Heteroaryl-triazole compounds as pesticides

Abstract

To provide intermediates for synthesizing heteroaryl-triazole compounds for use in the control of pests in plant protection and for the control of ectoparasites on animals.SOLUTION: This invention discloses, for example, a compound represented by the following formula, or 3-chloro-5-[(methylsulfonyl)methyl]benzoic acid, 3-(cyanomethyl)-5-(methylsulfonyl)benzoic acid, 5-[5-[(1S)-1-aminoethyl]-1,2,4-triazol-1-yl]pyrazine-2-carbonitrile hydrochloride, 2-chloro-6-(1-cyano-1-methyl-ethyl)pyridine-4-carboxylic acid, 6-[5-[(1S)-1-aminoethyl]-3-cyclopropyl-1,2,4-triazol-1-yl]pyrimidine-4-carbonitrile hydrochloride, and the like.SELECTED DRAWING: None

Description

[Technical Field]

[0001] The present invention includes novel heteroaryl-triazole compounds, such compounds Formulations and compositions, as well as animal pests in plant protection, which their use in the control of insects (including arthropods and insects) and in the control of ectoparasites of animals This application relates to their use for the treatment of ulcerative colitis. [Background technology]

[0002] Formula (I) [R 3b Certain heteroaryl-triazole compounds represented by the formula [=hydrogen] are It is disclosed in WO2017 / 192385 for use in controlling ectoparasites in animals. Pests in the field of pest control, including arthropods and insects, as well as in the field of plant protection WO2019 / 170626 and W2019 / 21519 regarding the use in the control of 8. Furthermore, patent applications WO2019 / 197468 and WO2019 / 2 01835, WO2019 / 202077 and WO2019 / 206799 include animal For use in the control of ectoparasites and pests in the field of plant protection (which Certain heteroaryl-triarylamines for controlling insects (including arthropods and insects) sol compounds are disclosed in WO2020 / 002563 and WO2020 / 0533. 64, WO2020 / 053365, WO2020 / 079198, WO2020 / 09 4363, WO2020 / 169445, WO2020 / 182649, WO2020 / 188014, WO2020 / 188027 and WO2020 / 193341 include azo All of these compounds have been described for use as insecticides. It is possible to do this.

[0003] Modern plant protection products and veterinary ectoparasiticides offer a wide range of benefits, e.g., efficacy, durability, spectrum Torque and resistance breaking characteristics Many requirements must be met. The combinatorial possibilities of the active compounds, in addition to the cost involved in synthesizing them, play a role. Furthermore, resistance may develop. For all these reasons, new crop protection compositions or Therefore, the search for veterinary ectoparasiticides cannot be considered complete, and there are many compounds that are being developed in comparison with known compounds. In comparison, there is a constant demand for new compounds with improved properties, at least in terms of individual aspects. It is being done. [Prior art documents] [Patent documents]

[0004] [Patent Document 1] WO2017 / 192385 [Patent Document 2] WO2019 / 170626 [Patent Document 3] WO2019 / 215198 [Patent Document 4] WO2019 / 197468 [Patent Document 5] WO2019 / 201835 [Patent Document 6] WO2019 / 202077 [Patent Document 7] WO2019 / 206799 [Patent Document 8] WO2020 / 002563 [Patent Document 9] WO2020 / 053364 [Patent Document 10] WO2020 / 053365 [Patent Document 11] WO2020 / 079198 [Patent Document 12] WO2020 / 094363 [Patent Document 13] WO2020 / 169445 [Patent Document 14] WO2020 / 182649 [Patent Document 15] WO2020 / 188014 [Patent Document 16] WO2020 / 188027 [Patent Document 17] WO2020 / 193341 Summary of the Invention [Problem to be solved by the invention]

[0005] The object of the present invention is to provide compounds that broaden the spectrum of pesticides in various respects. The purpose was to provide [Means for solving the problem]

[0006] Therefore, the present invention provides a compound of general formula (I) [ka] [In the formula (configuration 1-1): X is O or S; Y is a direct bond or an optionally substituted CH; R 1 is hydrogen; C1-C6 alkyl [wherein the alkyl is -CN, -CONH2, Substituted with one substituent selected from -COOH, -NO2 and -Si(CH3)3 C1-C6 haloalkyl; C2-C6 alkenyl; C2-C6 haloalkenyl C2-C6 alkynyl;C2-C6 haloalkynyl;C3-C4 cycloalkyl-C 1-C2 alkyl- [wherein the C3-C4 cycloalkyl is substituted with one or two halogen atoms] oxetan-3-yl-CH2- or benzyl [wherein which may be substituted with a halogen atom or a C1-C3 haloalkyl. ; R 2 is phenyl, pyridine, pyrimidine, pyrazine or pyridazine, wherein The phenyl, pyridine, pyrimidine, pyrazine or pyridazine has a total of 1 to 3 substituents. and wherein the substituent is substituted with either of the carbons adjacent to the carbon bonded to the C=X group. and at least one and at most three substituents are not present on any carbon atom. Hydroxy and optionally substituted C3-C6 cycloalkanes Coxy, -OCO-C1-C3 alkyl, -OSO2-C1-C6 alkyl, C2-C4 alkenyl, C2-C4 haloalkenyl, phenoxy and heterocyclyloxy; and C1-C3 alkyl, C1-C3 haloalkyl, C1-C3 haloalkoxy, C1- C3 alkoxy, C2-C4 alkenyloxy and C2-C4 haloalkenyloxy wherein the C1-C3 alkyl, C1-C3 haloalkyl, C1-C3 haloalkoxy, C 1-C3 alkoxy, C2-C4 alkenyloxy and C2-C4 haloalkenyloxy teeth, =O (oxo), =S (thiono), hydroxy, -CN, -COOH, -CSNH 2, -NO2, -NH2, -SF5, -SiMe3; and C3-C6 cycloalkyl, C3-C6 halo, optionally substituted in either case C1-C6 alkoxy, C1-C6 haloalkoxy, C1-C6 ... Kilthio, C1-C6 alkylsulfinyl, C1-C6 alkylsulfonyl, C3-C 6Cycloalkylkylthio, C3-C6 cycloalkylsulfinyl, C3-C6 cyclo C1-C6 haloalkylsulfonyl, C1-C6 haloalkylthio, C1-C6 haloalkylsulfonyl Nyl, C1-C6 haloalkylsulfonyl, -OCONH-C1-C6 alkyl, -NH (C1-C6 alkyl), -N(C1-C6 alkyl)2, -CONR 41 R 42 , -N R 42 COR 41 , -CO2C1-C6 alkyl, -C(=NOC1-C6 alkyl)H , —C(═NOC1-C6 alkyl)-C1-C6 alkyl; and Optionally substituted phenyl and heterocyclyl, wherein the heterocyclyl is , saturated and partially unsaturated 4- to 10-membered heterocyclyl, 5-membered heteroaryl, 6-membered hetero selected from the group consisting of aryl, 9-membered heteroaryl, and 10-membered heteroaryl; substituted with 1 to 3 substituents selected from the group consisting of: independently selected from Group A consisting of: and, The remaining substituents in the cases 1 and 2 are: Halogen, hydroxy, -NH2, -CN, SF5, -COOH, -CONH2, - NO2; and C1-C3 alkyl, C1-C3 haloalkyl, which may be substituted in any case; ru, C1-C3 alkoxy, C1-C3 haloalkoxy, C1-C3 haloalkylthio; each independently selected from Group B consisting of: R 3a , R 3b teeth, Hydrogen, halogens and -CN; and C1-C6 alkyl [wherein the alkyl is selected from the group consisting of halogen, hydroxy, -CN, -C OOH, -CONH2, -NO2, -NH2, optionally substituted C 1-C6 alkyl, C3-C6 cycloalkyl, C1-C6 alkoxy, C1-C6 alkoxy C1-C6 alkylsulfinyl, C1-C6 alkylsulfonyl, -NH( C1-C6 alkyl), -N(C1-C6 alkyl)2, -NHCO-C1-C6 alkyl -N(C1-C6 alkyl)CO-C1-C6 alkyl, -CO2C1-C6 alkyl -CONH(C1-C6 alkyl) and -CON(C1-C6 alkyl) and optionally substituted with 1 to 3 substituents independently selected from the group C3-C6 cycloalkyl, C1-C6 halo, which may be substituted in either case; Alkyl, C2-C6 alkenyl, C2-C6 haloalkenyl, C2-C6 alkynyl; and, benzyl, wherein the phenyl substituents are halogen, hydroxy, -CN, -COO H, -CONH2, -NO2, -NH2, -SF5, and in any case, substituted Optionally, C1-C6 alkyl, C1-C6 alkoxy, C1-C6 alkylthio, C 1-C6 alkylsulfinyl and C1-C6 alkylsulfonyl, respectively and heterocyclyl-C1-C6 alkyl, wherein the heterocyclyl substituent is 4 to 1 0-membered saturated and partially unsaturated heterocyclyl, 5-membered heteroaryl and 6-membered heteroaryl wherein each of these is selected from the group consisting of halogen, ═O(oxo), ), hydroxy, -CN, -COOH, -CONH2, -NO2, -NH2, and C1-C6 alkyl and C1-C6 alkoxy, optionally substituted in any case; and optionally substituted with 1 to 3 substituents independently selected from the group consisting of: independently selected from the group consisting of: Or, R 3a , R 3b are halogens, -CN, any of the carbons to which they are attached. optionally substituted C1-C6 alkyl, C1-C6 alkoxy and C1-C 6-haloalkoxy, optionally forming a C3-C6 carbocyclic or 3- to 6-membered heterocyclic ring system; R 4 is pyridine, pyrimidine, pyrazine or pyridazine, wherein the pyridine , pyrimidine, pyrazine or pyridazine is halogen, hydroxy, C1-C3 alkyl , C3-C4 cycloalkyl, C1-C3 haloalkyl, C1-C3 alkoxy substituted with 2-3 substituents independently selected from the group; Or, R 4 is pyridine, pyrimidine, pyrazine or pyridazine, wherein the pyridine , pyrimidine, pyrazine or pyridazine is substituted with a total of 1 to 3 substituents, and at least one and up to three substituents are -CN, -COOH, -NO2, -SF5, -NH2, substituted C3-C4 chloroalkyl; and C1-C3 alkyl and C1-C3 alkoxy [wherein each of these is -N H2, -OH, -NO2, -CN, -SH, CO2C1-C4 alkyl, -CONH2, SF5, -SO2NH2, C3-C4 cycloalkyl, C2-C4 alkenyl, C5-C 6 cycloalkenyl, C2-C4 alkynyl, -NH(C1-C6 alkyl), -N(C 1-C6 alkyl)2, N-C1-C4 alkanoylamino, C1-C4 alkoxy, C 1-C4 haloalkoxy, C2-C4 alkenyloxy, C2-C4 alkynyloxy, C3-C4 cycloalkoxy, C5-C6 cycloalkenyloxy, C1-C4 alkoxy C2-C4 alkenyloxycarbonyl, C2-C4 alkynyloxycarbonyl Carbonyl, C6-,C 10 -,C 14 -Aryloxycarbonyl, C1-C4 alkano C2-C4 alkenylcarbonyl, C2-C4 alkynylcarbonyl, C6-, C 10 -,C 14 -arylcarbonyl, C1-C4 alkylthio, C1-C4 haloalkyl thio, C3-C4 cycloalkylthio, C2-C4 alkenylthio, C5-C6 cyclo Alkenylthio, C2-C4 alkynylthio, C1-C4 alkylsulfinyl, C1- C4 haloalkylsulfinyl, C1-C4 alkylsulfonyl, C1-C4 haloalkyl -Sulfonyl, -SO2-NH(C1-C6 alkyl), -SO2-N(C1-C6 alkyl alkyl)2, C1-C4 alkylphosphinyl, C1-C4 alkylphosphonyl, N-C1 -C4 alkylaminocarbonyl, N,N-di-C1-C4 alkylaminocarbonyl, N-C1-C4 alkanoylaminocarbonyl, N-C1-C4 alkanoyl-N-C1 -C4 alkylaminocarbonyl, C6-,C 10 -,C 14 -aryl, C6-, C1 0-,C 14 -aryloxy, benzyl, benzyloxy, benzylthio, C6-, C 10 -,C14 -arylthio, C6-,C 10 -,C 14 -arylamino, benzyl Amino, heterocyclyl, heteroaryl and trialkylsilyl, and Substituents bonded via an alkyl group, such as C1-C4 alkylidene (e.g., methylidene or ethylidene), oxo group, imino group, and substituted imino group, substituted with 1 to 3 selected substituents; and -CO2-C1-C6 alkyl, C5-C6, optionally substituted in each case Cycloalkyl, C4-C6 alkyl, C4-C6 haloalkyl, C4-C6 alkoxy , C1-C6 haloalkoxy, C1-C6 alkylthio, C1-C6 alkylsulfini C1-C6 alkylsulfonyl, C3-C6 cycloalkylsulfanyl, C3-C 6 cycloalkylsulfinyl, C3-C6 cycloalkylsulfonyl, C1-C6 halo Alkylthio, C1-C6 haloalkylsulfinyl, C1-C6 haloalkylsulfonyl C2-C4 alkenylsulfanyl, C2-C4 alkenylsulfinyl, C2-C 4 Alkenylsulfonyl, C2-C4 Alkynylsulfanyl, C2-C4 Alkynyls sulfinyl, C2-C4 alkynylsulfonyl, phenylsulfanyl, phenylsulf S-C1-C6 alkylsulfinimidoyl, S-C3 -C6 cycloalkylsulfinimidoyl, S-C2-C6 alkenylsulfinimidoyl Doyle, S-C2-C6 alkynylsulfinimidoyl, S-phenylsulfinimido Doyle, S-C1-C6 alkylsulfonimidoyl, S-C3-C6 cycloalkylsulfonyl S-C2-C6 Alkenyl Sulfonimidoyl, S-C2-C6 Alkenyl Sulfonimidoyl, S-phenylsulfonimidoyl, -NH(C1-C6 alkyl alkyl), -N(C1-C6 alkyl)2, -C(=NOC1-C6 alkyl)H, -C( =NOC1-C6 alkyl)-C1-C6 alkyl, phenyl and 5-6 membered heteroaryl and The following substructures S1 to S6: [ka] [where: the bond to the pyridine, pyrimidine, pyrazine, or pyridazine is marked with a #; and Z is CO or CS, and Y 1 is independently selected from CO or SO2 ; R 41 is hydrogen or C1-C6 alkyl which may be substituted in either case, C1-C6 haloalkyl, C3-C6 cycloalkyl, -C1-C6 alkyl-C3-C 6 cycloalkyl and phenyl; R 42 is hydrogen or C1-C6 alkyl which may be substituted in either case, C1-C6 haloalkyl and C3-C6 cycloalkyl; R 43 is C1-C6 alkyl, C1-C6 halo, which may be substituted in either case. independently selected from C3-C6 cycloalkyl, C3-C6 cycloalkyl and phenyl; independently selected from Group A consisting of: and, The remaining substituents in the cases 1 and 2 are: halogen and hydroxy; and C1-C6 alkyl, C3-C6 cycloalkenyl, optionally substituted in either case alkyl, C1-C6 haloalkyl and C1-C6 alkoxy; each independently selected from Group B consisting of: Or, R 4 is a 5-membered heteroaryl, wherein the heteroaryl is Halogen, hydroxy, -CN, -COOH, -NO2, -SF5, -NH2; and , -CO2-C1-C6 alkyl, C1-C6, optionally substituted in either case Alkyl, C3-C6 cycloalkyl, C1-C6 haloalkyl, C1-C6 alkoxy , C1-C6 haloalkoxy, C1-C6 alkylthio, C1-C6 alkylsulfini C1-C6 alkylsulfonyl, C3-C6 cycloalkylsulfanyl, C3-C 6 cycloalkylsulfinyl, C3-C6 cycloalkylsulfonyl, C1-C6 halo Alkylthio, C1-C6 haloalkylsulfinyl, C1-C6 haloalkylsulfonyl C2-C4 alkenylsulfanyl, C2-C4 alkenylsulfinyl, C2-C 4 Alkenylsulfonyl, C2-C4 Alkynylsulfanyl, C2-C4 Alkynyls sulfinyl, C2-C4 alkynylsulfonyl, phenylsulfanyl, phenylsulf S-C1-C6 alkylsulfinimidoyl, S-C3 -C6 cycloalkylsulfinimidoyl, S-C2-C6 alkenylsulfinimidoyl Doyle, S-C2-C6 alkynylsulfinimidoyl, S-phenylsulfinimido Doyle, S-C1-C6 alkylsulfonimidoyl, S-C3-C6 cycloalkylsulfonyl S-C2-C6 Alkenyl Sulfonimidoyl, S-C2-C6 Alkenyl Sulfonimidoyl, S-phenylsulfonimidoyl, -NH(C1-C6 alkyl alkyl), -N(C1-C6 alkyl)2, -C(=NOC1-C6 alkyl)H, -C( =NOC1-C6 alkyl)-C1-C6 alkyl, phenyl and 5-6 membered heteroaryl and Substructures S1-S6, where the bond to the 5-membered heteroaryl is marked with a #, and Z is CO or CS, and Y 1 is independently selected from CO or SO2 be]; and optionally substituted with 1 to 3 substituents independently selected from the group consisting of: Or, R 4 is a 4- to 10-membered saturated or partially unsaturated heterocyclyl, a 9-membered heteroaryl, and and 10-membered heteroaryl, wherein are, respectively, Halogen, =O(oxo), =S(thiono), hydroxy, -CN, -COOH, - SO2NH2, -CONH2, -CSNH2, -NO2, -SF5, -NH2; and -CO2-C1-C6 alkyl, C1-C6, optionally substituted in either case Alkyl, C3-C6 cycloalkyl, C3-C6 cycloalkyl-C1-C6 alkyl , C1-C6 haloalkyl, C1-C6 alkoxy, C1-C6 haloalkoxy, C1- C6 alkylthio, C1-C6 alkylsulfinyl, C1-C6 alkylsulfonyl, C3-C6 cycloalkylsulfanyl, C3-C6 cycloalkylsulfinyl, C3 -C6 cycloalkylsulfonyl, C1-C6 haloalkylthio, C1-C6 haloalkyl C1-C6 haloalkylsulfonyl, C2-C4 alkenylsulfanily C2-C4 alkenylsulfinyl, C2-C4 alkenylsulfonyl, C2-C4 Alkynylsulfanyl, C2-C4 alkynylsulfinyl, C2-C4 alkynyls sulfonyl, phenylsulfanyl, phenylsulfinyl, phenylsulfonyl, SC 1-C6 alkylsulfinimidoyl, S-C3-C6 cycloalkylsulfinimidoyl Doyle, S-C2-C6 alkenylsulfinimidoyl, S-C2-C6 alkynylsulfinyl Sulfinimidoyl, S-phenylsulfinimidoyl, S-C1-C6 alkylsulfinimidoyl S-C3-C6 Cycloalkylsulfonimidoyl, S-C2-C6 Arylsulfonimidoyl Alkenylsulfonimidoyl, S-C2-C6 alkynylsulfonimidoyl, S-phenyl Nilsulfonimidoyl, -NH(C1-C6 alkyl), -N(C1-C6 alkyl) 2. -C(=NOC1-C6 alkyl)H, -C(=NOC1-C6 alkyl)-C1- C6 alkyl, phenyl and 5-6 membered heteroaryl; and Substructures S1 and S6, where the bond to the heterocyclic ring is marked with a #, and Z is CO or CS, and Y 1 is independently selected from CO or SO2 ru]; and optionally substituted with 1 to 3 substituents independently selected from the group consisting of: R 5 teeth, Hydrogen, halogens; and C3-C6 cycloalkyl, C1-C6 alkoxy, optionally substituted in either case; Koxy, C1-C6 haloalkoxy, (C1-C6 alkoxy)2CH-, -CO2C1 -C6 alkyl, -C(=NOC1-C6 alkyl)H, -C(=NOC1-C6 alkyl (C1-C6 alkyl); and C1-C6 alkyl and C1-C6 haloalkyl [wherein the C1-C6 alkyl and and C1-C6 haloalkyl are Halogen, =O (oxo), =S (thiono), hydroxy, -CN, -NO2, - SF5, -SiMe3; and C3-C6 cycloalkyl, C1-C6 alkyl, optionally substituted in either case alkoxy, C1-C6 haloalkoxy; and optionally substituted with 1 to 3 substituents independently selected from the group consisting of: selected from the group consisting of The present invention provides a compound represented by the formula:

[0007] The present invention further provides a compound represented by general formula (I) [wherein (structure 1-2): X is O or S; Y is a direct bond or an optionally substituted CH; R 1 is hydrogen; C1-C6 alkyl [wherein the alkyl is -CN, -CONH2, Substituted with one substituent selected from -COOH, -NO2 and -Si(CH3)3 C1-C6 haloalkyl; C2-C6 alkenyl; C2-C6 haloalkenyl C2-C6 alkynyl;C2-C6 haloalkynyl;C3-C4 cycloalkyl-C 1-C2 alkyl- [wherein the C3-C4 cycloalkyl is substituted with one or two halogen atoms] oxetan-3-yl-CH2- or benzyl [wherein which may be substituted with a halogen atom or a C1-C3 haloalkyl. ; R 2 is phenyl, pyridine, pyrimidine, pyrazine or pyridazine, wherein The phenyl, pyridine, pyrimidine, pyrazine or pyridazine has a total of 1 to 3 substituents. and wherein the substituent is substituted with either of the carbons adjacent to the carbon bonded to the C=X group. and at least one and at most two substituents are not present on any carbon atom. C3-C6 cycloalkoxy, wherein the cycloalkoxy is Halogen, =O (oxo), -CN, C1-C6 alkyl, C3-C6 cycloalkyl, C3-C6 halocycloalkyl , C1-C6 alkoxy, C1-C6 haloalkoxy, C1-C6 alkylthio, C1- C6 alkylsulfinyl, C1-C6 alkylsulfonyl, C3-C6 cycloalkyl kylthio, C3-C6 cycloalkylsulfinyl, C3-C6 cycloalkylsulfonyl optionally substituted with 1 to 2 substituents selected from the group consisting of yl; Or, C1-C6 alkyl, wherein the alkyl is -CN, C3-C6 cycloalkyl, C3-C6 halocycloalkyl, C1-C6 alkoxy C1-C6 haloalkoxy, C1-C6 alkylthio, C1-C6 alkylsulfonyl C1-C6 alkylsulfonyl, C3-C6 cycloalkylkylthio, C3-C 6 cycloalkylsulfinyl, C3-C6 cycloalkylsulfonyl substituted with one or two substituents selected from the group consisting of: Or, C1-C6 alkylcarbonyl and C3-C6 cycloalkylcarbonyl [wherein C1-C6 alkylcarbonyl and C3-C6 cycloalkylcarbonyl are Halogen, -CN, C3-C6 cycloalkyl, C3-C6 halocycloalkyl, C1-C6 alkyl Thio, C1-C6 alkylsulfinyl, C1-C6 alkylsulfonyl, C3-C6 thio C3-C6 cycloalkylsulfinyl, C3-C6 cycloa and optionally substituted with 1 to 2 substituents selected from the group consisting of alkylsulfonyl; Or, C1-C6 alkoxy, wherein the alkoxy is =O(oxo), -CN, C3-C6 cycloalkyl, C3-C6 halocycloalkyl, C1-C6 alkoxy C1-C6 haloalkoxy, C1-C6 alkylthio, C1-C6 alkylsulfonyl C1-C6 alkylsulfonyl, C3-C6 cycloalkylkylthio, C3-C 6 cycloalkylsulfinyl, C3-C6 cycloalkylsulfonyl substituted with one or two substituents selected from the group consisting of: Or, C1-C6 haloalkyl, wherein the haloalkyl is =O(oxo), -CN, C3-C6 cycloalkyl, C3-C6 halocycloalkyl, C1-C6 alkoxy C1-C6 haloalkoxy, C1-C6 alkylthio, C1-C6 alkylsulfonyl C1-C6 alkylsulfonyl, C3-C6 cycloalkylkylthio, C3-C 6 cycloalkylsulfinyl, C3-C6 cycloalkylsulfonyl substituted with one or two substituents selected from the group consisting of: Or, C1-C6 haloalkoxy, wherein the haloalkoxy is =O(oxo), -CN, C3-C6 cycloalkyl, C3-C6 halocycloalkyl, C1-C6 alkoxy C1-C6 haloalkoxy, C1-C6 alkylthio, C1-C6 alkylsulfonyl C1-C6 alkylsulfonyl, C3-C6 cycloalkylkylthio, C3-C 6 cycloalkylsulfinyl, C3-C6 cycloalkylsulfonyl substituted with one or two substituents selected from the group consisting of: Or, C2-C6 alkenyloxy [wherein the alkenyloxy is Halogen, -CN, C3-C6 cycloalkyl, C3-C6 halocycloalkyl, C1-C6 alkoxy C1-C6 haloalkoxy, C1-C6 alkylthio, C1-C6 alkylsulfonyl C1-C6 alkylsulfonyl, C3-C6 cycloalkylkylthio, C3-C 6 cycloalkylsulfinyl, C3-C6 cycloalkylsulfonyl substituted with one or two substituents selected from the group consisting of: Or, C1-C6 alkylSO2O- [wherein the alkylSO2O- is Halogen, -CN, C3-C6 cycloalkyl, C3-C6 halocycloalkyl, C1-C6 alkoxy C1-C6 haloalkoxy, C1-C6 alkylthio, C1-C6 alkylsulfonyl C1-C6 alkylsulfonyl, C3-C6 cycloalkylkylthio, C3-C 6 cycloalkylsulfinyl, C3-C6 cycloalkylsulfonyl substituted with one or two substituents selected from the group consisting of: Or, Phenyl-C1-C3 haloalkyl and phenyl-C1-C3 alkoxy, where: The phenyl is Halogen, -CN, C1-C6 alkyl, C3-C6 cycloalkyl, C3-C6 halocycloalkyl , C1-C6 alkoxy, C1-C6 haloalkoxy, C1-C6 alkylthio, C1- C6 alkylsulfinyl, C1-C6 alkylsulfonyl, C3-C6 cycloalkyl kylthio, C3-C6 cycloalkylsulfinyl, C3-C6 cycloalkylsulfonyl and optionally substituted with 1 to 3 substituents independently selected from the group consisting of aryl, aryl, aryl, aryl and aryl; Or, Heterocyclyloxy and heterocyclyl-C1-C3 alkoxy, wherein the hetero The heterocyclyl includes saturated and partially unsaturated 4- to 6-membered heterocyclyl, 5-membered heteroaryl, 6-membered heteroaryl, each of which is selected from the group consisting of: Halogen, -CN, C1-C6 alkyl, C3-C6 cycloalkyl, C3-C6 halocycloalkyl , C1-C6 alkoxy, C1-C6 haloalkoxy, C1-C6 alkylthio, C1- C6 alkylsulfinyl, C1-C6 alkylsulfonyl, C3-C6 cycloalkyl kylthio, C3-C6 cycloalkylsulfinyl, C3-C6 cycloalkylsulfonyl and optionally substituted with 1 to 3 substituents independently selected from the group consisting of methyl, ... independently selected from the group consisting of: and, The remaining optional substituents are: Hydrogen, halogen, hydroxy, -NH2, -CN, -NO2, C1-C3 alkyl, C1-C3 haloalkyl, C1-C3 alkoxy, C1-C3 haloalkoxy, C1-C 3 alkylthio, C1-C3 alkylsulfinyl, C1-C3 alkylsulfonyl, C 3-C4 cycloalkylkylthio, C3-C4 cycloalkylsulfinyl, C3-C 4Cycloalkylsulfonyl, C1-C3 haloalkylthio, C1-C3 haloalkyls sulfinyl and C1-C3 haloalkylsulfonyl; selected from the group consisting of: R 3a , R 3b teeth, Hydrogen, halogens and -CN; and C1-C6 alkyl [wherein the alkyl is selected from the group consisting of halogen, hydroxy, -CN, -C OOH, -CONH2, -NO2, -NH2, optionally substituted C 1-C6 alkyl, C3-C6 cycloalkyl, C1-C6 alkoxy, C1-C6 alkoxy C1-C6 alkylsulfinyl, C1-C6 alkylsulfonyl, -NH( C1-C6 alkyl), -N(C1-C6 alkyl)2, -NHCO-C1-C6 alkyl -N(C1-C6 alkyl)CO-C1-C6 alkyl, -CO2C1-C6 alkyl -CONH(C1-C6 alkyl) and -CON(C1-C6 alkyl) and optionally substituted with 1 to 3 substituents independently selected from the group C3-C6 cycloalkyl, C1-C6 halo, which may be substituted in either case; Alkyl, C2-C6 alkenyl, C2-C6 haloalkenyl, C2-C6 alkynyl; and, benzyl, wherein the phenyl substituents are halogen, hydroxy, -CN, -COO H, -CONH2, -NO2, -NH2, -SF5, and in any case, substituted Optionally, C1-C6 alkyl, C1-C6 alkoxy, C1-C6 alkylthio, C 1-C6 alkylsulfinyl and C1-C6 alkylsulfonyl, respectively and heterocyclyl-C1-C6 alkyl, wherein the heterocyclyl substituent is 4 to 1 0-membered saturated and partially unsaturated heterocyclyl, 5-membered heteroaryl and 6-membered heteroaryl wherein each of these is selected from the group consisting of halogen, ═O(oxo), ), hydroxy, -CN, -COOH, -CONH2, -NO2, -NH2, and C1-C6 alkyl and C1-C6 alkoxy, optionally substituted in any case; and optionally substituted with 1 to 3 substituents independently selected from the group consisting of: independently selected from the group consisting of: Or, R 3a , R 3b are halogens, -CN, any of the carbons to which they are attached. optionally substituted C1-C6 alkyl, C1-C6 alkoxy and C1-C 6-haloalkoxy, optionally forming a C3-C6 carbocyclic or 3- to 6-membered heterocyclic ring system; R 4 is the following substructure T1 to T6: [ka] wherein the bond to the triazole is marked with a #; where: X 1 is the following substructure S4-a [ka] [where: the bond to the pyridine, pyrimidine, pyrazine, or thiazole is marked with a #; R 41 is hydrogen or C1-C6 alkyl which may be substituted in either case, C1-C6 haloalkyl, C3-C6 cycloalkyl, -C1-C6 alkyl-C3-C 6 cycloalkyl and phenyl; R 42 is hydrogen or C1-C6 alkyl which may be substituted in either case, C1-C6 haloalkyl and C3-C6 cycloalkyl] and; X 2 -CN or X1 and; R 5 teeth, Hydrogen, halogens; and C1-C6 alkyl, C1-C6 haloalkyl, which may be substituted in any case; C3-C6 cycloalkyl, C1-C6 alkoxy, C1-C6 haloalkoxy, C1-C6 alkoxy)2CH-, -CO2C1-C6 alkyl, -C(=NOC1-C 6 alkyl)H, -C(=NOC1-C6 alkyl)-C1-C6 alkyl will be done] The present invention provides a compound represented by the formula:

[0008] The compounds of formula (I) may further be prepared by reacting any diastereomers or enantiomers that exist. and N-oxomers and E / Z isomers, as well as salts and N-oxomers of the compounds of formula (I). The present invention also includes the use of insecticides and their applications for controlling pests.

[0009] Preferred definitions of radicals for the formulae specified above and below are as follows: Please see below.

[0010] The present invention further provides a compound represented by general formula (I) [wherein (structure 1-3): X is O or S; Y is a direct bond or an optionally substituted CH; R 1 is hydrogen; C1-C6 alkyl [wherein the alkyl is -CN, -CONH2, Substituted with one substituent selected from -COOH, -NO2 and -Si(CH3)3 C1-C6 haloalkyl; C2-C6 alkenyl; C2-C6 haloalkenyl C2-C6 alkynyl;C2-C6 haloalkynyl;C3-C4 cycloalkyl-C 1-C2 alkyl- [wherein the C3-C4 cycloalkyl is substituted with one or two halogen atoms] oxetan-3-yl-CH2- or benzyl [wherein which may be substituted with a halogen atom or a C1-C3 haloalkyl. ; R 2 is phenyl, pyridine, pyrimidine, pyrazine or pyridazine, wherein The phenyl, pyridine, pyrimidine, pyrazine or pyridazine has a total of 1 to 3 substituents. and wherein the substituent is substituted with either of the carbons adjacent to the carbon bonded to the C=X group. and at least one and at most two substituents are not present on any carbon atom. C3-C6 cycloalkoxy, wherein the cycloalkoxy is Halogen, =O (oxo), -CN, C1-C6 alkyl, C3-C6 cycloalkyl, C3-C6 halocycloalkyl , C1-C6 alkoxy, C1-C6 haloalkoxy, C1-C6 alkylthio, C1- C6 alkylsulfinyl, C1-C6 alkylsulfonyl, C3-C6 cycloalkyl kylthio, C3-C6 cycloalkylsulfinyl, C3-C6 cycloalkylsulfonyl optionally substituted with 1 to 2 substituents selected from the group consisting of yl; Or, C1-C6 alkyl, wherein the alkyl is -CN, C3-C6 cycloalkyl, C3-C6 halocycloalkyl, C1-C6 alkoxy C1-C6 haloalkoxy, C1-C6 alkylthio, C1-C6 alkylsulfonyl C1-C6 alkylsulfonyl, C3-C6 cycloalkylkylthio, C3-C 6 cycloalkylsulfinyl, C3-C6 cycloalkylsulfonyl substituted with one or two substituents selected from the group consisting of: Or, C1-C6 alkylcarbonyl and C3-C6 cycloalkylcarbonyl [wherein C1-C6 alkylcarbonyl and C3-C6 cycloalkylcarbonyl are Halogen, -CN, C3-C6 cycloalkyl, C3-C6 halocycloalkyl, C1-C6 alkyl Thio, C1-C6 alkylsulfinyl, C1-C6 alkylsulfonyl, C3-C6 thio C3-C6 cycloalkylsulfinyl, C3-C6 cycloa and optionally substituted with 1 to 2 substituents selected from the group consisting of alkylsulfonyl; Or, C1-C6 alkoxy, wherein the alkoxy is =O(oxo), -CN, C3-C6 cycloalkyl, C3-C6 halocycloalkyl, C1-C6 alkoxy C1-C6 haloalkoxy, C1-C6 alkylthio, C1-C6 alkylsulfonyl C1-C6 alkylsulfonyl, C3-C6 cycloalkylkylthio, C3-C 6 cycloalkylsulfinyl, C3-C6 cycloalkylsulfonyl substituted with one or two substituents selected from the group consisting of: Or, C1-C6 haloalkyl, wherein the haloalkyl is =O(oxo), -CN, C3-C6 cycloalkyl, C3-C6 halocycloalkyl, C1-C6 alkoxy C1-C6 haloalkoxy, C1-C6 alkylthio, C1-C6 alkylsulfonyl C1-C6 alkylsulfonyl, C3-C6 cycloalkylkylthio, C3-C 6 cycloalkylsulfinyl, C3-C6 cycloalkylsulfonyl substituted with one or two substituents selected from the group consisting of: Or, C1-C6 haloalkoxy, wherein the haloalkoxy is =O(oxo), -CN, C3-C6 cycloalkyl, C3-C6 halocycloalkyl, C1-C6 alkoxy C1-C6 haloalkoxy, C1-C6 alkylthio, C1-C6 alkylsulfonyl C1-C6 alkylsulfonyl, C3-C6 cycloalkylkylthio, C3-C 6 cycloalkylsulfinyl, C3-C6 cycloalkylsulfonyl substituted with one or two substituents selected from the group consisting of: Or, C2-C6 alkenyloxy [wherein the alkenyloxy is Halogen, -CN, C3-C6 cycloalkyl, C3-C6 halocycloalkyl, C1-C6 alkoxy C1-C6 haloalkoxy, C1-C6 alkylthio, C1-C6 alkylsulfonyl C1-C6 alkylsulfonyl, C3-C6 cycloalkylkylthio, C3-C 6 cycloalkylsulfinyl, C3-C6 cycloalkylsulfonyl substituted with one or two substituents selected from the group consisting of: Or, C1-C6 alkylSO2O- [wherein the alkylSO2O- is Halogen, -CN, C3-C6 cycloalkyl, C3-C6 halocycloalkyl, C1-C6 alkoxy C1-C6 haloalkoxy, C1-C6 alkylthio, C1-C6 alkylsulfonyl C1-C6 alkylsulfonyl, C3-C6 cycloalkylkylthio, C3-C 6 cycloalkylsulfinyl, C3-C6 cycloalkylsulfonyl substituted with one or two substituents selected from the group consisting of: Or, Phenyl-C1-C3 haloalkyl and phenyl-C1-C3 alkoxy, where: The phenyl is Halogen, -CN, C1-C6 alkyl, C3-C6 cycloalkyl, C3-C6 halocycloalkyl , C1-C6 alkoxy, C1-C6 haloalkoxy, C1-C6 alkylthio, C1- C6 alkylsulfinyl, C1-C6 alkylsulfonyl, C3-C6 cycloalkyl kylthio, C3-C6 cycloalkylsulfinyl, C3-C6 cycloalkylsulfonyl and optionally substituted with 1 to 3 substituents independently selected from the group consisting of methyl, ... Or, Heterocyclyloxy and heterocyclyl-C1-C3 alkoxy, wherein the hetero The heterocyclyl includes saturated and partially unsaturated 4- to 6-membered heterocyclyl, 5-membered heteroaryl, 6-membered heteroaryl, each of which is selected from the group consisting of: Halogen, -CN, C1-C6 alkyl, C3-C6 cycloalkyl, C3-C6 halocycloalkyl , C1-C6 alkoxy, C1-C6 haloalkoxy, C1-C6 alkylthio, C1- C6 alkylsulfinyl, C1-C6 alkylsulfonyl, C3-C6 cycloalkyl kylthio, C3-C6 cycloalkylsulfinyl, C3-C6 cycloalkylsulfonyl and optionally substituted with 1 to 3 substituents independently selected from the group consisting of methyl, ... independently selected from the group consisting of: and, The remaining optional substituents are: Hydrogen, halogen, hydroxy, -NH2, -CN, -NO2, C1-C3 alkyl, C3-C6-cycloalkyl, C1-C3 haloalkyl, C1-C3 alkoxy, C1- C3 haloalkoxy, C1-C3 alkylthio, C1-C3 alkylsulfinyl, C1 -C3 alkylsulfonyl, C3-C4 cycloalkylkylthio, C3-C4 cycloa C3-C4 cycloalkylsulfonyl, C1-C3 haloalkylthio O, C1-C3 haloalkylsulfinyl and C1-C3 haloalkylsulfonyl; selected from the group consisting of: R 3a , R 3b teeth, Hydrogen, halogens and -CN; and C1-C6 alkyl [wherein the alkyl is selected from the group consisting of halogen, hydroxy, -CN, -C OOH, -CONH2, -NO2, -NH2, optionally substituted C 1-C6 alkyl, C3-C6 cycloalkyl, C1-C6 alkoxy, C1-C6 alkoxy C1-C6 alkylsulfinyl, C1-C6 alkylsulfonyl, -NH( C1-C6 alkyl), -N(C1-C6 alkyl)2, -NHCO-C1-C6 alkyl -N(C1-C6 alkyl)CO-C1-C6 alkyl, -CO2C1-C6 alkyl -CONH(C1-C6 alkyl) and -CON(C1-C6 alkyl) and optionally substituted with 1 to 3 substituents independently selected from the group C3-C6 cycloalkyl, C1-C6 halo, which may be substituted in either case; Alkyl, C2-C6 alkenyl, C2-C6 haloalkenyl, C2-C6 alkynyl; and, benzyl, wherein the phenyl substituents are halogen, hydroxy, -CN, -COO H, -CONH2, -NO2, -NH2, -SF5, and in any case, substituted Optionally, C1-C6 alkyl, C1-C6 alkoxy, C1-C6 alkylthio, C 1-C6 alkylsulfinyl and C1-C6 alkylsulfonyl, respectively and heterocyclyl-C1-C6 alkyl, wherein the heterocyclyl substituent is 4 to 1 0-membered saturated and partially unsaturated heterocyclyl, 5-membered heteroaryl and 6-membered heteroaryl wherein each of these is selected from the group consisting of halogen, ═O(oxo), ), hydroxy, -CN, -COOH, -CONH2, -NO2, -NH2, and C1-C6 alkyl and C1-C6 alkoxy, optionally substituted in any case; and optionally substituted with 1 to 3 substituents independently selected from the group consisting of: independently selected from the group consisting of: Or, R 3a , R 3b are halogens, -CN, any of the carbons to which they are attached. optionally substituted C1-C6 alkyl, C1-C6 alkoxy and C1-C 6-haloalkoxy, optionally forming a C3-C6 carbocyclic or 3- to 6-membered heterocyclic ring system; R 4 is the following substructure T1 to T6: [ka] wherein the bond to the triazole is marked with a #; where: X 1 is the following substructure S4-a [ka] [where: the bond to the pyridine, pyrimidine, pyrazine, or thiazole is marked with a #; R 41 is hydrogen or C1-C6 alkyl which may be substituted in either case, C1-C6 haloalkyl, C3-C6 cycloalkyl, -C1-C6 alkyl-C3-C 6 cycloalkyl and phenyl; R 42 is hydrogen or C1-C6 alkyl which may be substituted in either case, C1-C6 haloalkyl and C3-C6 cycloalkyl] and; X 2 -CN or X 1 and; R 5 teeth, Hydrogen, halogens; and C1-C6 alkyl, C1-C6 haloalkyl, which may be substituted in any case; C3-C6 cycloalkyl, C1-C6 alkoxy, C1-C6 haloalkoxy, C1-C6 alkoxy)2CH-, -CO2C1-C6 alkyl, -C(=NOC1-C 6 alkyl)H, -C(=NOC1-C6 alkyl)-C1-C6 alkyl will be done] The present invention provides a compound represented by the formula:

[0011] The compounds of formula (I) may further be prepared by reacting any diastereomers or enantiomers that exist. and N-oxomers and E / Z isomers, as well as salts and N-oxomers of the compounds of formula (I). The present invention also includes the use of insecticides and their applications for controlling pests.

[0012] Preferred definitions of radicals for the formulae specified above and below are as follows: Please see below. DETAILED DESCRIPTION OF THE INVENTION

[0013] Preferred is(Configuration 2-1), formula (I) [wherein, X is O or S; Y is a direct bond or CH; R 1 is hydrogen; C1-C3 alkyl [wherein the alkyl is -CN, -CONH2, Substituted with one substituent selected from -COOH, -NO2 and -Si(CH3)3 C1-C3 haloalkyl; C2-C4 alkenyl; C2-C4 haloalkenyl C2-C4 alkynyl;C2-C4 haloalkynyl;C3-C4 cycloalkyl-C 1-C2 alkyl- [wherein the C3-C4 cycloalkyl is substituted with one or two halogen atoms] oxetan-3-yl-CH2-; or benzyl [which may be substituted with an atom]; wherein the benzyl may be substituted with a halogen atom or a C1-C3 haloalkyl. ] and; R 2 is phenyl, pyridine, pyrimidine, pyrazine or pyridazine, wherein The phenyl, pyridine, pyrimidine, pyrazine or pyridazine has a total of 1 to 3 substituents. and wherein the substituent is substituted with either of the carbons adjacent to the carbon bonded to the C=X group. and at least one and at most two substituents are not present on any carbon atom. Hydroxy and C3-C6 cycloalkoxy, -OCO-C1-C3 alkyl, -OSO2-C1-C4 alkyl, C2-C4 alkenyl, C2-C4 haloalkenyl; and, Phenoxy and heterocyclyloxy, wherein the heterocyclyl is saturated and partially Consists of 4-6 membered heterocyclyl, 5 membered heteroaryl, and 6 membered heteroaryl and the phenoxy or heterocyclyloxy is selected from the group consisting of halogen, —CN, each independently selected from the group consisting of C1-C3 alkyl and C1-C3 haloalkyl and C1-C3 alkyl, C1-C3 haloalkyl, C1-C3 haloalkoxy, C1- C3 alkoxy, C2-C4 alkenyloxy and C2-C4 haloalkenyloxy wherein the C1-C3 alkyl, C1-C3 haloalkyl, C1-C3 haloalkoxy, C 1-C3 alkoxy, C2-C4 alkenyloxy and C2-C4 haloalkenyloxy teeth, Halogen, =O(oxo), =S(thiono), hydroxy, -CN, -COOH, -CSNH2, -NO2, -NH2, -SF5, -SiMe3, and C3-C6 cycloalkyl, C3-C6 halocycloalkyl, C1-C4 alkoxy C1-C4 haloalkoxy, C1-C4 alkylthio, C1-C4 alkylsulfonyl C1-C4 alkylsulfonyl, C3-C6 cycloalkylkylthio, C3-C 6 cycloalkylsulfinyl, C3-C6 cycloalkylsulfonyl, C1-C4 halo Alkylthio, C1-C4 haloalkylsulfinyl, C1-C4 haloalkylsulfonyl -OCONH-C1-C4 alkyl, -NH(C1-C4 alkyl), -N(C1- C4 alkyl)2, -CONR 41 R 42 , -NR 42 COR 41 , -CO2C1-C4 Alkyl, -C(=NOC1-C4 alkyl)H, -C(=NOC1-C4 alkyl)- substituted with 1 to 3 substituents selected from the group consisting of C1-C4 alkyl; and , Phenyl-C1-C3 alkyl, phenyl-C1-C3 haloalkyl, phenyl-C 1-C3 haloalkoxy, phenyl-C1-C3 alkoxy, heterocyclyl-C1-C 3 alkyl, heterocyclyl-C1-C3 haloalkyl, heterocyclyl-C1-C3 halo heterocyclyl-C1-C3 alkoxy, heterocyclyl-C1-C3 alkoxy, wherein the heterocyclyl is Saturated and partially unsaturated 5- to 6-membered heterocyclyl, 5-membered heteroaryl, 6-membered heteroarylene and wherein said phenyl or heterocyclyl is selected from the group consisting of halogen, , =O(oxo), -CN, C1-C4 alkyl, C3-C4 cycloalkyl, C1- Select independently from the group consisting of C4 haloalkyl, C1-C4 alkoxy, C1-C4 haloalkoxy optionally substituted with 1 to 3 substituents selected arbitrarily; independently selected from Group A consisting of: and, The remaining substituents in the cases 1 and 2 are: Halogen, -CN, SF5-NO2, C1-C3 alkyl, C1-C3 haloalkyl , C1-C3 alkoxy, C1-C3 haloalkoxy and C1-C3 haloalkylthio; each independently selected from Group B consisting of: R 3a , R 3b teeth, Hydrogen, halogens and -CN; and C1-C4 alkyl [wherein the alkyl is hydroxy, -CN, -COOH, - CONH2, -NO2, -NH2, C1-C4 alkyl, C3-C6 cycloalkyl, C 1-C4 haloalkyl, C1-C4 alkoxy, C1-C4 haloalkoxy, C1-C4 Alkylthio, C1-C4 alkylsulfinyl, C1-C4 alkylsulfonyl, C1 -C4 haloalkylthio, C1-C4 haloalkylsulfinyl, C1-C4 haloalkyl and optionally substituted with 1 to 3 substituents independently selected from the group consisting of arylsulfonyl, ]; and C3-C6 cycloalkyl [wherein the cycloalkyl is selected from the group consisting of halogen, -CN, -C OOH, -CONH2, C1-C4 alkyl, C1-C4 haloalkyl, C3-C6 cycloalkyl C1-C4 haloalkoxy, C1-C4 alkoxy, and C1-C4 haloalkyl [wherein the haloalkyl is hydroxy, -CN, C3- From the group consisting of C6 cycloalkyl, C1-C4 alkoxy, C1-C4 haloalkoxy optionally substituted with 1 to 2 selected substituents; independently selected from the group consisting of: R 4 is pyridine, pyrimidine, pyrazine or pyridazine, wherein the pyridine , pyrimidine, pyrazine or pyridazine is Halogen, hydroxy, C1-C3 alkyl, C3-C4 cycloalkyl, C1-C 3 haloalkyl, C1-C3 alkoxy, and 2 to 3 substituted alkyl groups independently selected from the group consisting of substituted with a group; Or, R 4 is pyridine, pyrimidine, pyrazine or pyridazine, wherein the pyridine , pyrimidine, pyrazine or pyridazine is substituted with a total of 1 to 3 substituents, and at least one and at most two substituents are -CN, -COOH, -NO2, -SF5, -NH2, substituted C3-C4 chloroalkyl; and C1-C3 alkyl and C1-C3 alkoxy [wherein each of these is -C N, -CO2C1-C4 alkyl, -CONH2, SF5, -SO2NH2, C3-C4 Cycloalkyl, -NH(C1-C4 alkyl), -N(C1-C4 alkyl)2, N- C1-C4 alkanoylamino, C1-C4 alkoxy, C1-C4 haloalkoxy, C 1-C4 alkoxycarbonyl, C6-,C 10 -,C 14 -aryloxycarbonyl , C1-C4 alkanoyl, C1-C4 alkylthio, C1-C4 haloalkylthio, C 3-C4 cycloalkylthio, C1-C4 alkylsulfinyl, C1-C4 haloalkyl sulfinyl, C1-C4 alkylsulfonyl, C1-C4 haloalkylsulfonyl, -SO2-NH(C1-C4 alkyl), -SO2-N(C1-C4 alkyl)2, N- C1-C4 alkylaminocarbonyl, N,N-di-C1-C4 alkylaminocarbonyl N-C1-C4 alkanoylaminocarbonyl, N-C1-C4 alkanoyl-N- C1-C4 alkylaminocarbonyl, heterocyclyl, heteroaryl, and double Substituents attached via a bond, such as C1-C4 alkylidene (e.g., methylidene) methylamine or ethylidene), oxo group, imino group and substituted imino group. substituted with 1 to 2 substituents independently selected from and -CO2-C1-C4 alkyl, C4-C6 haloalkyl, C1-C4 haloalkoxy C1-C4 alkylthio, C1-C4 alkylsulfinyl, C1-C4 alkylsulfinyl sulfonyl, C3-C6 cycloalkylsulfanyl, C3-C6 cycloalkylsulfonyl C3-C6 cycloalkylsulfonyl, C1-C4 haloalkylthio, C1-C4 Haloalkylsulfinyl, C1-C4 haloalkylsulfonyl, -NH(C1-C4 alkyl -N(C1-C4 alkyl), -C(=NOC1-C4 alkyl)H, -C (=NOC1-C4 alkyl)-C1-C4 alkyl; and Phenyl and 5-6 membered heteroaryl [wherein the phenyl or 5-6 membered heteroaryl The alkyl group is selected from halogen, -CN, and optionally substituted C1-C4 alkyl groups. Alkyl, C3-C6 cycloalkyl, C1-C3 haloalkyl, C1-C3 alkoxy , C1-C3 haloalkoxy, C1-C3 alkylthio, C1-C3 alkylsulfini C1-C3 alkylsulfonyl, C3-C6 cycloalkylthio, C3-C6 cyclo Alkyl sulfinyl, C3-C6 cycloalkylsulfonyl, C1-C3 haloalkyl Thio, C1-C3 haloalkylsulfinyl and C1-C3 haloalkylsulfonyl and The following substructures S1 to S6: [ka] [where: the bond to the pyridine, pyrimidine, pyrazine, or pyridazine is marked with a #; and Z is CO or CS, and Y 1 is independently selected from CO or SO2 ; R 41 is hydrogen or C1-C4 alkyl which may in any case be substituted, C1-C4 haloalkyl, C3-C6 cycloalkyl, C1-C4 alkyl-C3-C6 cycloalkyl and phenyl; R 42 represents hydrogen and optionally substituted C1-C4 alkyl in either case. , C1-C4 haloalkyl and C3-C6 cycloalkyl; R43 is optionally substituted C1-C4 alkyl, C1-C4 halo independently selected from C3-C6 cycloalkyl, C3-C6 cycloalkyl and phenyl; independently selected from Group A consisting of: and, The remaining substituents in the cases 1 and 2 are: halogen and hydroxy; and C1-C4 alkyl, C3-C6 cycloalkyl, C1-C4 haloalkyl and C1 -C4 alkoxy; each independently selected from Group B consisting of: Or, R 4 is a 5-membered heteroaryl, wherein the heteroaryl is Halogen, hydroxy, -CN, -COOH, -NO2, -SF5, -NH2; and , -CO2-C1-C4 alkyl, C1-C4 alkyl, C3-C6 cycloalkyl, C1-C4 haloalkyl, C1-C4 alkoxy, C1-C4 haloalkoxy, C1-C 4 alkylthio, C1-C4 alkylsulfinyl, C1-C4 alkylsulfonyl, C 3-C6 cycloalkylsulfanyl, C3-C6 cycloalkylsulfinyl, C3- C6 cycloalkylsulfonyl, C1-C4 haloalkylthio, C1-C4 haloalkyl Sulfinyl, C1-C4 haloalkylsulfonyl, -NH(C1-C4 alkyl), - N(C1-C4 alkyl)2, -C(=NOC1-C4 alkyl)H, -C(=NOC1 -C4 alkyl)-C1-C4 alkyl; and Phenyl and 5-6 membered heteroaryl [wherein the phenyl or 5-6 membered heteroaryl The alkyl group is selected from halogen, -CN, and optionally substituted C1-C4 alkyl groups. Alkyl, C3-C6 cycloalkyl, C1-C3 haloalkyl, C1-C3 alkoxy , C1-C3 haloalkoxy, C1-C3 alkylthio, C1-C3 alkylsulfini C1-C3 alkylsulfonyl, C3-C6 cycloalkylthio, C3-C6 cyclo Alkyl sulfinyl, C3-C6 cycloalkylsulfonyl, C1-C3 haloalkyl Thio, C1-C3 haloalkylsulfinyl and C1-C3 haloalkylsulfonyl; and Beauty, Substructures S1-S6, where the bond to the 5-membered heteroaryl is marked with a #, and Z is CO or CS, and Y 1 is independently selected from CO or SO2 be]; and optionally substituted with 1 to 3 substituents independently selected from the group consisting of: R 5 teeth, Hydrogen, halogens; and C3-C6 cycloalkyl, C1-C4 alkoxy, C1-C4 haloalkoxy, ( C1-C4 alkoxy)2CH-, -CO2C1-C4 alkyl, -C(=NOC1-C 4 alkyl)H, —C(═NOC1-C4 alkyl)-C1-C4 alkyl; and C1-C4 alkyl and C1-C4 haloalkyl [wherein the C1-C4 alkyl and and C1-C4 haloalkyl are Halogen, =O (oxo), =S (thiono), hydroxy, -CN, -NO2, - SF5, -SiMe3; and C3-C6 cycloalkyl, C1-C6 alkyl, optionally substituted in either case alkoxy, C1-C6 haloalkoxy; and optionally substituted with 1 to 3 substituents selected from the group consisting of selected from the group consisting of It is a compound represented by the formula:

[0014] Preferred is (Configuration 2-2), and further, a compound represented by the formula (I) [wherein X is O or S; Y is a direct bond or CH; R 1 is hydrogen; C1-C3 alkyl [wherein the alkyl is -CN, -CONH2, Substituted with one substituent selected from -COOH, -NO2 and -Si(CH3)3 C1-C3 haloalkyl; C2-C4 alkenyl; C2-C4 haloalkenyl C2-C4 alkynyl;C2-C4 haloalkynyl;C3-C4 cycloalkyl-C 1-C2 alkyl- [wherein the C3-C4 cycloalkyl is substituted with one or two halogen atoms] oxetan-3-yl-CH2-; or benzyl [which may be substituted with an atom]; wherein the benzyl may be substituted with a halogen atom or a C1-C3 haloalkyl. ] and; R 2 is phenyl, pyridine, pyrimidine, pyrazine or pyridazine, wherein The phenyl, pyridine, pyrimidine, pyrazine or pyridazine has a total of 1 to 3 substituents. and wherein the substituent is substituted with either of the carbons adjacent to the carbon bonded to the C=X group. and at least one and at most two substituents are not present on any carbon atom. C3-C6 cycloalkoxy, wherein the cycloalkoxy is Halogen, =O (oxo), -CN, C1-C3 alkyl, C3-C4 cycloalkyl, C3-C4 halocycloalkyl , C1-C3 alkoxy, C1-C3 haloalkoxy, C1-C3 alkylthio, C1- C3 alkylsulfinyl, C1-C3 alkylsulfonyl, C3-C4 cycloalkyl kylthio, C3-C4 cycloalkylsulfinyl, C3-C4 cycloalkylsulfonyl optionally substituted with 1 to 2 substituents selected from the group consisting of yl; Or, C1-C3 alkyl, wherein the alkyl is -CN, C3-C4 cycloalkyl, C3-C4 halocycloalkyl, C1-C3 haloal Coxy, C1-C3 alkylthio, C1-C3 alkylsulfinyl, C1-C3 alkyl C3-C4 cycloalkylsulfonyl, C3-C4 cycloalkylkylthio, C3-C4 cycloalkylsulf 1 to 2 substituents selected from the group consisting of C3-C4 cycloalkylsulfonyl is replaced by]; Or, C1-C3 alkylcarbonyl and C3-C6 cycloalkylcarbonyl [wherein The C1-C3 alkylcarbonyl and C3-C6 cycloalkylcarbonyl are Halogen, -CN, C3-C4 cycloalkyl, C3-C4 halocycloalkyl, C1-C3 alkyl Thio, C1-C3 alkylsulfinyl, C1-C3 alkylsulfonyl, C3-C4 thio C3-C4 cycloalkylsulfinyl, C3-C4 cycloa and optionally substituted with 1 to 2 substituents selected from the group consisting of alkylsulfonyl; Or, C1-C3 alkoxy, wherein the alkoxy is =O(oxo), -CN, C3-C4 cycloalkyl, C3-C4 halocycloalkyl, C1-C3 alkoxy C1-C3 haloalkoxy, C1-C3 alkylthio, C1-C3 alkylsulfonyl C1-C3 alkylsulfonyl, C3-C4 cycloalkylkylthio, C3-C 4 cycloalkylsulfinyl, C3-C4 cycloalkylsulfonyl substituted with one or two substituents selected from the group consisting of: Or, C1-C3 haloalkyl, wherein the haloalkyl is =O(oxo), -CN, C3-C4 cycloalkyl, C3-C4 halocycloalkyl, C1-C3 alkoxy C1-C3 haloalkoxy, C1-C3 alkylthio, C1-C3 alkylsulfonyl C1-C3 alkylsulfonyl, C3-C4 cycloalkylkylthio, C3-C 4 cycloalkylsulfinyl, C3-C4 cycloalkylsulfonyl substituted with one or two substituents selected from the group consisting of: Or, C1-C3 haloalkoxy, wherein the haloalkoxy is =O(oxo), -CN, C3-C4 cycloalkyl, C3-C4 halocycloalkyl, C1-C3 alkoxy C1-C3 haloalkoxy, C1-C3 alkylthio, C1-C3 alkylsulfonyl C1-C3 alkylsulfonyl, C3-C4 cycloalkylkylthio, C3-C 4 cycloalkylsulfinyl, C3-C4 cycloalkylsulfonyl substituted with one or two substituents selected from the group consisting of: Or, C2-C4 alkenyloxy [wherein the alkenyloxy is halogens, -CN, and C3-C4 cycloalkyl, C3-C4 halocycloalkyl, C1-C3 alkoxy C1-C3 haloalkoxy, C1-C3 alkylthio, C1-C3 alkylsulfonyl C1-C3 alkylsulfonyl, C3-C4 cycloalkylkylthio, C3-C 4 cycloalkylsulfinyl, C3-C4 cycloalkylsulfonyl substituted with one or two substituents selected from the group consisting of: Or, C1-C3 alkylSO2O- [wherein the alkylSO2O- is halogens, -CN, and C3-C4 cycloalkyl, C3-C4 halocycloalkyl, C1-C3 alkoxy C1-C3 haloalkoxy, C1-C3 alkylthio, C1-C3 alkylsulfonyl C1-C3 alkylsulfonyl, C3-C4 cycloalkylkylthio, C3-C 4 cycloalkylsulfinyl, C3-C4 cycloalkylsulfonyl substituted with one or two substituents selected from the group consisting of: Or, Phenyl-C1-C3 haloalkyl and phenyl-C1-C3 alkoxy, where: The phenyl is Halogen, -CN, C1-C3 alkyl, C3-C4 cycloalkyl, C3-C4 halocycloalkyl , C1-C3 alkoxy, C1-C3 haloalkoxy, C1-C3 alkylthio, C1- C3 alkylsulfinyl, C1-C3 alkylsulfonyl, C3-C4 cycloalkyl kylthio, C3-C4 cycloalkylsulfinyl, C3-C4 cycloalkylsulfonyl and optionally substituted with 1 to 3 substituents independently selected from the group consisting of methyl, ... Or, Heterocyclyloxy and heterocyclyl-C1-C3 alkoxy, wherein the hetero The heterocyclyl includes saturated and partially unsaturated 4- to 6-membered heterocyclyl, 5-membered heteroaryl, 6-membered heteroaryl, each of which is selected from the group consisting of: Halogen, -CN, C1-C3 alkyl, C3-C4 cycloalkyl, C3-C4 halocycloalkyl , C1-C3 alkoxy, C1-C3 haloalkoxy, C1-C3 alkylthio, C1- C3 alkylsulfinyl, C1-C3 alkylsulfonyl, C3-C4 cycloalkyl kylthio, C3-C4 cycloalkylsulfinyl, C3-C4 cycloalkylsulfonyl and optionally substituted with 1 to 3 substituents independently selected from the group consisting of methyl, ... independently selected from the group consisting of: and, The remaining optional substituents are: Hydrogen, halogen, hydroxy, -NH2, -CN, -NO2, C1-C3 alkyl, C1-C3 haloalkyl, C1-C3 alkoxy, C1-C3 haloalkoxy, C1-C 3 alkylthio, C1-C3 alkylsulfinyl, C1-C3 alkylsulfonyl, C 3-C4 cycloalkylkylthio, C3-C4 cycloalkylsulfinyl, C3-C 4Cycloalkylsulfonyl, C1-C3 haloalkylthio, C1-C3 haloalkyls sulfinyl and C1-C3 haloalkylsulfonyl; selected from the group consisting of: R 3a , R 3b teeth, Hydrogen, halogens and -CN; and C1-C4 alkyl [wherein the alkyl is hydroxy, halogen, -CN, -CO OH, -CONH2, -NO2, -NH2, C1-C4 alkyl, C3-C6 cycloalkenyl alkyl, C1-C4 haloalkyl, C1-C4 alkoxy, C1-C4 haloalkoxy, C 1-C4 alkylthio, C1-C4 alkylsulfinyl, C1-C4 alkylsulfonyl C1-C4 haloalkylthio, C1-C4 haloalkylsulfinyl, C1-C4 halo and substituted with 1 to 3 substituents independently selected from the group consisting of alkylsulfonyl, alkylphenylsulfonyl, aryl ... may be]; and C3-C6 cycloalkyl [wherein the cycloalkyl is selected from the group consisting of halogen, -CN, -C OOH, -CONH2, C1-C4 alkyl, C1-C4 haloalkyl, C3-C6 cycloalkyl C1-C4 haloalkoxy, C1-C4 alkoxy, and C1-C4 haloalkyl [wherein the haloalkyl is hydroxy, -CN, C3- From the group consisting of C6 cycloalkyl, C1-C4 alkoxy, C1-C4 haloalkoxy optionally substituted with 1 to 2 selected substituents; independently selected from the group consisting of: R 4 is the following substructure T1 to T6: [ka] wherein the bond to the triazole is marked with a #; where: X 1 is the following substructure S4-a [ka] [where: the bond to the pyridine, pyrimidine, pyrazine, or thiazole is marked with a #; R 41 is hydrogen or C1-C4 alkyl which may in any case be substituted, C1-C4 haloalkyl, C3-C6 cycloalkyl, C1-C4 alkyl-C3-C6 cycloalkyl and phenyl; R 42 represents hydrogen and optionally substituted C1-C4 alkyl in either case. , C1-C4 haloalkyl and C3-C6 cycloalkyl] and; X 2 -CN or X 1 and; R 5 teeth, Hydrogen, halogens; and C1-C4 alkyl, C1-C4 haloalkyl, C3-C6 cycloalkyl, C1- C4 alkoxy, C1-C4 haloalkoxy, (C1-C4 alkoxy)2CH-, -C O2C1-C4 alkyl, -C(=NOC1-C4 alkyl)H, -C(=NOC1-C 4 alkyl)-C1-C4 alkyl] It is a compound represented by the formula:

[0015] Preferred is (Configuration 2-3), and further, a compound represented by formula (I) [wherein X is O or S; Y is a direct bond or CH; R 1 is hydrogen; C1-C3 alkyl [wherein the alkyl is -CN, -CONH2, Substituted with one substituent selected from -COOH, -NO2 and -Si(CH3)3 C1-C3 haloalkyl; C2-C4 alkenyl; C2-C4 haloalkenyl C2-C4 alkynyl;C2-C4 haloalkynyl;C3-C4 cycloalkyl-C 1-C2 alkyl- [wherein the C3-C4 cycloalkyl is substituted with one or two halogen atoms] oxetan-3-yl-CH2-; or benzyl [which may be substituted with an atom]; wherein the benzyl may be substituted with a halogen atom or a C1-C3 haloalkyl. ] and; R 2 is phenyl, pyridine, pyrimidine, pyrazine or pyridazine, wherein The phenyl, pyridine, pyrimidine, pyrazine or pyridazine has a total of 1 to 3 substituents. and wherein the substituent is substituted with either of the carbons adjacent to the carbon bonded to the C=X group. and at least one and at most two substituents are not present on any carbon atom. C3-C6 cycloalkoxy, wherein the cycloalkoxy is Halogen, =O (oxo), -CN, C1-C3 alkyl, C3-C4 cycloalkyl, C3-C4 halocycloalkyl , C1-C3 alkoxy, C1-C3 haloalkoxy, C1-C3 alkylthio, C1- C3 alkylsulfinyl, C1-C3 alkylsulfonyl, C3-C4 cycloalkyl kylthio, C3-C4 cycloalkylsulfinyl, C3-C4 cycloalkylsulfonyl optionally substituted with 1 to 2 substituents selected from the group consisting of yl; Or, C1-C3 alkyl, wherein the alkyl is -CN, C3-C4 cycloalkyl, C3-C4 halocycloalkyl, C1-C3 haloal Coxy, C1-C3 alkylthio, C1-C3 alkylsulfinyl, C1-C3 alkyl C3-C4 cycloalkylsulfonyl, C3-C4 cycloalkylkylthio, C3-C4 cycloalkylsulf 1 to 2 substituents selected from the group consisting of C3-C4 cycloalkylsulfonyl is replaced by]; Or, C1-C3 alkylcarbonyl and C3-C6 cycloalkylcarbonyl [wherein The C1-C3 alkylcarbonyl and C3-C6 cycloalkylcarbonyl are Halogen, -CN, C3-C4 cycloalkyl, C3-C4 halocycloalkyl, C1-C3 alkyl Thio, C1-C3 alkylsulfinyl, C1-C3 alkylsulfonyl, C3-C4 thio C3-C4 cycloalkylsulfinyl, C3-C4 cycloa and optionally substituted with 1 to 2 substituents selected from the group consisting of alkylsulfonyl; Or, C1-C3 alkoxy, wherein the alkoxy is =O(oxo), -CN, C3-C4 cycloalkyl, C3-C4 halocycloalkyl, C1-C3 alkoxy C1-C3 haloalkoxy, C1-C3 alkylthio, C1-C3 alkylsulfonyl C1-C3 alkylsulfonyl, C3-C4 cycloalkylkylthio, C3-C 4 cycloalkylsulfinyl, C3-C4 cycloalkylsulfonyl substituted with one or two substituents selected from the group consisting of: Or, C1-C3 haloalkyl, wherein the haloalkyl is =O(oxo), -CN, C3-C4 cycloalkyl, C3-C4 halocycloalkyl, C1-C3 alkoxy C1-C3 haloalkoxy, C1-C3 alkylthio, C1-C3 alkylsulfonyl C1-C3 alkylsulfonyl, C3-C4 cycloalkylkylthio, C3-C 4 cycloalkylsulfinyl, C3-C4 cycloalkylsulfonyl substituted with one or two substituents selected from the group consisting of: Or, C1-C3 haloalkoxy, wherein the haloalkoxy is =O(oxo), -CN, C3-C4 cycloalkyl, C3-C4 halocycloalkyl, C1-C3 alkoxy C1-C3 haloalkoxy, C1-C3 alkylthio, C1-C3 alkylsulfonyl C1-C3 alkylsulfonyl, C3-C4 cycloalkylkylthio, C3-C 4 cycloalkylsulfinyl, C3-C4 cycloalkylsulfonyl substituted with one or two substituents selected from the group consisting of: Or, C2-C4 alkenyloxy [wherein the alkenyloxy is halogens, -CN, and C3-C4 cycloalkyl, C3-C4 halocycloalkyl, C1-C3 alkoxy C1-C3 haloalkoxy, C1-C3 alkylthio, C1-C3 alkylsulfonyl C1-C3 alkylsulfonyl, C3-C4 cycloalkylkylthio, C3-C 4 cycloalkylsulfinyl, C3-C4 cycloalkylsulfonyl substituted with one or two substituents selected from the group consisting of: Or, C1-C3 alkylSO2O- [wherein the alkylSO2O- is halogens, -CN, and C3-C4 cycloalkyl, C3-C4 halocycloalkyl, C1-C3 alkoxy C1-C3 haloalkoxy, C1-C3 alkylthio, C1-C3 alkylsulfonyl C1-C3 alkylsulfonyl, C3-C4 cycloalkylkylthio, C3-C 4 cycloalkylsulfinyl, C3-C4 cycloalkylsulfonyl substituted with one or two substituents selected from the group consisting of: Or, Phenyl-C1-C3 haloalkyl and phenyl-C1-C3 alkoxy, where: The phenyl is Halogen, -CN, C1-C3 alkyl, C3-C4 cycloalkyl, C3-C4 halocycloalkyl , C1-C3 alkoxy, C1-C3 haloalkoxy, C1-C3 alkylthio, C1- C3 alkylsulfinyl, C1-C3 alkylsulfonyl, C3-C4 cycloalkyl kylthio, C3-C4 cycloalkylsulfinyl, C3-C4 cycloalkylsulfonyl and optionally substituted with 1 to 3 substituents independently selected from the group consisting of methyl, ... Or, Heterocyclyloxy and heterocyclyl-C1-C3 alkoxy, wherein the hetero The heterocyclyl includes saturated and partially unsaturated 4- to 6-membered heterocyclyl, 5-membered heteroaryl, 6-membered heteroaryl, each of which is selected from the group consisting of: Halogen, -CN, C1-C3 alkyl, C3-C4 cycloalkyl, C3-C4 halocycloalkyl , C1-C3 alkoxy, C1-C3 haloalkoxy, C1-C3 alkylthio, C1- C3 alkylsulfinyl, C1-C3 alkylsulfonyl, C3-C4 cycloalkyl kylthio, C3-C4 cycloalkylsulfinyl, C3-C4 cycloalkylsulfonyl and optionally substituted with 1 to 3 substituents independently selected from the group consisting of methyl, ... independently selected from the group consisting of: and, The remaining optional substituents are: Hydrogen, halogen, hydroxy, -NH2, -CN, -NO2, C1-C3 alkyl, C3-C6 cycloalkyl, C1-C3 haloalkyl, C1-C3 alkoxy, C1-C 3 haloalkoxy, C1-C3 alkylthio, C1-C3 alkylsulfinyl, C1- C3 alkylsulfonyl, C3-C4 cycloalkylkylthio, C3-C4 cycloalky alkylsulfinyl, C3-C4 cycloalkylsulfonyl, C1-C3 haloalkylthio , C1-C3 haloalkylsulfinyl and C1-C3 haloalkylsulfonyl; selected from the group consisting of: R 3a , R 3b teeth, Hydrogen, halogens and -CN; and C1-C4 alkyl [wherein the alkyl is hydroxy, halogen, -CN, -CO OH, -CONH2, -NO2, -NH2, C1-C4 alkyl, C3-C6 cycloalkenyl alkyl, C1-C4 haloalkyl, C1-C4 alkoxy, C1-C4 haloalkoxy, C 1-C4 alkylthio, C1-C4 alkylsulfinyl, C1-C4 alkylsulfonyl C1-C4 haloalkylthio, C1-C4 haloalkylsulfinyl, C1-C4 halo and substituted with 1 to 3 substituents independently selected from the group consisting of alkylsulfonyl, alkylphenylsulfonyl, aryl ... may be]; and C3-C6 cycloalkyl [wherein the cycloalkyl is selected from the group consisting of halogen, -CN, -C OOH, -CONH2, C1-C4 alkyl, C1-C4 haloalkyl, C3-C6 cycloalkyl C1-C4 haloalkoxy, C1-C4 alkoxy, and C1-C4 haloalkyl [wherein the haloalkyl is hydroxy, -CN, C3- From the group consisting of C6 cycloalkyl, C1-C4 alkoxy, C1-C4 haloalkoxy optionally substituted with 1 to 2 selected substituents; independently selected from the group consisting of: R 4 is the following substructure T1 to T6: [ka] wherein the bond to the triazole is marked with a #; where: X 1 is the following substructure S4-a [ka] [where: the bond to the pyridine, pyrimidine, pyrazine, or thiazole is marked with a #; R 41 is hydrogen or C1-C4 alkyl which may in any case be substituted, C1-C4 haloalkyl, C3-C6 cycloalkyl, C1-C4 alkyl-C3-C6 cycloalkyl and phenyl; R 42 represents hydrogen and optionally substituted C1-C4 alkyl in either case. , C1-C4 haloalkyl and C3-C6 cycloalkyl] and; X 2 -CN or X 1 and; R 5 teeth, Hydrogen, halogens; and C1-C4 alkyl, C1-C4 haloalkyl, C3-C6 cycloalkyl, C1- C4 alkoxy, C1-C4 haloalkoxy, (C1-C4 alkoxy)2CH-, -C O2C1-C4 alkyl, -C(=NOC1-C4 alkyl)H, -C(=NOC1-C 4 alkyl)-C1-C4 alkyl] It is a compound represented by the formula:

[0016] Even more preferable is (Configuration 3-1), formula (I) [wherein, X is O or S; Y is a direct bond; R 1 is hydrogen; C1-C3 alkyl, wherein the alkyl is selected from the group consisting of -CN, -NO2 and - Si(CH3)3]; C3-C4 cyclohexyl cycloalkyl-C1-C2 alkyl-, wherein the C3-C4 cycloalkyl is one or optionally substituted with two halogen atoms; or benzyl, wherein the benzyl is , optionally substituted with a halogen atom or a C1-C3 haloalkyl; R 2 is phenyl or pyridine, wherein the phenyl or pyridine is one to two It may be substituted with a substituent, provided that the substituent is not adjacent to the carbon bonded to the C=X group. and at least one and at most two substituents are not present on any carbon atom that is Hydroxy and C3-C6 cycloalkoxy, -OCO-C1-C3 alkyl, -OSO2-C1-C3 alkyl, C2-C4 alkenyl, C2-C4 haloalkenyl; and, Phenoxy, wherein the phenoxy is selected from halogen, —CN, C1-C3 alkyl, and substituted with 1 to 2 substituents each independently selected from the group consisting of C1-C3 haloalkyl; may be substituted]; and heterocyclyloxy, wherein the heterocyclyl contains one oxygen atom; saturated 4- to 6-membered heterocyclyl; and C1-C3 alkyl, C1-C3 haloalkyl, C1-C3 haloalkoxy, C1- C3 alkoxy, C2-C4 alkenyloxy and C2-C4 haloalkenyloxy wherein the C1-C3 alkyl, C1-C3 haloalkyl, C1-C3 haloalkoxy, C 1-C3 alkoxy, C2-C4 alkenyloxy and C2-C4 haloalkenyloxy teeth, Halogen, ═O (oxo), —CN; and C3-C4 cycloalkyl, C3-C4 halocycloalkyl, C1-C3 alkoxy C1-C3 haloalkoxy, C1-C3 alkylthio, C1-C3 alkylsulfonyl C1-C3 alkylsulfonyl, C3-C4 cycloalkylkylthio, C3-C 4 cycloalkylsulfinyl, C3-C4 cycloalkylsulfonyl and Phenyl-C1-C3 haloalkyl, phenyl-C1-C3 alkoxy and heterocycloalkyl acryl-C1-C3 alkyl, wherein the heterocyclyl is pyrazolyl, triazolyl, and tetrazolyl, and said phenyl or heterocyclyl is selected from the group consisting of Halogen, ═O (oxo), -CN, C1-C3 alkyl, C3-C4 cycloalkyl, The group consisting of C1-C3 haloalkyl, C1-C3 alkoxy, and C1-C3 haloalkoxy and heterocyclyl-C1-C3 alkoxy, wherein the heterocyclyl is substituted with one oxygen atom; selected from the group consisting of saturated 4- to 6-membered heterocyclyl containing atoms; independently selected from Group A consisting of: and, The remaining optional substituents are: Halogen, hydroxy, -NH2, -CN, SF5, -COOH, -CONH2, - NO2, C1-C3 alkyl, C1-C3 haloalkyl, C1-C3 alkoxy, C1- C3 haloalkoxy and C1-C3 haloalkylthio; selected from Group B consisting of: R 3a , R 3b is hydrogen; C1-C3 alkyl [wherein the alkyl is halogen, - Independently selected from the group consisting of CN, C3-C4 cycloalkyl, and C1-C3 alkoxy optionally substituted with 1 to 3 substituents; C3-C4 cycloalkyl; C1-C 3 haloalkyl; R 4 is pyridine, pyrimidine, pyrazine or thiazole, wherein the pyridine , pyrimidine, pyrazine or thiazole is substituted with a total of 1 to 2 substituents, The substituent of 1 is -CN, -NO2, -NH2, substituted C3-C4 cycloalkyl, C1-C 4 haloalkoxy, C1-C3 alkylthio, C1-C3 alkylsulfinyl, C1- C3 alkylsulfonyl, C3-C4 cycloalkylsulfanyl, C3-C4 cycloa C3-C4 cycloalkylsulfonyl, C1-C3 haloalkylthio O, C1-C3 haloalkylsulfinyl, C1-C3 haloalkylsulfonyl, -CO 2C1-C3 alkyl, -C(=NOC1-C3 alkyl)H, -C(=NOC1-C3 alkyl)-C1-C3 alkyl; and The following substructures S1, S2, S4 and S5: [ka] [where: The bond to the pyridine, pyrimidine, pyrazine, pyridazine or thiazole is marked with a #. and Z is CO or CS]: Selected from Group A consisting of: and, The remaining optional substituents are: halogen, -CN; and C1-C3 alkyl, C3-C4 cycloalkyl, C1-C3 haloalkyl, C1- C3 alkoxy, C1-C3 haloalkoxy, C1-C3 alkylthio, C1-C3 alkoxy alkylsulfinyl, C1-C3 alkylsulfonyl, C1-C3 haloalkylthio, C1 -C3 haloalkylsulfinyl, C1-C3 haloalkylsulfonyl, C3-C4 cycloalkyl C3-C4 cycloalkylsulfanyl, C3-C4 cycloalkylsulfinyl, C3-C4 cycloalkylsulfanyl rucylsulfonyl; selected from Group B consisting of: R 41 is hydrogen, C1-C3 alkyl, C1-C3 haloalkyl and C3-C4 cycloalkyl. is roalkyl; R 42 is hydrogen, C1-C3 alkyl and C1-C3 haloalkyl; R 43 is C1-C3 alkyl, C1-C3 haloalkyl and C3-C4 cycloalkyl It is a kill; R 5 is hydrogen, halogen, C1-C3 alkyl, C1-C3 haloalkyl, C3-C4 cycloalkyl or C1-C3 alkoxy. It is a compound represented by the formula:

[0017] Likewise, it is even more preferable to (Configuration 3-2), formula (I) [wherein, X is O or S; Y is a direct bond; R 1 is hydrogen; C1-C3 alkyl, wherein the alkyl is selected from the group consisting of -CN, -NO2 and - Si(CH3)3]; C3-C4 cyclohexyl cycloalkyl-C1-C2 alkyl-, wherein the C3-C4 cycloalkyl is one or optionally substituted with two halogen atoms; or benzyl, wherein the benzyl is , optionally substituted with a halogen atom or a C1-C3 haloalkyl; R 2 is phenyl or pyridine, wherein the phenyl or pyridine is one to two substituted with a substituent, provided that the substituent is adjacent to the carbon bonded to the C=X group; and at least one and at most two substituents are C3-C6 cycloalkoxy, wherein the cycloalkoxy is 1 to 2 substituents selected from the group consisting of halogen, -CN, and C1-C3 alkyl may be replaced by]; Or, C1-C3 alkyl, wherein the alkyl is -CN, C3-C4 cycloalkyl, C3-C4 halocycloalkyl, C1-C3 alkoxy C1-C3 haloalkoxy, C1-C3 alkylthio, C1-C3 alkylsulfonyl C1-C3 alkylsulfonyl, C3-C4 cycloalkylkylthio, C3-C 4 cycloalkylsulfinyl, C3-C4 cycloalkylsulfonyl substituted with one or two substituents selected from the group consisting of: Or, C1-C3 alkylcarbonyl and C3-C4 cycloalkylcarbonyl [wherein The alkylcarbonyl and cycloalkylcarbonyl are Halogen, -CN, C3-C4 cycloalkyl, C3-C4 halocycloalkyl may be substituted with 1 to 2 substituents; Or, C1-C3 alkoxy, wherein the alkoxy is =O(oxo), -CN, C3-C4 cycloalkyl, C3-C4 halocycloalkyl, C1-C3 alkoxy C1-C3 haloalkoxy, C1-C3 alkylthio, C1-C3 alkylsulfonyl C1-C3 alkylsulfonyl, C3-C4 cycloalkylkylthio, C3-C 4 cycloalkylsulfinyl, C3-C4 cycloalkylsulfonyl substituted with one or two substituents selected from the group consisting of: Or, C1-C3 haloalkyl, wherein the haloalkyl is =O(oxo), -CN, C3-C4 cycloalkyl, C3-C4 halocycloalkyl, C1-C3 alkoxy C1-C3 haloalkoxy, C1-C3 alkylthio, C1-C3 alkylsulfonyl C1-C3 alkylsulfonyl, C3-C4 cycloalkylkylthio, C3-C 4 cycloalkylsulfinyl, C3-C4 cycloalkylsulfonyl substituted with one or two substituents selected from the group consisting of: Or, C1-C3 haloalkoxy, wherein the haloalkoxy is =O(oxo), -CN, C3-C4 cycloalkyl, C3-C4 halocycloalkyl, C1-C3 alkoxy C1-C3 haloalkoxy, C1-C3 alkylthio, C1-C3 alkylsulfonyl C1-C3 alkylsulfonyl, C3-C4 cycloalkylkylthio, C3-C 4 cycloalkylsulfinyl, C3-C4 cycloalkylsulfonyl substituted with one or two substituents selected from the group consisting of: Or, C2-C4 alkenyloxy [wherein the alkenyloxy is halogens, -CN, and C3-C4 cycloalkyl, C3-C4 halocycloalkyl, C1-C3 alkoxy C1-C3 haloalkoxy, C1-C3 alkylthio, C1-C3 alkylsulfonyl C1-C3 alkylsulfonyl, C3-C4 cycloalkylkylthio, C3-C 4 cycloalkylsulfinyl, C3-C4 cycloalkylsulfonyl substituted with one or two substituents selected from the group consisting of: Or, C1-C3 alkylSO2O- [wherein the alkylSO2O- is halogens, -CN, and C3-C4 cycloalkyl, C3-C4 halocycloalkyl, C1-C3 alkoxy C1-C3 haloalkoxy, C1-C3 alkylthio, C1-C3 alkylsulfonyl C1-C3 alkylsulfonyl, C3-C4 cycloalkylkylthio, C3-C 4 cycloalkylsulfinyl, C3-C4 cycloalkylsulfonyl substituted with one or two substituents selected from the group consisting of: Or, Phenyl-C1-C3 haloalkyl and phenyl-C1-C3 alkoxy, where: The phenyl is Halogen, -CN, C1-C3 alkyl, C3-C4 cycloalkyl, C1-C3 haloalkyl, C1 -C3 alkoxy, C1-C3 haloalkoxy, and optionally substituted with a substituent of the formula: Or, Heterocyclyloxy and heterocyclyl-C1-C3 alkoxy, wherein the hetero Heterocyclyl is a member of the group consisting of saturated 4- to 6-membered heterocyclyls containing one oxygen atom. and the heterocyclyl phenyl is Halogen, -CN, C1-C3 alkyl, C3-C4 cycloalkyl, C1-C3 haloalkyl, C1 -C3 alkoxy, C1-C3 haloalkoxy, and optionally substituted with a substituent of the formula: independently selected from the group consisting of: and, The remaining optional substituents are: Hydrogen, halogen, hydroxy, -NH2, -CN, -NO2, C1-C3 alkyl, C1-C3 haloalkyl, C1-C3 alkoxy, C1-C3 haloalkoxy, C1-C 3 alkylthio, C1-C3 alkylsulfinyl, C1-C3 alkylsulfonyl, C 3-C4 cycloalkylkylthio, C3-C4 cycloalkylsulfinyl, C3-C 4Cycloalkylsulfonyl, C1-C3 haloalkylthio, C1-C3 haloalkyls sulfinyl and C1-C3 haloalkylsulfonyl; selected from the group consisting of: R 3a , R 3b is hydrogen; C1-C3 alkyl [wherein the alkyl is halogen, - CN, C3-C4 cycloalkyl, C1-C3 alkoxy, C1-C3 haloalkyl and optionally substituted with 1 to 3 substituents independently selected from the group consisting of Independently selected; R 4 is the following substructure T1 to T6: [ka] wherein the bond to the triazole is marked with a #; where: X 1 is the following substructure S4-a [ka] [where: the bond to the pyridine, pyrimidine, pyrazine, or thiazole is marked with a #; R 41 is hydrogen, C1-C3 alkyl, C1-C3 cyanoalkyl, C1-C3 haloa alkyl and C3-C4 cycloalkyl; R42 is hydrogen, C1-C3 alkyl and C1-C3 haloalkyl] and; X 2 -CN or X 1 and; R 5 is hydrogen, halogen, C1-C3 alkyl, C1-C3 haloalkyl, C3-C4 cycloalkyl or C1-C3 alkoxy. It is a compound represented by the formula:

[0018] Likewise, it is even more preferable to (Configuration 3-3), formula (I) [wherein, X is O or S; Y is a direct bond; R 1 is hydrogen; C1-C3 alkyl, wherein the alkyl is selected from the group consisting of -CN, -NO2 and - Si(CH3)3]; C3-C4 cyclohexyl cycloalkyl-C1-C2 alkyl-, wherein the C3-C4 cycloalkyl is one or optionally substituted with two halogen atoms; or benzyl, wherein the benzyl is , optionally substituted with a halogen atom or a C1-C3 haloalkyl; R 2 is phenyl or pyridine, wherein the phenyl or pyridine is one to two substituted with a substituent, provided that the substituent is adjacent to the carbon bonded to the C=X group; and at least one and at most two substituents are C3-C6 cycloalkoxy, wherein the cycloalkoxy is 1 to 2 substituents selected from the group consisting of halogen, -CN, and C1-C3 alkyl may be replaced by]; Or, C1-C3 alkyl, wherein the alkyl is -CN, C3-C4 cycloalkyl, C3-C4 halocycloalkyl, C1-C3 alkoxy C1-C3 haloalkoxy, C1-C3 alkylthio, C1-C3 alkylsulfonyl C1-C3 alkylsulfonyl, C3-C4 cycloalkylkylthio, C3-C 4 cycloalkylsulfinyl, C3-C4 cycloalkylsulfonyl substituted with one or two substituents selected from the group consisting of: Or, C1-C3 alkylcarbonyl and C3-C4 cycloalkylcarbonyl [wherein The alkylcarbonyl and cycloalkylcarbonyl are Halogen, -CN, C3-C4 cycloalkyl, C3-C4 halocycloalkyl may be substituted with 1 to 2 substituents; Or, C1-C3 alkoxy, wherein the alkoxy is =O(oxo), -CN, C3-C4 cycloalkyl, C3-C4 halocycloalkyl, C1-C3 alkoxy C1-C3 haloalkoxy, C1-C3 alkylthio, C1-C3 alkylsulfonyl C1-C3 alkylsulfonyl, C3-C4 cycloalkylkylthio, C3-C 4 cycloalkylsulfinyl, C3-C4 cycloalkylsulfonyl substituted with one or two substituents selected from the group consisting of: Or, C1-C3 haloalkyl, wherein the haloalkyl is =O(oxo), -CN, C3-C4 cycloalkyl, C3-C4 halocycloalkyl, C1-C3 alkoxy C1-C3 haloalkoxy, C1-C3 alkylthio, C1-C3 alkylsulfonyl C1-C3 alkylsulfonyl, C3-C4 cycloalkylkylthio, C3-C 4 cycloalkylsulfinyl, C3-C4 cycloalkylsulfonyl substituted with one or two substituents selected from the group consisting of: Or, C1-C3 haloalkoxy, wherein the haloalkoxy is =O(oxo), -CN, C3-C4 cycloalkyl, C3-C4 halocycloalkyl, C1-C3 alkoxy C1-C3 haloalkoxy, C1-C3 alkylthio, C1-C3 alkylsulfonyl C1-C3 alkylsulfonyl, C3-C4 cycloalkylkylthio, C3-C 4 cycloalkylsulfinyl, C3-C4 cycloalkylsulfonyl substituted with one or two substituents selected from the group consisting of: Or, C2-C4 alkenyloxy [wherein the alkenyloxy is halogens, -CN, and C3-C4 cycloalkyl, C3-C4 halocycloalkyl, C1-C3 alkoxy C1-C3 haloalkoxy, C1-C3 alkylthio, C1-C3 alkylsulfonyl C1-C3 alkylsulfonyl, C3-C4 cycloalkylkylthio, C3-C 4 cycloalkylsulfinyl, C3-C4 cycloalkylsulfonyl substituted with one or two substituents selected from the group consisting of: Or, C1-C3 alkylSO2O- [wherein the alkylSO2O- is halogens, -CN, and C3-C4 cycloalkyl, C3-C4 halocycloalkyl, C1-C3 alkoxy C1-C3 haloalkoxy, C1-C3 alkylthio, C1-C3 alkylsulfonyl C1-C3 alkylsulfonyl, C3-C4 cycloalkylkylthio, C3-C 4 cycloalkylsulfinyl, C3-C4 cycloalkylsulfonyl substituted with one or two substituents selected from the group consisting of: Or, Phenyl-C1-C3 haloalkyl and phenyl-C1-C3 alkoxy, where: The phenyl is Halogen, -CN, C1-C3 alkyl, C3-C4 cycloalkyl, C1-C3 haloalkyl, C1 -C3 alkoxy, C1-C3 haloalkoxy, and optionally substituted with a substituent of the formula: Or, Heterocyclyloxy and heterocyclyl-C1-C3 alkoxy, wherein the hetero Heterocyclyl is a member of the group consisting of saturated 4- to 6-membered heterocyclyls containing one oxygen atom. and the heterocyclyl phenyl is Halogen, -CN, C1-C3 alkyl, C3-C4 cycloalkyl, C1-C3 haloalkyl, C1 -C3 alkoxy, C1-C3 haloalkoxy, and optionally substituted with a substituent of the formula: independently selected from the group consisting of: and, The remaining optional substituents are: Hydrogen, halogen, hydroxy, -NH2, -CN, -NO2, C1-C3 alkyl, C3-C6 cycloalkyl, C1-C3 haloalkyl, C1-C3 alkoxy, C1-C 3 haloalkoxy, C1-C3 alkylthio, C1-C3 alkylsulfinyl, C1- C3 alkylsulfonyl, C3-C4 cycloalkylkylthio, C3-C4 cycloalky alkylsulfinyl, C3-C4 cycloalkylsulfonyl, C1-C3 haloalkylthio , C1-C3 haloalkylsulfinyl and C1-C3 haloalkylsulfonyl; selected from the group consisting of: R 3a , R 3b is hydrogen; C1-C3 alkyl [wherein the alkyl is halogen, - CN, C3-C4 cycloalkyl, C1-C3 alkoxy, C1-C3 haloalkyl and optionally substituted with 1 to 3 substituents independently selected from the group consisting of Independently selected; R 4 is the following substructure T1 to T6: [ka] wherein the bond to the triazole is marked with a #; where: X 1 is the following substructure S4-a [ka] [where: the bond to the pyridine, pyrimidine, pyrazine, or thiazole is marked with a #; R 41 is hydrogen, C1-C3 alkyl, C1-C3 cyanoalkyl, C1-C3 haloa alkyl and C3-C4 cycloalkyl; R 42 is hydrogen, C1-C3 alkyl and C1-C3 haloalkyl] and; X 2 -CN or X 1 and; R 5 is hydrogen, halogen, C1-C3 alkyl, C1-C3 haloalkyl, C3-C4 cycloalkyl or C1-C3 alkoxy. It is a compound represented by the formula:

[0019] Particularly preferred is(Configuration 4-1) is a compound represented by the formula (I) [wherein X is O; Y is a direct bond; R 1 is hydrogen; R 2 The following substructure Q1: [ka] [where the bond to the C=X-group is marked with a #] Selected from; R 21 teeth, Hydroxy, cyanomethyl, 1-cyanoethyl, 2-cyanopropan-2-yl, Chloropropyl (difluoromethyl), (methylsulfanyl)methyl, (methylsulfonyl)methyl (methylsulfonyl)methyl, 2-ethoxy-1,1-difluoro-2- oxo-ethyl, (methylsulfanyl)methoxy, (methylsulfinyl)methoxy, (Methylsulfonyl)methoxy, 1-cyano-1-methyl-ethoxy, oxetane-3- yloxy, tetrahydro-2H-pyran-4-yloxy, tetrahydro-2H-pyran (3,3-dichloroprop-2-en-1-yl)oxy, (2 ,3,3-trichloroprop-2-en-1-yl)oxy, (2,2-difluorocyclohexane (2,2-dichlorocyclopropyl)methoxy, (1,2,2-dichlorocyclopropyl)methoxy, (trichlorocyclopropyl)methoxy, cyclopropyloxy, cyclobutyloxy, cyclopropyl Chloropentyloxy, cyclopropylmethoxy, 2,2-dichlorovinyl, (3,4-di Methyl-5-oxo-4,5-dihydro-1H-1,2,4-triazol-1-yl methyl, acetoxy, cyclopropylcarbonyl, methanesulfonyloxy; or Benzyloxy, 1-phenylethoxy, phenoxy, pyrazol-1-ylmethyl or difluoro(phenyl)methyl [wherein the benzyloxy, 1-phenylethoxy , phenoxy, pyrazol-1-ylmethyl or difluoro(phenyl)methyl are halo selected from the group consisting of aryl, CN, C1-C3 alkyl, and C1-C3 haloalkyl and optionally substituted with a substituent selected from the group consisting of: R 22 is hydrogen, fluorine, chlorine, bromine, methyl, ethyl, n-propyl, isopropyl difluoromethyl, trifluoromethyl, difluoromethoxy or trifluoromethan It is Kishi; R 3a is hydrogen; R 3b is selected from the group consisting of hydrogen and methyl; R 4 is composed of the following substructures S50, S51 and S52: [ka] [wherein the bond to the triazole is marked with a #] Selected from one of; X 41 -CN and -CONR 41 R 42 Selected from; X 42 -CN and -CONR 41 R 42 Selected from; X 43 -CN, -NO2 and -CONR 41 R 42 Selected from; R 41 is hydrogen, methyl, ethyl or cyclopropyl; R 42 is hydrogen, methyl or ethyl; R 5 is hydrogen, methyl, ethyl, cyclopropyl, methoxy or ethoxy. It is a compound represented by the formula:

[0020] Likewise particularly preferred are (Configuration 4-2), formula (I) [wherein, X is O; Y is a direct bond; R 1 is hydrogen; R 2 is composed of the following substructures Q1 and Q2: [ka] [where the bond to the C=X-group is marked with a #] Selected from; where: R 21 cyclopropyloxy, (2,2-dichlorocyclopropyl)oxy, cyclopropyloxy Anomethyl, 2-cyanopropan-2-yl, cyclopropyl(difluoromethyl), 2 -cyanopropan-2-yloxy, cyclopropylmethoxy, (2,2-difluorosilyl) (2,2-dichlorocyclopropyl)methoxy, (3,3-dichlorocyclopropyl)methoxy chloroprop-2-en-1-yl)oxy, (2,3,3-trichloroprop-2-en (1-phenyl)oxy; R 22 is hydrogen, fluorine, chlorine, bromine, iodine, difluoromethyl, trifluoromethyl methyl, difluoromethoxy, trifluoromethoxy, methylsulfonyl, difluoromethyl sulfonyl or trifluoromethylsulfonyl; R 3a is hydrogen; R 3b is hydrogen or methyl; R 4 is the following substructure T1 to T6: [ka] [wherein the bond to the triazole is marked with a #] Selected from one of; where: X 1 is the following substructure S4-a: [ka] [where: the bond to the pyridine, pyrimidine, pyrazine, or thiazole is marked with a #; R 41 is hydrogen, methyl, ethyl or cyclopropyl; R 42 is hydrogen, methyl or ethyl] and; X 2 -CN or X 1 and; R 5 is hydrogen, methyl, ethyl or cyclopropyl. It is a compound represented by the formula:

[0021] Likewise particularly preferred are (Configuration 4-3), formula (I) [wherein, X is O; Y is a direct bond; R 1 is hydrogen; R 2 is composed of the following substructures Q1 and Q2: [ka] [where the bond to the C=X-group is marked with a #] Selected from; where: R 21 cyclopropyloxy, (2,2-dichlorocyclopropyl)oxy, cyclopropyloxy 2-Cyanopropan-2-yl, cyclopropyl(difluoromethyl), cyclopropyl Cyclopropylcarbonyl, 2-cyanopropan-2-yloxy, cyclopropylmethoxy (2,2-difluorocyclopropyl)methoxy, (2,2-dichlorocyclopropyl) (3,3-dichloroprop-2-en-1-yl)oxy, (2,3,3 -trichloroprop-2-en-1-yl)oxy, difluoro-(4-fluorophenyl) (I)methyl; R 22 is hydrogen, fluorine, chlorine, bromine, iodine, cyclopropyl, difluoromethyl , trifluoromethyl, difluoromethoxy, trifluoromethoxy, methylsulfonyl , difluoromethylsulfonyl or trifluoromethylsulfonyl; R 3a is hydrogen; R 3b is hydrogen or methyl; R 4 is the following substructure T1 to T6: [ka] [wherein the bond to the triazole is marked with a #] Selected from one of; where: X 1 is the following substructure S4-a: [ka] [where: the bond to the pyridine, pyrimidine, pyrazine, or thiazole is marked with a #; R 41 is hydrogen, methyl, ethyl or cyclopropyl; R 42 is hydrogen, methyl or ethyl] and; X 2 -CN or X 1 and; R 5 is hydrogen, methyl, ethyl or cyclopropyl. It is a compound represented by the formula:

[0022] Very particularly preferred are (Configuration 5-1), formula (I) [wherein, X is O; Y is a direct bond; R 1 is hydrogen; R 2 is 3-(1-cyanoethyl)phenyl, 3-(2,3,3-trichloroallyl) oxy)-5-(trifluoromethyl)phenyl, 3-(2-cyanopropan-2-yl) -5-(trifluoromethoxy)phenyl, 3-(2-cyanopropan-2-yl)-5 -(trifluoromethyl)phenyl, 3-(2-cyanopropan-2-yl)-5-iso Propylphenyl, 3-(3,3-dichloroallyloxy)-5-(trifluoromethyl )phenyl, 3-(cyanomethyl)-5-fluorophenyl, 3-(cyanomethyl)phenyl 3-(cyclopropylmethoxy)-5-methylphenyl, 3-(methylsulfinyl) (trifluoromethyl)phenyl, 3-(oxan-4-ylmethoxy)-5-(trifluoromethyl)phenyl 3-(oxan-4-yloxy)-5-(trifluoromethyl)phenyl (trifluoromethyl)phenyl, 3-[(2,2-dichlorocyclopropyl)methoxy ]-5-(trifluoromethyl)phenyl, 3-[(2-chlorophenyl)methoxy]- 5-(trifluoromethyl)phenyl, 3-[(3-chlorophenyl)methoxy]-5- (trifluoromethyl)phenyl, 3-[(4-chlorophenyl)methoxy]-5-(trifluoromethyl)phenyl (trifluoromethyl)phenyl, 3-[1-(2-chlorophenyl)ethoxy]-5-(trifluoromethyl)phenyl (trifluoromethyl)phenyl, 3-[1-(3-chlorophenyl)ethoxy]-5-(trifluoromethyl)phenyl (trifluoromethyl)phenyl, 3-[1-(4-chlorophenyl)ethoxy]-5-(trifluoromethyl)phenyl (trifluoromethyl)phenyl, 3-acetyloxy-5-chlorophenyl, 3-benzyl Oxy-5-(trifluoromethyl)phenyl, 3-bromo-5-(2,2-dichloroethene phenyl, 3-bromo-5-(2,3,3-trichloroallyloxy) Phenyl, 3-bromo-5-[difluoro-(4-fluorophenyl)methyl]phenyl , 3-bromo-5-cyclopropyloxyphenyl, 3-chloro-5-(2-cyanopropyl) 3-chloro-5-(4-chlorophenoxy)phenyl, 3- Chloro-5-(4-fluorophenoxy)phenyl, 3-chloro-5-(cyanomethyl) Phenyl, 3-chloro-5-(cyclopropylcarbonyl)phenyl, 3-chloro-5- (methylsulfonylmethyl)phenyl, 3-chloro-5-[(3,4-dimethyl-5-o 4,5-dihydro-1H-1,2,4-triazol-1-ylmethyl]phenyl 3-chloro-5-[[4-(trifluoromethyl)-1H-pyrazol-1-yl] methyl]phenyl, 3-chloro-5-methylsulfonyloxyphenyl, 3-chloro-5 -phenoxyphenyl, 3-cyclobutyloxy-5-methylphenyl, 3-cyclopentene 3-hydroxy-5-methylphenyl, 3-hydroxy-5-(trifluoromethyl)phenyl phenyl or 3-methyl-5-(oxetan-3-yloxy)phenyl; R 3a is hydrogen; R 3b is methyl; R 4 5-cyanopyridin-2-yl, 5-cyano-1,3-thiazol-2-yl , 5-(dimethylaminocarbonyl)-1,3-thiazol-2-yl or 5-nitro- 1,3-thiazol-2-yl; R 5 is hydrogen, methyl, cyclopropyl or methoxy. It is a compound represented by the formula:

[0023] Likewise very particularly preferred are (Configuration 5-2), formula (I) [wherein, X is O; Y is a direct bond; R 1 is hydrogen; R 2 teeth, 3-Bromo-5-(cyclopropoxy)phenyl, 3-cyclopropyloxy-5- (trifluoromethoxy)phenyl, 3-bromo-5-(2,2-dichlorocyclopropyl) (aryl)oxyphenyl, 3-chloro-5-(cyanomethyl)phenyl, 3-(cyanomethyl)-5-(trifluoromethyl)phenyl 3-chloro-5-(2-cyanopropan-2-yl)phenyl, 3-chloro-5-(2-cyanopropan-2-yl)phenyl 3-(2-cyanopropan-2-yl)-5-(trifluoromethyl)phenyl, 3 -(2-cyanopropan-2-yl)-5-(trifluoromethoxy)phenyl, 3-( 2-cyanopropan-2-yl)-5-methylsulfonylphenyl, 3-chloro-5-(2-cyanopropan-2-yloxy)phenyl, 3-bromo- 5-(2-cyanopropan-2-yloxy)phenyl, 3-bromo-5-[cyclopropyl(difluoro)methyl]phenyl, 3-Bromo-5-[(2,2-difluorocyclopropyl)methoxy]phenyl, 3 -bromo-5-[(2,2-dichlorocyclopropyl)methoxy]phenyl, 3-[(2 ,2-dichlorocyclopropyl)methoxy]-5-(trifluoromethyl)phenyl, 3-[(2,3,3-trichloroprop-2-en-1-yl)oxy]-5-(trichloroprop-2-en-1-yl)oxy (trifluoromethyl)phenyl, 3-bromo-5-[(2,3,3-trichloropropane-2 -en-1-yl)oxy]phenyl, or 2-chloro-6-(2-cyanopropan-2-yl)pyridin-4-yl; R 3a is hydrogen; R 3b is methyl; R 4 is 5-[[ethyl(methyl)amino]carbonyl]pyridin-2-yl, 5- Anopyrazin-2-yl, 6-cyanopyrimidin-4-yl, 6-(aminocarbonyl) Pyrimidin-4-yl, 5-cyano-1,3-thiazol-2-yl, 5-(methylcarbamate) bamoyl)-1,3-thiazol-2-yl or 5-(dimethylaminocarbonyl)-1 ,3-thiazol-2-yl; R 5 is hydrogen, methyl or cyclopropyl. It is a compound represented by the formula:

[0024] Likewise very particularly preferred are (Configuration 5-3), formula (I) [wherein, X is O; Y is a direct bond; R 1 is hydrogen; R 2 teeth, 3-Bromo-5-(cyclopropoxy)phenyl, 3-cyclopropyloxy-5- (trifluoromethoxy)phenyl, 3-bromo-5-(2,2-dichlorocyclopropyl) (aryl)oxyphenyl, 3-chloro-5-(cyanomethyl)phenyl, 3-(cyanomethyl)-5-(trifluoromethyl)phenyl 3-chloro-5-(2-cyanopropan-2-yl)phenyl, 3-chloro-5-(2-cyanopropan-2-yl)phenyl 3-(2-cyanopropan-2-yl)-5-(trifluoromethyl)phenyl, 3 -(2-cyanopropan-2-yl)-5-(trifluoromethoxy)phenyl, 3-( 2-cyanopropan-2-yl)-5-methylsulfonylphenyl, 3-chloro-5-(cyclopropylcarbonyl)phenyl, 3-chloro-5-(2-cyanopropan-2-yloxy)phenyl, 3-bromo- 5-(2-cyanopropan-2-yloxy)phenyl, 3-Bromo-5-[cyclopropyl(difluoro)methyl]phenyl, 3-(2-cyclopropyl) (anopropan-2-yloxy)-5-cyclopropylphenyl, 3-Bromo-5-[(2,2-difluorocyclopropyl)methoxy]phenyl, 3 -bromo-5-[(2,2-dichlorocyclopropyl)methoxy]phenyl, 3-[(2 ,2-dichlorocyclopropyl)methoxy]-5-(trifluoromethyl)phenyl, 3-[(2,3,3-trichloroprop-2-en-1-yl)oxy]-5-(trichloroprop-2-en-1-yl)oxy (trifluoromethyl)phenyl, 3-bromo-5-[(2,3,3-trichloropropane-2 -en-1-yl)oxy]phenyl, 3-bromo-5-[difluoro-(4-fluorophenyl)methyl]phenyl, or , 2-chloro-6-(2-cyanopropan-2-yl)pyridin-4-yl; R 3a is hydrogen; R 3b is methyl; R 4 is 5-[[ethyl(methyl)amino]carbonyl]pyridin-2-yl, 5- Anopyrazin-2-yl, 6-cyanopyrimidin-4-yl, 6-(aminocarbonyl) Pyrimidin-4-yl, 6-(methylaminocarbonyl)pyrimidin-4-yl, 5-(methylaminocarbonyl)pyrimidin-4-yl Ano-1,3-thiazol-2-yl, 5-(methylcarbamoyl)-1,3-thiazo 5-(dimethylaminocarbonyl)-1,3-thiazol-2-yl or 5-(dimethylaminocarbonyl)-1,3-thiazol-2-yl can be; R 5 is hydrogen, methyl or cyclopropyl. It is a compound represented by the formula:

[0025] In a further preferred embodiment, the present invention provides a compound of formula (I') [ka] [In the formula, the structural element R 1 , R 2 , R 3a , R 3b , R 4 , R 5 and Y is in the configuration (1-1) The meaning or structure given in (2-1) The meaning or structure given in (3 -1) or the meaning given in the structure (4-1) or have the meaning given in structure (5-1). The present invention relates to a compound represented by the formula:

[0026] In a further preferred embodiment, the present invention provides a compound of formula (I') [ka] [In the formula, the structural element R 1 , R 2 , R 3a , R 3b , R 4 , R 5 and Y is in the configuration (1-2) The meaning or structure given in (2-2) The meaning or structure given in (3 -2) or the meaning given in (4-2) or have the meaning given in structure (5-2). The present invention relates to a compound represented by the formula:

[0027] In a further preferred embodiment, the present invention provides a compound of formula (I″) [ka] [During the ceremony, R 3b is C1-C3 alkyl, particularly preferably Me, and R 3a teeth , H; and Structural element R 1 , R 2 , R 4 , R 5 and Y has the meaning given in the structure (1-1). The meaning or structure given in (2-1) is given in (3-1) In the given meaning or structure (4-1) in the given meaning or structure (5-1) has the meaning given to it. The present invention relates to a compound represented by the formula:

[0028] In a further preferred embodiment, the present invention provides a compound of formula (I″) [ka] [During the ceremony, R 3b is C1-C3 alkyl, particularly preferably Me, and R 3a teeth , H; and Structural element R 1 , R 2 , R 4 , R 5 and Y has the meaning given in the structure (1-2). The meaning or structure given in (2-2) is given in (3-2) In the given meaning or structure (4-2) In the given meaning or structure (5-2) has the meaning given to it. The present invention relates to a compound represented by the formula:

[0029] In a further preferred embodiment, the present invention provides a compound of formula (I″) [ka] [During the ceremony, R 3b is C1-C3 alkyl, particularly preferably Me, and R 3a teeth , H; and Structural element R 1 , R 2 , R 4 , R 5 and Y has the meaning given in the structure (1-3). The meaning or structure (3-3) is given in the taste or structure (2-3) In the given meaning or structure (4-3) In the given meaning or structure (5-3) has the meaning given to it. The present invention relates to a compound represented by the formula:

[0030] In a further preferred embodiment, the present invention provides a compound of formula (I''') [ka] [During the ceremony, R 3b is C1-C3 alkyl, particularly preferably Me, and R 3a teeth , H; and Structural element R 1 , R 2 , R 4 , R 5 and Y has the meaning given in the structure (1-1). The meaning or structure given in (2-1) is given in (3-1) In the given meaning or structure (4-1) in the given meaning or structure (5-1) has the meaning given to it. The present invention relates to a compound represented by the formula:

[0031] In a further preferred embodiment, the present invention provides a compound of formula (I''') [ka] [During the ceremony, R 3b is C1-C3 alkyl, particularly preferably Me, and R 3a teeth , H; and Structural element R 1 , R 2 , R 4 , R 5 and Y has the meaning given in the structure (1-2). The meaning or structure given in (2-2) is given in (3-2) In the given meaning or structure (4-2) In the given meaning or structure (5-2) has the meaning given to it. The present invention relates to a compound represented by the formula:

[0032] In a further preferred embodiment, the present invention provides a compound of formula (I''') [ka] [During the ceremony, R 3b is C1-C3 alkyl, particularly preferably Me, and R 3a teeth , H; and Structural element R 1 , R 2 , R 4 , R 5 and Y has the meaning given in the structure (1-3). The meaning or structure (3-3) is given in the taste or structure (2-3) In the given meaning or structure (4-3) In the given meaning or structure (5-3) has the meaning given to it. The present invention relates to a compound represented by the formula:

[0033] Additionally, the present invention encompasses the following intermediate compounds and their salts (see Table 2): ): Intermediate 5A: 3-chloro-5-(2-cyanopropan-2-yl)benzoic acid; Intermediate 9A: 3-chloro-5-(cyclopropylcarbonyl)benzoic acid; Intermediate 10A: 3-[(methylsulfinyl)methoxy]-5-(trifluoromethyl) benzoic acid; Intermediate 25A: 3-(cyanomethyl)-5-(trifluoromethoxy)benzoic acid; Intermediate 26A: 3-(2-cyanopropan-2-yl)-5-(trifluoromethyl) Sodium benzoate / 3-(2-cyanopropan-2-yl)-5-(trifluoromethyl)benzoate (Methoxy)benzoic acid; Intermediate 28A: 3-bromo-5-(2,2-dichlorovinyl)benzoic acid; Intermediate 35A: 3-bromo-5-[difluoro(4-fluorophenyl)methyl]anhydride zoic acid; Intermediate 48A: 3-chloro-5-[(methylsulfonyl)methyl]benzoic acid; Intermediate 50A: 3-(cyclopropoxy)-5-(trifluoromethoxy)benzoic acid ; Intermediate 51A: 3-bromo-5-(1-cyano-1-methyl-ethoxy)benzoic acid; Intermediate 52A: 3-chloro-5-(1-cyano-1-methyl-ethoxy)benzoic acid; Intermediate 54A: 5-[5-[(1S)-1-aminoethyl]-1,2,4-triazo [1-yl]pyrazine-2-carbonitrile hydrochloride; Intermediate 58A: 6-[5-[(1S)-1-aminoethyl]-3-cyclopropyl- 1,2,4-triazol-1-yl]pyrimidine-4-carbonitrile hydrochloride; Intermediate 59A: 6-[5-[(1S)-1-aminoethyl]-3-cyclopropyl- 1,2,4-triazol-1-yl]pyrimidine-4-carboxamide hydrochloride; Intermediate 60A: 3-chloro-6-(1-cyano-1-methyl-ethyl)pyridine-4 -carboxylic acids; Intermediate 61A: 6-{5-[(1S)-1-aminoethyl]-3-methyl-1H-1 ,2,4-triazol-1-yl}-N-ethyl-N-methylnicotinamide hydrochloride; Intermediate 69A: 3-(cyanomethyl)-5-(methylsulfonyl)benzoic acid; Intermediate 70A: 3-(2-cyanopropan-2-yl)-5-(methylsulfonyl) benzoic acid; Intermediate 72A: 3-(1-cyano-1-methyl-ethoxy)-5-cyclopropyl- Benzoic acid.

[0034] The compound represented by formula (I) may exist in the form of stereoisomers depending on the type of substituents. i.e., geometric and / or optical isomeric forms or isomeric mixtures in various compositions. Although, generally, only for compounds of formula (I) Although discussed herein, the present invention does not include the pure stereoisomers and their derivatives. and any desired mixture of

[0035] However, according to the present invention, it is preferred to use an optically active compound of formula (I). Stereoisomeric forms and salts thereof are used.

[0036] Thus, the present invention provides a method for controlling pests (which includes arthropods, and in particular insects). for the removal of enantiomers and diastereomers, both pure and their mixtures. do.

[0037] Where appropriate, the compounds of formula (I) may exist in different polymorphic forms or can exist as a mixture of different polymorphic forms. Both pure polymorphs and polymorphic mixtures are It is provided by and can be used in accordance with the present invention.

[0038] definition Those skilled in the art will understand that when the expressions "a" or "an" are used in this application, even if the Even if not explicitly stated, "one," "one or more," or "at least one" may be used depending on the context. " I know that it can mean ".

[0039] For all structures described herein, including ring systems and groups, adjacent atoms may be -O It must not be -O- or -OS-.

[0040] Structures with variable numbers of possible carbon atoms (C atoms) are intended to be more specific. In this application, C 炭素原子の下限 -C 炭素原子の上限 Structure (C LL -C UL For example, alkyl groups may be composed of 3 to 10 carbon atoms. In that case, C3-C 10 -alkyl. It is composed of carbon atoms and heteroatoms. The resulting ring structure can be described as an "LL-UL membered" structure. An example of a six-membered ring structure is toluene. It is a methyl group-substituted six-membered ring structure.

[0041] Collective terms for substituents, e.g., C LL -C UL -alkyl may be a complex substituent, e.g. C LL -C UL -Cycloalkyl-CLL -C UL -If it is at the end of alkyl, The first component of the substituent, e.g., C LL -C UL -Cycloalkyl is the same as and independently, the latter substituents, e.g., C LL -C UL -Al The term "cyclic group" as used herein refers to chemical groups, ring systems, and cyclic radicals. All the collective words that are LL -C UL By adding "LL~UL member" It can be stated more specifically.

[0042] In the definitions of the symbols given in the formula above, a set of substituents generally representative of the following is provided: used the word.

[0043] Halogen is an element of the 7th main group, preferably fluorine, chlorine, bromine and iodine, more preferably Preferably it concerns fluorine, chlorine and bromine, even more preferably fluorine and chlorine.

[0044] Examples of heteroatoms are N, O, S, P, B, Si. Preferably, the term "heteroatom" is used. " relates to N, S and O.

[0045] According to the present invention, "alkyl", either alone or as part of a chemical group, preferably represents 1 Straight or branched chain hydrocarbons having up to 6 carbon atoms, such as methyl, ethyl, n- Propyl, isopropyl, n-butyl, isobutyl, s-butyl, t-butyl, pentyl , 1-methylbutyl, 2-methylbutyl, 3-methylbutyl, 1,2-dimethylpropyl , 1,1-dimethylpropyl, 2,2-dimethylpropyl, 1-ethylpropyl, hexyl 1-methylpentyl, 2-methylpentyl, 3-methylpentyl, 4-methylpentyl 1,2-dimethylpropyl, 1,3-dimethylbutyl, 1,4-dimethylbutyl, 2 ,3-dimethylbutyl, 1,1-dimethylbutyl, 2,2-dimethylbutyl, 3,3-di Methylbutyl, 1,1,2-trimethylpropyl, 1,2,2-trimethylpropyl, 1 -ethylbutyl and 2-ethylbutyl. Alkyl having 1 to 4 carbon atoms, e.g. For example, methyl, ethyl, n-propyl, isopropyl, n-butyl, Isobutyl, sec-butyl or t-butyl are also preferred. Alkyl according to the present invention is defined as one or more The substituted groups may be the same or different radicals as above.

[0046] According to the present invention, "alkenyl", either alone or as part of a chemical group, preferably A straight or branched chain hydrocarbon having 2 to 6 carbon atoms and at least one double bond , for example, vinyl, 2-propenyl, 2-butenyl, 3-butenyl, 1-methyl-2-propenyl, propenyl, 2-methyl-2-propenyl, 2-pentenyl, 3-pentenyl, 4-pentenyl 1-methyl-2-butenyl, 2-methyl-2-butenyl, 3-methyl-2-butenyl 1-methyl-3-butenyl, 2-methyl-3-butenyl, 3-methyl-3-butenyl , 1,1-dimethyl-2-propenyl, 1,2-dimethyl-2-propenyl, 1-ethyl -2-propenyl, 2-hexenyl, 3-hexenyl, 4-hexenyl, 5-hexenyl , 1-methyl-2-pentenyl, 2-methyl-2-pentenyl, 3-methyl-2-pentenyl 4-methyl-2-pentenyl, 3-methyl-3-pentenyl, 4-methyl-3-pentenyl pentenyl, 1-methyl-4-pentenyl, 2-methyl-4-pentenyl, 3-methyl-4 -pentenyl, 4-methyl-4-pentenyl, 1,1-dimethyl-2-butenyl, 1,1 -dimethyl-3-butenyl, 1,2-dimethyl-2-butenyl, 1,2-dimethyl-3- Butenyl, 1,3-dimethyl-2-butenyl, 2,2-dimethyl-3-butenyl, 2,3 -dimethyl-2-butenyl, 2,3-dimethyl-3-butenyl, 1-ethyl-2-butenyl 1-ethyl-3-butenyl, 2-ethyl-2-butenyl, 2-ethyl-3-butenyl , 1,1,2-trimethyl-2-propenyl, 1-ethyl-1-methyl-2-propenyl and 1-ethyl-2-methyl-2-propenyl. Aryl having 2 to 4 carbon atoms. phenyl, for example, inter alia, 2-propenyl, 2-butenyl or 1-methyl-2-propenyl; Alkenyl according to the present invention is preferably one or more of the same or different It may be substituted with a radical such as

[0047] According to the present invention, "alkynyl", either alone or as part of a chemical group, preferably A straight or branched chain hydrocarbon having 2 to 6 carbon atoms and at least one triple bond , for example, 2-propynyl, 2-butynyl, 3-butynyl, 1-methyl-2-propynyl , 2-pentynyl, 3-pentynyl, 4-pentynyl, 1-methyl-3-butynyl, 2- Methyl-3-butynyl, 1-methyl-2-butynyl, 1,1-dimethyl-2-propynyl , 1-ethyl-2-propynyl, 2-hexynyl, 3-hexynyl, 4-hexynyl, 5 -hexynyl, 1-methyl-2-pentynyl, 1-methyl-3-pentynyl, 1-methyl -4-pentynyl, 2-methyl-3-pentynyl, 2-methyl-4-pentynyl, 3-methyl 4-pentynyl, 4-methyl-2-pentynyl, 1,1-dimethyl-3-butynyl , 1,2-dimethyl-3-butynyl, 2,2-dimethyl-3-butynyl, 1-ethyl-3 -butynyl, 2-ethyl-3-butynyl, 1-ethyl-1-methyl-2-propynyl and 2,5-hexadinyl. Alkynyl having 2 to 4 carbon atoms, for example, Also preferred are ethynyl, 2-propynyl, and 2-butynyl-2-propenyl. The alkynyl groups defined above may be substituted with one or more identical or different radicals. .

[0048] According to the present invention, "cycloalkyl" is preferred, either alone or as part of a chemical group. Monocyclic, bicyclic or tricyclic hydrocarbons having 3 to 10 carbon atoms, e.g., cyclohexane, Propyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, cyclobutyl octyl, bicyclo[2.2.1]heptyl, bicyclo[2.2.2]octyl or adamantyl represents cycloalkyl having 3, 4, 5, 6 or 7 carbon atoms, e.g. For example, cyclopropyl or cyclobutyl are particularly preferred. Alkyl can be substituted with one or more identical or different radicals.

[0049] According to the present invention, "alkylcycloalkyl" preferably has 4 to 10 or 4 to 7 alkyl groups. monocyclic, bicyclic or tricyclic alkylcycloalkyl having carbon atoms, for example, ethylcyclopropyl, ethylcyclopropyl, isopropylcyclobutyl, 3-methylcyclopropyl It represents cyclopentyl and 4-methylcyclohexyl. alkylcycloalkyl, such as, inter alia, ethylcyclopropyl or 4-methylcyclopropyl; Cyclohexyl and the like are also preferred. Alkylcycloalkyl according to the present invention is one or more identical or may be substituted with a different radical.

[0050] According to the present invention, "cycloalkylalkyl" preferably has 4 to 10 or 4 to 7 alkyl groups. monocyclic, bicyclic or tricyclic cycloalkylalkyl having carbon atoms, for example, Cyclopropylmethyl, cyclobutylmethyl, cyclopentylmethyl, cyclohexylmethyl cyclopentylethyl and cyclopentylethyl. alkylalkyl, such as, inter alia, cyclopropylmethyl or cyclobutylmethyl; Cycloalkylalkyl according to the present invention is preferably one or more of the same or different The group may be substituted with any of the following radicals:

[0051] According to the present invention, "hydroxyalkyl" preferably has 1 to 6 carbon atoms. , straight or branched chain alcohols, such as methanol, ethanol, n-propanol, Isopropanol, n-butanol, isobutanol, s-butanol and t-butanol Hydroxyalkyl groups having 1 to 4 carbon atoms are also preferred. The hydroxyalkyl groups may be substituted with one or more identical or different radicals. do.

[0052] According to the present invention, "alkoxy" preferably refers to straight or is a branched O-alkyl, for example, methoxy, ethoxy, n-propoxy, isopropoxy It represents 1-4 carbon atoms, n-butoxy, isobutoxy, s-butoxy, and t-butoxy. Alkoxy groups containing one or more identical alkyl groups are also preferred. They may be substituted with the same or different radicals.

[0053] According to the present invention, "alkylthio" or "alkylsulfanyl" preferably means 1 to Straight or branched chain S-alkyl having 6 carbon atoms, for example, methylthio, ethyl Thio, n-propylthio, isopropylthio, n-butylthio, isobutylthio, s-butylthio alkylthio and t-butylthio. Alkylthio groups having 1 to 4 carbon atoms are also preferred. Alkylthio groups according to the present invention may be substituted with one or more identical or different radicals. may be substituted with

[0054] According to the present invention, "alkylsulfinyl" preferably has 1 to 6 carbon atoms. straight-chain or branched alkylsulfinyl, for example, methylsulfinyl, ethylsulfinyl; sulfinyl, n-propylsulfinyl, isopropylsulfinyl, n-butylsulfinyl isobutylsulfinyl, s-butylsulfinyl and t-butylsulfinyl Also preferred are alkylsulfinyl groups having 1 to 4 carbon atoms. The alkylsulfinyl group may be substituted with one or more identical or different radicals. and encompasses both enantiomers.

[0055] According to the present invention, "alkylsulfonyl" preferably has 1 to 6 carbon atoms. , straight or branched alkylsulfonyl, for example, methylsulfonyl, ethylsulfonyl, n-propylsulfonyl, isopropylsulfonyl, n-butylsulfonyl, isobutyl sulfonyl, s-butylsulfonyl and t-butylsulfonyl. Alkylsulfonyl groups having 1 alkyl groups are also preferred. The substituted groups may be the same or different.

[0056] According to the present invention, "cycloalkylthio" or "cycloalkylsulfanyl" is preferably -S-cycloalkyl, preferably having 3 to 6 carbon atoms, such as cyclopropyl Thio, cyclobutylthio, cyclopentylthio, cyclohexylthio. 3 to 5 Cycloalkylthio groups having carbon atoms are also preferred. Cycloalkylthio groups according to the present invention may be substituted with one or more identical or different radicals.

[0057] According to the present invention, "cycloalkylsulfinyl" preferably has 3 to 6 carbon atoms. -S(O)-cycloalkyl, for example, cyclopropylsulfinyl, cyclo represents butylsulfinyl, cyclopentylsulfinyl, and cyclohexylsulfinyl Cycloalkylsulfinyl groups having 3 to 5 carbon atoms are also preferred. A cycloalkylsulfinyl group may be substituted with one or more identical or different radicals. It can be exchanged and includes both enantiomers.

[0058] According to the present invention, "cycloalkylsulfonyl" preferably has 3 to 6 carbon atoms. -SO2-cycloalkyl, for example, cyclopropylsulfonyl, cyclobutyl Sulfonyl, cyclopentylsulfonyl, cyclohexylsulfonyl. 3 to 5 Cycloalkylsulfonyl groups having carbon atoms are also preferred. The sulfonyl groups may be substituted with one or more identical or different radicals.

[0059] According to the present invention, "phenylthio" or "phenylsulfanyl" means -S-phenyl phenylthio. The phenylthio groups according to the present invention may be one or more identical or or may be substituted with a different radical.

[0060] According to the present invention, "phenylsulfinyl" refers to -S(O)-phenyl, e.g., phenyl The phenylsulfinyl group according to the present invention may be one or more identical or different radicals and both enantiomers can be Contains.

[0061] According to the present invention, "phenylsulfonyl" refers to -SO2-phenyl, e.g., phenyl The phenylsulfonyl group according to the present invention may be one or more identical or different. It may be substituted with a radical which is

[0062] According to the present invention, "alkylcarbonyl" includes methylcarbonyl, ethylcarbonyl, n-Propylcarbonyl, isopropylcarbonyl, s-butylcarbonyl and t-butylcarbonyl linear or branched alkyl groups, preferably having 2 to 7 carbon atoms, such as alkylcarbonyl; It represents alkyl-C(=O). Alkylcarbonyl having 1 to 4 carbon atoms is also preferred. Alkylcarbonyl according to the invention may be substituted with one or more identical or different radicals. can be exchanged.

[0063] According to the present invention, "alkoxycarbonyl" alone or as a component of a chemical group means an alkoxycarbonyl group. The alkoxy moiety preferably has 1 to 6 carbon atoms or 1 to 4 carbon atoms. linear or branched alkoxycarbonyl, for example, methoxycarbonyl, ethoxycarbonyl; carbonyl, n-propoxycarbonyl, isopropoxycarbonyl, s-butoxycarbonyl The alkoxycarbonyl group according to the present invention represents one or more alkoxycarbonyl groups. The substituted groups may be the same or different radicals as above.

[0064] According to the present invention, "alkylaminocarbonyl" preferably has 1 to 6 alkyl moieties. straight-chain or branched-chain alkylaminocarbonyl groups having 1 to 4 carbon atoms; Nyl, for example, methylaminocarbonyl, ethylaminocarbonyl, n-propylamino carbonyl, isopropylaminocarbonyl, s-butylaminocarbonyl and t-butylaminocarbonyl The alkylaminocarbonyl group according to the present invention represents one or more identical aminocarbonyl groups. or may be substituted with a different radical.

[0065] According to the present invention, "N,N-dialkylaminocarbonyl" is preferred for the alkyl moiety. or straight or branched chain N,N-dicarboxylic acids having 1 to 6 carbon atoms or 1 to 4 carbon atoms Alkylaminocarbonyl, for example, N,N-dimethylaminocarbonyl, N,N-diaminocarbonyl N,N-di(n-propylamino)carbonyl, N,N-di(isopropylamino)carbonyl N,N-di-(s-butylamino)carbonyl and N,N-di-(s-propylamino)carbonyl The N,N-dialkylaminocarbonyl group according to the present invention may be one or more identical or different. It may be substituted with a radical which is

[0066] According to the present invention, "aryl" preferably refers to an alkyl group having 6 to 14, especially 6 to 10, ring carbon atoms. monocyclic, bicyclic or polycyclic aromatic systems having rings, for example phenyl, naphthyl, aryl, tolyl, phenanthrenyl, and preferably phenyl. Fused polycyclic systems in which the attachment site is on the aromatic system, e.g., tetrahydronaphthyl, indenyl The aryl group according to the present invention also represents one or more aryl groups. The substituted groups may be the same or different radicals as above.

[0067] An example of a substituted aryl is arylalkyl, which is a C1-C4-alkyl group. C6-C 14 - one or more identical or different in the aryl moiety Examples of such arylalkyls include benzophenone, ... Examples include diphenyl and phenyl-1-ethyl.

[0068] According to the present invention, the term "polycyclic" rings includes fused, bridged and spirocyclic carbon rings. It refers to rings and heterocycles, as well as ring systems linked via single or double bonds.

[0069] According to the present invention, a "heterocycle", a "heterocyclic ring" or a "heterocyclic ring system" is at least At least one carbon atom is a heteroatom (preferably N, O, S, P, B, Si, Se) and is substituted with a heteroatom selected from the group consisting of saturated, unsaturated or heteroaromatic at least one ring of the aryl group, wherein the ring is unsubstituted or substituted; The bond site is on a ring atom. Unless otherwise specified, the heterocyclic ring preferably has 3 to 9 rings in the heterocyclic ring. atoms (particularly, 3 to 6 ring atoms) and one or more (preferably, 1 to 4, particularly, 1 or 2 or 3) heteroatoms (preferably heteroatoms selected from the group consisting of N, O and S) The heterocyclic ring usually contains two oxygen atoms, but the two oxygen atoms must not be directly adjacent. containing up to four nitrogen atoms and / or up to two oxygen atoms and / or up to two sulfur atoms In the case of optionally substituted heterocyclyl, the invention also includes polycyclic ring systems, e.g. , 8-azabicyclo[3.2.1]octanyl, 1-azabicyclo[2.2.1]heptyl 1-oxa-5-azaspiro[2.3]hexyl or 2,3-dihydro-1H-yne This also includes dolls.

[0070] Heterocyclyl groups according to the invention include, for example, piperidinyl, piperazinyl, morpholinyl, methyl ... Linyl, pyrrolidinyl, imidazolinyl, imidazolidinyl, thiazolidinyl, oxazo Lysinyl, dioxolanyl, dioxolyl, pyrazolidinyl, tetrahydrofuranyl, di Hydrofuranyl, oxetanyl, oxiranyl, azetidinyl, aziridinyl, oxazetanyl oxaziridinyl, oxazepanyl, oxazinanyl, azepanyl, oxopyridine dioxopyrrolidinyl, oxomorpholinyl, oxopiperazinyl and oxo Cepanil, etc.

[0071] Of particular interest are heteroaryl, i.e., heteroaromatic systems. The term "heteroaryl" refers to heteroaromatic compounds, i.e., heterocycles, which are encompassed by the above definition of heterocycle. It represents a fully unsaturated aromatic heterocyclic compound. Preferred is one selected from the above group. having up to three (preferably one or two) identical or different heteroatoms; Heteroaryl according to the present invention is, for example, furyl, thienyl, phenyl ... Triazolyl, imidazolyl, 1,2,3-triazolyl and 1,2,4-triazolyl, isoxazolyl, thiazolyl, isothiazolyl, 1,2,3-oxadiazolyl, 1,3 ,4-oxadiazolyl, 1,2,4-oxadiazolyl and 1,2,5-oxadiazolyl Aryl, azepinyl, pyrrolyl, pyridyl, pyridazinyl, pyrimidinyl, pyrazinyl, 1 ,3,5-triazinyl, 1,2,4-triazinyl and 1,2,3-triazinyl, 1 ,2,4-oxazinyl, 1,3,2-oxazinyl, 1,3,6-oxazinyl and 1 ,2,6-oxazinyl, oxepinyl, thiepinyl, 1,2,4-triazolonyl, and and 1,2,4-diazepinyl. Heteroaryl groups according to the present invention are those containing one or more of the same The substituents may be the same or different radicals.

[0072] According to the present invention, the substituent =O (oxo) is a substituent that is a substituted or unsubstituted aryl group, i.e., two hydrogen atoms of a methylene (CH2) group or is for the lone electron pairs of sulfur, nitrogen and phosphorus atoms that have only non-hydrogen substituents. For example, the radical C2-alkyl can be substituted, for example, by ═O (oxo). The heterocycle thietan-3-yl- is, for example, -COCH3. =O (oxo) group to give 1-oxothietan-3-yl or two = Substitution with an O (oxo) group results in 1,1-dioxothietan-3-yl.

[0073] According to the present invention, the substituent =S (thiono) is attached to two hydrogen atoms of a methylene (CH2) group. For example, the radical C2-alkyl can be replaced by, for example, =S(thiono ) to give -CSCH3.

[0074] As used herein, the expression "optionally substituted" means that the substituted The group may or may not be substituted with further substituents. means.

[0075] The term "optionally substituted" refers to a group / substituent, e.g., alkyl, Alkenyl, alkynyl, alkoxy, alkylthio, alkylsulfinyl, alkyl sulfonyl, cycloalkyl, aryl, phenyl, benzyl, heterocyclyl and hetero This means that the aryl radicals and the like are substituted, for example, means a substituted radical derived from a base structure that is not one substituent or a plurality of substituents, preferably 1, 2, 3, 4, 5, 6 or 7 substituents ) is, for example, amino, hydroxyl, halogen, nitro, cyano, isocyano, mercapto, Buto, isothiocyanato, C1-C4-carboxyl, carbonamido, SF5, amino Sulfonyl, C1-C4-alkyl, C1-C4-haloalkyl, C3-C4-cycloalkyl C2-C4-alkenyl, C5-C6-cycloalkenyl, C2-C4-alkyl Nyl, N-mono-C1-C4-alkylamino, N,N-di-C1-C4-alkylamino N-C1-C4-alkanoylamino, C1-C4-alkoxy, C1-C4-halo Alkoxy, C2-C4-alkenyloxy, C2-C4-alkynyloxy, C3-C 4-Cycloalkoxy, C5-C6-cycloalkenyloxy, C1-C4-alkoxy Carbonyl, C2-C4-alkenyloxycarbonyl, C2-C4-alkynyloxy Carbonyl, C6-aryloxycarbonyl, C 10 -aryloxycarbonyl, C 14 -aryloxycarbonyl, C1-C4-alkanoyl, C2-C4-alkenyl Carbonyl, C2-C4-alkynylcarbonyl, C6-arylcarbonyl, C 10 - Arylcarbonyl, C 14 -arylcarbonyl, C1-C4-alkylthio, C1- C4-haloalkylthio, C3-C4-cycloalkylthio, C2-C4-alkenylthio O, C5-C6-cycloalkenylthio, C2-C4-alkynylthio, C1-C4-a alkylsulfinyl (wherein both enantiomers of the C1-C4-alkylsulfinyl group C1-C4-haloalkylsulfinyl (wherein C1-C4-haloalkylsulfinyl is included), both enantiomers of the alkylsulfinyl group are included), C1-C4-alkyl C1-C4-haloalkylsulfonyl, N-mono-C1-C4-alkyl Aminosulfonyl, N,N-di-C1-C4-alkylaminosulfonyl, C1-C4- alkylphosphinyl, C1-C4-alkylphosphonyl (wherein C1-C4-alkyl Both the C1-C4-alkylphosphonyl and C1-C4-alkylphosphonyl enantiomers are included. N-C1-C4-alkylaminocarbonyl, N,N-di-C1-C4-alkyl Aminocarbonyl, N-C1-C4-alkanoylaminocarbonyl, N-C1-C4- Alkanoyl-N-C1-C4-alkylaminocarbonyl, C6-aryl, C 10 - Aryl, C 14 -aryl, C6-aryloxy, C10 -aryloxy, C 14 -aryloxy, benzyl, benzyloxy, benzylthio, C6-arylthio, C 10 -arylthio, C 14 -arylthio, C6-arylamino, C 10 -aryl Amino, C 14 -arylamino, benzylamino, heterocyclyl and trialkylamino alkyl, substituents attached through a double bond (e.g., C1-C4-alkylidene (e.g., methylidene or ethylidene), oxo group, imino group and substituted imino group). When two or more radicals form one or more rings, they are selected from the group consisting of: , carbocyclic, heterocyclic, saturated, partially saturated, unsaturated (including, for example, aromatic rings) The substituents listed above can be any of the substituents listed above and can be further substituted. Substituents ("first substituent level"), if they contain hydrocarbonaceous moieties, wherein further substituents ("second substituent level"), such as halogen, hydroxyl, Amino, nitro, cyano, isocyano, azido, acylamino, oxo and imino groups The term "substituted" refers to a group consisting of aryl, aryls ... The "(optionally)" group preferably includes only one or two substitution levels. Includes.

[0076] Halogen-substituted or halogenated chemical groups (e.g., alkyl or alkoxy) is substituted with one halogen or up to the maximum possible number of substituents. Such groups are also called halo groups (e.g., haloalkyl). In the case of poly-halogen substitution, the halogen atoms may be the same or different. They may all be bonded to one carbon atom or may be bonded to multiple carbon atoms. Halogen is in particular fluorine, chlorine, bromine or iodine, and is preferably Preferably, it is fluorine, chlorine or bromine, more preferably fluorine. The halogen-substituted group is monohalocycloalkyl, e.g., 1-fluorocycloalkyl. 2-fluorocyclopropyl or 1-fluorocyclobutyl, monohaloal Chlorethyl, e.g., 2-chloroethyl, 2-fluoroethyl, 1-chloroethyl, 1-fluoroethyl chloroethyl, chloromethyl or fluoromethyl, perhaloalkyl, for example trichloromethyl methyl or trifluoromethyl or CF2CF3, polyhaloalkyl, e.g., difluoro Methyl, 2-fluoro-2-chloroethyl, dichloromethyl, 1,1,2,2-tetrafluoroethane Further examples of haloalkyl include fluoroethyl and 2,2,2-trifluoroethyl. , trichloromethyl, chlorodifluoromethyl, dichlorofluoromethyl, chloromethyl , bromomethyl, 1-fluoroethyl, 2-fluoroethyl, 2,2-difluoroethyl , 2,2,2-trifluoroethyl, 2,2,2-trichloroethyl, 2-chloro-2, 2-difluoroethyl, pentafluoroethyl, 3,3,3-trifluoropropyl and Pentafluoro-t-butyl is preferred. Preferred are those having 1 to 4 carbon atoms and fluorine or chlorine. and bromine, and 1 to 9 (preferably 1 to 5) the same or different Particularly preferred are haloalkyls having one or two carbon atoms. Atoms and 1 to 5 identical or different halogens selected from fluorine and chlorine haloalkyl having atoms such as difluoromethyl, trifluoromethyl, among others; or 2,2-difluoroethyl). Further examples of halogen-substituted compounds are: is haloalkoxy, for example, OCF3, OCHF2, OCH2F, OCF2CF3, O CH2CF3, OCH2CHF2 and OCH2CH2Cl, haloalkylsulfanyl, For example, difluoromethylthio, trifluoromethylthio, trichloromethylthio, chloromethylthio Fluorodifluoromethylthio, 1-fluoroethylthio, 2-fluoroethylthio, 2,2- Difluoroethylthio, 1,1,2,2-tetrafluoroethylthio, 2,2,2-trifluoroethylthio Fluoroethylthio or 2-chloro-1,1,2-trifluoroethylthio, haloalkyl sulfinyl, for example, difluoromethylsulfinyl, trifluoromethylsulfinyl nyl, trichloromethylsulfinyl, chlorodifluoromethylsulfinyl, 1-fluoro Oroethylsulfinyl, 2-fluoroethylsulfinyl, 2,2-difluoroethyl Sulfinyl, 1,1,2,2-tetrafluoroethylsulfinyl, 2,2,2-tri Fluoroethylsulfinyl and 2-chloro-1,1,2-trifluoroethylsulfinyl haloalkylsulfinyl, for example, difluoromethylsulfinyl, trifluoromethylsulfinyl, trichloromethylsulfinyl, chlorodifluoromethylsulfinyl, 1-fluoroethylsulfinyl, 2-fluoroethylsulfinyl, 2,2- difluoroethylsulfinyl, 1,1,2,2-tetrafluoroethylsulfinyl, 2,2,2-Trifluoroethylsulfinyl and 2-chloro-1,1,2-trifluoro haloethylsulfinyl, haloalkylsulfonyl groups, for example, difluoromethylsulfonyl trifluoromethylsulfonyl, trichloromethylsulfonyl, chlorodifluoromethyl Fluoroethylsulfonyl, 1-fluoroethylsulfonyl, 2-fluoroethylsulfonyl, 2, 2-difluoroethylsulfonyl, 1,1,2,2-tetrafluoroethylsulfonyl, 2,2,2-trifluoroethylsulfonyl and 2-chloro-1,1,2-trifluoro It is ethylsulfonyl.

[0077] In the case of radicals having carbon atoms, preference is given to radicals having 1 to 4 carbon atoms, especially 1 or Generally, halogens (e.g., fluorine and chlorine) , (C1-C4) alkyl (preferably methyl or ethyl), (C1-C4) haloal alkyl (preferably trifluoromethyl), (C1-C4)alkoxy (preferably methyl), (C1-C4)haloalkoxy, nitro and cyano. Particularly preferred are the substituents methyl, methoxy, fluorine, and chlorine.

[0078] Substituted amino (for example, mono- or di-substituted amino) can be, for example, alkyl. one or two selected from the group consisting of aryl, hydroxy, amino, alkoxy, acyl and aryl; Substituted amino radicals N-substituted by identical or different radicals of means a radical selected from the group consisting of: -dialkylamino (e.g., methylamino, ethylamino, N,N-dimethylamino, N,N-diethylamino, N,N-di-n-propylamino, N,N-diisopropylamino amino or N,N-dibutylamino), N-monoalkoxyalkylamino or N,N-di Alkoxyalkylamino groups (e.g., N-methoxymethylamino, N-methoxyethyl Amino, N,N-di(methoxymethyl)amino or N,N-di(methoxyethyl)amino ), N-monoarylamino and N,N-diarylamino, e.g., optionally substituted Good aniline, acylamino, N,N-diacylamino, N-alkyl-N-aryl amino, N-alkyl-N-acylamino and, furthermore, saturated N-heterocycles; and, preferred are alkyl radicals having 1 to 4 carbon atoms; The aryl is preferably phenyl or substituted phenyl; and for acyl, The definitions given further below apply, preferably (C1-C4)-alkano The same applies to substituted hydroxylamino or hydrazino. will be done.

[0079] The substituted amino may further be a quaternary amino having four organic substituents on the nitrogen atom. This also includes monium compounds (salts).

[0080] The optionally substituted phenyl is preferably unsubstituted phenyl or or halogen, (C1-C4)-alkyl, (C1-C4)-alkoxy, (C1-C 4)-alkoxy-(C1-C4)-alkoxy, (C1-C4)-alkoxy-(C1 -C4)-Alkyl, (C1-C4)-Haloalkyl, (C1-C4)-Haloalkoxy , (C1-C4)-alkylthio, (C1-C4)-haloalkylthio, (C1-C4) -Alkylsulfinyl, (C1-C4)-haloalkylsulfinyl, (C1-C4) -Alkylsulfonyl, (C1-C4)-haloalkylsulfonyl, cyano, isocyano and nitro, substituted or polysubstituted (preferably up to trisubstituted) phenyl, for example, o-triphenyl; m-tolyl and p-tolyl, dimethylphenyl, 2-chlorophenyl, 3-chlorophenyl phenyl and 4-chlorophenyl, 2-fluorophenyl, 3-fluorophenyl and 4- Fluorophenyl, 2-trifluoromethylphenyl, 3-trifluoromethylphenyl and 4-trifluoromethylphenyl, and 4-trichloromethylphenyl, 2,4- Dichlorophenyl, 3,5-dichlorophenyl, 2,5-dichlorophenyl and 2,3- Dichlorophenyl, o-methoxyphenyl, m-methoxyphenyl and p-methoxyphenyl and 4-heptafluorophenyl.

[0081] The optionally substituted cycloalkyl is preferably an unsubstituted cycloalkyl. or halogen, cyano, (C1-C4)-alkyl, (C1-C4)-alanyl Alkoxy, (C1-C4)-alkoxy-(C1-C4)-alkoxy, (C1-C4) -alkoxy-(C1-C4)-alkyl, (C1-C4)-haloalkyl and (C1- C4)-haloalkoxy, Cycloalkyl mono- or polysubstituted (preferably up to three) with dialkyl , in particular cycloalkyl substituted by one or two (C1-C4)-alkyl radicals is.

[0082] The compounds of the present invention may be present in preferred embodiments. The embodiments can be combined with each other. It does not include combinations that would be excluded based on expert knowledge. For example, combinations of three or more adjacent Ring structures containing oxygen atoms of the formula: are excluded.

[0083] Isomers The compound represented by formula (I) may exist in the form of a geometric isomer depending on the type of the substituent. and / or in the form of optically active isomers or corresponding isomeric mixtures in various compositions. These stereoisomers can also exist in the form of enantiomers, diastereomers, etc. The present invention therefore provides pure stereoisomers and Any mixtures of these isomers are included.

[0084] Methods and Uses The present invention also relates to a method for controlling pests, wherein the method comprises administering a compound of formula (I): The compound is then allowed to act on the pests and / or their habitat. is practiced in agriculture and forestry and in the protection of materials. Preferably, methods for surgical or therapeutic treatment of the human or animal body and methods for treating human or animal diseases. Diagnostic methods performed on the body of an animal are excluded from the above methods.

[0085] The present invention further relates to compounds of formula (I) as pesticides, in particular as crop protection agents. The present invention also relates to the use of compounds that are

[0086] In the context of this application, the term "pesticide" is used in each case. always also encompasses the term "crop protection agent".

[0087] Good tolerance by plants, desirable toxicity to warm-blooded animals, and good The compounds of formula (I) that exhibit environmental compatibility are capable of mitigating biotic and abiotic stressors. It is suitable for protecting plants and plant organs against loess factors and for increasing yields. It is suitable for improving the quality of crops and is also useful in agriculture and horticulture. in livestock farming, in aquaculture, in forests, in gardens and leisure facilities, in stored products Pests encountered in the protection of materials and materials, and in the field of hygiene, in particular insects, It is suitable for controlling arachnids, helminths, especially nematodes, and mollusks.

[0088] In the context of this patent application, the term "hygiene" refers to the prevention of diseases (especially infectious diseases) Any and all means, methods and practices aimed at preventing, and the prevention of, human and animal Helps protect health and / or the environment and / or maintains cleanliness It is understood to mean any and all means, methods and implementations. means for cleaning, disinfecting and sterilizing, e.g. For example, textile or hard surfaces (especially glass, wood, concrete, porcelain, ceramic) Hand tools for cleaning surfaces made of plastic or even metal(s). means for disinfecting and sterilizing the same and for preventing sanitary pests and / or Means for ensuring that the waste remains free are included. In this connection, preferably, surgical or therapeutic procedures that can be performed on the human or animal body are also included. Devices and diagnostic methods performed on the human or animal body fall within the scope of protection according to the invention. are excluded from the scope.

[0089] The term "field of hygiene" therefore includes those areas in which such hygienic means, methods and practices are important. All areas, technical and industrial applications, such as kitchens, bakeries, airports, bathrooms, Regarding hygiene in swimming pools, department stores, hotels, hospitals, livestock sheds, livestock farms, etc. This includes all areas, technical fields and industrial applications that are relevant to the present invention.

[0090] Therefore, the term "sanitary pest" refers to insects whose presence is problematic in the field of hygiene, especially those is understood to mean one or more pests that are problematic for health reasons. The main purpose is to avoid or minimize the presence of sanitary pests in the field of hygiene. Controlling and / or avoiding or minimizing contact with sanitary pests This is especially important for preventing outbreaks and for tackling existing outbreaks. This can be achieved by applying insecticides that can be used for both It is also possible to use preparations that avoid or reduce contact with pests. Examples of live pests include the organisms listed below.

[0091] Thus, the term "hygienic protection" includes such hygienic means, methods and practices. This includes all actions that maintain and / or improve the quality of the product.

[0092] The compounds of formula (I) can preferably be used as pesticides They are effective against normally sensitive and resistant species and at all developmental stages. The pests may include the following: can: Pests of the Arthropoda phylum, in particular the Arachnida class, e.g., Acarus species ( Acarus spp., e.g., Acarus siro, Ake Aceria kuko, Aceria sherdonii ldoni), Aculops spp., Acul us spp.), e.g., Aculus fockeui , Aculus schlechtendali, Ann Amblyomma spp., Amphitetranychus bienensii Amphitetranychus viennensis, Argus species gas spp.), Boophilus spp., Brevipal Brevipalpus spp., e.g., Brevipalpus hoenisis (Brevipalpus phoenicis), Bryobia graminoum (Bryo bia graminum), Bryobia praetiosa (Bryobia praet iosa), Centruroides spp., Coriopsis Chorioptes spp., Derman yssus gallinae), Dermatophagoides pteronyssinus (Derma tophagoides pteronyssinus), Dermatophagoides phagoides Dermatophagoides farinae, Dermacentor species ( Dermacentor spp.), Eotetranych spp. us spp.), e.g., Eotetranychu hykoriae s hicoriae), Epitrimerus pyri , Eutetranychus spp., e.g., Euteto Eutetranychus banksi, Eriophyes genus Species (Eriophyes spp.), e.g., Eriophyes pili (Eriophy es pyri), Glycyphagus domesticus (Glycyphagus dome sticus), Halotydeus destru ctor), Hemitarsonemus spp., e.g. For example, Hemitarsonemus latus (= Poly Polyphagotarsonemus latus ), Hyalomma spp., Ixodes spp. spp.), Latrodectus spp., Loxoskelet Loxosceles spp., Neutrombicula autumnalis utrombicula autumnalis, Nuphersa species spp.), Oligonychus spp., e.g., Oligonychus spp. Oligonychus coffeae, Oligonychus coffeae Oligonychus coniferarum, Oligonychus i Oligonychus ilicis, Oligonychus indicus gonychus indicus, Oligonyx mangiferus (Oligony chus mangiferus), Oligonychus platensis (Oligonych us pratensis), Oligonychus punicae (Oligonychus pu nicae), Oligonychus yothersi ), Ornithodorus spp., Ornithonisus spp. (Ornithonyssus spp.), Panonychus spp. spp.), e.g., Panonychus citri (=Me Metatetranychus citri, Panonic Panonychus ulmi (=Met atetranychus ulmi), Phyllocopterta oleivora (Phyll ocoptruta oleivora), Platytetranychus multidigitalis (Pl atytetranychus multidigituli), Polyphagotarsonem Polyphagotarsonemus latus, Psoroptes genus species (Psoroptes spp.), Rhipicephalus spp. spp.), Rhizoglyphus spp., Sarcoptes Sarcoptes spp., Scorpio maurus maurus, Steneotarsonemus sp p.), Steneotarsonemus spi nki), Tarsonemus spp., e.g., Tarsonemus Tarsonemus confusus, Tarsonemus pallidus (Tarsonemus pallidus), Tetranych species us spp.), e.g., Tetranychus canadensis (Tetranychus c anadensis), Tetranychus cinnabarinus (Tetranychus ci nnabarinus), Tetranychus tu rkestani), Tetranychus urticae ae), Trombicula alfredduge si), Vaejovis spp., Basate lycopersici ( Vasates lycopersici); From the class Chilopoda, for example, the genus Geophilus spp.), Scutigera spp.; of the order Collembola or class Collembola, e.g., Onychiurus albicilla Onychiurus armatus; Sminturus viridis nthurus viridis); From the class Diplopoda, for example, Blaniurus guttulatus ulus guttulatus); From the class Insecta, for example, from the order Blattodea, for example , Blatta orientalis, Blatta a Blattella asahinai, Blattella germanica ttella germanica), Leucophaea maderae (Leucophae a maderae), Loboptera decipiens (Loboptera decipi ens), Neostylopyga rhombifolia (Neostylopyga rhombi folia), Panchlora spp., Parcobratta spp. (Parcoblatta spp.), Periplaneta spp. spp.), e.g., Periplaneta americana (Periplaneta americana) cana), Periplaneta australasiae (Periplaneta austr alasiae), Pycnoscelus surinamensis (Pycnoscelus suri namensis), Supella longipalpa ; Coleoptera, e.g., Acalinma vitatum ymma vittatum), Acanthocerides obtectus (Acanthosc elides obtectus), Adoretus spp. Aethina tumida, Agelastica arnii astica alni), Agrilus spp., e.g. Agrilus planipennis, Agrilus planipennis Coxalis (Agrilus coxalis), Agrilus bilineatus (Agri agrilus bilineatus, agrilus anx ius), Agriotes spp., e.g., Agriotes . Linneatus (Agriotes linneatus), Agriotes mancus (A griotes mancus, Agriotes obscurus bscurus), Alphitobius diaperinus (Alphitobius dia perinus, Amphimallon solusticialis lstitialis), Anobium punctat um), Anomala dubia, Anoplophora species plophora spp.), e.g., Anoplophora glabripennis (Anopl ophora glabripennis), Anthonomus species spp.), e.g., Anthonomus grandis is), Anthrenus spp., Apio spp. n spp.), Apogonia spp., Atus haemoru Hoidales (Athous haemorrhoidales), Atmaria species (At omaria spp., e.g., Atomaria lin earis), Attagenus spp., Balis caerulescens Baris caerulescens, Brucizius obtectus chidius obtectus), Bruchus spp., e.g. For example, Bruchus pisorum, Bruchus rufimanu Bruchus rufimanus, Cassida spp. ), Cerotoma trifurcata, Ceutrine Ceutorrhynchus spp., e.g. Ceutorrhynchus reed Millis (Ceutorrhynchus assimilis), Ceutorhynchus qua Quadridens (Ceutorrhynchus quadridens), Ceutorhynchus Ceutorrhynchus rapae, Chaetochnema species tocnema spp.), e.g., Chaetocnema confinis (Chaetocn ema confinis), Chaetocnema denticulata (Chaetocnema denticulata), Chaetocnema ectipa (Chaetocnema ect ypa), Cleonus mendicus, Conoderus Conoderus spp., Cosmopolite spp. s spp.), e.g., Cosmopolites sorgizus (Cosmopolites s ordidus), Costelytra zealan deer (Costelytra zealan dica), Ctenicera spp., Curculio spp. Curculio spp., e.g., Curculio cariae (Curculio cariae) yae), Curculio caryatrypes , Curculio obtusus, Curculio saii (Curculio sayi), Cryptolestes ferrugineus (Cryptol estes ferrugineus), Cryptolestes pusillus (Cryptol estes pusillus), Cryptorhynchus lapati (Cryptorhync hus lapathi), Cryptorhynchus mangiferae (Cryptorhyn chus mangiferae), Cylindrocopturus species (Cylindroco pturus spp.), Cylindrocopturus adspersus (Cylindro copturus adspersus, Cylindrocopturus fullnisii (Cyli ndrocopturus furnissi, Dendroctonus species (Dendro ctonus spp.), e.g., Dendroctonus ponderosae (Dendroc tonus ponderosae), Dermestes spp. .), Diabrotica spp., e.g., Diabrotica . Balteata (Diabrotica balteata), Diabrotica barberi (D iabrotica barberi), diabrotica undecimpunctata howal Diabrotica undecimpunctata howardi, Diaphora Diabrotica undecimpunctata undecimpunctata (Diabrotica un decimpunctata undecimpunctata), Diabrotica Bill Ghyfella virgifera (Diabrotica virgifera virgife ra), Diabrotica virgifera zeae (Diabrotica virgife ra zeae), Dichocrocis spp., Dichocrocis Dicladistella armigera, Diloboderus species (D iloboderus spp.), Epicaerus spp. ), Epilachna spp., e.g., Epilachna borealis Epilachna borealis, Epilachna varivestis chna varivestis), Epitrix spp., For example, Epitrix cucumeris, Epitri Epitrix fuscula, Epitrix hiruchipennis ( Epitrix hirtipennis, Epitrix subcrinitae (Epitr ix subcrinita), Epitrix tuberis (Epitrix tuber is), Faustinus spp., Gybium psiloidea Gibbium psylloides, Gnathocerus cornutus ocerus cornutus, Hellula undalis Heteronychus arator, Heteronychus arator Heteronyx spp., Hoplia argentea argentea), Hylamorpha elegans ns), Hylotrupes bajulus, Hypera Hypera postica, Hypomaceae eces squamosus), Hypothenemus sp. p.), e.g., Hypothenemus hampei , Hypothenemus obscurus, Hypo Hypothenemus pubescens, Lacnoste Lachnosterna consanguinea, La Lasioderma serricorne, latex Latheticus oryzae, Lathri dius spp.), Lema spp., Leptinotarsa decemline Atta (Leptinotarsa decemlineata), Leucoptera species (L eucoptera spp.), e.g., Leucoptera copheera (Leucopt era coffeella), Limonius ecty pus, Lissorhoptrus oryzophilus ophilus), Listronotus spp. (= Hippe Hyperodes spp., Lixus spp. , Luperodes spp., Luperomorpha xanthodera ( Luperomorpha xanthodera), Lyctus spp. pp.), Megacyllene spp., e.g. Robiniae (Megacyllene robiniae), Megacelis species (Meg ascelis spp.), Melanotus spp., e.g. For example, Melanotus longulus oregonensis (Melanotus longulus oregonensis, Meligethes aeneus eus), Melolontha spp., e.g., Melolontha Melolontha melolontha, Migdolus species dolus spp.), Monochamus spp., Naupa Naupactus xanthographus, Nec Necrobia spp., Neogaleru cella spp.), Niptus hololeucus (Niptus hololeucu s), Oryctes rhinoceros, Oryzaev Oryzaephilus surinamensis, O Oryzaphagus oryzae, Othiorhynchus genus Species (Otiorhynchus spp.), e.g., Otiorhynchus cribricollis (Otiorhynchus cribricollis), Otiorhynchus ligusti Otiorhynchus ligustici, Otiorhynchus ovatus tiorhynchus ovatus), Othiorhynchus rugosostialus (Ot iorhynchus rugosostriarus), Othiorhynchus sulcatus (Otiorhynchus sulcatus), Oulema sp. p.), e.g., Oulema melanopus, Oulema Oulema oryzae, Oxycetonia jukunda etonia jucunda, Phaedon cochleareae chleariae), Phyllophaga spp., Phyllophaga helleri, Phyllotoreta species (P hyllotreta spp.), e.g., Phyllotreta armolasiae (Phyl lotreta armoraciae, Phyllotreta pusilla (Phyllotre ta pusilla), Phyllotreta ramosa a), Phyllotreta striolata, Popillia japonica, Premnotrypes species (Premnotrypes spp.), Prostephanus torncatus (Pros tephanus truncatus), Psylliodes sp. spp.), e.g., Psylliodes affini s ), Psylliodes chrysocephal a), Psylliodes punctulata, Ptinus spp., Rhizobius ventralis us ventralis), Rhizopertha dominica (Rhizopertha dominica) inica), Rhynchophorus spp., Rhynchophorus Rhynchophorus ferrugineus, Phalaenopsis Rhynchophorus palmarum, Scoritus Scolytus spp., e.g., Scolytus multistriatus (Sc olytus multistriatus), Sinoxylon perforans (Sino xylon perforans, Sitophilus spp. .), for example, Sitophilus granariu s), Sitophilus linearis, Sitof Sitophilus oryzae, Sitophilus zeamais (Sitophilus zeamais), Sphenophorus species rus spp.), Stegobium paniceum (Stegobium paniceu m), Sternechus spp., e.g., Sternechus Sternechus paludatus, Syphiletes species mphyletes spp.), Tanymecus spp., For example, Tanymecus dilaticollis , Tanymecus indicus, Tanymecus Paris Tanymecus palliatus, Tenebrio molitor brio molitor, Tenebrioides mauretanicus (Tenebrioi des mauretanicus, Tribolium spp. .), for example, Tribolium audax, Tribo Tribolium castaneum, Tribolium castaneum Tribolium confusum, Trogoderma species erma spp.), Tychius spp., Xylotrex spp. Xylotrechus spp., Zabrus spp., For example, Zabrus tenebrioides; Dermaptera, for example, Anisolabis maritime solabis maritime), Forficula auricularia (Forficu la auricularia, Labidura riparia ia); Diptera, e.g., Aedes spp., e.g. Aedes aegypti, Aedes albopictus (Aedes albopictus), Aedes sti cticus, Aedes vexans, Agromyza species (Agromyza spp.), e.g., Agromyza frontera (Agromyza frontella), Agromyza parvicornis (Agromyza parvi cornis), Anastrepha spp., Anopheles Anopheles spp., e.g., Anopheles quadrimaculatus (Anopheles quadrimaculatus), Anopheles gumbiae (Anopheles gambiae), Asphondylia species a spp.), Bactrocera spp., e.g. Bactrocera cucurbitae, Bactrocera La dorsalis (Bactrocera dorsalis), Bactrocera oleae (Bactrocera oleae), Bibio hortulanus (Bibio hort ulanus), Calliphora erythrocephala cephala), Calliphora vicina, Serratia Ceratitis capitata, Chironomus species onomus spp., Chrysomya spp., Chryso Chrysops spp., Chrysozona pluvialis ona pluvialis), Cochliomya spp. , Contarinia spp., e.g., Contarinia jo Johnsoni (Contarinia johnsoni), Contarinia nasturtii (C ontarinia nasturtii), Contari nia pyrivora), Contarinia scruzi (Contarinia sch ulzi), Contarinia sorghicola ), Contarinia tritici, Cordylovia Anthropophaga (Cordylobia anthropophaga), Krikoto Cricotopus sylvestris, Cricotopus species (Culex spp.), e.g., Culex pipiens s), Culex quinquefasciatus us), Culicoides spp., Culicateta spp. iseta spp.), Cuterebra spp., Dacus Dacus oleae, Dasineura spp. ), for example, Dasineura brassicae, De Delia spp., e.g., Delia antqua iqua), Delia coarctata, Delia flora Delia florilega, Delia plat ura), Delia radicum, Dermatobia hominis (Dermatobia hominis), Drosophila species spp.), e.g., Drosphila melanogaster (Drosphila mela nogaster, Drosophila suzukii ), Echinocnemus spp., Eureia hercules Ray (Euleia heraclei), Fannia spp. , Gasterophilus spp., Glossina spp. Glossina spp.), Haematopota spp. ), Hydrellia spp., Hydrellia griseola (Hy drellia griseola, Hylemya spp., Hippobosca spp., Hypoderma spp. ma spp.), Liriomyza spp., e.g. Liriomyza brassicae, Liriomyza phidobu Liriomyza huidobrensis, Liriomyza sativae ( Liriomyza sativae), Lucilia spp., For example, Lucilia cuprina, Lutozomyia species ( Lutzomyia spp., Mansonia spp., Mu Musca spp., e.g., Musca domestica estica), Musca domestica vi cina), Oestrus spp., Oscinella fritillaria (Os cinella frit), Paratanytarsus species spp.), Paralauterborniella subcinctus (Paralauterborni ella subcincta), Pegomia or Pegomia species Pegomyia spp., e.g., Pegomyia bet ae), Pegomya hyoscyami, Pegomya ru Pegomya rubivora, Phlebotom species us spp.), Phorbia spp., Pho rmia spp.), Piophila casei, Platycodon Platyparea poeciloptera, Project Prodiplosis spp., Psila rosae osae), Rhagoletis spp., e.g. Rhagoletis cingulata, Rhagoletis completa (Rhagoletis completa), Rhagoletis fausta (Rhagol etis fausta), Rhagoletis inferens (Rhagoletis i ndifferens), Rhagoletis menda x), Rhagoletis pomonella, Sarcof Sarcophaga spp., Simulium spp. pp.), for example, Simulium meridiona le), Stomoxys spp., Tabanus spp. s spp.), Tetanopus spp., Ti pula spp.), e.g. Tipula paludosa , Tipula simplex, Toxotrypana curvica Uda (Toxotrypana curvicauda); Hemiptera, e.g., Acissia acaciaevaileianae (Acizzia acaciaebaileyanae), Acizzia dodonaeae ( Acizzia dodonaeae, Acizzia uncatatoides (Acizzia uncatoides), Acrida turrita, Achillea Acyrthosiphon spp., e.g., Acyrthosiphon pis Acyrthosiphon pisum, Acrogoni species a spp.), Aeneolamia spp., Agonocena Agonoscena spp., Aleurocanthus spp. thus spp.), Aleyrodes proletella (Aleyrodes prolet ella), Aleurolobus barodensis (Aleurolobus baroden sis), Aleurothrix flocco sus), Allocaridara malayensis (Allocaridara malayen sis), Amrasca spp., e.g., Amrasca biguts Amrasca bigutulla, Amrasca devastans a devastans, Anuraphis cardu i), Aonidiella spp., e.g., Aonidiella Aonidiella aurantii, Aonidiella citrina ( Aonidiella citrina, Aonidiella inornata (Aonidie lla inornata), Aphanostigma pili (Aphanostigma pili) iri), Aphis spp., e.g., Aphis citricola (A Aphis citricola, Aphis craccivora ora), Aphis fabae, Aphis holvesi his forbesi), Aphis glycines, Aphis gossypii, Aphis hederae s hederae), Aphis illinoise nsis), Aphis middletoni, Aphis Aphis nasturtii, Aphis nerii erii), Aphis pomi, Aphis spiraecola his spiraecola), Aphis viburniphila niphila), Arboridia apicalis ), Arytainilla spp., Aspidiella spp. pidiella spp.), Aspidiotus spp. ), e.g., Aspidiotus nerii, Atanus Atanus spp., Aulacorthum solani solani), Bemisia tabaci, Blastopusilla Blastopsylla occidentalis, Borei Boreioglycaspis melaleuca e), Brachycaudus helichrysi ), Brachycolus spp., Brevicoryne brassicae Brevicoryne brassicae, Cacopsy lla spp.), e.g., Cacopsylla pyri cola), Calligypona marginata , Capulinia spp., Carneocephala fulgida (C arneocephala fulgida), Ceratovacuna lanigera (Cerato vacuna lanigera), Cercopidae, Ceropla Ceroplastes spp., Chaetosiphon fragaehorii (C haetosiphon fragaefolii), Chionaspis tegalensis (C hionaspis tegalensis), Chlorita onukii (Chlorita onukii), Chondracris rosea, Chromaphis juglandicola , Chrysomphalus aonidum, Chrysomphalus ficus, Chrysomphalina Mbira (Cicadulina mbila), Coccomytilus harii (Coccom ytilus halli), Coccus spp., e.g. Coccus hesperidum, Coccus longulosus Coccus longulus, Coccus pseudomagnoliarum (Coccus pseudomagnoliarum), Coccus virilis idis), Cryptomyzus ribis, Cryptomyzus ribis Cryptoneossa spp., Cten arytaina spp.), Dalbulus spp., Zia Dialeurodes chittendeni, Dialeurodes chittendeni Dialeurodes citri, Dialeurodes citri aphorina citri), Diaspis spp., Jiu Diuraphis spp., Doralis sp. p.), Drosicha spp., Dysaph spp. is spp.), e.g., Dysaphis apiifolia olia), Dysaphis plantaginea ), Dysaphis tulipae, Dysmicoccus spp. (Dysmicoccus spp.), Empoasca spp. .), for example, Empoasca abrupta, Em Empoasca fabae, Empoasca marigna poasca maligna), Empoasca sola na), Empoasca stevensi, Erioso Eriosoma spp., e.g., Eriosoma americanum soma americanum, Eriosoma lanigerum nigerum), Eriosoma pyricola, E Erythroneura spp., Eucalyptolima spp. ucalyptolyma spp.), Euphyllura spp. pp.), Euscelis bilobatus, Ferri Ferrisia spp., Fiorinia sp. p.), Furcaspis oceanica, Geoco Geococcus coffeae, Glycaspis species (Gl ycaspis spp.), Heteropsylla cubana (Heteropsylla cu bana), Heteropsylla spinulosa a), Homalodisca coagulata, Hyalopterus arundinis, Hyalopterus arundinis Hyalopterus pruni, Icery species a spp.), e.g., Icerya purchasi, I Idiocerus spp., Idioscopus spp. opus spp.), Laodelphax striatellus triatellus), Lecanium spp., e.g. Lecanium corni (= Parthenolecanium corni ( Parthenolecanium corni), Lepidosafes species osaphes spp.), e.g., Lepidosaphes ulmi (Lepidosaph es ulmi), Lipaphis erysimi, Rojo Leucasspis japonica (Lopholeucaspis japonica), Rico Lycorma delicatula, Macrosiphum species crosiphum spp.), e.g., Macrosiphum euphorbiae (Macro siphum euphorbiae, Macrosiphum lily m lilii), Macrosiphum rosae, Ma Macrosteles facifrons, Maha Narva spp., Melanaphis sacchari phis sacchari), Metcalfiella species (Metcalfiella s pp.), Metcalfa pruinosa, Metopo Metopolophium dirhodum, Moneria Monellia costalis, Monelliopsis pecanis nelliopsis pecanis), Myzus spp., e.g. Myzus ascalonicus, Myzus cerasi (Myzus cerasi), Myzus ligustri , Myzus ornatus, Myzu persicae s persicae), Myzus nicotianae , Nasonovia ribisnigri, Neomass Neomaskellia spp., Nephotetchchis spp. tettix spp.), e.g., Nephote tettix cincticeps (Nephote ttix cincticeps), Nephotettix nigropictus (Nephote ttix nigropictus), Nettigonicera spectre (Nettigoni clla spectra), Nilaparvata lugens (Nilaparvata lu gens), Oncometopia spp., Orthezia Orthezia praelonga, Oxya chinensis ya chinensis), Pachypsylla spp., Parabemisia myricae, Paratoliosa genus Species (Paratrioza spp.), e.g., Paratrioza cockleri (Para trioza cockerelli), Parlatoria spp. pp.), Pemphigus spp., e.g., Pemphigus Pemphigus bursarius, Pemphigus popplii Pemphigus populivenae, Peregrinus mykiss (Pe regrinus maidis), Perkinsiella species spp.), Phenacoccus spp., e.g. Na Phenacoccus madeirensis, pro Phloeomyzus passerinii, Holod Phorodon humuli, Phylloxera species ra spp.), e.g., Phylloxera devastratrichis devastatrix, Phylloxera notabilis (Phylloxera no tabilis), Pinnaspis aspidistrae (Pinnaspis aspid istrae), Planococcus spp., e.g. Planococcus citri, Prosopidopsilla Flava (Prosopidopsylla flava), Protopulvinaria pyrifolia Lummis (Protopulvinaria pyriformis), Pseudauracus Pseudaulacaspis pentagona, Pseudaulacaspis pentagona Pseudococcus spp., e.g., Pseudococcus ka Pseudococcus calceolariae, Pseudococcus Pseudococcus comstocki, Pseudococcus comstocki Pseudococcus longispinus, Pseudococcus longispinus Pseudococcus maritimus, Pseudococcus Pseudococcus viburni, Psilopsis genus Psyllopsis spp., Psylla spp., e.g. For example, Psylla buxi, Psylla mal i), Psylla pyri, Pteromal species us spp.), Pulvinaria spp., Pillilla spp. (Pyrilla spp.), Quadraspidio tus spp.), e.g., Quadraspiziotus juglansregiae (Quad raspidiotus juglansregiae), Quadraspidiotus male Treaeformis (Quadraspidiotus ostreaeformis), Quadraspidiotus pernisiosus ciosus), Quesada gigas, Lastrococus Rastrococcus spp., Rhopalosi spp. phum spp.), e.g., Rhopalosiphum maydis maidis), Rhopalosiphum oxyacanthae (Rhopalosiphum o xyacanthae), Rhopalosiphum padi ), Rhopalosiphum rufiabdminare (Rhopalosiphum rufiabd ominale), Saissetia spp., e.g., Saissetia Saissetia coffeae, Saissetia miranda (S Saissetia miranda), Saissetia neglecta (Saissetia neglecta), Saissetia oleae, Ska Scaphoideus titanus, Scaphoideus g Schizaphis graminum, Serenaspizus alticulata Selenaspidus articulatus, Siph flava a flava), Sitobion avenae, Sogata Sogata spp., Sogatella fucifera rcifera), Sogatodes spp., Stictocepha La Festina (Stictocephala festina), Siphoninus philippinarum Siphoninus phillyreae, Tenaraphala maraiensi Tenalapha malayensis, Tetragonocephalus species tragonocephela spp.), Tinocaris cariaehoriae (Tino callis caryaefoliae), Tomaspis sp. p.), Toxoptera spp., e.g., Toxoptera Toxoptera aurantii, Toxoptera citricidus (Toxoptera citricidus), Trialeurodes vaporariorum ( Trialeurodes vaporariorum, Trioza species spp.), e.g., Trioza diospyri, Chi Typhlocyba spp., Unaspis spp. spp.), Viteus vitifolii, Zigina spp. (Zygina spp.); The suborder Heteroptera, for example, Aelia spp. pp.), Anasa tristis, Anthethiopsis spp. species (Antestiopsis spp.), Boisea spp. , Blissus spp., Calocoris spp. spp.), Campylomma livida, Caveleri Cavelerius spp., Cimex spp. , e.g., Cimex adjunctus, Cimex Hemipterus (Cimex hemipterus), Cimex rectularius (C Cimex lectularius), Cimex pilos ellus), Collaria spp., Creontiades jill Creontiades dilutus, Dasynu piperis s piperis), Dichelops furcatus s), Diconocoris hewetti, Diconocoris hewetti Dysdercus spp., Euschistus spp. us spp.), e.g., Euschistus herous s), Euschistus servus, Euschistus Euschistus tristigmus, Euschistus Euschistus variolarius, Eurydema genus species (Eurydema spp.), Eurygaster sp p.), Halyomorpha halys, Heliopal Heliopeltis spp., Horci as nobilellus), Leptocorisa spp. ), Leptocorisa varicornis, Leptoglossus occidentalis is), Leptoglossus phyllopus ), Lygocoris spp., e.g., Lygocoris pubulnii Lygocoris pabulinus, Lygus spp. For example, Lygus elisus, Lygus hesperus gus hesperus, Lygus lineolari s), Macropes excavatus, Megaco Megacopta cribraria, Miridae dae), Monalonion atratum, Nezha Nezara spp., e.g., Nezara virizura idula), Nysius spp., Oebalus spp. us spp.), Pentomidae, Piesma quadrata (P iesma quadrata), Piezodorus spp. ), for example, Piezodorus guildinii ), Psallus spp., Pseu dacysta persea), Rhodnius spp., Sahlbergella singularis, Scaptocoris castanea, Scotinoho Scotinophora spp., Stepha nitis nashi), Tibraca spp., Triatoma spp. Species (Triatoma spp.); Hymenoptera, for example, Acromyrmecichus species rmex spp.), Athalia spp., e.g., Athalia Athalia rosae, Atta spp., Campo Camponotus spp., Dolichovespula spp. vespula spp.), Diprion spp., e.g. Diprion similis, Hoplopha species locampa spp.), e.g., Hoplocampa kookaei (Hoplocampa cookei), Hoplocampa testud inea), Lasius spp., Linepithema (Iridiomyrmecium Linepithema (Iridiomyrmex) humile , Monomorium pharaonis, Parato Paratrechina spp., Paravespra spp. spula spp.), Plagiolepis spp., Sirex spp., e.g., Sirex noctilio noctilio, Solenopsis invicta a), Tapinoma spp., Technomyrmecides albipes ( Technomyrmex albipes, Urocerus species pp.), Vespa spp., e.g., Vespa crabro a crabro), Wasmannia auropunctata (Wasmannia auro punctata), Xeris spp.; Isopoda, e.g., Armadillidium vulgare (Arma dillidium vulgare, Oniscus asellus ellus), Porcellio scaber; From the order Isoptera, for example, Coptotermes species mes spp.), e.g., Coptotermes formosanus formosanus, Cornitermes cumulans (Cornitermes c umulans), Cryptotermes spp., Incisitermes spp., Ka lotermes spp.), Microtermes oveci (Microtermes o besi), Nasutitermes spp., Odontothe Odontotermes spp., Porote rmes spp.), Reticulitermes spp. .), for example, Reticulitermes flavipes (Reticulitermes fla vipes, Reticulitermes hes perus); Lepidoptera, e.g., Achro ia grisella), Acronicta major ), Adoxophyes spp., e.g., Adoxophyes Adoxophyes orana, Aedes leucomelas ia leucomelas), Agrotis spp., e.g. , Agrotis segetum, Agrotis epsilon (Agrotis ipsilon), Alabama spp., e.g. For example, Alabama argillacea, Amieloi Amyelois transitella, Anarthia species (A narsia spp.), Anticarsia spp., For example, Anticarsia gemmatalis ), Argyroploce spp., Autographa spp. Autographa spp.), Barathra brassicae (Barathra bra ssicae), Blastodacna atra, Boll Borbo cinnara, Bulatrix tulbergii cculatrix thurberiella), Bupa piniarius (Bupa lus piniarius), Busseola spp., Kako Cacoecia spp., Caloptilia teivora lia theivora), Capua reticulana ), Carpocapsa pomonella, Carposi Carposina niponensis, Carposina niponensis Mata (Cheimatobia brumata), Chilo spp. For example, Chilo plejadellus, Chilo sp lessaris (Chilo suppressalis), Coleucis pariana (Cho reutis pariana), Choristoneura sp. spp.), Chrysodeixis chalcites es), Clysia ambiguella, Cunafaro Cnaphalocerus spp., Cnaphalocerus medinarii Cnaphalocrocis medinalis, Cnephasia species phasia spp.), Conopomorpha spp. ), Conotrachelus spp., Copitarsia spp. (Copitarsia spp.), Cydia spp., e.g. Cydia nigricana, Cydia pomonella a pomonella), Dalaca noctuides ), Diaphania spp., Dipa ropsis spp.), Diatraea saccharalis (Diatraea sacc haralis), Dioryctria spp., e.g. Dioryctria zimmermani, Airy Earias spp., Ecdytropha aurantium lopha aurantium, Elasmopalpus lignocellus (Elasmop alpus lignosellus), Eldana saccharina charina), Ephestia spp., e.g. Ephestia elutella, Ephestia quaeniae Ephestia kuehniella, Epinotia species spp.), Epiphyas postvittan a), Erannis spp., Oerskobiella musculana (E rschoviella musculana), Etiella sp. p.), Eudocima spp., Eulia spp. spp.), Eupoecilia ambiguel la), Euproctis spp., e.g. Euproctis chrysorrhoea, Euproctis species (Euxoa spp.), Feltia spp., Galleria meliloti Galleria mellonella, Gracilaria species laria spp.), Grapholitha spp., e.g. For example, Grapholita molesta, Grapholita pu Grapholita prunivora, Hedyl spp. epta spp.), Helicoverpa spp., e.g. For example, Helicoverpa armigera, Helicoverpa Helicoverpa zea, Heliothi species s spp.), e.g., Heliothis virescens ens), Hepialus spp., e.g., Hepialus hum Hepialus humuli, Hoffmannophila pseudospletera (Ho fmannophila pseudospretella, Homoeosoma species (Ho moeosoma spp.), Homona spp., Hyponomeuta Padella (Hyponomeuta padella), Kakiboria flavofasciata (Kakivoria flavofasciata), Lampid spp. es spp.), Laphygma spp., Raspeiresia Laspeyresia molesta, Leucinodes orbonaris ( Leucinodes orbonalis, Leucoptera species a spp.), e.g., Leucoptera coff eella), Lithocolletis spp., e.g. Lithocolletis blancardella a), Lithophane antennata, Robe Lobesia spp., e.g., Lobesia botlana botrana), Loxagrotis albi costa), Lymantria spp., e.g., Lymantria Lymantria dispar, Lyonetia species ia spp.), e.g., Lyonetia clerke lla), Malacosoma neustria, Ma Maruca testulalis, Mamestra brassicae (Mamestra brassicae), Melanitis leda (Melanitis leda), Mocis spp., Monopis obviera is obviella), Mythimna separata ), Nemapogon cloacellus, Nymph Nymphula spp., Oiketicus sp. p.), Omphisa spp., Opero spp. phtera spp., Oria spp., Ort haga spp.), Ostrinia spp., e.g. Ostrinia nubilalis, Panolis francis Panolis flammea, Parnara spp. , Pectinophora spp., e.g., Pectinophora . Gossypiella (Pectinophora gossypiella), Perileucoptera Perileucoptera spp., Phthorimaea spp. imaea spp.), e.g., Phthorimaea operculella (Phthorimae a operculella), Phyllocnist is citrella), Phyllonorycter spp. pp.), e.g., Phyllonorycter brancaldera (Phyllonorycter blancardella, Phyllonor ycter crataegella), Pieris spp., e.g. For example, Pieris rapae, Platinota strutanana atynota stultana), Plodia interpunctella (Plodia interpunctella), Plusia spp., Plutella Xylostella (Plutella xylostella) (= Plutella macripen) Varnish (Plutella maculipennis), Podesi species a spp.), e.g., Podesia syringae , Prays spp., Prodenia spp. .), Protoparce spp., Pseudaletia spp. seudaletia spp., e.g., Pseu daletia unipuncta), Pseudoplusia includens (Pseu doplusia includens, Pyrausta nubilalis nubilalis), Rachiplusia nu, Skoe Schoenobius spp., e.g., Schoenobius bipun Cutifer (Schoenobius bipunctifer), Silpophaga species ( Scirpophaga spp.), e.g., Scirpophaga innotata (Scirp ophaga innotata), Scotia segetum m), Sesamia spp., e.g., Sesamia inferens (Sesamia inferens), Sparganothi s spp.), Spodoptera spp., e.g. Spodoptera eradiana, Spodoptera eradiana Spodoptera exigua, Spodoptera frugiperda (Sp odoptera frugiperda), Spodoptera praefica (Spodo ptera praefica), Stathmopoda spp. .), Stenoma spp., Stomopteryx subsesivera ( Stomopteryx subsecivella, Synantedon species (Synan thedon spp.), Tecia solanivora , Thaumetopoea spp., Termecia gemmata Squirrel (Thermesia gemmatalis), Tinea croacella (Tinea cloacella), Tinea pellionella , Tineola bisselliella, Tortoriche Tortrix spp., Trichophaga tapetum a tapetzella), Trichoplusia spp. .), e.g., Trichoplusia ni, Tripoliza Incertulas (Tryporyza incertulas), Ivy absoluta (T uta absoluta), Viracola spp.; Orthoptera or Saltatoria, for example, Aketa Acheta domesticus, Dichlopulus species roplus spp.), Gryllotalpa spp., For example, Gryllotalpa gryllotalpa a), Hieroglyphus spp., Locusta spp. ocusta spp.), e.g., Locusta migratoria (Locusta mig ratoria, Melanoplus spp., e.g. Melanoplus devastator, Paratra Paratlanticus ussuriensis, Schistocerca gregaria; From the order Phthiraptera, for example, Damalinia species ia spp.), Haematopinus spp., Rhino Linognathus spp., Pedicul us spp.), Phylloxera vasta trix), Phthirus pubis, Trichodectes species (Trichodectes spp.); From the order Psocoptera, for example, Lepinotus species tus spp.), Liposcelis spp.; From the order Siphonaptera, for example, Ceratophyllus species phyllus spp.), Ctenocephalides spp. spp.), e.g., Ctenocephalides canis (Ctenocephalide s canis), Ctenocephalides felis (Ctenocephalides felis), Pulex irritans, Tunga pene Tunga penetrans, Xenops ylla cheopis); Thysanoptera, e.g., Anaphotryps obscurus Anaphothrips obscurus, Variothrips biformis (B aliothrips biformis), Caetanahothrips leeuweni (Ch aetanaphothrips leeuweni), Drepanothrips leeuweni ( Drepanothrips reuteri), Enneothrips flavens (En neothrips flavens), Frankliniella species lla spp.), e.g., Frankliniella fusca (Frankliniella fusca), Frankliniella occidentalis (Frankliniella occidentalis), Franklinie sculptosa (Franklinie lla schultzei), Frankliniela tritici (Frankliniel la tritici), Frankliniella bassinii (Frankliniella vaccinii), Frankliniella williamsii (Frankliniella williamsi), Haplothrips spp., He Heliothrips spp., Heliothrips femora Squirrel (Hercinothrips femoralis), Chacothrips species (Kak othrips spp.), Rhipiphorothrips cruentatus (Rhipiphor othrips cruentatus), Scirtothri species ps spp.), Taeniothrips cardamomum damomi), Thrips spp., e.g., Thrips palmi (Thrips palmi), Thrips tabaci; Zygentoma (=Thysanura), e.g., Ctenolepisma Genus species (Ctenolepisma spp.), Lepisma saccharina (Lepisma saccharina), Lepismodes inquilinus (Lepismodes i nquilinus, Thermobia domestica ca); From the class Symphyla, for example, Scutigere species lla spp.), e.g., Scutigerella inmaculata immaculata); Pests of the phylum Mollusca, e.g., Bivalvia For example, Dreissena spp.; and also Gastropoda, for example, Arion spp. .), for example, Arion ater rufus, Bio Biomphalaria spp., Bulinus spp. us spp.), Deroceras spp., e.g. Deroceras laeve, Galba spp. ), Lymnaea spp., Oncomelania spp. lania spp.), Pomacea spp., Succinea spp. (Succinea spp.); Plant pests of the phylum Nematoda (i.e., plant-parasitic nematodes), especially Aggrenota Aglenchus spp., e.g., Aglenchus agricola (A glenchus agricola), Anguina spp. For example, Anguina tritici, Aphelenkoi Aphelenchoides spp., e.g., Aphelenchoides Aphelenchoides arachidis, Aphelenchoide Aphelenchoides fragariae, Belonolli Mus species (Belonolaimus spp.), e.g., Belonolaimus gracilis Belonolaimus gracilis, Belonolaimus longicaudatus Belonolaimus longicaudatus, Belonolaimus norvegicus Toni (Belonolaimus nortoni), Bursafelencus species (Bur saphelenchus spp.), e.g., Bursaphelenchus coccophyllus ( Bursaphelenchus cocophilus), Bursaphelenchus elegans Mus (Bursaphelenchus eremus), Bursaphelenchus xylo Bursaphelenchus xylophilus, Cacopaurus genus Cacopaurus spp., e.g., Cacopaurus pestis (Cacop aurus pestis), Criconemella spp. ), for example, Criconemella curvata, Criconemella onoensis, Crico Criconemella ornata, Criconemella lucius Criconemella rusium, Criconemella xenoplakis (Cr iconemella xenoplax)(=Mesocriconema xenoplakis(Me socriconema xenoplax), Criconnemoides species (Cricon emoides spp.), e.g., Cricon emoides ferniae (Cricon emoides ferniae), Criconemoides onoense (Criconem oides onoense), Criconemoides ornatum (Criconemoi des ornatum), Ditylenchus spp. For example, Ditylenchus dipsaci, Dolicho Dolichodorus spp., Globodera spp. ra spp.), e.g., Globodera pallida ), Globodera rostochiensis ), Helicotylenchus spp., e.g. Helicotylenchus dihystera , Hemicriconemoides spp., Hemi Hemicycliophora spp., Heterodera spp. eterodera spp.), e.g., Heterodera avenae (Heteroder a avenae), Heterodera glycine s), Heterodera schachtii, Hills Hirschmaniella spp., Hoplolimus spp. oplolaimus spp.), Longidorus spp. .), e.g., Longidorus africanu s), Meloidogyne spp., e.g., Meloidogyne Meloidogyne chitwoodi, Meloidogyne phala Rachis (Meloidogyne fallax), Meloidogyne hapula (Meloi dogyne hapla), Meloidogyne incognita (Meloidogyne incognita), Meloinema spp., Nacobbus Nacobbus spp., Neotylenchus spp. spp.), Paralongidorus spp., Paraphelenchus spp., Paratrichodorus spp. Species (Paratrichodorus spp.), e.g., Paratrichodorus minor (Paratrichodorus minor), Paratylenchus species (Paraty lenchus spp.), Pratylenchus spp. .), for example, Pratylenchus penetrance (Pratylenchus penetrance) rans), Pseudohalenchus spp., Psilenchus spp., Punct odera spp.), Quinisulcius spp. ), Radopholus spp., e.g., Radopholus citro Radopholus citrophilus, Radopholus similis ( Radopholus similis), Rotylenchu spp. lus spp.), Rotylenchus spp., Scute Scutellonema spp., Subanguina spp. uina spp.), Trichodorus spp., e.g. For example, Trichodorus obtusus, Trichodorus Trichodorus primitivus, Chilencolyne Tylenchorhynchus spp., e.g., Tylenchorhynchus Tylenchorhynchus annulatus, Chilench Tylenchulus spp., e.g., Tylenchulus semipennetra ance (Tylenchulus semipenetrans), Xiphinema species (X iphinema spp.), e.g., Xiphinema index (Xiphinem a index).

[0093] The compounds of formula (I) may optionally be used to remove the May also be used as an herbicide, safener, growth regulator or agent for improving plant properties or a microbicide or gametocide e) as, for example, fungicides, antifungal agents, c) Bactericides or viricides (which also include agents acting against viroids) or to treat MLO (mycoplasma-like organisms) and RLO (rickettsiae Where appropriate, they may also be used as agents against other activating compounds. They can also be used as intermediates or precursors for the synthesis of products.

[0094] Formulation / Usage Form The present invention further relates to formulations, in particular formulations for controlling unwanted animal pests. The formulations can be applied to animal pests and / or their habitats.

[0095] The formulations of the present invention are available in "ready-for-use" form. The formulation can be provided to the end user, i.e., the plant or seed can be sprayed with a spray device or It can be applied directly by suitable equipment such as dusting equipment. Alternatively, the formulation can be Provided to the end user in the form of a concentrate that must be diluted, preferably with water, before use Therefore, unless otherwise indicated, the expression "preparation" refers to such a concentrated whereas the expression "use form" refers to a "ready-to-use" solution, i.e., means the end user as such diluted formulation.

[0096] The formulations of the present invention can be prepared in a conventional manner, for example by incorporating the compounds of the present invention into the formulations disclosed herein. It can be prepared by mixing with one or more suitable adjuvants, such as those listed in can.

[0097] The formulations comprise at least one compound of the invention and at least one agriculturally suitable adjuvant. (e.g., carrier(s) and / or surfactant(s)) .

[0098] Carriers are generally inert, solid or liquid, natural or synthetic organic or inorganic substances. Such carriers generally are suitable for application of the compounds, e.g., to plants, plant parts or seeds. Examples of suitable solid carriers include, but are not limited to, ammonium salts, in particular ammonium sulfate, ammonium phosphate and ammonium nitrate, natural Rock flours, such as kaolin, clay, talc, chalk, quartz, attapulgite, montmorillonite Lilonite and diatomaceous earth, silica gel, and synthetic rock flours, e.g., micronized silica, aluminum Examples of solid carriers typically useful for preparing granules include silicates and silicates. includes, but is not limited to, crushed and fractionated natural rocks, such as calcite, marble, and light Stone, meerschaum and dolomite, synthetic granules consisting of inorganic and organic powders, and organic materials, e.g. Granules made from materials such as burlap, paper, sawdust, coconut shells, corn cobs and tobacco stems Examples of suitable liquid carriers include, but are not limited to, water, organic solvents, and Examples of suitable solvents include polar and non-polar organic solvents. Chemical liquids, such as those selected from the following types: aromatic and non-aromatic carbon Hydrogen compounds (e.g., cyclohexane, paraffins, alkylbenzenes, xylene, thiazolinone, benzene, tetrahydronaphthylene, alkylnaphthalenes, chlorinated aromatic compounds or chlorine chloroaliphatic hydrocarbons, such as chlorobenzenes, chloroethylenes or methylene chloride; Alcohols and polyols, which may optionally be substituted, It may be methylated and / or esterified, e.g., ethanol , propanol, butanol, benzyl alcohol, cyclohexanol or glycol ), ketones (e.g., acetone, methyl ethyl ketone, methyl isobutyl ketone, cyclohexanone, cyclohexanone, esters (which includes fats and oils) and (poly)ethers, unsubstituted and substituted amines, amides (e.g. For example, dimethylformamide or fatty acid amides) and their esters, lactams ( For example, N-alkylpyrrolidones (especially N-methylpyrrolidone) and lactones, Sulfones and sulfoxides (e.g., dimethyl sulfoxide), of plant or animal origin oils, nitriles (alkylnitriles, e.g., acetonitrile, propionotrile, butyronitrile, or aromatic nitriles (e.g., benzonitrile), carbonate esters (cyclic carbonates, such as ethylene carbonate, propylene carbonate, butylene carbonate, or Dialkyl carbonates, such as dimethyl carbonate, diethyl carbonate, dipropyl carbonate, carbonate dibutyl carbonate, dioctyl carbonate). The carrier is a liquefied gas extender, i.e., Liquids that are gases in the It can also be propane, nitrogen, carbon dioxide, and the like.

[0099] Preferred solid carriers are selected from clay, talc and silica.

[0100] Preferred liquid carriers are water, fatty acid amides and their esters, aromatic and non-aromatic carbons. Hydrogen esters, lactams, lactones, carbonates, ketones, (poly)ethers are selected.

[0101] The amount of carrier typically ranges from 1 to 99.99% by weight of the formulation, preferably from 5 to 99.9% by weight, more preferably 10 to 99.5% by weight, and most preferably Preferably, it is in the range of 20 to 99% by weight.

[0102] The liquid carrier typically comprises in the range of 20 to 90% by weight of the formulation, for example 30 to 80% by weight. It exists within the range of %.

[0103] The solid carrier typically comprises in the range of 0 to 50% by weight of the formulation, preferably 5 to 45% by weight. %, for example, in the range of 10 to 30% by weight.

[0104] If the formulation contains two or more carriers, the approximate range refers to the total amount of carriers. do.

[0105] The surfactant may be ionic (cationic or anionic), zwitterionic or non-ionic. surfactants, such as ionic or nonionic emulsifiers, foam formers, dispersants, wetting agents; Examples of suitable surfactants include: Examples include, but are not limited to, polyacrylic acid. salts of ethoxylated poly(α-substituted) acrylate derivatives, salts of lignosulfonic acid (e.g. , sodium lignosulfonate), phenolsulfonic acid or naphthalenesulfonic acid salts of ethyl alcohol or fatty acids or fatty amines, Polycondensation products of ethylene oxide and / or propylene oxide (polyoxyethylene fatty acid esters) ethers, such as castor oil ethoxylates, polyoxyethylene fatty alcohol ethers, For example, alkylaryl polyglycol ethers), substituted phenols (preferably or alkylphenols or arylphenols), salts of sulfosuccinates, Taurine derivatives (preferably alkyl taurates), polyethoxylated alcohols or are phosphate esters of polyethoxylated phenols, fatty esters of polyols (e.g., fatty acid esters of glycerol or sorbitol or sucrose), sulfates (e.g. , alkyl sulfates and alkyl ether sulfates), sulfonates (e.g., alkyl benzoates, aryl sulfonates and alkyl benzene sulfonates), Sulfonated polymer of phthalene / formaldehyde, phosphate ester, protein hydrolyzate solution, lignosulfite waste liquor and methylcellulose. References to salts in this paragraph are Preferably, the respective alkali salts, alkaline earth metal salts and ammonium salts are indicated. do.

[0106] Preferred surfactants are ethoxylated poly(α-substituted) acrylate derivatives, alcohols Polycondensation polymers of ethylene oxide and / or propylene oxide containing polyoxyethylene Ethylene fatty acid ester, alkylbenzene sulfonate, naphthalene / formaldehyde sulfonated polymers of polyoxyethylene fatty acid esters, e.g., castor oil ethoxylates, Select from esters, sodium lignosulfonates and arylphenol ethoxylates will be done.

[0107] The amount of surfactant is typically in the range of 5 to 40% by weight of the formulation, for example 10 to 20 The range is % by weight.

[0108] Further examples of suitable adjuvants include: water repellents, desiccants, binders. (adhesives, tackifiers, fixatives, e.g., carboxymethyl cellulose, and powders or natural and synthetic polymers in the form of granules or latex, e.g., arabic gums, polyvinyl alcohol and polyvinyl acetate, natural phospholipids such as cephalin and lecithin, and synthetic phospholipids, polyvinylpyrrolidone and tylose), thickeners and Secondary thickeners (e.g., cellulose ethers, acrylic acid derivatives, xanthan gum, modified clays, e.g., products available under the name Bentone, and micronized silica), stabilizing agents (e.g., cryostabilizers), preservatives (e.g., dichlorophen, benzyl alcohol hemiphosphates), Lumar, 1,2-benzisothiazolin-3-one, 2-methyl-4-isothiazoline -3-one), antioxidants, light stabilizers, especially UV stabilizers, or chemical and / or is another agent that improves physical stability), dyes or pigments (e.g., inorganic pigments, e.g., Iron oxide, titanium oxide and Prussian Blue; organic dyes, alizarin dyes, azo dyes and metal phthalocyanine dyes), antifoaming agents (e.g., antifoaming agents and magnesium stearate), antifreeze agents, adhesives, gibberellins, and , processing aids, mineral and vegetable oils, aromatic substances, waxes, nutrients (including iron salts, manganese salts, boric acid salts, (including trace nutrients such as copper, cobalt, molybdenum, and zinc salts), protective Colloids, thixotropic materials, penetrating agents, sequestering agents, and complexing agents x former).

[0109] The choice of the adjuvant depends on the intended method of application of the compound of the invention and / or the physical properties of the compound. Furthermore, the adjuvant depends on the properties of the preparation or the use form prepared from the preparation. Selected to impart special properties (technical, physical and / or biological properties) The choice of adjuvants can customize the formulation to suit specific needs. It can be customized.

[0110] The formulations contain an insecticidally / acaricidally / nematicidally effective amount of a compound(s) of the present invention. The term "effective amount" refers to the amount of a substance or material used to control harmful insects / mites / nematodes on cultivated plants. It represents an amount that is sufficient in protection and does not cause substantial damage to the treated plants. Such amounts can vary within wide limits and depend on a variety of factors, e.g., The species of insect / mite / nematode to be controlled, the cultivated plants or materials treated, the climatic conditions and the type of plant used The formulations according to the present invention typically contain 0.01 to 99% by weight of the compound of the present invention. %, preferably 0.05 to 98% by weight, more preferably 0.1 to 95% by weight, More preferably, the compound of the present invention is present in an amount of 0.5 to 90% by weight, and most preferably, in an amount of 1 to 80% by weight. The formulation may contain two or more compounds of the present invention. In this case, the approximate range represents the total amount of the compound of the present invention.

[0111] The formulations of the present invention may be solutions (e.g., aqueous solutions), emulsions, aqueous and oily suspensions. Liquids, powders (e.g., wettable powders, soluble powders), dusts, pastes, granules (e.g., Soluble granules, granules for broadcasting, suspoemulsion formulations, and formulations impregnated with the compound of the present invention. natural or synthetic products, fertilizers, and also microencapsulated in polymeric materials. The compounds of the present invention can be in any conventional formulation type, such as those It can be in suspended, emulsified or dissolved form. Examples of formulation types are solutions, water-soluble concentrates (e.g., SL, LS), and dispersible concentrates (DC). , suspensions and suspension formulations (e.g., SC, OD, OF, FS), emulsions (e.g., EC), Emulsions (e.g., EW, EO, ES, ME, SE), capsules (e.g., CS , ZC), pastes, pastels, wettable powders or dusts (e.g., WP, SP, WS, DP , DS), compression molding agent (e.g., BR, TB, DT), granules (e.g., (e.g., WG, SG, GR, FG, GG, MG), insecticidal products (e.g., LN), and Gel formulations (e.g., GW, GF) for treating plant propagation materials (e.g., seeds) These and further formulation types are designated by the Food and Agriculture Organization of the United Nations (FAO) The outline is defined in the "Catalogue of pesticides for mulation types and international coding System”, Technical Monograph No. 2, 6th Ed. May 2008, Croplife International It is being done.

[0112] Preferably, the formulation of the present invention is in the form of one of the following types: EC, SC, FS, SE, OD, WG, WP, CS, more preferably EC, SC, OD, WG, C S.

[0113] Examples of formulation types and further details regarding their preparation are provided below. When more than one compound of the invention is present, the approximate amount of a compound of the invention is This refers to the total amount of any two or more of the additional ingredients of the formulation. If representatives of the above (e.g., wetting agents, binders) are present, such ingredients are also It is used.

[0114] (i) Water-soluble thickeners (SL, LS) 10 to 60% by weight of at least one compound of the present invention and 5 to 15% by weight of a surfactant ( For example, polycondensation of ethylene oxide and / or propylene oxide containing alcohols. The mixture) is added to water and / or a water-soluble solvent (e.g., proton exchange solvent) in an amount such that the total amount becomes 100% by weight. Alcohols such as pyrene glycol, or carbonates such as propylene carbonate) Dissolve. Before application, dilute the concentrate with water.

[0115] (ii) Dispersible Thickener (DC) 5 to 25% by weight of at least one compound of the present invention and 1 to 10% by weight of a surfactant and and / or binder (e.g., polyvinylpyrrolidone) in such a way that the total amount is 100% by weight. Dissolve in a small amount of organic solvent (e.g., cyclohexanone). Dilute with water to obtain a dispersion. is obtained.

[0116] (iii) Emulsifiable concentrate (EC) 15 to 70% by weight of at least one compound of the present invention and 5 to 10% by weight of a surfactant ( For example, a mixture of calcium dodecylbenzenesulfonate and castor oil ethoxylate , a water-insoluble organic solvent (e.g., an aromatic hydrocarbon or Fatty acid amide) and, if necessary, additional water-soluble solvent. An emulsion is obtained.

[0117] (iv) Emulsifying agents (EW, EO, ES) 5 to 40% by weight of at least one compound of the present invention and 1 to 10% by weight of a surfactant (e.g. For example, a mixture of calcium dodecylbenzenesulfonate and castor oil ethoxylate, or ethylene oxide and / or propylene glycol with or without alcohol Polycondensation of ethylene oxide) in 20 to 40% by weight of a water-insoluble organic solvent (e.g., aromatic carbon This mixture is dissolved in an emulsifier so that the total amount becomes 100% by weight. The resulting formulation is a homogeneous emulsion. The solution can be further diluted with water.

[0118] (v) Suspensions and suspension preparations (v-1) Water-based (SC, FS) In a suitable grinding device (e.g., a stirred ball mill), 20 to 60% by weight of the at least one of the compounds of the present invention is mixed. At least one compound is added to 2 to 10% by weight of a surfactant (e.g., sodium lignosulfonate). and polyoxyethylene fatty alcohol ether), 0.1 to 2% by weight of a thickener (e.g., Addition of a mixture of granules (e.g., xanthan gum) and water and grinding results in a fine suspension of the active substance. The active ingredient is diluted with water to improve its stability. In FS type formulations, up to 40% by weight of binder (e.g. polyvinyl alcohol) is used. Add the alcohol.

[0119] (v-2) Oil-based (OD, OF) In a suitable grinding device (e.g., a stirred ball mill), 20 to 60% by weight of the at least one of the compounds of the present invention is mixed. At least one compound is added to 2 to 10% by weight of a surfactant (e.g., sodium lignosulfonate). and polyoxyethylene fatty alcohol ether), 0.1 to 2% by weight of a thickener (e.g., For example, modified clay, especially Bentone or silica, and an organic carrier are added and milled. A finely divided active substance oil suspension is obtained. The organic carrier is added in an amount of 100% by weight. Upon dilution with water, a stable dispersion of the active substance is obtained.

[0120] (vi) Water dispersible granules and water-soluble granules (WG, SG) 1 to 90% by weight (preferably 20 to 80% by weight, most preferably 50 to 80% by weight) ) at least one compound of the present invention, and sodium alkylnaphthylsulfonate) and optionally a carrier material, and then finely milled. and using typical technical equipment (e.g. extrusion granulation, spray drying granulation, fluidized bed granulation). The surfactant and carrier material are mixed in a total amount of 10% or more to form a water dispersible granule or a water-soluble granule. 0% by weight. Dilution with water gives a stable dispersion or A solution is obtained.

[0121] (vii) Wettable powders and water-soluble powders (WP, SP, WS) 50 to 80% by weight of at least one compound of the present invention in a rotor-stator mill , 1 to 20% by weight of a surfactant (e.g., sodium lignosulfonate, alkyl naphthyl sodium sulfonate) and a solid carrier (e.g., sodium benzoate) in an amount such that the total amount is 100% by weight. Add silica gel and grind. Dilution with water produces a stable dispersion or solution of the active substance. is obtained.

[0122] (viii) Gel preparations (GW, GF) In a stirred ball mill, 5 to 25% by weight of at least one compound of the present invention is mixed with 3 to 10 % by weight of a surfactant (e.g., sodium lignosulfonate), 1-5% by weight of a binder ( For example, carboxymethyl cellulose) and an amount of water to make the total amount 100% by weight. This gives a fine suspension of the active substance. , a stable suspension of the active substance is obtained.

[0123] (ix) Microemulsifiers (MEs) 5 to 20% by weight of at least one compound of the present invention is dissolved in 5 to 30% by weight of an organic solvent blend. (e.g., fatty acid dimethylamide and cyclohexanone), 10-25 wt.% surfactant Agent blends (e.g., polyoxyethylene fatty alcohol ethers and arylphenols) ethoxylate) and water in an amount sufficient to bring the total to 100% by weight. Stir for 1 hour to allow the spontaneous formation of a thermodynamically stable microemulsion.

[0124] (x) Microcapsules (CS) 5 to 50% by weight of at least one compound of the present invention, 0 to 40% by weight of a water-insoluble organic solvent (e.g., aromatic hydrocarbons), 2 to 15% by weight of an acrylic monomer (e.g., methyl methacrylate) The oil phase, which contains a protective coating, is Disperse the polymer in an aqueous solution of a polymer (e.g., polyvinyl alcohol). Poly(meth)acrylate microcapsules are produced by radical polymerization initiated by an agent. Alternatively, 5 to 50% by weight of at least one compound of the present invention, 0 to 40% by weight of % by weight of water-insoluble organic solvent (e.g., aromatic hydrocarbon) and isocyanate monomer (e.g., For example, diphenylmethene-4,4'-diisocyanate) is added to the oil phase by the protective coating. The polymer is dispersed in an aqueous solution of a polyvinyl alcohol (e.g., polyvinyl alcohol), thereby forming a poly Urea microcapsules are formed. Optionally, a polyamine (e.g., hexamethylene Polyurea microcapsules are also formed when a diamine (C) is added to the monomer. S It accounts for 1 to 10% of the total weight of the formulation.

[0125] (xi) Dustable powders (DP, DS) 1 to 10% by weight of at least one compound of the present invention is finely ground to a total of 100% by weight. The mixture is intimately mixed with a suitable amount of solid carrier (e.g., finely divided kaolin).

[0126] (xii) Granules (GR, FG) 0.5 to 30% by weight of at least one compound of the present invention is finely ground, and the total amount is 100% by weight. and combined with an amount of a solid support (e.g., silicate) such that

[0127] (xiii) Ultra-low volume liquids )(UL) 1 to 50% by weight of at least one compound of the present invention, so that the total amount is 100% by weight. The compound is dissolved in an amount of an organic solvent (e.g., an aromatic hydrocarbon).

[0128] Formulation types (i) to (xiii) may optionally contain further adjuvants, for example, 0.1 to 1% by weight of preservative, 0.1 to 1% by weight of antifoaming agent, 0.1 to 1% by weight of dye and / or pigment and 5 to 10% by weight of an antifreeze agent.

[0129] mixture The compounds of formula (I) may be used, for example, in combination with a prolonged action to broaden the spectrum of action. To increase the duration, speed of action, and repulsion Use one or more suitable fungicides, fungicides, or fungicides to prevent the development of resistance. Bactericides, acaricides, molluscicides, nematicides, insecticides, microbiocides oculars), beneficial species, herbicides, fertilizers, bird repellents, plant enhancers (phytotoni c) in mixtures with sterilants, safeners, semiochemicals and / or plant growth regulators Furthermore, such active compound combinations can be used to improve plant growth. and / or tolerance to abiotic factors (e.g., high or low temperatures), Improving tolerance to drought or increased water content or soil salinity Furthermore, it is possible to improve flowering and fruiting performance, and germination ability. It is also possible to optimize the strength and root development, and to facilitate harvesting, It is possible to improve yield, influence maturity and It is also possible to improve the quality and / or nutritional value of the harvested produce. It may also increase shelf life and / or improve the processability of the harvested product It is also possible to do this.

[0130] Additionally, the compounds of formula (I) may be used in combination with other active compounds or semiochemicals (e.g., derivatives). attractants, and / or bird repellents, and / or plant activators, and / or growth regulators, and The compound represented by formula (I) can also be present in a mixture with a fertilizer (and / or fertilizer). The compounds are used to improve plant characteristics (e.g., growth, yield, and quality of the crop). It is also possible to use

[0131] In a particular embodiment according to the invention, the compound of formula (I) is present in the formulation or In the use forms prepared from such formulations, further compounds (preferably those described below) may be present. It exists in a mixed state with other compounds (compounds listed).

[0132] When one of the compounds described below can exist in various tautomeric forms , and in each case, even if not explicitly mentioned, these forms are equally included. Furthermore, all named mixing partners are possible due to their functional groups. If possible, salts can also be formed with suitable bases or acids.

[0133] Insecticides / Acaricides / Nematicides The active compounds identified herein by "common names" are known and For example, the pesticide handbook ("The Pesticide Manual” 16th Ed., British Cro p Protection Council 2012) or It can be found on the internet (e.g., http: / / www.alanw ood.net / pesticides). The classification was The latest IRAC Mode of Action Classification It is based on the "Scheme".

[0134] (1) Acetylcholinesterase (AChE) inhibitors, preferably Carbamates, including alanycarb, aldicarb, bendiocarb, and benflaca Rub, butocarboxim, butoxycarboxim, carbaryl, carbofuran, carbos fluphen, ethiofencarb, fenobucarb, formetanate, furathiocarb, ibuprofen Soprocarb, methiocarb, methomyl, metolcarb, oxamyl, pirimicarb, Lopoxur, thiodicarb, thiofanox, triazamate, trimethacarb, XM C and xylylcarb; or Organic phosphate esters, such as acephate, azamethiphos, azinphos-ethyl, Azinphos-methyl, cadusafos, chlorethoxyphos, chlorfenvinphos, chlor Mephos, chlorpyrifos-methyl, coumaphos, cyanophos, demeton-S-methyl, dimethicone Azinone, dichlorvos / DDVP, dicrotophos, dimethoate, dimethylvinphos, Disulfoton, EPN, Ethion, Ethoprophos, Famfur, Fenamiphos, Fen Nitrothion, fenthion, fosthiazate, heptenophos, imidazophos, isofen Nphos, O-(methoxyaminothiophosphoryl) salicylate isopropyl, isoxathio malathion, mecarbam, methamidophos, methidathion, mevinphos, monocrotophos methicone, naled, omethoate, oxydemeton-methyl, parathion-methyl, phenthoate phosalone, phorate, phosalone, phosmet, phosphamidon, phoxim, pirimiphos-methionine le, profenofos, propetamfos, prothiofos, pyraclofos, pyridaphenthio quinalphos, sulfotep, tebupirimfos, temephos, terbufos, tetrachlor Selected from vinphos, thiometon, triazophos, trichlorfon and vamidothion .

[0135] (2) GABA-regulated chloride channel blockers, preferably Cyclodiene-organochlorine, selected from chlordane and endosulfan or Phenylpyrazoles (fiproles), which consist of ethiprole and fipronil are selected.

[0136] (3) sodium channel modulators, preferably Pyrethroids, which include acrinathrin, allethrin, and d-cis-trans allethrin d-transallethrin, bifenthrin, bioallethrin, bioallethrin s- Cyclopentenyl isomers, bioresmethrin, cycloprothrin, cyfluthrin, beta -Cyfluthrin, cyhalothrin, lambda-cyhalothrin, gamma-cyhalothrin, cyper Methrin, alpha-cypermethrin, beta-cypermethrin, theta-cypermethrin cypermethrin, zeta-cypermethrin, cyphenothrin [(1R)-trans-isomer], delta Methrin, empenthrin [(EZ)-(1R)-isomer], esfenvalerate, Tofenprox, fenpropathrin, fenvalerate, flucythrinate, flu Methrin, Tau-fluvalinate, Halfenprox, Imiprothrin, Kadetrin , momfluorotrin, permethrin, phenothrin [(1R)-trans-isomer], Prallethrin, pyrethrins (pyrethrum), resmethrin, Silaf Luofen, Tefluthrin, Tetramethrin, Tetramethrin [(1R)-isomer], selected from larometrin and transfluthrin; or DDT; or methoxychlor.

[0137] (4) Nicotinic acetylcholine receptor (nAChR) competitive modulators, preferably Or, Neonicotinoids, which include acetamiprid, clothianidin, dinotefuran, and imipenem. selected from dacloprid, nitenpyram, thiacloprid and thiamethoxam; or , nicotine; or sulfoximines, which are selected from sulfoxaflor; or butenolides, which are selected from flupyradifurone; or Mesoionics, which are selected from triflumezopyrim.

[0138] (5) Nicotinic acetylcholine receptor (nAChR) allosteric modulators (Part I), preferably Spinosyns, which are selected from spinetoram and spinosad.

[0139] (6) Allosteric modulation of glutamate-regulated chloride channels (GluCl) Tar, preferably Avermectins / milbemycins, which include abamectin, emamectin benzoate The compound is selected from the group consisting of lepimectin and milbemectin.

[0140] (7) Juvenile hormone mimetics, preferably Juvenile hormone analogs selected from hydroprene, kinoprene and methoprene. or Fenoxycarb; or pyriproxyfen.

[0141] (8) Various unspecified (multi-site) inhibitors, preferably Alkyl halides, selected from methyl bromide and other alkyl halides or Chloropicrin; or sulfuryl fluoride; or borax; or tartar emetic; or Methyl isocyanate generating substances, which are diazomet and metham are selected.

[0142] (9) Chordotonal organ TRPV channel modulators, preferably pyridine azomethanes, selected from pymetrozine and pyrifluquinazone; Or, Pyropenes, which are selected from afidopyropenes.

[0143] (10) Mite growth inhibitors that act on CHS1, such as clofentezine and hexyl It is selected from azox, diflovidazine and etoxazole.

[0144] (11) A microbial disruptor of the insect gut membrane, Bacillus thuringiensis Bacillus thuringiensis subsp. ecies israelensis), Bacillus sphaericus sphaericus), Bacillus thuringiensis subsp. aizawai (Baci Illus thuringiensis subspecies aizawai), Bacillus thuringiensis subsp. kurstaki (Bacillus thuringiensis nsis subspecies kurstaki), Bacillus thuringiensis subspecies tenebrionis (Bacillus thuringiensis subspecies cies tenebrionis) and Bt plant proteins (which include Cry1Ab, Cry1Ac, Cry1Fa, Cry1A.105, Cry2Ab, Vip3A, mCr y3A, Cry3Ab, Cry3Bb and Cry34Ab1 / 35Ab1 ) is selected.

[0145] (12) Inhibitors of mitochondrial ATP synthase, preferably an ATP disruptor, which is selected from diafenthiuron; or Organotin compounds, which consist of azocyclotin, cyhexatin and fenbutatin oxide selected; or Propargite; or tetradifon.

[0146] (13) Uncouplers of oxidative phosphorylation by disrupting the proton gradient, which It is selected from lorfenapir, DNOC and sulfluramide.

[0147] (14) Nicotinic acetylcholine receptor channel blockers, such as bensultat cartap, cartap hydrochloride, thiocylam and thiosultap sodium The compound is selected from the group consisting of ammonium, ammonium hydroxide, ammonium nitrate ...

[0148] (15) A chitin biosynthesis inhibitor acting on CHS1, preferably Benzoyl urea compounds, including bistrifluron, chlorfluazuron, and diflubenzuron Flucycloxuron, Flufenoxuron, Hexaflumuron, Lufenuron, Nova The compound is selected from fluron, noviflumuron, teflubenzuron and triflumuron.

[0149] (16) Chitin biosynthesis inhibitors (type 1), which are selected from buprofezin do.

[0150] (17) Molting disruptors (especially for Diptera, i.e., for dipterans), which is selected from cyromazine.

[0151] (18) Ecdysone receptor agonists, preferably Diacylhydrazines, which include chromafenozide, halofenozide, and methoxyfenozide. tetrazolidinone and tebufenozide.

[0152] (19) Octopamine receptor agonists, which are selected from amitraz.

[0153] (20) Mitochondrial complex III electron transport inhibitors, such as hydramethylnon, It is selected from acequinocyl, fluacrypyrim and bifenazate.

[0154] (21) Mitochondrial complex I electron transport inhibitors, preferably METI acaricides and insecticides, which include fenazaquin, fenpyroximate, pyrimidin, selected from difen, pyridaben, tebufenpyrad and tolfenpyrad; or Rotenone (Derris).

[0155] (22) Voltage-dependent sodium channel blockers, preferably an oxadiazine, selected from indoxacarb; or Semicarbazones, which are selected from metaflumizone.

[0156] (23) Acetyl-CoA carboxylase inhibitors, preferably Tetronic acid derivatives and tetramic acid derivatives, such as spirodiclofen, spiromethicone, The compound is selected from the group consisting of phen, spiropydione and spirotetramat.

[0157] (24) Mitochondrial complex IV electron transport inhibitors, preferably Phosphide-based compounds, which include aluminum phosphide, calcium phosphide, phosphine and phosphorus or zinc chloride; Cyanides, including calcium cyanide, potassium cyanide, and sodium cyanide is selected from.

[0158] (25) Mitochondrial complex II electron transport inhibitors, preferably β-ketonitrile derivatives, which are selected from cyenopyrafen and cyflumetofen. or Carboxanilides, which are selected from piflubumid.

[0159] (28) Ryanodine receptor modulators, preferably Diamides, including chlorantraniliprole, cyantraniliprole, and cyclanilic acid The hydroxybenzoate is selected from riprole, flubendiamide and tetraliniprole.

[0160] (29) Chordotonal organ modulators (target sites undefined), which are The compound is selected from the group consisting of amides.

[0161] (30) GABA-regulated chloride channel allosteric modulators, preferably , Metadiamides, which are selected from broflanilide; or Isoxazoles, which are selected from fluxametamide.

[0162] (31) Baculovirus, preferably Granulosis viruses (GVs), which are transmitted by the codling moth (Cydia pomonella) GV and codling moth (Thaumatotibia leucotreta) (G V); or Nuclear polyhedrosis viruses (NPVs), which are transmitted by the velvet bean caterpillar (Anticarsi a gemmatalis) MNPV and Helicoverpa armigera migera) NPV is selected.

[0163] (32) Nicotinic acetylcholine receptor allosteric modulators (site II) ), which is selected from the GS-omega / kappa HXTX-Hv1a peptide.

[0164] (33) An additional active compound selected from the following: acinonapir, afoxoxo Rayner, azadirachtin, benclothiaz, benzoximate, benzpyrimoxane, Bromopropylate, quinomethionate, chloroprallethrin ethrin), cryolite, cyclobutriflurum (cyclobutriflurum) trifluram or Cyclobutrifen (CAS 1460292-16-3), cycloxapride, cyetopyrafen (Cyetpyr afen), cyhalodiamide, dichloromesothiazide, di Cofol, dimpropyridaz, ε-metofluthrin, ε- Momfluthrin (epsilon-momfluthrin), flometoquin, fluazam Indolizine, Fluensulfone, Flufenerim, Flufenoxystrobin, Fluf Diprole, Fluhexafon, Fluopyram, Flupirimine, Fluralaner, Fufenozy Fupentiofenox (CAS 1472050 -04-6), guadipyr, heptafluthrin, imidacloth, iprodione, isocyanate Cloceram, κ-bifenthrin, κ-tefluthrin, lotilaner, meperfluthrin, Oxazosulfil, paichongding, pyridalyl, Pirifluquinazone, pyriminostrobin, spirobudiclofen lofen), tetramethylfluthrin, tetrachlorantraniliprole, tigoranel (tigolaner), thioxazaphen, thiofluoximate (thiofluo ximate), iodomethane, triflupentoxide e) (CAS 1472050-04-6); and Bacillus firmus (Bac illus firmus)-based preparation (I-1582, BioNeem, Vo tivo), and further the following compound: 1-{2-fluoro-4-methyl-5-[ (2,2,2-trifluoroethyl)sulfinyl]phenyl}-3-(trifluoromethyl (ethyl)-1H-1,2,4-triazol-5-amine (WO2006 / 043635 (known from others) (CAS 885026-50-6), {1'-[(2E)-3-(4-chloro phenyl)prop-2-en-1-yl]-5-fluorospiro[indole-3,4' -piperidine]-1(2H)-yl}(2-chloropyridin-4-yl)methanone (WO 2003 / 106457) (CAS 637360-23-7), 2-chloro- N-[2-{1-[(2E)-3-(4-chlorophenyl)prop-2-en-1-yl ]piperidin-4-yl}-4-(trifluoromethyl)phenyl]isonicotinamide (known from WO2006 / 003494) (CAS 872999-66-1), 3-( 4-chloro-2,6-dimethylphenyl)-4-hydroxy-8-methoxy-1,8-di Azaspiro[4.5]dec-3-en-2-one (known from WO2010052161) (CAS 1225292-17-0), 3-(4-chloro-2,6-dimethylphenyl )-8-Methoxy-2-oxo-1,8-diazaspiro[4.5]dec-3-ene-4- yl ethyl carbonate (known from EP2647626) (CAS 1440516- 42-6), 4-(but-2-yn-1-yloxy)-6-(3,5-dimethylpiperidinyl) (Zin-1-yl)-5-fluoropyrimidine (known from WO2004 / 099160) ( CAS 792914-58-0), PF1364 (already listed in JP2010 / 018586) (CAS 1204776-60-2), (3E)-3-[1-[(6-chloro-3 -pyridyl)methyl]-2-pyridylidene]-1,1,1-trifluoro-propane-2 -on (known from WO2013 / 144213) (CAS 1461743-15-6) , N-[3-(benzylcarbamoyl)-4-chlorophenyl]-1-methyl-3-(phenyl) (trifluoroethyl)-4-(trifluoromethyl)-1H-pyrazole-5-carboxamide Samid (known from WO2010 / 051926) (CAS 1226889-14-0) , 5-bromo-4-chloro-N-[4-chloro-2-methyl-6-(methylcarbamoyl )phenyl]-2-(3-chloro-2-pyridyl)pyrazole-3-carboxamide (C Known from N103232431) (CAS 1449220-44-3), 4-[5-( 3,5-dichlorophenyl)-4,5-dihydro-5-(trifluoromethyl)-3-isopropyl [isoxazolyl]-2-methyl-N-(cis-1-oxido-3-thietanyl)benzal 4-[5-(3,5-dichlorophenyl)-4,5-dihydro-5-(trifluoromethyl) [2-methyl-N-(trans-1-oxide)-3-isoxazolyl]-2-methyl-N-(trans-1-oxide)-3-isoxazolyl -thietanyl)benzamide and 4-[(5S)-5-(3,5-dichlorophenyl)- 4,5-Dihydro-5-(trifluoromethyl)-3-isoxazolyl]-2-methyl -N-(cis-1-oxide-3-thietanyl)benzamide (WO2013 / 0503 17A1) (CAS 1332628-83-7), N-[3-chloro-1-( 3-pyridinyl)-1H-pyrazol-4-yl]-N-ethyl-3-[(3,3,3- (+)-N-[3-chloro-1-(trifluoropropyl)sulfinyl]propanamide -(3-pyridinyl)-1H-pyrazol-4-yl]-N-ethyl-3-[(3,3, 3-trifluoropropyl)sulfinyl]propanamide and (-)-N-[3-chloro 1-(3-pyridinyl)-1H-pyrazol-4-yl]-N-ethyl-3-[(3 ,3,3-trifluoropropyl)sulfinyl]propanamide (WO2013 / 16 2715A2, WO2013 / 162716A2, US2014 / 0213448A1 (known from others) (CAS 1477923-37-7), 5-[[(2E)-3-chloro-2- propen-1-yl]amino]-1-[2,6-dichloro-4-(trifluoromethyl) Phenyl]-4-[(trifluoromethyl)sulfinyl]-1H-pyrazole-3-carboxylate Carbonitrile (known from CN101337937A) (CAS 1105672-77- 2), 3-bromo-N-[4-chloro-2-methyl-6-[(methylamino)thioxomethoxone [ethyl]phenyl]-1-(3-chloro-2-pyridinyl)-1H-pyrazole-5-chlor Voxamide, (Liudaibenjiaxuanan, from CN103109816A Known) (CAS 1232543-85-9); N-[4-chloro-2-[[(1,1- Dimethylethyl)amino]carbonyl]-6-methylphenyl]-1-(3-chloro-2 -pyridinyl)-3-(fluoromethoxy)-1H-pyrazole-5-carboxamide ( Known from WO2012 / 034403A1) (CAS 1268277-22-0), N -[2-(5-amino-1,3,4-thiadiazol-2-yl)-4-chloro-6-methyl 3-bromo-1-(3-chloro-2-pyridinyl)-1H-pyrazole -5-carboxamide (known from WO2011 / 085575A1) (CAS 1233 882-22-8), 4-[3-[2,6-dichloro-4-[(3,3-dichloro-2- propen-1-yl)oxy]phenoxy]propoxy]-2-methoxy-6-(trifluoromethyl)prop ... (fluoromethyl)pyrimidine (known from CN101337940A) (CAS 11081 84-52-6); (2E)- and 2(Z)-2-[2-(4-cyanophenyl)-1- [3-(trifluoromethyl)phenyl]ethylidene]-N-[4-(difluorometh- (Ci)phenyl]hydrazinecarboxamide (known from CN101715774A) (CA S 1232543-85-9);3-(2,2-dichloroethenyl)-2,2-dimethyl 4-(1H-benzimidazol-2-yl)phenyl-cyclopropanecarboxylic acid Ester (known from CN103524422A) (CAS 1542271-46-4) ;(4aS)-7-chloro-2,5-dihydro-2-[[(methoxycarbonyl)[4- [(trifluoromethyl)thio]phenyl]amino]carbonyl]indeno[1,2-e [1,3,4]oxadiazine-4a(3H)-carboxylic acid methyl ester (CN10 2391261A) (CAS 1370358-69-2); 6-deoxy-3 -O-ethyl-2,4-di-O-methyl-,1-[N-[4-[1-[4-(1,1,2 ,2,2-pentafluoroethoxy)phenyl]-1H-1,2,4-triazole-3 -yl]phenyl]carbamate]-α-L-mannopyranose (US2014 / 027 5503A1) (CAS 1181213-14-8); 8-(2-cyclopropyl) (4-trifluoromethyl-phenoxy)-3-(6-trifluoromethyl)-2-methoxy-4-trifluoromethyl-phenoxy -pyridazin-3-yl)-3-aza-bicyclo[3.2.1]octane (CAS 12 53850-56-4), (8-anti)-8-(2-cyclopropylmethoxy-4-thiazolinone (trifluoromethyl-phenoxy)-3-(6-trifluoromethyl-pyridazin-3-yl) (aryl)-3-aza-bicyclo[3.2.1]octane (CAS 933798-27-7) , (8-syn)-8-(2-cyclopropylmethoxy-4-trifluoromethyl-pheno Oxy)-3-(6-trifluoromethyl-pyridazin-3-yl)-3-aza-bicyclo [3.2.1] Octane (WO2007040280A1, WO2007040282A 1) (CAS 934001-66-8), N-[3-chloro-1-(3-pyridyl) N-ethyl-3-[(3,3,3-trifluoromethylphenyl)-1H-pyrazol-4-yl]-N ... (Oropropyl)thio]-propanamide (WO2015 / 058021A1, WO201 5 / 058028A1) (CAS 1477919-27-9), and N-[ 4-(aminothioxomethyl)-2-methyl-6-[(methylamino)carbonyl]phenyl [Nyl]-3-bromo-1-(3-chloro-2-pyridinyl)-1H-pyrazole-5-carboxylate Ruboxamide (known from CN103265527A) (CAS 1452877-50- 7), 5-(1,3-dioxan-2-yl)-4-[[4-(trifluoromethyl)furan [phenyl]methoxy]-pyrimidine (known from WO2013 / 115391A1) (CAS 1449021-97-9), 3-(4-chloro-2,6-dimethylphenyl)-8- Methoxy-1-methyl-1,8-diazaspiro[4.5]decane-2,4-dione (WO Known from 2014 / 187846A1) (CAS 1638765-58-8), 3-( 4-chloro-2,6-dimethylphenyl)-8-methoxy-1-methyl-2-oxo-1 ,8-Diazaspiro[4.5]dec-3-en-4-ylcarbonic acid ethyl ester (WO2 010 / 066780A1, WO2011151146A1) (CAS 122 9023-00-0), 4-[(5S)-5-(3,5-dichloro-4-fluorophenyl -4,5-dihydro-5-(trifluoromethyl)-3-isoxazolyl]-N- [(4R)-2-Ethyl-3-oxo-4-isoxazolidinyl]-2-methyl- Zuamide (known from WO2011 / 067272 and WO2013 / 050302) (CA S 1309959-62-3).

[0165] disinfectant Active ingredients identified herein by "common name" are known and For example, see "The Pesticide Manual (16th Ed.Bri or listed in the National Crop Protection Council (Nat. Or you can search the internet (e.g. www.alanwood.n et / pesticides ).

[0166] All biocidal mixtures named in classes (1) to (15) are If the functional groups allow it, it may also be possible to form salts with suitable bases or acids. All mixing partners named in classes (1) to (15) are to be used where appropriate. may include tautomeric forms.

[0167] (1) Inhibitors of ergosterol biosynthesis, e.g., (1.001) cyproconazole , (1.002) Difenoconazole, (1.003) Epoxiconazole, (1.00 4) Fenhexamid, (1.005) Fenpropidin, (1.006) Fenpropid Morph, (1.007) fenpyrazamine, (1.008) fluquinconazole, (1. 009) Flutriafol, (1.010) Imazalil, (1.011) Imazalil sulfate , (1.012) Ipconazole, (1.013) Metconazole, (1.014) Miconazole Ibutanil, (1.015) Paclobutrazol, (1.016) Prochloraz, (1. 017) Propiconazole, (1.018) Prothioconazole, (1.019) Pyriso Xazol, (1.020) Spiroxamine, (1.021) Tebuconazole, (1.0 22) Tetraconazole, (1.023) Triadimenol, (1.024) Tridemol F, (1.025) Triticonazole, (1.026) (1R,2S,5S)-5-(4 -chlorobenzyl)-2-(chloromethyl)-2-methyl-1-(1H-1,2,4-trimethylbenzyl) (1S,2R,5R)triazol-1-ylmethyl)cyclopentanol, (1.027)(1S,2R,5R )-5-(4-chlorobenzyl)-2-(chloromethyl)-2-methyl-1-(1H-1 ,2,4-triazol-1-ylmethyl)cyclopentanol, (1.028)(2R )-2-(1-chlorocyclopropyl)-4-[(1R)-2,2-dichlorocyclopropyl pyryl]-1-(1H-1,2,4-triazol-1-yl)butan-2-ol, (1 .029)(2R)-2-(1-chlorocyclopropyl)-4-[(1S)-2,2-dichloro Chlorocyclopropyl]-1-(1H-1,2,4-triazol-1-yl)butane- 2-ol, (1.030)(2R)-2-[4-(4-chlorophenoxy)-2-(thiazolinone] [1H-1,2,4-trifluoromethyl)phenyl]-1-(1H-1,2,4-triazol-1-yl) Propan-2-ol, (1.031)(2S)-2-(1-chlorocyclopropyl)-4 -[(1R)-2,2-dichlorocyclopropyl]-1-(1H-1,2,4-triazo (1.032)(2S)-2-(1-chlorocyclohexane)-1-ylbutan-2-ol (1H-1,2-dichloropropyl)-4-[(1S)-2,2-dichlorocyclopropyl]-1-(1H-1, 2,4-triazol-1-yl)butan-2-ol, (1.033)(2S)-2- [4-(4-chlorophenoxy)-2-(trifluoromethyl)phenyl]-1-(1H -1,2,4-triazol-1-yl)propan-2-ol, (1.034)(R -[3-(4-chloro-2-fluorophenyl)-5-(2,4-difluorophenyl) -1,2-oxazol-4-yl](pyridin-3-yl)methanol, (1.035 )(S)-[3-(4-chloro-2-fluorophenyl)-5-(2,4-difluorophenyl) (phenyl)-1,2-oxazol-4-yl](pyridin-3-yl)methanol, (1 .036) [3-(4-chloro-2-fluorophenyl)-5-(2,4-difluorophenyl) (phenyl)-1,2-oxazol-4-yl](pyridin-3-yl)methanol, (1 .037)1-({(2R,4S)-2-[2-chloro-4-(4-chlorophenoxy) phenyl]-4-methyl-1,3-dioxolan-2-yl}methyl)-1H-1,2, 4-Triazole, (1.038)1-({(2S,4S)-2-[2-chloro-4-( 4-chlorophenoxy)phenyl]-4-methyl-1,3-dioxolan-2-yl}methyl (1.039)1-{[3-(2-chlorophenyl)-1H-1,2,4-triazole (phenyl)-2-(2,4-difluorophenyl)oxiran-2-yl]methyl}-1H -1,2,4-triazol-5-yl thiocyanate, (1.040)1-{[rel (2R,3R)-3-(2-chlorophenyl)-2-(2,4-difluorophenyl)o Xylan-2-yl]methyl}-1H-1,2,4-triazol-5-ylthiocyanate ester, (1.041)1-{[rel(2R,3S)-3-(2-chlorophenyl)-2 -(2,4-difluorophenyl)oxiran-2-yl]methyl}-1H-1,2,4 -triazol-5-yl thiocyanate, (1.042)2-[(2R,4R,5R) -1-(2,4-dichlorophenyl)-5-hydroxy-2,6,6-trimethylhepta benzo-4-yl]-2,4-dihydro-3H-1,2,4-triazole-3-thione, ( 1.043)2-[(2R,4R,5S)-1-(2,4-dichlorophenyl)-5-hydroxybenzoate Hydroxy-2,6,6-trimethylheptan-4-yl]-2,4-dihydro-3H-1 ,2,4-triazole-3-thione, (1.044)2-[(2R,4S,5R)-1 -(2,4-dichlorophenyl)-5-hydroxy-2,6,6-trimethylheptane- 4-yl]-2,4-dihydro-3H-1,2,4-triazole-3-thione, (1. 045)2-[(2R,4S,5S)-1-(2,4-dichlorophenyl)-5-hydro [2,4-dihydro-3H-1,2-xy-2,6,6-trimethylheptan-4-yl]-2,4-dihydro- ,4-triazole-3-thione, (1.046)2-[(2S,4R,5R)-1-( 2,4-dichlorophenyl)-5-hydroxy-2,6,6-trimethylheptane-4- yl]-2,4-dihydro-3H-1,2,4-triazole-3-thione, (1.04 7) 2-[(2S,4R,5S)-1-(2,4-dichlorophenyl)-5-hydroxy -2,6,6-trimethylheptan-4-yl]-2,4-dihydro-3H-1,2,4 -triazole-3-thione, (1.048)2-[(2S,4S,5R)-1-(2, 4-dichlorophenyl)-5-hydroxy-2,6,6-trimethylheptan-4-yl ]-2,4-dihydro-3H-1,2,4-triazole-3-thione, (1.049) 2-[(2S,4S,5S)-1-(2,4-dichlorophenyl)-5-hydroxy-2 ,6,6-trimethylheptan-4-yl]-2,4-dihydro-3H-1,2,4-trimethylheptan-4-yl Triazole-3-thione, (1.050) 2-[1-(2,4-dichlorophenyl)-5 -Hydroxy-2,6,6-trimethylheptan-4-yl]-2,4-dihydro-3H -1,2,4-triazole-3-thione, (1.051)2-[2-chloro-4-(2 ,4-dichlorophenoxy)phenyl]-1-(1H-1,2,4-triazole-1- (1.052) 2-[2-chloro-4-(4-chlorophenoxy)-2-yl]propan-2-ol [1H-1,2,4-triazol-1-yl]butane-2- ol, (1.053) 2-[4-(4-chlorophenoxy)-2-(trifluoromethyl [1H-1,2,4-triazol-1-yl]phenyl]-1-(1H-1,2,4-triazol-1-yl)butan-2-ol (1.054) 2-[4-(4-chlorophenoxy)-2-(trifluoromethyl) Phenyl]-1-(1H-1,2,4-triazol-1-yl)pentan-2-ol , (1.055) Mefentrifluconazole, (1.056) 2-{[3-(2-chloro (2,4-difluorophenyl)-2-(2,4-difluorophenyl)oxiran-2-yl]methyl}- 2,4-Dihydro-3H-1,2,4-triazole-3-thione, (1.057)2- {[rel(2R,3R)-3-(2-chlorophenyl)-2-(2,4-difluorophenyl) (phenyl)oxiran-2-yl]methyl}-2,4-dihydro-3H-1,2,4-trimethyl Azole-3-thione, (1.058)2-{[rel(2R,3S)-3-(2-chloro (2,4-difluorophenyl)-2-(2,4-difluorophenyl)oxiran-2-yl]methyl}- 2,4-Dihydro-3H-1,2,4-triazole-3-thione, (1.059)5- (4-chlorobenzyl)-2-(chloromethyl)-2-methyl-1-(1H-1,2,4 -triazol-1-ylmethyl)cyclopentanol, (1.060)5-(allyl 1-{[3-(2-chlorophenyl)-2-(2,4-difluorophenyl 1H-1,2,4-triazole, (1.061 )5-(allylsulfanyl)-1-{[rel(2R,3R)-3-(2-chlorophenoxy) 2-(2,4-difluorophenyl)oxiran-2-yl]methyl}-1H- 1,2,4-Triazole, (1.062) 5-(arylsulfanyl)-1-{[re l(2R,3S)-3-(2-chlorophenyl)-2-(2,4-difluorophenyl) Oxiran-2-yl]methyl}-1H-1,2,4-triazole, (1.063)N '-(2,5-dimethyl-4-{[3-(1,1,2,2-tetrafluoroethoxy)fluorene (phenyl)sulfanyl}phenyl)-N-ethyl-N-methylimidoformamide, (1 .064)N'-(2,5-dimethyl-4-{[3-(2,2,2-trifluoroethoxy (iii)phenyl]sulfanyl}phenyl)-N-ethyl-N-methylimidoformamide , (1.065)N'-(2,5-dimethyl-4-{[3-(2,2,3,3-tetrafluoroethylene (fluoropropoxy)phenyl]sulfanyl}phenyl)-N-ethyl-N-methylimide N'-(2,5-dimethyl-4-{[3-(pentafluoromethyl)methyl] ... (Oroethoxy)phenyl]sulfanyl}phenyl)-N-ethyl-N-methylimido Fluoramide, (1.067)N'-(2,5-dimethyl-4-{3-[(1,1,2,2 -tetrafluoroethyl)sulfanyl]phenoxy}phenyl)-N-ethyl-N-methyl Thilimidoformamide, (1.068)N'-(2,5-dimethyl-4-{3-[(2 ,2,2-trifluoroethyl)sulfanyl]phenoxy}phenyl)-N-ethyl- N-Methylimidoformamide, (1.069)N'-(2,5-dimethyl-4-{3- [(2,2,3,3-tetrafluoropropyl)sulfanyl]phenoxy}phenyl) -N-ethyl-N-methylimidoformamide, (1.070)N'-(2,5-dimethyl 4-{3-[(pentafluoroethyl)sulfanyl]phenoxy}phenyl)-N -Ethyl-N-methylimidoformamide, (1.071)N'-(2,5-dimethyl- 4-phenoxyphenyl)-N-ethyl-N-methylimidoformamide, (1.072 )N'-(4-{[3-(difluoromethoxy)phenyl]sulfanyl}-2,5-di (1.073)N'-methylphenyl)-N-ethyl-N-methylimidoformamide (4-{3-[(difluoromethyl)sulfanyl]phenoxy}-2,5-dimethyl (1.074)N'-[5-phenyl-N-ethyl-N-methylimidoformamide Bromo-6-(2,3-dihydro-1H-inden-2-yloxy)-2-methylpyridin N'-{(2-methyl-3-yl)-N-ethyl-N-methylimidoformamide, (1.075)N ... 4-[(4,5-dichloro-1,3-thiazol-2-yl)oxy]-2,5-dimethyl phenyl}-N-ethyl-N-methylimidoformamide, (1.076)N'-{5 -Bromo-6-[(1R)-1-(3,5-difluorophenyl)ethoxy]-2-methyl {pyridin-3-yl}-N-ethyl-N-methylimidoformamide, (1.077) N'-{5-bromo-6-[(1S)-1-(3,5-difluorophenyl)ethoxy] -2-methylpyridin-3-yl}-N-ethyl-N-methylimidoformamide, (1 .078)N'-{5-bromo-6-[(cis-4-isopropylcyclohexyl)oxy] ci]-2-methylpyridin-3-yl}-N-ethyl-N-methylimidoformamide, (1.079)N'-{5-bromo-6-[(trans-4-isopropylcyclohexyl) (I)oxy]-2-methylpyridin-3-yl}-N-ethyl-N-methylimidoform Amide, (1.080)N'-{5-bromo-6-[1-(3,5-difluorophenyl )Ethoxy]-2-methylpyridin-3-yl}-N-ethyl-N-methylimidoform a Mido, (1.081) Ipfentrifluconazole zole), (1.082) 2-[4-(4-chlorophenoxy)-2-(trifluoro methyl)phenyl]-1-(1H-1,2,4-triazol-1-yl)propane-2 -ol, (1.083)2-[6-(4-bromophenoxy)-2-(trifluoromethyl) [1,2,4-triazol-1-yl]-3-pyridyl]-1-(1,2,4-triazol-1-yl)propane-2- ol, (1.084) 2-[6-(4-chlorophenoxy)-2-(trifluoromethyl -3-pyridyl]-1-(1,2,4-triazol-1-yl)propan-2-ol (1.085) 3-[2-(1-chlorocyclopropyl)-3-(3-chloro-2 -fluoro-phenyl)-2-hydroxy-propyl]imidazole-4-carbonitri and (1.086) 4-[[6-[rac-(2R)-2-(2,4-difluoro phenyl)-1,1-difluoro-2-hydroxy-3-(5-thioxo-4H-1,2 ,4-triazol-1-yl)propyl]-3-pyridyl]oxy]benzonitrile.

[0168] (2) Inhibitors of the respiratory chain at complex I or complex II, e.g., (2.001)beta Nzovindiflupyr, (2.002) bixafen, (2.003) boscalid, (2. 004) Carboxin, (2.005) Fluopyram, (2.006) Flutolanil, ( 2.007) Fluxapyroxad, (2.008) Furametpyr, (2.009) Isoflurane etamide, (2.010) isopyrazam (anti-epimeric enantiomer 1R,4 S,9S), (2.011) isopyrazam (anti-epimeric enantiomer 1S, 4R,9R), (2.012) isopyrazam (anti-epimer racemic compound 1RS ,4SR,9SR), (2.013) isopyrazam (syn-epimer racemic compound (1 RS, 4SR, 9RS) and the anti-epimer racemic compound (1RS, 4SR, 9SR) (2.014) Isopyrazam (syn-epimeric enantiomers 1R,4 S,9R), (2.015) isopyrazam (syn-epimeric enantiomer 1S,4 R,9S), (2.016) isopyrazam (syn-epimer racemic compound 1RS,4 SR,9RS), (2.017) Penflufen, (2.018) Penthiopyrad, (2 .019) Pydiflumetofen, (2.020) Pyraziflumid, (2.021) Sedaki San, (2.022) 1,3-dimethyl-N-(1,1,3-trimethyl-2,3-dihydro- dro-1H-inden-4-yl)-1H-pyrazole-4-carboxamide, (2.0 23) 1,3-dimethyl-N-[(3R)-1,1,3-trimethyl-2,3-dihydro -1H-inden-4-yl]-1H-pyrazole-4-carboxamide, (2.024 )1,3-dimethyl-N-[(3S)-1,1,3-trimethyl-2,3-dihydro-1 H-inden-4-yl]-1H-pyrazole-4-carboxamide, (2.025)1 -methyl-3-(trifluoromethyl)-N-[2'-(trifluoromethyl)biphenyl [2-fluoro-2-yl]-1H-pyrazole-4-carboxamide, (2.026) 2-fluoro -6-(trifluoromethyl)-N-(1,1,3-trimethyl-2,3-dihydro-1 H-inden-4-yl)benzamide, (2.027) 3-(difluoromethyl)-1 -methyl-N-(1,1,3-trimethyl-2,3-dihydro-1H-indene-4-yl) (2.028) IMPYRFLUXAMIDE, ( 2.029) 3-(difluoromethyl)-1-methyl-N-[(3S)-1,1,3-trifluoromethyl] Trimethyl-2,3-dihydro-1H-inden-4-yl]-1H-pyrazole-4-carboxylate Ruboxamide, (2.030) Fluindapyr, (2.031) 3-(difluoromethyl )-N-[(3R)-7-fluoro-1,1,3-trimethyl-2,3-dihydro-1H -inden-4-yl]-1-methyl-1H-pyrazole-4-carboxamide, (2. 032) 3-(Difluoromethyl)-N-[(3S)-7-fluoro-1,1,3-trimethyl- Methyl-2,3-dihydro-1H-inden-4-yl]-1-methyl-1H-pyrazo Fluoro-4-carboxamide, (2.033) 5,8-difluoro-N-[2-(2-fluoro) 4-{[4-(trifluoromethyl)pyridin-2-yl]oxy}phenyl)ethyl quinazolin-4-amine, (2.034) N-(2-cyclopentyl-5-fluoro (benzyl)-N-cyclopropyl-3-(difluoromethyl)-5-fluoro-1-methyl N-(2-tert-butyl)-1H-pyrazole-4-carboxamide, (2.035)N-(2-tert-butyl) (5-methylbenzyl)-N-cyclopropyl-3-(difluoromethyl)-5-fluoro- Oro-1-methyl-1H-pyrazole-4-carboxamide, (2.036)N-(2- tert-Butylbenzyl)-N-cyclopropyl-3-(difluoromethyl)-5-fluoro Fluoro-1-methyl-1H-pyrazole-4-carboxamide, (2.037)N-(5 -chloro-2-ethylbenzyl)-N-cyclopropyl-3-(difluoromethyl)-5 -Fluoro-1-methyl-1H-pyrazole-4-carboxamide, (2.038)N- (5-chloro-2-isopropylbenzyl)-N-cyclopropyl-3-(difluoromethyl) (2.0)-5-fluoro-1-methyl-1H-pyrazole-4-carboxamide 39)N-[(1R,4S)-9-(dichloromethylene)-1,2,3,4-tetrahydrofuran 1,4-Methanonaphthalen-5-yl]-3-(difluoromethyl)-1-methyl- 1H-Pyrazole-4-carboxamide, (2.040)N-[(1S,4R)-9-( Dichloromethylene)-1,2,3,4-tetrahydro-1,4-methanonaphthalene-5- yl]-3-(difluoromethyl)-1-methyl-1H-pyrazole-4-carboxamide (2.041)N-[1-(2,4-dichlorophenyl)-1-methoxypropane- 2-yl]-3-(difluoromethyl)-1-methyl-1H-pyrazole-4-carboxamide N-[2-chloro-6-(trifluoromethyl)benzyl]-N -Cyclopropyl-3-(difluoromethyl)-5-fluoro-1-methyl-1H-pyra 2.043)N-[3-chloro-2-fluoro-6-( Trifluoromethyl)benzyl]-N-cyclopropyl-3-(difluoromethyl)-5 -Fluoro-1-methyl-1H-pyrazole-4-carboxamide, (2.044)N- [5-chloro-2-(trifluoromethyl)benzyl]-N-cyclopropyl-3-(di Fluoromethyl)-5-fluoro-1-methyl-1H-pyrazole-4-carboxamide , (2.045) N-cyclopropyl-3-(difluoromethyl)-5-fluoro-1- Methyl-N-[5-methyl-2-(trifluoromethyl)benzyl]-1H-pyrazole -4-carboxamide, (2.046) N-cyclopropyl-3-(difluoromethyl) -5-fluoro-N-(2-fluoro-6-isopropylbenzyl)-1-methyl-1H -pyrazole-4-carboxamide, (2.047) N-cyclopropyl-3-(difluoromethyl) (2-isopropyl-5-methylbenzyl)-5-fluoro-N-(2-isopropyl-5-methylbenzyl)-1-methyl thyl-1H-pyrazole-4-carboxamide, (2.048)N-cyclopropyl-3 -(Difluoromethyl)-5-fluoro-N-(2-isopropylbenzyl)-1-methyl N-cyclopropyl-1H-pyrazole-4-carbothioamide, (2.049) N-cyclopropyl-3 -(Difluoromethyl)-5-fluoro-N-(2-isopropylbenzyl)-1-methyl N-cyclopropyl-1H-pyrazole-4-carboxamide, (2.050) N-cyclopropyl-3- (Difluoromethyl)-5-fluoro-N-(5-fluoro-2-isopropylbenzyl )-1-Methyl-1H-pyrazole-4-carboxamide, (2.051)N-cyclopropanediol propyl-3-(difluoromethyl)-N-(2-ethyl-4,5-dimethylbenzyl)- 5-Fluoro-1-methyl-1H-pyrazole-4-carboxamide, (2.052)N -Cyclopropyl-3-(difluoromethyl)-N-(2-ethyl-5-fluorobenzene (2.05)-5-fluoro-1-methyl-1H-pyrazole-4-carboxamide 3) N-Cyclopropyl-3-(difluoromethyl)-N-(2-ethyl-5-methylbenzyl) (2. 054) N-Cyclopropyl-N-(2-cyclopropyl-5-fluorobenzyl)-3 -(Difluoromethyl)-5-fluoro-1-methyl-1H-pyrazole-4-carboxylate N-cyclopropyl-N-(2-cyclopropyl-5-methylbenzamide) Benzyl)-3-(difluoromethyl)-5-fluoro-1-methyl-1H-pyrazole- 4-Carboxamide, (2.056) N-cyclopropyl-N-(2-cyclopropylbenzamide) Benzyl)-3-(difluoromethyl)-5-fluoro-1-methyl-1H-pyrazole- 4-Carboxamide, (2.057) pyrapropoin.

[0169] (3) Inhibitors of the respiratory chain at complex III, for example (3.001) Ametoctra Gin, (3.002) Amisulbrom, (3.003) Azoxystrobin, (3.00 4) Coumethoxystrobin, (3.005) Moxystrobin, (3.006) Cyazofamid, (3.007) Dimoxystrobin , (3.008) Enoxastrobin, (3.009) Famoxadone, (3.010) Fenamidon, (3.011) Flufenoxystrobin obin), (3.012) Fluoxastrobin, (3.013) Kresoxime-methionine Le, (3.014) metominostrobin, (3.015) orysastrobin, (3.01 6) Picoxystrobin, (3.017) Pyraclostrobin, (3.018) Pyramet Strobin, (3.019) pyraoxystrobin, (3.020) trifloxystrobin Bin, (3.021)(2E)-2-{2-[({[(1E)-1-(3-{[(E)- 1-Fluoro-2-phenylvinyl]oxy}phenyl)ethylidene]amino}oxy) methyl]phenyl}-2-(methoxyimino)-N-methylacetamide, (3.022 )(2E,3Z)-5-{[1-(4-chlorophenyl)-1H-pyrazol-3-yl ]oxy}-2-(methoxyimino)-N,3-dimethylpent-3-enamide, (3 .023)(2R)-2-{2-[(2,5-dimethylphenoxy)methyl]phenyl} -2-Methoxy-N-methylacetamide, (3.024)(2S)-2-{2-[(2 ,5-dimethylphenoxy)methyl]phenyl}-2-methoxy-N-methylacetami do, (3.025) fenpicoxamid, (3.026) mandestrobin, (3.02 7) N-(3-ethyl-3,5,5-trimethylcyclohexyl)-3-formamide 2-Hydroxybenzamide, (3.028)(2E,3Z)-5-{[1-(4-chloro (2-fluorophenyl)-1H-pyrazol-3-yl]oxy}-2-(methoxy imino)-N,3-dimethylpent-3-enamide, (3.029){5-[3-(2 ,4-dimethylphenyl)-1H-pyrazol-1-yl]-2-methylbenzyl} carbamate Methyl tetraprole, (3.030) Methyl tetraprole, (3.031) Florylpicoxane Samid.

[0170] (4) Mitosis and cell division inhibitors, for example, (4.001) carbendazim, ( 4.002) Diethofencarb, (4.003) Ethaboxam, (4.004) Fluo Picolide, (4.005) Pencycuron, (4.006) Thiabendazole, (4.00 7) Thiophanate-methyl, (4.008) Zoxamide, (4.009) 3-chloro- 4-(2,6-difluorophenyl)-6-methyl-5-phenylpyridazine, (4.0 10) 3-chloro-5-(4-chlorophenyl)-4-(2,6-difluorophenyl) -6-Methylpyridazine, (4.011) 3-chloro-5-(6-chloropyridine-3- yl)-6-methyl-4-(2,4,6-trifluorophenyl)pyridazine, (4.0 12) 4-(2-bromo-4-fluorophenyl)-N-(2,6-difluorophenyl) )-1,3-dimethyl-1H-pyrazol-5-amine, (4.013)4-(2-bromo (2-bromo-6-fluorophenyl)-N-(2-bromo-4-fluorophenyl)-1,3-di Methyl-1H-pyrazol-5-amine, (4.014) 4-(2-bromo-4-fluoro (2-bromophenyl)-N-(2-bromophenyl)-1,3-dimethyl-1H-pyrazole-5 -amine, (4.015) 4-(2-bromo-4-fluorophenyl)-N-(2-chloro (4-fluorophenyl)-1,3-dimethyl-1H-pyrazol-5-amine, .016) 4-(2-bromo-4-fluorophenyl)-N-(2-chlorophenyl)- 1,3-Dimethyl-1H-pyrazol-5-amine, (4.017) 4-(2-bromo- (4-fluorophenyl)-N-(2-fluorophenyl)-1,3-dimethyl-1H-pi 4-(2-chloro-4-fluorophenyl)-N-thiazol-5-amine, (4.018) -(2,6-difluorophenyl)-1,3-dimethyl-1H-pyrazol-5-amine , (4.019) 4-(2-chloro-4-fluorophenyl)-N-(2-chloro-6- Fluorophenyl)-1,3-dimethyl-1H-pyrazol-5-amine, (4.020 )4-(2-chloro-4-fluorophenyl)-N-(2-chlorophenyl)-1,3- Dimethyl-1H-pyrazol-5-amine, (4.021) 4-(2-chloro-4-fluoro (2-fluorophenyl)-N-(2-fluorophenyl)-1,3-dimethyl-1H-pyrazole -5-Amine, (4.022) 4-(4-chlorophenyl)-5-(2,6-difluoro phenyl)-3,6-dimethylpyridazine, (4.023)N-(2-bromo-6-fluoro (2-chloro-4-fluorophenyl)-4-(2-chloro-4-fluorophenyl)-1,3-dimethyl-1H -pyrazol-5-amine, (4.024)N-(2-bromophenyl)-4-(2-chlorophenyl)- (4-fluorophenyl)-1,3-dimethyl-1H-pyrazol-5-amine, 4.025)N-(4-chloro-2,6-difluorophenyl)-4-(2-chloro-4 -fluorophenyl)-1,3-dimethyl-1H-pyrazol-5-amine.

[0171] (5) Compounds capable of acting at multiple sites, e.g., (5.001) Bordeaux mixture, (5. 002) Captafol, (5.003) Captan, (5.004) Chlorothalonil, ( 5.005) Copper hydroxide, (5.006) Copper naphthenate, (5.007) Copper oxide, (5.0 08) Basic copper chloride, (5.009) Copper(2+) sulfate, (5.010) Dithianon, (5 .011) Dodine, (5.012) Folpet, (5.013) Mancozeb, (5.014 ) Maneb, (5.015) Metiram, (5.016) Metiram zinc (metiram zinc), (5.017) copper oxine, (5.018) propineb, (5.019) sulfur Yellow and sulfur agents, for example, calcium polysulfide, (5.020) thiuram, (5.021) di Neb, (5.022) Ziram, (5.023) 6-ethyl-5,7-dioxo-6,7- Dihydro-5H-pyrrolo[3',4':5,6][1,4]dithiino[2,3-c][1 ,2]Thiazole-3-carbonitrile.

[0172] (6) Compounds capable of inducing host defenses, e.g., (6.001) acibenzolar-S -methyl, (6.002) isotianil, (6.003) probenazole, (6.004 )Tiadinil.

[0173] (7) Inhibitors of amino acid and / or protein biosynthesis, e.g., (7.001) cysteine Prodinil, (7.002) Kasugamycin, (7.003) Kasugamycin Hydrochloride Hydrate substance, (7.004) oxytetracycline, (7.005) pyrimethanil, (7.00 6) 3-(5-fluoro-3,3,4,4-tetramethyl-3,4-dihydroisoquinone (1-phenyl)quinoline.

[0174] (8) Inhibitors of ATP production, for example, (8.001) silthiofam.

[0175] (9) Inhibitors of cell wall synthesis, for example, (9.001) benthiavalicarb, (9.0 02) Dimethomorph, (9.003) Flumorph, (9.004) Iprovalicarb, ( 9.005) Mandipropamid, (9.006) Pyrimorph, ( 9.007) Valifenalate, (9.008) (2E)-3-(4-tert-butyl (phenyl)-3-(2-chloropyridin-4-yl)-1-(morpholin-4-yl)propionate L-2-en-1-one, (9.009)(2Z)-3-(4-tert-butylphenyl) (2-chloropyridin-4-yl)-1-(morpholin-4-yl)propan- -2-en-1-on.

[0176] (10) Inhibitors of lipid and membrane synthesis, for example, (10.001) propamocarb, ( 10.002) Propamocarb hydrochloride, (10.003) Tolclofos-methyl.

[0177] (11) Inhibitors of melanin biosynthesis, for example, (11.001) tricyclazole, ( 11.002) 2,2,2-trifluoroethyl {3-methyl-1-[(4-methylbenzoyl) (zoyl)amino]butan-2-yl}carbamate.

[0178] (12) Inhibitors of nucleic acid synthesis, for example, (12.001) benalaxyl, (12.00 2) Benalaxyl-M (chiralaxyl), (12.003) Metalaxyl, (12.00 4) Metalaxyl-M (mefenoxam).

[0179] (13) Signal transduction inhibitors, for example, (13.001) fludioxonil, (1 3.002) Iprodione, (13.003) Procymidone, (13.004) Proquina Zide, (13.005) quinoxyfen, (13.006) vinclozolin.

[0180] (14) Compounds that can act as uncouplers, e.g., (14.001) fluazinam , (14.002) Meptylzinocap.

[0181] (15) Additional fungicides selected from the group consisting of: (15.001) A Bucidic acid, (15.002) Benthazole, (15.003) Bethoxadin, (15 .004) capsimycin, (15.005) carvone, (1 5.006) Chinomethionate, (15.007) Kufraneb, (15.008) Sifr Fenamide, (15.009) Cymoxanil, (15.010) Cyprosulfamide, ( 15.011) Flutianil, (15.012) Fosetyl-aluminum, (15.01 3) Fosetyl-calcium, (15.014) Fosetyl-sodium, (15.015) Methyl isothiocyanate, (15.016) Metrafenone, (15.017) Mildy Omycin, (15.018) Natamycin, (15.019) Dimethyldithiocarbamate Nickel phosphate, (15.020) nitroisopropyl, (15.021) oxamo Oxamocarb, (15.022) Oxathiapiproline, (15.02 3) Oxyfenthiin, (15.024) Pentachlorophen phenols and their salts, (15.025) phosphorous acid and its salts, (15.026) propamocal Propamocarb-fosetylate, (15.027 ) Pyriophenone (chlazafenone), (15.028) Tebufloquine, (15.029) tecloftalam, (15.030) tolnifanide, ( 15.031)1-(4-{4-[(5R)-5-(2,6-difluorophenyl)-4 ,5-dihydro-1,2-oxazol-3-yl]-1,3-thiazol-2-yl} Piperidin-1-yl)-2-[5-methyl-3-(trifluoromethyl)-1H-pyra [4-[(5S)-5-(2-[(2-isopropyl-1-yl)ethanone], (15.032)1-(4-{4-[(5S)-5-(2 ,6-difluorophenyl)-4,5-dihydro-1,2-oxazol-3-yl]- 1,3-thiazol-2-yl}piperidin-1-yl)-2-[5-methyl-3-(thiazol-2-yl)] (trifluoromethyl)-1H-pyrazol-1-yl]ethanone, (15.033) 2-( 6-benzylpyridin-2-yl)quinazoline, (15.034) dipimethitrone, (1 5.035) 2-[3,5-bis(difluoromethyl)-1H-pyrazol-1-yl] -1-[4-(4-{5-[2-(prop-2-yn-1-yloxy)phenyl]-4 ,5-dihydro-1,2-oxazol-3-yl}-1,3-thiazol-2-yl) Piperidin-1-yl]ethanone, (15.036) 2-[3,5-bis(difluoromethyl) ethyl)-1H-pyrazol-1-yl]-1-[4-(4-{5-[2-chloro-6-( (2-yn-1-yloxy)phenyl]-4,5-dihydro-1,2-oxazo {1,3-thiazol-3-yl}-1,3-thiazol-2-yl)piperidin-1-yl]ethanone, (15.037) 2-[3,5-bis(difluoromethyl)-1H-pyrazole-1-yl] 1-[4-(4-{5-[2-fluoro-6-(prop-2-yn-1-yloxy] (phenyl)-4,5-dihydro-1,2-oxazol-3-yl}-1,3-thia (15.038)2-[6-(3-(2-yl)piperidin-1-yl]ethanone, -fluoro-4-methoxyphenyl)-5-methylpyridin-2-yl]quinazoline, ( 15.039)2-{(5R)-3-[2-(1-{[3,5-bis(difluoromethyl )-1H-pyrazol-1-yl]acetyl}piperidin-4-yl)-1,3-thiazo 4,5-dihydro-1,2-oxazol-5-yl}-3-chloro Phenyl methanesulfonate, (15.040)2-{(5S)-3-[2-(1-{ [3,5-bis(difluoromethyl)-1H-pyrazol-1-yl]acetyl}piperi

[0043] [1,3-thiazol-4-yl]-4,5-dihydro-1,2-oxo {5-chloro-1,2-benzotriazol-5-yl}-3-chlorophenyl methanesulfonate, (15.041) Pflufenoquine, (15.042) 2-{2-fluoro-6-[(8-fluoro-2- Methylquinolin-3-yl)oxy]phenyl}propan-2-ol, (15.043 ) Fluoxapiproline, (15.044) 2-{3-[2-(1-{[3,5-bis( Difluoromethyl)-1H-pyrazol-1-yl]acetyl}piperidin-4-yl) -1,3-thiazol-4-yl]-4,5-dihydro-1,2-oxazol-5-yl {phenyl}phenyl methanesulfonate, (15.045) 2-phenylphenol and salts, (15.046) 3-(4,4,5-trifluoro-3,3-dimethyl-3,4-dihydro (Isoquinolin-1-yl)quinoline, (15.047) quinofumelin melin), (15.048) 4-amino-5-fluoropyrimidin-2-ol (alternatively Mutant form: 4-amino-5-fluoropyrimidin-2(1H)-one), (15.04 9) 4-oxo-4-[(2-phenylethyl)amino]butanoic acid, (15.050) 5 -Amino-1,3,4-thiadiazole-2-thiol, (15.051) 5-chloro- N'-Phenyl-N'-(prop-2-yn-1-yl)thiophene 2-sulfonohydride Razide, (15.052) 5-fluoro-2-[(4-fluorobenzyl)oxy]pyridine 5-Fluoro-2-[(4-methylbenzyl)amino]-4-amine, (15.053) 9-Fluoro-2,2-dimethyl-5-pyrimidin-4-amine, (15.054) -(Quinolin-3-yl)-2,3-dihydro-1,4-benzoxazepine, (15. 055) but-3-yn-1-yl{6-[({[(Z)-(1-methyl-1H-tetramethyl (5-phenyl)methylene]amino}oxy)methyl]pyridin-2-yl {2Z}carbamate, (15.056)(2Z)-3-amino-2-cyano-3-phenyl Ethyl acrylate, (15.057) Phenazine-1-carboxylic acid, (15.058) 3 , 4,5-trihydroxybenzoic acid propyl, (15.059) quinolin-8-ol, (15.060) Quinolin-8-ol sulfate (2:1), (15.061) {6 -[({[(1-methyl-1H-tetrazol-5-yl)(phenyl)methylene]amino tert-Butyl]pyridin-2-yl}carbamate, (15.0 62) 5-Fluoro-4-imino-3-methyl-1-[(4-methylphenyl)sulfonyl] 1H-3,4-dihydropyrimidin-2(1H)-one, (15.063) aminopyridine phenoxy)-5-(2-chloro-4-(2-fluorophenoxy)-5- Methylphenyl]-N-ethyl-N-methylimidoformamide), (15.065) ( N'-(2-chloro-5-methyl-4-phenoxyphenyl)-N-ethyl-N-methyl imidoformamide), (15.066)(2-{2-[(7,8-difluoro-2-methyl (chiruquinolin-3-yl)oxy]-6-fluorophenyl}propan-2-ol), (15.067) (5-bromo-1-(5,6-dimethylpyridin-3-yl)-3,3 -dimethyl-3,4-dihydroisoquinoline), (15.068)(3-(4,4-difluoroisoquinoline), Fluoro-5,5-dimethyl-4,5-dihydrothieno[2,3-c]pyridin-7-yl )quinoline), (15.069)(1-(4,5-dimethyl-1H-benzimidazole) -1-yl)-4,4-difluoro-3,3-dimethyl-3,4-dihydroisoquinoline ), (15.070) 8-fluoro-3-(5-fluoro-3,3-dimethyl-3,4- Dihydroisoquinolin-1-yl)quinolone, (15.071) 8-fluoro-3-(5 -Fluoro-3,3,4,4-tetramethyl-3,4-dihydroisoquinolin-1-yl )Quinolone, (15.072)3-(4,4-difluoro-3,3-dimethyl-3,4- Dihydroisoquinolin-1-yl)-8-fluoroquinoline, (15.073)(N-methyl N-phenyl-4-[5-(trifluoromethyl)-1,2,4-oxadiazo]thyl (15.074) (methyl {4-[5-(trifluoromethyl-3-yl]benzamide) methyl)-1,2,4-oxadiazol-3-yl]phenyl}carbamate), (1 5.075)(N-{4-[5-(trifluoromethyl)-1,2,4-oxadiazo (15.076) N-methyl-3-ylbenzyl}cyclopropanecarboxamide 4-(5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl)benzyl N-[(E)-methoxyiminomethyl]-4-[5-(triazol-2-yl)methyl]-4-[(methylaminomethyl) ... (trifluoromethyl)-1,2,4-oxadiazol-3-yl]benzamide, (15 .078)N-[(Z)-Methoxyiminomethyl]-4-[5-(trifluoromethyl) -1,2,4-oxadiazol-3-yl]benzamide, (15.079)N-[4 -[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]phenyl ]Cyclopropanecarboxamide, (15.080)N-(2-fluorophenyl)-4 -[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]benzal amide, (15.081) 2,2-difluoro-N-methyl-2-[4-[5-(trifluoromethyl)-2,2-difluoro-N-methyl ... (1,2,4-oxadiazol-3-yl)phenyl]acetamide, (1,2,4-oxadiazol-3-yl)phenyl]acetamide, 15.082) N-Allyl-N-[[4-[5-(trifluoromethyl)-1,2,4- Oxadiazol-3-yl)phenyl]methyl]acetamide, (15.083)N- [(E)-N-Methoxy-C-methyl-carbonimidoyl]-4-(5-(trifluoromethyl) 1,2,4-oxadiazol-3-yl]-benzamide, (15.08 4) N-[(Z)-N-methoxy-C-methyl-carbonimidoyl]-4-[5-(trimethylsilyl) (trifluoromethyl)-1,2,4-oxadiazol-3-yl]benzamide, (15 .085)N-Allyl-N-[[4-[5-(trifluoromethyl)-1,2,4-oxo Sadiazol-3-yl]phenyl]-methyl]propanamide, (15.086) 4, 4-Dimethyl-1-[[4-[5-(trifluoromethyl)-1,2,4-oxadiazo N-methyl-3-ylphenylmethylpyrrolidin-2-one, (15.087) 4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]benzoyl Benzenecarbothioamide, (15.088) 5-methyl-1-[[4-[5-(trifluoromethyl) (1,2,4-Oxadiazol-3-yl)phenyl]methyl]pyrrolidine N-((2,3-difluoro-4-[(5-(trifluoromethyl)-2-one) (trimethyl)-1,2,4-oxadiazol-3-yl]phenyl]methyl]-3,3, 3-Trifluoro-propanamide, (15.090) 1-methoxy-1-methyl-3- [[4-[5-(trifluoromethyl}-1,2,4-oxadiazol-3-yl] phenyl]methyl]urea, (15.091) 1,1-diethyl-3-[[4-[5-(triphenylmethyl)urea Fluoromethyl {1,2,4-oxadiazol-3-yl]phenyl]methyl]urea , (15.092)N-[[4-[5-(trifluoromethyl)-1,2,4-oxazolidinyl] Azol-3-yl]phenyl]methyl]propanamide, (15.093) N-Methoxy cis-N-[[4-[5-(trifluoromethyl)-1,2,4-oxadiazole-3- 1-Methoxyphenylmethylcyclopropanecarboxamide, (15.094) 3-methyl-1-[[4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl] phenyl]methyl]urea, (15.095)N-methoxy-N-[[ 4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]phenyl N,2-Dimethoxy-N -[[4-[5-(trifluoromethyl}-1,2,4-oxadiazol-3-yl] centre N-ethyl-2-methyl-N-[[phenylmethyl]propanamide, (15.097) 4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl)phenyl methyl]propanamide, (15.098) 1-methoxy-3-methyl-1-[[4 -[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]phenyl ]methyl]urea, (15.099) 1,3-dimethoxy-1-[[4-[5-(trifluoromethyl) (1,2,4-oxadiazol-3-yl)phenyl]methyl]urea, ( 15.100) 3-Ethyl-1-methoxy-1-[[4-[5-(trifluoromethyl) -1,2,4-Oxadiazol-3-yl]phenyl]methyl]urea, (15.101 )1-[[4-[5-(trifluoromethyl)-1,2,4-oxadiazole-3-yl phenyl]phenyl]methyl]piperidin-2-one, (15.102) 4,4-dimethyl-2 -[[4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl] Phenyl]methyl]isoxazolidin-3-one, (15.103) 5,5-dimethyl -2-[[4-[5-(trifluoromethyl)-1,2,4-oxadiazole-3-yl] [phenyl]phenyl]methyl]isoxazolidin-3-one, (15.104) 3,3-dimethyl 1-[[4-[5-(trifluoromethyl)-1,2,4-oxadiazole-3 -yl]phenyl]methyl]piperidin-2-one, (15.105) 1-[[3-fluro Oro-4-(5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl) -phenyl]methyl]azepan-2-one, (15.106) 4,4-dimethyl-2-[ [4-(5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]- phenyl]methyl]isoxazolidin-3-one, (15.107) 5,5-dimethyl- 2-[[4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl ]phenyl]methyl]isoxazolidin-3-one, (15.108)(1-{4-[ 5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]benzyl}- 1H-pyrazol-4-yl) ethyl acetate, (15.109) N,N-dimethyl-1-{ 4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]benzene {1H-1,2,4-triazole-3-amine, and (15.110)N-{2 ,3-Difluoro-4-[5-(trifluoromethyl)-1,2,4-oxadiazole -3-yl]benzyl}butanamide.

[0182] Biological pesticides as mixture components The compounds of formula (I) may be combined with a biological pesticide.

[0183] Biological pesticides include, inter alia, bacteria, fungi, yeasts, plant extracts and microbial pesticides. The term "enzyme" includes products (e.g., proteins and secondary metabolites) formed by the enzyme.

[0184] Biological pesticides include bacteria, e.g., spore-forming bacteria, root-colonizing bacteria, and These include bacteria that act as pesticides, fungicides or nematicides, and bacteria that act as biological insecticides, fungicides or nematicides.

[0185] The above-mentioned bacteria are used or can be used as biological pesticides. An example is the following: Bacillus amyloliquefaciens iens strain FZB42 (DSM 231179) or Bacillus cereus (Bac Bacillus cereus), especially B. cereus strain CN CM I-1562, or Bacillus firmus strain I-1582 (accession number CNCM I-1582), or Bacillus pumilus (B Acillus pumilus), in particular strain GB34 (accession number ATCC 7008 14) and strain QST2808 (accession number NRRL B-30087), or Bacillus Bacillus subtilis, in particular strain GB03 (accession number ATCC SD-1397) or Bacillus subtilis tilis strain QST713 (accession number NRRL B-21661), or Bacillus Bacillus subtilis strain OST 30002 (accession number NRRL B-50421), Bacillus thuringiensis (Bacillus thuringiensis uringiensis), especially Bacillus thuringiensis subsp. israerensis B. thuringiensis subspecies israelensi s) (antigenic type H-14) strain AM65-52 (accession number ATCC 1276), or Bacillus thuringiensis subspecies Aizawai (B. thuringiensis subsp. aizawai), in particular strain ABTS-1857 (SD-1372), Bacillus thuringiensis subsp. kurstaki (B. thuringiensis s subsp. kurstaki) strain HD-1, or Bacillus thuringiensis Subspecies tenebrionis (B. thuringiensis subsp. tene brionis strain NB 176 (SD-5428), Pasteuria penetrans (P asteuria penetrans), Pasteuria species (Pasteuria s pp.) (Rotylenchulus reniformis (Rotylenchulus reniformis rmis)-PR3 (accession number ATCC SD-5834), Streptomyces Streptomyces microflavus strain AQ612 1 (= QRD 31.013, NRRL B-50550), Streptomyces galli Streptomyces galbus strain AQ 6047 (accession number NRR L 30232).

[0186] Fungi and yeasts that are or can be used as biological pesticides Examples of classes are: Beauveria bassiana, specifically strain ATCC 74040, Coniothyrium minitans (Coniothyrium minita ns), in particular, strain CON / M / 91-8 (accession number DSM-9660), Lecanisiriu Lecanicillium spp., in particular strain HRO LEC 12, Lecanicillium lecanii (formerly known as Known as Verticillium lecanii In particular, strain KV01, Metarhizium anisopliae (Metarhizium anisopliae), in particular strain F52 (DSM3884 / ATCC 90448) , Metschnikowia fructico la), in particular, strain NRRL Y-30752, Paecilomyces fumosoroseus (Pae cilomyces fumosoroseus) (Current: Isaria fumosorosea (I saria fumosorosea), in particular the strain IFPC 200613 or the strain Ap opka 97 (accession number ATCC 20874), Paecilomyces lilacinus (P aecilomyces lilacinus), especially Paecilomyces lilacinus ( P. lilacinus) strain 251 (AGAL 89 / 030550), Talaromyces Talaromyces flavus, especially strain V117b, Trichoderma Trichoderma atroviride, especially strain SC 1 (Accession number CBS 122089), Trichoderma harzianum (Trichod erma harzianum), especially Trichoderma harzianum riffai (T. harzianum rifai)T39 (accession number CNCM I-952).

[0187] Viruses that are or can be used as biological pesticides An example is the following: Smaller apple tortrix (Adoxophyes orana) granulosis virus (GV) , codling moth (Cydia pomonella) granulosis virus (GV), tobacco Helicoverpa armigera nuclear polyhedrosis virus (NPV), Spodoptera exigua mNPV, Spodoptera exigua (Spodoptera frugiperda) mNPV, Egyptian armyworm (Afri can cotton leafworm)(Spodoptera littoral is) NPV.

[0188] added as an "inoculum" to a plant or plant part or plant organ, Bacteria and fungi that promote plant growth and plant health through certain properties are also included. Examples that can be given are: Agrobacterium spp., Azorhizobium Azorhizobium caulinodans, Azospirill Azospirillum spp., Azotobacter spp. cter spp.), Bradyrhizobium spp. .), Burkholderia spp., especially Burkholderia Burkholderia cepacia (formerly known as Pseudomonas cepacia) Monas cepacia (formerly known as Pseudomonas cepacia), Gigaspora spp. or Gigaspora monosporum (Gi gaspora monosporum), Glomus spp., Laccaria spp., Lactobacillus buchneri obacillus buchneri, Paraglomus species spp.), Pisolithus tinctorus , Pseudomonas spp., Rhizobium spp. zobium spp.), especially Rhizobium trifolii (Rhizobium tr ifolii), Rhizopogon spp., Scleroderma Scleroderma spp., Suillus spp. ), Streptomyces spp.

[0189] Plant extracts that are or can be used as biological pesticides and products formed by microorganisms (which include proteins and secondary metabolites) ) is the following: Garlic (Allium sativum), Wormwood (Artemisia absinthium) inthium, azadirachtin, Biokeeper WP, Cassia nigricans, Celastrus Celastrus angulatus, American antler plant (C henopodium anthelminticum), chitin, Armour-Ze n, Dryopteris filix-mas, Horsetail (Equi setum arvense), Fortune Aza, Fungastop, Hea ds Up (Quinopodium quinoa saponin extract), insect repellent Chrysanthemum (Pyrethrum / Pyrethrins), Surinam bittersweet (Quassia amara), Quercus, Quillaja, Rega lia, ("Requiem TM Insecticide), rotenone, riania / Ryanodine, Symphytum officinale, Artemisia (Tanacetum vulgare), Thymol, Triact 70, TriCo n, nasturtium (Tropaeulum majus), nettle (Urtic a dioica), Veratrin, European mistletoe (Viscum album ), Brassicaceae extracts, especially rapeseed flour or mustard flour and bio-insecticidal / acaricidal active substances obtained from olive oil, in particular e.g. Charcoal, the active ingredient in products bearing the brand name FLiPPER® Chain length C 16 -C 20 Unsaturated fats / carboxylic acids with

[0190] Safeners as blend components The compounds of formula (I) can be used as safeners, e.g., benoxacor, cloquintocet, (-mexyl), cyometrinil, cyprosulfamide, dichlormid, fenchlor (-ethyl), fenclorim, flurazole, fluxofenim, furilazole , Isoxadifen (-ethyl), Mefenpyr (-diethyl), Naphthalic anhydride, Xabetrinil, 2-methoxy-N-({4-[(methylcarbamoyl)amino]phenyl (phenyl)sulfonyl)benzamide (CAS 129531-12-0), 4-(dichloroaza Cetyl)-1-oxa-4-azaspiro[4.5]decane (CAS 71526-07- 3), 2,2,5-trimethyl-3-(dichloroacetyl)-1,3-oxazolidine ( It can be combined with other compounds such as CAS 52836-31-4.

[0191] Plants and plant parts All plants and plant parts can be treated according to the invention, where the plants are desirable and undesirable wild or crop plants (including naturally occurring crop plants) All plants and plant parts such as cereals (wheat, rice, triticale, barley, rye, oats), corn, soybeans, potatoes, sugar beets, sugar Squid, tomato, pepper, cucumber, melon, carrot, watermelon, onion, lettuce, Spinach, leeks, kidney beans, Brassica oleracea) (e.g., cabbage) and other vegetable species, cotton, tobacco, rapeseed, etc. and, in addition, fruit plants (fruit-bearing plants, apples, pears, citrus fruits and grapevines). ) etc. Crop plants are those obtained by conventional breeding and optimization methods. The plant may be a plant capable of producing the desired product or may be obtained by biotechnological and genetic engineering methods. or a plant obtainable by a combination of the above methods. Such crop plants also include transgenic plants, It also includes plant varieties that may or may not be protected by variety ownership rights. Plants include all stages of development, such as seeds, seedlings, and young plants (immature plants). The term should be understood to mean the mature plant. Plant parts include shoots, leaves, flowers, etc. is understood to mean all parts and organs of the plant, both above-ground and below-ground, such as the roots and Examples that may be mentioned include leaves, needles, stems, trunks, flowers, fruiting bodies, fruits and seeds, as well as and further including tubers, roots and rhizomes. Harvested plants or harvested plant parts, and vegetative propagation organs al) and reproductive organs (generative propagation mater ial), such as seedlings, tubers, rhizomes, cuttings and seeds, also include plant parts. is included in the part.

[0192] The treatment according to the invention of plants and plant parts with compounds of formula (I) can be carried out in the conventional manner. By various treatment methods, for example, immersion, spraying, vaporization, fogging, scattering, The compounds may be applied directly to the plant or plant parts by application, injection, etc., or by injecting the compounds into the surrounding area of the plant or plant parts. , by acting on the environment or storage space, Also, in the case of propagation material, especially seeds, may also be achieved by applying one or more coatings.

[0193] As already mentioned above, all plants and their parts can be treated according to the invention. In a preferred embodiment, wild plant species and plant cultivars, or hybrids or progeny, can be used. Plant species and plant cultivars obtained by conventional biological breeding methods such as rotoplast fusion, In yet another preferred embodiment, the portions are further processed. Transgenics obtained by genetic engineering methods, sometimes in combination with conventional methods. Plants and plant cultivars (genetically modified organisms) and their parts are treated. rts) or "parts of plants" or "parts of plants" The invention is particularly preferably are treated with plants of conventional varieties that are commercially available or in use, respectively. Plant varieties are developed by conventional breeding or by mutagenesis or recombinant DNA techniques. is understood to mean a plant with new properties ("traits") obtained by artifical means. They can be cultivars, varieties, biotypes or genotypes.

[0194] Transgenic plants, seed treatments and integration events According to the invention, the compounds of formula (I) are advantageously administered to transgenic plants, Receiving genetic material that confers advantageous and / or useful characteristics (traits) on plant varieties or plant parts. can be used to treat those plants, plant varieties or plant parts that have been harvested. Thus, the present invention relates to one or more recombinant traits or transgenic events or It is contemplated that these combinations may be combined. A transgenic event occurs at a specific location (locus) within a chromosome in the plant genome. It is created by inserting a specific recombinant DNA molecule. A new DNA sequence, called an "instance," is formed and the inserted recombinant DNA molecule and Adjacent to / flanking both ends of the inserted DNA These traits are characterized by a certain amount of genomic DNA (ng). Transgenic events include, but are not limited to, pest resistance, water availability, efficiency, yield performance, drought tolerance, seed quality, improved nutritional quality, hybrid seed production and and herbicide tolerance, where the trait is a trait or transgenic Such advantageous and / or useful properties are measured in comparison to plants lacking vents. Specific examples of traits include improved plant growth, vigor, stress tolerance, and uprightness. dability, lodging resistance, nutrient uptake, plant nutrition and / or yield, in particular improved growth, increased tolerance to high or low temperatures, drought or water or soil salinity levels Improved resistance to thrombus, enhanced flowering performance, improved ease of harvesting, accelerated maturation , increased yield, improved quality and / or improved nutritional value of the harvested product, Improved shelf life and / or improved processability of the resulting product, and reduced risk of pests and harmful microorganisms. organisms (e.g. insects, arachnids, nematodes, mites, slugs and snails) Improved resistance or tolerance to

[0195] The characteristics of resistance or tolerance to such harmful animals and harmful microorganisms (especially insects) Among the DNA sequences encoding the proteins to be provided, those that are widely described in the literature and are well known in the art are particularly Bacillus thuringiensis (Ba) encoding the Bt protein, which is well known to those and genetic material derived from C. thuringiensis. In addition, proteins extracted from bacteria such as Photorhabdus In particular, the following qualities are also mentioned (WO97 / 17432 and WO98 / 08932): Bt Cry proteins or VIP proteins (which include CrylA, C ryIAb, CryIAc, CryIIA, CryIIIA, CryIIIB2, Cry 9c Cry2Ab, Cry3Bb and CryIF proteins) or exhibits toxicity and fragments thereof, as well as hybrids or combinations thereof, in particular , CrylF protein or a hybrid derived from CrylF protein (e.g., hybrid lid CrylA-CrylF protein or its toxic fragment), Cryl A type protein or a toxic fragment thereof, preferably a CrylAc protein or hybrids derived from CrylAc proteins (e.g., hybrid CrylAb- CrylAc protein), or CrylAb or Bt2 protein or toxic a fragment thereof, a Cry2Ae, Cry2Af or Cry2Ag protein, or a fragment thereof that exhibits toxicity, a CrylA.105 protein, or a flag thereof that exhibits toxicity ment, VIP3Aa19 protein, VIP3Aa20 protein, COT202 or VIP3A protein produced in the COT203 cotton event, "Estruch et al. (1996), Proc Natl Acad Sci US A. 28;93(11):5389-94, or Toxic fragments thereof, Cry proteins as described in WO2001 / 47952 Protein, insecticidal protein (WO9) derived from Xenorhabdus 8 / 50427), an insecticidal tactic derived from Serratia Proteins (especially those derived from Serratia entomophila) insecticidal protein), or from various species of the genus Photorhabdus insecticidal proteins, such as the photolabs described in WO98 / 08932; (Photorhabdus). The sequences that are known (especially those fragments that show toxicity) and some amino acids ( Any variant of these proteins, which differ in 1 to 10, preferably 1 to 5) Mutations or deletions of signal peptides (e.g., plastid signal peptides) or other transcription factors Any mutant or mutant form of such a protein fused to a protein or peptide. Mutants are also encompassed herein.

[0196] Another particularly important example of such a property is the addition of one or more herbicides (e.g., imidazolinone Resistance to benzophenone, sulfonylureas, glyphosate or phosphinothricin The aim is to confer the trait of resistance to specific herbicides on transformed plant cells and plants. Among the DNA sequences encoding proteins that contribute to the development of the present invention, mention may be made in particular of: The method described in WO2009 / 152359 confers resistance to rufosinate herbicides. The bar gene or PAT gene or Streptomyces coelicolor (Strep tomyces coelicolor) gene, herbicides targeting EPSPS (especially and suitable EPSPS ( 5 -Enolpyruvylshikimate-3-phosphate synthase ), a gene encoding glyphosate A gene encoding glyphosate-n-acetyltransferase or glyphosate Genes encoding hydroxylase reductases. Further suitable herbicide tolerance traits include: At least one ALS (acetolactate synthase) inhibitor (e.g., WO2 007 / 024782), mutant Arabidopsis ALS / AHAS gene (e.g., U.S. Patent No. 6,855,533), 2,4-D (2,4-dihydroxybenzoates), 2,4-D-monooxygenase, which confers resistance to chlorophenoxyacetic acid, was found to be involved in the The genes that regulate the dicamba (3,6-dichloro-2-methoxybenzoic acid) A gene encoding dicamba monooxygenase that confers resistance.

[0197] Yet another particularly important example of such a property is, for example, systemic acquired resistance (SAR), Stemin, phytoalexins, inducers and even resistance genes and the proteins and toxins expressed thereby to combat plant pathogenic fungi, bacteria and / or is improved resistance to viruses.

[0198] Transgenic plants or plant cultivars which can preferably be treated according to the invention Particularly useful transgenic events in Event 531 / PV-GHBK04 (cotton, insect control, WO2002 / 0406 77), Event 1143-14A (cotton, insect control, undeposited Event 1143-51B (as described in WO2006 / 128569); , insect control, not deposited, described in WO2006 / 128570); Cent 1445 (cotton, herbicide resistant, not deposited, US-A2002-120964 or described in WO2002 / 034946); Event 17053 (rice, weed control) Drug-resistant, PTA-9843, described in WO2010 / 117737 Event 17314 (rice, herbicide resistant, deposited as PTA-9844) (described in WO2010 / 117735); Event 281-24-23 6 (cotton, insect control-herbicide resistance, deposited as PTA-6233, WO200 5 / 103266 or US-A2005-216969); Event 3 006-210-23 (cotton, insect control-herbicide resistance, deposited as PTA-6233 The invention is described in US-A2007-143876 or WO2005 / 103266. Event 3272 (corn, quality traits, PTA-9972) The deposited Event 33391 (wheat, herbicide resistant, deposited as PTA-2347) (described in WO2002 / 027004), Event 40416 ( Maize, insect control-herbicide resistant, deposited as ATCC PTA-11508 as described in WO11 / 075593); Event 43A47 (corn , insect control-herbicide resistance, deposited as ATCC PTA-11509, WO2 011 / 075595); Event 5307 (corn, insect control) , which has been deposited as ATCC PTA-9561 and is described in WO2010 / 077816 Event ASR-368 (bentgrass, herbicide resistant, ATCC PT A-4816, US-A2006-162007 or WO2004 / 053062); Event B16 (corn, herbicide resistance, accession (not listed in US-A2003-126634); Event BPS- CV127-9 (soybean, herbicide resistant, deposited under NCIMB No. 41603) as described in WO2010 / 080829); Event BLRl (Brassica napus, Restoration of male sterility, deposited as NCIMB 41193, WO2005 / 074 671), Event CE43-67B (cotton, insect control, DSM AC C2724, US-A2009-217423 or WO2006 / 128573); Event CE44-69D (cotton, insect control, deposited Event CE44 -69D (cotton, insect control, not deposited, described in WO2006 / 128571 Event CE46-02A (cotton, insect control, not deposited, WO200 6 / 128572); Event COT102 (cotton, insect control, deposited Not described in US-A2006-130175 or WO2004 / 039986 Event COT202 (cotton, insect control, not deposited, US-A20 07-067868 or WO2005 / 054479); Event CO T203 (cotton, insect control, not deposited, described in WO2005 / 054480 Event DAS21606-3 / 1606 (soybean, herbicide tolerance, PTA -11028, described in WO2012 / 033794), Event DAS40278 (maize, herbicide resistant, ATCC PTA-10244 Deposited as described in WO2011 / 022469); Event DA S-44406-6 / pDAB8264.44.06.l (soybean, herbicide tolerance, PTA -11336, described in WO2012 / 075426), Event DAS-14536-7 / pDAB8291.45.36.2 (soybean, herbicide Resistance, deposited as PTA-11335, described in WO2012 / 075429 Event DAS-59122-7 (corn, insect control - herbicide resistance, Deposited as ATCC PTA 11384, US-A2006-070139 Event DAS-59132 (corn, insect control - herbicide resistant) (not deposited, described in WO2009 / 100188); Event DA S68416 (soybean, herbicide resistant, deposited under ATCC PTA-10442) as described in WO2011 / 066384 or WO2011 / 066360); Event DP-098140-6 (Maize, Herbicide Tolerant, ATCC PTA-82 96, US-A2009-137395 or WO08 / 11201 9); Event DP-305423-1 (soybean, quality traits, No deposits have been made in US Pat. No. 2008-312082 or WO2008 / 054747 Event DP-32138-1 (corn, hybridization) The strain has been deposited as ATCC PTA-9158, US-A2009-021 0970 or described in WO2009 / 103049); Event DP-3560 43-5 (soybean, herbicide resistant, deposited as ATCC PTA-8287, U S-A2010-0184079 or WO2008 / 002872); Event EE-I (eggplant, insect control, not deposited, described in WO07 / 091277 Event Fil 17 (corn, herbicide resistant, ATCC 2090 31, US-A2006-059581 or WO98 / 04414 Event FG72 (soybean, herbicide resistant, PTA-11041 and (described in WO2011 / 063413), event GA2 1 (corn, herbicide resistant, deposited as ATCC 209033, US- A2005-086719 or WO98 / 044140); Event G G25 (maize, herbicide resistant, deposited as ATCC 209032, U S-A2005-188434 or WO98 / 044140); GHB119 (cotton, insect control-herbicide resistance, deposited as ATCC PTA-8398) (described in WO2008 / 151780); Event GHB614 ( Cotton, herbicide resistant, deposited as ATCC PTA-6878, US-A201 0-050282 or W02007 / 017186); Event GJ1 1 (corn, herbicide resistant, deposited as ATCC 209030, US- A2005-188434 or WO98 / 044140); Event G M RZ13 (sugar beet, virus resistant, deposited under NCIMB-41601) Event H7-1 (sugar beet, excluding Herbicide resistance, deposited as NCIMB 41158 or NCIMB 41159, as described in US-A2004-172669 or WO2004 / 074492); Event JOPLINl (wheat, disease resistance, not deposited, US-A2008-0 64032); Event LL27 (soybean, herbicide resistant, NCIMB4 1658, WO2006 / 108674 or US-A2008-3 20616); Event LL55 (soybean, herbicide resistance, NCIMB 41660, WO2006 / 108675 or US-A2008- 196127); Event LLcotton25 (cotton, herbicide resistance, Deposited as ATCC PTA-3343, WO2003 / 013224 or U S A2003-097687); Event LLRICE06 (rice, Herbicide resistance, deposited as ATCC 203353, US 6,468,747 or WO2000 / 026345); event LLRice62 (rice , herbicide resistant, deposited as ATCC 203352, WO2000 / 0263 45), event LLRICE601 (rice, herbicide resistance, ATCC PTA-2600, US-A2008-2289060 or WO2 000 / 026356); Event LY038 (corn, quality The traits related to the strain are deposited as ATCC PTA-5623, US-A2007-0 28322 or WO2005 / 061720); Event MIR162 (Maize, insect control, deposited as PTA-8166, US-A2009 -300784 or WO2007 / 142840); Event MIR6 04 (corn, insect control, not deposited, US-A2008-167456 or is described in WO2005 / 103301); Event MON15985 (cotton, Insect control, deposited as ATCC PTA-2516, US-A2004-25 0317 or described in WO2002 / 100163); Event MON810 ( Maize, insect control, not deposited, described in US-A2002-102582 Event MON863 (corn, insect control, ATCC PTA-26 05, WO2004 / 011601 or US-A2006-095 986); Event MON87427 (corn, pollination control, AT CC PTA-7899, which is described in WO2011 / 062904 Event MON87460 (maize, stress tolerance, ATCC PTA -8910, WO2009 / 111263 or US-A2011- 0138504); Event MON87701 (Soybean, Insect Control, A US-A2009-130071, deposited as TCC PTA-8194, or WO2009 / 064652); event MON87705 (soybean, Quality traits - herbicide tolerance, deposited as ATCC PTA-9241, U S-A2010-0080887 or WO2010 / 037016); Event MON87708 (soybean, herbicide resistant, ATCC PTA-9670) (as described in WO2011 / 034704); Event MON877 12 (soybean, yield, deposited as PTA-10296, WO2012 / 051 199), Event MON87754 (soybean, quality traits, A The compound described in WO2010 / 024976 has been deposited as TCC PTA-9385. Event MON87769 (soybean, quality traits, ATCC PTA -8911, US-A2011-0067141 or WO2009 / 102873); Event MON88017 (corn, insect control Herbicide resistance, deposited as ATCC PTA-5582, US-A2008 -028482 or WO2005 / 059103); Event MON8 8 913 (cotton, herbicide resistant, deposited as ATCC PTA-4854, WO2 004 / 072235 or US-A2006-059590); Event MON88302 (Brassica napus, herbicide resistant, deposited as PTA-10955) , described in WO2011 / 153186), event MON88701 (cotton, Herbicide resistance, deposited as PTA-11754, WO2012 / 134808 described), Event MON89034 (corn, insect control, ATCC P TA-7455, WO07 / 140256 or US-A2008- 260932); Event MON89788 (soybean, herbicide resistance, A US-A2006-282915, deposited as TCC PTA-6708, or WO2006 / 130436); Event MS1 1 (Brassica napus, pollination Controlled-herbicide resistance, deposited as ATCC PTA-850 or PTA-2485 Event MS8 (oilseed rape, pollination) Controlled-herbicide resistance, deposited as ATCC PTA-730, WO2001 / 0 41558 or US-A2003-188347); Event NK60 3 (corn, herbicide resistant, deposited as ATCC PTA-2478, U S-A2007-292854); Event PE-7 (rice, insect control , not deposited, described in WO2008 / 114282); Event RF3 (Brassica napus, pollination control-herbicide resistance, deposited as ATCC PTA-730, as described in WO2001 / 041558 or US-A2003-188347); Event RT73 (Brassica napus, herbicide resistant, not deposited, WO2002 / 0368 31 or US-A2008-070260); Event SYHT0H2 / SYN-000H2-5 (soybean, herbicide resistant, deposited as PTA-11226) (described in WO2012 / 082548), Event T227-1 (Tensa B, herbicide resistance, not deposited, WO2002 / 44407 or US-A2009- 265817); Event T25 (corn, herbicide resistant, deposited Not described in US-A2001-029014 or WO2001 / 051654 Event T304-40 (cotton, insect control - herbicide resistance, ATCC PTA -8171, US-A2010-077501 or WO2008 / 122406); Event T342-142 (cotton, insect control, deposited Not listed in WO2006 / 128568); Event TC1507 ( Maize, insect control-herbicide resistant, not deposited, US-A2005-0392 26 or WO2004 / 099447); Event VIP1034 ( Corn, insect control-herbicide resistance, deposited as ATCC PTA-3925 , described in WO2003 / 052073), Event 32316 (corn , insect control-herbicide resistance, deposited as PTA-11507, WO2011 / 0 84632), Event 4114 (Corn, Insect Control - Herbicide Tolerant PTA-11506, and described in WO2011 / 084621. Event EE-GM3 / FG72 (soybean, herbicide resistant, ATCC accession number P TA-11041) (This may be Event EE-GM1 / LL27 or Event EE-GM2 / LL55 (stacked with the same) (WO2011 / 063413A2) , event DAS-68416-4 (soybean, herbicide resistant, ATCC accession number PTA-1 0442, WO2011 / 066360Al), Event DAS-68416-4 (Die , herbicide resistance, ATCC accession number PTA-10442, WO2011 / 066384A l), Event DP-040416-8 (Maize, Insect Control, ATCC Accession No. P TA-11508, WO2011 / 075593Al), Event DP-043A47- 3 (corn, insect control, ATCC accession number PTA-11509, WO2011 / 0 75595Al), Event DP-004114-3 (Corn, Insect Control, ATC C Accession No. PTA-11506, WO2011 / 084621Al), Event DP-0 32316-8 (corn, insect control, ATCC accession number PTA-11507, WO 2011 / 084632Al), Event MON-88302-9 (Brassica napus, herbicide-resistant Sex, ATCC accession number PTA-10955, WO2011 / 153186Al), event DAS-21606-3 (soybean, herbicide resistant, ATCC accession number PTA-11028 , WO2012 / 033794A2), Event MON-87712-4 (soybean, quality Traits related to the genotype, ATCC Accession No. PTA-10296, WO2012 / 051199A2 ), Event DAS-44406-6 (soybean, stacked herbicide resistance, ATCC Accession No. PTA-11336, WO2012 / 075426Al), Event DAS-14 536-7 (soybean, stacked herbicide resistance, ATCC accession number PTA-11335 , WO2012 / 075429Al), Event SYN-000H2-5 (soybean, weed control Drug resistance, ATCC accession number PTA-11226, WO2012 / 082548A2), Bent DP-061061-7 (Brassica napus, herbicide resistant, accession number not available, WO2012 071039Al), Event DP-073496-4 (Brassica napus, herbicide resistant, Accession no. No. not available, US2012131692), Event 8264.44.06.1 (soybean, Stacked herbicide resistance, Accession No. PTA-11336, WO2012075426A 2), Event 8291.45.36.2 (soybean, stacked herbicide resistance, accession no. No. PTA-11335, WO2012075429A2), Event SYHT0H2 (D Size, ATCC Accession No. PTA-11226, WO2012 / 082548A2), MON88701 (cotton, ATCC accession number PTA-11754, WO2012 / 1 34808Al), event KK179-2 (alfalfa, ATCC accession number PTA -11833, WO2013 / 003558Al), event pDAB8264.42. 32.1 (soybean, stacked herbicide resistance, ATCC accession number PTA-11993, WO2013 / 010094Al), Event MZDT09Y (corn, ATCC Accession number PTA-13025, WO2013 / 012775Al).

[0199] Additionally, a list of such transgenic events is available at the United States Department of Agriculture (USDA) It is provided by the Animal and Plant Health Inspection Service (APHIS) and is available on the World Wide Web. Those websites " aphis.usda.gov " can be found at With respect to the application, the status of the list as it exists / existed on the filing date of this application is relevant. do.

[0200] The genes / events that confer the desired trait are reciprocally expressed in the transgenic plant. It is also possible for the genes to be present in any combination. Examples of plants include important crop plants, such as cereals (wheat, rice, triticale, barley, lamb, etc.). barley, oats), corn, soybeans, potatoes, sugar beets, sugarcane, tomatoes peas and other types of vegetables, cotton, tobacco, rapeseed, and also fruit plants. Examples include fruit-bearing plants (apples, pears, citrus fruits, and grapes). , corn, soybeans, wheat, rice, potatoes, cotton, sugarcane, tobacco and rapeseed Seeds are particularly important. Characters of particular importance include insects, arachnids, nematodes and slugs. Improved plant resistance to insects and snails, as well as resistance to one or more herbicides. The increased resistance of plants to the disease.

[0201] Preferably, of such plants, plant parts or plant seeds which can be treated according to the invention Commercially available examples include marketed products sold or marketed under the following trade names: (e.g., plant seeds): GENUITY®, DROUGHTGA RD (registered trademark), SMARTSTAX (registered trademark), RIB COMPLETE (registered trademark) Trademark), ROUNDUP READY (registered trademark), VT DOUBLE PRO (registered trademark) VT TRIPLE PRO (registered trademark), BOLLGARD II (registered trademark) ), ROUNDUP READY 2 YIELD (registered trademark), YIELDGARD ( ROUNDUP READY 2® XTEN DTM , INTA CTA RR2 PRO®, VISTIVE GOLD®, and / or Or XTENDFLEX TM .

[0202] Crop protection - types of treatment The treatment of plants and plant parts with compounds of formula (I) can be carried out in the same manner as conventional treatment methods. For example, by immersion, spraying, atomizing, irrigating, vaporizing, dusting, fogging, scattering, foaming, painting, etc. , spreading-on, injection, irrigation (drenching), point The compounds may be applied directly to the plants, such as by drip irrigation, or by applying the compounds to the surrounding areas of the plants and plant parts. , habitat or storage space, and also by injecting the reproductive organs (pro In the case of pesticides, especially seeds, dry seed treatment is also required. as a powder for seed treatment, a solution for liquid seed treatment, a water-soluble powder for slurry treatment, and as a coating. Furthermore, the compound represented by formula (I) may be treated by coating with one or more films. The compound is applied by ultra-low volume method. Alternatively, the application form or the compound represented by formula (I) itself may be applied to the soil. It is also possible to inject it into

[0203] A preferred direct treatment of plants is by foliar application (i.e., application of a compound of formula (I) to the foliage). In this case, the frequency of treatment and the amount of application shall be determined according to the level of occurrence of the pest. should be adapted according to the rules.

[0204] In the case of systemically active compounds, the compounds of formula (I) can also be transported via the root system. In this case, the plant will reach the plant even if the plant is exposed to the compound of formula (I) in relation to its habitat. This is done by applying a compound that has a specific function, for example, by irrigation. g) or by mixing into the soil or nutrient solution (i.e., in the place where the plants grow ( impregnating a liquid form of a compound of formula (I) into a soil or a hydroponic system, for example; or by soil application [i.e., by administering the compound of formula (I) according to the invention in solid form by applying the agent to the locus of the plants in a liquid form (for example in granular form) or by drip application ( Often referred to as "chemigation" (i.e., plant At a defined position in the vicinity of the compound of formula (I) according to the present invention, a compound of formula (I) containing varying amounts of water is added. Together, liquid applications over a specific period of time from the surface or underground drip line. In the case of rice crops, this can be achieved by applying the fertilizer in a solid form. A compound of formula (I) (e.g., as granules) is metered into a flooded rice paddy It can also be implemented by

[0205] Digital Technology The compounds of the invention may be used in conjunction with models to, for example, perform site-specific crop management, satellite Agriculture, precision farming or precision farming Models incorporated into computer programs for agriculture Such a model can be used in conjunction with profitability, sustainability and soil, weather, crops (e.g. type, growth stage, plant health) with the aim of optimizing environmental protection; condition), weeds (e.g., type, growth stage), diseases, pests, nutrients, water, moisture, biomass Using data from various sources such as satellite data and yields, we can identify the location of agricultural fields. In particular, such models can be used to optimize agronomic decisions. It helps to control the accuracy of pesticide application and to record the work carried out.

[0206] As an example, a model may be used to model pest infestations and to treat crop plants with a compound of the invention. If it is calculated that the recommended threshold for use has been reached, the The light compounds can be applied to crop plants.

[0207] Commercially available systems that include agronomic models include The Climate FieldScripts by Corporation TM , Xarvio by BASF TM , AGLogic manufactured by John Deere TM etc.

[0208] The compounds of the present invention can be used in farm vehicles (e.g., tractors, robots, helicopters, airplanes, etc.) , mounted on or contained within an unmanned aerial vehicle (UAV, e.g., drone, etc.) In combination with computerized spraying equipment such as spot spraying equipment or precision spraying equipment Such devices typically include an input sensor (e.g., a camera, etc.) and a processing unit, which is configured to analyze the input data, and Based on the analysis of the input data, the compound of the present invention is specifically administered to crop plants (respectively, weeds). (designed to provide a decision to apply in a specific and accurate manner). The use of such computerized spraying equipment usually requires the use of computerized systems to localize the recorded data. and location systems (e.g., GPS receivers) for guiding or controlling farm vehicles, information A geographic information system (GIS) is required to display the data on an easy-to-understand map, as well as the necessary information for spraying, etc. They also need suitable farm vehicles to carry out essential farm tasks.

[0209] For example, pests can be detected from images captured by a camera. The pests can be identified and / or classified based on the image. Image processing algorithms may be used in the classification and / or analysis. The algorithm is a machine learning algorithm, e.g., a trained neural network ( trained neutral network), decision trees, etc. , and artificial intelligence algorithms can be used. The compounds described can be applied only where necessary.

[0210] Seed treatment Control of pests by treating plant seeds has been known for a long time and is continually being improved. However, seed treatment has not always been satisfactorily resolved. Thus, during storage of the plants, after sowing or Eliminate or at least significantly reduce the need for additional post-emergence pesticide applications. It is desirable to develop methods for protecting seeds and germinating plants so that The active compounds used protect the plant from pest attacks without causing any damage to the plant itself. Optimize the amount of active compound used to ensure optimal protection of seeds and germinating plants In particular, seed treatment methods that use minimal amounts of pesticide to treat the seeds are also desirable. In order to achieve optimal protection of the plants and also of the germinating plants, Intrinsic insecticidal properties of insect-resistant or pest-tolerant transgenic plants Sexual or nematicidal properties should also be taken into consideration.

[0211] The present invention therefore relates in particular to a method for protecting seeds and germinating plants from attack by pests. The method also relates to a method for treating seeds with one of the compounds of formula (I): The method of the present invention for protecting seeds and germinating plants from attack by pests The method further comprises treating the seeds with a compound of formula (I) and a mixture of ingredients in one operation. The method also includes treating the seeds simultaneously or sequentially. It also includes a method in which the compound represented by I) and the mixed component are treated at different times. .

[0212] The present invention further provides a method for protecting seeds and the resulting plants from pests. It also relates to the use of a compound of formula (I) for treating children.

[0213] Furthermore, the present invention provides a compound of formula (I) according to the present invention, which is protected against pests. The present invention also relates to seeds treated with the compound. The present invention also relates to seeds treated simultaneously with the synthetic components. The present invention also relates to seeds treated at different times with the compound and the mixture components of formula (I). In the case of seeds treated at different times with different compounds and mixture components, the individual substances In this case, the compound of formula (I) may be present in a different layer on the surface of the polymer. The layers containing the components can optionally be separated by intermediate layers. Furthermore, the compound represented by formula (I) and the mixed component are used as a component of the coating or in addition to the coating. The present invention also relates to seeds to which the composition has been applied as a further layer or layers.

[0214] Furthermore, the present invention provides a method for reducing the abrasion of seeds by dust after treatment with a compound of formula (I). The present invention also relates to seeds that are subjected to a film coating process to prevent this.

[0215] One advantage of the systemically acting compounds of formula (I) is that they can be used to treat seeds. By treating the seeds, not only are the seeds themselves protected from pests, The fact is that the plants resulting from this treatment are also protected after emergence. This avoids the need to treat the crop directly shortly after sowing.

[0216] Treating seeds with a compound of formula (I) improves germination and The fact that sprouting may be enhanced should also be seen as a further advantage.

[0217] The use of the compounds of formula (I) is also particularly relevant to transgenic seeds. It is also considered advantageous that

[0218] Additionally, compounds of formula (I) may be used in combination with signal transduction techniques or compositions. It is also possible to use symbiotic organisms (e.g., rhizobia, mycorrhizal fungi and / or colonization by bacteria or endophytic bacteria or fungi) and / or nitrogen The immobilization is optimized.

[0219] The compounds of formula (I) are used in agriculture, in greenhouses, in forestry or in horticulture. It is particularly suitable for protecting the seeds of cereals (e.g. wheat, barley, rye, foxtail millet and oats), corn, cotton, soybean, rice , potato, sunflower, coffee, tobacco, canola, rapeseed, beet (e.g., lentils) and fodder beet), groundnut, vegetables (e.g., tomatoes, cucumbers, kidney beans ( beans), cruciferous vegetables, onions and lettuce, fruit plants, turf and ornamental seeds Cereals (e.g., wheat, barley, rye, and oats), corn, Treating the seeds of soybeans, cotton, canola, rapeseed, vegetables and rice is particularly important. do.

[0220] As already mentioned above, transgenic seeds with compounds of formula (I) The treatment of insecticides and / or nematicidal properties is also of particular importance. Plant seeds generally containing at least one heterologous gene that controls the expression of a peptide. These heterologous genes in the transgenic seeds are expressed in Bacillus s species, Rhizobium species, Pseudomonas s) species, Serratia species, Trichoderma species , Clavibacter species, Glomus species or Gli The present invention relates to the preparation of basil, which may be derived from a microorganism such as Gliocladium species. containing at least one heterologous gene derived from Bacillus sp. It is particularly suitable for treating transgenic seeds that are , derived from Bacillus thuringiensis It is a heterologous gene.

[0221] In the context of the present invention, the compounds of formula (I) are applied to the seeds. The seeds are treated in a state that is stable enough to avoid damage during treatment. The treatment can be carried out at any time between harvest and sowing. separated from the product and free of cobs, husks, petioles, husks, hairs or pulp, e.g. Seeds that have been harvested, purified, and dried to a moisture content that allows for storage Alternatively, after drying it can be treated with, for example, water and then dried again. In the case of rice seeds, rice embryos can be used. Use seeds that have been soaked, for example in water, until they reach a certain stage (pigeon breast stage). It is also possible to increase the concentration of the seeds, which stimulates germination and makes it more uniform.

[0222] When treating seeds, care should be taken to ensure that seed germination is not adversely affected or that the resulting plants are not damaged. The amount of compound of formula (I) applied to the seeds and / or further additives may be adjusted so as not to cause In general, care must be taken in selecting the amount of additive. This must be ensured, especially in the case of active compounds that may have phytotoxic effects at certain application rates. Not possible.

[0223] Generally, the compounds of formula (I) are applied to the seeds in a suitable formulation. Suitable formulations and methods for processing are known to those skilled in the art.

[0224] The compounds of formula (I) can be used in conventional seed dressing formulations, e.g. solutions, emulsions, and the like, such as a coating, suspension, powder, foam, slurry or other coating composition for seeds. It can be converted into a UV formulation and further converted into an ULV formulation.

[0225] These formulations can be prepared in known manner by incorporating the compounds of formula (I) in conventional excipients, e.g. , customary extenders, and further solvents or diluents, colorants, wetting agents, dispersants, emulsifiers, Mixing with an antifoaming agent, a preservative, a second thickener, an adhesive, gibberellins, etc., and further Prepare by mixing with water.

[0226] Colors that may be present in seed dressing formulations that can be used in accordance with the present invention The coloring agents are all coloring agents customary for such purposes. Dyes that dissolve in pigments or water can be used. n B," "CI Pigment Red 112" and "CI Solvent Examples of colorants include those known as "Red 1."

[0227] Useful compounds that may be present in seed dressing formulations that can be used in accordance with the present invention include: Suitable wetting agents include all wetting-promoting agents customarily used in the formulation of pesticidal active compounds. Preferably, alkyl naphthalene sulfonates, such as diisopropyl Naphthalene sulfonate or diisobutyl naphthalene sulfonate, etc., are used.

[0228] Useful compounds that may be present in seed dressing formulations that can be used in accordance with the present invention include: Suitable dispersing and / or emulsifying agents are non-ionic surfactants customarily used in the formulation of pesticide active ingredients. All dispersants are of the ionic, anionic and cationic types. Preferably, they are nonionic or Anionic dispersants or mixtures of nonionic and anionic dispersants are used. The nonionic dispersants that are used are, in particular, ethylene oxide / propylene oxide bromine. polymers, alkylphenol polyglycol ethers and tristyrylphenols tristryrylphenol polyglycol ethers and their Suitable anionic dispersants include, in particular, the phosphorylated or sulfated derivatives of Lignosulfonates, polyacrylates and arylsulfonates / formaldehyde It is a condensation product.

[0229] Antifoaming agents that may be present in seed dressing formulations that may be used in accordance with the present invention include: The foam-inhibiting agents are all foam-inhibiting substances customarily used for the formulation of pesticide active ingredients. For example, silicone antifoaming agents and magnesium stearate are used.

[0230] Preservatives that may be present in seed dressing formulations that can be used in accordance with the present invention An agent is any substance that can be used for that purpose in an agrochemical composition. Examples include dichlorophene and benzyl alcohol hemiformal.

[0231] A second agent that may be present in a seed dressing formulation that may be used in accordance with the present invention. The thickening agents are all substances that can be used for this purpose in agrochemical compositions. Cellulose derivatives, acrylic acid derivatives, xanthan, modified clay and finely divided silica are preferred. It's nice.

[0232] Adhesives that may be present in seed dressing formulations that can be used in accordance with the present invention The binders are all conventional binders that can be used in seed dressing products. , polyvinyl acetate, polyvinyl alcohol and tylose are preferred. can be done.

[0233] Zybele spp. which may be present in seed dressing formulations which may be used in accordance with the present invention. The gibberellins are preferably gibberellin A1, gibberellin A3 (=gibberellic acid), gibberellin A4 (=gibberellic acid), gibberellin A5 (=gibberellic acid), gibberellin A6 (=gibberellic acid), gibberellin A7 (=gibberellic acid), gibberellin A8 (=gibberellic acid), gibberellin A Gibberellin A4 and gibberellin A7; particularly preferably, gibberellic acid is used. Phosphorus is known (cf. R. Wegler "Chemie der Pfl anzenschutz- and Schadlingsbekampfungsmi ttel”, vol.2, Springer Verlag, 1970, pp. 401-412).

[0234] Seed dressing formulations that can be used in accordance with the present invention are suitable for a wide variety of seed types. It can be used directly or after prior dilution with water to treat the It can be used, for example, as a concentrate or diluted with water. The preparations that can be obtained from concentrated formulations by the process are those derived from cereals, e.g. wheat, barley, It can be used to dress seeds such as rye, oats and triticale. and also corn, rice, rapeseed, peas, beans, cotton , can also be used to dress sunflower, soybean and beet seeds, or It can be used to dress a wide variety of vegetable seeds. Seed dressing formulations that can be used in this way or their diluted application forms are It can also be used to dress the seeds of phenothiazines.

[0235] Seed dressing formulations that can be used according to the present invention or seed dressing formulations to which water has been added When treating seeds with a use form prepared by Any conventional mixing equipment is useful. Specifically, the procedure for seed dressing is as follows: The seeds are placed in a mixer, which may be operated batchwise or continuously. The specified amount of seed dressing formulation is added as is or after pre-dilution with water. and mix everything until the formulation is evenly distributed on the surface of the seeds. If appropriate, this is followed by a drying step.

[0236] The application rates of the seed dressing formulations that can be used according to the invention can vary within a relatively wide range. It can be considered that the specific content of the compound of formula (I) in the preparation and The application rate of the compound of formula (I) is generally 100 mg / kg of seeds. The amount is 0.001 to 50 g per kg of seeds, and preferably 0.01 to 15 g per kg of seeds.

[0237] animal health In the field of animal health, i.e. veterinary medicine, the compounds of formula (I) are It is active against parasites, especially against ectoparasites or endoparasites. "Endoparasites" include, inter alia, helminths and protozoa (e.g., coccidia). The parasite is typically and preferably an arthropod, in particular an insect or acarid. do.

[0238] In the field of veterinary medicine, compounds of formula (I) having a favorable degree of toxicity to warm-blooded animals are preferred. The compounds are used in animal breeding and livestock production in domestic animals, breeding animals, zoo animals, and research animals. Occurring in laboratory, experimental and domestic animals They are suitable for controlling all developmental stages or specific parasites of the parasite. It is active against the developmental stages of

[0239] Agricultural livestock can include, for example: mammals, e.g. Sheep, goats, horses, donkeys, camels, buffalo, rabbits, reindeer, fallow deer, and , especially cattle and pigs; or poultry, such as turkeys, ducks, geese, and and, in particular, chickens; or fish or crustaceans, for example fish in aquaculture. or crustaceans; or optionally insects, such as bees.

[0240] Domestic animals can include, for example: mammals, e.g. Hamsters, guinea pigs, rats, mice, chinchillas, ferrets, and especially Wild animals, cats; caged birds; reptiles; amphibians, or fish in an aquarium.

[0241] In certain embodiments, a compound of Formula (I) is administered to a mammal.

[0242] In another particular embodiment, the compounds of formula (I) are effective against birds, i.e., caged birds. , or, in particular, to poultry.

[0243] By using the compounds of formula (I) to control animal parasites, To reduce or prevent illness and mortality in animals and to improve performance e) To reduce or prevent the deterioration of (meat, milk, wool, leather, eggs, honey, etc.) It is intended that this will result in more economical and easier animal care and better A healthy animal state can be achieved.

[0244] The term "control" or "controlling" means As used herein in connection with the field of animal health, compounds of formula (I) and reducing the occurrence of individual parasites in infected animals to harmless levels. More specifically, "control" means being effective in reducing the When used in the present invention, the compounds of formula (I) kill individual parasites. and is effective in inhibiting its growth or inhibiting its proliferation. do.

[0245] Representative arthropods include, but are not limited to: R: From the order Anoplurida, for example, Haematopinus species atopinus spp.), Linognathus spp. ), Pediculus spp., Phtirus spp. spp.), Solenopotes spp.; Order Mallophagida and suborder Amblycelina cerina and the suborder Ischnocerina, e.g., Bobi Bovicola spp., Damalina spp. ), Felicola spp.; Lepik entron spp.), Menopon spp., Trichodectes Trichodectes spp., Trimenopon spp. on spp.), Trinoton spp., Wernechiella spp. species (Werneckiella spp.); Diptera and Nematocerina From the suborder Brachycerina, for example, Aedes species spp.), Anopheles spp., Achilotus spp. Atylotus spp., Braula spp., Calliphora spp. Calliphora spp., Chrysomyia spp. pp.), Chrysops spp., Culex spp. spp.), Culicoides spp., Eucimurium Eusimulium spp., Fannia spp. , Gasterophilus spp., Glossina spp. lossina spp.), Haematobia spp., Haematopota spp., Hippo bosca spp.), Hybomitra spp., Hydrota Hydrotaea spp., Hypoderma spp. pp.), Lipoptena spp., Lucilia spp. lia spp.), Lutzomyia spp., Merophaga Melophagus spp., Morellia spp. .), Musca spp., Odagmia spp. .), Oestrus spp., Phillipomia spp. ipomyia spp., Phlebotomus spp. , Rhinoestrus spp., Sarcophaga spp. rcophaga spp.), Simulium spp., Stomoxys spp., Tabanus spp. ), Tipula spp., Wilhelmia spp. spp.), Wohlfahrtia spp.; From the order Siphonapterida, for example, Ceratophilus species tophyllus spp.), Ctenocephalides spp. des spp.), Pulex spp., Tunga spp. spp.), Xenopsylla spp.; From the order Heteropterida, for example, Cim ex spp.), Panstrongylus spp. , Rhodnius spp., Triatoma spp. spp.); and harmful and sanitary pests of the order Blattaria (Blattarida).

[0246] Additionally, among arthropods, examples include, but are not limited to, the following mites: You can: Acari (Acarina) and Metastigmatidae mata), for example, Argasidae, for example, Argus species ( Argas spp., Ornithodorus spp. , Otobius spp., Ixodidae, e.g. For example, Amblyomma spp., Dermacentor spp. ermacentor spp.), Haemaphysalis spp. s spp.), Hyalomma spp., Ixodes spp. xodes spp.), Rhipicephalus (Boophilus) spp. lus(Boophilus) spp.), Rhipicephalus spp. alus spp. (the original genus of multihost mites); Mesostigmatidae ta), for example, Dermanyssus spp., Ornithoptera Ornithonyssus spp., Pneumonisus spp. monyssus spp.), Raillietia spp. , Sternostoma spp., Tropilaelapus spp. Tropilaelaps spp., Varroa spp.; Actinedida (Prostigmata), e.g., Acara Acarapis spp., Cheyletiell spp. a spp.), Demodex spp., Listrophorus spp. Listrophorus spp., Myobia spp., Ne Neotrombicula spp., Ornithocheirretia spp. species (Ornithocheyletia spp.), Psore rgates spp.), Trombicula spp.; and Acaridida (Astigmata), e.g., Acarus Acarus spp., Caloglyphus spp. .), Chorioptes spp., Cyt odites spp.), Hypodectes spp., Knemidocoptes spp., Laminosioptes spp. (Laminosioptes spp.), Notoedres spp. spp.), Otodectes spp., Psoroptes spp. Psoroptes spp., Pterolichus spp. .), Sarcoptes spp., Trixacarus spp. ixacarus spp.), Tyrophagus spp. .

[0247] Representative parasitic protozoa include, but are not limited to, the following: You can: Subphylum Mastigophora (Flagellata), e.g. For example: Metamonada: Diplomonad da), for example, Giardia spp., Spironucleus spp. species (Spironucleus spp.); Parabasala: Trichomonadida da), for example, Histomonas spp., Pentatric Pentatrichomonas spp., Tetratrichomonas spp. species (Tetratrichomonas spp.), Trichomonas species (Tricho monas spp.), Tritrichomonas sp. p); Euglenozoa: Order Trypanosomatida matida), for example, Leishmania spp., Trypanosoma spp.; Sarcomastigophora (Rhizopodia) da)), for example, Entamoebidae, for example, Entamoebidae Entamoeba spp., Centramo ebidae), e.g., Acanthamoeba sp., Euamoebidae, e.g., Hartmanella species nella sp.); Alveolata, e.g., Apicomplexa mplexa) (Sporozoa), e.g., Cryptosporidium spp. (Cryptosporidium spp.); Eimeriida ), for example, Besnoitia spp., Cystoisospora Cystoisospora spp., Eimeria spp. pp.), Hammondia spp., Isospora spp. spora spp.), Neospora spp., Sarcosis Sarcocystis spp., Toxoplasma spp. sma spp.); Adeleida, e.g., Hepatozoon spp. species (Hepatozoon spp.), Klossiella sp. p.); Haemosporida, e.g., Leucocytozoa Leucocytozoon spp., Plasmodium spp. dium spp.); of the order Piroplasmida, e.g. Babesia spp., Ciliophora spp. spp.), Echinozoon spp., Theileria spp. Theileria spp.; Vesibuliferidae a) for example, Balantidium spp., Bukist Nella species (Buxtonella spp.); Microspora, e.g., Encephalitzoon species ephalitozoon spp.), Enterocytozoon spp. ozoon spp.), Globidium spp., Nosema Nosema spp. and also, for example, Myxozoa spp. oa spp.).

[0248] Helminths that are pathogenic to humans or animals include, for example, Acanthopanax hocephala), Nematoda, Pentastoma and Platyhelminthes (platyhelmintha) [e.g., monogenea, cestodes ( cestodes and trematodes.

[0249] Representative helminths include, but are not limited to: : Monogenea: e.g., Dactylogyrus species rus spp.), Gyrodactylus spp., Microbothrium spp., Po lystoma spp.), Troglocephalus spp. spp.); Cestodes: Order Pseudophyllid ea), for example: Bothridium spp., Diphyllo Diphyllobothrium spp., Diphlogonoporus spp. species (Diplogonoporus spp.), Ichthyobothrium spp. yobothrium spp.), Ligula spp., Cystose Schistocephalus spp., Spirometra spp. irometra spp.); From the order Cyclophyllida, for example: Andira spp. (Andyra spp.), Anoplocephala spp. pp.), Avitellina spp., Be rtiella spp.), Cittotaenia spp. , Davainea spp., Diorchis spp. spp.), Diplopylidium spp., Dipi Dipylidium spp., Echinococcus spp. coccus spp., Echinocotyle spp. , Echinolepis spp., Hyda tigera spp.), Hymenolepis spp., Joyeuxiella spp., Mesocestoides spp. (Mesocestoides spp.), Moniezia sp. p.), Paranoplocephala spp., La Raillietina spp., Stiles spp. ia spp.), Taenia spp., Th ysaniezia spp.), Thysanosoma spp. ); Trematodes: of the subclass Digenea, for example: Austrobilharzia spp., Brachyraima Brachylaima spp., Calicophoron spp. on spp.), Catatropis spp., Chronorchis Clonorchis spp., Collyriclu m spp.), Cotylophoron spp., Cyclococcus Elm species (Cyclocoelum spp.), Dicro coelium spp.), Diplostomum spp. ), Echinochasmus spp., Echinochasmus spp. Echinoparyphium spp., Echinostoma spp. ostoma spp.), Eurytrema spp., Fa Fasciola spp., Fascioli spp. des spp.), Fasciolopsis spp., Fischoederius spp., Gastrothyrax Gastrothylacus spp., Gigantobilharzia spp. antobilharzia spp.), Gigantocot yle spp.), Heterophyes spp., Hypo Hypoderaeum spp., Leucochloridium spp. ucochloridium spp.), Metagonimus spp. spp.), Metorchis spp., Nanophyetus spp. (Nanophyetus spp.), Notocotylus spp. spp.), Opisthorchis spp., Ornithobia Ornithobilharzia spp., Paragonimus spp. Paragonimus spp., Paramphist omum spp.), Plagiorchis spp., Po Posthodiplostomum spp., Prost Prosthogonimus spp., Schistosoma spp. stosoma spp.), Trichobilharzi spp. a spp.), Troglotrema spp., Typhloco Elm species (Typhlocoelum spp.); Nematodes: of the order Trichinellida For example: Capillaria spp., Eucoleus spp. ucoleus spp.), Paracapillaria spp. pp.), Trichinella spp., Trichomosoides spp. Species (Trichomosoides spp.), Trichuris sp. spp.); From the order Tylenchida, for example: Micronema species onema spp.), Parastrongyloi spp. des spp.), Strongyloides spp. ); Order Rhabditina, for example: Aerulostrongylus Aelurostrongylus spp., Amido stomum spp.), Ancylostoma spp. , Angiostrongylus spp., Bronchus Bronchonema spp., Bunostomum spp. mum spp.), Chabertia spp., Cooperia spp. Cooperia spp., Cooperioides spp. spp.), Crenosoma spp., Cyatostomum spp. (Cyathostomum spp.), Cyclococcus spp. rcus spp.), Cyclodontostomum spp. spp.), Cyclocercus spp., Silico Stephanus spp. (Cylicostephanus spp.), Cylindrophallin Cylindropharynx spp., Cys tocaulus spp.), Dictyocaulus spp. pp.), Elaphostrongylus spp. , Filaroides spp., Globocephalus spp. lobocephalus spp.), Graphidium spp. spp.), Gyalocephalus spp., fly fly Haemonchus spp., Heligmosomoides spp. mosomoides spp.), Hyostrongylus spp. us spp.), Marshallagia spp., Meta Strongylus spp. (Metastrongylus spp.), Muellerius spp. ( Muellerius spp., Necator spp., Nema Nematodirus spp., Neostrongylus spp. strongylus spp., Nippostron gylus spp.), Obeliscoides spp. ), Oesophagodontus spp., Oeso Oesophagostomum spp., Orlanus spp. Ollulanus spp.; Ornithostrongylus spp. ongylus spp.), Oslerus spp., Oslerus Ostertagia spp., Paracooperia spp. peria spp.), Paraclenosoma spp. ), Parafilaroides spp., Parelaphos Parelaphostrongylus spp., Pneumoca Pneumocaulus spp., Pneumostrongylus spp. neumostrongylus spp.), Poteriostomum spp. stomum spp.), Protostrongylu s spp.), Spicocaulus spp., Stepha Stephanurus spp., Strongylus spp. ylus spp.), Syngamus spp., Terador's heron Teladorsagia spp., Trichonema spp. a spp.), Trichostrongylus sp. p.), Triodontophorus spp., Toro Troglostrongylus spp., Unshinari Uncinaria spp.; In the order Spirurida, for example: Acanthocheironema spp. Acanthocheilonema spp.), Anisakis spp. spp.), Ascaridia spp.; Ascaris spp. Ascaris spp.), Ascarops spp., Ascarops Aspiculuris spp., Baylisascaris spp. lisascaris spp.), Brugia spp., Serco Cercopithifilaria spp., Crassicauda Crassicauda spp., Dipetalonema spp. ma spp.), Dirofilaria spp., Drac Dracunculus spp.; Draschia spp. a spp.), Enterobius spp., filariasis Filaria spp., Gnathostoma sp. p.), Gongylonema spp., Habronema spp. abronema spp.), Heterakis spp.; Litomosoides spp., Loa spp. .), Onchocerca spp., Oxyuris spp. yuris spp.), Parabronema spp., Parafilaria spp., Parascaris spp. scaris spp.), Passalurus spp., Physaloptera spp., Probstomaillia spp. robstmayria spp., Pseudofilaria spp. ria spp.), Setaria spp., Scutella spp. Skjrabinema spp., Spirocerca spp. spp.), Stephanofilaria spp. , Strongyluris spp., Syphasia spp. hacia spp.), Thelazia spp., Toxaskari Toxascaris spp., Toxocara sp. p.), Wuchereria spp.; Phylum Acantocephala: Order Oligocene anthorhynchida, for example: Macra canthorhynchus spp.), Prosthen orchis spp.; Moniliformida ), for example: Moniliformis spp.; From the order Polymorphida, for example: Filicoris species licollis spp.); Coleoptera (Echinorhynchida) ), for example, Acanthocephalus spp. , Echinorhynchus spp., Leptorhynchoides Leptorhynchoides spp.; Phylum Pentastoma: Order Porocephali da), for example, Linguatula spp.

[0250] In the field of veterinary medicine and in animal husbandry, the administration of compounds of formula (I) , by methods commonly known in the art, e.g., in the form of a suitable preparation. The administration is carried out enterally, parenterally, transdermally or intranasally. Can be administered methaphylactically or therapeutically .

[0251] Thus, one embodiment of the present invention provides a compound of formula (I) for use as a medicament. Pertaining to things.

[0252] Another embodiment is an antiendoparasitic agent. t) a compound of formula (I) for use as a

[0253] Another particular embodiment is for use as an anti-helmintic agent. and more particularly nematicides, flatwormicides, cidal agent, acanthocephalic agent as a pentastomicidal agent The present invention relates to a compound of formula (I) for use in

[0254] Another particular embodiment is as an antiprotozoal agent. The present invention relates to a compound of formula (I) for use in

[0255] Another embodiment is an antiectoparasitic agent. In particular, for use as arthropodicides and more particularly for use as insecticides or acaricides. The present invention relates to a compound represented by formula (I) for use in the treatment of a pulmonary arthritis.

[0256] A further aspect of the present invention is a method for treating a stomach ulcer by administering to a subject a composition comprising an effective amount of at least one compound of formula (I) and A veterinary preparation containing at least one of the following: and excipients (e.g., solid or liquid diluents), pharmaceutically acceptable adjuvants (e.g., surfactants), especially pharmaceutically acceptable surfactants customarily used in veterinary formulations. excipients that may be used and / or pharmaceutically acceptable excipients customarily used in veterinary formulations. Aids in obtaining.

[0257] A related aspect of the invention is a method for preparing the veterinary formulations described herein. wherein the method comprises administering at least one compound of formula (I) to a pharmaceutically acceptable carrier. acceptable excipients and / or adjuvants (especially pharmaceuticals customarily used in veterinary preparations) and / or veterinary formulations. The method includes mixing the composition with a pharmaceutical composition containing the compound (a pharmaceutical composition containing the compound and a ...).

[0258] Another particular embodiment of the present invention is an ectoparasiticide formulation according to the above embodiment. siticidal formulations and endoparasiticide formulations Veterinary formulations selected from the group consisting of parasiticidal formulations Preparations, more particularly anthelmintic preparations, antiprotozoal preparations formulations and arthropodicides Veterinary formulations selected from the group of , nematicide preparations, flatworm-killing preparations (platyhelminthicidal for mulations), acanthocephalic veterinary drug preparations (acanthocephalicidal formulations, pentastomicidal formulations (pentastomicidal f Veterinary preparations selected from the group consisting of insecticide formulations and acaricide formulations. and methods for preparing them.

[0259] Another aspect is directed to parasitic infections, particularly the ectoparasites and endoparasites described herein. a method for treating an infection by a parasite selected from the group of organisms, said method comprising: and administering to an animal (particularly a non-human animal) in need of such treatment an effective amount of a compound of formula (I) By applying the compound.

[0260] Another aspect is directed to parasitic infections, particularly the ectoparasites and endoparasites described herein. a method for treating an infection by a parasite selected from the group of organisms, said method comprising: , as defined herein, in animals (particularly non-human animals) in need of such treatment. By applying veterinary preparations.

[0261] Another aspect relates to parasitic infections in animals (particularly non-human animals), particularly those described herein. Treatment of infections caused by parasites selected from the group of ectoparasites and endoparasites described The present invention relates to the use of a compound of formula (I) in

[0262] In the context of the field of animal health or veterinary medicine, the term "treatment" refers to prophylaxis. This includes preventative, metaphylactic or therapeutic treatment.

[0263] In a particular embodiment, for the field of veterinary medicine, at least one compound of formula (I) Mixtures of compounds with other active ingredients (especially endoparasiticides and ectoparasiticides) is provided.

[0264] In the field of animal health, a "mixture" is a mixture of two (or more) different active ingredients. It does not merely mean that the active ingredients are formulated into a common formulation and thereby applied together. It also refers to a product that does not contain a single active compound but contains a separate formulation for each active compound. If more than two active compounds are applied, all active compounds should be formulated in a common formulation. Alternatively, all active compounds can be formulated in separate formulations; In other words, some of the active compounds are formulated together and some of the active compounds are formulated separately. In separate formulations, the active compounds are applied separately. The application can be either sequential or sequential.

[0265] The active compounds identified herein by "common name" are known and For example, as described in the "Pesticide Manual" (see above). or can be found on the internet (e.g., http: / / www.alanwood.net / pesticides).

[0266] Representative active ingredients selected from the group of ectoparasiticides as mixing partners include: including, but not limited to, the insecticides and acaricides detailed above. Further active ingredients that may be used are listed in the current IRA C Mode of Action Classification Scheme” According to the above classification based on: (1) acetylcholinesterase (AC) hE) inhibitors; (2) GABA-regulated chloride channel blockers; (3) sodium channel (4) Nicotinic acetylcholine receptor (nAChR) competitive modulators (5) Nicotinic acetylcholine receptor (nAChR) allosteric (6) Glutamate-regulated chloride channel (GluCl) allosterol (7) Juvenile hormone mimetics; (8) Various unspecified (multiple) (9) Chordotonal organ modulators; (10) Mite growth inhibitors; (12) Mites Inhibitors of mitochondrial ATP synthase, e.g., ATP disruptors; (13) protease inhibitors; Uncoupler of oxidative phosphorylation by disrupting the ATP gradient; (14) Nicotinic acetate Chiral receptor channel blockers; (15) Chitin biosynthesis inhibitors (type 0); (1 6) Chitin biosynthesis inhibitors (type 1); (17) Molting disruptors (especially Diptera ( (i.e., against Diptera); (18) Ecdysone receptor agonists; (19) Octopamine receptor agonists (21) Mitochondrial complex I electron transport inhibitors; (25) Mitochondrial Complex II electron transport inhibitors; (20) Mitochondrial complex III electron transport inhibitors; (2 2) Voltage-dependent sodium channel blockers; (23) Acetyl-CoA carboxylase (28) Ryanodine receptor modulators; (30) GABA-regulated chloride channel Channel allosteric modulators.

[0267] Active compounds with unknown or unspecified mechanisms of action, e.g., fentrif phenanil, fenoxacrim, cycloprene, chlorobenzilate, chlordimeform, Rubendimine, dicyclanil, amidoflumet, chinomethionate, triatene, clo Thiazoben, tetrasulfur, potassium oleate, petroleum, methoxadiazone, gossypurule, Flutensin, bromopropylate, cryolite; Another class of compounds, e.g., butacarb, dimethylane, cloethocarb, phosphocarb Bu, Pirimiphos (-ethyl), Parathion (-ethyl), Methacrifos, o-Salicylic Acid Isopropyl, trichlorfon, tigolaner, sulprofos, Ropafos, Cebufos, Pyridathione, Protoate, Diclofenthion, Demeton-S -Methyl sulfone, isazofos, cyanofenphos, dialifos, carbophenothion, Altatiophos, Allomfenvinphos (-methyl), Azinphos (-ethyl), Chlor Pyriphos (-ethyl), phosmetiran, iodofenphos, dioxabenzophos, hormon Thione, fonofos, flupyrazophos, fensulfothion, etrimphos; Organochlorine compounds, such as camphechlor, lindane, heptachlor; or phenyl Pyrazoles, such as acetoprole, pyrafluprole, pyriprole, vaniliprole or isoxazolines, such as sarolaner, afoxolane Le, lotilaner, fluralaner; Pyrethroids, such as (cis-, trans-) metofluthrin, profluthrin, Flufenprox, flubrocythrinate, fubufenprox, fenflutri Protrifenbut, Pyresmethrin, RU15525, Teralethrin, Cis-less Methrin, heptafluthrin, bioethanomethrin, biopermethrin, fenpyritri cis-cypermethrin, cis-permethrin, clocithrin, cyhalothrin (lambda -), clovaporthrin, or halogenated hydrocarbons (HCHs); Neonicotinoids, for example, nithiazine; Dichloromezotiaz, triflumezopyrim; Macrocyclic lactones, such as nemadectin, ivermectin, latidectin, moxide Cutin, Selamectin, Eprinomectin, Doramectin, Emamectin Benzoate; rubemycin oxime; Triplene, epofenonane, diofenolan; Biological agents, hormones, or pheromones, e.g., natural products, e.g., tree thuringiensin, codlemone, or neem components; Dinitrophenols, such as dinocap, dinobuton, binapacryl; Benzoylureas, for example, fluazuron, penfluron; Amidine derivatives such as chlormebuform, cymia Zoll, Demiditraz; Bee hive varroa acaricide icides), for example, organic acids, e.g., formic acid, oxalic acid.

[0268] Representative active ingredients selected from the group of endoparasiticides as mixing partners include: These include, but are not limited to, compounds with anthelmintic activity and compounds with antiprotozoal activity. can.

[0269] The anthelmintic active compound includes, but is not limited to, the following nematicidal active compounds, suction-killing compounds, Insecticidal and / or cestocidal compounds may be mentioned, for example: From the class of macrocyclic lactones, for example: eprinomectin, abamectin, nemadectin Moxidectin, Doramectin, Selamectin, Lepimectin, Latidectin, Mil Vermectin, ivermectin, emamectin, milbemycin; From the class of the benzimidazoles and probenzimidazoles, for example: Oxyben oxibendazole, mebendazole, triclabendazole Iclabendazole, thiophanate, parbene parbendazole, oxfendazole e), netobimin, fenbendazole, febantel, thiabe thiabendazole, cyclobendazole, cambendazole, Albendazole-sulfoxide, albendazole, flubendazole; from the class of depsipeptides, preferably from the class of cyclic depsipeptides, in particular The class of 24-membered cyclic depsipeptides, for example: emodepsid e), PF1022A; From the class of the tetrahydropyrimidines, for example: morantel, pyrantel, oxanthine Le; From the class of the imidazothiazoles, for example: butamisole, levamisole, tetramiso Rule; From the class of aminophenylamidines, for example: amidantel, deacylated amidantel le (dAMD), tribendimidine; From the class of aminoacetonitriles, for example: monepantel ; From the class of the paraherquamides, for example: paraherquamide, delquantel; From the class of salicylanilides, for example: tribromosalan, bromoxanide, bromine Anide, clioxanide, closantel, niclosamide, oxyclozanide, rafoxa Nido; From the class of substituted phenols, for example: nitroxynil, bithionol, diisophenone hexachlorophene, niclofolan, meniclofolan ); ...

Claims

1. Formula (I) 【Chemical 1】 [During the ceremony, X is O or S; Y is a direct bond or an optionally substituted CH ２ and R １ is hydrogen; C １ -C ６ Alkyl [wherein the alkyl is -CN, -CONH ２ , -COOH, -NO ２ and -Si(CH ３ ) ３ substituted with one substituent selected from may be]; C １ -C ６ Haloalkyl; C ２ -C ６ Alkenyl; C ２ -C ６ Haloarkeni Lu; C ２ -C ６ Alkynyl; C ２ -C ６ Haloalkynyl; C ３ -C ４ Cycloalkyl-C １ -C ２ alkyl-[wherein the C ３ -C ４ Cycloalkyl is a group containing one or two halogen atoms. oxetan-3-yl-CH ２ - or benzyl [where , which are halogen atoms or C １ -C ３ and optionally substituted with haloalkyl. ； R ２ is phenyl, pyridine, pyrimidine, pyrazine or pyridazine, wherein The phenyl, pyridine, pyrimidine, pyrazine or pyridazine has a total of 1 to 3 substituents. and wherein the substituent is substituted with either of the carbons adjacent to the carbon bonded to the C=X group. is not present on any carbon atom, and at least one and at most two substituents are C ３ -C ６ Cycloalkoxy, wherein the cycloalkoxy is Halogen, ═O (oxo), —CN, C １ -C ６ Alkyl, C ３ -C ６ Cycloalkyl, C ３ -C ６ Halocycloalkyl , C １ -C ６ Alkoxy, C １ -C ６ Haloalkoxy, C １ -C ６ Alkylthio, C １ - C ６ Alkylsulfinyl, C １ -C ６ Alkylsulfonyl, C ３ -C ６ cycloalkyl kylthio, C ３ -C ６ Cycloalkylsulfinyl, C ３ -C ６ Cycloalkylsulfonates and optionally substituted with 1 to 2 substituents selected from the group consisting of aryl, aryl, aryl, aryl and aryl; Or, C １ -C ６ alkyl, wherein the alkyl is -CN, C ３ -C ６ Cycloalkyl, C ３ -C ６ Halocycloalkyl, C １ -C ６ Alcoki C, C １ -C ６ Haloalkoxy, C １ -C ６ Alkylthio, C １ -C ６ Alkyl sulfide Nill, C. １ -C ６ Alkylsulfonyl, C ３ -C ６ Cycloalkylthio, C ３ -C ６ Cycloalkylsulfinyl, C ３ -C ６ cycloalkylsulfonyl substituted with one or two substituents selected from the group consisting of: Or, C １ -C ６ Alkylcarbonyl and C ３ -C ６ Cycloalkylcarbonyl [wherein C １ -C ６ Alkylcarbonyl and C ３ -C ６ Cycloalkylcarbonyl is Halogen, -CN, C ３ -C ６ Cycloalkyl, C ３ -C ６ Halocycloalkyl, C １ -C ６ Alkyl Chio, C １ -C ６ Alkylsulfinyl, C １ -C ６ Alkylsulfonyl, C ３ -C ６ S Chloroalkylthio, C ３ -C ６ Cycloalkylsulfinyl, C ３ -C ６ Cycloa and optionally substituted with 1 to 2 substituents selected from the group consisting of alkylsulfonyl; Or, C １ -C ６ Alkoxy, wherein the alkoxy is ═O (oxo), —CN, C ３ -C ６ Cycloalkyl, C ３ -C ６ Halocycloalkyl, C １ -C ６ Alcoki C, C １ -C ６ Haloalkoxy, C １ -C ６ Alkylthio, C １ -C ６ Alkyl sulfide Nill, C. １ -C ６ Alkylsulfonyl, C ３ -C ６ Cycloalkylthio, C ３ -C ６ Cycloalkylsulfinyl, C ３ -C ６ cycloalkylsulfonyl substituted with one or two substituents selected from the group consisting of: Or, C １ -C ６ haloalkyl, wherein said haloalkyl is ═O (oxo), —CN, C ３ -C ６ Cycloalkyl, C ３ -C ６ Halocycloalkyl, C １ -C ６ Alcoki C, C １ -C ６ Haloalkoxy, C １ -C ６ Alkylthio, C １ -C ６ Alkyl sulfide Nill, C. １ -C ６ Alkylsulfonyl, C ３ -C ６ Cycloalkylthio, C ３ -C ６ Cycloalkylsulfinyl, C ３ -C ６ cycloalkylsulfonyl substituted with one or two substituents selected from the group consisting of: Or, C １ -C ６ haloalkoxy, wherein said haloalkoxy is ═O (oxo), —CN, C ３ -C ６ Cycloalkyl, C ３ -C ６ Halocycloalkyl, C １ -C ６ Alcoki C, C １ -C ６ Haloalkoxy, C １ -C ６ Alkylthio, C １ -C ６ Alkyl sulfide Nill, C. １ -C ６ Alkylsulfonyl, C ３ -C ６ Cycloalkylthio, C ３ -C ６ Cycloalkylsulfinyl, C ３ -C ６ cycloalkylsulfonyl substituted with one or two substituents selected from the group consisting of: Or, C ２ -C ６ alkenyloxy, wherein the alkenyloxy is Halogen, -CN, C ３ -C ６ Cycloalkyl, C ３ -C ６ Halocycloalkyl, C １ -C ６ Alcoki C, C １ -C ６ Haloalkoxy, C １ -C ６ Alkylthio, C １ -C ６ Alkyl sulfide Nill, C. １ -C ６ Alkylsulfonyl, C ３ -C ６ Cycloalkylthio, C ３ -C ６ Cycloalkylsulfinyl, C ３ -C ６ cycloalkylsulfonyl substituted with one or two substituents selected from the group consisting of: Or, C １ -C ６ Alkyl SO ２ O- [wherein the alkylSO ２ O- is Halogen, -CN, C ３ -C ６ Cycloalkyl, C ３ -C ６ Halocycloalkyl, C １ -C ６ Alcoki C, C １ -C ６ Haloalkoxy, C １ -C ６ Alkylthio, C １ -C ６ Alkyl sulfide Nill, C. １ -C ６ Alkylsulfonyl, C ３ -C ６ Cycloalkylthio, C ３ -C ６ Cycloalkylsulfinyl, C ３ -C ６ cycloalkylsulfonyl substituted with one or two substituents selected from the group consisting of: Or, Phenyl-C １ -C ３ Haloalkyl and phenyl-C １ -C ３ Alkoxy [wherein: The phenyl is Halogen, -CN, C １ -C ６ Alkyl, C ３ -C ６ Cycloalkyl, C ３ -C ６ Halocycloalkyl , C １ -C ６ Alkoxy, C １ -C ６ Haloalkoxy, C １ -C ６ Alkylthio, C １ - C ６ Alkylsulfinyl, C １ -C ６ Alkylsulfonyl, C ３ -C ６ cycloalkyl kylthio, C ３ -C ６ Cycloalkylsulfinyl, C ３ -C ６ Cycloalkylsulfonates and optionally substituted with 1 to 3 substituents independently selected from the group consisting of aryl, aryl, aryls ... Or, Heterocyclyloxy and heterocyclyl-C １ -C ３ Alkoxy [wherein the Irocyclyl includes saturated and partially unsaturated 4- to 6-membered heterocyclyl, 5-membered heteroaryl, 6-membered heteroaryl, each of which is selected from the group consisting of: Halogen, -CN, C １ -C ６ Alkyl, C ３ -C ６ Cycloalkyl, C ３ -C ６ Halocycloalkyl , C １ -C ６ Alkoxy, C １ -C ６ Haloalkoxy, C １ -C ６ Alkylthio, C １ - C ６ Alkylsulfinyl, C １ -C ６ Alkylsulfonyl, C ３ -C ６ cycloalkyl kylthio, C ３ -C ６ Cycloalkylsulfinyl, C ３ -C ６ Cycloalkylsulfonates and optionally substituted with 1 to 3 substituents independently selected from the group consisting of aryl, aryl, aryls ... are independently selected from the group consisting of: and, The remaining optional substituents are: Hydrogen, halogen, hydroxy, -NH ２ , -CN, -NO ２ , C １ -C ３ Alkyl, C ３ -C ６ -cycloalkyl, C １ -C ３ Haloalkyl, C １ -C ３ Alkoxy, C １ - C ３ Haloalkoxy, C １ -C ３ Alkylthio, C １ -C ３ Alkylsulfinyl, C １ -C ３ Alkylsulfonyl, C ３ -C ４ Cycloalkylthio, C ３ -C ４ Cycloa alkylsulfinyl, C ３ -C ４ Cycloalkylsulfonyl, C １ -C ３ Haloalkyl O, C １ -C ３ Haloalkylsulfinyl and C １ -C ３ Haloalkylsulfonyl; selected from the group consisting of: R ３ａ , R ３ｂ teeth, hydrogen, halogens and —CN; and C １ -C ６ Alkyl [wherein the alkyl is selected from the group consisting of halogen, hydroxy, —CN, —C OOH, -CONH ２ , -NO ２ , -NH ２ , optionally substituted C in either case １ -C ６ Alkyl, C ３ -C ６ Cycloalkyl, C １ -C ６ Alkoxy, C １ -C ６ Al Kirchio, C. １ -C ６ Alkylsulfinyl, C １ -C ６ Alkylsulfonyl, -NH( C １ -C ６ alkyl), -N(C １ -C ６ alkyl) ２ , -NHCO-C １ -C ６ Archi Ru, -N(C １ -C ６ alkyl)CO-C １ -C ６ Alkyl, —CO ２ C １ -C ６ Archi -CONH(C １ -C ６ alkyl) and -CON(C １ -C ６ alkyl) ２ Consists of optionally substituted with 1 to 3 substituents independently selected from the group and, In either case, optionally substituted C ３ -C ６ Cycloalkyl, C １ -C ６ Halo Alkyl, C ２ -C ６ Alkenyl, C ２ -C ６ Haloalkenyl, C ２ -C ６ Alkynyl; and, benzyl, wherein the phenyl substituents are halogen, hydroxy, —CN, —COO H, -CONH ２ , -NO ２ , -NH ２ , -SF ５ , and in either case replaced May be C １ -C ６ Alkyl, C １ -C ６ Alkoxy, C １ -C ６ Alkylthio, C １ -C ６ Alkylsulfinyl and C １ -C ６ alkylsulfonyl and optionally substituted with 1 to 5 independently selected substituents; and, Heterocyclyl-C １ -C ６ alkyl [wherein the heterocyclyl substituent is 4 to 1 0-membered saturated and partially unsaturated heterocyclyl, 5-membered heteroaryl and 6-membered heteroaryl wherein each of these is selected from the group consisting of halogen, ═O (oxo), ), hydroxy, —CN, —COOH, —CONH ２ , -NO ２ , -NH ２ , as well as In either case, optionally substituted C １ -C ６ Alkyl and C １ -C ６ From alkoxy and optionally substituted with 1 to 3 substituents independently selected from the group consisting of: are independently selected from the group consisting of: Or, R ３ａ , R ３ｂ together with the carbon to which they are attached, halogen, -CN, any optionally substituted C １ -C ６ Alkyl, C １ -C ６ Alkoxy and C １ -C ６ substituted with 1 to 2 substituents each independently selected from the group consisting of haloalkoxy; May be C ３ -C ６ - forming a carbocyclic or 3- to 6-membered heterocyclic ring system; R ４ is composed of the following substructures T1 to T6: 【Chemistry 2】 wherein the bond to the triazole is marked with a #; where: X １ is the following substructure S4-a 【Chemistry 3】 [where: The bond to the pyridine, pyrimidine, pyrazine, or thiazole is marked with a #; R ４１ is hydrogen or optionally substituted C １ -C ６ Alkyl, C １ -C ６ Haloalkyl, C ３ -C ６ Cycloalkyl, —C １ -C ６ Alkyl-C ３ -C ６ cycloalkyl and phenyl; R ４２ is hydrogen or optionally substituted C １ -C ６ Alkyl, C １ -C ６ Haloalkyl and C ３ -C ６ is cycloalkyl] and X ２ is -CN or X １ and R ５ teeth, Hydrogen, halogens; and, In either case, optionally substituted C １ -C ６ Alkyl, C １ -C ６ Hello Aruki Lu, C ３ -C ６ Cycloalkyl, C １ -C ６ Alkoxy, C １ -C ６ Haloalkoxy, ( C １ -C ６ alkoxy) ２ CH—, —CO ２ C １ -C ６ Alkyl, -C(=NOC １ -C ６ alkyl)H, -C(=NOC １ -C ６ alkyl)-C １ -C ６ Selected from the group of alkyl will be done] A compound represented by the formula:

2. X is O or S; Y is a direct bond or CH ２ and R １ is hydrogen; C １ -C ３ Alkyl [wherein the alkyl is -CN, -CONH ２ , -COOH, -NO ２ and -Si(CH ３ ) ３ substituted with one substituent selected from may be]; C １ -C ３ Haloalkyl; C ２ -C ４ Alkenyl; C ２ -C ４ Haloarkeni Lu; C ２ -C ４ Alkynyl; C ２ -C ４ Haloalkynyl; C ３ -C ４ Cycloalkyl-C １ -C ２ alkyl-[wherein the C ３ -C ４ Cycloalkyl is a group containing one or two halogen atoms. oxetan-3-yl-CH ２ -; or benzyl [ wherein the benzyl is a halogen atom or １ -C ３ Optionally substituted with haloalkyl ] and R ２ is phenyl, pyridine, pyrimidine, pyrazine or pyridazine, wherein The phenyl, pyridine, pyrimidine, pyrazine or pyridazine has a total of 1 to 3 substituents. and wherein the substituent is substituted with either of the carbons adjacent to the carbon bonded to the C=X group. is not present on any carbon atom, and at least one and at most two substituents are C ３ -C ６ Cycloalkoxy, wherein the cycloalkoxy is Halogen, ═O (oxo), —CN, C １ -C ３ Alkyl, C ３ -C ４ Cycloalkyl, C ３ -C ４ Halocycloalkyl , C １ -C ３ Alkoxy, C １ -C ３ Haloalkoxy, C １ -C ３ Alkylthio, C １ - C ３ Alkylsulfinyl, C １ -C ３ Alkylsulfonyl, C ３ -C ４ cycloalkyl kylthio, C ３ -C ４ Cycloalkylsulfinyl, C ３ -C ４ Cycloalkylsulfonates and optionally substituted with 1 to 2 substituents selected from the group consisting of aryl, aryl, aryl, aryl and aryl; Or, C １ -C ３ alkyl, wherein the alkyl is -CN, C ３ -C ４ Cycloalkyl, C ３ -C ４ Halocycloalkyl, C １ -C ３ Haloal Kokisi, C. １ -C ３ Alkylthio, C １ -C ３ Alkylsulfinyl, C １ -C ３ Archi sulfonyl, C ３ -C ４ Cycloalkylthio, C ３ -C ４ Cycloalkylsulfur Finil, C ３ -C ４ 1 to 2 substituents selected from the group consisting of cycloalkylsulfonyl is replaced by]; Or, C １ -C ３ Alkylcarbonyl and C ３ -C ６ Cycloalkylcarbonyl [wherein The C １ -C ３ Alkylcarbonyl and C ３ -C ６ Cycloalkylcarbonyl is Halogen, -CN, C ３ -C ４ Cycloalkyl, C ３ -C ４ Halocycloalkyl, C １ -C ３ Alkyl Chio, C １ -C ３ Alkylsulfinyl, C １ -C ３ Alkylsulfonyl, C ３ -C ４ S Chloroalkylthio, C ３ -C ４ Cycloalkylsulfinyl, C ３ -C ４ Cycloa and optionally substituted with 1 to 2 substituents selected from the group consisting of alkylsulfonyl; Or, C １ -C ３ Alkoxy, wherein the alkoxy is ═O (oxo), —CN, C ３ -C ４ Cycloalkyl, C ３ -C ４ Halocycloalkyl, C １ -C ３ Alcoki C, C １ -C ３ Haloalkoxy, C １ -C ３ Alkylthio, C １ -C ３ Alkyl sulfide Nill, C. １ -C ３ Alkylsulfonyl, C ３ -C ４ Cycloalkylthio, C ３ -C ４ Cycloalkylsulfinyl, C ３ -C ４ cycloalkylsulfonyl substituted with one or two substituents selected from the group consisting of: Or, C １ -C ３ haloalkyl, wherein said haloalkyl is ═O (oxo), —CN, C ３ -C ４ Cycloalkyl, C ３ -C ４ Halocycloalkyl, C １ -C ３ Alcoki C, C １ -C ３ Haloalkoxy, C １ -C ３ Alkylthio, C １ -C ３ Alkyl sulfide Nill, C. １ -C ３ Alkylsulfonyl, C ３ -C ４ Cycloalkylthio, C ３ -C ４ Cycloalkylsulfinyl, C ３ -C ４ cycloalkylsulfonyl substituted with one or two substituents selected from the group consisting of: Or, C １ -C ３ haloalkoxy, wherein said haloalkoxy is ═O (oxo), —CN, C ３ -C ４ Cycloalkyl, C ３ -C ４ Halocycloalkyl, C １ -C ３ Alcoki C, C １ -C ３ Haloalkoxy, C １ -C ３ Alkylthio, C １ -C ３ Alkyl sulfide Nill, C. １ -C ３ Alkylsulfonyl, C ３ -C ４ Cycloalkylthio, C ３ -C ４ Cycloalkylsulfinyl, C ３ -C ４ cycloalkylsulfonyl substituted with one or two substituents selected from the group consisting of: Or, C ２ -C ４ alkenyloxy, wherein the alkenyloxy is Halogen, —CN, and C ３ -C ４ Cycloalkyl, C ３ -C ４ Halocycloalkyl, C １ -C ３ Alcoki C, C １ -C ３ Haloalkoxy, C １ -C ３ Alkylthio, C １ -C ３ Alkyl sulfide Nill, C. １ -C ３ Alkylsulfonyl, C ３ -C ４ Cycloalkylthio, C ３ -C ４ Cycloalkylsulfinyl, C ３ -C ４ cycloalkylsulfonyl substituted with one or two substituents selected from the group consisting of: Or, C １ -C ３ Alkyl SO ２ O- [wherein the alkylSO ２ O- is Halogen, —CN, and C ３ -C ４ Cycloalkyl, C ３ -C ４ Halocycloalkyl, C １ -C ３ Alcoki C, C １ -C ３ Haloalkoxy, C １ -C ３ Alkylthio, C １ -C ３ Alkyl sulfide Nill, C. １ -C ３ Alkylsulfonyl, C ３ -C ４ Cycloalkylthio, C ３ -C ４ Cycloalkylsulfinyl, C ３ -C ４ cycloalkylsulfonyl substituted with one or two substituents selected from the group consisting of: Or, Phenyl-C １ -C ３ Haloalkyl and phenyl-C １ -C ３ Alkoxy [wherein: The phenyl is Halogen, -CN, C １ -C ３ Alkyl, C ３ -C ４ Cycloalkyl, C ３ -C ４ Halocycloalkyl , C １ -C ３ Alkoxy, C １ -C ３ Haloalkoxy, C １ -C ３ Alkylthio, C １ - C ３ Alkylsulfinyl, C １ -C ３ Alkylsulfonyl, C ３ -C ４ cycloalkyl kylthio, C ３ -C ４ Cycloalkylsulfinyl, C ３ -C ４ Cycloalkylsulfonates and optionally substituted with 1 to 3 substituents independently selected from the group consisting of aryl, aryl, aryls ... Or, Heterocyclyloxy and heterocyclyl-C １ -C ３ Alkoxy [wherein the Irocyclyl includes saturated and partially unsaturated 4- to 6-membered heterocyclyl, 5-membered heteroaryl, 6-membered heteroaryl, each of which is selected from the group consisting of: Halogen, -CN, C １ -C ３ Alkyl, C ３ -C ４ Cycloalkyl, C ３ -C ４ Halocycloalkyl , C １ -C ３ Alkoxy, C １ -C ３ Haloalkoxy, C １ -C ３ Alkylthio, C １ - C ３ Alkylsulfinyl, C １ -C ３ Alkylsulfonyl, C ３ -C ４ cycloalkyl kylthio, C ３ -C ４ Cycloalkylsulfinyl, C ３ -C ４ Cycloalkylsulfonates and optionally substituted with 1 to 3 substituents independently selected from the group consisting of aryl, aryl, aryls ... are independently selected from the group consisting of: and, The remaining optional substituents are: Hydrogen, halogen, hydroxy, -NH ２ , -CN, -NO ２ , C １ -C ３ Alkyl, C ３ -C ６ Cycloalkyl, C １ -C ３ Haloalkyl, C １ -C ３ Alkoxy, C １ -C ３ Haloalkoxy, C １ -C ３ Alkylthio, C １ -C ３ Alkylsulfinyl, C １ - C ３ Alkylsulfonyl, C ３ -C ４ Cycloalkylthio, C ３ -C ４ Cycloal Chilsulfinyl, C ３ -C ４ Cycloalkylsulfonyl, C １ -C ３ Haloalkylthio , C １ -C ３ Haloalkylsulfinyl and C １ -C ３ Haloalkylsulfonyl; selected from the group consisting of: R ３ａ , R ３ｂ teeth, hydrogen, halogens and —CN; and C １ -C ４ Alkyl [wherein the alkyl is hydroxy, halogen, —CN, —CO OH, -CONH ２ , -NO ２ , -NH ２ , C １ -C ４ Alkyl, C ３ -C ６ Cycloal Kill, C １ -C ４ Haloalkyl, C １ -C ４ Alkoxy, C １ -C ４ Haloalkoxy, C １ -C ４ Alkylthio, C １ -C ４ Alkylsulfinyl, C １ -C ４ Alkyl sulfonyl Lu, C １ -C ４ Haloalkylthio, C １ -C ４ Haloalkylsulfinyl, C １ -C ４ Ha and substituted with 1 to 3 substituents independently selected from the group consisting of alkylsulfonyl, alkylphenylsulfonyl, aryl ... may be]; and C ３ -C ６ Cycloalkyl [wherein the cycloalkyl is selected from the group consisting of halogen, —CN, —C OOH, -CONH ２ , C １ -C ４ Alkyl, C １ -C ４ Haloalkyl, C ３ -C ６ Shik Roalkyl, C １ -C ４ Alkoxy, C １ -C ４ haloalkoxy and C １ -C ４ Haloalkyl [wherein the haloalkyl is hydroxy, —CN, C ３ - C ６ Cycloalkyl, C １ -C ４ Alkoxy, C １ -C ４ From the group consisting of haloalkoxy optionally substituted with 1 to 2 selected substituents; are independently selected from the group consisting of: R ４ is composed of the following substructures T1 to T6: 【Chemistry 4】 wherein the bond to the triazole is marked with a #; where: X １ is the following substructure S4-a 【Chemistry 5】 [where: The bond to the pyridine, pyrimidine, pyrazine, or thiazole is marked with a #; R ４１ is hydrogen or optionally substituted C １ -C ４ Alkyl, C １ -C ４ Haloalkyl, C ３ -C ６ Cycloalkyl, C １ -C ４ Alkyl-C ３ -C ６ cycloalkyl and phenyl; R ４２ represents hydrogen and optionally substituted C １ -C ４ Alkyl , C １ -C ４ Haloalkyl and C ３ -C ６ is cycloalkyl] and X ２ is -CN or X １ and R ５ teeth, hydrogen, halogens; and C １ -C ４ Alkyl, C １ -C ４ Haloalkyl, C ３ -C ６ Cycloalkyl, C １ - C ４ Alkoxy, C １ -C ４ Haloalkoxy, (C １ -C ４ alkoxy) ２ CH-, -C O ２ C １ -C ４ Alkyl, -C(=NOC １ -C ４ alkyl)H, -C(=NOC １ -C ４ alkyl)-C １ -C ４ selected from the group of alkyl; The compound of claim 1.

3. X is O or S; Y is a direct bond; R １ is hydrogen; C １ -C ３ Alkyl [wherein the alkyl is —CN, —NO ２ and- Si(CH ３ ) ３ and optionally substituted with one substituent selected from the group consisting of: ３ -C ４ Shik alkyl-C １ -C ２ alkyl-[wherein the C ３ -C ４ Cycloalkyl may be one or optionally substituted with two halogen atoms; or benzyl [wherein the benzyl is , a halogen atom or C １ -C ３ optionally substituted with haloalkyl; R ２ is phenyl or pyridine, wherein the phenyl or pyridine is one to two substituted with a substituent, provided that the substituent is adjacent to the carbon bonded to the C=X group; and at least one and at most two substituents are C ３ -C ６ Cycloalkoxy, wherein the cycloalkoxy is Halogen, -CN, C １ -C ３ 1 to 2 substituents selected from the group consisting of alkyl may be substituted with]; Or, C １ -C ３ alkyl, wherein the alkyl is -CN, C ３ -C ４ Cycloalkyl, C ３ -C ４ Halocycloalkyl, C １ -C ３ Alcoki C, C １ -C ３ Haloalkoxy, C １ -C ３ Alkylthio, C １ -C ３ Alkyl sulfide Nill, C. １ -C ３ Alkylsulfonyl, C ３ -C ４ Cycloalkylthio, C ３ -C ４ Cycloalkylsulfinyl, C ３ -C ４ cycloalkylsulfonyl substituted with one or two substituents selected from the group consisting of: Or, C １ -C ３ Alkylcarbonyl and C ３ -C ４ Cycloalkylcarbonyl [wherein The alkylcarbonyl and cycloalkylcarbonyl are Halogen, -CN, C ３ -C ４ Cycloalkyl, C ３ -C ４ halocycloalkyl optionally substituted with 1 to 2 substituents selected from the group consisting of methyl, ... Or, C １ -C ３ Alkoxy, wherein the alkoxy is ═O (oxo), —CN, C ３ -C ４ Cycloalkyl, C ３ -C ４ Halocycloalkyl, C １ -C ３ Alcoki C, C １ -C ３ Haloalkoxy, C １ -C ３ Alkylthio, C １ -C ３ Alkyl sulfide Nill, C. １ -C ３ Alkylsulfonyl, C ３ -C ４ Cycloalkylthio, C ３ -C ４ Cycloalkylsulfinyl, C ３ -C ４ cycloalkylsulfonyl substituted with one or two substituents selected from the group consisting of: Or, C １ -C ３ haloalkyl, wherein said haloalkyl is ═O (oxo), —CN, C ３ -C ４ Cycloalkyl, C ３ -C ４ Halocycloalkyl, C １ -C ３ Alcoki C, C １ -C ３ Haloalkoxy, C １ -C ３ Alkylthio, C １ -C ３ Alkyl sulfide Nill, C. １ -C ３ Alkylsulfonyl, C ３ -C ４ Cycloalkylthio, C ３ -C ４ Cycloalkylsulfinyl, C ３ -C ４ cycloalkylsulfonyl substituted with one or two substituents selected from the group consisting of: Or, C １ -C ３ haloalkoxy, wherein said haloalkoxy is ═O (oxo), —CN, C ３ -C ４ Cycloalkyl, C ３ -C ４ Halocycloalkyl, C １ -C ３ Alcoki C, C １ -C ３ Haloalkoxy, C １ -C ３ Alkylthio, C １ -C ３ Alkyl sulfide Nill, C. １ -C ３ Alkylsulfonyl, C ３ -C ４ Cycloalkylthio, C ３ -C ４ Cycloalkylsulfinyl, C ３ -C ４ cycloalkylsulfonyl substituted with one or two substituents selected from the group consisting of: Or, C ２ -C ４ alkenyloxy, wherein the alkenyloxy is Halogen, -CN, C ３ -C ４ Cycloalkyl, C ３ -C ４ Halocycloalkyl, C １ -C ３ Alcoki C, C １ -C ３ Haloalkoxy, C １ -C ３ Alkylthio, C １ -C ３ Alkyl sulfide Nill, C. １ -C ３ Alkylsulfonyl, C ３ -C ４ Cycloalkylthio, C ３ -C ４ Cycloalkylsulfinyl, C ３ -C ４ cycloalkylsulfonyl substituted with one or two substituents selected from the group consisting of: Or, C １ -C ３ Alkyl SO ２ O- [wherein the alkylSO ２ O- is Halogen, -CN, C ３ -C ４ Cycloalkyl, C ３ -C ４ Halocycloalkyl, C １ -C ３ Alcoki C, C １ -C ３ Haloalkoxy, C １ -C ３ Alkylthio, C １ -C ３ Alkyl sulfide Nill, C. １ -C ３ Alkylsulfonyl, C ３ -C ４ Cycloalkylthio, C ３ -C ４ Cycloalkylsulfinyl, C ３ -C ４ cycloalkylsulfonyl substituted with one or two substituents selected from the group consisting of: Or, Phenyl-C １ -C ３ Haloalkyl and phenyl-C １ -C ３ Alkoxy [wherein: The phenyl is Halogen, -CN, C １ -C ３ Alkyl, C ３ -C ４ Cycloalkyl, C １ -C ３ Haloalkyl, C １ -C ３ Alkoxy, C １ -C ３ 1 to 3 independently selected from the group consisting of haloalkoxy and optionally substituted with a substituent of the formula: Or, Heterocyclyloxy and heterocyclyl-C １ -C ３ Alkoxy [wherein the Heterocyclyl is selected from the group consisting of saturated 4- to 6-membered heterocyclyls containing one oxygen atom. and the heterocyclyl phenyl is Halogen, -CN, C １ -C ３ Alkyl, C ３ -C ４ Cycloalkyl, C １ -C ３ Haloalkyl, C １ -C ３ Alkoxy, C １ -C ３ 1 to 3 independently selected from the group consisting of haloalkoxy and optionally substituted with a substituent of the formula: are independently selected from the group consisting of: and, The remaining optional substituents are: Hydrogen, halogen, hydroxy, -NH ２ , -CN, -NO ２ , C １ -C ３ Alkyl, C ３ -C ６ Cycloalkyl, C １ -C ３ Haloalkyl, C １ -C ３ Alkoxy, C １ -C ３ Haloalkoxy, C １ -C ３ Alkylthio, C １ -C ３ Alkylsulfinyl, C １ - C ３ Alkylsulfonyl, C ３ -C ４ Cycloalkylthio, C ３ -C ４ Cycloal Chilsulfinyl, C ３ -C ４ Cycloalkylsulfonyl, C １ -C ３ Haloalkylthio , C １ -C ３ Haloalkylsulfinyl and C １ -C ３ Haloalkylsulfonyl; selected from the group consisting of: R ３ａ , R ３ｂ is hydrogen; C １ -C ３ Alkyl [wherein the alkyl is halogen, - C.N., C. ３ -C ４ Cycloalkyl, C １ -C ３ Alkoxy, C １ -C ３ From haloalkyl and optionally substituted with 1 to 3 substituents independently selected from the group consisting of Independently selected; R ４ is composed of the following substructures T1 to T6: 【Chemistry 6】 wherein the bond to the triazole is marked with a #; where: X １ is the following substructure S4-a 【Chemistry 7】 [where: The bond to the pyridine, pyrimidine, pyrazine, or thiazole is marked with a #; R ４１ is hydrogen, C １ -C ３ Alkyl, C １ -C ３ Cyanoalkyl, C １ -C ３ Hello Rukill and C ３ -C ４ is cycloalkyl; R ４２ is hydrogen, C １ -C ３ Alkyl and C １ -C ３ haloalkyl] and X ２ is -CN or X １ and R ５ is hydrogen, halogen, C １ -C ３ Alkyl, C １ -C ３ Haloalkyl, C ３ -C ４ Cycloalkyl or C １ -C ３ is alkoxy; 3. The compound of claim 1 or 2.

4. X is O; Y is a direct bond; R １ is hydrogen; R ２ is represented by the following substructures Q1 and Q2: 【Chemistry 8】 [where the bond to the C=X-group is marked with a #] Selected from: where: R ２１ is cyclopropyloxy, (2,2-dichlorocyclopropyl)oxy, cyclopropyloxy 2-cyanopropan-2-yl, cyclopropyl(difluoromethyl), cyclopropyl(difluoromethyl) cyclopropylcarbonyl, 2-cyanopropan-2-yloxy, cyclopropylmethoxy (2,2-difluorocyclopropyl)methoxy, (2,2-dichlorocyclopropyl) (3,3-dichloroprop-2-en-1-yl)oxy, (2,3,3 -trichloroprop-2-en-1-yl)oxy, difluoro-(4-fluorophenyl) (methyl)methyl; R ２２ is hydrogen, fluorine, chlorine, bromine, iodine, cyclopropyl, difluoromethyl , trifluoromethyl, difluoromethoxy, trifluoromethoxy, methylsulfonyl , difluoromethylsulfonyl or trifluoromethylsulfonyl; R ３ａ is hydrogen; R ３ｂ is hydrogen or methyl; R ４ is composed of the following substructures T1 to T6: 【Chemistry 9】 where the bond to the triazole is marked with a #. selected from one of: where: X １ is the following substructure S4-a: 【Chemistry 10】 [where: The bond to the pyridine, pyrimidine, pyrazine, or thiazole is marked with a #; R ４１ is hydrogen, methyl, ethyl or cyclopropyl; R ４２ is hydrogen, methyl or ethyl. and X ２ is -CN or X １ and R ５ is hydrogen, methyl, ethyl or cyclopropyl; The compound according to any one of claims 1 to 3.

5. X is O; Y is a direct bond; R １ is hydrogen; R ２ is 3-bromo-5-(cyclopropoxy)phenyl, 3-cyclopropyloxy -5-(trifluoromethoxy)phenyl, 3-bromo-5-(2,2-dichlorocyclo propyl)oxyphenyl, 3-chloro-5-(cyanomethyl)phenyl, 3-(cyano methyl)-5-(trifluoromethoxy)phenyl, 3-chloro-5-(2-cyanopropyl 3-(2-cyanopropan-2-yl)phenyl, 3-(2-cyanopropan-2-yl)-5-(trifluoromethyl)phenyl 3-(2-cyanopropan-2-yl)-5-(trifluoromethyl)phenyl, 3-(2-cyanopropan-2-yl)-5-methylsulfonylphenyl 3-chloro-5-(cyclopropylcarbonyl)phenyl, 3-chloro-5-(2- cyanopropan-2-yloxy)phenyl, 3-bromo-5-(2-cyanopropane- 2-yloxy)phenyl, 3-bromo-5-[cyclopropyl(difluoro)methyl] Phenyl, 3-(2-cyanopropan-2-yloxy)-5-cyclopropylphenyl , 3-bromo-5-[(2,2-difluorocyclopropyl)methoxy]phenyl, 3- Bromo-5-[(2,2-dichlorocyclopropyl)methoxy]phenyl, 3-[(2, 2-dichlorocyclopropyl)methoxy]-5-(trifluoromethyl)phenyl, 3- [(2,3,3-trichloroprop-2-en-1-yl)oxy]-5-(trifluoromethyl) 3-bromo-5-[(2,3,3-trichloroprop-2-ene- 1-yl)oxy]phenyl, 3-bromo-5-[difluoro-(4-fluorophenyl ) methyl]phenyl, or 2-chloro-6-(2-cyanopropan-2-yl)pyridin benzo-4-yl; R ３ａ is hydrogen; R ３ｂ is methyl; R ４ is 5-[[ethyl(methyl)amino]carbonyl]pyridin-2-yl, 5- Anopyrazin-2-yl, 6-cyanopyrimidin-4-yl, 6-(aminocarbonyl) Pyrimidin-4-yl, 6-(methylaminocarbonyl)pyrimidin-4-yl, 5-(methylaminocarbonyl)pyrimidin-4-yl Ano-1,3-thiazol-2-yl, 5-(methylcarbamoyl)-1,3-thiazo 5-(dimethylaminocarbonyl)-1,3-thiazol-2-yl, or 5-(dimethylaminocarbonyl)-1,3-thiazol-2-yl le; R ５ is hydrogen, methyl or cyclopropyl; The compound according to any one of claims 1 to 4.

6. Formula (I″) 【Chemistry 11】 [During the ceremony, R ３ｂ is C １ -C ３ alkyl, particularly preferably Me, and R ３ａ teeth , H; and Structural element R １ , R ２ , R ４ , R ５ and Y has the meaning given in the structure (1-3). The meaning or structure given in taste or structure (2-3) is given in meaning or structure (3-3) In the given meaning or structure (4-3) In the given meaning or structure (5-3) has the meaning given to it. The compound according to any one of claims 1 to 5, characterized in that it has a structure represented by:

7. Formula (I''') 【Chemistry 12】 [During the ceremony, R ３ｂ is C １ -C ３ alkyl, particularly preferably Me, and R ３ａ teeth , H; and Structural element R １ , R ２ , R ４ , R ５ and Y has the meaning given in the structure (1-3). The meaning or structure given in taste or structure (2-3) is given in meaning or structure (3-3) In the given meaning or structure (4-3) In the given meaning or structure (5-3) has the meaning given to it. The compound according to any one of claims 1 to 5, characterized in that it has a structure represented by:

8. The compound 3-chloro-5-(2-cyanopropan-2-yl)benzoic acid, 3-chloro- 5-(Cyclopropylcarbonyl)benzoic acid, 3-[(methylsulfinyl)methoxy] -5-(trifluoromethyl)benzoic acid, 3-(cyanomethyl)-5-(trifluoromethyl)benzoic acid 3-(2-cyanopropan-2-yl)-5-(trifluoromethoxy)benzoic acid, Sodium benzoate, 3-bromo-5-(2,2-dichlorovinyl)benzoic acid, 3- Bromo-5-[difluoro(4-fluorophenyl)methyl]benzoic acid, 3-chloro-5 -[(methylsulfonyl)methyl]benzoic acid, 3-(cyclopropoxy)-5-(trifluoromethyl)benzoic acid 3-Bromo-5-(1-cyano-1-methyl-ethoxy)benzoic acid, 3-Bromo-5-(1-cyano-1-methyl-ethoxy)benzoic acid benzoic acid, 3-chloro-5-(1-cyano-1-methyl-ethoxy)benzoic acid, 5-[5- [(1S)-1-aminoethyl]-1,2,4-triazol-1-yl]pyrazine-2 -carbonitrile hydrochloride, 6-[5-[(1S)-1-aminoethyl]-3-cyclopropyl pyr-1,2,4-triazol-1-yl]pyrimidine-4-carbonitrile hydrochloride, 6-[5-[(1S)-1-aminoethyl]-3-cyclopropyl-1,2,4-triazol-1,2,4-triazol-2,3-diol [0043] pyrimidine-4-carboxamide hydrochloride, 3-chloro-6-(1-chloro-1-yl)pyrimidine-4-carboxamide hydrochloride, 6-{5-[(1S)-1-amino-1-methyl-ethyl)pyridine-4-carboxylic acid, [aminoethyl]-3-methyl-1H-1,2,4-triazol-1-yl}-N-ethyl -N-methylnicotinamide hydrochloride, 3-(cyanomethyl)-5-(methylsulfonyl) Benzoic acid, 3-(2-cyanopropan-2-yl)-5-(methylsulfonyl)benzoic acid , 3-(1-cyano-1-methyl-ethoxy)-5-cyclopropyl-benzoic acid, and Those salts.

9. Formulations, in particular pesticide formulations, comprising a compound of formula (I) according to any one of claims 1 to 7 The formulation comprises at least one compound.

10. It further comprises at least one bulking agent and / or at least one surfactant. The formulation of claim 9.

11. The compound of formula (I) is mixed with at least one further active compound.

11. The formulation according to claim 9 or 10, characterized in that

12. A method for controlling pests (especially insects), comprising the step of: (I) or the formulation according to any one of claims 9 to 11, or the method characterized by acting on the habitat of such organisms.

13. the pest is a pest and includes an insect or arachnid; 13. The method according to claim 12, characterized in that the pest is an insect or an arachnid. The method described.

14. A compound of formula (I) according to any one of claims 1 to 7 for controlling pests. Use of a formulation according to any one of claims 9 to 11.

15. The pests include insects or arachnids, or the pests are insects or 15. The use according to claim 14, characterized in that the animal is an arachnid.

16. 16. Use according to claim 14 or 15 in crop protection.

17. 16. Use according to claim 14 or 15 in the field of animal health.

18. A method for protecting seeds or germinating plants from pests (especially insects), comprising: A compound represented by formula (I) according to any one of claims 1 to 7 or any one of claims 9 to 11 said method of protecting, comprising the step of contacting said compound with the formulation described above.

19. Seeds obtained by the method of claim 18.

Images