６ ) alkenyloxy, C １ ~C ６ Alkynyloxy, halo(C ２ ~C ６ ) alkynyloxy, hydroxy, C １ ~C ６ Alkylcarbonyloxy, C １ ~C ６ Alkoxycarbonyloxy, C １ ~C ６ Alkyl sulfonyloxy, halo(C １ ~C ６ ) alkylsulfonyloxy, —OC(O)N(R ２６ ) R ２７ , C １ ~C ６ Alkylthio, C １ ~C ６ Alkylsulfinyl, C １ ~C ６ Alkyl sulfonyl, halo(C １ ~C ６ ) alkylthio, halo(C １ ~C ６ ) alkylsulfinyl, halo(C １ ~C ６ ) alkylsulfonyl, C ２ ~C ６ Alkenylthio, C ２ ~C ６ Alkenylsulfinyl, C ２ ~C ６ Alkenylsulfonyl, halo(C ２ ~C ６ ) alkenylthio, halo(C ２ ~C ６ ) alkenylsulfinyl, halo(C ２ ~C ６ ) alkenylsulfonyl, C ２ ~C ６ Alkynylthio, C ２ ~C ６ Alkynylsulfinyl, C ２ ~C ６ Alkynylsulfonyl, halo(C ２ ~C ６ ) alkynylthio, halo(C ２ ~C ６ ) alkynylsulfinyl, halo(C ２ ~C ６ ) alkynylsulfonyl, —SO ３ H, -S(O) ２ N (R ２８ ) R ２９ , -SC≡N, -S(O)(=NR ３０ ) R ３１ , -SF ５ , -N(R ３２ ) R ３３ , -N=S(O)(R ５４ ) R ５５ , formyl, carboxy, C １ ~C ６ Alkylcarbonyl, halo(C １ ~C ６ ) alkylcarbonyl, C １ ~C ６ Alkoxycarbonyl, halo(C １ ~C ６ ) alkoxycarbonyl, —C(O)N(R ３５ ) R ３６ , -C(=NOR １２ ) R １３ , Tori (C １ ~C ６ ) alkylsilyl, R ７ (C １ ~C ６ ) alkyl, R １６ (C １ ~C ６ ) alkoxy, C ３ ~C ６ Cycloalkyl, R ５８ (C ３ ~C ６ ) cycloalkyl, cyano, nitro, E-1 to E-56, E-61 to E-83, -O-(E-1) to -O-(E-63), -O-(E-65) to -O-(E-70), -O-(E-72) to -O-(E-80), -S-(E-1) to -S-(E-63), -S-(E-65) to -S-(E-70), -S-(E-72) to -S-(E-80), -S(O)-(E-1) to -S(O)-(E-83), -S(O) ２ -(E-1)~-S(O) ２ -(E-83), -C(O)-(E-1) to -C(O)-(E-83), -N=N-(E-1) to -N=N-(E-63), -N=N-(E-65) to -N=N-(E-70), or -N=N-(E-72) to -N=N-(E-80), Z １ In the above relationship, when t2 represents an integer of 2, t3 represents an integer of 2 or 3, t4 represents an integer of 2, 3 or 4, and t5 represents an integer of 2, 3, 4 or 5, each of Z １ may be the same as or different from each other, E １ is a halogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl, C １ ~C ６ Alkoxy, C １ ~C ６ Alkylthio, halo(C １ ~C ６ ) alkylthio, C １ ~C ６ Alkylsulfinyl, C １ ~C ６ represents alkylsulfonyl or cyano; E １ In the above relationship, when t2 represents an integer of 2, t3 represents an integer of 2 or 3, t4 represents an integer of 2, 3 or 4, and t5 represents an integer of 2, 3, 4 or 5, each E １ may be the same as or different from each other, E ３ is a hydrogen atom, C １ ~C ６ Alkyl or halo(C １ ~C ６ ) represents alkyl, R ７ is C １ ~C ６ Alkoxy (C １ ~C ６ ) alkoxy, cyano, C １ ~C ６ Alkoxy, C １ ~C ６ Alkylcarbonyloxy, carboxy, C １ ~C ６ Alkylcarbonyl, C １ ~C ６ Alkoxycarbonyl, —C(O)N(R ３７ ) R ３８ , -N(R ３９ ) R ４０ , C １ ~C ６ Alkylthio, C １ ~C ６ alkylsulfonyl or E-1 to E-83; R １６ is C １ ~C ６ Alkylthio, C １ ~C ６ Alkylsulfinyl, C １ ~C ６ Alkylsulfonyl, —C(O)N(R ４１ ) R ４２ , C １ ~C ６ Alkoxy, halo (C １ ~C ６ ) alkoxy, C １ ~C ６ Alkoxy (C １ ~C ６ ) alkoxy, E-1 to E-83, or —C(O)—(E-1) to —C(O)—(E-83), R １２ is a hydrogen atom, C １ ~C ６ Alkyl or halo(C １ ~C ６ ) represents alkyl, R １３ is a hydrogen atom, C １ ~C ６ Alkyl or halo(C １ ~C ６ ) represents alkyl, Z ３ is a hydrogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl, C １ ~C ６ Alkoxy (C １ ~C ６ ) alkyl, C １ ~C ６ Alkylcarbonyl, halo(C １ ~C ６ ) alkylcarbonyl, C １ ~C ６ Alkoxycarbonyl or halo(C １ ~C ６ ) represents alkoxycarbonyl; R ２６ is a hydrogen atom or C １ ~C ６ represents alkyl, R ２７ is a hydrogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl or C ３ ~C ６ represents cycloalkyl, R ２８ is a hydrogen atom or C １ ~C ６ represents alkyl, R ２９ is a hydrogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl, C ３ ~C ６ Cycloalkyl, C １ ~C ６ Alkylcarbonyl, halo(C １ ~C ６ ) alkylcarbonyl or C １ ~C ６ represents an alkoxycarbonyl; R ３０ is a hydrogen atom, C １ ~C ６ Alkyl or halo(C １ ~C ６ ) represents alkyl, R ３１ is C １ ~C ６ Alkyl or halo(C １ ~C ６ ) represents alkyl, R ３２ is a hydrogen atom or C １ ~C ６ represents alkyl, R ３３ is a hydrogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl, C １ ~C ６ Alkylcarbonyl, halo(C １ ~C ６ ) alkylcarbonyl, C １ ~C ６ Alkoxycarbonyl, halo(C １ ~C ６ ) alkoxycarbonyl, C １ ~C ６ Alkylaminocarbonyl, di(C １ ~C ６ ) alkylaminocarbonyl, —C(O)NHC(O)OR ３４ , -C(S)NHC(O)OR ３４ or C １ ~C ６ represents alkylsulfonyl, R ３４ is C １ ~C ６ represents alkyl, R ３５ is a hydrogen atom or C １ ~C ６ represents alkyl, R ３６ is a hydrogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl or C ３ ~C ６ represents cycloalkyl, R ３７ is a hydrogen atom or C １ ~C ６ represents alkyl, R ３８ is a hydrogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl or C ３ ~C ６ represents cycloalkyl, R ３９ is a hydrogen atom, C １ ~C ６ Alkyl or halo(C １ ~C ６ ) represents alkyl, R ４０ is a hydrogen atom, C １ ~C ６ Alkyl, C １ ~C ６ Alkylcarbonyl or C １ ~C ６ represents an alkoxycarbonyl; R ４１ is a hydrogen atom or C １ ~C ６ represents alkyl, R ４２ is a hydrogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl or C ３ ~C ６ represents cycloalkyl, R ５４ is C １ ~C ６ represents alkyl, R ５５ is C １ ~C ６ represents alkyl, R ５８ is a halogen atom, C １ ~C ６ represents alkoxy or cyano; J represents J-1′ or J-2′; A １ is a nitrogen atom or CR １ｃ represents G is -N(R ２１ ) R ２２ , -C(=NOR ６７ ) R ６８ , R ６９ (C １ ~C ６ ) alkyl or G-1′ to G-160′, R ２１ is a hydrogen atom, C １ ~C ６ Alkyl or halo(C １ ~C ６ ) represents alkyl, R ２２ is a hydrogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl, C ２ ~C ６ Alkenyl, halo(C ２ ~C ６ ) alkenyl, C ２ ~C ６ Alkynyl, halo(C ２ ~C ６ ) alkynyl, R ２３ (C １ ~C ６ ) alkyl or M-1 to M-82, R ２３ is C １ ~C ６ Alkoxy, C １ ~C ６ Alkylcarbonyl, C １ ~C ６ Alkoxycarbonyl, hydroxy, cyano, C １ ~C ６ Alkylamino, di(C １ ~C ６ ) alkylamino, C １ ~C ６ Alkylcarbonylamino, C １ ~C ６ alkoxycarbonylamino or M-1 to M-82, R ６７ is a hydrogen atom, C １ ~C ６ Alkyl or halo(C １ ~C ６ ) represents alkyl, R ６８ is a hydrogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl or M-1 to M-82, R ６９ M-1 to M-82, -N(R ７０ ) R ７１ , -C(=O)N(R ７２ ) R ７３ or -C(=NOR ７４ ) R ７５ represents R ７０ is a hydrogen atom or C １ ~C ６ represents alkyl, R ７１ is -C(=O)R ７６ represents R ７６ is C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl or M-1 to M-82, R ７２ is a hydrogen atom or C １ ~C ６ represents alkyl, R ７３ represents M-1 to M-82, R ７４ is a hydrogen atom or C １ ~C ６ represents alkyl, R ７５ is a hydrogen atom, C １ ~C ６ Alkyl or C ３ ~C ６ represents cycloalkyl, Z ２ is a halogen atom, C １ ~C ６ Alkyl, C ２ ~C ６ Alkenyl, C ２ ~C ６ Alkynyl, halo(C １ ~C ６ ) alkyl, halo (C ２ ~C ６ ) alkenyl, halo(C ２ ~C ６ ) alkynyl, C １ ~C ６ Alkoxy, halo (C １ ~C ６ ) alkoxy, C ２ ~C ６ Alkenyloxy, halo(C ２ ~C ６ ) alkenyloxy, C ２ ~C ６ Alkynyloxy, halo(C ２ ~C ６ ) alkynyloxy, hydroxy, C １ ~C ６ Alkylcarbonyloxy, C １ ~C ６ Alkoxycarbonyloxy, C １ ~C ６ Alkyl sulfonyloxy, halo(C １ ~C ６ ) alkylsulfonyloxy, —OC(O)N(R ６０ ) R ６１ , C １ ~C ６ Alkylthio, C １ ~C ６ Alkylsulfinyl, C １ ~C ６ Alkyl sulfonyl, halo(C １ ~C ６ ) alkylthio, halo(C １ ~C ６ ) alkylsulfinyl, halo(C １ ~C ６ ) alkylsulfonyl, C ２ ~C ６ Alkenylthio, C ２ ~C ６ Alkenylsulfinyl, C ２ ~C ６ Alkenylsulfonyl, halo(C ２ ~C ６ ) alkenylthio, halo(C ２ ~C ６ ) alkenylsulfinyl, halo(C ２ ~C ６ ) alkenylsulfonyl, C ２ ~C ６ Alkynylthio, C ２ ~C ６ Alkynylsulfinyl, C ２ ~C ６ Alkynylsulfonyl, halo(C ２ ~C ６ ) alkynylthio, halo(C ２ ~C ６ ) alkynylsulfinyl, halo(C ２ ~C ６ ) alkynylsulfonyl, —SO ３ H, -S(O) ２ N (R ４８ ) R ４９ , -SC≡N, -S(O)(=NR ５２ ) R ５３ , -SF ５ , -N(R ４４ ) R ４５ , -N=S(O)(R ５６ ) R ５７ , formyl, carboxy, C １ ~C ６ Alkylcarbonyl, halo(C １ ~C ６ ) alkylcarbonyl, C １ ~C ６ Alkoxycarbonyl, halo(C １ ~C ６ ) alkoxycarbonyl, —C(O)N(R ４６ ) R ４７ , -C(=NOR １４ ) R １５ , Tori (C １ ~C ６ ) alkylsilyl, R ２４ (C １ ~C ６ ) alkyl, R ２５ (C １ ~C ６ ) alkoxy, C ３ ~C ６ Cycloalkyl, R ５９ (C ３ ~C ６ ) cycloalkyl, cyano, nitro, M-1 to M-56, M-61 to M-82, —O-(M-1) to —O-(M-63), —O-(M-65) to —O-(M-70), or —O-(M-72) to —O-(M-80), Z ２ In the above relationship, when t2 represents an integer of 2, t3 represents an integer of 2 or 3, t4 represents an integer of 2, 3 or 4, and t5 represents an integer of 2, 3, 4 or 5, each of Z ２ may be the same as or different from each other, Alternatively, t4 represents an integer of 2, and two Z ２ When two Z ２ together form oxo, -CH ２ CH ２ -, -OCH ２ CH ２ O-, -OCH ２ CH ２ CH ２ O-, = NOR ４３ , =NN(R ６３ ) R ６４ or =NN=C(R ６５ ) R ６６ represents R ４３ is a hydrogen atom or C １ ~C ６ represents alkyl, R ２４ is C １ ~C ６ Alkoxy, hydroxy or -N(R ５０ ) R ５１ represents R ２５ is C １ ~C ６ represents alkoxy or M-1 to M-82; M １ is a halogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl, C １ ~C ６ Alkoxy, C １ ~C ６ Alkylthio, halo(C １ ~C ６ ) alkylthio, C １ ~C ６ Alkylsulfinyl, C １ ~C ６ represents alkylsulfonyl or cyano; M １ In the above relationship, when t2 represents an integer of 2, t3 represents an integer of 2 or 3, t4 represents an integer of 2, 3 or 4, and t5 represents an integer of 2, 3, 4 or 5, each of M １ may be the same as or different from each other, M ３ is a hydrogen atom, C １ ~C ６ Alkyl or halo(C １ ~C ６ ) represents alkyl, R １４ is a hydrogen atom, C １ ~C ６ Alkyl or halo(C １ ~C ６ ) represents alkyl, R １５ is a hydrogen atom, C １ ~C ６ Alkyl or halo(C １ ~C ６ ) represents alkyl, Z ４ is a hydrogen atom, C １ ~C ６ Alkyl, C １ ~C ６ Alkylcarbonyl, C １ ~C ６ Alkoxycarbonyl, C １ ~C ６ Alkoxy (C １ ~C ６ ) alkyl or C １ ~C ６ represents alkylsulfonyl, R ４４ is a hydrogen atom, C １ ~C ６ Alkyl or halo(C １ ~C ６ ) represents alkyl, R ４５ is a hydrogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl, C １ ~C ６ Alkylcarbonyl, halo(C １ ~C ６ ) alkylcarbonyl, C １ ~C ６ Alkoxycarbonyl, halo(C １ ~C ６ ) alkoxycarbonyl, C １ ~C ６ Alkyl sulfonyl or halo(C １ ~C ６ ) represents alkylsulfonyl, R ４６ is a hydrogen atom or C １ ~C ６ represents alkyl, R ４７ is a hydrogen atom, C １ ~C ６ Alkyl or halo(C １ ~C ６ ) represents alkyl, R ４８ is a hydrogen atom, C １ ~C ６ Alkyl or halo(C １ ~C ６ ) represents alkyl, R ４９ is a hydrogen atom, C １ ~C ６ Alkyl or halo(C １ ~C ６ ) represents alkyl, R ５０ is a hydrogen atom or C １ ~C ６ represents alkyl, R ５１ is a hydrogen atom, C １ ~C ６ Alkyl, C １ ~C ６ Alkylcarbonyl, halo(C １ ~C ６ ) alkylcarbonyl, C １ ~C ６ Alkoxycarbonyl, halo(C １ ~C ６ ) alkoxycarbonyl, C １ ~C ６ Alkyl sulfonyl or halo(C １ ~C ６ ) represents alkylsulfonyl, R ５２ is a hydrogen atom or C １ ~C ６ represents alkyl, R ５３ is C １ ~C ６ represents alkyl, R ５６ is C １ ~C ６ represents alkyl, R ５７ is C １ ~C ６ represents alkyl, R ５９ is a halogen atom, C １ ~C ６ represents alkoxy or cyano; R ６０ is a hydrogen atom or C １ ~C ６ represents alkyl, R ６１ is a hydrogen atom, C １ ~C ６ Alkyl or halo(C １ ~C ６ ) represents alkyl, R ６３ is a hydrogen atom or C １ ~C ６ represents alkyl, R ６４ is a hydrogen atom, C １ ~C ６ Alkyl, C １ ~C ６ Alkylcarbonyl, halo(C １ ~C ６ ) alkylcarbonyl, C １ ~C ６ Alkoxycarbonyl, halo(C １ ~C ６ ) alkoxycarbonyl, C １ ~C ６ Alkyl sulfonyl or halo(C １ ~C ６ ) represents alkylsulfonyl, R ６５ is a hydrogen atom or C １ ~C ６ represents alkyl, R ６６ is C １ ~C ６ represents alkyl, R １ represents a hydrogen atom, a halogen atom, or C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl, C １ ~C ６ Alkoxy, hydroxy, C １ ~C ６ Alkylthio, C １ ~C ６ Alkylsulfinyl, C １ ~C ６ Alkyl sulfonyl, halo(C １ ~C ６ ) alkylthio, halo(C １ ~C ６ ) alkylsulfinyl, halo(C １ ~C ６ ) alkylsulfonyl, —N(R １ｄ ) R １ｅ , cyano or nitro; R １ａ represents a hydrogen atom, a halogen atom, or C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl, C １ ~C ６ Alkoxy, hydroxy, -N(R １ｄ ) R １ｅ , cyano or nitro; R １ｂ represents a hydrogen atom, a halogen atom, or C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl, C １ ~C ６ Alkoxy, hydroxy, -N(R １ｄ ) R １ｅ , cyano or nitro; R １ｃ represents a hydrogen atom, a halogen atom, or C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl, C １ ~C ６ Alkoxy, hydroxy, -N(R １ｄ ) R １ｅ , cyano or nitro; R １ｄ is a hydrogen atom or C １ ~C ６ represents alkyl, R １ｅ is a hydrogen atom or C １ ~C ６ represents alkyl, R ２ is a hydrogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl, C ２ ~C ６ Alkenyl, C ２ ~C ６ Alkynyl, C ３ ~C ６ cycloalkyl, —C(O)R ４ , -C(O)OR ５ , or R ６７ (C １ ~C ６ ) represents alkyl, R ６７ is C １ ~C ６ Alkoxy, C １ ~C ６ Alkylthio, C １ ~C ６ Alkylsulfinyl, C １ ~C ６ alkylsulfonyl, cyano, or V-1 to V-82; V １ is a halogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl, C １ ~C ６ Alkoxy, C １ ~C ６ Alkylthio, C １ ~C ６ Alkylsulfinyl, C １ ~C ６ represents alkylsulfonyl, cyano or nitro, V １ In the above relationship, when t2 represents an integer of 2, t3 represents an integer of 2 or 3, t4 represents an integer of 2, 3 or 4, and t5 represents an integer of 2, 3, 4 or 5, each of V １ may be the same as or different from each other, V ３ is a hydrogen atom, C １ ~C ６ Alkyl or halo(C １ ~C ６ ) represents alkyl, R ４ is C １ ~C ６ Alkyl, C ２ ~C ６ Alkenyl, C ２ ~C ６ Alkynyl, C １ ~C ６ Alkylcarbonyl, C １ ~C ６ Alkoxycarbonyl, C １ ~C ６ Alkylamino, di(C １ ~C ６ ) alkylamino, R ６ (C １ ~C ６ ) alkyl or V-1 to V-82; R ５ is C １ ~C ６ Alkyl, C ２ ~C ６ Alkenyl, C ２ ~C ６ Alkynyl, R ９ (C １ ~C ６ ) alkyl, V-1 to V-63, V-65 to V-70, or V-72 to V-80; R ６ is a halogen atom, C １ ~C ６ represents alkoxy, cyano, nitro, or V-1 to V-82; R ９ is a halogen atom, C １ ~C ６ represents alkoxy, cyano, nitro, or V-1 to V-82; n represents an integer of 0, 1 or 2; (iii) When Q is Q-C, Q-C is C １ ~C ６ Alkyl, R １７ (C １ ~C ６ ) alkyl, —N(R １８ ) R １９ , -OR ６２ or Q-1 to Q-82; R １７ is a halogen atom, C １ ~C ６ represents alkoxy or E-1 to E-83; R １８ is a hydrogen atom, C １ ~C ６ Alkyl or C ２ ~C ６ represents alkenyloxycarbonyl, R １９ are E-1 to E-63, E-65 to E-70, E-72 to E-80, C １ ~C ６ Alkyl, C １ ~C ６ Alkylcarbonyl, C １ ~C ６ Alkoxycarbonyl, C １ ~C ６ Alkylsulfonyl or R ２０ (C １ ~C ６ ) represents alkyl, R ２０ represents E-1 to E-83, R ６２ is a hydrogen atom or C １ ~C ６ represents alkyl, Z １ is a halogen atom, C １ ~C ６ Alkyl, C ２ ~C ６ Alkenyl, C ２ ~C ６ Alkynyl, halo(C １ ~C ６ ) alkyl, halo (C ２ ~C ６ ) alkenyl, halo(C ２ ~C ６ ) alkynyl, C １ ~C ６ Alkoxy, halo (C １ ~C ６ ) alkoxy, C ２ ~C ６ Alkenyloxy, halo(C ２ ~C ６ ) alkenyloxy, C ２ ~C ６ Alkynyloxy, halo(C ２ ~C ６ ) alkynyloxy, hydroxy, C １ ~C ６ Alkylcarbonyloxy, C １ ~C ６ Alkoxycarbonyloxy, C １ ~C ６ Alkyl sulfonyloxy, halo(C １ ~C ６ ) alkylsulfonyloxy, —OC(O)N(R ２６ ) R ２７ , C １ ~C ６ Alkylthio, C １ ~C ６ Alkylsulfinyl, C １ ~C ６ Alkyl sulfonyl, halo(C １ ~C ６ ) alkylthio, halo(C １ ~C ６ ) alkylsulfinyl, halo(C １ ~C ６ ) alkylsulfonyl, C ２ ~C ６ Alkenylthio, C ２ ~C ６ Alkenylsulfinyl, C ２ ~C ６ Alkenylsulfonyl, halo(C ２ ~C ６ ) alkenylthio, halo(C ２ ~C ６ ) alkenylsulfinyl, halo(C ２ ~C ６ ) alkenylsulfonyl, C ２ ~C ６ Alkynylthio, C ２ ~C ６ Alkynylsulfinyl, C ２ ~C ６ Alkynylsulfonyl, halo(C ２ ~C ６ ) alkynylthio, halo(C ２ ~C ６ ) alkynylsulfinyl, halo(C ２ ~C ６ ) alkynylsulfonyl, —SO ３ H, -S(O) ２ N (R ２８ ) R ２９ , -SC≡N, -S(O)(=NR ３０ ) R ３１ , -SF ５ , -N(R ３２ ) R ３３ , -N=S(O)(R ５４ ) R ５５ , formyl, carboxy, C １ ~C ６ Alkylcarbonyl, halo(C １ ~C ６ ) alkylcarbonyl, C １ ~C ６ Alkoxycarbonyl, halo(C １ ~C ６ ) alkoxycarbonyl, —C(O)N(R ３５ ) R ３６ , -C(=NOR １２ ) R １３ , Tori (C １ ~C ６ ) alkylsilyl, R ７ (C １ ~C ６ ) alkyl, R １６ (C １ ~C ６ ) alkoxy, C ３ ~C ６ Cycloalkyl, R ５８ (C ３ ~C ６ ) cycloalkyl, cyano, nitro, E-1 to E-56, E-61 to E-83, -O-(E-1) to -O-(E-63), -O-(E-65) to -O-(E-70), -O-(E-72) to -O-(E-80), -S-(E-1) to -S-(E-63), -S-(E-65) to -S-(E-70), -S-(E-72) to -S-(E-80), -S(O)-(E-1) to -S(O)-(E-83), -S(O) ２ -(E-1)~-S(O) ２ -(E-83), -C(O)-(E-1) to -C(O)-(E-83), -N=N-(E-1) to -N=N-(E-63), -N=N-(E-65) to -N=N-(E-70), or -N=N-(E-72) to -N=N-(E-80), Z １ In the above relationship, when t2 represents an integer of 2, t3 represents an integer of 2 or 3, t4 represents an integer of 2, 3 or 4, and t5 represents an integer of 2, 3, 4 or 5, each of Z １ may be the same as or different from each other, E １ is a halogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl, C １ ~C ６ Alkoxy, C １ ~C ６ Alkylthio, halo(C １ ~C ６ ) alkylthio, C １ ~C ６ Alkylsulfinyl, C １ ~C ６ represents alkylsulfonyl or cyano; E １ In the above relationship, when t2 represents an integer of 2, t3 represents an integer of 2 or 3, t4 represents an integer of 2, 3 or 4, and t5 represents an integer of 2, 3, 4 or 5, each E １ may be the same as or different from each other, E ３ is a hydrogen atom, C １ ~C ６ Alkyl or halo(C １ ~C ６ ) represents alkyl, R ７ is C １ ~C ６ Alkoxy (C １ ~C ６ ) alkoxy, cyano, C １ ~C ６ Alkoxy, C １ ~C ６ Alkylcarbonyloxy, carboxy, C １ ~C ６ Alkylcarbonyl, C １ ~C ６ Alkoxycarbonyl, —C(O)N(R ３７ ) R ３８ , -N(R ３９ ) R ４０ , C １ ~C ６ Alkylthio, C １ ~C ６ alkylsulfonyl or E-1 to E-83; R １６ is C １ ~C ６ Alkylthio, C １ ~C ６ Alkylsulfinyl, C １ ~C ６ Alkylsulfonyl, —C(O)N(R ４１ ) R ４２ , C １ ~C ６ Alkoxy, halo (C １ ~C ６ ) alkoxy, C １ ~C ６ Alkoxy (C １ ~C ６ ) alkoxy, E-1 to E-83, or —C(O)—(E-1) to —C(O)—(E-83), R １２ is a hydrogen atom, C １ ~C ６ Alkyl or halo(C １ ~C ６ ) represents alkyl, R １３ is a hydrogen atom, C １ ~C ６ Alkyl or halo(C １ ~C ６ ) represents alkyl, Z ３ is a hydrogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl, C １ ~C ６ Alkoxy (C １ ~C ６ ) alkyl, C １ ~C ６ Alkylcarbonyl, halo(C １ ~C ６ ) alkylcarbonyl, C １ ~C ６ Alkoxycarbonyl or halo(C １ ~C ６ ) represents alkoxycarbonyl; R ２６ is a hydrogen atom or C １ ~C ６ represents alkyl, R ２７ is a hydrogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl or C ３ ~C ６ represents cycloalkyl, R ２８ is a hydrogen atom or C １ ~C ６ represents alkyl, R ２９ is a hydrogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl, C ３ ~C ６ Cycloalkyl, C １ ~C ６ Alkylcarbonyl, halo(C １ ~C ６ ) alkylcarbonyl or C １ ~C ６ represents an alkoxycarbonyl; R ３０ is a hydrogen atom, C １ ~C ６ Alkyl or halo(C １ ~C ６ ) represents alkyl, R ３１ is C １ ~C ６ Alkyl or halo(C １ ~C ６ ) represents alkyl, R ３２ is a hydrogen atom or C １ ~C ６ represents alkyl, R ３３ is a hydrogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl, C １ ~C ６ Alkylcarbonyl, halo(C １ ~C ６ ) alkylcarbonyl, C １ ~C ６ Alkoxycarbonyl, halo(C １ ~C ６ ) alkoxycarbonyl, C １ ~C ６ Alkylaminocarbonyl, di(C １ ~C ６ ) alkylaminocarbonyl, —C(O)NHC(O)OR ３４ , -C(S)NHC(O)OR ３４ or C １ ~C ６ represents alkylsulfonyl, R ３４ is C １ ~C ６ represents alkyl, R ３５ is a hydrogen atom or C １ ~C ６ represents alkyl, R ３６ is a hydrogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl or C ３ ~C ６ represents cycloalkyl, R ３７ is a hydrogen atom or C １ ~C ６ represents alkyl, R ３８ is a hydrogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl or C ３ ~C ６ represents cycloalkyl, R ３９ is a hydrogen atom, C １ ~C ６ Alkyl or halo(C １ ~C ６ ) represents alkyl, R ４０ is a hydrogen atom, C １ ~C ６ Alkyl, C １ ~C ６ Alkylcarbonyl or C １ ~C ６ represents an alkoxycarbonyl; R ４１ is a hydrogen atom or C １ ~C ６ represents alkyl, R ４２ is a hydrogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl or C ３ ~C ６ represents cycloalkyl, R ５４ is C １ ~C ６ represents alkyl, R ５５ is C １ ~C ６ represents alkyl, R ５８ is a halogen atom, C １ ~C ６ represents alkoxy or cyano; J represents J-1 to J-52; Z ５ is a hydrogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl, C １ ~C ６ Alkoxy (C １ ~C ６ ) alkyl, C １ ~C ６ Alkylcarbonyl, halo(C １ ~C ６ ) alkylcarbonyl, C １ ~C ６ Alkoxycarbonyl, halo(C １ ~C ６ ) alkoxycarbonyl, C １ ~C ６ Alkyl sulfonyl or halo(C １ ~C ６ ) represents alkylsulfonyl, R １ represents a hydrogen atom, a halogen atom, or C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl, C １ ~C ６ Alkoxy, hydroxy, C １ ~C ６ Alkylthio, C １ ~C ６ Alkylsulfinyl, C １ ~C ６ Alkyl sulfonyl, halo(C １ ~C ６ ) alkylthio, halo(C １ ~C ６ ) alkylsulfinyl, halo(C １ ~C ６ ) alkylsulfonyl, —N(R １ｄ ) R １ｅ , cyano or nitro; R １ａ represents a hydrogen atom, a halogen atom, or C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl, C １ ~C ６ Alkoxy, hydroxy, -N(R １ｄ ) R １ｅ , cyano or nitro; R １ｂ represents a hydrogen atom, a halogen atom, or C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl, C １ ~C ６ Alkoxy, hydroxy, -N(R １ｄ ) R １ｅ , cyano or nitro; R １ｃ represents a hydrogen atom, a halogen atom, or C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl, C １ ~C ６ Alkoxy, hydroxy, -N(R １ｄ ) R １ｅ , cyano or nitro; R １ｄ is a hydrogen atom or C １ ~C ６ represents alkyl, R １ｅ is a hydrogen atom or C １ ~C ６ represents alkyl, G is -N(R ２１ ) R ２２ , -C(=NOR ６７ ) R ６８ , R ６９ (C １ ~C ６ ) alkyl or G-1′ to G-160′, R ２１ is a hydrogen atom, C １ ~C ６ Alkyl or halo(C １ ~C ６ ) represents alkyl, R ２２ is a hydrogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl, C ２ ~C ６ Alkenyl, halo(C ２ ~C ６ ) alkenyl, C ２ ~C ６ Alkynyl, halo(C ２ ~C ６ ) alkynyl, R ２３ (C １ ~C ６ ) alkyl or M-1 to M-82, R ２３ is C １ ~C ６ Alkoxy, C １ ~C ６ Alkylcarbonyl, C １ ~C ６ Alkoxycarbonyl, hydroxy, cyano, C １ ~C ６ Alkylamino, di(C １ ~C ６ ) alkylamino, C １ ~C ６ Alkylcarbonylamino, C １ ~C ６ alkoxycarbonylamino or M-1 to M-82, R ６７ is a hydrogen atom, C １ ~C ６ Alkyl or halo(C １ ~C ６ ) represents alkyl, R ６８ is a hydrogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl or M-1 to M-82, R ６９ M-1 to M-82, -N(R ７０ ) R ７１ , -C(=O)N(R ７２ ) R ７３ or -C(=NOR ７４ ) R ７５ represents R ７０ is a hydrogen atom or C １ ~C ６ represents alkyl, R ７１ is -C(=O)R ７６ represents R ７６ is C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl or M-1 to M-82, R ７２ is a hydrogen atom or C １ ~C ６ represents alkyl, R ７３ represents M-1 to M-82, R ７４ is a hydrogen atom or C １ ~C ６ represents alkyl, R ７５ is a hydrogen atom, C １ ~C ６ Alkyl or C ３ ~C ６ represents cycloalkyl, Z ４ is a hydrogen atom, C １ ~C ６ Alkyl, C １ ~C ６ Alkoxy (C １ ~C ６ ) alkyl, C １ ~C ６ Alkylcarbonyl, C １ ~C ６ Alkoxycarbonyl or C １ ~C ６ represents alkylsulfonyl, Z ２ is a halogen atom, C １ ~C ６ Alkyl, C ２ ~C ６ Alkenyl, C ２ ~C ６ Alkynyl, halo(C １ ~C ６ ) alkyl, halo (C ２ ~C ６ ) alkenyl, halo(C ２ ~C ６ ) alkynyl, C １ ~C ６ Alkoxy, halo (C １ ~C ６ ) alkoxy, C ２ ~C ６ Alkenyloxy, halo(C ２ ~C ６ ) alkenyloxy, C ２ ~C ６ Alkynyloxy, halo(C ２ ~C ６ ) alkynyloxy, hydroxy, C １ ~C ６ Alkylcarbonyloxy, C １ ~C ６ Alkoxycarbonyloxy, C １ ~C ６ Alkyl sulfonyloxy, halo(C １ ~C ６ ) alkylsulfonyloxy, —OC(O)N(R ６０ ) R ６１ , C １ ~C ６ Alkylthio, C １ ~C ６ Alkylsulfinyl, C １ ~C ６ Alkyl sulfonyl, halo(C １ ~C ６ ) alkylthio, halo(C １ ~C ６ ) alkylsulfinyl, halo(C １ ~C ６ ) alkylsulfonyl, C ２ ~C ６ Alkenylthio, C ２ ~C ６ Alkenylsulfinyl, C ２ ~C ６ Alkenylsulfonyl, halo(C ２ ~C ６ ) alkenylthio, halo(C ２ ~C ６ ) alkenylsulfinyl, halo(C ２ ~C ６ ) alkenylsulfonyl, C ２ ~C ６ Alkynylthio, C ２ ~C ６ Alkynylsulfinyl, C ２ ~C ６ Alkynylsulfonyl, halo(C ２ ~C ６ ) alkynylthio, halo(C ２ ~C ６ ) alkynylsulfinyl, halo(C ２ ~C ６ ) alkynylsulfonyl, —SO ３ H, -S(O) ２ N (R ４８ ) R ４９ , -SC≡N, -S(O)(=NR ５２ ) R ５３ , -SF ５ , -N(R ４４ ) R ４５ , -N=S(O)(R ５６ ) R ５７ , formyl, carboxy, C １ ~C ６ Alkylcarbonyl, halo(C １ ~C ６ ) alkylcarbonyl, C １ ~C ６ Alkoxycarbonyl, halo(C １ ~C ６ ) alkoxycarbonyl, —C(O)N(R ４６ ) R ４７ , -C(=NOR １４ ) R １５ , Tori (C １ ~C ６ ) alkylsilyl, R ２４ (C １ ~C ６ ) alkyl, R ２５ (C １ ~C ６ ) alkoxy, C ３ ~C ６ Cycloalkyl, R ５９ (C ３ ~C ６ ) cycloalkyl, cyano, nitro, M-1 to M-56, M-61 to M-82, —O-(M-1) to —O-(M-63), —O-(M-65) to —O-(M-70), or —O-(M-72) to —O-(M-80), n represents an integer of 0, 1, or 2; Z ２ In the above relationship, when t2 represents an integer of 2, t3 represents an integer of 2 or 3, t4 represents an integer of 2, 3 or 4, and t5 represents an integer of 2, 3, 4 or 5, each of Z ２ may be the same as or different from each other, Alternatively, t4 represents an integer of 2, and two Z ２ When two Z ２ together form oxo, -CH ２ CH ２ -, -OCH ２ CH ２ O-, -OCH ２ CH ２ CH ２ O-, = NOR ４３ , =NN(R ６３ ) R ６４ or =NN=C(R ６５ ) R ６６ represents R ４３ is a hydrogen atom or C １ ~C ６ represents alkyl, R ２４ is C １ ~C ６ Alkoxy, hydroxy or -N(R ５０ ) R ５１ represents R ２５ is C １ ~C ６ represents alkoxy or M-1 to M-82; M １ is a halogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl, C １ ~C ６ Alkoxy, C １ ~C ６ Alkylthio, halo(C １ ~C ６ ) alkylthio, C １ ~C ６ Alkylsulfinyl, C １ ~C ６ represents alkylsulfonyl or cyano; M １ In the above relationship, when t2 represents an integer of 2, t3 represents an integer of 2 or 3, t4 represents an integer of 2, 3 or 4, and t5 represents an integer of 2, 3, 4 or 5, each of M １ may be the same as or different from each other, M ３ is a hydrogen atom, C １ ~C ６ Alkyl or halo(C １ ~C ６ ) represents alkyl, R １４ is a hydrogen atom, C １ ~C ６ Alkyl or halo(C １ ~C ６ ) represents alkyl, R １５ is a hydrogen atom, C １ ~C ６ Alkyl or halo(C １ ~C ６ ) represents alkyl, R ４４ is a hydrogen atom, C １ ~C ６ Alkyl or halo(C １ ~C ６ ) represents alkyl, R ４５ is a hydrogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl, C １ ~C ６ Alkylcarbonyl, halo(C １ ~C ６ ) alkylcarbonyl, C １ ~C ６ Alkoxycarbonyl, halo(C １ ~C ６ ) alkoxycarbonyl, C １ ~C ６ Alkyl sulfonyl or halo(C １ ~C ６ ) represents alkylsulfonyl, R ４６ is a hydrogen atom or C １ ~C ６ represents alkyl, R ４７ is a hydrogen atom, C １ ~C ６ Alkyl or halo(C １ ~C ６ ) represents alkyl, R ４８ is a hydrogen atom, C １ ~C ６ Alkyl or halo(C １ ~C ６ ) represents alkyl, R ４９ is a hydrogen atom, C １ ~C ６ Alkyl or halo(C １ ~C ６ ) represents alkyl, R ５０ is a hydrogen atom or C １ ~C ６ represents alkyl, R ５１ is a hydrogen atom, C １ ~C ６ Alkyl, C １ ~C ６ Alkylcarbonyl, halo(C １ ~C ６ ) alkylcarbonyl, C １ ~C ６ Alkoxycarbonyl, halo(C １ ~C ６ ) alkoxycarbonyl, C １ ~C ６ Alkyl sulfonyl or halo(C １ ~C ６ ) represents alkylsulfonyl, R ５２ is a hydrogen atom or C １ ~C ６ represents alkyl, R ５３ is C １ ~C ６ represents alkyl, R ５６ is C １ ~C ６ represents alkyl, R ５７ is C １ ~C ６ represents alkyl, R ５９ is a halogen atom, C １ ~C ６ represents alkoxy or cyano; R ６０ is a hydrogen atom or C １ ~C ６ represents alkyl, R ６１ is a hydrogen atom, C １ ~C ６ Alkyl or halo(C １ ~C ６ ) represents alkyl, R ６３ is a hydrogen atom or C １ ~C ６ represents alkyl, R ６４ is a hydrogen atom, C １ ~C ６ Alkyl, C １ ~C ６ Alkylcarbonyl, halo(C １ ~C ６ ) alkylcarbonyl, C １ ~C ６ Alkoxycarbonyl, halo(C １ ~C ６ ) alkoxycarbonyl, C １ ~C ６ Alkyl sulfonyl or halo(C １ ~C ６ ) represents alkylsulfonyl, R ６５ is a hydrogen atom or C １ ~C ６ represents alkyl, R ６６ is C １ ~C ６ represents alkyl, R ２ is a hydrogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl, C ２ ~C ６ Alkenyl, C ２ ~C ６ Alkynyl, C ３ ~C ６ cycloalkyl, —C(O)R ４ , -C(O)OR ５ or R ６７ (C １ ~C ６ ) represents alkyl, R ６７ is C １ ~C ６ Alkoxy, C １ ~C ６ Alkylthio, C １ ~C ６ Alkylsulfinyl, C １ ~C ６ alkylsulfonyl, cyano, or V-1 to V-82; V １ is a halogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl, C １ ~C ６ Alkoxy, C １ ~C ６ Alkylthio, C １ ~C ６ Alkylsulfinyl, C １ ~C ６ represents alkylsulfonyl, cyano or nitro, V １ In the above relationship, when t2 represents an integer of 2, t3 represents an integer of 2 or 3, t4 represents an integer of 2, 3 or 4, and t5 represents an integer of 2, 3, 4 or 5, each of V １ may be the same as or different from each other, V ３ is a hydrogen atom, C １ ~C ６ Alkyl or halo(C １ ~C ６ ) represents alkyl, R ４ is C １ ~C ６ Alkyl, C ２ ~C ６ Alkenyl, C ２ ~C ６ Alkynyl, C １ ~C ６ Alkylcarbonyl, C １ ~C ６ Alkoxycarbonyl, C １ ~C ６ Alkylamino, di(C １ ~C ６ ) alkylamino, R ６ (C １ ~C ６ ) alkyl or V-1 to V-82; R ５ is C １ ~C ６ Alkyl, C ２ ~C ６ Alkenyl, C ２ ~C ６ Alkynyl, R ９ (C １ ~C ６ ) alkyl, V-1 to V-63, V-65 to V-70, or V-72 to V-80; R ６ is a halogen atom, C １ ~C ６ represents alkoxy, cyano, nitro, or V-1 to V-82; R ９ is a halogen atom, C １ ~C ６ represents alkoxy, cyano, nitro, or V-1 to V-82; When Q is Q-A, Q-B, or Q-C, R ３ is a hydrogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl, C ２ ~C ６ Alkenyl, C ２ ~C ６ Alkynyl, C ３ ~C ６ Cycloalkyl or C １ ~C ６ represents alkylcarbonyl, X represents an oxygen atom or a sulfur atom; Y represents an oxygen atom or a sulfur atom; t1 represents an integer of 0 or 1; t2 represents an integer of 0, 1, or 2; t3 represents an integer of 0, 1, 2 or 3; t4 represents an integer of 0, 1, 2, 3, or 4; t5 represents an integer of 0, 1, 2, 3, 4, or 5; d1 represents an integer of 0 or 1; d2 represents an integer of 0, 1 or 2; d3 represents an integer of 0, 1, 2 or 3; d4 represents an integer of 0, 1, 2, 3, or 4; and d5 represents an integer of 0, 1, 2, 3, 4 or 5.] or a salt thereof. Q is QA, QB or QC; (i) If Q is Q-A, then: Q-A is C １ ~C ６ Alkyl, R １７ (C １ ~C ６ ) alkyl, —N(R １８ ) R １９ , Q-1, Q-2, Q-3, Q-4, Q-5, Q-6, Q-8, Q-9, Q-10, Q-12, Q-13, Q-14, Q-15, Q-19, Q-20, Q-21, Q-22, Q-23, Q-24, Q-25, Q-26, Q-28, Q-29, Q-31, Q-34, Q-35, Q-37, Q-38, Q-39, Q-40, Q-42, Q-44, Q-45, Q-46, Q-47, Q-49, Q-50, Q-51, Q-52, Q-53, Q-55, Q-56, Q-59 or Q-60; J represents J-1 to J-27; G is G-1, G-2, G-3, G-4, G-5, G-7, G-8, G-9, G-11, G-12, G-13, G-14, G-15, G-16, G-17, G-18, G- 19, G-20, G-25, G-26, G-28, G-29, G-33, G-35, G-36, G-37, G-40, G-41, G-42, G-44 or G-46; R １７ is a halogen atom, C １ ~C ６ alkoxy, E-1 or E-60; R １８ is C １ ~C ６ Alkyl or C ２ ~C ６ represents alkenyloxycarbonyl, R １９ is E-1, C １ ~C ６ Alkoxycarbonyl or R ２０ (C １ ~C ６ ) represents alkyl, R ２０ represents E-1, Z １ is a halogen atom, C １ ~C ６ Alkyl, C ２ ~C ６ Alkenyl, C ２ ~C ６ Alkynyl, halo(C １ ~C ６ ) alkyl, C １ ~C ６ Alkoxy, halo (C １ ~C ６ ) alkoxy, C ２ ~C ６ Alkenyloxy, C ２ ~C ６ Alkynyloxy, hydroxy, C １ ~C ６ Alkylcarbonyloxy, —OC(O)N(R ２６ ) R ２７ , C １ ~C ６ Alkylthio, C １ ~C ６ Alkyl sulfonyl, halo(C １ ~C ６ ) alkylthio, halo(C １ ~C ６ ) alkylsulfonyl, —S(O) ２ N (R ２８ ) R ２９ , -SC≡N, -S(O)(=NR ３０ ) R ３１ , -SF ５ , -N(R ３２ ) R ３３ , carboxy, C １ ~C ６ Alkylcarbonyl, halo(C １ ~C ６ ) alkylcarbonyl, C １ ~C ６ Alkoxycarbonyl, —C(O)N(R ３５ ) R ３６ , R ７ (C １ ~C ６ ) alkyl, R １６ (C １ ~C ６ ) alkoxy, C ３ ~C ６ Cycloalkyl, cyano, nitro, E-1, E-50, —O-(E-1), —O-(E-2), —O-(E-3), —O-(E-12), —O-(E-14), —S-(E-1), —S(O) ２ -(E-1), -C(O)-(E-1), -C(O)-(E-64), -C(O)-(E-71), -C(O)-(E-81), -C(O)-(E-82), -C(O)-(E-83) or -N=N-(E-1), Z １ In the above relationship, when t2 represents an integer of 2, t3 represents an integer of 2 or 3, t4 represents an integer of 2, 3 or 4, and t5 represents an integer of 2, 3, 4 or 5, each of Z １ may be the same as or different from each other, E １ is a halogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl, C １ ~C ６ Alkoxy, C １ ~C ６ represents alkylthio or cyano; E １ In the above relationship, when t2 represents an integer of 2, t3 represents an integer of 2 or 3, t4 represents an integer of 2, 3 or 4, and t5 represents an integer of 2, 3, 4 or 5, each E １ may be the same as or different from each other, E ３ is C １ ~C ６ represents alkyl, R ７ is C １ ~C ６ Alkoxy (C １ ~C ６ ) alkoxy, cyano, C １ ~C ６ Alkoxy, carboxy, —C(O)N(R ３７ ) R ３８ , -N(R ３９ ) R ４０ , C １ ~C ６ alkylsulfonyl or E-1, R １６ is C １ ~C ６ Alkylsulfonyl, —C(O)N(R ４１ ) R ４２ , C １ ~C ６ Alkoxy, C １ ~C ６ Alkoxy (C １ ~C ６ ) alkoxy, E-1 or —C(O)—(E-81), R ２ is a hydrogen atom, C １ ~C ６ Alkyl, —C(O)R ４ or -C(O)OR ５ represents R ４ is C １ ~C ６ alkyl, V-1 or V-19; R ５ is C １ ~C ６ represents alkyl, Z ３ is C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl or C １ ~C ６ Alkoxy (C １ ~C ６ ) represents alkyl, R ２６ is C １ ~C ６ represents alkyl, R ２７ is C １ ~C ６ represents alkyl, R ２９ is a hydrogen atom, C １ ~C ６ Alkyl or C １ ~C ６ represents alkylcarbonyl, R ３０ is C １ ~C ６ represents alkyl, R ３１ is C １ ~C ６ represents alkyl, R ３３ is C １ ~C ６ Alkyl, C １ ~C ６ Alkylcarbonyl, C １ ~C ６ Alkoxycarbonyl, C １ ~C ６ Alkylaminocarbonyl, —C(S)NHC(O)OR ３４ or C １ ~C ６ represents alkylsulfonyl, R ３６ is a hydrogen atom or C １ ~C ６ represents alkyl, R ３８ is a hydrogen atom or C １ ~C ６ represents alkyl, R ３９ is a hydrogen atom or C １ ~C ６ represents alkyl, R ４０ is C １ ~C ６ Alkyl or C １ ~C ６ represents an alkoxycarbonyl; R ４１ is C １ ~C ６ represents alkyl, R ４２ is C １ ~C ６ represents alkyl, Z ５ is C １ ~C ６ represents alkyl, R １ represents a hydrogen atom, a halogen atom, or C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl, C １ ~C ６ Alkoxy, hydroxy, C １ ~C ６ Alkylthio or C １ ~C ６ represents alkylsulfinyl, R １ａ represents a hydrogen atom, R １ｂ represents a hydrogen atom, R １ｃ represents a hydrogen atom, a halogen atom, or a halo(C １ ~C ６ ) represents alkyl, Z ２ is a halogen atom, C １ ~C ６ Alkyl, C ２ ~C ６ Alkenyl, halo(C １ ~C ６ ) alkyl, C １ ~C ６ Alkoxy, halo (C １ ~C ６ ) alkoxy, hydroxy, C １ ~C ６ Alkylcarbonyloxy, C １ ~C ６ Alkylthio, C １ ~C ６ Alkylsulfinyl, C １ ~C ６ Alkyl sulfonyl, halo(C １ ~C ６ ) alkylthio, —S(O) ２ N (R ４８ ) R ４９ , -N(R ４４ ) R ４５ , carboxy, C １ ~C ６ Alkylcarbonyl, C １ ~C ６ Alkoxycarbonyl, —C(O)N(R ４６ ) R ４７ , -C(=NOR １４ ) R １５ , Tori (C １ ~C ６ ) alkylsilyl, R ２４ (C １ ~C ６ ) alkyl, R ２５ (C １ ~C ６ ) alkoxy, C ３ ~C ６ represents cycloalkyl, cyano, nitro, M-1, or —O-(M-1); Z ２ In the above relationship, when t2 represents an integer of 2, t3 represents an integer of 2 or 3, t4 represents an integer of 2, 3 or 4, and t5 represents an integer of 2, 3, 4 or 5, each of Z ２ may be the same as or different from each other, R ２５ is C １ ~C ６ represents alkoxy or M-1, M １ is a halogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl or C １ ~C ６ represents alkoxy, M １ In the above relationship, when t2 represents an integer of 2, t3 represents an integer of 2 or 3, t4 represents an integer of 2, 3 or 4, and t5 represents an integer of 2, 3, 4 or 5, each of M １ may be the same as or different from each other, R １４ is C １ ~C ６ represents alkyl, R １５ is C １ ~C ６ represents alkyl, R ４４ is a hydrogen atom or C １ ~C ６ represents alkyl, R ４５ is C １ ~C ６ Alkyl, C １ ~C ６ Alkylcarbonyl or C １ ~C ６ represents an alkoxycarbonyl; R ４８ is a hydrogen atom or C １ ~C ６ represents alkyl, R ４９ is a hydrogen atom or C １ ~C ６ represents alkyl, R ５１ is C １ ~C ６ Alkyl or C １ ~C ６ represents alkylsulfonyl; (ii) When Q is Q-B, Q-B is C １ ~C ６ Alkyl, R １７ (C １ ~C ６ ) alkyl, —N(R １８ ) R １９ , Q-1, Q-2, Q-3, Q-4, Q-5, Q-6, Q-8, Q-9, Q-10, Q-12, Q-13, Q-14, Q-15, Q-19, Q-20, Q-21, Q-22, Q-23, Q-24, Q-25, Q-26, Q-28, Q-29, Q-31, Q-34, Q-35, Q-37, Q-38, Q-39, Q-40, Q-42, Q-44, Q-45, Q-46, Q-47, Q-49, Q-50, Q-51, Q-52, Q-53, Q-55, Q-56, Q-59 or Q-60; J represents J-1′ or J-2′; A １ is a nitrogen atom or CR １ｃ represents G is -N(R ２１ ) R ２２ , -C(=NOR ６７ ) R ６８ , R ６９ (C １ ~C ６ ) alkyl, G-1′ to G-28′, G-40′, G-68′, G-69′, G-157′ or G-159′; R １７ is a halogen atom, C １ ~C ６ alkoxy, E-1 or E-60; R １８ is C １ ~C ６ Alkyl or C ２ ~C ６ represents alkenyloxycarbonyl, R １９ is E-1, C １ ~C ６ Alkoxycarbonyl or R ２０ (C １ ~C ６ ) represents alkyl, R ２０ represents E-1, Z １ is a halogen atom, C １ ~C ６ Alkyl, C ２ ~C ６ Alkenyl, C ２ ~C ６ Alkynyl, halo(C １ ~C ６ ) alkyl, C １ ~C ６ Alkoxy, halo (C １ ~C ６ ) alkoxy, C ２ ~C ６ Alkenyloxy, C ２ ~C ６ Alkynyloxy, hydroxy, C １ ~C ６ Alkylcarbonyloxy, —OC(O)N(R ２６ ) R ２７ , C １ ~C ６ Alkylthio, C １ ~C ６ Alkyl sulfonyl, halo(C １ ~C ６ ) alkylthio, halo(C １ ~C ６ ) alkylsulfonyl, —S(O) ２ N (R ２８ ) R ２９ , -SC≡N, -S(O)(=NR ３０ ) R ３１ , -SF ５ , -N(R ３２ ) R ３３ , carboxy, C １ ~C ６ Alkylcarbonyl, halo(C １ ~C ６ ) alkylcarbonyl, C １ ~C ６ Alkoxycarbonyl, —C(O)N(R ３５ ) R ３６ , R ７ (C １ ~C ６ ) alkyl, R １６ (C １ ~C ６ ) alkoxy, C ３ ~C ６ Cycloalkyl, cyano, nitro, E-1, E-50, —O-(E-1), —O-(E-2), —O-(E-3), —O-(E-12), —O-(E-14), —S-(E-1), —S(O) ２ -(E-1), -C(O)-(E-1), -C(O)-(E-64), -C(O)-(E-71), -C(O)-(E-81), -C(O)-(E-82), -C(O)-(E-83) or -N=N-(E-1), Z １ In the above relationship, when t2 represents an integer of 2, t3 represents an integer of 2 or 3, t4 represents an integer of 2, 3 or 4, and t5 represents an integer of 2, 3, 4 or 5, each of Z １ may be the same as or different from each other, E １ is a halogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl, C １ ~C ６ Alkoxy, C １ ~C ６ represents alkylthio or cyano; E １ In the above relationship, when t2 represents an integer of 2, t3 represents an integer of 2 or 3, t4 represents an integer of 2, 3 or 4, and t5 represents an integer of 2, 3, 4 or 5, each E １ may be the same as or different from each other, E ３ is C １ ~C ６ represents alkyl, R ７ is C １ ~C ６ Alkoxy (C １ ~C ６ ) alkoxy, cyano, C １ ~C ６ Alkoxy, carboxy, —C(O)N(R ３７ ) R ３８ , -N(R ３９ ) R ４０ , C １ ~C ６ alkylsulfonyl or E-1, R １６ is C １ ~C ６ Alkylsulfonyl, —C(O)N(R ４１ ) R ４２ , C １ ~C ６ Alkoxy, C １ ~C ６ Alkoxy (C １ ~C ６ ) alkoxy, E-1 or —C(O)—(E-81), R ２ is a hydrogen atom, C １ ~C ６ Alkyl, —C(O)R ４ or -C(O)OR ５ represents R ４ is C １ ~C ６ alkyl, V-1 or V-19; R ５ is C １ ~C ６ represents alkyl, Z ３ is C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl or C １ ~C ６ Alkoxy (C １ ~C ６ ) represents alkyl, R ２６ is C １ ~C ６ represents alkyl, R ２７ is C １ ~C ６ represents alkyl, R ２９ is a hydrogen atom, C １ ~C ６ Alkyl or C １ ~C ６ represents alkylcarbonyl, R ３０ is C １ ~C ６ represents alkyl, R ３１ is C １ ~C ６ represents alkyl, R ３３ is C １ ~C ６ Alkyl, C １ ~C ６ Alkylcarbonyl, C １ ~C ６ Alkoxycarbonyl, C １ ~C ６ Alkylaminocarbonyl, —C(S)NHC(O)OR ３４ or C １ ~C ６ represents alkylsulfonyl, R ３６ is a hydrogen atom or C １ ~C ６ represents alkyl, R ３８ is a hydrogen atom or C １ ~C ６ represents alkyl, R ３９ is a hydrogen atom or C １ ~C ６ represents alkyl, R ４０ is C １ ~C ６ Alkyl or C １ ~C ６ represents an alkoxycarbonyl; R ４１ is C １ ~C ６ represents alkyl, R ４２ is C １ ~C ６ represents alkyl, R １ represents a hydrogen atom, a halogen atom, or C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl, C １ ~C ６ Alkoxy, hydroxy, C １ ~C ６ Alkylthio or C １ ~C ６ represents alkylsulfinyl, R １ａ represents a hydrogen atom, R １ｂ represents a hydrogen atom, R １ｃ represents a hydrogen atom, a halogen atom, or a halo(C １ ~C ６ ) represents alkyl, R ２１ is a hydrogen atom or C １ ~C ６ represents alkyl, R ２２ is C １ ~C ６ Alkyl, C ２ ~C ６ Alkenyl, C ２ ~C ６ Alkynyl, R ２３ (C １ ~C ６ ) alkyl, M-57, M-60, M-61 or M-81; R ２３ is C １ ~C ６ Alkoxy, C １ ~C ６ Alkoxycarbonyl, hydroxy, cyano, C １ ~C ６ represents alkylamino or M-1, R ６７ is C １ ~C ６ represents alkyl, R ６８ is C １ ~C ６ represents alkyl or M-1, R ６９ are M-1, M-2, M-14, -N(R ７０ ) R ７１ , -C(=O)N(R ７２ ) R ７３ or -C(=NOR ７４ ) R ７５ represents R ７０ represents a hydrogen atom, R ７６ is C １ ~C ６ represents alkyl or M-1, R ７２ represents a hydrogen atom, R ７３ represents M-1, R ７４ is C １ ~C ６ represents alkyl, R ７５ is C ３ ~C ６ represents cycloalkyl, Z ２ is a halogen atom, C １ ~C ６ Alkyl, C ２ ~C ６ Alkenyl, halo(C １ ~C ６ ) alkyl, C １ ~C ６ Alkoxy, halo (C １ ~C ６ ) alkoxy, hydroxy, C １ ~C ６ Alkylcarbonyloxy, C １ ~C ６ Alkylthio, C １ ~C ６ Alkylsulfinyl, C １ ~C ６ Alkyl sulfonyl, halo(C １ ~C ６ ) alkylthio, —S(O) ２ N (R ４８ ) R ４９ , -N(R ４４ ) R ４５ , carboxy, C １ ~C ６ Alkylcarbonyl, C １ ~C ６ Alkoxycarbonyl, —C(O)N(R ４６ ) R ４７ , -C(=NOR １４ ) R １５ , Tori (C １ ~C ６ ) alkylsilyl, R ２４ (C １ ~C ６ ) alkyl, R ２５ (C １ ~C ６ ) alkoxy, C ３ ~C ６ represents cycloalkyl, cyano, nitro, M-1, or —O-(M-1); Z ２ In the above relationship, when t2 represents an integer of 2, t3 represents an integer of 2 or 3, t4 represents an integer of 2, 3 or 4, and t5 represents an integer of 2, 3, 4 or 5, each of Z ２ may be the same as or different from each other, Alternatively, t4 represents an integer of 2, and two Z ２ When two Z ２ together form oxo, -CH ２ CH ２ -, -OCH ２ CH ２ O- or =NOR ４３ represents R ２５ is C １ ~C ６ represents alkoxy or M-1, M １ is a halogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl or C １ ~C ６ represents alkoxy, M １ In the above relationship, when t2 represents an integer of 2, t3 represents an integer of 2 or 3, t4 represents an integer of 2, 3 or 4, and t5 represents an integer of 2, 3, 4 or 5, each of M １ may be the same as or different from each other, R １４ is C １ ~C ６ represents alkyl, R １５ is C １ ~C ６ represents alkyl, R ４４ is a hydrogen atom or C １ ~C ６ represents alkyl, R ４５ is C １ ~C ６ Alkyl, C １ ~C ６ Alkylcarbonyl or C １ ~C ６ represents an alkoxycarbonyl; R ４８ is a hydrogen atom or C １ ~C ６ represents alkyl, R ４９ is a hydrogen atom or C １ ~C ６ represents alkyl, R ５１ is C １ ~C ６ Alkyl or C １ ~C ６ represents alkylsulfonyl; (iii) When Q is Q-C, Q-C is C １ ~C ６ Alkyl, R １７ (C １ ~C ６ ) alkyl, —N(R １８ ) R １９ , Q-1, Q-2, Q-3, Q-4, Q-5, Q-6, Q-8, Q-9, Q-10, Q-12, Q-13, Q-14, Q-15, Q-19, Q-20, Q-21, Q-22, Q-23, Q-24, Q-25, Q-26, Q-28, Q-29, Q-31, Q-34, Q-35, Q-37, Q-38, Q-39, Q-40, Q-42, Q-44, Q-45, Q-46, Q-47, Q-49, Q-50, Q-51, Q-52, Q-53, Q-55, Q-56, Q-59 or Q-60; J represents J-1 to J-27; G is -N(R ２１ ) R ２２ , -C(=NOR ６７ ) R ６８ , R ６９ (C １ ~C ６ ) alkyl, G-1′ to G-28′, G-40′, G-68′, G-69′, G-157′ or G-159′; R １７ is a halogen atom, C １ ~C ６ alkoxy, E-1 or E-60; R １８ is C １ ~C ６ Alkyl or C ２ ~C ６ represents alkenyloxycarbonyl, R １９ is E-1, C １ ~C ６ Alkoxycarbonyl or R ２０ (C １ ~C ６ ) represents alkyl, R ２０ represents E-1, Z １ is a halogen atom, C １ ~C ６ Alkyl, C ２ ~C ６ Alkenyl, C ２ ~C ６ Alkynyl, halo(C １ ~C ６ ) alkyl, C １ ~C ６ Alkoxy, halo (C １ ~C ６ ) alkoxy, C ２ ~C ６ Alkenyloxy, C ２ ~C ６ Alkynyloxy, hydroxy, C １ ~C ６ Alkylcarbonyloxy, —OC(O)N(R ２６ ) R ２７ , C １ ~C ６ Alkylthio, C １ ~C ６ Alkyl sulfonyl, halo(C １ ~C ６ ) alkylthio, halo(C １ ~C ６ ) alkylsulfonyl, —S(O) ２ N (R ２８ ) R ２９ , -SC≡N, -S(O)(=NR ３０ ) R ３１ , -SF ５ , -N(R ３２ ) R ３３ , carboxy, C １ ~C ６ Alkylcarbonyl, halo(C １ ~C ６ ) alkylcarbonyl, C １ ~C ６ Alkoxycarbonyl, —C(O)N(R ３５ ) R ３６ , R ７ (C １ ~C ６ ) alkyl, R １６ (C １ ~C ６ ) alkoxy, C ３ ~C ６ Cycloalkyl, cyano, nitro, E-1, E-50, —O-(E-1), —O-(E-2), —O-(E-3), —O-(E-12), —O-(E-14), —S-(E-1), —S(O) ２ -(E-1), -C(O)-(E-1), -C(O)-(E-64), -C(O)-(E-71), -C(O)-(E-81), -C(O)-(E-82), -C(O)-(E-83) or -N=N-(E-1), Z １ In the above relationship, when t2 represents an integer of 2, t3 represents an integer of 2 or 3, t4 represents an integer of 2, 3 or 4, and t5 represents an integer of 2, 3, 4 or 5, each of Z １ may be the same as or different from each other, E １ is a halogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl, C １ ~C ６ Alkoxy, C １ ~C ６ represents alkylthio or cyano; E １ In the above relationship, when t2 represents an integer of 2, t3 represents an integer of 2 or 3, t4 represents an integer of 2, 3 or 4, and t5 represents an integer of 2, 3, 4 or 5, each E １ may be the same as or different from each other, E ３ is C １ ~C ６ represents alkyl, R ７ is C １ ~C ６ Alkoxy (C １ ~C ６ ) alkoxy, cyano, C １ ~C ６ Alkoxy, carboxy, —C(O)N(R ３７ ) R ３８ , -N(R ３９ ) R ４０ , C １ ~C ６ alkylsulfonyl or E-1, R １６ is C １ ~C ６ Alkylsulfonyl, —C(O)N(R ４１ ) R ４２ , C １ ~C ６ Alkoxy, C １ ~C ６ Alkoxy (C １ ~C ６ ) alkoxy, E-1 or —C(O)—(E-81), R ２ is a hydrogen atom, C １ ~C ６ Alkyl, —C(O)R ４ or -C(O)OR ５ represents R ４ is C １ ~C ６ alkyl, V-1 or V-19; R ５ is C １ ~C ６ represents alkyl, Z ３ is C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl or C １ ~C ６ Alkoxy (C １ ~C ６ ) represents alkyl, R ２６ is C １ ~C ６ represents alkyl, R ２７ is C １ ~C ６ represents alkyl, R ２９ is a hydrogen atom, C １ ~C ６ Alkyl or C １ ~C ６ represents alkylcarbonyl, R ３０ is C １ ~C ６ represents alkyl, R ３１ is C １ ~C ６ represents alkyl, R ３３ is C １ ~C ６ Alkyl, C １ ~C ６ Alkylcarbonyl, C １ ~C ６ Alkoxycarbonyl, C １ ~C ６ Alkylaminocarbonyl, —C(S)NHC(O)OR ３４ or C １ ~C ６ represents alkylsulfonyl, R ３６ is a hydrogen atom or C １ ~C ６ represents alkyl, R ３８ is a hydrogen atom or C １ ~C ６ represents alkyl, R ３９ is a hydrogen atom or C １ ~C ６ represents alkyl, R ４０ is C １ ~C ６ Alkyl or C １ ~C ６ represents an alkoxycarbonyl; R ４１ is C １ ~C ６ represents alkyl, R ４２ is C １ ~C ６ represents alkyl, Z ５ is C １ ~C ６ represents alkyl, R １ represents a hydrogen atom, a halogen atom, or C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl, C １ ~C ６ Alkoxy, hydroxy, C １ ~C ６ Alkylthio or C １ ~C ６ represents alkylsulfinyl, R １ａ represents a hydrogen atom, R １ｂ represents a hydrogen atom, R １ｃ represents a hydrogen atom, a halogen atom, or a halo(C １ ~C ６ ) represents alkyl, R ２１ is a hydrogen atom or C １ ~C ６ represents alkyl, R ２２ is C １ ~C ６ Alkyl, C ２ ~C ６ Alkenyl, C ２ ~C ６ Alkynyl, R ２３ (C １ ~C ６ ) alkyl, M-57, M-60, M-61 or M-81; R ２３ is C １ ~C ６ Alkoxy, C １ ~C ６ Alkoxycarbonyl, hydroxy, cyano, C １ ~C ６ represents alkylamino or M-1, R ６７ is C １ ~C ６ represents alkyl, R ６８ is C １ ~C ６ represents alkyl or M-1, R ６９ are M-1, M-2, M-14, -N(R ７０ ) R ７１ , -C(=O)N(R ７２ ) R ７３ or -C(=NOR ７４ ) R ７５ represents R ７０ represents a hydrogen atom, R ７６ is C １ ~C ６ represents alkyl or M-1, R ７２ represents a hydrogen atom, R ７３ represents M-1, R ７４ is C １ ~C ６ represents alkyl, R ７５ is C ３ ~C ６ represents cycloalkyl, Z ２ is a halogen atom, C １ ~C ６ Alkyl, C ２ ~C ６ Alkenyl, halo(C １ ~C ６ ) alkyl, C １ ~C ６ Alkoxy, halo (C １ ~C ６ ) alkoxy, hydroxy, C １ ~C ６ Alkylcarbonyloxy, C １ ~C ６ Alkylthio, C １ ~C ６ Alkylsulfinyl, C １ ~C ６ Alkyl sulfonyl, halo(C １ ~C ６ ) alkylthio, —S(O) ２ N (R ４８ ) R ４９ , -N(R ４４ ) R ４５ , carboxy, C １ ~C ６ Alkylcarbonyl, C １ ~C ６ Alkoxycarbonyl, —C(O)N(R ４６ ) R ４７ , -C(=NOR １４ ) R １５ , Tori (C １ ~C ６ ) alkylsilyl, R ２４ (C １ ~C ６ ) alkyl, R ２５ (C １ ~C ６ ) alkoxy, C ３ ~C ６ represents cycloalkyl, cyano, nitro, M-1, or —O-(M-1); Z ２ In the above relationship, when t2 represents an integer of 2, t3 represents an integer of 2 or 3, t4 represents an integer of 2, 3 or 4, and t5 represents an integer of 2, 3, 4 or 5, each of Z ２ may be the same as or different from each other, Alternatively, t4 represents an integer of 2, and two Z ２ When two Z ２ together form oxo, -CH ２ CH ２ -, -OCH ２ CH ２ O- or =NOR ４３ represents R ２５ is C １ ~C ６ represents alkoxy or M-1, M １ is a halogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl or C １ ~C ６ represents alkoxy, M １ In the above relationship, when t2 represents an integer of 2, t3 represents an integer of 2 or 3, t4 represents an integer of 2, 3 or 4, and t5 represents an integer of 2, 3, 4 or 5, each of M １ may be the same as or different from each other, R １４ is C １ ~C ６ represents alkyl, R １５ is C １ ~C ６ represents alkyl, R ４４ is a hydrogen atom or C １ ~C ６ represents alkyl, R ４５ is C １ ~C ６ Alkyl, C １ ~C ６ Alkylcarbonyl or C １ ~C ６ represents an alkoxycarbonyl; R ４８ is a hydrogen atom or C １ ~C ６ represents alkyl, R ４９ is a hydrogen atom or C １ ~C ６ represents alkyl, R ５１ is C １ ~C ６ Alkyl or C １ ~C ６ represents alkylsulfonyl; When Q is Q-A, Q-B, or Q-C, R ３ represents a hydrogen atom, 2. The aryltetrahydropyridine compound or a salt thereof according to claim 1, wherein Y represents an oxygen atom. Q is QA, QB or QC; (i) If Q is Q-A, then: Q-A represents Q-1, Q-2, Q-3, Q-4, Q-9, Q-12 or Q-14; J represents J-1 to J-27; G is G-1, G-2, G-3, G-4, G-5, G-7, G-8, G-9, G-11, G-12, G-13, G-14, G-15, G-16, G-17, G-18, G- 19, G-20, G-25, G-26, G-28, G-29, G-33, G-35, G-36, G-37, G-40, G-41, G-42, G-44 or G-46; Z １ is a halogen atom, C １ ~C ６ Alkyl, C １ ~C ６ represents alkoxy or cyano; Z １ In the above relationship, when t2 represents an integer of 2, t3 represents an integer of 2 or 3, t4 represents an integer of 2, 3 or 4, and t5 represents an integer of 2, 3, 4 or 5, each of Z １ may be the same as or different from each other, R ２ is a hydrogen atom or C １ ~C ６ represents alkyl, Z ３ is C １ ~C ６ represents alkyl, R １ is a hydrogen atom, halo (C １ ~C ６ ) alkyl, C １ ~C ６ represents alkoxy or hydroxy, R １ｃ represents a hydrogen atom, Z ４ is C １ ~C ６ represents alkyl, X represents an oxygen atom; (ii) When Q is Q-B, Q-B represents Q-1, Q-2, Q-3, Q-4, Q-5, Q-6, Q-8, Q-9, Q-10, Q-12, Q-14, Q-15, Q-19, Q-22, Q-23, Q-24, Q-25, Q-26, Q-28, Q-29, Q-34, Q-35, Q-37, Q-38, Q-40, Q-42, Q-44, Q-45, Q-46, Q-47, Q-49, Q-50, Q-51, Q-52, Q-55 or Q-56; G is -N(R ２１ ) R ２２ , R ６９ (C １ ~C ６ ) alkyl, G-1′, G-2′, G-5′, G-6′, G-9′, G-10′, G-11′ or G-19′; Z １ is a halogen atom, C ２ ~C ６ Alkenyl, C ２ ~C ６ Alkynyl, halo(C １ ~C ６ ) alkyl, C １ ~C ６ Alkoxy, halo (C １ ~C ６ ) alkoxy, C ２ ~C ６ Alkenyloxy, C ２ ~C ６ Alkynyloxy, hydroxy, C １ ~C ６ Alkylcarbonyloxy, —OC(O)N(R ２６ ) R ２７ , C １ ~C ６ Alkylthio, C １ ~C ６ Alkyl sulfonyl, halo(C １ ~C ６ ) alkylthio, halo(C １ ~C ６ ) alkylsulfonyl, —S(O) ２ N (R ２８ ) R ２９ , -SC≡N, -S(O)(=NR ３０ ) R ３１ , -N(R ３２ ) R ３３ , carboxy, C １ ~C ６ Alkylcarbonyl, halo(C １ ~C ６ ) alkylcarbonyl, C １ ~C ６ Alkoxycarbonyl, —C(O)N(R ３５ ) R ３６ , R ７ (C １ ~C ６ ) alkyl, R １６ (C １ ~C ６ ) alkoxy, C ３ ~C ６ Cycloalkyl, cyano, nitro, E-1, E-50, —O-(E-1), —O-(E-2), —O-(E-3), —O-(E-14), —S-(E-1), —S(O) ２ -(E-1), -C(O)-(E-1), -C(O)-(E-64), -C(O)-(E-71), -C(O)-(E-81), -C(O)-(E-82), -C(O)-(E-83) or -N=N-(E-1), Z １ In the above relationship, when t2 represents an integer of 2, t3 represents an integer of 2 or 3, t4 represents an integer of 2, 3 or 4, and t5 represents an integer of 2, 3, 4 or 5, each of Z １ may be the same as or different from each other, R ２ is a hydrogen atom, -C(O)R ４ or -C(O)OR ５ represents R ２８ represents a hydrogen atom, R ２９ is a hydrogen atom or C １ ~C ６ represents alkylcarbonyl, R ３３ is C １ ~C ６ Alkyl, C １ ~C ６ Alkylcarbonyl, C １ ~C ６ Alkoxycarbonyl, C １ ~C ６ Alkylaminocarbonyl or —C(S)NHC(O)OR ３４ represents R １ｃ represents a hydrogen atom, R ２１ is C １ ~C ６ represents alkyl, R ２２ is C １ ~C ６ Alkyl or C ２ ~C ６ represents alkenyl, Z ２ is a halogen atom or C １ ~C ６ represents alkyl, Z ２ In the above relationship, when t2 represents an integer of 2, t3 represents an integer of 2 or 3, t4 represents an integer of 2, 3 or 4, and t5 represents an integer of 2, 3, 4 or 5, each of Z ２ may be the same as or different from each other, Alternatively, t4 represents an integer of 2, and two Z ２ When two Z ２ Let's get together -CH ２ CH ２ represents -, M １ represents a halogen atom, M １ In the above relationship, when t2 represents an integer of 2, t3 represents an integer of 2 or 3, t4 represents an integer of 2, 3 or 4, and t5 represents an integer of 2, 3, 4 or 5, each of M １ may be identical to each other or different from each other; (iii) When Q is Q-C, Q-C is C １ ~C ６ Alkyl, R １７ (C １ ~C ６ ) alkyl, —N(R １８ ) R １９ , Q-1, Q-2, Q-3, Q-4, Q-5, Q-9, Q-12, Q-13, Q-14, Q-20, Q-21, Q-23, Q-29, Q-31, Q-39, Q-53, Q-59 or Q-60; J represents J-1, J-5, J-6, J-10, J-12, J-17, J-18, J-19 or J-24; G is -N(R ２１ ) R ２２ , -C(=NOR ６７ ) R ６８ , G-1′ to G-9′, G-12′ to G-28′, G-40′, G-68′, G-69′, G-157′ or G-159′; Z １ is a halogen atom, C １ ~C ６ Alkyl, C １ ~C ６ Alkoxy, halo (C １ ~C ６ ) alkoxy, C １ ~C ６ Alkylthio, —S(O) ２ N (R ２８ ) R ２９ , -SF ５ , -N(R ３２ ) R ３３ , carboxy, C １ ~C ６ Alkoxycarbonyl, —C(O)N(R ３５ ) R ３６ , R １６ (C １ ~C ６ ) alkoxy, C ３ ~C ６ represents cycloalkyl, cyano, E-1, —O-(E-1) or —O-(E-12); Z １ In the above relationship, when t2 represents an integer of 2, t3 represents an integer of 2 or 3, t4 represents an integer of 2, 3 or 4, and t5 represents an integer of 2, 3, 4 or 5, each of Z １ may be the same as or different from each other, E １ is a halogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl or C １ ~C ６ represents alkoxy, E １ In the above relationship, when t2 represents an integer of 2, t3 represents an integer of 2 or 3, t4 represents an integer of 2, 3 or 4, and t5 represents an integer of 2, 3, 4 or 5, each E １ may be the same as or different from each other, R １６ represents E-1, R ２ represents a hydrogen atom or —C(O)OR ５ represents Z ３ is C １ ~C ６ represents alkyl, R ２８ is C １ ~C ６ represents alkyl, R ２９ is C １ ~C ６ represents alkyl, R ３２ represents a hydrogen atom, R ３３ is C １ ~C ６ Alkylcarbonyl or C １ ~C ６ represents alkylsulfonyl, R ３５ represents a hydrogen atom, R ３６ is C １ ~C ６ represents alkyl, R １ represents a hydrogen atom or a halogen atom, R ２２ is C １ ~C ６ Alkyl, C ２ ~C ６ Alkynyl, R ２３ (C １ ~C ６ ) alkyl, M-57, M-60, M-61 or M-81; Z ２ is a halogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl, C １ ~C ６ Alkoxy, C １ ~C ６ Alkylsulfonyl, C １ ~C ６ represents alkoxycarbonyl or cyano; Z ２ In the above relationship, when t2 represents an integer of 2, t3 represents an integer of 2 or 3, t4 represents an integer of 2, 3 or 4, and t5 represents an integer of 2, 3, 4 or 5, each of Z ２ may be the same as or different from each other, Alternatively, t4 represents an integer of 2, and two Z ２ When two Z ２ together form oxo, -CH ２ CH ２ -, -OCH ２ CH ２ O- or =NOR ４３ represents 3. The aryltetrahydropyridine compound or a salt thereof according to claim 2, wherein X represents an oxygen atom. Q is QA, QB or QC; (i) If Q is Q-A, then: J represents J-1, J-5, J-6, J-8, J-10, J-14, J-15, J-17, J-18, J-19, J-21, J-22, J-23, J-24, J-25, J-26 or J-27; G represents G-1, G-3, G-4, G-5, G-7, G-9, G-11, G-12, G-13, G-14, G-15, G-16, G-17, G-18, G-19, G-20, G-25, G-26, G-28, G-29, G-35, G-36, G-37, G-40, G-41, G-42, G-44 or G-46; represents Z ２ is a halogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl, C １ ~C ６ Alkoxy, C １ ~C ６ Alkylthio, C １ ~C ６ Alkylsulfinyl, C １ ~C ６ Alkylsulfonyl, —N(R ４４ ) R ４５ , C １ ~C ６ Alkoxycarbonyl, C ３ ~C ６ represents cycloalkyl, cyano, nitro, M-1, or —O-(M-1); Z ２ In the above relationship, when t2 represents an integer of 2, t3 represents an integer of 2 or 3, t4 represents an integer of 2, 3 or 4, and t5 represents an integer of 2, 3, 4 or 5, each of Z ２ may be the same as or different from each other, R ４５ is C １ ~C ６ Alkyl or C １ ~C ６ The aryltetrahydropyridine compound or a salt thereof according to claim 3, wherein the aryltetrahydropyridine compound or the salt thereof represents alkylcarbonyl. Q is QA or QC; (i) If Q is Q-A, then: Q-A is C １ ~C ６ Alkyl, R １７ (C １ ~C ６ ) alkyl, —N(R １８ ) R １９ , Q-1, Q-2, Q-3, Q-4, Q-5, Q-9, Q-12, Q-13, Q-14, Q-20, Q-21, Q-23, Q-29, Q-31, Q-39, Q-53, Q-59 or Q-60; J represents J-1 to J-27; Z １ is a halogen atom, C １ ~C ６ Alkyl, C １ ~C ６ Alkoxy, halo (C １ ~C ６ ) alkoxy, C １ ~C ６ Alkylthio, —S(O) ２ N (R ２８ ) R ２９ , -SF ５ , -N(R ３２ ) R ３３ , carboxy, C １ ~C ６ Alkoxycarbonyl, —C(O)N(R ３５ ) R ３６ , R １６ (C １ ~C ６ ) alkoxy, C ３ ~C ６ represents cycloalkyl, cyano, E-1, —O-(E-1) or —O-(E-12); Z １ In the above relationship, when t2 represents an integer of 2, t3 represents an integer of 2 or 3, t4 represents an integer of 2, 3 or 4, and t5 represents an integer of 2, 3, 4 or 5, each of Z １ may be the same as or different from each other, E １ is a halogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl or C １ ~C ６ represents alkoxy, E １ In the above relationship, when t2 represents an integer of 2, t3 represents an integer of 2 or 3, t4 represents an integer of 2, 3 or 4, and t5 represents an integer of 2, 3, 4 or 5, each E １ may be the same as or different from each other, R １６ represents E-1, R ２ is a hydrogen atom, C １ ~C ６ Alkyl or —C(O)OR ５ represents Z ３ is C １ ~C ６ represents alkyl, R ２８ is C １ ~C ６ represents alkyl, R ２９ is C １ ~C ６ represents alkyl, R ３２ represents a hydrogen atom, R ３３ is C １ ~C ６ Alkylcarbonyl or C １ ~C ６ represents alkylsulfonyl, R ３５ represents a hydrogen atom, R ３６ is C １ ~C ６ represents alkyl, R １ represents a hydrogen atom, a halogen atom, a halo (C １ ~C ６ ) alkyl, C １ ~C ６ represents alkoxy or hydroxy; (iii) When Q is Q-C, Q-C is C １ ~C ６ Alkyl, R １７ (C １ ~C ６ ) alkyl, —N(R １８ ) R １９ , Q-1, Q-2, Q-3, Q-4, Q-5, Q-9, Q-12, Q-13, Q-14, Q-20, Q-21, Q-23, Q-29, Q-31, Q-39, Q-53, Q-59 or Q-60; J represents J-1 to J-27; G is -N(R ２１ ) R ２２ , -C(=NOR ６７ ) R ６８ , G-1′ to G-9′, G-12′ to G-28′, G-40′, G-68′, G-69′, G-157′ or G-159′; Z １ is a halogen atom, C １ ~C ６ Alkyl, C １ ~C ６ Alkoxy, halo (C １ ~C ６ ) alkoxy, C １ ~C ６ Alkylthio, —S(O) ２ N (R ２８ ) R ２９ , -SF ５ , -N(R ３２ ) R ３３ , carboxy, C １ ~C ６ Alkoxycarbonyl, —C(O)N(R ３５ ) R ３６ , R １６ (C １ ~C ６ ) alkoxy, C ３ ~C ６ represents cycloalkyl, cyano, E-1, —O-(E-1) or —O-(E-12); Z １ In the above relationship, when t2 represents an integer of 2, t3 represents an integer of 2 or 3, t4 represents an integer of 2, 3 or 4, and t5 represents an integer of 2, 3, 4 or 5, each of Z １ may be the same as or different from each other, E １ is a halogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl or C １ ~C ６ represents alkoxy, E １ In the above relationship, when t2 represents an integer of 2, t3 represents an integer of 2 or 3, t4 represents an integer of 2, 3 or 4, and t5 represents an integer of 2, 3, 4 or 5, each E １ may be the same as or different from each other, R １６ represents E-1, R ２ is a hydrogen atom, C １ ~C ６ Alkyl or —C(O)OR ５ represents Z ３ is C １ ~C ６ represents alkyl, R ２８ is C １ ~C ６ represents alkyl, R ２９ is C １ ~C ６ represents alkyl, R ３２ represents a hydrogen atom, R ３３ is C １ ~C ６ Alkylcarbonyl or C １ ~C ６ represents alkylsulfonyl, R ３５ represents a hydrogen atom, R ３６ is C １ ~C ６ represents alkyl, R ２２ is C １ ~C ６ Alkyl, C ２ ~C ６ Alkynyl, R ２３ (C １ ~C ６ ) alkyl, M-57, M-60, M-61 or M-81; R １ represents a hydrogen atom, a halogen atom, a halo (C １ ~C ６ ) alkyl, C １ ~C ６ represents alkoxy or hydroxy; When Q is either Q-A or Q-C, 3. The aryltetrahydropyridine compound or a salt thereof according to claim 2, wherein X represents an oxygen atom. Q is QA or QC; (i) If Q is Q-A, then: J represents J-1, J-5, J-6, J-8, J-10, J-12, J-14, J-15, J-17, J-18, J-19, J-21, J-22, J-23, J-24, J-25, J-26 or J-27; G represents G-1, G-3, G-4, G-5, G-7, G-9, G-11, G-12, G-13, G-14, G-15, G-16, G-17, G-18, G-19, G-20, G-25, G-26, G-28, G-29, G-35, G-36, G-37, G-40, G-41, G-42, G-44 or G-46; Z ２ is a halogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl, C １ ~C ６ Alkoxy, C １ ~C ６ Alkylthio, C １ ~C ６ Alkylsulfinyl, C １ ~C ６ Alkylsulfonyl, —N(R ４４ ) R ４５ , C １ ~C ６ Alkoxycarbonyl, C ３ ~C ６ represents cycloalkyl, cyano, nitro, M-1, or —O-(M-1); Z ２ In the above relationship, when t2 represents an integer of 2, t3 represents an integer of 2 or 3, t4 represents an integer of 2, 3 or 4, and t5 represents an integer of 2, 3, 4 or 5, each of Z ２ may be the same as or different from each other, R ４５ is C １ ~C ６ Alkyl or C １ ~C ６ represents alkylcarbonyl; (iii) When Q is Q-C, J represents J-1, J-5, J-6, J-8, J-10, J-12, J-14, J-15, J-17, J-18, J-19, J-21, J-22, J-23, J-24, J-25, J-26 or J-27; Z ２ is a halogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl, C １ ~C ６ Alkoxy, C １ ~C ６ Alkylthio, C １ ~C ６ Alkylsulfinyl, C １ ~C ６ Alkylsulfonyl, —N(R ４４ ) R ４５ , C １ ~C ６ Alkoxycarbonyl, C ３ ~C ６ represents cycloalkyl, cyano, nitro, M-1, or —O-(M-1); Z ２ In the above relationship, when t2 represents an integer of 2, t3 represents an integer of 2 or 3, t4 represents an integer of 2, 3 or 4, and t5 represents an integer of 2, 3, 4 or 5, each of Z ２ may be the same as or different from each other, Alternatively, t4 represents an integer of 2, and two Z ２ When two Z ２ together form oxo, -CH ２ CH ２ -, -OCH ２ CH ２ O- or =NOR ４３ represents R ４５ is C １ ~C ６ Alkyl or C １ ~C ６ The aryltetrahydropyridine compound or a salt thereof according to claim 5, wherein the aryltetrahydropyridine compound or the salt thereof represents alkylcarbonyl. Q is Q-B or Q-C; (ii) When Q is Q-B, R ２ is a hydrogen atom, -C(O)R ４ or -C(O)OR ５ represents Z ２ is a halogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl, C １ ~C ６ Alkoxy, C １ ~C ６ Alkylsulfonyl, C １ ~C ６ represents alkoxycarbonyl or cyano; Z ２ In the above relationship, when t2 represents an integer of 2, t3 represents an integer of 2 or 3, t4 represents an integer of 2, 3 or 4, and t5 represents an integer of 2, 3, 4 or 5, each of Z ２ may be the same as or different from each other, Alternatively, t4 represents an integer of 2, and two Z ２ When two Z ２ together form oxo, -CH ２ CH ２ -, -OCH ２ CH ２ O- or =NOR ４３ represents; (iii) When Q is Q-C, J represents J-1, J-5, J-6, J-10, J-12, J-17, J-18, J-19 or J-24; R ２ is a hydrogen atom, -C(O)R ４ or -C(O)OR ５ represents Z ２ is a halogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl, C １ ~C ６ Alkoxy, C １ ~C ６ Alkylsulfonyl, C １ ~C ６ represents alkoxycarbonyl or cyano; Z ２ In the above relationship, when t2 represents an integer of 2, t3 represents an integer of 2 or 3, t4 represents an integer of 2, 3 or 4, and t5 represents an integer of 2, 3, 4 or 5, each of Z ２ may be the same as or different from each other, Alternatively, t4 represents an integer of 2, and two Z ２ When two Z ２ together form oxo, -CH ２ CH ２ -, -OCH ２ CH ２ O- or =NOR ４３ The aryltetrahydropyridine compound or a salt thereof according to claim 2, wherein Q is QA, QB or QC; (i) If Q is Q-A, then: Q-A represents Q-1, Q-2, Q-3, Q-4, Q-6, Q-9, Q-10, Q-12 or Q-14; Z １ is a halogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl, C １ ~C ６ represents alkoxy or cyano; Z １ In the above relationship, when t2 represents an integer of 2, t3 represents an integer of 2 or 3, t4 represents an integer of 2, 3 or 4, and t5 represents an integer of 2, 3, 4 or 5, each of Z １ may be the same as or different from each other, Z ３ is C １ ~C ６ represents alkyl, J is J-1, J-2, J-3, J-4, J-5, J-6, J-7, J-8, J-9, J-10, J-11, J-12, J-13, J-14, Represents J-15, J-16, J-17, J-18, J-19, J-20, J-21, J-22, J-23, J-24, J-25 or J-26, Z ５ is C １ ~C ６ represents alkyl, R １ａ represents a hydrogen atom, R １ｂ represents a hydrogen atom, R １ｃ represents a hydrogen atom, G represents G-1, G-2, G-3, G-5, G-7, G-14, G-19, G-25, G-26, G-35 or G-41; Z ２ is a halogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl, C １ ~C ６ Alkoxy, C １ ~C ６ Alkylthio, C １ ~C ６ Alkylsulfinyl, C １ ~C ６ Alkylsulfonyl, —N(R ４４ ) R ４５ , C １ ~C ６ Alkoxycarbonyl, C ３ ~C ６ represents cycloalkyl, cyano or nitro, Z ２ In the above relationship, when t2 represents an integer of 2, t3 represents an integer of 2 or 3, t4 represents an integer of 2, 3 or 4, and t5 represents an integer of 2, 3, 4 or 5, each of Z ２ may be the same as or different from each other, R ４４ is a hydrogen atom or C １ ~C ６ represents alkyl, R ４４ and R ４５ In the relationship, R ４４ When represents a hydrogen atom, R ４５ is C １ ~C ６ represents alkylcarbonyl, R ４４ is C １ ~C ６ When it represents alkyl, R ４５ is C １ ~C ６ represents alkyl, Z ４ is C １ ~C ６ represents alkyl, R １ represents a hydrogen atom, a halogen atom, a halo (C １ ~C ６ ) alkyl, C １ ~C ６ represents alkyl or hydroxy; R ２ is a hydrogen atom, C １ ~C ６ Alkyl or —C(O)OR ５ represents R ５ is C １ ~C ６ represents alkyl; (ii) When Q is Q-B, Q-B represents Q-1, Q-2, Q-3, Q-4, Q-5, Q-6, Q-8, Q-9, Q-12, Q-14 or Q-15; Z １ is a halogen atom, C １ ~C ６ Alkyl, C ２ ~C ６ Alkenyl, C ２ ~C ６ Alkynyl, halo(C １ ~C ６ ) alkyl, C １ ~C ６ Alkoxy, halo (C １ ~C ６ ) alkoxy, C １ ~C ６ Alkenyloxy, C １ ~C ６ Alkynyloxy, C １ ~C ６ Alkylthio, C １ ~C ６ Alkyl sulfonyl, halo(C １ ~C ６ ) alkylthio, —N(R ３２ ) R ３３ , C １ ~C ６ Alkylcarbonyl, C １ ~C ６ Alkoxycarbonyl, —C(O)N(R ３５ ) R ３６ , C ３ ~C ６ Cycloalkyl, R ７ (C １ ~C ６ ) alkyl, R １６ (C １ ~C ６ ) represents alkoxy, cyano or nitro; Z １ In the above relationship, when t2 represents an integer of 2, t3 represents an integer of 2 or 3, t4 represents an integer of 2, 3 or 4, and t5 represents an integer of 2, 3, 4 or 5, each of Z １ may be the same as or different from each other, R ７ is C １ ~C ６ Alkoxy or C １ ~C ６ Alkoxy (C １ ~C ６ ) represents alkoxy; R １６ is C １ ~C ６ represents alkoxy, R ３２ is a hydrogen atom or C １ ~C ６ represents alkyl, R ３２ and R ３３ In the relationship, R ３２ When represents a hydrogen atom, R ３３ is C １ ~C ６ Alkylcarbonyl, C １ ~C ６ Alkoxycarbonyl or C １ ~C ６ represents alkylaminocarbonyl, R ３２ is C １ ~C ６ When it represents alkyl, R ３３ is C １ ~C ６ represents alkyl, R ３５ is C １ ~C ６ represents alkyl, R ３６ is C １ ~C ６ represents alkyl, Z ３ is C １ ~C ６ Alkyl or halo(C １ ~C ６ ) represents alkyl, J represents J-1′ or J-2′; A １ is a nitrogen atom or CR １ｃ represents R １ａ represents a hydrogen atom, R １ｂ represents a hydrogen atom, R １ｃ represents a hydrogen atom, G represents G-1′, G-2′, G-5′, G-6′, G-9′, G-10′, or G-11′; Z ２ is a halogen atom or C １ ~C ６ represents alkyl, Z ２ In the relationship, when t4 represents an integer of 2, 3 or 4, each Z ２ may be the same as or different from each other, R １ represents a hydrogen atom, a halogen atom, or a halo(C １ ~C ６ ) represents alkyl, R ２ is a hydrogen atom, C １ ~C ６ Alkyl, —C(O)R ４ or -C(O)OR ５ represents R ４ is C １ ~C ６ alkyl, V-1 or V-19; R ５ is C １ ~C ６ represents alkyl; (iii) When Q is Q-C, Q-C represents Q-1, Q-2, Q-3, Q-4, Q-6, Q-9, Q-12 or Q-14; Z １ is a halogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl, C １ ~C ６ Alkoxy, —C(O)N(R ３５ ) R ３６ , -N(R ３２ ) R ３３ , cyano or nitro; Z １ In the above relationship, when t2 represents an integer of 2, t3 represents an integer of 2 or 3, t4 represents an integer of 2, 3 or 4, and t5 represents an integer of 2, 3, 4 or 5, each of Z １ may be the same as or different from each other, R ３５ represents a hydrogen atom, R ３６ is C １ ~C ６ represents alkyl, R ３２ represents a hydrogen atom, R ３３ is C １ ~C ６ represents alkylcarbonyl, Z ３ is C １ ~C ６ represents alkyl, J represents J-1, J-5, J-6, J-10, J-17, J-18, J-19 or J-24; R １ represents a hydrogen atom or a halogen atom, G represents G-1′, G-2′, G-3′, G-4′, G-5′, G-6′, G-7′, G-8′, G-9′, G-12′, G-13′, G-14′, G-15′, or G-16′; R １ａ represents a hydrogen atom, R １ｂ represents a hydrogen atom, R １ｃ represents a hydrogen atom, Z ４ is a hydrogen atom, C １ ~C ６ Alkyl, C １ ~C ６ Alkoxy (C １ ~C ６ ) alkyl, C １ ~C ６ Alkylcarbonyl or C １ ~C ６ represents an alkoxycarbonyl; Z ２ is a halogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl, C １ ~C ６ represents alkoxy, cyano or nitro, n represents an integer of 0, 1, or 2; Z ２ In the relationship, when t4 represents an integer of 2, 3 or 4, each Z ２ may be the same as or different from each other, Alternatively, t4 represents an integer of 2, and two Z ２ When two Z ２ together represent oxo, R ２ is a hydrogen atom, C １ ~C ６ Alkyl or —C(O)OR ５ represents R ５ is C １ ~C ６ represents alkyl; When Q is Q-A, Q-B, or Q-C, R ３ represents a hydrogen atom, X represents an oxygen atom or a sulfur atom; Y represents an oxygen atom or a sulfur atom; t2 represents an integer of 0, 1, or 2; t3 represents an integer of 0, 1, 2 or 3; t4 represents an integer of 0, 1, 2, 3, or 4; t5 represents an integer of 0, 1, 2, 3, 4, or 5; d3 represents an integer of 0, 2. The aryltetrahydropyridine compound or a salt thereof according to claim 1, wherein d5 represents an integer of 0. Q is QA, QB or QC; (i) If Q is Q-A, then: Q-A represents Q-1, Q-2, Q-3, Q-4, Q-9 or Q-12; Z １ represents a halogen atom or cyano; J represents J-1, J-5, J-6, J-8, J-10, J-15, J-17, J-18, J-19, J-21, J-22, J-23, J-24, J-25 or J-26; G represents G-1, G-3, G-5, G-7, G-14, G-19, G-25, G-26, G-35 or G-41; Z ２ is a halogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl, C １ ~C ６ Alkoxy, C １ ~C ６ Alkylthio, C １ ~C ６ Alkylsulfonyl, —N(R ４４ ) R ４５ , C １ ~C ６ Alkoxycarbonyl, C ３ ~C ６ represents cycloalkyl, cyano or nitro, R １ is a hydrogen atom, halo (C １ ~C ６ ) alkyl or hydroxy; R ２ is a hydrogen atom or C １ ~C ６ represents alkyl, Y represents an oxygen atom; (ii) When Q is Q-B, R ２ is a hydrogen atom, -C(O)R ４ or -C(O)OR ５ represents; (iii) When Q is Q-C, Q represents Q-1, Q-2, Q-3, Q-4, Q-9, Q-12 or Q-14; Z １ is a halogen atom, —C(O)N(R ３５ ) R ３６ , -N(R ３２ ) R ３３ or cyano, Z ２ is a halogen atom, C １ ~C ６ Alkyl, halo (C １ ~C ６ ) alkyl or C １ ~C ６ represents alkoxy, R ２ represents a hydrogen atom or —C(O)OR ５ represents Y represents an oxygen atom; 9. The aryltetrahydropyridine compound or a salt thereof according to claim 8, wherein X represents an oxygen atom in any of QA, QB and QC.

2. The aryltetrahydropyridine compound or a salt thereof according to claim 1, wherein Q is QA. The aryltetrahydropyridine compound or a salt thereof according to claim 1, wherein Q is QB. The aryltetrahydropyridine compound or a salt thereof according to claim 1, wherein Q is QC. 　 G is -N(R ２１ ) R ２２ The aryltetrahydropyridine compound or a salt thereof according to claim 1, wherein:

2. The aryltetrahydropyridine compound or a salt thereof according to claim 1, wherein G is G-1, G-3 or G-7.

2. The aryltetrahydropyridine compound or a salt thereof according to claim 1, wherein G is G-1′, G-2′, G-5′, G-6′, G-9′, G-13′, G-19′, or G-27′. Q is QA, QB or QC; (i) If Q is Q-A, then: J represents J-1, J-10, J-17 or J-19; (ii) When Q is Q-B, A １ represents a nitrogen atom; (iii) When Q is Q-C, 2. The aryltetrahydropyridine compound or a salt thereof according to claim 1, wherein J is J-1, J-10, J-17 or J-19. Q is QA, QB or QC; (i) If Q is Q-A, then: Q-A represents Q-1, Q-2, Q-3, Q-4, Q-12 or Q-14; (ii) When Q is Q-B, Q-B represents Q-1, Q-2, Q-3, Q-4, Q-12 or Q-14; (iii) When Q is Q-C, 2. The aryltetrahydropyridine compound or a salt thereof according to claim 1, wherein QC is Q-1, Q-2, Q-3, Q-4, Q-12 or Q-14. 　 A pest control agent comprising, as an active ingredient, one or more selected from the aryltetrahydropyridine compounds and salts thereof according to any one of claims 1 to 17.

18. A pesticide comprising, as an active ingredient, one or more selected from the aryltetrahydropyridine compounds and salts thereof according to any one of claims 1 to 17.

18. An agent for controlling internal or external parasites of mammals or birds, comprising one or more compounds selected from the aryltetrahydropyridine compounds and salts thereof according to any one of claims 1 to 17 as active ingredients.

21. The control agent according to claim 20, wherein the ectoparasite is a flea or acar.

18. An insecticide or acaricide comprising, as an active ingredient, one or more aryltetrahydropyridine compounds and salts thereof according to any one of claims 1 to 17. 　 A seed treatment agent comprising, as an active ingredient, one or more selected from the aryltetrahydropyridine compounds and salts thereof according to any one of claims 1 to 17. 　 The seed treatment agent according to claim 23, wherein the seed treatment is carried out by immersion treatment. 　 A soil treatment agent comprising, as an active ingredient, one or more aryltetrahydropyridine compounds and salts thereof according to any one of claims 1 to 17. 　 The soil treatment agent according to claim 25, wherein the soil treatment is carried out by soil drench treatment.

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