Heterocyclic compounds for combating invertebrate pests

Abstract

The invention relates to heterocyclic compounds of formula (I) wherein the variables have the meanings as defined in the specification, to compositions comprising them, to active compound combinations comprising them, and to their use for protecting growing plants and animals from attack or infestation by invertebrate pests, furthermore, to seed comprising such compounds.

Description

[0001] Heterocyclic compounds for combating invertebrate pests

[0002] Description

[0003] The invention relates to heterocyclic compounds of formula I

[0004]

[0005] wherein

[0006] B1is N or CRB1;

[0007] B2is N or CRB2;

[0008] B3is N or CRB3;

[0009] B4is N or CRB4;

[0010] with the proviso that not more than two of B1, B2, B3, or B4are N;

[0011] W is O, S, or N-RN;

[0012] RNis H, or Ci-C4-alkyl, wherein the alkyl moiety is unsubstituted or substituted with one or more halogen;

[0013] Q is a group Q1, Q2, Q3, Q4, or Q5

[0014]

[0015] Q1Q2Q3Q4or Q5wherein # is the bond to the -C(W)- spacer, and § is the bond to the 6-membered ring; RB1, RB2, RB3, and RB4independently of each other are H, halogen, N3, OH, CN, NO2, -SCN, -SF5, Ci-C6-alkyl, Ci-C6-alkoxy, C2-C6-alkenyl, tri-Ci-C6-alkylsilyl, C2-C6-alkynyl, Ci-C6-alkoxy- Ci-C4-alkyl, Ci-C6-alkoxy-Ci-C4-alkoxy, C3-C6-cycloalkyl, C3-C6-cycloalkoxy, C3-C6- cycloalkyl-Ci-C4-alkyl, Ci-C4-alkyl-C3-C6-cycloalkoxy, wherein the alkyl, alkoxy, alkenyl, alkynyl, cycloalkyl and cycloalkoxy moieties are unsubstituted or substituted with one or more halogen; C(=O)-ORa, NRbRc, Ci-C6-alkylene-NRbRc, O-Ci-C6-alkylene-NRbRc, Ci- C6-alkylene-CN, NH-Ci-C6-alkylene-NRbRc, C(=O)-NRbRc, C(=O)-Rd, SO2NRbRc, or S(=O)mRe, phenyl, phenoxy, phenylcarbonyl, phenylthio, or -CH2-phenyl, wherein the phenyl rings are unsubstituted or substituted with one or more Rf;

[0016] R1a, R1b, and R1cindependently of each other are H, halogen, N3, OH, CN, NO2, -SCN, -SF5, Ci-C6-alkyl, Ci-C6-alkoxy, C2-C6-alkenyl, tri-Ci-C6-alkylsilyl, C2-C6-alkynyl, Ci-C6-alkoxy- Ci-C4-alkyl, Ci-C6-alkoxy-Ci-C4-alkoxy, C3-C6-cycloalkyl, C3-C6-cycloalkoxy, C3-C6- cycloalkyl-Ci-C4-alkyl, C3-C6-cycloalkoxy-Ci-C4-alkyl, wherein the alkyl, alkoxy, alkenyl, alkynyl, cycloalkyl and cycloalkoxy moieties are unsubstituted or substituted with one or more halogen; C(=O)-ORa, NRbRc, Ci-C6-alkylene-NRbRc, O-Ci-C6-alkylene-NRbRc, Ci- C6-alkylene-CN, NH-Ci-C6-alkylene-NRbRc, C(=O)-NRbRc, C(=O)-Rd, SO2NRbRc, or S(=O)mRe, phenyl, phenoxy, phenylcarbonyl, phenylthio or -CH2-phenyl, wherein phenyl rings are unsubstituted or substituted with one or more Rf; or R1aand R1b, or R1band R1c, form together with the carbon atoms to which they are bonded a 5- or 6-membered partially unsaturated heterocyclic ring, which is unsubstituted or substituted with one or more halogen, CN, Ci-C4-alkyl, or Ci-C4-haloalkyl;

[0017] m is 0, 1, or 2;

[0018] R2is a moiety of formula X-Y-Z-T-R3; wherein

[0019] X is a single bond;

[0020] -(C(Rxa)2)P-, wherein p is an integer of 1 to 3, preferably 1 or 2;

[0021] -(C(Rxa)2)0-NRxc-, wherein o is an integer of 1 or 2 and N is bound to Y; or -NRXC-;

[0022] Y is -CRya=N-, wherein the N is bound to Z;

[0023] -NRyc-C(=O)-, wherein C(=O) is bound to Z; or

[0024] -NRyc-C(=S)-, wherein C(=S) is bound to Z;

[0025] Z is -NRZC-C(=O)-, wherein C(=O) is bound to T;

[0026] -NRzc-C(=S)-, wherein C(=S) is bound to T;

[0027] -N=C(S-Rza)-, wherein T is bound to the carbon atom; or

[0028] -NRzc-C(S-Rza)=, wherein T is bound to the carbon atom;

[0029] T is O, N or N-RT;

[0030] R3is aryl, aryl-Ci-C4-alkyl, hetaryl, or hetaryl-Ci-C4-alkyl, wherein the aryl or hetaryl rings are unsubstituted or substituted with one or more R9and wherein the hetaryl is a 5- or 6- membered monocyclic hetaryl or a 8-, 9- or 10-membered bicyclic hetaryl;

[0031] and wherein

[0032] Rxa, Ryaare, identical or different, H, halogen, Ci-C6-alkyl, Ci-C6-alkoxy, C2-C6-alkenyl, C2- C6-alkynyl, Ci-C6-alkoxy-Ci-C4-alkyl, C3-C6-cycloalkyl, Ci-C4-alkyl-C3-C6-cycloalkyl, Ci- C4-alkyl-C3-C6-cycloalkoxy, wherein the alkyl, alkoxy, alkenyl, alkynyl, cycloalkyl and cycloalkoxy moieties are unsubstituted or substituted with one or more halogen;

[0033] Rxc, Ryc, Rzcare, identical or different, H, Ci-C6-alkyl, C2-C6-alkenyl, C2-C6-alkynyl, Ci-C4-alkyl- Ci-C6-alkoxy, C3-C6-cycloalkyl, Ci-C4-alkyl-C3-C6-cycloalkyl, Ci-C4-alkyl-C3-C6- cycloalkoxy, or -NRbRc, wherein the alkyl, alkoxy, alkenyl, alkynyl, cycloalkyl and cycloalkoxy moieties are unsubstituted or substituted with one or more halogen;

[0034] RTis H, Ci-C6-alkyl, C2-C6-alkenyl, C2-C6-alkynyl, Ci-C4-alkyl-Ci-C6-alkoxy, C3-C6-cycloalkyl, C3-C6-cycloalkyl-Ci-C4-alkyl, C3-C6-cycloalkoxy-Ci-C4-alkyl, wherein the alkyl, alkoxy, alkenyl, alkynyl, cycloalkyl and cycloalkoxy moieties are unsubstituted or substituted with one or more halogen;

[0035] Rzais H, Ci-C6-alkyl, Ci-C6-alkoxy, C2-C6-alkenyl, tri-Ci-C6-alkylsilyl, C2-C6-alkynyl, Ci-C4- alkyl-Ci-C6-alkoxy, C3-C6-cycloalkyl, Ci-C4-alkyl-C3-C6-cycloalkoxy, Ci-C4-alkyl-C3-C6- cycloalkyl, wherein the alkyl, alkoxy, alkenyl, alkynyl, cycloalkyl and cycloalkoxy moieties are unsubstituted or substituted with one or more halogen; Ci-C6-alkylene-NRbRc, Ci-C6- alkylene-CN, C(=O)-NRbRc, C(=O)-Rd, phenyl, phenylcarbonyl, or -CH2-phenyl, wherein the phenyl rings are unsubstituted or substituted with one or more Rf;

[0036] Rzatogether with RTor Rzcif present, may form a linear Ci-C6-alkylene or a linear C2-C6- alkenylene group, where in the linear Ci-C6-alkylene and the linear C2-C6-alkenylene a CH2moiety is optionally replaced by a carbonyl and / or wherein 1 or 2 CH2moieties are optionally replaced by O or S and / or wherein the linear Ci-C6-alkylene and the linear C2- C6-alkenylene are unsubstituted or substituted with one or more Rh; Ra, Rband Rcare, identical or different, H, Ci-C6-alkyl, C2-C6-alkenyl, C2-C6-alkynyl, Ci-C6- alkoxy-Ci-C4-alkyl, C3-C6-cycloalkyl, C3-C6-cycloalkyl-Ci-C4-alkyl, C3-C6-cycloalkoxy-Ci- C4-alkyl, wherein the alkyl, alkoxy, alkenyl, alkynyl, cycloalkyl and cycloalkoxy moieties are unsubstituted or substituted with one or more halogen, Ci-C6-alkylene-CN, phenyl, or -CH2-phenyl, wherein the phenyl rings are unsubstituted or substituted with one or more Rf;

[0037] Rdis H, Ci-C6-alkyl, C2-C6-alkenyl, C2-C6-alkynyl, Ci-C6-alkoxy-Ci-C4-alkyl, C3-C6-cycloalkyl, C3-C6-cycloalkyl-Ci-C4-alkyl, C3-C6-cycloalkoxy-Ci-C4-alkyl, wherein the alkyl, alkoxy, alkenyl, alkynyl, cycloalkyl and cycloalkoxy moieties are unsubstituted or substituted with one or more halogen; phenyl, or-CH2-phenyl, wherein the phenyl rings are unsubstituted or substituted with one or more Rf;

[0038] Reis Ci-C6-alkyl, C3-C6-cycloalkyl, C3-C6-cycloalkyl-Ci-C4-alkyl, wherein the alkyl, cycloalkyl moieties are unsubstituted or substituted with one or more halogen; phenyl or -CH2- phenyl, wherein the phenyl rings are unsubstituted or substituted with one or more Rf; Rfis halogen, N3, OH, CN, NO2, -SON, -SF5, Ci-C6-alkyl, Ci-C6-alkoxy, C2-C6-alkenyl, tri-Ci-C6-alkylsilyl, C2-C6-alkynyl, Ci-C6-alkoxy-Ci-C4-alkyl, Ci-C6-alkoxy-Ci-C4-alkoxy, C3-C6- cycloalkyl, C3-C6-cycloalkoxy, C3-C6-cycloalkyl-Ci-C4-alkyl, C3-C6-cycloalkoxy-Ci-C4- alkyl, wherein the alkyl, alkoxy, alkenyl, alkynyl, cycloalkyl and cycloalkoxy moieties are unsubstituted or substituted with one or more halogen;

[0039] Rgis halogen, N3, OH, CN, NO2, -SCN, -SF5, Ci-C6-alkyl, Ci-C6-alkoxy, C2-C6-alkenyl, tri-Ci-C6-alkylsilyl, C2-C6-alkynyl, Ci-C6-alkoxy-Ci-C4-alkyl, Ci-C4-alkyl-Ci-C6-alkoxy, Ci-C6- alkoxy-Ci-C4-alkoxy, C3-C6-cycloalkyl, C3-C6-cycloalkoxy, C3-C6-cycloalkyl-Ci-C4-alkyl, C3-C6-cycloalkoxy-Ci-C4-alkyl, wherein the alkyl, alkoxy, alkenyl, alkynyl, cycloalkyl and cycloalkoxy moieties are unsubstituted or substituted with one or more halogen; C(=O)- ORa, NRbRc, Ci-C6-alkylene-NRbRc, O-Ci-C6-alkylene-NRbRc, Ci-C6-alkylene-CN, NH-Ci- C6-alkylene-NRbRc, C(=O)-NRbRc, C(=O)-Rd, SO2NRbRc, or S(=O)mRe;

[0040] Rhis halogen, OH, Ci-C6-alkyl, C3-C6-cycloalkyl, or CN; and

[0041] the N-oxides, stereoisomers, tautomers, and agriculturally or veterinarily acceptable salts thereof.

[0042] The invention also provides an agricultural composition comprising at least one compound of formula I, a stereoisomer thereof and / or an agriculturally acceptable salt thereof and at least one liquid and / or solid carrier, especially at least one inert liquid and / or solid agriculturally acceptable carrier.

[0043] The invention also provides a veterinary composition comprising at least one compound of formula I, a stereoisomer thereof and / or a veterinarily acceptable salt thereof and at least one liquid and / or solid carrier, especially at least one inert veterinarily liquid and / or solid acceptable carrier.

[0044] The invention also provides a method for controlling invertebrate pests which method comprises treating the pests, their food supply, their habitat or their breeding ground or a cultivated plant, plant propagation materials (such as seed), soil, area, material or environment in which the pests are growing or may grow, or the materials, cultivated plants, plant propagation materials (such as seed), soils, surfaces or spaces to be protected from pest attack or infestation with a pesticidally effective amount of a compound of formula I or a salt thereof as defined herein.

[0045] The present invention also relates to plant propagation material, in particular seed, comprising at least one compound of formula I and / or an agriculturally acceptable salt thereof. The invention further relates to a method for treating or protecting an animal from infestation or infection by parasites which comprises bringing the animal in contact with a parasiticidally effective amount of a compound of formula I or a veterinarily acceptable salt thereof. Bringing the animal in contact with the compound I, its salt orthe veterinary composition of the invention means applying or administering it to the animal.

[0046] WO2013 / 009791, WO2020 / 163146, WO2021 / 013561, and WO / 2024 / 061768 describe structurally closely related active compounds. These compounds are mentioned to be useful for combating invertebrate pests.

[0047] Nevertheless, there remains a need for highly effective and versatile agents for combating invertebrate pests. It is therefore an object of the present invention to provide compounds having a good pesticidal activity and showing a broad activity spectrum against a large number of different invertebrate pests, especially against difficult to control pests, such as insects.

[0048] It has been found that these objects can be achieved by compounds of formula I as depicted and defined below, and by their stereoisomers, salts, tautomers and N-oxides, in particular their agriculturally acceptable salts.

[0049] Compounds of formula I, in particular wherein R2is R2-2 (compounds of formula II), can be obtained from Compounds III via a carbonyl substitution reaction with compound i.

[0050]

[0051] wherein Q is Q2, Q3, orQ4This transformation is usually carried out at temperatures of from -20°C to +120 °C, preferably from 0°C to 25°C, in an inert solvent, in the presence of a base [cf. WO2020163146], Suitable solvents are aliphatic hydrocarbons such as pentane, hexane, cyclohexane, and petrol ether, aromatic hydrocarbons such as toluene, o-, m-, and p-xylene, halogenated hydrocarbons such as methylene chloride, chloroform, and chlorobenzene, ethers such as diethylether, diisopropylether, tert. -butylmethylether (MTBE), dioxane, anisole, and tetrahydrofuran (THF), nitrils such as acetonitrile, and propionitrile, alcohols such as methanol (MeOH), ethanol (EtOH), n-propanol, isopropanol, n-butanol, and tert. -butanol, moreover dimethyl sulphoxide (DMSO), dimethyl formamide (DMF), and dimethylacetamide (DMA), preferably ethers such as THF. It is also possible to use mixtures of the solvents mentioned.

[0052] Suitable bases are, in general, inorganic compounds, such as alkali metal and alkaline earth metal hydroxides, such as lithium hydroxide, sodium hydroxide, potassium hydroxide and calcium hydroxide, alkali metal and alkaline earth metal oxides, such as lithium oxide, sodium oxide, calcium oxide, and magnesium oxide, alkali metal and alkaline earth metal hydrides, such as lithium hydride, sodium hydride, potassium hydride and calcium hydride, alkali metal and alkaline earth metal carbonates, such as lithium carbonate, potassium carbonate and calcium carbonate, and also alkali metal bicarbonates, such as sodium bicarbonate, moreover organic bases, for example tertiary amines, such as trimethylamine, triethylamine, diisopropylethylamine and N-methylpiperidine, pyridine, substituted pyridines, such as collidine, lutidine and 4- dimethylaminopyridine, and also bicyclic amines. Particular preference is given to alkali metal carbonates, such as potassium carbonate. The bases are generally employed in catalytic amounts; however, they can also be used in equimolar amounts, in excess or, if appropriate, as solvent.

[0053] The starting materials are generally reacted with one another in equimolar amounts. In terms of yield, it may be advantageous to employ an excess of II, based on III.

[0054] Compounds II can be obtained from Compounds IV via a carbonyl addition reaction. Suitable reagents are carbonyl transfer reagents such as phosgene, diphosgene or carbonyldiimidazole.

[0055]

[0056] wherein Q is Q5

[0057] This transformation is usually carried out at temperatures of from -20°C to +120°C, preferably from 0°C to 50°C, in an inert solvent, in the presence of a base [cf. WO2024061768], Suitable solvents are aliphatic hydrocarbons such as pentane, hexane, cyclohexane, and petrol ether, aromatic hydrocarbons such as toluene, o-, m-, and p-xylene, halogenated hydrocarbons such as methylene chloride, chloroform, and chlorobenzene, ethers such as diethylether, diisopropylether, tert. -butylmethylether (MTBE), dioxane, anisole, and tetrahydrofuran (THF), nitrils such as acetonitrile, and propionitrile, ketons such as acetone, methyl ethyl ketone, diethyl ketone, and tert. -butyl methyl ketone, alcohols such as methanol (MeOH), ethanol (EtOH), n-propanol, isopropanol, n-butanol, and tert. -butanol, moreover dimethyl sulphoxide (DMSO), dimethyl formamide (DMF), and dimethylacetamide (DMA), preferably nitrils such as acetonitrile. It is also possible to use mixtures of the solvents mentioned.

[0058] Suitable bases are, in general, inorganic compounds, such as alkali metal and alkaline earth metal hydroxides, such as lithium hydroxide, sodium hydroxide, potassium hydroxide and calcium hydroxide, alkali metal and alkaline earth metal oxides, such as lithium oxide, sodium oxide, calcium oxide, and magnesium oxide, alkali metal and alkaline earth metal hydrides, such as lithium hydride, sodium hydride, potassium hydride and calcium hydride, alkali metal and alkaline earth metal carbonates, such as lithium carbonate, potassium carbonate and calcium carbonate, and also alkali metal bicarbonates, such as sodium bicarbonate, moreover organic bases, for example tertiary amines, such as trimethylamine, triethylamine, diisopropylethylamine and N-methylpiperidine, pyridine, substituted pyridines, such as collidine, lutidine and 4-dimethylaminopyridine, and also bicyclic amines. Particular preference is given to alkali metal carbonates, such as potassium carbonate. The bases are generally employed in catalytic amounts; however, they can also be used in equimolar amounts, in excess or, if appropriate, as solvent.

[0059] The starting materials are generally reacted with one another in equimolar amounts. In terms of yield, it may be advantageous to employ an excess of I and / or the carbonylating agent, based on IV. Compounds III can be obtained from Compounds IV via an acylation reaction. Suitable reagents are aryl chloroformates such as phenyl chloroform ate.

[0060] w

[0061]

[0062] herein Q is Q2, Q3, or Q4

[0063] This transformation is usually carried out at temperatures of from -20°C to +120°C, preferably from 0°C to 25°C, in an inert solvent, in the presence of a base [cf. WO2024061768], Suitable solvents are aliphatic hydrocarbons such as pentane, hexane, cyclohexane, and petrol ether, aromatic hydrocarbons such as toluene, o-, m-, and p-xylene, halogenated hydrocarbons such as methylene chloride, chloroform, and chlorobenzene, ethers such as diethylether, diisopropylether, tert. -butylmethylether (MTBE), dioxane, anisole, and tetrahydrofuran (THF), nitrils such as acetonitrile, and propionitrile, ketons such as acetone, methyl ethyl ketone, diethyl ketone, and tert. -butyl methyl ketone, alcohols such as methanol (MeOH), ethanol (EtOH), n-propanol, isopropanol, n-butanol, and tert. -butanol, moreover dimethyl sulphoxide (DMSO), dimethyl formamide (DMF), and dimethylacetamide (DMA), preferably ethers such as tetrahydrofuran (THF). It is also possible to use mixtures of the solvents mentioned.

[0064] Suitable bases are, in general, inorganic compounds, such as alkali metal and alkaline earth metal hydrides, such as lithium hydride, sodium hydride, potassium hydride and calcium hydride, alkali metal and alkaline earth metal carbonates, such as lithium carbonate, potassium carbonate and calcium carbonate, and also alkali metal bicarbonates, such as sodium bicarbonate, moreover organic bases, for example tertiary amines, such as trimethylamine, triethylamine, diisopropylethylamine and N-methylpiperidine, pyridine, substituted pyridines, such as collidine, lutidine and 4-dimethylaminopyridine, and also bicyclic amines. Particular preference is given to organic bases, such as triethylamine. The bases are generally employed in catalytic amounts; however, they can also be used in equimolar amounts, in excess or, if appropriate, as solvent. The starting materials are generally reacted with one another in equimolar amounts. In terms of yield, it may be advantageous to employ an excess of the chloroform ate, based on IV.

[0065] Compounds IV can be obtained from Compounds V via a Suzuki reaction. Suitable reagents are compounds ii.

[0066]

[0067] wherein h is 0 or 1 wherein Q is Q3or Q4

[0068] This transformation is usually carried out at temperatures offrom25°C to 120°C, preferably from 50°C to 110°C, in an inert solvent, in the presence of a base and a catalyst [cf. WO2013147183], Suitable solvents are aliphatic hydrocarbons such as pentane, hexane, cyclohexane, and petrol ether, aromatic hydrocarbons such as toluene, o-, m-, and p-xylene, halogenated hydrocarbons such as methylene chloride, chloroform, and chlorobenzene, ethers such as diethylether, diisopropylether, tert. -butylmethylether (MTBE), dioxane, anisole, and tetrahydrofura (THF), nitrils such as acetonitrile, and propionitrile, alcohols such as methanol (MeOH), ethanol (EtOH), n-propanol, isopropanol, n-butanol, and tert. -butanol, moreover dimethyl sulphoxide (DMSO), dimethyl formamide (DMF), and dimethylacetamide (DMA), and water, preferably aromatic hydrocarbons such as toluene and water. It is also possible to use mixtures of the solvents mentioned.

[0069] Suitable bases are, in general, inorganic compounds, such as alkali metal and alkaline earth metal hydroxides, such as lithium hydroxide, sodium hydroxide, potassium hydroxide and calcium hydroxide, alkali metal and alkaline earth metal oxides, such as lithium oxide, sodium oxide, calcium oxide, and magnesium oxide, alkali metal and alkaline earth metal carbonates, such as lithium carbonate, potassium carbonate and calcium carbonate, and also alkali metal bicarbonates, such as sodium bicarbonate, moreover organic bases, for example tertiary amines, such as trimethylamine, triethylamine, diisopropylethylamine and N-methylpiperidine, pyridine, substituted pyridines, such as collidine, lutidine and 4-dimethylaminopyridine, and also bicyclic amines. Particular preference is given to alkali metal carbonates, such potassium carbonate. The bases are generally employed in catalytic amounts; however, they can also be used in equimolar amounts, in excess or, if appropriate, as solvent.

[0070] Suitable catalysts are in general Palladium catalyst systems - preferably in combination with a phosphine ligand such as palladium acetate and triphenylphosphine, tetrakis(triphenylphosphine)palladium, dichloro[1,1'-bis(diphenylphosphino)ferrocene]pal-ladium(ll), dichlorobis(triphenylphosphine)palladium. The catalyst systems are generally employed in catalytic amounts; however, they can also be used in equimolar amounts, or in excess.

[0071] The starting materials are generally reacted with one another in equimolar amounts. In terms of yield, it may be advantageous to employ an excess of ii, based on V.

[0072] Compounds VI can be obtained from Compounds VII via an amide coupling reaction. Suitable reagents are compounds Hi.

[0073]

[0074] wherein h is 0 or 1

[0075] This transformation is usually carried out at temperatures of from -20°C to +120°C, preferably from 0°C to 80°C, in an inert solvent, in the presence of a base [cf. WO2021262684], Suitable solvents are aliphatic hydrocarbons such as pentane, hexane, cyclohexane, and petrol ether, aromatic hydrocarbons such as toluene, o-, m-, and p-xylene, halogenated hydrocarbons such as methylene chloride, chloroform, and chlorobenzene, ethers such as diethylether, diisopropylether, tert. -butylmethylether (MTBE), dioxane, anisole, and tetrahydrofuran (THF), nitrils such as acetonitrile, and propionitrile, moreover dimethyl sulphoxide (DMSO), dimethyl formamide (DMF), and dimethylacetamide (DMA), preferably aromatic hydrocarbons such as toluene and halogenated hydrocarbons such as methylene chloride. It is also possible to use mixtures of the solvents mentioned. Suitable bases are, in general, inorganic compounds, such as alkali metal and alkaline earth metal hydroxides, such as lithium hydroxide, sodium hydroxide, potassium hydroxide and calcium hydroxide, alkali metal and alkaline earth metal hydrides, such as lithium hydride, sodium hydride, potassium hydride and calcium hydride, alkali metal and alkaline earth metal carbonates, such as lithium carbonate, potassium carbonate and calcium carbonate, and also

[0076] alkali metal bicarbonates, such as sodium bicarbonate, moreover organic bases, for example tertiary amines, such as trimethylamine, triethylamine, diisopropylethylamine and N-methylpiperidine, pyridine, substituted pyridines, such as collidine, lutidine and 4-dimethylaminopyridine, and also bicyclic amines. Particular preference is given to alkali metal carbonates, such as potassium carbonate. The bases are generally employed in catalytic amounts; however, they can also be used in equimolar amounts, in excess or, if appropriate, as solvent.

[0077] The starting materials are generally reacted with one another in equimolar amounts. In terms of yield, it may be advantageous to employ an excess of iii, based on VII.

[0078] Compounds IV can be obtained from Compounds VIII via a reduction reaction. Suitable reducing agents are hydrogen gas in the presence of a metal catalyst or a nonprecious metal in the presence of acid, or other reducing agents such as sodium dithionite.

[0079]

[0080] wherein Q is Q2, or Q5

[0081] Conditions for Q1and Q2:

[0082] This transformation is usually carried out at temperatures of from 0°C to 120°C, preferably from 25°C to 100°C, in an inert solvent, in the presence of a catalyst [cf. Long et al, European Journal of Medicinal Chemistry (2021), 213, 113215],

[0083] Suitable solvents are aliphatic hydrocarbons such as pentane, hexane, cyclohexane, and petrol ether, aromatic hydrocarbons such as toluene, o-, m-, and p-xylene, halogenated hydrocarbons such as methylene chloride, chloroform, and chlorobenzene, ethers such as diethylether, diisopropylether, tert. -butylmethylether (MTBE), dioxane, anisole, and tetrahydrofuran (THF), nitrils such as acetonitrile, and propionitrile, ketons such as acetone, methyl ethyl ketone, diethyl ketone, and tert. -butyl methyl ketone, alcohols such as methanol (MeOH), ethanol (EtOH), n-propanol, isopropanol, n-butanol, and tert. -butanol, moreover dimethyl sulphoxide (DMSO), dimethyl formamide (DMF), and dimethylacetamide (DMA), and water, preferably alcohols such as methanol. It is also possible to use mixtures of the solvents mentioned.

[0084] Suitable metal catalysts are, in general, metal catalysts, such as Palladium and platinum on charcoal, or Raney nickel. Particular preference is given to Raney nickel. The catalysts are generally employed in catalytic amounts; however, they can also be used in equimolar amounts, in excess or, if appropriate, as solvent.

[0085] The starting materials are generally reacted with one another in equimolar amounts. In terms of yield, it may be advantageous to employ an excess of catalyst, based on VII. Conditions for Q5:

[0086] This transformation is usually carried out at temperatures of from -20°C to 120°C, preferably from 0°C to 110°C, in an inert solvent, in the presence of a reducing agent [cf. WO2013080222], Suitable solvents are aliphatic hydrocarbons such as pentane, hexane, cyclohexane, and petrol ether, aromatic hydrocarbons such as toluene, o-, m-, and p-xylene, ethers such as diethylether, diisopropylether, tert. -butylmethylether (MTBE), dioxane, anisole, and tetrahydrofuran (THF), nitrils such as acetonitrile, and propionitrile, alcohols such as methanol (MeOH), ethanol (EtOH), n-propanol, isopropanol, n-butanol, and tert. -butanol, moreover dimethyl sulphoxide (DMSO), dimethyl formamide (DMF), and dimethylacetamide (DMA), and water, preferably alcohols such as methanol. It is also possible to use mixtures of the solvents mentioned.

[0087] Suitable reducing agents are, in general, nonprecious metals in the presence of acid or ammonium chloride such as the following combinations Iron and zinc in the presence of ammonium chloride and acetic acid. The reducing agents are generally employed in stoichiometric amounts; however, they can also be used in excess or, if appropriate, as solvent.

[0088] Compounds IX can be obtained from Compounds X or from Compounds XI via an amide coupling reaction. Suitable reagents are acid chlorides such as compounds iv.

[0089]

[0090] wherein A is N or CH Q is Q1, Q2, or Q5

[0091] W = O

[0092] This transformation is usually carried out at temperatures of from -20°C to +120°C, preferably from 0°C to 80°C, in an inert solvent, in the presence of a base [cf. WO2021262684], Suitable solvents are aliphatic hydrocarbons such as pentane, hexane, cyclohexane, and petrol ether, aromatic hydrocarbons such as toluene, o-, m-, and p-xylene, halogenated hydrocarbons such as methylene chloride, chloroform, and chlorobenzene, ethers such as diethylether, diisopropylether, tert. -butylmethylether (MTBE), dioxane, anisole, and tetrahydrofuran (THF), nitrils such as acetonitrile, and propionitrile, moreover dimethyl sulphoxide (DMSO), dimethyl formamide (DMF), and dimethylacetamide (DMA), preferably aromatic hydrocarbons such as toluene and halogenated hydrocarbons such as methylene chloride. It is also possible to use mixtures of the solvents mentioned.

[0093] Suitable bases are, in general, inorganic compounds, such as alkali metal and alkaline earth metal hydroxides, such as lithium hydroxide, sodium hydroxide, potassium hydroxide and calcium hydroxide, alkali metal and alkaline earth metal hydrides, such as lithium hydride, sodium hydride, potassium hydride and calcium hydride, alkali metal and alkaline earth metal carbonates, such as lithium carbonate, potassium carbonate and calcium carbonate, and also

[0094] alkali metal bicarbonates, such as sodium bicarbonate, moreover organic bases, for example tertiary amines, such as trimethylamine, triethylamine, diisopropylethylamine and N-methylpiperidine, pyridine, substituted pyridines, such as collidine, lutidine and 4-dimethylaminopyridine, and also bicyclic amines. Particular preference is given to alkali metal carbonates, such as potassium carbonate. The bases are generally employed in catalytic amounts; however, they can also be used in equimolar amounts, in excess or, if appropriate, as solvent.

[0095] The starting materials are generally reacted with one another in equimolar amounts. In terms of yield, it may be advantageous to employ an excess of iv, based on X or XI.

[0096] Compounds X can be obtained from Compounds XII via an Ullman coupling reaction, followed by deprotection of the Boc-group under standard conditions. Suitable reagents are compounds v.

[0097] o

[0098]

[0099] This transformation is usually carried out at temperatures of from 0°C to 120°C, preferably from 40°C to 120°C, in an inert solvent, in the presence of a base and a catalyst [cf. WO2023098656], Suitable solvents are aliphatic hydrocarbons such as pentane, hexane, cyclohexane, and petrol ether, aromatic hydrocarbons such as toluene, o-, m-, and p-xylene, halogenated hydrocarbons such as methylene chloride, chloroform, and chlorobenzene, ethers such as diethylether, diisopropylether, tert. -butylmethylether (MTBE), dioxane, anisole, and tetrahydrofuran (THF), nitrils such as acetonitrile, and propionitrile, ketons such as acetone, methyl ethyl ketone, diethyl ketone, and tert. -butyl methyl ketone, alcohols such as methanol (MeOH), ethanol (EtOH), n-propanol, isopropanol, n-butanol, and tert. -butanol, moreover dimethyl sulphoxide (DMSO), dimethyl formamide (DMF), and dimethylacetamide (DMA), preferably ethers such as dioxane. It is also possible to use mixtures of the solvents mentioned.

[0100] Suitable bases are, in general, inorganic compounds, such as alkali metal and alkaline earth metal hydroxides, such as lithium hydroxide, sodium hydroxide, potassium hydroxide and calcium hydroxide, alkali metal and alkaline earth metal oxides, such as lithium oxide, sodium oxide, calcium oxide, and magnesium oxide, alkali metal and alkaline earth metal hydrides, such as lithium hydride, sodium hydride, potassium hydride and calcium hydride, alkali metal and alkaline earth metal carbonates, such as lithium carbonate, potassium carbonate and calcium carbonate, and also alkali metal bicarbonates, such as sodium bicarbonate, alkali metal phosphates such as sodium phosphate or potassium phosphate, moreover organic bases, for example tertiary amines, such as trimethylamine, triethylamine, diisopropylethylamine and N-methylpiperidine, pyridine, substituted pyridines, such as collidine, lutidine and 4-dimethylaminopyridine, and also bicyclic amines. Particular preference is given to alkali metal phosphates such as sodium phosphate. The bases are generally employed in catalytic amounts; however, they can also be used in equimolar amounts, in excess or, if appropriate, as solvent.

[0101] Suitable catalysts are in general Cuprous iodide, cuprous cyanide or cuprous oxide. The catalysts are generally employed in catalytic amounts; however, they can also be used in equimolar amounts, or in excess.

[0102] The starting materials are generally reacted with one another in equimolar amounts. In terms of yield, it may be advantageous to employ an excess of v, based on XII.

[0103] The Boc deprotection can be performed using standard conditions, as for example described in March’s Advanced Organic Chemistry 6th edition, Michael B. Smith and Jerry March. Compounds XI can be obtained from Compounds XIII via a nucleophilic aromatic substitution reaction, followed by deprotection of the Boc group under standard conditions. Suitable reagents are compounds vi.

[0104]

[0105] XIII XI

[0106] wherein A is N

[0107] This transformation is usually carried out at temperatures offrom25°C to 150°C, preferably from 50°C to 120°C, in an inert solvent, in the presence of a base [cf. Russell et al, RSC Advances (2015), 5(113), 93433-93437],

[0108] Suitable solvents are aliphatic hydrocarbons such as pentane, hexane, cyclohexane, and petrol ether, aromatic hydrocarbons such as toluene, o-, m-, and p-xylene, halogenated hydrocarbons such as methylene chloride, chloroform, and chlorobenzene, ethers such as diethylether, diisopropylether, tert. -butylmethylether (MTBE), dioxane, anisole, and tetrahydrofuran (THF), nitrils such as acetonitrile, and propionitrile, ketons such as acetone, methyl ethyl ketone, diethyl ketone, and tert. -butyl methyl ketone, alcohols such as methanol (MeOH), ethanol (EtOH), n-propanol, isopropanol, n-butanol, and tert. -butanol, moreover dimethyl sulphoxide (DMSO), dimethyl formamide (DMF), and dimethylacetamide (DMA), preferably nitrils such as acetonitrile. It is also possible to use mixtures of the solvents mentioned.

[0109] Suitable bases are, in general, inorganic compounds, such as alkali metal and alkaline earth metal hydrides, such as lithium hydride, sodium hydride, potassium hydride and calcium hydride, alkali metal and alkaline earth metal carbonates, such as lithium carbonate, potassium carbonate and calcium carbonate, and also alkali metal bicarbonates, such as sodium bicarbonate, moreover organic bases, for example tertiary amines, such as trimethylamine, triethylamine, diisopropylethylamine and N-methylpiperidine, pyridine, substituted pyridines, such as collidine, lutidine and 4-dimethylaminopyridine, and also bicyclic amines. Particular preference is given to alkali metal carbonates, such as potassium carbonate. The bases are generally employed in catalytic amounts; however, they can also be used in equimolar amounts, in excess or, if appropriate, as solvent.

[0110] The starting materials are generally reacted with one another in equimolar amounts. In terms of yield, it may be advantageous to employ an excess of vi, based on XIII.

[0111] The Boc deprotection can be performed using standard conditions, as for example described in March’s Advanced Organic Chemistry 6th edition, Michael B. Smith and Jerry March.

[0112] Compounds XIV can be obtained from Compounds XV via a cyclization reaction. Suitable reagents are alpha halogenated acetic acid derivatives.

[0113]

[0114] This transformation is usually carried out at temperatures of from -20°C to 120°C, preferably from 25°C to 110°C, in an inert solvent, in the presence of a base [cf. Trotsko et al, Molecules (2019), 24(17), 3029], Suitable solvents are aliphatic hydrocarbons such as pentane, hexane, cyclohexane, and petrol ether, aromatic hydrocarbons such as toluene, o-, m-, and p-xylene, halogenated hydrocarbons such as methylene chloride, chloroform, and chlorobenzene, ethers such as diethylether, diisopropylether, tert. -butylmethylether (MTBE), dioxane, anisole, and tetrahydrofuran (THF), nitrils such as acetonitrile, and propionitrile, ketons such as acetone, methyl ethyl ketone, diethyl ketone, and tert. -butyl methyl ketone, alcohols such as methanol (MeOH), ethanol (EtOH), n-propanol, isopropanol, n-butanol, and tert. -butanol, moreover dimethyl sulphoxide (DMSO), dimethyl formamide (DMF), and dimethylacetamide (DMA), preferably alcohols such as methanol. It is also possible to use mixtures of the solvents mentioned.

[0115] Suitable bases are, in general, inorganic compounds, such as alkali metal and alkaline earth metal hydroxides, such as lithium hydroxide, sodium hydroxide, potassium hydroxide and calcium hydroxide, alkali metal and alkaline earth metal hydrides, such as lithium hydride, sodium hydride, potassium hydride and calcium hydride, alkali metal acetates such as sodium acetate, alkali metal and alkaline earth metal carbonates, such as lithium carbonate, potassium carbonate and calcium carbonate, and also alkali metal bicarbonates, such as sodium bicarbonate, moreover organic bases, for example tertiary amines, such as trimethylamine, triethylamine, diisopropylethylamine and N-methylpiperidine, pyridine, substituted pyridines, such as collidine, lutidine and 4-dimethylaminopyridine, and also bicyclic amines. Particular preference is given to alkali metal acetates such as sodium acetate. The bases are generally employed in catalytic amounts; however, they can also be used in equimolar amounts, in excess or, if appropriate, as solvent. The starting materials are generally reacted with one another in equimolar amounts. In terms of yield, it may be advantageous to employ an excess of alpha halogenated acetic acid derivatives, based on XV.

[0116] Compounds lllb can be obtained from Compounds Illa via a thionylation reaction. A suitable reagent is Lawesson’s reagent.

[0117]

[0118] wherein Q is Q1, Q2, Q3, or Q4This transformation is usually carried out at temperatures offrom25°C to 120°C, preferably from 50°C to 120°C, in an inert solvent, in the presence of Lawesson’s reagent [cf. W02004018439], Suitable solvents are aromatic hydrocarbons such as toluene, o-, m-, and p-xylene, halogenated hydrocarbons such as methylene chloride, chloroform, and chlorobenzene, preferably aromatic hydrocarbons such as toluene. It is also possible to use mixtures of the solvents mentioned. The starting materials are generally reacted with one another in equimolar amounts. In terms of yield, it may be advantageous to employ an excess of Lawesson’s reagent, based on Illa.

[0119] Compounds Ila can be obtained from Compounds XX via the following reaction sequence.

[0120]

[0121] The transformation from XX to XXI is usually carried out analogues to the transformation from VIII to IV. The transformation from XXI to XXII is usually carried out analogues to the transformation from IV to III. The transformation from XXII to XXIII is usually carried out analogues to the transformation from IV to II. The transformation from XXIII to XXIV is usually carried out under standart Boc-deprotection condition known to the skilled person and as described in various literature references, e.g., reference book March’s Advanced Organic Chemistry 6th edition, Michael B. Smith and Jerry March.

[0122] Compounds Ila can be obtained from Compounds XXIV via an imidation reaction. Suitable reagents are compounds of formula XXVII. This transformation is usually carried out at temperatures of from 0°C to 110°C, preferably from 25°C to 80°C, in an inert solvent, in the presence of an acid [cf. Eur. J. Med. Chem. (1977), 12(4), 365-369],

[0123] Suitable solvents are ethers such as diethylether, diisopropylether, tert. -butylmethylether (MTBE), dioxane, anisole, and tetrahydrofurane (THF), nitrils such as acetonitrile, and propionitrile, alcohols such as methanol (MeOH), ethanol (EtOH), n-propanol, isopropanol, n-butanol, and tert. -butanol, moreover dimethyl sulphoxide (DMSO), dimethyl formamide (DMF), and dimethylacetamide (DMA), and water preferably alcohols such as methanol or ethanor or water. It is also possible to use mixtures of the solvents mentioned.

[0124] Suitable acids and acidic catalysts are in general anorganic acids such as hydrofluoric acid, hydrochloric acid, hydrobromic acid, sulphuric acid und perchloric acid, Lewis acids, such as boron tri fluoride, aluminium tri chloride, iron III chloride, tin IV chloride, titanium IV chloride and zinc II chloride, moreover organic acids such as formic acid, acetic acid, propionic acid, oxalic acid, toluene sulphonic acid, benzene sulphonic acid, camphor sulphonic acid, citric acid, and trifluoro acetic acid. The acids are generally employed in catalytic amounts; however, they can also be used in equimolar amounts, in excess or, if appropriate, as solvent. The starting materials are generally reacted with one another in equimolar amounts. In terms of yield, it may be advantageous to employ an excess of XXVII, based on XXIV.

[0125] Compounds XXVII can be obtained from Compounds XXVI via an alkylation reaction. Suitable reagents are methyl iodide. Compounds XXVII are typically obtained as the hydroiodide salt

[0126] Hl

[0127]

[0128] XXVI XXVII

[0129] This transformation is usually carried out at temperatures of from 0°C to 120°C, preferably from 25°C to 110°C, in an inert solvent, in the presence of an alkylating agent such as methyl iodide [cf. Bioorganic & Medicinal Chemistry (2001), 10(1), 41-46],

[0130] Suitable solvents are ethers such as diethylether, diisopropylether, tert. -butylmethylether (MTBE), dioxane, anisole, and tetrahydrofurane (THF), ketons such as acetone, methyl ethyl ketone, diethyl ketone, and tert. -butyl methyl ketone, preferably ketons and ethers such as acetone and THF. It is also possible to use mixtures of the solvents mentioned.

[0131] The starting materials are generally reacted with one another in equimolar amounts. In terms of yield, it may be advantageous to employ an excess of methyl iodide, based on XXVI.

[0132] The starting materials required for preparing the compounds I are commercially available or known from the literature [cf. WO2020163146] or can be prepared in accordance with the literature cited.

[0133] The reaction mixtures are worked up in a customary manner, for example by mixing with water, separating the phases and, if appropriate, chromatographic purification of the crude products. Some of the intermediates and end products are obtained in the form of colorless or slightly brownish viscous oils which are purified or freed from volatile components under reduced pressure and at moderately elevated temperature. If the intermediates and end products are obtained as solids, purification can also be carried out by recrystallization or digestion.

[0134] If individual compounds I cannot be obtained by the routes described above, they can be prepared by derivatization of other compounds I.

[0135] However, if the synthesis yields mixtures of isomers, a separation is generally not necessarily required since in some cases the individual isomers can be interconverted during work-up for use or during application (for example under the action of light, acids or bases). Such conversions may also take place after use, for example in the treatment of plants in the treated plant, or in the invertebrate pest to be controlled.

[0136] The organic moieties groups mentioned in the above definitions of the variables are - like the term halogen - collective terms for individual listings of the individual group members. The prefix Cn-Cm indicates in each case the possible number of carbon atoms in the group.

[0137] The term “partially or fully substituted” by a radical means that in general the group is substituted with same or different radicals. The term “halogen” denotes in each case fluorine, bromine, chlorine, or iodine, in particular fluorine, chlorine, or bromine.

[0138] The term "alkyl" as used herein and in the alkyl moieties of alkylamino, alkylcarbonyl, alkylthio, alkylsulfinyl, alkylsulfonyl and alkoxyalkyl denotes in each case a straight-chain or branched alkyl group having usually from 1 to 10 carbon atoms, frequently from 1 to 6 carbon atoms, preferably 1 to 4 carbon atoms, more preferably from 1 to 3 carbon atoms. Examples of an alkyl group are methyl (Me), ethyl (Et), n-propyl (n-Pr), iso-propyl, n-butyl, 2-butyl, iso-butyl, tert-butyl, n-pentyl, 1 -methylbutyl, 2 methylbutyl, 3 methylbutyl, 2,2-dimethylpropyl, 1 ethylpropyl, n-hexyl, 1,1-dimethyl-propyl, 1,2-dimethylpropyl, 1 -methylpentyl, 2-methylpentyl, 3-methylpentyl, 4-methylpentyl, 1,1 -dimethylbutyl, 1,2-dimethylbutyl, 1,3-dimethylbutyl, 2,2-dimethylbutyl, 2,3-dimethylbutyl, 3,3-dimethylbutyl, 1 -ethylbutyl, 2-ethylbutyl, 1,1,2-trimethylpropyl, 1,2,2-trimethylpropyl, 1-ethyl-1 -methylpropyl, and 1-ethyl-2-methylpropyl.

[0139] The term "haloalkyl" as used herein and in the haloalkyl moieties of haloalkylcarbonyl, haloalkoxycarbonyl, haloalkylthio, haloalkylsulfonyl, haloalkylsulfinyl, haloalkoxy and haloalkoxyalkyl, denotes in each case a straight-chain or branched alkyl group having usually from 1 to 10 carbon atoms, frequently from 1 to 6 carbon atoms, preferably from 1 to 4 carbon atoms, wherein the hydrogen atoms of this group are partially or totally replaced with halogen atoms. Preferred haloalkyl moieties are selected from Ci-C4-haloalkyl, more preferably from Ci-C3-haloalkyl orCi-C2-haloalkyl, in particular from Ci-C2-fluoroalkyl such as fluoromethyl, difluoromethyl, trifluoromethyl, 1 -fluoroethyl, 2-fluoroethyl, 2,2 difluoroethyl, 2,2,2-trifluoroethyl, pentafluoroethyl, and the like.

[0140] The term "alkoxy" as used herein denotes in each case a straight-chain or branched alkyl group which is bonded via an oxygen atom and has usually from 1 to 10 carbon atoms, frequently from 1 to 6 carbon atoms, preferably 1 to 4 carbon atoms. Examples of an alkoxy group are methoxy, ethoxy, n-propoxy, iso-propoxy, n-butyloxy, 2-butyloxy, iso-butyloxy, tert. -butyloxy, and the like. The term "alkoxyalkyl" as used herein refers to alkyl usually comprising 1 to 10, frequently 1 to 4, preferably 1 to 2 carbon atoms, wherein 1 carbon atom carries an alkoxy radical usually comprising 1 to 4, preferably 1 or 2 carbon atoms as defined above. Examples are CH2OCH3, CH2-OC2H5, 2-(methoxy)ethyl, and 2-(ethoxy)ethyl.

[0141] The term "haloalkoxy" as used herein denotes in each case a straight-chain or branched alkoxy group having from 1 to 10 carbon atoms, frequently from 1 to 6 carbon atoms, preferably 1 to 4 carbon atoms, wherein the hydrogen atoms of this group are partially or totally replaced with halogen atoms, in particular fluorine atoms. Preferred haloalkoxy moieties include C1-C4-haloalkoxy, in particular Ci-C2-fluoroalkoxy, such as fluoromethoxy, difluoromethoxy, trifluoromethoxy, 1 fluoroethoxy, 2-fluoroethoxy, 2,2 difluoroethoxy, 2,2,2-trifluoroethoxy, 2-chloro-2-fluoroethoxy, 2-chloro-2,2-difluoro-ethoxy, 2,2dichloro-2-fluorethoxy, 2,2,2-trichloroethoxy, pentafluoroethoxy and the like.

[0142] The term "alkylthio "(alkylsulfanyl: alkyl-S-)" as used herein refers to a straight-chain or branched saturated alkyl group having 1 to 10 carbon atoms, preferably 1 to 4 carbon atoms (= Ci-C4-alkylthio), more preferably 1 to 3 carbon atoms, which is attached via a sulfur atom. The term "haloalkylthio" as used herein refers to an alkylthio group as mentioned above wherein the hydrogen atoms are partially or fully substituted by fluorine, chlorine, bromine and / or iodine. The term "alkylsulfinyl" (alkylsulfoxyl: Ci-C6-alkyl-S(O)-), as used herein refers to a straightchain or branched saturated alkyl group (as mentioned above) having 1 to 10 carbon atoms, preferably 1 to 4 carbon atoms (= Ci-C4-alkylsulfinyl), more preferably 1 to 3 carbon atoms bonded through the sulfur atom of the sulfinyl group at any position in the alkyl group.

[0143] The term "haloalkylsulfinyl" as used herein refers to an alkylsulfinyl group as mentioned above wherein the hydrogen atoms are partially or fully substituted by fluorine, chlorine, bromine and / or iodine.

[0144] The term "alkylsulfonyl" (alkyl-S(O)2-) as used herein refers to a straight-chain or branched saturated alkyl group having 1 to 10 carbon atoms, preferably 1 to 4 carbon atoms (= C1-C4-alkylsulfonyl), preferably 1 to 3 carbon atoms, which is bonded via the sulfur atom of the sulfonyl group at any position in the alkyl group.

[0145] The term "haloalkylsulfonyl" as used herein refers to an alkylsulfonyl group as mentioned above wherein the hydrogen atoms are partially or fully substituted by fluorine, chlorine, bromine and / or iodine.

[0146] The term "alkylcarbonyl" refers to an alkyl group as defined above, which is bonded via the carbon atom of a carbonyl group (C=O) to the remainder of the molecule.

[0147] The term "haloalkylcarbonyl" refers to an alkylcarbonyl group as mentioned above, wherein the hydrogen atoms are partially or fully substituted by fluorine, chlorine, bromine and / or iodine. The term "alkoxycarbonyl" refers to an alkylcarbonyl group as defined above, which is bonded via an oxygen atom to the remainder of the molecule.

[0148] The term "haloalkoxycarbonyl” refers to an alkoxycarbonyl group as mentioned above, wherein the hydrogen atoms are partially or fully substituted by fluorine, chlorine, bromine and / or iodine. The term "alkenyl" as used herein denotes in each case a singly unsaturated hydrocarbon radical having usually 2 to 10, frequently 2 to 6, preferably 2 to 4 carbon atoms, e.g. vinyl, allyl (2-propen-1-yl), 1 -propen-1 -yl, 2 propen-2-yl, methallyl (2-methylprop-2-en-1-yl), 2-buten-1-yl, 3-buten-1-yl, 2-penten-1-yl, 3-penten-1-yl, 4-penten-1-yl, 1-methylbut-2-en-1-yl, 2-ethylprop-2-en-1 -yl and the like.

[0149] The term "haloalkenyl" as used herein refers to an alkenyl group as defined above, wherein the hydrogen atoms are partially or totally replaced with halogen atoms.

[0150] The term "alkynyl" as used herein denotes in each case a singly unsaturated hydrocarbon radical having usually 2 to 10, frequently 2 to 6, preferably 2 to 4 carbon atoms, e.g. ethynyl, propargyl (2-propyn-1-yl), 1-propyn-1-yl, 1-methylprop-2-yn-1-yl), 2-butyn-1-yl, 3-butyn-1-yl, 1-pentyn-1-yl, 3-pentyn-1-yl, 4-pentyn-1-yl, 1-methylbut-2-yn-1-yl, 1-ethylprop-2-yn-1-yl and the like. The term "haloalkynyl" as used herein refers to an alkynyl group as defined above, wherein the hydrogen atoms are partially or totally replaced with halogen atoms.

[0151] The term "cycloalkyl" as used herein and in the cycloalkyl moieties of cycloalkoxy and cycloalkylthio denotes in each case a monocyclic cycloaliphatic radical having usually from 3 to 10 or from 3 to 6 carbon atoms, such as cyclopropyl (c-C3H5), cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, cyclooctyl, cyclononyl and cyclodecyl or cyclopropyl, cyclobutyl, cyclopentyl and cyclohexyl.

[0152] The term "halocycloalkyl" as used herein and in the halocycloalkyl moieties of halocycloalkoxy and halocycloalkylthio denotes in each case a monocyclic cycloaliphatic radical having usually from 3 to 10 C atoms or 3 to 6 C atoms, wherein at least one, e.g. 1, 2, 3, 4 or 5 of the hydrogen atoms, are replaced by halogen, in particular by fluorine or chlorine. Examples are 1- and 2-flu-orocyclopropyl, 1,2-, 2,2- and 2,3-difluorocyclopropyl, 1,2,2-trifluorocyclopropyl, 2, 2,3,3-tetrafluorocyclpropyl, 1- and 2-chlorocyclopropyl, 1,2-, 2,2- and 2,3-dichlorocyclopropyl, 1,2,2-trichlorocyclopropyl, 2,2,3,3-tetrachlorocyclpropyl, 1-,2- and 3-fluorocyclopentyl, 1,2-, 2,2-, 2,3-, 3,3-, 3,4-, 2,5-difluorocyclopentyl, 1-,2- and 3-chlorocyclopentyl, 1,2-, 2,2-, 2,3-, 3,3-, 3,4-, 2,5-dichlorocyclopentyl and the like.

[0153] The term “halocycloalkenyl” as used herein and in the halocycloalkenyl moieties of halocycloalkenyloxy and halocycloalkenylthio denotes in each case a monocyclic singly unsaturated non-aromatic radical having usually from 3 to 10, e.g. 3 or 4 or from 5 to 10 carbon atoms, preferably from 3- to 8 carbon atoms, wherein at least one, e.g. 1, 2, 3, 4 or 5 of the hydrogen atoms, are replaced by halogen, in particular by fluorine or chlorine. Examples are 3,3-difluorocyclopropen-1-yl and 3,3-dichlorocyclopropen-1-yl.

[0154] The term "cycloalkenylalkyl" refers to a cycloalkenyl group as defined above which is bonded via an alkyl group, such as a Ci-C5-alkyl group or a Ci-C4-alkyl group, in particular a methyl group (= cycloalkenylmethyl), to the remainder of the molecule.

[0155] The term “carbocycle” or “carbocyclyl” includes in general a 3- to 12-membered, preferably a 3-to 8-membered or a 5- to 8-membered, more preferably a 5- or 6-membered monocyclic, non-aromatic ring comprising 3 to 12, preferably 3 to 8 or 5 to 8, more preferably 5 or 6 carbon atoms. Preferably, the term “carbocycle” covers cycloalkyl and cycloalkenyl groups as defined above. The term “heterocycle” or "heterocyclyl" includes in general 3- to 12-membered, preferably 3- to 6-membered, in particular 6-membered monocyclic heterocyclic non-aromatic radicals. The heterocyclic non-aromatic radicals usually comprise 1, 2, 3, 4 or 5, preferably 1, 2 or 3 heteroatoms selected from N, O and S as ring members, wherein S-atoms as ring members may be present as S, SO or SO2. Examples of 5- or 6-membered heterocyclic radicals comprise saturated or unsaturated, non-aromatic heterocyclic rings, such as oxiranyl, oxetanyl, thietanyl, thietanyl-S-oxid (S-oxothietanyl), thietanyl-S-dioxid (S-dioxothiethanyl), pyrrolidinyl, pyrrolinyl, pyrazolinyl, tetrahydrofuranyl, dihydrofuranyl, 1,3-dioxolanyl, thiolanyl, S-oxothiolanyl, S-dioxothiolanyl, dihydrothienyl, S-oxodihydrothienyl, S-dioxodihydrothienyl, oxazolidinyl, oxazolinyl, thiazolinyl, oxathiolanyl, piperidinyl, piperazinyl, pyranyl, dihydropyranyl, tetrahydropyranyl, 1,3- and 1,4-dioxanyl, thiopyranyl, S. oxothiopyranyl, S-dioxothiopyranyl, dihydrothiopyranyl, S-oxodihydrothiopyranyl, S-dioxodihydrothiopyranyl, tetrahydrothiopyranyl, S-oxotetrahydrothiopyranyl, S-dioxotetrahydrothiopyranyl, morpholinyl, thiomorpholinyl, S-oxothiomorpholinyl, S-dioxothiomorpholinyl, thiazinyl and the like. Examples for heterocyclic ring also comprising 1 or 2 carbonyl groups as ring members comprise pyrrolidin-2-onyl, pyrrolidin-2,5-dionyl, imidazolidin-2-onyl, oxazolidin-2-onyl, thiazolidin-2-only, and the like.

[0156] The term "hetaryl" includes monocyclic 5- or 6-membered heteroaromatic radicals comprising as ring members 1, 2, 3 or 4 heteroatoms selected from N, O and S. N- or S-containing hetaryl groups may be present as positively charged onium, and form together with a neighbouring atom a mesoionic entity. Examples of 5- or 6 membered heteroaromatic radicals include pyridyl, i.e. 2-, 3-, or 4 pyridyl, pyrimidinyl, i.e. 2, 4- or 5-pyrimidinyl, pyrazinyl, pyridazinyl, i.e. 3- or 4 pyridazinyl, thienyl, i.e. 2- or 3-thienyl, furyl, i.e. 2-or 3-furyl, pyrrolyl, i.e. 2- or 3 pyrrolyl, oxazolyl, i.e. 2-, 3- or 5-oxazolyl, isoxazolyl, i.e. 3-, 4- or 5-isoxazolyl, thiazolyl, i.e. 2-, 3- or 5-thiazolyl, isothiazolyl, i.e. 3-, 4- or 5 isothiazolyl, pyrazolyl, i.e. 1-, 3-, 4- or 5-pyrazolyl, i.e. 1-, 2-, 4- or 5-imidazolyl, oxadiazolyl, e.g. 2- or 5 [1,3,4]oxadiazolyl, 4- or 5-(1,2,3-oxadiazol)yl, 3- or 5-(1,2,4-oxadiazol)yl, 2- or 5 (1,3,4-thiadiazol)yl, thiadiazolyl, e.g. 2- or 5-(1,3,4-thiadiazol)yl, 4- or 5 (1,2,3 thiadiazol)yl, 3- or5-(1,2,4-thiadiazol)yl, triazolyl, e.g. 1H-, 2H- or3H 1,2,3 triazol-4-yl, 2H-triazol-3-yl, 1 H-, 2H-, or 4H-1,2,4-triazolyl and tetrazolyl, i.e. 1 H- or 2H tetrazolyl. The term "hetaryl" also includes bicyclic 8 to 10-membered heteroaromatic radicals comprising as ring members 1, 2 or 3 heteroatoms selected from N, O and S, wherein a 5- or 6-membered heteroaromatic ring is fused to a phenyl ring or to a 5- or 6-membered heteroaromatic radical. Examples of a 5- or 6-membered heteroaromatic ring fused to a phenyl ring or to a 5- or 6-membered heteroaromatic radical include benzofuranyl, benzothienyl, indolyl, indazolyl, benzimidazolyl, benzoxathiazolyl, benzoxadiazolyl, benzothiadiazolyl, benzoxazinyl, chinolinyl, isochinolinyl, purinyl, 1,8-naphthyridyl, pteridyl, pyrido[3,2 d]pyrimidyl or pyridoimidazolyl and the like. These fused hetaryl radicals may be bonded to the remainder of the molecule via any ring atom of 5- or 6-membered heteroaromatic ring or via a carbon atom of the fused phenyl moiety.

[0157] The terms "heterocyclylalkyl" and "hetarylalkyl" refer to heterocyclyl or hetaryl, respectively, as defined above which are bonded via a Ci-C5-alkyl group or a Ci-C4-alkyl group, in particular a methyl group (= heterocyclylmethyl or hetarylmethyl, respectively), to the remainder of the molecule.

[0158] The term “arylalkyl” and "phenylalkyl" refer to aryl as defined above and phenyl, respectively, which are bonded via Ci-C5-alkyl group or a Ci-C4-alkyl group, in particular a methyl group (= arylmethyl or phenylmethyl), to the remainder of the molecule, examples including benzyl, 1-phenylethyl, 2-phenylethyl, 2-phenoxyethyl etc.

[0159] The terms “alkylene”, “cycloalkylene”, “heterocycloalkylene”, “alkenylene”, “cycloalkenylene”, “heterocycloalkenylene” and “alkynylene” refer to alkyl, cycloalkyl, heterocycloalkyl, alkenyl, cycloalkenyl, heterocycloalkenyl and alkynyl as defined above, respectively, which are bonded to the remainder of the molecule, via two atoms, preferably via two carbon atoms, of the respective group, so that they represent a linker between two moieties of the molecule.

[0160] In a particular embodiment, the variables of the compounds of the formula I have the following meanings, these meanings, both on their own and in combination with one another, being particular embodiments of the compounds of the formula I.

[0161] It is understood that the various embodiments of compounds of formula I also include the N-oxide, stereoisomer, tautomer, agriculturally or veterinarily acceptable salt thereof.

[0162] Embodiments and preferred compounds of the invention for use in pesticidal methods and for insecticidal application purposes are outlined in the following paragraphs.

[0163] With respect to the variables, embodiments of the intermediates correspond to those of the compounds of the formula I.

[0164] In various embodiments, R2is R2-1, and W is O. Such compounds correspond to compounds of formula 11. A

[0165] B1-B2

[0166] Q—

[0167] sB-B3N— N R3

[0168] o N

[0169]

[0170] S,

[0171] In various embodiments, R2is R2-2, and W is O. Such compounds correspond to compounds of formula II. B

[0172]

[0173] In various embodiments, R2is R2-4, and W is O. Such compounds correspond to compounds of formula II. C

[0174]

[0175] In various embodiments, B1is CRB1, B2is CRB2, B3is CRB3, and B4is CRB4.

[0176] In various embodiments, B1is N, B2is CRB2, B3is CRB3, and B4is CRB4.

[0177] In various embodiments, B1is CRB1, B2is N, B3is CRB3, and B4is CRB4.

[0178] In various embodiments, B1is N, B2is CRB2, B3is CRB3, and B4is N.

[0179] In various embodiments, B1is N, B2is CRB2, B3is N, and B4is CRB4.

[0180] In various embodiments, B1is CRB1, B2is N, B3is N, and B4is CRB4.

[0181] In various embodiments, B1is CH, B2is CH, B3is CH, and B4is CH.

[0182] In various embodiments, B1is N, B2is CH, B3is CH, and B4is CH.

[0183] In various embodiments, B1is CH, B2is N, B3is CH, and B4is CH.

[0184] In various embodiments, B1is N, B2is CH, B3is CH, and B4is N.

[0185] In various embodiments, B1is N, B2is CH, B3is N, and B4is CH.

[0186] In various embodiments, B1is CH, B2is N, B3is N, and B4is CH.

[0187] In various embodiments, B1is CCI, B2is CH, B3is CH, and B4is CH.

[0188] In various embodiments, B1is CH, B2is CCI, B3is CH, and B4is CH.

[0189] In various embodiments, B1is CF, B2is CH, B3is CH, and B4is CH.

[0190] In various embodiments, B1is CH, B2is CF, B3is CH, and B4is CH.

[0191] In various embodiments, X is a single bond, Y is -CRya=N-, wherein the N is bound to Z, Z is -N=C(S-Rza)-, wherein T is bound to the carbon atom, and T is N-RT, wherein Rzatogether with RTforms a linear Ci-C6-alkylene group, preferably C2alkylene group, where in the linear Ci-C6-alkylene a CH2moiety is replaced by a carbonyl and wherein the linear Ci-C6-alkylene is unsubstituted or substituted with one or more Rh, and Ryais preferably H.

[0192] In various embodiments, X is a single bond, Y is -NRyc-C(=O)-, wherein C(=O) is bound to Z, Z is -N=C(S-Rza)-, wherein T is bound to the carbon atom, and T is N-RT, wherein Rzatogether with RTforms a linear Ci-C6-alkylene group, preferably C2alkylene group, where in the linear Ci-C6-alkylene a CH2moiety is replaced by a carbonyl and wherein the linear Ci-C6-alkylene is unsubstituted or substituted with one or more Rh, and Rycis preferably H.

[0193] In various embodiments, X is -(C(Rxa)2)p-, wherein p is 2, Y is -NRyc-C(=O)-, wherein C(=O) is bound to Z, Z is -N=C(S-Rza)-, wherein T is bound to the carbon atom, and T is N-RT, wherein Rzatogether with RTforms a linear Ci-C6-alkylene group, preferably C2alkylene group, where in the linear Ci-C6-alkylene a CH2moiety is replaced by a carbonyl and wherein the linear Ci-C6-alkylene is unsubstituted or substituted with one or more Rh, and all Rxaand Rycare preferably H. In various embodiments, X is -(C(Rxa)2)0-NRxc-, wherein o is 1 and N is bound to Y, Y is -NRyc-C(=O)-, wherein C(=O) is bound to Z, Z is -N=C(S-Rza)-, wherein T is bound to the carbon atom, and T is N-RT, wherein Rzatogether with RTforms a linear Ci-C6-alkylene group, preferably C2alkylene group, where in the linear Ci-C6-alkylene a CH2moiety is replaced by a carbonyl and wherein the linear Ci-C6-alkylene is unsubstituted or substituted with one or more Rh, wherein one Rxa, Rxcand Rycare preferably H and the other Rxais preferably methyl, or wherein one Rxaand Rycare preferably H and the other Rxaand Rxcare preferably methyl.

[0194] In various embodiments, X is -(C(Rxa)2)0-NRxc-, wherein o is 1 and N is bound to Y, Y is -NRyc-C(=O)-, wherein C(=O) is bound to Z, Z is -NRZC-C(=S)-, wherein C(=S) is bound to T, and T is N-RT, wherein one Rxa, Rxc, Ryc, Rzcand RTare preferably H and the other Rxais preferably methyl, or wherein one Rxa, Ryc, Rzcand RTare preferably H and the other Rxaand Rxcare preferably methyl.

[0195] In various embodiments, X is -(C(Rxa)2)p-, wherein p is 1, Y is -NRyc-C(=O)-, wherein C(=O) is bound to Z, Z is -NRZC-C(=S)-, wherein C(=S) is bound to T, and T is N-RT, wherein one Rxa, Rzcand RTare preferably H, the other Rxais preferably methyl, and Rycis preferably -NH2.

[0196] In various embodiments, X is -(C(Rxa)2)0-NRxc-, wherein o is 1 and N is bound to Y, Y is -NRyc-C(=O)-, wherein C(=O) is bound to Z, Z is -NRZC-C(=S)-, wherein C(=S) is bound to T, and T is N-RT, wherein one Rxa, Ryc, Rzcand RTare preferably H and the other Rxaand Rxcare preferably methyl.

[0197] In various embodiments, X is -(C(Rxa)2)0-NRxc-, wherein o is 1 and N is bound to Y, Y is -NRyc-C(=O)-, wherein C(=O) is bound to Z, Z is -N=C(S-Rza)-, wherein T is bound to the carbon atom, and T is N-RT, wherein Rzatogether with RTforms a linear Ci-C6-alkylene group, preferably C2alkylene group, where in the linear Ci-C6-alkylene a CH2moiety is replaced by a carbonyl and wherein the linear Ci-C6-alkylene is unsubstituted or substituted with one or more Rh, and one Rxaand Rycare preferably H and the other Rxaand Rxcare preferably methyl.

[0198] In various embodiments, X is a single bond, Y is -CRya=N-, wherein the N is bound to Z, Z is -NRZC— C(=S)—, wherein C(=S) is bound to T and T is N-RT, wherein Rya, Rzc, and RTare preferably H.

[0199] In various embodiments, X is a single bond, Y is -NRyc-C(=O)-, wherein C(=O) is bound to Z, Z is -NRzc-C(=S)-, wherein C(=S) is bound to T and T is N-RT, wherein Ryc, Rzc, and RTare preferably H.

[0200] In various embodiments, R3is monocyclic or bicyclic aryl substituted with one or more Rs, preferably phenyl, naphthyl, or pyridinyl optionally substituted with one or more Rs. In various embodiments, RB1, RB2, RB3, and RB4independently of each other are H, halogen, N3, OH, CN, NO2, -SCN, -SF5, C1-C6-alkyl, C1-C6-alkoxy, C2-C6-alkenyl, tri-C1-C6-alkylsilyl, C2-C6-alkynyl, C1-C4-alkyl-C1-C6-alkoxy, C1-C6-alkoxy-C1-C4-alkoxy, C3-C6-cycloalkyl, C3-C6-cycloalkoxy, C3-C6-cycloalkyl-Ci-C4-alkyl, Ci-C4-alkyl-C3-C6-cycloalkoxy, wherein the alkyl, alkoxy, alkenyl, alkynyl, cycloalkyl and cycloalkoxy moieties are unsubstituted or substituted with one or more halogen; C(=O)-ORa, NRbRc, Ci-C6-alkylene-NRbRc, O-Ci-C6-alkylene-NRbRc, Ci-C6-alkylene-CN, NH-Ci-C6-alkylene-NRbRc, C(=O)-NRbRc, C(=O)-Rd, SO2NRbRc, or S(=O)mRe, phenyl, phenoxy, phenylcarbonyl, phenylthio, or -CH2-phenyl, wherein the phenyl rings are unsubstituted or substituted with one or more Rf;

[0201] In various embodiments, R1a, R1b, and R1cindependently of each other are H, halogen, N3, OH, CN, NO2, -SCN, -SF5, C1-C6-alkyl, C1-C6-alkoxy, C2-C6-alkenyl, tri-C1-C6-alkylsilyl, C2-C6-alkynyl, C1-C4-alkyl-C1-C6-alkoxy, C1-C6-alkoxy-C1-C4-alkoxy, C3-C6-cycloalkyl, C3-C6-cycloalkoxy, C3-C6-cycloalkyl-Ci-C4-alkyl, C3-C6-cycloalkoxy-C1-C4-alkyl, wherein the alkyl, alkoxy, alkenyl, alkynyl, cycloalkyl and cycloalkoxy moieties are unsubstituted or substituted with one or more halogen; C(=O)-ORa, NRbRc, Ci-C6-alkylene-NRbRc, O-Ci-C6-alkylene-NRbRc, Ci-C6-alkylene-CN, NH-Ci-C6-alkylene-NRbRc, C(=O)-NRbRc, C(=O)-Rd, SO2NRbRc, or S(=O)mRe, phenyl, phenoxy, phenylcarbonyl, phenylthio or-CH2-phenyl, wherein phenyl rings are unsubstituted or substituted with one or more Rf;

[0202] In various embodiments, R1aand R1b, or R1band R1c, form together with the carbon atoms to which they are bonded a 5- or 6-membered partially unsaturated heterocyclic ring, which contains 1 or 2 heteroatoms selected from N, O, S, and which is unsubstituted or substituted with one or more halogen, CN, Ci-C4-alkyl, or Ci-C4-haloalkyl; preferably wherein the heterocyclic ring contains two O atoms.

[0203] In various embodiments, R1a, R1b, and R1cindependently of each other are halogen, OH, Ci-C6-alkyl, Ci-C6-haloalkyl, Ci-C6-alkoxy, Ci-C6-haloalkoxy, or S-Re.

[0204] In various embodiments, Reis Ci-C6-alkyl, C3-C6-cycloalkyl, C3-C6-cycloalkyl-Ci-C4-alkyl, wherein the alkyl, cycloalkyl moieties are unsubstituted or substituted with one or more halogen.

[0205] In various embodiments, RB1, RB2, RB3, and RB4independently of each other are H, halogen, Ci-C6-alkyl, Ci-C6-alkoxy, C2-C6-alkenyl, C2-C6-alkynyl, wherein the alkyl, alkoxy, alkenyl, alkynyl, moieties are unsubstituted or substituted with one or more halogen, preferably H, F, Cl, Br, OCF3, OCHF2, OCH3, or OCH2CH3.

[0206] In various embodiments, R1a, R1b, and R1cindependently of each other are halogen, OH, Ci-C6-alkyl, Ci-C6-haloalkyl, Ci-C6-alkoxy, Ci-C6-haloalkoxy, or S-Re; and

[0207] Reis Ci-C6-alkyl, C3-C6-cycloalkyl, C3-C6-cycloalkyl-Ci-C4-alkyl, wherein the alkyl, cycloalkyl moieties are unsubstituted or substituted with one or more halogen; and

[0208] RB1, RB2, RB3, and RB4independently of each other are H, halogen, Ci-C6-alkyl, Ci-C6-alkoxy, C2-C6-alkenyl, C2-C6-alkynyl, wherein the alkyl, alkoxy, alkenyl, alkynyl, moieties are unsubstituted or substituted with one or more halogen.

[0209] In various embodiments, R2is selected from the following groups o s R2-3, R2-6,

[0210]

[0211] R2-10. In various embodiments, R3is selected from the following groups

[0212]

[0213]

[0214] R3-22,

[0215] R3-25,

[0216]

[0217]

[0218] preferably, wherein R3is R3-1, R3-29, R3-30, or R3-31.

[0219] In one preferred embodiment, the invention relates to compounds of Table I, or the N-oxide, stereoisomer, tautomer, agriculturally or veterinarily acceptable salt thereof.

[0220] In particular with a view to their use, preference is given to the compounds of formula I compiled in the tables below. Each of the groups mentioned for a substituent in the tables is furthermore per se, independently of the combination in which it is mentioned, a particularly preferred aspect of the substituent in question.

[0221] Table 1: Compounds of formula I in which R1ais H, R1cis H, W is O, R2is R2-1, R3is R3-1, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0222] Table 2: Compounds of formula I in which R1ais H, R1cis H, W is O, R2is R2-2, R3is R3-1, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0223] Table 3: Compounds of formula I in which R1ais H, R1cis H, W is O, R2is R2-3, R3is R3-1, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0224] Table 4: Compounds of formula I in which R1ais H, R1cis H, W is O, R2is R2-4, R3is R3-1, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0225] Table 5: Compounds of formula I in which R1ais H, R1cis H, W is O, R2is R2-5, R3is R3-1, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A. Table 6: Compounds of formula I in which R1ais H, R1cis H, W is O, R2is R2-6, R3is R3-1, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0226] Table 7: Compounds of formula I in which R1ais H, R1cis H, W is O, R2is R2-7, R3is R3-1, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0227] Table 8: Compounds of formula I in which R1ais H, R1cis H, W is O, R2is R2-8, R3is R3-1, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0228] Table 9: Compounds of formula I in which R1ais H, R1cis H, W is O, R2is R2-9, R3is R3-1, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0229] Table 10: Compounds of formula I in which R1ais H, R1cis H, W is O, R2is R2-10, R3is R3-1, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0230] Table 11: Compounds of formula I in which R1ais H, R1cis H, W is O, R2is R2-1, R3is R3-29, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0231] Table 12: Compounds of formula I in which R1ais H, R1cis H, W is O, R2is R2-2, R3is R3-29, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0232] Table 13: Compounds of formula I in which R1ais H, R1cis H, W is O, R2is R2-3, R3is R3-29, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0233] Table 14: Compounds of formula I in which R1ais H, R1cis H, W is O, R2is R2-4, R3is R3-29, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0234] Table 15: Compounds of formula I in which R1ais H, R1cis H, W is O, R2is R2-5, R3is R3-29, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0235] Table 16: Compounds of formula I in which R1ais H, R1cis H, W is O, R2is R2-6, R3is R3-29, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0236] Table 17: Compounds of formula I in which R1ais H, R1cis H, W is O, R2is R2-7, R3is R3-29, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0237] Table 18: Compounds of formula I in which R1ais H, R1cis H, W is O, R2is R2-8, R3is R3-29, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0238] Table 19: Compounds of formula I in which R1ais H, R1cis H, W is O, R2is R2-9, R3is R3-29, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0239] Table 20: Compounds of formula I in which R1ais H, R1cis H, W is O, R2is R2-10, R3is R3-29, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A. Table 21: Compounds of formula I in which R1ais H, R1cis H, W is O, R2is R2-1, R3is R3-30, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0240] Table 22: Compounds of formula I in which R1ais H, R1cis H, W is O, R2is R2-2, R3is R3-30, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0241] Table 23: Compounds of formula I in which R1ais H, R1cis H, W is O, R2is R2-3, R3is R3-30, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0242] Table 24: Compounds of formula I in which R1ais H, R1cis H, W is O, R2is R2-4, R3is R3-30, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0243] Table 25: Compounds of formula I in which R1ais H, R1cis H, W is O, R2is R2-5, R3is R3-30, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0244] Table 26: Compounds of formula I in which R1ais H, R1cis H, W is O, R2is R2-6, R3is R3-30, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0245] Table 27: Compounds of formula I in which R1ais H, R1cis H, W is O, R2is R2-7, R3is R3-30, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0246] Table 28: Compounds of formula I in which R1ais H, R1cis H, W is O, R2is R2-8, R3is R3-30, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0247] Table 29: Compounds of formula I in which R1ais H, R1cis H, W is O, R2is R2-9, R3is R3-30, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0248] Table 30: Compounds of formula I in which R1ais H, R1cis H, W is O, R2is R2-10, R3is R3-30, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0249] Table 31: Compounds of formula I in which R1ais H, R1cis H, W is O, R2is R2-1, R3is R3-31, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0250] Table 32: Compounds of formula I in which R1ais H, R1cis H, W is O, R2is R2-2, R3is R3-31, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0251] Table 33: Compounds of formula I in which R1ais H, R1cis H, W is O, R2is R2-3, R3is R3-31, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0252] Table 34: Compounds of formula I in which R1ais H, R1cis H, W is O, R2is R2-4, R3is R3-31, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0253] Table 35: Compounds of formula I in which R1ais H, R1cis H, W is O, R2is R2-5, R3is R3-31, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A. Table 36: Compounds of formula I in which R1ais H, R1cis H, W is O, R2is R2-6, R3is R3-31, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0254] Table 37: Compounds of formula I in which R1ais H, R1cis H, W is O, R2is R2-7, R3is R3-31, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0255] Table 38: Compounds of formula I in which R1ais H, R1cis H, W is O, R2is R2-8, R3is R3-31, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0256] Table 39: Compounds of formula I in which R1ais H, R1cis H, W is O, R2is R2-9, R3is R3-31, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0257] Table 40: Compounds of formula I in which R1ais H, R1cis H, W is O, R2is R2-10, R3is R3-31, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0258] Table 41: Compounds of formula I in which R1ais F, R1cis H, W is O, R2is R2-1, R3is R3-1, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0259] Table 42: Compounds of formula I in which R1ais F, R1cis H, W is O, R2is R2-2, R3is R3-1, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0260] Table 43: Compounds of formula I in which R1ais F, R1cis H, W is O, R2is R2-3, R3is R3-1, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0261] Table 44: Compounds of formula I in which R1ais F, R1cis H, W is O, R2is R2-4, R3is R3-1, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0262] Table 45: Compounds of formula I in which R1ais F, R1cis H, W is O, R2is R2-5, R3is R3-1, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0263] Table 46: Compounds of formula I in which R1ais F, R1cis H, W is O, R2is R2-6, R3is R3-1, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0264] Table 47: Compounds of formula I in which R1ais F, R1cis H, W is O, R2is R2-7, R3is R3-1, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0265] Table 48: Compounds of formula I in which R1ais F, R1cis H, W is O, R2is R2-8, R3is R3-1, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0266] Table 49: Compounds of formula I in which R1ais F, R1cis H, W is O, R2is R2-9, R3is R3-1, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0267] Table 50: Compounds of formula I in which R1ais F, R1cis H, W is O, R2is R2-10, R3is R3-1, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A. Table 51: Compounds of formula I in which R1ais F, R1cis H, W is O, R2is R2-1, R3is R3-29, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0268] Table 52: Compounds of formula I in which R1ais F, R1cis H, W is O, R2is R2-2, R3is R3-29, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0269] Table 53: Compounds of formula I in which R1ais F, R1cis H, W is O, R2is R2-3, R3is R3-29, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0270] Table 54: Compounds of formula I in which R1ais F, R1cis H, W is O, R2is R2-4, R3is R3-29, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0271] Table 55: Compounds of formula I in which R1ais F, R1cis H, W is O, R2is R2-5, R3is R3-29, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0272] Table 56: Compounds of formula I in which R1ais F, R1cis H, W is O, R2is R2-6, R3is R3-29, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0273] Table 57: Compounds of formula I in which R1ais F, R1cis H, W is O, R2is R2-7, R3is R3-29, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0274] Table 58: Compounds of formula I in which R1ais F, R1cis H, W is O, R2is R2-8, R3is R3-29, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0275] Table 59: Compounds of formula I in which R1ais F, R1cis H, W is O, R2is R2-9, R3is R3-29, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0276] Table 60: Compounds of formula I in which R1ais F, R1cis H, W is O, R2is R2-10, R3is R3-29, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0277] Table 61: Compounds of formula I in which R1ais F, R1cis H, W is O, R2is R2-1, R3is R3-30, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0278] Table 62: Compounds of formula I in which R1ais F, R1cis H, W is O, R2is R2-2, R3is R3-30, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0279] Table 63: Compounds of formula I in which R1ais F, R1cis H, W is O, R2is R2-3, R3is R3-30, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0280] Table 64: Compounds of formula I in which R1ais F, R1cis H, W is O, R2is R2-4, R3is R3-30, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0281] Table 65: Compounds of formula I in which R1ais F, R1cis H, W is O, R2is R2-5, R3is R3-30, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A. Table 66: Compounds of formula I in which R1ais F, R1cis H, W is O, R2is R2-6, R3is R3-30, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0282] Table 67: Compounds of formula I in which R1ais F, R1cis H, W is O, R2is R2-7, R3is R3-30, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0283] Table 68: Compounds of formula I in which R1ais F, R1cis H, W is O, R2is R2-8, R3is R3-30, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0284] Table 69: Compounds of formula I in which R1ais F, R1cis H, W is O, R2is R2-9, R3is R3-30, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0285] Table 70: Compounds of formula I in which R1ais F, R1cis H, W is O, R2is R2-10, R3is R3-30, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0286] Table 71: Compounds of formula I in which R1ais F, R1cis H, W is O, R2is R2-1, R3is R3-31, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0287] Table 72: Compounds of formula I in which R1ais F, R1cis H, W is O, R2is R2-2, R3is R3-31, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0288] Table 73: Compounds of formula I in which R1ais F, R1cis H, W is O, R2is R2-3, R3is R3-31, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0289] Table 74: Compounds of formula I in which R1ais F, R1cis H, W is O, R2is R2-4, R3is R3-31, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0290] Table 75: Compounds of formula I in which R1ais F, R1cis H, W is O, R2is R2-5, R3is R3-31, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0291] Table 76: Compounds of formula I in which R1ais F, R1cis H, W is O, R2is R2-6, R3is R3-31, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0292] Table 77: Compounds of formula I in which R1ais F, R1cis H, W is O, R2is R2-7, R3is R3-31, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0293] Table 78: Compounds of formula I in which R1ais F, R1cis H, W is O, R2is R2-8, R3is R3-31, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0294] Table 79: Compounds of formula I in which R1ais F, R1cis H, W is O, R2is R2-9, R3is R3-31, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0295] Table 80: Compounds of formula I in which R1ais F, R1cis H, W is O, R2is R2-10, R3is R3-31, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A. Table 81: Compounds of formula I in which R1ais Cl, R1cis H, W is O, R2is R2-1, R3is R3-1, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0296] Table 82: Compounds of formula I in which R1ais Cl, R1cis H, W is O, R2is R2-2, R3is R3-1, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0297] Table 83: Compounds of formula I in which R1ais Cl, R1cis H, W is O, R2is R2-3, R3is R3-1, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0298] Table 84: Compounds of formula I in which R1ais Cl, R1cis H, W is O, R2is R2-4, R3is R3-1, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0299] Table 85: Compounds of formula I in which R1ais Cl, R1cis H, W is O, R2is R2-5, R3is R3-1, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0300] Table 86: Compounds of formula I in which R1ais Cl, R1cis H, W is O, R2is R2-6, R3is R3-1, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0301] Table 87: Compounds of formula I in which R1ais Cl, R1cis H, W is O, R2is R2-7, R3is R3-1, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0302] Table 88: Compounds of formula I in which R1ais Cl, R1cis H, W is O, R2is R2-8, R3is R3-1, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0303] Table 89: Compounds of formula I in which R1ais Cl, R1cis H, W is O, R2is R2-9, R3is R3-1, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0304] Table 90: Compounds of formula I in which R1ais Cl, R1cis H, W is O, R2is R2-10, R3is R3-1, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0305] Table 91: Compounds of formula I in which R1ais Cl, R1cis H, W is O, R2is R2-1, R3is R3-29, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0306] Table 92: Compounds of formula I in which R1ais Cl, R1cis H, W is O, R2is R2-2, R3is R3-29, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0307] Table 93: Compounds of formula I in which R1ais Cl, R1cis H, W is O, R2is R2-3, R3is R3-29, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0308] Table 94: Compounds of formula I in which R1ais Cl, R1cis H, W is O, R2is R2-4, R3is R3-29, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0309] Table 95: Compounds of formula I in which R1ais Cl, R1cis H, W is O, R2is R2-5, R3is R3-29, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A. Table 96: Compounds of formula I in which R1ais Cl, R1cis H, W is O, R2is R2-6, R3is R3-29, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0310] Table 97: Compounds of formula I in which R1ais Cl, R1cis H, W is O, R2is R2-7, R3is R3-29, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0311] Table 98: Compounds of formula I in which R1ais Cl, R1cis H, W is O, R2is R2-8, R3is R3-29, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0312] Table 99: Compounds of formula I in which R1ais Cl, R1cis H, W is O, R2is R2-9, R3is R3-29, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0313] Table 100: Compounds of formula I in which R1ais Cl, R1cis H, W is O, R2is R2-10, R3is R3- 29, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0314] Table 101: Compounds of formula I in which R1ais Cl, R1cis H, W is O, R2is R2-1, R3is R3-30, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0315] Table 102: Compounds of formula I in which R1ais Cl, R1cis H, W is O, R2is R2-2, R3is R3-30, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0316] Table 103: Compounds of formula I in which R1ais Cl, R1cis H, W is O, R2is R2-3, R3is R3-30, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0317] Table 104: Compounds of formula I in which R1ais Cl, R1cis H, W is O, R2is R2-4, R3is R3-30, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0318] Table 105: Compounds of formula I in which R1ais Cl, R1cis H, W is O, R2is R2-5, R3is R3-30, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0319] Table 106: Compounds of formula I in which R1ais Cl, R1cis H, W is O, R2is R2-6, R3is R3-30, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0320] Table 107: Compounds of formula I in which R1ais Cl, R1cis H, W is O, R2is R2-7, R3is R3-30, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0321] Table 108: Compounds of formula I in which R1ais Cl, R1cis H, W is O, R2is R2-8, R3is R3-30, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0322] Table 109: Compounds of formula I in which R1ais Cl, R1cis H, W is O, R2is R2-9, R3is R3-30, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0323] Table 110: Compounds of formula I in which R1ais Cl, R1cis H, W is O, R2is R2-10, R3is R3- 30, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A. Table 111: Compounds of formula I in which R1ais Cl, R1cis H, W is O, R2is R2-1, R3is R3-31, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0324] Table 112: Compounds of formula I in which R1ais Cl, R1cis H, W is O, R2is R2-2, R3is R3-31, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0325] Table 113: Compounds of formula I in which R1ais Cl, R1cis H, W is O, R2is R2-3, R3is R3-31, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0326] Table 114: Compounds of formula I in which R1ais Cl, R1cis H, W is O, R2is R2-4, R3is R3-31, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0327] Table 115: Compounds of formula I in which R1ais Cl, R1cis H, W is O, R2is R2-5, R3is R3-31, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0328] Table 116: Compounds of formula I in which R1ais Cl, R1cis H, W is O, R2is R2-6, R3is R3-31, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0329] Table 117: Compounds of formula I in which R1ais Cl, R1cis H, W is O, R2is R2-7, R3is R3-31, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0330] Table 118: Compounds of formula I in which R1ais Cl, R1cis H, W is O, R2is R2-8, R3is R3-31, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0331] Table 119: Compounds of formula I in which R1ais Cl, R1cis H, W is O, R2is R2-9, R3is R3-31, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0332] Table 120: Compounds of formula I in which R1ais Cl, R1cis H, W is O, R2is R2-10, R3is R3-31, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0333] Table 121: Compounds of formula I in which R1ais OCF3, R1cis H, W is O, R2is R2-1, R3is R3-1, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0334] Table 122: Compounds of formula I in which R1ais OCF3, R1cis H, W is O, R2is R2-2, R3is R3-1, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0335] Table 123: Compounds of formula I in which R1ais OCF3, R1cis H, W is O, R2is R2-3, R3is R3-1, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0336] Table 124: Compounds of formula I in which R1ais OCF3, R1cis H, W is O, R2is R2-4, R3is R3-1, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0337] Table 125: Compounds of formula I in which R1ais OCF3, R1cis H, W is O, R2is R2-5, R3is R3-1, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A. Table 126: Compounds of formula I in which R1ais OCF3, R1cis H, W is O, R2is R2-6, R3is R3-1, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0338] Table 127: Compounds of formula I in which R1ais OCF3, R1cis H, W is O, R2is R2-7, R3is R3-1, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0339] Table 128: Compounds of formula I in which R1ais OCF3, R1cis H, W is O, R2is R2-8, R3is R3-1, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0340] Table 129: Compounds of formula I in which R1ais OCF3, R1cis H, W is O, R2is R2-9, R3is R3-1, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0341] Table 130: Compounds of formula I in which R1ais OCF3, R1cis H, W is O, R2is R2-10, R3is R3-1, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0342] Table 131: Compounds of formula I in which R1ais OCF3, R1cis H, W is O, R2is R2-1, R3is R3-29, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0343] Table 132: Compounds of formula I in which R1ais OCF3, R1cis H, W is O, R2is R2-2, R3is R3-29, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0344] Table 133: Compounds of formula I in which R1ais OCF3, R1cis H, W is O, R2is R2-3, R3is R3-29, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0345] Table 134: Compounds of formula I in which R1ais OCF3, R1cis H, W is O, R2is R2-4, R3is R3-29, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0346] Table 135: Compounds of formula I in which R1ais OCF3, R1cis H, W is O, R2is R2-5, R3is R3-29, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0347] Table 136: Compounds of formula I in which R1ais OCF3, R1cis H, W is O, R2is R2-6, R3is R3-29, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0348] Table 137: Compounds of formula I in which R1ais OCF3, R1cis H, W is O, R2is R2-7, R3is R3-29, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0349] Table 138: Compounds of formula I in which R1ais OCF3, R1cis H, W is O, R2is R2-8, R3is R3-29, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0350] Table 139: Compounds of formula I in which R1ais OCF3, R1cis H, W is O, R2is R2-9, R3is R3-29, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0351] Table 140: Compounds of formula I in which R1ais OCF3, R1cis H, W is O, R2is R2-10, R3is R3-29, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A. Table 141: Compounds of formula I in which R1ais OCF3, R1cis H, W is O, R2is R2-1, R3is R3-30, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0352] Table 142: Compounds of formula I in which R1ais OCF3, R1cis H, W is O, R2is R2-2, R3is R3-30, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0353] Table 143: Compounds of formula I in which R1ais OCF3, R1cis H, W is O, R2is R2-3, R3is R3-30, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0354] Table 144: Compounds of formula I in which R1ais OCF3, R1cis H, W is O, R2is R2-4, R3is R3-30, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0355] Table 145: Compounds of formula I in which R1ais OCF3, R1cis H, W is O, R2is R2-5, R3is R3-30, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0356] Table 146: Compounds of formula I in which R1ais OCF3, R1cis H, W is O, R2is R2-6, R3is R3-30, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0357] Table 147: Compounds of formula I in which R1ais OCF3, R1cis H, W is O, R2is R2-7, R3is R3-30, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0358] Table 148: Compounds of formula I in which R1ais OCF3, R1cis H, W is O, R2is R2-8, R3is R3-30, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0359] Table 149: Compounds of formula I in which R1ais OCF3, R1cis H, W is O, R2is R2-9, R3is R3- 30, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0360] Table 150: Compounds of formula I in which R1ais OCF3, R1cis H, W is O, R2is R2-10, R3is R3-30, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0361] Table 151: Compounds of formula I in which R1ais OCF3, R1cis H, W is O, R2is R2-1, R3is R3- 31, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0362] Table 152: Compounds of formula I in which R1ais OCF3, R1cis H, W is O, R2is R2-2, R3is R3-31, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0363] Table 153: Compounds of formula I in which R1ais OCF3, R1cis H, W is O, R2is R2-3, R3is R3-31, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0364] Table 154: Compounds of formula I in which R1ais OCF3, R1cis H, W is O, R2is R2-4, R3is R3-31, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0365] Table 155: Compounds of formula I in which R1ais OCF3, R1cis H, W is O, R2is R2-5, R3is R3-31, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A. Table 156: Compounds of formula I in which R1ais OCF3, R1cis H, W is O, R2is R2-6, R3is R3-31, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0366] Table 157: Compounds of formula I in which R1ais OCF3, R1cis H, W is O, R2is R2-7, R3is R3-31, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0367] Table 158: Compounds of formula I in which R1ais OCF3, R1cis H, W is O, R2is R2-8, R3is R3-31, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0368] Table 159: Compounds of formula I in which R1ais OCF3, R1cis H, W is O, R2is R2-9, R3is R3-31, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0369] Table 160: Compounds of formula I in which R1ais OCF3, R1cis H, W is O, R2is R2-10, R3is R3-31, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0370] Table 161: Compounds of formula I in which R1ais CF3, R1cis H, W is O, R2is R2-1, R3is R3-1, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0371] Table 162: Compounds of formula I in which R1ais CF3, R1cis H, W is O, R2is R2-2, R3is R3-1, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0372] Table 163: Compounds of formula I in which R1ais CF3, R1cis H, W is O, R2is R2-3, R3is R3-1, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0373] Table 164: Compounds of formula I in which R1ais CF3, R1cis H, W is O, R2is R2-4, R3is R3-1, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0374] Table 165: Compounds of formula I in which R1ais CF3, R1cis H, W is O, R2is R2-5, R3is R3-1, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0375] Table 166: Compounds of formula I in which R1ais CF3, R1cis H, W is O, R2is R2-6, R3is R3-1, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0376] Table 167: Compounds of formula I in which R1ais CF3, R1cis H, W is O, R2is R2-7, R3is R3-1, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0377] Table 168: Compounds of formula I in which R1ais CF3, R1cis H, W is O, R2is R2-8, R3is R3-1, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0378] Table 169: Compounds of formula I in which R1ais CF3, R1cis H, W is O, R2is R2-9, R3is R3-1, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0379] Table 170: Compounds of formula I in which R1ais CF3, R1cis H, W is O, R2is R2-10, R3is R3-1, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A. Table 171: Compounds of formula I in which R1ais CF3, R1cis H, W is O, R2is R2-1, R3is R3-29, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0380] Table 172: Compounds of formula I in which R1ais CF3, R1cis H, W is O, R2is R2-2, R3is R3-29, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0381] Table 173: Compounds of formula I in which R1ais CF3, R1cis H, W is O, R2is R2-3, R3is R3-29, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0382] Table 174: Compounds of formula I in which R1ais CF3, R1cis H, W is O, R2is R2-4, R3is R3-29, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0383] Table 175: Compounds of formula I in which R1ais CF3, R1cis H, W is O, R2is R2-5, R3is R3-29, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0384] Table 176: Compounds of formula I in which R1ais CF3, R1cis H, W is O, R2is R2-6, R3is R3-29, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0385] Table 177: Compounds of formula I in which R1ais CF3, R1cis H, W is O, R2is R2-7, R3is R3-29, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0386] Table 178: Compounds of formula I in which R1ais CF3, R1cis H, W is O, R2is R2-8, R3is R3-29, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0387] Table 179: Compounds of formula I in which R1ais CF3, R1cis H, W is O, R2is R2-9, R3is R3-29, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0388] Table 180: Compounds of formula I in which R1ais CF3, R1cis H, W is O, R2is R2-10, R3is R3- 29, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0389] Table 181: Compounds of formula I in which R1ais CF3, R1cis H, W is O, R2is R2-1, R3is R3- 30, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0390] Table 182: Compounds of formula I in which R1ais CF3, R1cis H, W is O, R2is R2-2, R3is R3-30, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0391] Table 183: Compounds of formula I in which R1ais CF3, R1cis H, W is O, R2is R2-3, R3is R3-30, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0392] Table 184: Compounds of formula I in which R1ais CF3, R1cis H, W is O, R2is R2-4, R3is R3-30, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0393] Table 185: Compounds of formula I in which R1ais CF3, R1cis H, W is O, R2is R2-5, R3is R3-30, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A. Table 186: Compounds of formula I in which R1ais CF3, R1cis H, W is O, R2is R2-6, R3is R3-30, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0394] Table 187: Compounds of formula I in which R1ais CF3, R1cis H, W is O, R2is R2-7, R3is R3-30, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0395] Table 188: Compounds of formula I in which R1ais CF3, R1cis H, W is O, R2is R2-8, R3is R3-30, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0396] Table 189: Compounds of formula I in which R1ais CF3, R1cis H, W is O, R2is R2-9, R3is R3-30, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0397] Table 190: Compounds of formula I in which R1ais CF3, R1cis H, W is O, R2is R2-10, R3is R3- 30, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0398] Table 191: Compounds of formula I in which R1ais CF3, R1cis H, W is O, R2is R2-1, R3is R3- 31, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0399] Table 192: Compounds of formula I in which R1ais CF3, R1cis H, W is O, R2is R2-2, R3is R3-31, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0400] Table 193: Compounds of formula I in which R1ais CF3, R1cis H, W is O, R2is R2-3, R3is R3-31, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0401] Table 194: Compounds of formula I in which R1ais CF3, R1cis H, W is O, R2is R2-4, R3is R3-31, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0402] Table 195: Compounds of formula I in which R1ais CF3, R1cis H, W is O, R2is R2-5, R3is R3-31, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0403] Table 196: Compounds of formula I in which R1ais CF3, R1cis H, W is O, R2is R2-6, R3is R3-31, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0404] Table 197: Compounds of formula I in which R1ais CF3, R1cis H, W is O, R2is R2-7, R3is R3-31, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0405] Table 198: Compounds of formula I in which R1ais CF3, R1cis H, W is O, R2is R2-8, R3is R3-31, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0406] Table 199: Compounds of formula I in which R1ais CF3, R1cis H, W is O, R2is R2-9, R3is R3-31, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A.

[0407] Table 200: Compounds of formula I in which R1ais CF3, R1cis H, W is O, R2is R2-10, R3is R3-31, and the combination of R1b, Q, B1, B2, B3, and B4for a compound corresponds in each case to one row of Table A. Table A

[0408] No. R1bQ B1B2B3B4A-1 F Q1CH CH CH CH A-2 Cl Q1CH CH CH CH A-3 Br Q1CH CH CH CH A-4 OCF3Q1CH CH CH CH A-5 OCHF2Q1CH CH CH CH A-6 CN Q1CH CH CH CH A-7 OCH3Q1CH CH CH CH A-8 OCH2CH3Q1CH CH CH CH A-9 F Q2CH CH CH CH A-10 Cl Q2CH CH CH CH A-11 Br Q2CH CH CH CH A-12 OCF3Q2CH CH CH CH A-13 OCHF2Q2CH CH CH CH A-14 CN Q2CH CH CH CH A-15 OCH3Q2CH CH CH CH A-16 OCH2CH3Q2CH CH CH CH A-17 F Q3CH CH CH CH A-18 Cl Q3CH CH CH CH A-19 Br Q3CH CH CH CH A-20 OCF3Q3CH CH CH CH A-21 OCHF2Q3CH CH CH CH A-22 CN Q3CH CH CH CH A-23 OCH3Q3CH CH CH CH A-24 OCH2CH3Q3CH CH CH CH A-25 F Q4CH CH CH CH A-26 Cl Q4CH CH CH CH A-27 Br Q4CH CH CH CH A-28 OCF3Q4CH CH CH CH A-29 OCHF2Q4CH CH CH CH A-30 CN Q4CH CH CH CH A-31 OCH3Q4CH CH CH CH A-32 OCH2CH3Q4CH CH CH CH A-33 F Q5CH CH CH CH A-34 Cl Q5CH CH CH CH A-35 Br Q5CH CH CH CH A-36 OCF3Q5CH CH CH CH A-37 OCHF2Q5CH CH CH CH A-38 CN Q5CH CH CH CH A-39 OCH3Q5CH CH CH CH A-40 OCH2CH3Q5CH CH CH CH

[0409]

[0410] A-41 F Q1N CH CH CH No. R1bQ B1B2B3B4A-42 Cl Q1N CH CH CH A-43 Br Q1N CH CH CH A-44 OCF3Q1N CH CH CH A-45 OCHF2Q1N CH CH CH A-46 CN Q1N CH CH CH A-47 OCH3Q1N CH CH CH A-48 OCH2CH3Q1N CH CH CH A-49 F Q2N CH CH CH A-50 Cl Q2N CH CH CH A-51 Br Q2N CH CH CH A-52 OCF3Q2N CH CH CH A-53 OCHF2Q2N CH CH CH A-54 CN Q2N CH CH CH A-55 OCH3Q2N CH CH CH A-56 OCH2CH3Q2N CH CH CH A-57 F Q3N CH CH CH A-58 Cl Q3N CH CH CH A-59 Br Q3N CH CH CH A-60 OCF3Q3N CH CH CH A-61 OCHF2Q3N CH CH CH A-62 CN Q3N CH CH CH A-63 OCH3Q3N CH CH CH A-64 OCH2CH3Q3N CH CH CH A-65 F Q4N CH CH CH A-66 Cl Q4N CH CH CH A-67 Br Q4N CH CH CH A-68 OCF3Q4N CH CH CH A-69 OCHF2Q4N CH CH CH A-70 CN Q4N CH CH CH A-71 OCH3Q4N CH CH CH A-72 OCH2CH3Q4N CH CH CH A-73 F Q5N CH CH CH A-74 Cl Q5N CH CH CH A-75 Br Q5N CH CH CH A-76 OCF3Q5N CH CH CH A-77 OCHF2Q5N CH CH CH A-78 CN Q5N CH CH CH A-79 OCH3Q5N CH CH CH A-80 OCH2CH3Q5N CH CH CH A-81 F Q1CH N CH CH A-82 Cl Q1CH N CH CH A-83 Br Q1CH N CH CH

[0411]

[0412] A-84 OCF3Q1CH N CH CH No. R1bQ B1B2B3B4A-85 OCHF2Q1CH N CH CH A-86 CN Q1CH N CH CH A-87 OCH3Q1CH N CH CH A-88 OCH2CH3Q1CH N CH CH A-89 F Q2CH N CH CH A-90 Cl Q2CH N CH CH A-91 Br Q2CH N CH CH A-92 OCF3Q2CH N CH CH A-93 OCHF2Q2CH N CH CH A-94 CN Q2CH N CH CH A-95 OCH3Q2CH N CH CH A-96 OCH2CH3Q2CH N CH CH A-97 F Q3CH N CH CH A-98 Cl Q3CH N CH CH A-99 Br Q3CH N CH CH A- 100 OCF3Q3CH N CH CH A-101 OCHF2Q3CH N CH CH A- 102 CN Q3CH N CH CH A- 103 OCH3Q3CH N CH CH A- 104 OCH2CH3Q3CH N CH CH A- 105 F Q4CH N CH CH A- 106 Cl Q4CH N CH CH A- 107 Br Q4CH N CH CH A- 108 OCF3Q4CH N CH CH A- 109 OCHF2Q4CH N CH CH A-110 CN Q4CH N CH CH A-111 OCH3Q4CH N CH CH A-112 OCH2CH3Q4CH N CH CH A-113 F Q5CH N CH CH A-114 Cl Q5CH N CH CH A-115 Br Q5CH N CH CH A-116 OCF3Q5CH N CH CH A-117 OCHF2Q5CH N CH CH A-118 CN Q5CH N CH CH A-119 OCH3Q5CH N CH CH A- 120 OCH2CH3Q5CH N CH CH A- 121 F Q1N CH CH N A- 122 Cl Q1N CH CH N A- 123 Br Q1N CH CH N A- 124 OCF3Q1N CH CH N A- 125 OCHF2Q1N CH CH N A- 126 CN Q1N CH CH N

[0413]

[0414] A- 127 OCH3Q1N CH CH N No. R1bQ B1B2B3B4A- 128 OCH2CH3Q1N CH CH N A- 129 F Q2N CH CH N A- 130 Cl Q2N CH CH N A-131 Br Q2N CH CH N A- 132 OCF3Q2N CH CH N A- 133 OCHF2Q2N CH CH N A- 134 CN Q2N CH CH N A- 135 OCH3Q2N CH CH N A- 136 OCH2CH3Q2N CH CH N A- 137 F Q3N CH CH N A- 138 Cl Q3N CH CH N A- 139 Br Q3N CH CH N A- 140 OCF3Q3N CH CH N A-141 OCHF2Q3N CH CH N A- 142 CN Q3N CH CH N A- 143 OCH3Q3N CH CH N A- 144 OCH2CH3Q3N CH CH N A- 145 F Q4N CH CH N A- 146 Cl Q4N CH CH N A- 147 Br Q4N CH CH N A- 148 OCF3Q4N CH CH N A- 149 OCHF2Q4N CH CH N A- 150 CN Q4N CH CH N A-151 OCH3Q4N CH CH N A- 152 OCH2CH3Q4N CH CH N A- 153 F Q5N CH CH N A- 154 Cl Q5N CH CH N A- 155 Br Q5N CH CH N A- 156 OCF3Q5N CH CH N A- 157 OCHF2Q5N CH CH N A- 158 CN Q5N CH CH N A- 159 OCH3Q5N CH CH N A- 160 OCH2CH3Q5N CH CH N A- 161 F Q1CH N N CH A- 162 Cl Q1CH N N CH A- 163 Br Q1CH N N CH A- 164 OCF3Q1CH N N CH A- 165 OCHF2Q1CH N N CH A- 166 CN Q1CH N N CH A- 167 OCH3Q1CH N N CH A- 168 OCH2CH3Q1CH N N CH A- 169 F Q2CH N N CH

[0415]

[0416] A- 170 Cl Q2CH N N CH No. R1bQ B1B2B3B4A- 171 Br Q2CH N N CH A- 172 OCF3Q2CH N N CH A- 173 OCHF2Q2CH N N CH A- 174 CN Q2CH N N CH A- 175 OCH3Q2CH N N CH A- 176 OCH2CH3Q2CH N N CH A- 177 F Q3 CH N N CH A- 178 Cl Q3 CH N N CH A- 179 Br Q3 CH N N CH A- 180 OCF3Q3 CH N N CH A- 181 OCHF2Q3 CH N N CH A- 182 CN Q3 CH N N CH A- 183 OCH3Q3 CH N N CH A- 184 OCH2CH3Q3 CH N N CH A- 185 F Q4CH N N CH A- 186 Cl Q4CH N N CH A- 187 Br Q4CH N N CH A- 188 OCF3Q4CH N N CH A- 189 OCHF2Q4CH N N CH A- 190 CN Q4CH N N CH A-191 OCH3Q4CH N N CH A- 192 OCH2CH3Q4CH N N CH A- 193 F Q5CH N N CH A- 194 Cl Q5CH N N CH A- 195 Br Q5CH N N CH A- 196 OCF3Q5CH N N CH A- 197 OCHF2Q5CH N N CH A- 198 CN Q5CH N N CH A- 199 OCH3Q5CH N N CH A-200 OCH2CH3Q5CH N N CH A-201 F Q1N CH N CH A-202 Cl Q1N CH N CH A-203 Br Q1N CH N CH A-204 OCF3Q1N CH N CH A-205 OCHF2Q1N CH N CH A-206 CN Q1N CH N CH A-207 OCH3Q1N CH N CH A-208 OCH2CH3Q1N CH N CH A-209 F Q2N CH N CH A-210 Cl Q2N CH N CH A-211 Br Q2N CH N CH A-212 OCF3Q2N CH N CH

[0417]

[0418] A-213 OCHF2Q2N CH N CH No. R1bQ B1B2B3B4A-214 CN Q2N CH N CH A-215 OCH3Q2N CH N CH A-216 OCH2CH3Q2N CH N CH A-217 F Q3 N CH N CH A-218 Cl Q3 N CH N CH A-219 Br Q3 N CH N CH A-220 OCF3Q3 N CH N CH A-221 OCHF2Q3 N CH N CH A-222 CN Q3 N CH N CH A-223 OCH3Q3 N CH N CH A-224 OCH2CH3Q3 N CH N CH A-225 F Q4N CH N CH A-226 Cl Q4N CH N CH A-227 Br Q4N CH N CH A-228 OCF3Q4N CH N CH A- 229 OCHF2Q4N CH N CH A-230 CN Q4N CH N CH A-231 OCH3Q4N CH N CH A-232 OCH2CH3Q4N CH N CH A-233 F Q5N CH N CH A-234 Cl Q5N CH N CH A-235 Br Q5N CH N CH A-236 OCF3Q5N CH N CH A-237 OCHF2Q5N CH N CH A-238 CN Q5N CH N CH A-239 OCH3Q5N CH N CH A-240 OCH2CH3Q5N CH N CH A-241 F Q1CCI CH CH CH A-242 Cl Q1CCI CH CH CH A-243 Br Q1CCI CH CH CH A-244 OCF3Q1CCI CH CH CH A-245 OCHF2Q1CCI CH CH CH A-246 CN Q1CCI CH CH CH A-247 OCH3Q1CCI CH CH CH A-248 OCH2CH3Q1CCI CH CH CH A-249 F Q2CCI CH CH CH A-250 Cl Q2CCI CH CH CH A-251 Br Q2CCI CH CH CH A-252 OCF3Q2CCI CH CH CH A-253 OCHF2Q2CCI CH CH CH A-254 CN Q2CCI CH CH CH A-255 OCH3Q2CCI CH CH CH

[0419]

[0420] A-256 OCH2CH3Q2CCI CH CH CH No. R1bQ B1B2B3B4A-257 F Q3 CCI CH CH CH A-258 Cl Q3 CCI CH CH CH A-259 Br Q3 CCI CH CH CH A-260 OCF3Q3 CCI CH CH CH A- 261 OCHF2Q3 CCI CH CH CH A-262 CN Q3 CCI CH CH CH A-263 OCH3Q3 CCI CH CH CH A-264 OCH2CH3Q3 CCI CH CH CH A-265 F Q4CCI CH CH CH A-266 Cl Q4CCI CH CH CH A-267 Br Q4CCI CH CH CH A-268 OCF3Q4CCI CH CH CH A- 269 OCHF2 Q4CCI CH CH CH A-270 CN Q4CCI CH CH CH A-271 OCH3Q4CCI CH CH CH A-272 OCH2CH3Q4CCI CH CH CH A-273 F Q5CCI CH CH CH A-274 Cl Q5CCI CH CH CH A-275 Br Q5CCI CH CH CH A-276 OCF3Q5CCI CH CH CH A-277 OCHF2 Q5CCI CH CH CH A-278 CN Q5CCI CH CH CH A-279 OCH3Q5CCI CH CH CH A-280 OCH2CH3Q5CCI CH CH CH A-281 F Q1CH CCI CH CH A-282 Cl Q1CH CCI CH CH A-283 Br Q1CH CCI CH CH A-284 OCF3Q1CH CCI CH CH A-285 OCHF2 Q1CH CCI CH CH A-286 CN Q1CH CCI CH CH A-287 OCH3Q1CH CCI CH CH A-288 OCH2CH3Q1CH CCI CH CH A-289 F Q2CH CCI CH CH A-290 Cl Q2CH CCI CH CH A-291 Br Q2CH CCI CH CH A-292 OCF3Q2CH CCI CH CH A-293 OCHF2 Q2CH CCI CH CH A-294 CN Q2CH CCI CH CH A-295 OCH3Q2CH CCI CH CH A-296 OCH2CH3Q2CH CCI CH CH A-297 F Q3 CH CCI CH CH A-298 Cl Q3 CH CCI CH CH

[0421]

[0422] A-299 Br Q3 CH CCI CH CH No. R1bQ B1B2B3B4A-300 OCF3Q3 CH CCI CH CH A-301 OCHF2Q3 CH CCI CH CH A-302 CN Q3 CH CCI CH CH A-303 OCH3Q3 CH CCI CH CH A-304 OCH2CH3Q3 CH CCI CH CH A-305 F Q4CH CCI CH CH A-306 Cl Q4CH CCI CH CH A-307 Br Q4CH CCI CH CH A-308 OCF3Q4CH CCI CH CH A-309 OCHF2 Q4CH CCI CH CH A-310 CN Q4CH CCI CH CH A-311 OCH3Q4CH CCI CH CH A-312 OCH2CH3Q4CH CCI CH CH A-313 F Q5CH CCI CH CH A-314 Cl Q5CH CCI CH CH A-315 Br Q5CH CCI CH CH A-316 OCF3Q5CH CCI CH CH A-317 OCHF2 Q5CH CCI CH CH A-318 CN Q5CH CCI CH CH A-319 OCH3Q5CH CCI CH CH A-320 OCH2CH3Q5CH CCI CH CH A-321 F Q1CF CH CH CH A-322 Cl Q1CF CH CH CH A-323 Br Q1CF CH CH CH A-324 OCF3Q1CF CH CH CH A-325 OCHF2 Q1CF CH CH CH A-326 CN Q1CF CH CH CH A-327 OCH3Q1CF CH CH CH A-328 OCH2CH3Q1CF CH CH CH A-329 F Q2CF CH CH CH A-330 Cl Q2CF CH CH CH A-331 Br Q2CF CH CH CH A-332 OCF3Q2CF CH CH CH A-333 OCHF2 Q2CF CH CH CH A-334 CN Q2CF CH CH CH A-335 OCH3Q2CF CH CH CH A-336 OCH2CH3Q2CF CH CH CH A-337 F Q3 CF CH CH CH A-338 Cl Q3 CF CH CH CH A-339 Br Q3 CF CH CH CH A-340 OCF3Q3 CF CH CH CH A-341 OCHF2 Q3 CF CH CH CH

[0423]

[0424] A-342 CN Q3 CF CH CH CH No. R1bQ B1B2B3B4A-343 OCH3Q3 CF CH CH CH A-344 OCH2CH3Q3 CF CH CH CH A-345 F Q4CF CH CH CH A-346 Cl Q4CF CH CH CH A-347 Br Q4CF CH CH CH A-348 OCF3Q4CF CH CH CH A-349 OCHF2Q4CF CH CH CH A-350 CN Q4CF CH CH CH A-351 OCH3Q4CF CH CH CH A-352 OCH2CH3Q4CF CH CH CH A-353 F Q5CF CH CH CH A-354 Cl Q5CF CH CH CH A-355 Br Q5CF CH CH CH A-356 OCF3Q5CF CH CH CH A-357 OCHF2Q5CF CH CH CH A-358 CN Q5CF CH CH CH A-359 OCH3Q5CF CH CH CH A-360 OCH2CH3Q5CF CH CH CH A-361 F Q1CH CF CH CH A-362 Cl Q1CH CF CH CH A-363 Br Q1CH CF CH CH A-364 OCF3Q1CH CF CH CH A-365 OCHF2Q1CH CF CH CH A-366 CN Q1CH CF CH CH A-367 OCH3Q1CH CF CH CH A-368 OCH2CH3Q1CH CF CH CH A-369 F Q2CH CF CH CH A-370 Cl Q2CH CF CH CH A-371 Br Q2CH CF CH CH A-372 OCF3Q2CH CF CH CH A-373 OCHF2Q2CH CF CH CH A-374 CN Q2CH CF CH CH A-375 OCH3Q2CH CF CH CH A-376 OCH2CH3Q2CH CF CH CH A-377 F Q3 CH CF CH CH A-378 Cl Q3 CH CF CH CH A-379 Br Q3 CH CF CH CH A-380 OCF3Q3 CH CF CH CH A-381 OCHF2Q3 CH CF CH CH A-382 CN Q3 CH CF CH CH A-383 OCH3Q3 CH CF CH CH A-384 OCH2CH3Q3 CH CF CH CH

[0425]

[0426] A-385 F Q4CH CF CH CH No. R1bQ B1B2B3B4A-386 Cl Q4CH CF CH CH A-387 Br Q4CH CF CH CH A-388 OCF3Q4CH CF CH CH A-389 OCHF2Q4CH CF CH CH A-390 CN Q4CH CF CH CH A-391 OCH3Q4CH CF CH CH A-392 OCH2CH3Q4CH CF CH CH A-393 F Q5CH CF CH CH A-394 Cl Q5CH CF CH CH A-395 Br Q5CH CF CH CH A-396 OCF3Q5CH CF CH CH A-397 OCHF2 Q5CH CF CH CH A-398 CN Q5CH CF CH CH A-399 OCH3Q5CH CF CH CH A-400 OCH2CH3Q5CH CF CH CH A-401 H Q1CH CH CH CH A-402 H Q2CH CH CH CH A-403 H Q3 CH CH CH CH A-404 H Q4CH CH CH CH A-405 H Q5CH CH CH CH A-406 H Q1N CH CH CH A-407 H Q2N CH CH CH A-408 H Q3 N CH CH CH A-409 H Q4N CH CH CH A-410 H Q5N CH CH CH A-411 H Q1CH N CH CH A-412 H Q2CH N CH CH A-413 H Q3 CH N CH CH A-414 H Q4CH N CH CH A-415 H Q5CH N CH CH A-416 H Q1N CH CH N A-417 H Q2N CH CH N A-418 H Q3 N CH CH N A-419 H Q4N CH CH N A-420 H Q5N CH CH N A-421 H Q1CH N N CH A-422 H Q2CH N N CH A-423 H Q3 CH N N CH A-424 H Q4CH N N CH A-425 H Q5CH N N CH A-426 H Q1N CH N CH A-427 H Q2N CH N CH

[0427]

[0428] A-428 H Q3 N CH N CH No. R1bQ B1B2B3B4A-429 H Q4N CH N CH A-430 H Q5N CH N CH A-431 H Q1CCI CH CH CH A-432 H Q2CCI CH CH CH A-433 H Q3 CCI CH CH CH A-434 H Q4CCI CH CH CH A-435 H Q5CCI CH CH CH A-436 H Q1CH CCI CH CH A-437 H Q2CH CCI CH CH A-438 H Q3 CH CCI CH CH A-439 H Q4CH CCI CH CH A-440 H Q5CH CCI CH CH A-441 H Q1CF CH CH CH A-442 H Q2CF CH CH CH A-443 H Q3 CF CH CH CH A-444 H Q4CF CH CH CH A-445 H Q5CF CH CH CH A-446 H Q1CH CF CH CH A-447 H Q2CH CF CH CH A-448 H Q3 CH CF CH CH A-449 H Q4CH CF CH CH A-450 H Q5CH CF CH CH A-451 CF3Q1CH CH CH CH A-452 CF3Q2CH CH CH CH A-453 CF3Q3 CH CH CH CH A-454 CF3Q4CH CH CH CH A-455 CF3Q5CH CH CH CH A-456 CF3Q1N CH CH CH A-457 CF3Q2N CH CH CH A-458 CF3Q3 N CH CH CH A-459 CF3Q4N CH CH CH A-460 CF3Q5N CH CH CH A-461 CF3Q1CH N CH CH A-462 CF3Q2CH N CH CH A-463 CF3Q3 CH N CH CH A-464 CF3Q4CH N CH CH A-465 CF3Q5CH N CH CH A-466 CF3Q1N CH CH N A-467 CF3Q2N CH CH N A-468 CF3Q3 N CH CH N A-469 CF3Q4N CH CH N A-470 CF3Q5N CH CH N

[0429]

[0430] A-471 CF3Q1CH N N CH No. R1bQ B1B2B3B4

[0431] A-472 CF3Q2CH N N CH

[0432] A-473 CF3Q3 CH N N CH

[0433] A-474 CF3Q4CH N N CH

[0434] A-475 CF3Q5CH N N CH

[0435] A-476 CF3Q1N CH N CH

[0436] A-477 CF3Q2N CH N CH

[0437] A-478 CF3Q3 N CH N CH

[0438] A-479 CF3Q4N CH N CH

[0439] A-480 CF3Q5N CH N CH

[0440] A-481 CF3Q1CCI CH CH CH

[0441] A-482 CF3Q2CCI CH CH CH

[0442] A-483 CF3Q3 CCI CH CH CH

[0443] A-484 CF3Q4CCI CH CH CH

[0444] A-485 CF3Q5CCI CH CH CH

[0445] A-486 CF3Q1CH CCI CH CH

[0446] A-487 CF3Q2CH CCI CH CH

[0447] A-488 CF3Q3 CH CCI CH CH

[0448] A-489 CF3Q4CH CCI CH CH

[0449] A-490 CF3Q5CH CCI CH CH

[0450] A-491 CF3Q1CF CH CH CH

[0451] A-492 CF3Q2CF CH CH CH

[0452] A-493 CF3Q3 CF CH CH CH

[0453] A-494 CF3Q4CF CH CH CH

[0454] A-495 CF3Q5CF CH CH CH

[0455] A-496 CF3Q1CH CF CH CH

[0456] A-497 CF3Q2CH CF CH CH

[0457] A-498 CF3Q3 CH CF CH CH

[0458] A-499 CF3Q4CH CF CH CH

[0459]

[0460] A-500 CF3Q5CH CF CH CH

[0461] As used herein, the term “compound(s) of the invention” or “compound(s) according to the invention” refers to the compound(s) of formula (I) as defined above, which are also referred to as “compound(s) of formula I” or “compound(s) I” or “formula I compound(s)”, and includes their salts, tautomers, stereoisomers, and N-oxides.

[0462] Mixtures

[0463] The invention also relates to a mixture of at least one compound of the invention with at least one mixing partner. Preferred are binary mixtures of one compound of the invention as component I with one mixing partner herein as component II. Preferred weight ratios for such binary mixtures are from 5000: 1 to 1:5000, preferably from 1000: 1 to 1: 1000, more preferably from 100: 1 to 1: 100, particularly from 10:1 to 1:10. In such binary mixtures, components I and II may be used in equal amounts, or an excess of component I, or an excess of component II may be used. Mixing partners can be selected from pesticides, in particular insecticides, nematicides, and acaricides, fungicides, herbicides, plant growth regulators, fertilizers. Preferred mixing partners are insecticides, nematicides, and fungicides.

[0464] The following list M of pesticides, grouped according to the Mode of Action Classification of the Insecticide Resistance Action Committee (IRAC), together with which the compounds of the invention can be used and with which potential synergistic effects might be produced, illustrates the possible combinations:

[0465] M.1 AChE inhibitors: aldicarb, alanycarb, bendiocarb, benfuracarb, butocarboxim, butoxycarboxim, carbaryl, carbofuran, carbosulfan, ethiofencarb, fenobucarb, formetanate, furathiocarb, isoprocarb, methiocarb, methomyl, metolcarb, oxamyl, pirimicarb, propoxur, thiodicarb, thiofanox, trimethacarb, XMC, xylylcarb, triazamate; acephate, azamethiphos, azinphos-ethyl, azinphosmethyl, cadusafos, chlorethoxyfos, chlorfenvinphos, chlormephos, chlorpyrifos, chlorpyrifosmethyl, coumaphos, cyanophos, demeton-S-methyl, diazinon, dichlorvos / DDVP, dicrotophos, dimethoate, dimethylvinphos, disulfoton, EPN, ethion, ethoprophos, famphur, fenamiphos, fenitrothion, fenthion, fosthiazate, heptenophos, imicyafos, isofenphos, isopropyl O-(methoxyaminothio-phosphoryl) salicylate, isoxathion, malathion, mecarbam, methamidophos, methidathion, mevinphos, monocrotophos, naled, omethoate, oxydemeton-methyl, parathion, parathion-methyl, phenthoate, phorate, phosalone, phosmet, Phosphamidon, phoxim, pirimiphos-methyl, profenofos, propetamphos, prothiofos, pyraclofos, pyridaphenthion, quinalphos, sulfotep, tebupirimfos, temephos, terbufos, tetrachlorvinphos, thiometon, triazophos, trichlorfon, vamidothion;

[0466] M.2. GABA-gated chloride channel antagonists: cyclodiene organochlorine compounds: endosulfan, chlordane; phenylpyrazoles: ethiprole, fipronil, flufiprole, pyrafluprole, pyriprole; M.3 Sodium channel modulators: pyrethroids: acrinathrin, allethrin, d-cis-trans allethrin, d-trans allethrin, bifenthrin, kappa-bifenthrin, bioallethrin, bioallethrin S-cylclopentenyl, bio-resmethrin, cycloprothrin, cyfluthrin, beta-cyfluthrin, cyhalothrin, lambda-cyhalothrin, gamma-cyhalothrin, cypermethrin, alpha-cypermethrin, beta-cypermethrin, theta-cypermethrin, zeta-cypermethrin, cyphenothrin, deltamethrin, empenthrin, esfenvalerate, etofenprox, fenpropathrin, fenvalerate, flucythrinate, flumethrin, tau-fluvalinate, halfenprox, heptafluthrin, imiprothrin, meperfluthrin.metofluthrin, momfluorothrin, epsilon-momfluorothrin, permethrin, phenothrin, prallethrin, profluthrin, pyrethrin (pyrethrum), resmethrin, silafluofen, tefluthrin, kappa-tefluthrin, tetramethylfluthrin, tetramethrin, tralomethrin, transfluthrin; sodium channel modulators, e.g.: DDT, methoxychlor;

[0467] M.4 nAChR agonists: neonicotinoids: acetamiprid, clothianidin, cycloxaprid, dinotefuran, imidacloprid, nitenpyram, thiacloprid, thiamethoxam; 4,5-dihydro-N-nitro-1-(2-oxiranylmethyl)-1H-imidazol-2-amine, (2E-)-1-[(6-Chloropyridin-3-yl)methyl]-N'-nitro-2-pentylidenehydrazinecarbox-imidamide; 1-[(6-Chloropyridin-3-yl)methyl]-7-methyl-8-nitro-5-propoxy- 1,2, 3,5,6, 7-hexahydro-imidazo[1,2-a]pyridine; nicotine; sulfoxaflor; flupyradifurone; triflumezopyrim, fenmezoditiaz, flupyrimin, 1-[(2-chlorothiazol-5-yl)methyl]-3-(3,5-dimethylisoxazol-4-yl)pyrido[1,2-a]pyrimidine-2,4-dione;

[0468] M.5 Nicotinic acetylcholine receptor allosteric activators:spinosyns, e.g. spinosad or spineto-ram;

[0469] M.6 Chloride channel activators from the class of avermectins and milbemycins, e.g. abamectin, emamectin benzoate, ivermectin, lepimectin, or milbemectin; M.7 Juvenile hormone mimics, such as hydroprene, kino-prene, methoprene; fenoxycarb, or pyriproxyfen;

[0470] M.8 miscellaneous multi-site inhibitors: CH3Br, other alkyl halides, chloropicrin, sulfuryl fluoride, borax, tartar emetic;

[0471] M.9 Chordotonal organ TRPV channel modulators: afidopyropen, pymetrozine; pyrifluquinazon; M.10 Mite growth inhibitors: clofentezine, hexythiazox, diflovidazin, etoxazole;

[0472] M.11 Microbial disruptors of insect midgut membranes: bacillus thuringiensis, bacillus sphaericus, and insecticdal proteins they produce e.g.: bacillus thuringiensis subsp. israelensis, bacillus sphaericus, bacillus thuringiensis subsp. aizawai, bacillus thuringiensis subsp. kurstaki, bacillus thuringiensis subsp. tenebrionis, Bt crop proteins: CrylAb, CrylAc, CrylFa, Cry2Ab, mCry3A, Cry3Ab, Cry3Bb, Cry34 / 35Ab1;

[0473] M.12 Inhibitors of mitochondrial ATP synthase: diafenthiuron, organotin miticides, e.g.: azocyclotin, cyhexatin, fenbutatin oxide, propargite, tetradifon;

[0474] M.13 Uncouplers of oxidative phosphorylation via disruption of the proton gradient: chlorfenapyr, DNOC, sulfluramid;

[0475] M.14 nAChR channel blockers: nereistoxin analogues bensultap, cartap hydrochloride, thio-cyclam, thiosultap-sodium;

[0476] M.15 Inhibitors of the chitin biosynthesis type 0, e.g.: bistrifluron, chlorfluazuron, difluben-zuron, flucycloxuron, flufenoxuron, hexaflumuron, lufenuron, novaluron, noviflumuron, teflubenzuron, triflumuron;

[0477] M.16 Inhibitors of the chitin biosynthesis type 1: buprofezin;

[0478] M.17 Moulting disruptors: Dipteran, cyromazine;

[0479] M.18 Ecdyson receptor agonists, e.g.: methoxyfenozide, tebufenozide, halofenozide, fufeno-zide, chromafenozide;

[0480] M.19 Octopamin receptor agonists: amitraz;

[0481] M.20 Mitochondrial complex III electron transport inhibitors: hydramethylnon, acequinocyl, fluacrypyrim; bifenazate;

[0482] M.21 METI acaricides and insecticides, e.g.: fenazaquin, fen pyroxi mate, pyrimidifen, pyrida-ben, tebufenpyrad, tolfenpyrad, rotenone;

[0483] M.22 Voltage-dependent sodium channel blockers: indoxacarb, metaflumizone, N-(3-chloro-2-methyl-phenyl)-2-[(4-chlorophenyl)[4-[methyl(methylsulfonyl)amino]phenyl]-methylene]-hydrazinecarboxamide, N-[4-chloro-2-[[(1,1-dimethylethyl)amino]carbonyl]-6-methylphenyl]-1-(3-chloro-2-pyridinyl)-3-(fluoromethoxy)-1H-pyrazole-5-carboxamide, 2-[2-(4-cyanophenyl)-1-[3-(trifluoromethyl)phenyl]ethylidene]-N-[4-(difluoromethoxy)phenyl]-hydrazinecarboxamide;

[0484] M.23 Inhibitors of the of acetyl CoA carboxylase, e.g.: spirodiclofen, spiromesifen, spirotetramat; spiropidion; spirobudifen, 11-(4-chloro-2,6-dimethylphenyl)-12-hydroxy-1,4-dioxa-9-azadispiro[4.2.4.2]tetradec-11-en-10-one, spidoxamat;

[0485] M.24 Mitochondrial complex IV electron transport inhibitors: e.g. aluminium phosphide, calcium phosphide, zinc phosphide, cyanide;

[0486] M.25 Mitochondrial complex II electron transport inhibitors, e.g.: cyenopyrafen, cyflumetofen, cyetpyrafen, pyflubumide;

[0487] M.28 Ryanodine receptor-modulators: chlorantraniliprole, cyantraniliprole, cyclaniliprole, flubendiamide, fluchlordiniliprole, (R)-3-chloro-N1-{2-methyl-4-[1,2,2,2-tetrafluoro-1-(trifluoro-methyl)ethyl]phenyl}-N2-(1-methyl-2-methylsulfonylethyl)phthalamid, (S)-3-chloro-N1-{2-methyl-4-[1,2,2,2-tetrafluoro-1-(trifluoromethyl)ethyl]phenyl}-N2-(1-methyl-2-methylsulfonylethyl)phthal- amide, methyl-2-[3,5-dibromo-2-({[3-bromo-1-(3-chlorpyridin-2-yl)-1H-pyrazol-5-yl]carbonyl}ami-no)benzoyl]-1,2-dimethylhydrazine-carboxylate; N-[2-(5-amino-1,3,4-thiadiazol-2-yl)-4-chloro-6-methyl-phenyl]-3-bromo-1-(3-chloro-2-pyridinyl)-1H-pyrazole-5-carboxamide; 3-chloro-1-(3-chloro-2-pyridinyl)-N-[2,4-dichloro-6-[[(1-cyano-1-methylethyl)amino]carbonyl]phenyl]-1H-pyrazole-5-carboxamide; tetrachlorantraniliprole; tetraniliprole; tiorantraniliprole; N-[4-chloro-2-[[(1,1-dimethylethyl)amino]carbonyl]-6-methyl-phenyl]-1-(3-chloro-2-pyridinyl)-3-(fluoromethoxy)-1 H-pyrazole-5-carboxamide; cyhalodiamide; N-[2-(5-amino-1,3,4-thiadiazol-2-yl)-4-chloro-6-methylphenyl]-3-bromo-1-(3-chloro-2-pyridinyl)-1H-pyrazole-5-carboxamide, pioxaniliprole; M.29: Chordotonal organ Modulators: flonicamid, flumetnicam;

[0488] M.30: broflanilide; fluxametamide, isocycloseram, piperflanilide;

[0489] M.33 acynonapyr;

[0490] M. UN. Unknown mode of action: afoxolaner, azadirachtin, amidoflumet, ben-zoximate, bromopropylate, chinomethionat, cryolite, cyproflanilid, dicloromezotiaz, dicofol, dimpropyridaz, flufenerim, flometoquin, fluensulfone, fluhexafon, fluopyram, fluralaner, metaldehyde, metoxadiazone, mivorilaner, modoflaner, piperonyl butoxide, pyridalyl, tioxazafen, trifluenfuronate, umifoxolaner, 11-(4-chloro-2,6-dimethylphenyl)-12-hydroxy-1,4-dioxa-9-azadispiro[4.2.4.2]-tetradec-11-en-10-one, 3-(4’-fluoro-2,4-dimethylbiphenyl-3-yl)-4-hydroxy-8-oxa-1-azaspiro[4.5]dec-3-en-2-one, 1-[2-fluoro-4-methyl-5-[(2,2,2-trifluoroethyl)sulfinyl]phenyl]-3-(trifluoromethyl)-1H-1,2,4-triazole-5-amine, actives on basis of bacillus firmus (Votivo, 1-1582); fluazaindolizine; N-[5-[[2-bromo-6-chloro-4-[1,2,2,3,3,3-hexafluoro-1-(trifluoromethyl)-propyl]phe-nyl]carbamoyl]-2-cyano-phenyl]-4-cyano-2-methyl-benzamide; 4-cyano-N-[2-cyano-5-[[2,6-dichloro-4-[1,2,2,3,3,3-hexafluoro-1-(trifluoromethyl)-propyl]phenyl]carbamoyl]phenyl]-2-methyl-benzamide; 4-cyano-N-[2-cyano-5-[[2,6-dichloro-4-[1,2,2,2-tetrafluoro-1-(trifluoro-methyl)ethyl]phenyl]carbamoyl]phenyl]-2-methyl-benzamide; N-[5-[[2-bromo-6-chloro-4-[1, 2,2,2-tetrafluoro-1 -(trifluoromethyl) ethyl]phenyl]carbamoyl]-2-cyano-phenyl]-4-cyano-2-methyl-benzamide;

[0491] 1-[(6-chloro-3-pyridinyl)methyl]-1,2,3,5,6,7-hexahydro-5-methoxy-7-methyl-8-nitro-imidazo[1,2-a]pyridine; 1-[(6-chloropyridin-3-yl)methyl]-7-methyl-8-nitro-1,2,3,5,6,7-hexahydroimidazo[1,2-a]pyridin-5-ol; 1-[(6-chloro-3-pyridinyl)methyl]-1,2,3,5,6,7-hexahydro-5-methoxy-7-methyl-8-nitro-imidazo[1,2-a]pyridine; 2-(3-pyridinyl)-N-(2-pyrimidinylmethyl )-2H-indazole-5-carboxamide; tyclopyrazoflor; sarolaner, lotilaner; N-[4-chloro-3-[[(phenylmethyl)amino]carbonyl]phenyl]-1-methyl-3-(1,1,2,2,2-pentafluoroethyl)-4-(trifluoromethyl)-1H-pyrazole-5-carboxamide; N-[4-chloro-3-[[(phenylmethyl)amino]carbonyl]phenyl]-1 -methyl-3-(1, 1,2,2, 2-pentafluoroethyl)-4-(trifluoromethyl)-1H-pyrazole-5-carboxamide; 2-(3-ethylsulfonyl-2-pyridyl)-3-methyl-6-(tri-fluoromethyl)imidazo[4,5-b]pyridine, 2-[3-ethylsulfonyl-5-(trifluoromethyl)-2-pyridyl]-3-methyl-6-(trifluoromethyl)imidazo[4,5-b]pyridine; N-[4-chloro-3-(cyclopropylcarbamoyl)phenyl]-2-methyl-5-(1,1,2,2,2-pentafluoroethyl)-4-(trifluoromethyl)pyrazole-3-carboxamide, N-[4-chloro-3-[(1 -cyanocyclopropyl)carbamoyl]phenyl]-2-methyl-5-(1, 1,2,2,2-pentafluoroethyl)-4-(trifluorome-thyl)pyrazole-3-carboxamide; benzpyrimoxan; tigolaner; oxazosulfyl; [(2S,3R,4R,5S,6S)-3,5-dimethoxy-6-methyl-4-propoxy-tetrahydropyran-2-yl] N-[4-[1-[4-(trifluoromethoxy)phenyl]- 1,2,4-triazol-3-yl]phenyl]carbamate; [(2S,3R,4R,5S,6S)-3,4,5-trimethoxy-6-methyl-tetrahydropyran-2-yl] N-[4-[1-[4-(trifluoromethoxy)phenyl]-1,2,4-triazol-3-yl]phenyl]carbamate; [(2S,3R,4R,5S,6S)-3,5-dimethoxy-6-methyl-4-propoxy-tetrahydropyran-2-yl] N-[4-[1 -[4-(1, 1,2,2,2-pentafluoroethoxy)phenyl]-1,2,4-triazol-3-yl]phenyl]carbamate; [(2S,3R,4R,5S,6S)-3,4,5-trimethoxy-6-methyl-tetrahydropyran-2-yl] N-[4-[1-[4-(1,1,2,2,2-pentafluoroethoxy)phenyl]-1,2,4- triazol-3-yl]phenyl]carbamate; (2Z)-3-(2-isopropylphenyl)-2-[(E)-[4-[1-[4-(trifluorome-thoxy)phenyl]-1,2,4-triazol-3-yl]phenyl]methylenehydrazono]thiazolidin-4-one, (2Z)-3-(2-isopropylphenyl)-2-[(E)-[4-[1 -[4-(1, 1,2,2,2-pentafluoroethoxy)phenyl]-1,2,4-triazol-3-yl]phe-nyl]methylenehydrazono]thiazolidin-4-one, (2Z)-3-(2-isopropylphenyl)-2-[(E)-[4-[1 -[4-(1, 1,2,2,2-pentafluoroethoxy)phenyl]-1,2,4-triazol-3-yl]phenyl]methylenehydrazono]thiazolidin-4-one; 2-(6-chloro-3-ethylsulfonyl-imidazo[1,2-a]pyridin-2-yl)-3-methyl-6-(trifluoromethyl)imidazo[4,5-b]pyridine, 2-(6-bromo-3-ethylsulfonyl-imidazo[1,2-a]pyridin-2-yl)-3-methyl-6-(trifluoro-methyl)imidazo[4,5-b]pyridine, 2-(3-ethylsulfonyl-6-iodo-imidazo[1,2-a]pyridin-2-yl)-3-methyl-6-(trifluoromethyl)imidazo[4,5-b]pyridine, 2-(7-chloro-3-ethylsulfonyl-imidazo[1,2-a]pyridin-2-yl)-3-methyl-6-(trifluoromethyl)imidazo[4,5-b]pyridine, 2-(7-chloro-3-ethylsulfonyl-imidazo[1,2-a]pyri-din-2-yl)-3-methyl-6-(trifluoromethyl)imidazo[4,5-b]pyridine, 2-(3-ethylsulfonyl-7-iodo-imida-zo[1,2-a]pyridin-2-yl)-3-methyl-6-(trifluoromethyl)imidazo[4,5-b]pyridine, 3-ethylsulfonyl-6-iodo-2-[3-methyl-6-(trifluoromethyl)imidazo[4,5-b]pyridin-2-yl]imidazo[1,2-a]pyridine-8-carbonitrile, 2-[3-ethylsulfonyl-8-fluoro-6-(trifluoromethyl)imidazo[1,2-a]pyridin-2-yl]-3-methyl-6-(trifluoro-methyl)imidazo[4,5-b]pyridine, 2-[3-ethylsulfonyl-7-(trifluoromethyl)imidazo[1,2-a]pyridin-2-yl]-3-methyl-6-(trifluoromethylsulfinyl)imidazo[4,5-b]pyridine, 2-[3-ethylsulfonyl-7-(trifluoromethyl)imi-dazo[1,2-a]pyridin-2-yl]-3-methyl-6-(trifluoromethyl)imidazo[4,5-c]pyridine, 2-(6-bromo-3-ethyl-sulfonyl-imidazo[1,2-a]pyridin-2-yl)-6-(trifluoromethyl)pyrazolo[4,3-c]pyridine; N-[[2-fluoro-4-[(2S,3S)-2-hydroxy-3-(3,4,5-trichlorophenyl)-3-(trifluoromethyl)pyrrolidin-1-yl]phenyl]methyl]cy-clopropanecarboxamide; sulfiflumin; flupentiofenox, N-[3-chloro-1-(3-pyridyl)pyrazol-4-yl]-2-me-thylsulfonyl-propanamide, cyclobutrifluram; N-[4-chloro-3-[(1-cyanocyclopro-pyl)carbamoyl]phenyl]-2-methyl-4-methylsulfonyl-5-(1, 1,2,2,2-pentafluoroethyl)pyrazole-3-carboxamide, cyproflanilide, nicofluprole; 1,4-dimethyl-2-[2-(pyridin-3-yl)-2h-indazol-5-yl]-1,2,4-triazolidine-3, 5-dione, indazapyroxamet, tiapyrachlor, N-cyclopropyl-5-[(5S)-5-(3,5-dichloro-4-fluoro-phenyl)-5-(trifluoromethyl)-4H-isoxazol-3-yl]isoquinoline-8-carboxamide, 5-[(5S)-5-(3,5-dichloro-4-fluoro-phenyl)-5-(trifluoromethyl)-4H-isoxazol-3-yl]-N-(pyrimidin-2-ylmethyl)iso-quinoline-8-carboxamide, N-[1-(2,6-difluorophenyl)pyrazol-3-yl]-2-(trifluoromethyl)benzamide, 5-((1R,3R)-3-(3,5-Bis(trifluoromethyl)phenyl)-2,2-dichlorocyclopropane-1-carboxamido)-2-chloro-N-(3-(2,2-difluoroacetamido)-2,4-difluorophenyl)benzamide, 1-[6-(2,2-difluoro-7-methyl-[1,3]dioxolo[4,5-f]benzimidazol-6-yl)-5-ethylsulfonyl-3-pyridyl]cyclopropanecarbonitrile, 6-(5-cyclopropyl-3-ethylsulfonyl-2-pyridyl)-2,2-difluoro-7-methyl-[1,3]dioxolo[4,5-f]benzimidazole, Ledprona. Flupyroxystrobin, 3,5-bis(trifluoromethyl)-N-[(1S)-1-[1-[6-(trifluoromethyl)-4-pyrimidinyl]-1H-1,2,4-triazol-5-yl]ethyl]-benzamide, 2-(3-ethylsulfonyl-2-pyridyl)-5-(2,2,3,3,3-pentafluoropropoxy)pyrazine, 2-[3-ethylsulfonyl-6-(trifluoromethyl)pyrazolo[1,5-a]pyridin-2-yl]-3-methyl-6-(trifluoromethyl)imidazo[4,5-b]pyridine, 9-(methoxymethyl)-5-(3-pyridyl)-2-oxa-5,6,9,14-tetrazatricyclo[8.4.0.0A{3,7}]tetradeca-1 (10),3,6, 11,13-pentaen-8-one, bisulfufen, 2-[5-[(E)-2-chloro-3,3,3-trifluoro-prop-1-enyl]-1-methyl-imidazol-2-yl]-5-cyclopropyl-3-ethylsulfonyl-pyridine, cybenzoxasulfyl, isoflualanam;

[0492] Bentioflumin, Vadescana, (3Z)-1-[2-fluoro-4-[1-[4-(trifluoromethoxy)phenyl]-1,2,4-triazol-3-yl]phenyl]-3-[3-[5-methyl-2-(2,2,2-trifluoroethoxymethyl)phenyl]-4-oxo-thiazolidin-2-ylidene]urea, 1-[6-(2,2-difluoro-8-oxo-[1,3]dioxolo[4,5-g]chromen-7-yl)-5-ethylsulfonyl-3-pyridyl]cyclopropanecarbonitrile, 2-chloro-N-[(1S)-2-ethyl-1-methyl-butyl]furan-3-carboxamide, galquin, [5-cyclopropyl-2-[3-methyl-6-(trifluoromethyl)imidazo[4,5-b]pyridin-2-yl]-3-pyridyl]-ethyl-hydroxy-oxo-A6-sulfane, 4-[5-(3,5-dichloro-4-fluoro-phenyl)-5-(trifluoromethyl)-4H-isoxazol-3-yl]- 2-methyl-N-[1-(2,2,2-trifluoroethylcarbamoyl)cyclopropyl]benzamide, 3-[3-ethylsulfonyl-7- (trifluoromethyl)imidazo[1,2-a]pyridin-2-yl]-7-(trifluoromethyl)chromen-4-one,

[0493] The commercially available compounds M listed above may be found in The Pesticide Man-ual, 18th Edition, C. MacBean, British Crop Protection Council (2018), or http: / / bcpcdata.com / pesticide-manual.html, http: / / www.alanwood.net / pesticides.

[0494] The active compounds described by IUPAC nomenclature are known from CN103814937; WO2013 / 003977, W02007 / 101369, WO2018 / 177970, CN10171577, CN102126994, W02007 / 101540, W02007 / 043677, WO2011 / 085575, W02008 / 134969, WO2012 / 034403, W02006 / 089633, W02008 / 067911, W02006 / 043635, W02009 / 124707, WO2013 / 050317, WO2010 / 060379, WO2010 / 127926, WO2010 / 006713, WO2012 / 000896, W02007 / 101369, WO2012 / 143317, WO2015 / 038503, EP2910126, WO2015 / 059039, W02015 / 190316, WO2012 / 126766, W02009 / 102736, WO2013 / 116053, WO2018 / 052136, WO2015150252, W02020055955, WO2021158455, WO2013092350, WO201811111, EP3608311, WO2019236274, WO2013092350, WO 2018052136, W02009102736, WO2016174049, WO2012126766, CN106554335, WO2017054524, CN105153113, W02022072650; WO2018071327, W02022101502, WO2012158396, W02007079162, W02020013147, W02020097414, EP242081, WO2023058748, WO2017065228, EP3428166, WO2021029308, W02022009058, WO2017067500, W02020090585, WO2017146226, W02021043115, WO2023016278, W02021011722, WO2024126388, WO2024137594, EP4389739, WO2016096584, WO2024120137, WO2024188755, CN115925576, WO2024087613.

[0495] The following list of fungicides, in conjunction with which the compounds of the invention can be used, illustrates the possible combinations:

[0496] A) Respiration (C)

[0497] - complex III at Qosite (Qol, C3): azoxystrobin (A.1.1), bifemetstrobin (A.1.24), bifujunzhi (A.1.37), coumethoxystrobin (A.1.2), coumoxystrobin (A.1.3), dimoxystrobin (A.1.4), ene- stroburin (A.1.5), famoxadone (A.1.21), fenamidone (A.1.23), fenaminstrobin (A.1.6), flufen- oxystrobin (A.1.7), fluoxastrobin (A.1.8), kresoxim-methyl (A.1.9), mandestrobin (A.1.10), metominostrobin (A.1.11), metyltetraprole (A.1.25; member of MoA subgroup A), orysastrobin (A.1.12), picoxystrobin (A.1.13), pyraclostrobin (A.1.14), pyrametostrobin (A.1.15), pyraoxy- strobin (A.1.16), pyribencarb (A.1.19), pyriminostrobin (A.1.36), triclopyricarb (A.1.20), trifloxystrobin (A.1.17), 2-(2-(3-(2,6-dichlorophenyl)- 1 -methyl-allylideneaminooxymethyl)- phenyl)-2-methoxyimino- / V-methyl-acetamide (A.1.18), methyl- / V-[2-[(1,4-dimethyl-5-phenyl- pyrazol-3-yl)oxylmethyl]phenyl]- / V-methoxy-carbamate (A.1.22), (Z,2E)-5-[1-(2,4-dichloro- phenyl)pyrazol-3-yl]-oxy-2-methoxyimino- / V,3-dimethyl-pent-3-enamide (A.1.34), (Z,2E)-5-[1-(4-chlorophenyl)pyrazol-3-yl]oxy-2-methoxyimino- / V,3-dimethyl-pent-3-enamide (A.1.35), 2-(ortho-((2,5-dimethylphenyl-oxymethylen)phenyl)-3-methoxy-acrylic acid methylester (A.1.38), methyl (Z)-3-methoxy-2-[2-methyl-5-(3-propylpyrazol-1-yl)phenoxy]- prop-2-enoate, methyl (Z)-2-[5-(3-isopropylpyrazol-1-yl)-2-methyl-phenoxy]-3-methoxy-prop- 2-enoate, methyl (Z)-3-methoxy-2-[2-methyl-5-[3-(trifluoromethyl)pyrazol-1-yl]phenoxy]prop- 2-enoate, methyl (Z)-3-methoxy-2-[2-methyl-5-(4-propyltriazol-2-yl)phenoxy]prop-2-enoate, methyl (Z)-3-methoxy-2-[2-methyl-5-[4-(trifluoromethyl)triazol-2-yl]phenoxy]prop-2-enoate, methyl (Z)-2-[5-(4-isopropyltriazol-2-yl)-2-methyl-phenoxy]-3-methoxy-prop-2-enoate, methyl (Z)-2-(5-cyclobutyl-2-methyl-phenoxy)-3-methoxy-prop-2-enoate, methyl (Z)-2-(5-cyclopent-yl-2-methyl-phenoxy)-3-methoxy-prop-2-enoate, methyl (Z)-2-(5-cyclopropyl-2-methyl-phen-oxy)-3-methoxy-prop-2-enoate, methyl (Z)-2-(5-cyclohexyl-2-methyl-phenoxy)-3-methoxy- prop-2-enoate, methyl (E)-3-methoxy-2-[(2-methyl-5-phenyl-phenyl)methyl]prop-2-enoate, methyl (E)-3-methoxy-2-[[5-[(E)- / V-methoxy-C-methyl-carbonimidoyl]-2,4-dimethyl-phenyl]- methyl]prop-2-enoate; methyl (E)-2-[[5-(2-cyclopropylethynyl)-2,4-dimethyl-phenyl]methyl]-3-methoxy-prop-2-enoate; methyl (E)-3-methoxy-2-(2-phenyl-1,3-benzoxazol-4-yl)prop-2-enoate; methyl (E)-3-methoxy-2-(2-phenyl-1,3-benzothiazol-4-yl)prop-2-enoate; methyl (E)-3-methoxy-2-(2-phenyl-1,3-benzoxazol-7-yl)prop-2-enoate; methyl (Z)-2-[6-(2-cycloprop-ylethynyl)benzimidazol-1-yl]-3-methoxy-prop-2-enoate; methyl (Z)-3-methoxy-2-(6-phenyl- benzimidazol-1-yl)prop-2-enoate; methyl (Z)-2-(3-chloro-6-phenyl-indol-1-yl)-3-methoxy- prop-2-enoate; methyl (Z)-2-(2,3-dichloro-6-phenyl-indol-1-yl)-3-methoxy-prop-2-enoate; methyl (Z)-3-methoxy-2-[6-[(E)-methoxyiminomethyl]indol-1-yl]prop-2-enoate; methyl (Z)-3-methoxy-2-[6-[(E)- / V-methoxy-C-methyl-carbonimidoyl]indol-1-yl]prop-2-enoate, methyl / V-[[5-[1-(2,6-difluoro-4-isopropyl-phenyl)pyrazol-3-yl]-2-methyl-phenyl]methyl]carbamate, methyl / V-[[5-[1-(4-cyclopropyl-2,6-difluoro-phenyl)pyrazol-3-yl]-2-methyl-phenyl]methyl]-carbamate, methyl / V-[[5-[1 -(4-chloro-2,6-difluoro-phenyl)pyrazol-3-yl]-2-methyl-phenyl]- methyl]carbamate, methyl / V-[[5-[1 -[2,6-difluoro-4-(trifluoromethyl)phenyl]pyrazol-3-yl]- 2-methyl-phenyl]methyl]carbamate;

[0498] - complex III at Qi site (Qil, C4): cyazofamid (A.2.1), amisulbrom (A.2.2), [(6S,7R,8R)-8-benzyl-3-[(3-hydroxy-4-methoxy-pyridine-2-carbonyl)amino]-6-methyl-4,9-di-oxo-1, 5-dioxonan-7-yl]-2-methylpropanoate (A.2.3), fenpicoxamid (A.2.4), florylpicoxamid (A.2.5), metarylpicoxamid (A.2.6);

[0499] - complex II (SDHI, C2): benodanil (A.3.1), benzovindiflupyr (A.3.2), bixafen (A.3.3), boscalid (A.3.4), carboxin (A.3.5), cyclobutrifluram (A.3.24), fenfuram (A.3.6), fluopyram (A.3.7), flutolanil (A.3.8), fluxapyroxad (A.3.9), furametpyr (A.3.10), inpyrfluxam (A.3.22), isofetamid (A.3.11), isoflucypram (A.3.31), isopyrazam (A.3.12), mepronil (A.3.13), oxycarboxin (A.3.14), penflufen (A.3.15), penthiopyrad (A.3.16), pydiflumetofen (A.3.17), pyrapropoyne (A.3.23), pyraziflumid (A.3.18), sedaxane (A.3.19), tecloftalam (A.3.20), thiflu-zamide (A.3.21), fluindapyr (A.3.28), / V-[2-[2-chloro-4-(trifluoromethyl)phenoxy]phenyl]- 3-(difluoromethyl)-5-fluoro-1-methyl-pyrazole-4-carboxamide (A.3.29), methyl (E)-2-[2-[(5-cy-ano-2-methyl-phenoxy)methyl]phenyl]-3-methoxy-prop-2-enoate (A.3.30), 2-(difluoromethyl)- / V-(1,1,3-trimethyl-indan-4-yl)pyridine-3-carboxamide (A.3.32), 2-(difluoromethyl)- / V-[(3R)-1,1,3-trimethylindan-4-yl]pyridine-3-carboxamide (A.3.33), 2-(difluoromethyl)- / V-(3-ethyl-1,1-dimethyl-indan-4-yl)pyridine-3-carboxamide (A.3.34), 2-(difluoromethyl)- / V-[(3R)-3-ethyl-1,1-dimethyl-indan-4-yl]pyridine-3-carboxamide (A.3.35), 2-(difluoromethyl)- / V-(1,1-dimethyl-3-propyl-indan-4-yl)pyridine-3-carboxamide (A.3.36), 2-(difluoromethyl)- / V-[(3R)-1,1-dimethyl-3-propyl-indan-4-yl]pyridine-3-carboxamide (A.3.37), 2-(difluoromethyl)-A / -(3-isobutyl- 1,1-dimethyl-indan-4-yl)pyridine-3-carboxamide (A.3.38), 2-(difluoromethyl)- / V-[(3R)-3-isobutyl-1,1-dimethyl-indan-4-yl]pyridine-3-carboxamide (A.3.39);

[0500] - complex I NADH oxido-reductase (C1): diflumetorim (A.4.1);

[0501] - uncouplers (C5): binapacryl (A.4.2), dinobuton (A.4.3), dinocap (AAA), fluazinam (A.4.5), meptyldinocap (A.4.6), ferimzone (A.4.7);

[0502] - inhibitors of ox. phosphorylation (C6): fentin salts, e.g. fentin-acetate (A.4.8), fentin chloride (A.4.9) or fentin hydroxide (A.4.10); - ATP transport: silthiofam (A.4.11);

[0503] - quinone inside and outside inhibitor stigmatellin binding type (QioSI; C8): ametoctradin (A.5.1);

[0504] B) Sterol biosynthesis (G)

[0505] - C14 demethylase (DMI, G1): triazoles: azaconazole (B.1.1), bitertanol (B.1.2), bromucon-azole (B.1.3), cyproconazole (B.1.4), difenoconazole (B.1.5), diniconazole (B.1.6), dinicon-azole-M (B.1.7), epoxiconazole (B.1.8), fenbuconazole (B.1.9), fluoxytioconazole (B.1.33), fluquinconazole (B.1.10), flusilazole (B.1.11), flutriafol (B.1.12), hexaconazole (B.1.13), imi-benconazole (B.1.14), ipconazole (B.1.15), ipfentrifluconazole (B.1.37), mefentrifluconazole (B.1.38), metconazole (B.1.17), myclobutanil (B.1.18), oxpoconazole (B.1.19), paclobutrazole (B.1.20), penconazole (B.1.21), propiconazole (B.1.22), prothioconazole (B.1.23), simeconazole (B.1.24), tebuconazole (B.1.25), tetraconazole (B.1.26), triadimefon (B.1.27), triadimenol (B.1.28), triticonazole (B.1.29), uniconazole (B.1.30), 2-(2,4-difluorophenyl)-1, 1 -difluoro-3-(tetrazol-1 -yl)- 1 -[5-[4-(2,2,2-trifluoroethoxy)phenyl]-2-pyridyl]propan-2-ol (B.1.31), 2-(2,4-difluorophenyl)-1,1-difluoro-3-(tetrazol-1-yl)-1-[5-[4-(trifluoromethoxy)phenyl]- 2-pyridyl]propan-2-ol (B.1.32), 2-(chloromethyl)-2-methyl-5-(p-tolylmethyl)-1-(1,2,4-triazol- 1-ylmethyl)cyclopentanol (B.1.43), 4-[[6-[2-(2,4-difluorophenyl)-1,1-difluoro-2-hydroxy- 3-(1,2,4-triazol-1-yl)propyl]-3-pyridyl]oxy]benzonitrile (B.1.53), 2-[6-(4-bromophenoxy)- 2-(trifluoromethyl)-3-pyridyl]-1-(1,2,4-triazol-1-yl)propan-2-ol (B.1.54), 2-[6-(4-chlorophen-oxy)-2-(trifluoromethyl)-3-pyridyl]-1-(1,2,4-triazol-1-yl)propan-2-ol (B.1.55), (2R)-2-[4-(4-chlo-rophenoxy)-2-(trifluoromethyl)phenyl]-1-(1,2,4-triazol-1-yl)propan-2-ol, (2S)-2-[4-(4-chlo-rophenoxy)-2-(trifluoromethyl)phenyl]-1-(1,2,4-triazol-1-yl)propan-2-ol, methyl 2-[2-chloro- 4-(4-chlorophenoxy)phenyl]-2-hydroxy-3-(1,2,4-triazol-1-yl)propanoate (B.1.56), 2-[2-chloro-4-(4-chlorophenoxy)phenyl]-2-hydroxy-3-(1,2,4-triazol-1-yl)propanoic acid (B.1.57); imidazoles: imazalil (B.1.44), pefurazoate (B.1.45), prochloraz (B.1.46), triflumizole (B.1.47); pyrimidines, pyridines, piperazines: fenarimol (B.1.49), pyrifenox (B.1.50), triforine (B.1.51), [3-(4-chloro-2-fluoro-phenyl)-5-(2,4-difluorophenyl)isoxazol-4-yl]-(3-pyridyl)methanol (B.1.52);

[0506] - delta14-reductase (G2): aldimorph (B.2.1), dodemorph (B.2.2), dodemorph-acetate (B.2.3), fenpropidin (B.2.6), fenpropimorph (B.2.4), piperalin (B.2.7), spiroxamine (B.2.8), tridemorph (B.2.5);

[0507] - 3-keto reductase (G3): fenhexamid (B.3.1), fenpyrazamine (B.3.2);

[0508] - other: chlorphenomizole (B.4.1);

[0509] C)Nucleic acids metabolism (A)

[0510] - RNA polymerase I (A1): benalaxyl (C.1.1), benalaxyl-M (C.1.2), kiralaxyl (C.1.3), metalaxyl (C.1.4), metalaxyl-M (C.1.5), ofurace (C.1.6), oxadixyl (C.1.7);

[0511] - adenosine deaminase (A2): bupirimate (C.2.4), 5-fluoro-2-(p-tolylmethoxy)pyrimidin-4-amine (C.2.6), 5-fluoro-2-(4-fluorophenylmethoxy)pyrimidin-4-amine (C.2.7), 5-fluoro-2-(4-chlorophenylmethoxy)pyrimidin-4-amine (C.2.8);

[0512] - DNA / RNA synthesis (A3): 5-fluorocytosine (C.2.5), hymexazole (C.2.1), octhilinone (C.2.2),

[0513] - gyrase (A4): oxolinic acid (C.2.3);

[0514] - dihydroorotate dehydrogenase (DHODH; A5): ipflufenoquin (C.5.1), quinofumelin (C.5.2), feneptamidoquin (C.5.3);

[0515] D)Cytoskeleton and motor protein (B) - tubulin polymerization (MBC; B1): benomyl (D.1.1), carbendazim (D.1.2), fuberidazole (D.1.3), pyridachlometyl (D.1.6), thiabendazole (D.1.4), thiophanate-methyl (D.1.5), / V-ethyl- 2-[(3-ethynyl-8-methyl-6-quinolyl)oxy]butanamide (D.1.8), / V-ethyl-2-[(3-ethynyl-8-methyl- 6-quinolyl)oxy]-2-methylsulfanyl-acetamide (D.1.9), 2-[(3-ethynyl-8-methyl-6-quinolyl)oxy]- / V-(2-fluoroethyl)butanamide (D.1.10), 2-[(3-ethynyl-8-methyl-6-quinolyl)oxy]- / V-(2-fluoroeth-yl)-2-methoxy-acetamide (D.1.11), 2-[(3-ethynyl-8-methyl-6-quinolyl)oxy]- / V-propyl-butanamide (D.1.12), 2-[(3-ethynyl-8-methyl-6-quinolyl)oxy]-2-methoxy- / V-propyl-acetamide (D.1.13), 2-[(3-ethynyl-8-methyl-6-quinolyl)oxy]-2-methylsulfanyl- / V-propyl-acetamide (D.1.14), 2-[(3-ethynyl-8-methyl-6-quinolyl)oxy]- / V-(2-fluoroethyl)-2-methylsulfanyl-acetamide (D.1.15), 4-(2-bromo-4-fluoro-phenyl)- / V-(2-chloro-6-fluoro-phenyl)-2,5-dimethyl-pyrazol- 3-amine (D.1.16), 4-(2-bromo-4-fluorophenyl)- / V-(2-fluoro-6-nitrophenyl)-1,3-dimethyl 1H-pyrazol-5-amine, 4-(2-chloro-4,6-difluorophenyl)- / V-(2-fluoro-6-nitrophenyl)-1,3-dimethyl 1H-pyrazol-5-amine, 4-(2-chloro-4-fluorophenyl)- / V-(2-fluoro-6-nitrophenyl)-3-ethyl-1 -methyl 1H-pyrazol-5-amine, 4-(2-chloro-4-fluorophenyl)- / V-(2-fluoro-4-methyl-6-nitrophenyl)-1,3-di methyl-1 H-pyrazol-5-amine, 4-(2-chloro-4-fluorophenyl)- / V-(2-fluoro-6-nitrophenyl)-1,3-di methyl-1 H-pyrazol-5-amine, 4-(2,4-difluorophenyl)- / V-(2-fluoro-6-nitrophenyl)-1,3-dimethyl 1H-pyrazol-5-amine;

[0516] - tubulin polymerization (B2): diethofencarb (D.2.1),

[0517] - tubulin polymersation (B3): ethaboxam (D.2.2), zoxamide (D.2.5);

[0518] - cell division (B4): pencycuron (D.2.3);

[0519] - spectrin-like proteins (B5): fluopicolide (D.2.4), fluopimomide (D.2.9);

[0520] - actin / myosin / fimbrin function (B6): metrafenone (D.2.6), phenamacril (D.2.8), pyriofenone (D.2.7);

[0521] E)Amino acids and protein synthesis (D)

[0522] - methionine synthesis (D1): cyprodinil (E.1.1), mepanipyrim (E.1.2), pyrimethanil (E.1.3); - ribosome, termination step (D2): blasticidin-S (E.2.1);

[0523] - ribosome initiation step (D3): kasugamycin (E.2.2), kasugamycin hydrochloride-hydrate (E.2.3);

[0524] - ribosome initiation step (D4): streptomycin (E.2.5);

[0525] - ribosome elongation step (D5): mildiomycin (E.2.4), oxytetracyclin (E.2.6);

[0526] F) Signal transduction

[0527] - mechanism unknown (E1): proquinazid (F.2.2), quinoxyfen (F.2.1);

[0528] - MAP / histidine kinase os-2 (E2): fludioxonil (F.1.5);

[0529] - MAP / histidine kinase os-1 (E3): iprodione (F.1.2), procymidone (F.1.3), vinclozolin (F.1.4); G) Lipid synthesis or transport I membrane (F)

[0530] - methyl transferase (F2): edifenphos (G.1.1), iprobenfos (G.1.2), isoprothiolane (G.1.4); pyrazophos (G.1.3);

[0531] - cell peroxidation (F3): biphenyl (G.2.5), chloroneb (G.2.6), dicloran (G.2.1), etridiazole (G.2.7), quintozene (G.2.2), tecnazene (G.2.3), tolclofos-methyl (G.2.4);

[0532] - cell membrane permeability (F4): propamocarb (G.4.1);

[0533] - ergosterol binding (F8): natamycin;

[0534] - oxysterol binding protein (F9): fluoxapiprolin (G.5.3), oxathiapiprolin (G.5.1), 4-[1-[2-[3-(di-fluoromethyl)-5-methyl-pyrazol-1-yl]acetyl]-4-piperidyl]- / V-tetralin-1-yl-pyridine-2-carboxamide (G.5.4), 4-[1 -[2-[3,5-bis(difluoromethyl)pyrazol-1 -yl]acetyl]-4-piperidyl]- / V-tetralin-1 -yl-pyri-dine-2-carboxamide (G.5.5), 4-[1-[2-[3-(difluoromethyl)-5-(trifluoromethyl)pyrazol-1-yl]acetyl]- 4-piperidyl]- / V-tetralin-1-yl-pyridine-2-carboxamide (G.5.6), 4-[1-[2-[5-cyclopropyl-3-(difluoro-methyl)pyrazol-1-yl]acetyl]-4-piperidyl]- / V-tetralin-1-yl-pyridine-2-carboxamide (G.5.7), 4-[1 -[2-[5-methyl-3-(trifluoromethyl)pyrazol-1 -yl]acetyl]-4-piperidyl]-A / -tetralin-1 -yl-pyridine-2-carboxamide (G.5.8), 4-[1-[2-[5-(difluoromethyl)-3-(trifluoromethyl)pyrazol-1 -yl]acetyl]-4-pi-peridyl]- / V-tetralin-1-yl-pyridine-2-carboxamide (G.5.9), 4-[1-[2-[3,5-bis(trifluoromethyl)pyr-azol-1-yl]acetyl]-4-piperidyl]- / V-tetralin-1-yl-pyridine-2-carboxamide (G.5.10), (4-[1-[2-[5-cy-clopropyl-3-(trifluoromethyl)pyrazol-1-yl]acetyl]-4-piperidyl]- / V-tetralin-1-yl-pyridine-2-carbox-amide (G.5.11), (1-(4-(4-(5-(2,6-dichlorophenyl)-4,5-dihydroisoxazol-3-yl)thiazol-2-yl)piper-idin-1-yl)-2-((3-trifluoromethyl)pyrazin-2-yl)oxy)ethan-1-one, 1-(4-(4-(5-(2-chloro-6-fluoro-phenyl)-4,5-dihydroisoxazol-3-yl)thiazol-2-yl)piperidin-1-yl)-2-((3-trifluoromethyl)pyridin-2-yl)-oxy)ethan-1-one, te / Y-butyl 4-(4-(5-(2-bromo-6-fluorophenyl)-4,5-dihydroisoxazol-3-yl)thiazol-2-yl)piperidin-1 -carboxylate, ((2-(3-(2-(1-(2-(3,5-bis(trifluoromethyl)-1 H-pyrazol-1 -yl)acetyl)-piperidin-4-yl)thiazol-4-yl)-4,5-dihydroisoxazo-5-yl)-3-fluorophenyl)imino)dimethyl-A6-sulfa-none, ((2-(3-(2-(1-(2-(3,5-bis(difluoromethyl)-1 H-pyrazol-1 -yl)acetyl)piperidin-4-yl)thiazol-4-yl)-4,5-dihydroisoxazo-5-yl)-3-fluorophenyl)imino)dimethyl-A6-sulfanone,

[0535] ((2-(3-(2-(1 -(2-(3,5-bis(difluoromethyl)-1 H-pyrazol-1 -yl)acetyl)piperidin-4-yl)thiazol-4-yl)- 4.5-dihydroisoxazo-5-yl)-3-chorophenyl)imino)(isopropyl)(methyl)-A6-sulfanone,

[0536] ((2-(3-(2-(1-(2-(3,5-bis(trifluoromethyl)-1 H-pyrazol-1 -yl)acetyl)piperidin-4-yl)thiazol-4-yl)- 4.5-dihydroisoxazo-5-yl)-3-fluorophenyl)imino)(isopropyl)(methyl)-A6-sulfanone,

[0537] ((2-(3-(2-(1-(2-(3,5-bis(difluoromethyl)-1 H-pyrazol-1 -yl)acetyl)piperidin-4-yl)thiazol-4-yl)- 4.5-dihydroisoxazo-5-yl)-3-(trifluoromethyl)phenyl)imino)dimethyl-A6-sulfanone, ((3-fluoro- 2-(3-(2-(1-(2-(5-methyl-3-(trifluoromethyl)-1 H-pyrazol-1 -yl)acetyl)piperidin-4-yl)thiazol-4-yl)- 4.5-dihydroisoxazo-5-yl)-phenyl)imino)dimethyl-A6-sulfanone;

[0538] H)Multi Site Activity (M)

[0539] - inorganics (M01): Bordeaux mixture (H.1.1), copper (H.1.2), copper acetate (H.1.3), copper hydroxide (H.1.4), copper oxychloride (H.1.5), basic copper sulfate (H.1.6), sulfur (H.1.7);

[0540] - dithiocarbamates and relatives: ferbam (H.2.1), mancozeb (H.2.2), maneb (H.2.3), metam (H.2.4), metiram (H.2.5), propineb (H.2.6), thiram (H.2.7), zineb (H.2.8), ziram (H.2.9), zinc thiazole (H.2.10);

[0541] - organochlorine compounds (M04, M05, M06, M08): anilazine (H.3.1), captafol (H.3.3), captan (H.3.4), chlorothalonil (H.3.2), dichlofluanid (H.3.6), dichlorophen (H.3.7), folpet (H.3.5), hexachlorobenzene (H.3.8), pentachlorphenole (H.3.9) and its salts, phthalide (H.3.10), tolylfluanid (H.3.11);

[0542] - guanidines, quinones, quinoxalines, maleimides, thiocarbamates (M07, M09, M10, M11, M12): chinomethionat (H.4.13), dithianon (H.4.9), fluoroimide (H.4.11), guanidine (H.4.1), guazatine (H.4.4), guazatine-acetate (H.4.5), iminoctadine (H.4.6), iminoctadine-triacetate (H.4.7), iminoctadine-tris(albesilate) (H.4.8), methasulfocarb (H.4.12), 2,6-dimethyl-1H,5H-[1,4]dithiino[2,3-c:5,6-c']dipyrrole-1,3,5,7(2H,6H)-tetraone (H.4.10),

[0543] I) Cell wall biosynthesis (H) and melanin synthesis in cell wall (I)

[0544] - chitin synthase (H4): polyoxin B (1.1.2);

[0545] - cellulose synthase (H5): benthiavalicarb (1.3.5), dimethomorph (1.3.1), flumorph (1.3.2), iprovalicarb (1.3.6), mandipropamid (1.3.3), pyrimorph (1.3.4), valifenalate (1.3.7);

[0546] - reductase in melanin synthesis (MBI-R; 11) pyroquilon (1.2.1), tricyclazole (1.2.2);

[0547] - dehydratase in melanin synthesis (MBI-D, I2); carpropamid (1.2.3), dicyclomet (1.2.4), fenoxanil (1.2.5);

[0548] - polyketide synthase in melanin synthesis (MBI-P, I3): tolprocarb (1.2.6);

[0549] J) Plant defence induction (P1 to P8)

[0550] - salicylate-related (P01-P03, P08): acibenzolar-S-methyl (J.1.1), probenazole (J.1.2), isotianil (J.1.3), tiadinil (J.1.4), dichlobentiazox (J.1.13); phosphonates (P07): fosetyl (J.1.6), fosetyl-aluminum (J.1.7), phosphorous acid and its salts (J.1.8), calcium phosphonate (J.1.11), potassium phosphonate (J.1.12); others: potassium or sodium bicarbonate (J.1.9), 4-cyclopropyl- / V-(2,4-dimethoxyphenyl)thiadiazole-5-carboxamide (J.1.10);

[0551] K) Unknown mode of action (U)

[0552] - aminopyrifen (K.1.54), benziothiazolinone (K.1.48), bromothalonil (K.1.49), bronopol (K.1.1), cyflufenamid (K.1.3), cymoxanil (K.1.4), dazomet (K.1.5), debacarb (K.1.6), diclomezine (K.1.8), difenzoquat (K.1.9), difenzoquat-methylsulfate (K.1.10), diphenylamin (K.1.11), dodine, dodine free base (K.1.18), fenitropan (K.1.12), flufenoxadiazam (K.1.58) [MoA proposed: class II histone deacetylase inhibitor], flumetover (K.1.14), flumetylsulforim (K.1.60), flusulfamide (K.1.15), flutianil (K.1.16), harpin (K.1.17), nitrapyrin (K.1.19), nitrothal-isopropyl (K.1.20), oxine-copper (K.1.22), picarbutrazox (K.1.41), pyrisoxazole (K.1.37), seboctylamine (K.1.61), tebufloquin (K.1.24), tecloftalam (K.1.25), triazoxide (K.1.26), validamycin (K.1.2); / V-(4-(4-chloro-3-trifluoromethyl-phenoxy)-2,5-dimethyl-phenyl)- / V-ethyl- / V-methyl formamidine (K.1.27), / V-(4-(4-fluoro-3-trifluoromethyl-phenoxy)-2,5-dimethyl-phenyl)- / V-ethyl- / V-methyl formamidine (K.1.28), / V-[4-[[3-[(4-chlorophenyl)methyl]-1,2,4-thia-diazol-5-yl]oxy]-2,5-dimethyl-phenyl]- / V-ethyl- / V-methyl-formamidine (K.1.29), / V-(5-bromo-6-indan-2-yloxy-2-methyl-3-pyridyl)- / V-ethyl- / V-methyl-formamidine (K.1.30), / V-[5-bromo-6-[1-(3,5-difluorophenyl)ethoxy]-2-methyl-3-pyridyl]- / V-ethyl- / V-methyl-formamidine (K.1.31), / V-[5-bromo-6-(4-isopropylcyclohexoxy)-2-methyl-3-pyridyl]- / V-ethyl- / V-methyl-formamidine (K.1.32), / V-[5-bromo-2-methyl-6-(1-phenylethoxy)-3-pyridyl]- / V-ethyl- / V-methyl-formamidine (K.1.33), / V-(2-methyl-5-trifluoromethyl-4-(3-trimethylsilanyl-propoxy)-phenyl)- / V-ethyl- / V-methyl formamidine (K.1.34), / V-(5-difluoromethyl-2-methyl-4-(3-trimethylsilanyl-propoxy)-phenyl)- / V-ethyl- / V-methyl formamidine (K.1.35), 2-(4-chloro-phenyl)- / V-[4-(3,4-dimethoxy-phenyl)-isoxazol-5-yl]-2-prop-2-ynyloxy-acetamide (K.1.36), 3-[5-(4-methylphenyl)-2,3-di-methyl-isoxazolidin-3-yl]-pyridine (K.1.38), 5-chloro-1-(4,6-dimethoxy-pyrimidin-2-yl)-2-meth-yl-1H-benzoimidazole (K.1.39), ethyl (Z)-3-amino-2-cyano-3-phenyl-prop-2-enoate (K.1.40), pentyl / V-[6-[[(Z)-[(1-methyltetrazol-5-yl)-phenyl-methylene]amino]oxymethyl]-2-pyridyl]carba-mate (K.1.42), but-3-ynyl / V-[6-[[(Z)-[(1-methyltetrazol-5-yl)-phenyl-methylene]amino]oxy-methyl]-2-pyridyl]carbamate (K.1.43), 2-(6-benzyl-2-pyridyl)quinazoline (K.1.50), 2-[6-(3-flu-oro-4-methoxy-phenyl)-5-methyl-2-pyridyl]quinazoline (K.1.51), / V-(2,5-dimethyl-4-phenoxy-phenyl)- / V-ethyl- / V-methyl-formamidine (K.1.53), / V-[5-bromo-2-methyl-6-(1-methyl-2-prop-oxy-ethoxy)-3-pyridyl]- / V-ethyl- / V-methyl-formamidine (K.1.56), / V'-[4-(4,5-dichlorothiazol-2-yl)oxy-2,5-dimethyl-phenyl]- / V-ethyl- / V-methyl-formamidine (K.1.57), / V-methyl-4-[5-(tri-fluoromethyl)-1,2,4-oxadiazol-3-yl]benzenecarbothioamide (K.1.59), / V-methoxy- / V-[[4-[5-(tri-fluoromethyl)-1,2,4-oxadiazol-3-yl]phenyl]methyl]cyclopropanecarboxamide (K.1.61), / V-((4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]phenyl)methyl)propanamide (K.1.62), 3,3,3-tri-fluoro- / V-[[3-fluoro-4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]phenyl]methyl]propanamide (K.1.63), 3,3,3-trifluoro- / V-[[2-fluoro-4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]phenyl]methyl]-propanamide (K.1.64), / V-[2,3-difluoro-4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]benzyl]-butanamide (K.1.65), / V-[[2,3-difluoro-4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]phenyl]- methyl]-3,3,3-trifluoro-propanamide (K.1.66), 1-methoxy-1-methyl-3-[[4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]phenyl]methyl]urea (K.1.67), 1, 1 -diethyl-3-[[4-[5-[trifluoromethyl]- 1.2.4-oxadiazol-3-yl]phenyl]methyl]urea (K.1.68), / V,2-dimethoxy- / V-[[4-[5-(trifluoromethyl)- 1.2.4-oxadiazol-3-yl]phenyl]methyl]propanamide (K.1.69), / V-ethyl-2-methyl- / V-[[4-[5-(trifluoro-methyl)-1,2,4-oxadiazol-3-yl]phenyl]methyl]propanamide (K.1.70), 1-methoxy-3-methyl- 1-[[4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]phenyl]methyl]urea (K.1.71), 1 -[[4-[5-(trifluoro-methyl)-1,2,4-oxadiazol-3-yl]phenyl]methyl]pyrrolidin-2-one (K.1.72), 1 -[[4-[5-(trifluoro-methyl)-1,2,4-oxadiazol-3-yl]phenyl]methyl]piperidin-2-one (K.1.73), 4-[[4-[5-(trifluoromethyl)- 1.2.4-oxadiazol-3-yl]phenyl]methyl]morpholin-3-one (K.1.74), 4,4-dimethyl-2-[[4-[5-(trifluoro-methyl)-1,2,4-oxadiazol-3-yl]phenyl]methyl]isoxazolidin-3-one (K.1.75), 2-[[4-[5-(trifluoro-methyl)-1,2,4-oxadiazol-3-yl]phenyl]methyl]isoxazolidin-3-one (K.1.76), 5,5-dimethyl- 2-[[4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]phenyl]methyl]isoxazolidin-3-one (K.1.77), 3,3-dimethyl-1-[[4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]phenyl]methyl]piperidin-2-one (K.1.78), 2-[[4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]phenyl]methyl]oxazinan-3-one (K.1.79), 1-[[3-fluoro-4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]phenyl]methyl]azepan-2-one (K.1.80), 4,4-dimethyl-1-[[4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]phenyl]methyl]pyrrolidin- 2-one (K.1.81), 5-methyl-1-[[4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]phenyl]methyl]-pyrrolidin-2-one (K.1.82), ethyl 1-[[4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]phenyl]methyl]-pyrazole-4-carboxylate (K.1.83), / V-methyl-1-[[4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]-phenyl]methyl]pyrazole-4-carboxamide (K.1.84), / V, / V-dimethyl-1-[4-[5-(trifluoromethyl)- 1.2.4-oxadiazol-3-yl]benzyl]-1 H-1,2,4-triazol-3-amine (K.1.85), / V-methoxy- / V-methyl-1-[[4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]phenyl]methyl]pyrazole-4-carboxamide (K.1.86), propyl-1-[[4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]phenyl]methyl]pyrazole-4-carboxamide (K.1.87), / V-methoxy-1-[[4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]phenyl]methyl]pyrazole- 4-carboxamide (K.1.88), / V-allyl- / V-[[4-[5-(trifluoromethyl)- 1,2,4-oxadiazol-3-yl]phen-yl]methyl]propanamide (K.1.89), 3-ethyl-1-methoxy-1-[[4-[5-(trifluoromethyl)-1,2,4-oxadiazol- 3-yl]phenyl]methyl]urea (K.1.90), 1,3-dimethoxy-1-[[4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]phenyl]methyl]urea (K.1.91), / V-allyl- / V-[[4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]phenyl]methyl]acetamide (K.1.92), / V-[4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]-benzyl]cyclopropanecarboxamide (K.1.93), 1-methyl-3-[[4-[5-(trifluoromethyl)-1,2,4-oxadi-azol-3-yl]phenyl]methyl]urea (K.1.94), / V'-[2-chloro-4-(2-fluorophenoxy)-5-methyl-phenyl]- / V-ethyl- / V-methyl-formamidine (K.1.95), / V-[2-chloro-4-[(4-methoxy-phenyl)methyl]-5-methyl-phenyl]- / V-ethyl- / V-methyl-formamidine (K.1.96), / V'-[2-chloro-4-[(4-cyano-phenyl)methyl]- 5-methyl-phenyl]- / V-ethyl- / V-methyl-formamidine (K.1.97), / V'-[2,5-dimethyl-4-(o-tolylmethyl)-phenyl]- / V-ethyl-N-methyl-formamidine (K.1.98), 6-chloro-3-(3-cyclopropyl-2-fluoro-phenoxy)- / V-[2-(2,4-dimethylphenyl)-2,2-difluoro-ethyl]-5-methyl-pyridazine-4-carboxamide (K.1.99), 3-(3-bromo-2-fluoro-phenoxy)-6-chloro- / V-[2-(2-chloro-4-methyl-phenyl)-2,2-difluoro-ethyl]-5-methyl-pyridazine-4-carboxamide (K.1.100), 6-chloro- / V-[2-(2-chloro-4-methyl-phenyl)-2,2-difluoro-ethyl]-3-(3-cyclopropyl-2-fluoro-phenoxy)-5-methyl-pyridazine-4-carboxamide (K.1.101), 6-chloro-3-(3-cyclopropyl-2-fluoro-phenoxy)- / V-[2-(3,4-dimethylphenyl)-2,2-diflu-oro-ethyl]-5-methyl-pyridazine-4-carboxamide (K.1.102), 6-chloro-3-(3-chloro-2-fluoro-phen-oxy)- / V-[2-(2,4-dimethylphenyl)-2,2-difluoro-ethyl]-5-methyl-pyridazine-4-carboxamide (K.1.103), / V-[2-(2-bromo-4-methyl-phenyl)-2,2-difluoro-ethyl]-6-chloro-3-(3-cyclopropyl-2-flu-oro-phenoxy)-5-methyl-pyridazine-4-carboxamide (K.1.104), 2-[cyano-(2,6-difluoro-4-pyri-dyl)amino]-5-methyl- / V-spiro[3.4]octan-3-yl-thiazole-4-carboxamide, 2-[acetyl-(2,6-difluoro- 4-pyridyl)amino]- / V-(2,2-dimethylcyclobutyl)-5-methyl-thiazole-4-carboxamide, 2-[(2,6-di- fluoro-4-pyridyl)-(2-methoxyacetyl)amino]- / V-(2,2-dimethylcyclobutyl)-5-methyl-thiazole- 4-carboxamide, 2-[cyano-(2,6-difluoro-4-pyridyl)amino]- / V-(2,2-dimethylcyclobutyl)-5-methyl- thiazole-4-carboxamide, / V-[1-[[3-[2-(5-fluoro-2-methoxy-phenyl)-2-hydroxy-ethyl]- 5-[(Z)- / V-isopropoxy-C-methyl-carbonimidoyl]-2,6-dioxo-pyrimidin-1-yl]methyl]-2-methyl- propyl]-2-methyl-propanamide, / V-[1-[[3-[2-(5-fluoro-2-methoxy-phenyl)-2-hydroxy-ethyl]- 5-[(Z)- / V-isopropoxy-C-methyl-carbonimidoyl]-2,6-dioxo-pyrimidin-1-yl]methyl]-2-methyl- propyl]-2,2-dimethyl-propanamide, / V-[2-[3-[2-(5-fluoro-2-methoxy-phenyl)-2-hydroxy-ethyl]- 5-[(Z)- / V-isopropoxy-C-methyl-carbonimidoyl]-2,6-dioxo-pyrimidin-1-yl]-1-methyl-ethyl]- 2-methyl-propanamide, / V-[2-[3-[2-hydroxy-2-(2-methoxyphenyl)ethyl]-5-[(Z)- / V-isopropoxy- C-methyl-carbonimidoyl]-2,6-dioxo-pyrimidin-1-yl]-1-methyl-ethyl]-2-methyl-propanamide, / V-[2-[3-[2-(2-cyanoethoxy)-2-(5-fluoro-2-methoxy-phenyl)ethyl]-5-[(Z)- / V-isopropoxy-C-meth- yl-carbonimidoyl]-2,6-dioxo-pyrimidin-1-yl]-1-methyl-ethyl]-2-methyl-propanamide, rac-3-[3-(3-chloro-2-fluoro-phenoxy)-6-methyl-pyridazin-4-yl]-5-[(2-chloro-4-methyl-phenyl)- methyl]-5,6-dihydro-4H-1,2,4-oxadiazine, (5S)-3-[3-(3-chloro-2-fluoro-phenoxy)-6-methyl- pyridazin-4-yl]-5-[(2-chloro-4-methyl-phenyl)methyl]-5,6-dihydro-4 / - / -1,2,4-oxadiazine, (5R)-3-[3-(3-chloro-2-fluoro-phenoxy)-6-methyl-pyridazin-4-yl]-5-[(2-chloro-4-methyl-phenyl)- methyl]-5,6-dihydro-4H-1,2,4-oxadiazine, 2-(4-fluorophenoxy)-1-[4-[5-(trifluoromethyl)- 1,2,4-oxadiazol-3-yl]phenyl]ethanone, 2-[(6-fluoro-3-pyridyl)oxy]-1-[4-[5-(trifluoromethyl)- 1,2,4-oxadiazol-3-yl]phenyl]ethanone, 2-(4-fluoroanilino)-1-[4-[5-(trifluoromethyl)-1,2,4-oxa- diazol-3-yl]phenyl]ethenone, ethyl 1-[[4-[[2-(trifluoromethyl)-1,3-dioxolan-2-yl]methoxy]- phenyl]methyl]-1 H-pyrazole-4-carboxylate, ethyl 1 -[[4-[[(1 Z)-2-ethoxy-3,3,3-trifluoro- 1 -pro- pen-1 -yl]oxy]phenyl]methyl]-1H-pyrazole-4-carboxylate;

[0553] The fungicides described by common names, their preparation and their activity e.g. against harmful fungi is known (cf.: http: / / www.alanwood.net / pesticides / ); these substances are commercially available.

[0554] The active substances, their preparation and their activity e.g. against fungi is known (www.bcpcpesticidecompendium.bcpc.org / ); many of them are commercially available. Compounds defined by IUPAC nomenclature, their preparation and pesticidal activity are also known (e.g. Can. J. Plant Sci. 48(6), 587-94, 1968; EP-141 317; EP-152031; EP-226917; EP-243970; EP-256503; EP-428941; EP-532022; EP-1 028 125; EP-1 035 122; EP-1 201 648; EP-1 122244, JP2002316902; DE19650197; DE10021412; DE102005009458; US 3,296,272; US 3,325,503; WO 98 / 46608; WO 99 / 14187; WO 99 / 24413; WO 99 / 27783; WO 00 / 29404; WO 00 / 46148; WO 00 / 65913; WO 01 / 54501; WO 01 / 56358; WO 02 / 22583; WO 02 / 40431; WO 03 / 10149; WO 03 / 11853; WO 03 / 14103; WO 03 / 16286; WO 03 / 53145; WO 03 / 61388; WO 03 / 66609; WO 03 / 74491; WO 04 / 49804; WO 04 / 83193; WO 05 / 120234; WO 05 / 123689; WO 05 / 123690; WO 05 / 63721; WO 05 / 87772; WO 05 / 87773; WO 06 / 15866; WO 06 / 87325; WO 06 / 87343; WO 07 / 82098; WO 07 / 90624, WO 10 / 139271, WO 11 / 028657, WO 12 / 168188, WO 07 / 006670, WO 11 / 77514; WO 13 / 047749, WO 10 / 069882, WO 13 / 047441, WO 03 / 16303, WO 09 / 90181, WO 13 / 007767, WO 13 / 010862, WO 13 / 127704, WO 13 / 024009, WO 13 / 24010, WO 13 / 047441, WO 13 / 162072, WO 13 / 092224, WO 11 / 135833, CN 1907024, CN 1456054, CN 103387541, CN 1309897, WO 12 / 84812, CN 1907024, WO 09094442, WO 14 / 60177, WO 13 / 116251, WO 08 / 013622, WO 15 / 65922, WO 94 / 01546, EP 2865265, WO 07 / 129454, WO 12 / 165511, WO 11 / 081174, WO 13 / 47441, WO 16 / 156241, WO 16 / 162265, WO 23 / 99460, WO 21 / 244950, WO 21 / 244951, WO 22 / 130188, WO 22 / 243810, WO 21 / 255070, WO 21 / 176057, WO 21 / 153754, JP2023064110, JP2022153603, JP2022046550, JP2022031355, WO 22 / 249074, WO 23 / 046861, WO 18 / 177894, WO 20 / 212513, WO 20 / 097012, US 2023 / 0069915.

[0555] Suitable mixing partners for the compounds of the invention also include biopesticides.

[0556] Biopesticides have been defined as a form of pesticides based on micro-organisms (bacteria, fungi, viruses, nematodes, etc.) or natural products (compounds, e.g. metabolites, proteins, or extracts from biological or other natural sources) (U. S. Environmental Protection Agency: http: / / www.epa.gov / pesticides / biopesticides / ). Biopesticides fall into two major classes, microbial and biochemical pesticides:

[0557] (1) Microbial pesticides consist of bacteria, fungi or viruses (and often include the metabolites that bacteria and fungi produce). Entomopathogenic nematodes are also classified as microbial pesticides, even though they are multi-cellular.

[0558] (2) Biochemical pesticides are naturally occurring substances or or structurally-similar and functionally identical to a naturally-occurring substance and extracts from biological sources that control pests or provide other crop protection uses as defined below, but have non-toxic mode of actions (e.g. growth or developmental regulation, attractants, repellents or defence activators (e.g. induced resistance) and are relatively non-toxic to mammals.

[0559] The following list of biopesticides, in conjunction with which the compounds of the invention can be used, illustrates the possible combinations:

[0560] L) Biopesticides

[0561] L1) Microbial pesticides with fungicidal, bactericidal, viricidal and / or plant defense activator activity: Ampelomyces quisqualis, Aspergillus flavus, Aureobasidium pullulans, Bacillus altitudinis, B. amyloliquefaciens, B. amyloliquefaciens ssp. plantarum (also referred to as B. velezensis), B. megaterium, B. mojavensis, B. mycoides, B. pumilus, B. simplex, B. solisalsi, B. subtilis, B. subtilis var. amyloliquefaciens, B. velezensis, Candida oleophila, C. saitoana, Clavibacter michiganensis (bacteriophages), Coniothyrium minitans, Cryphonectria parasitica, Cryptococcus albidus, Dilophosphora alopecuri, Fusarium oxysporum, Clonostachys rosea f. catenulate (also named Gliocladium catenulatum), Gliocladium roseum, Lysobacter antibioticus, L. enzymogenes, Metschnikowia fructicola, Microdochium dimerum, Microsphaeropsis ochracea, Muscodor albus, Paenibacillus alvei, Paenibacillus epiphyticus, P. polymyxa, Pantoea vagans, Penicillium bilaiae, Phlebiopsis gigantea, Pseudomonas sp., Pseudomonas chloraphis, Pseudozyma flocculosa, Pichia anomala, Pythium oligandrum, Sphaerodes mycoparasitica, Streptomyces griseoviridis, S. lydicus, S. violaceusniger, Talaromyces flavus, Trichoderma asperelloides, T. asperellum, T. atroviride, T. fertile, T. gamsii, T. harmatum, T. harzianum, T. polysporum, T. stromaticum, T. virens, T. viride, Typhula phacorrhiza, Ulocladium oudemansii, Verticillium dahliae, zucchini yellow mosaic virus (avirulent strain);

[0562] L2) Biochemical pesticides with fungicidal, bactericidal, viricidal and / or plant defense activator activity: harpin protein, plant oils (BM3): tea tree oil, orange oil (L.2.1), eugenol, limonene (L.2.2), geraniol (L.2.3), thymol (L.2.4); Reynoutria sachalinensis extract, aureobasidin (in particular aureobasidin A (L.2.5)), ambruticin (L.2.6), bafilomycin (L.2.7) (in particular bafilomycin A1, B1 and C1), chlorflavonin (L.2.8), cinnamaldehyde (L.2.9), natamycin (L.2.10; F8); L3) Microbial pesticides with insecticidal, acaricidal, molluscidal and / or nematicidal activity: Agrobacterium radiobacter, Bacillus cereus, B. firmus, B. thuringiensis, B. thuringiensis ssp. aizawai, B. t. ssp. israelensis, B. t. ssp. galleriae, B. t. ssp. kurstaki, B. t. ssp. tenebrionis, Beauveria bassiana, B. brongniartii, Burkholderia spp., Chromobacterium subtsugae, Cydia pomonella granulovirus (CpGV), Cryptophlebia leucotreta granulovirus (CrleGV), Flavobacterium spp., Helicoverpa armigera nucleopolyhedrovirus (HearNPV), Helicoverpa zea nucleopolyhedrovirus (HzNPV), Helicoverpa zea single capsid nucleopolyhedrovirus (HzSNPV), Heterorhabditis bacteriophora, Isaria fumosorosea, Lecanicillium longisporum, L. muscarium, Metarhizium anisopliae, M. anisopliae var. anisopliae, M. anisopliae var. acridum, Nomuraea rileyi, Paecilomyces fumosoroseus, P. lilacinus, Paenibacillus popilliae, Pasteuria spp., P. nishizawae, P. penetrans, P. ramosa, P. thornea, P. usgae, Pseudomonas fluorescens, Spodoptera littoralis nucleopolyhedrovirus (SpliNPV), Steinernema carpocapsae, S. feltiae, S. kraussei, Streptomyces galbus, S. microflavus- L4) Biochemical pesticides with insecticidal, acaricidal, molluscidal, pheromone and / or nematicidal activity: L-carvone, citral, (E, Z)-7,9-dodecadien-1-yl acetate, ethyl formate, (E, Z)-2,4-ethyl decadienoate (pear ester), (Z, Z, E)-7,11,13-hexadecatrienal, heptyl butyrate, isopropyl myristate, lavanulyl senecioate, cis-jasmone, 2-methyl-1 -butanol, methyl eugenol, methyl jasmonate, (E, Z)-2,13-octadecadien-1-ol, (E, Z)-2,13-octadecadien-1-ol acetate, (E, Z)-3,13-octadecadien-1-ol, (R)-1-octen-3-ol, pentatermanone, (E, Z, Z)-3,8,11-tetradecatrienyl acetate, (Z, E)-9,12-tetradecadien-1-yl acetate, (Z)-7-tetradecen-2-one, (Z)-9-tetradecen-1-yl acetate, (Z)-11-tetradecenal, (Z)-11-tetra- decen-1-ol, extract of Chenopodium ambrosiodes, Neem oil, Quillay extract;

[0563] L5) Microbial pesticides with plant stress reducing, plant growth regulator, plant growth promoting and / or yield enhancing activity: Azospirillum amazonense, A. brasilense, A. lipoferum, A. irakense, A. halopraeferens, Bradyrhizobium spp., B. elkanii, B. japonicum, B. liaoningense, B. lupini, Delftia acidovorans, Glomus intraradices, Mesorhizobium spp., Rhizobium leguminosarum bv. phaseoli, R. I. bv. trifolii, R. I. bv. viciae, R. tropic!, Sinorhizobium meliloti.

[0564] The biopesticides from group L1) and / or L2) may also have insecticidal, acaricidal, molluscidal, pheromone, nematicidal, plant stress reducing, plant growth regulator, plant growth promoting and / or yield enhancing activity. The biopesticides from group L3) and / or L4) may also have fungicidal, bactericidal, viricidal, plant defense activator, plant stress reducing, plant growth regulator, plant growth promoting and / or yield enhancing activity. The biopesticides from group L5) may also have fungicidal, bactericidal, viricidal, plant defense activator, insecticidal, acaricidal, molluscidal, pheromone and / or nematicidal activity.

[0565] Many of these biopesticides have been deposited under deposition numbers mentioned herein (the prefices e.g. ATCC or DSM referto the acronym of the respective culture collection, for details see e.g. here: http: / / www. wfcc.info / ccinfo / collection / by_acronym / ), are referred to in literature, registered and / or are commercially available: mixtures of Aureobasidium pullulans DSM 14940 and DSM 14941 isolated in 1989 in Konstanz, Germany (e.g. blastospores in BlossomProtect® from bio-ferm GmbH, Austria), Azospirillum brasilense Sp245 originally isolated in wheat region of South Brazil (Passo Fundo) at least prior to 1980 (BR 11005; e.g. GELFIX® Gram neas from BASF Agricultural Specialties Ltd., Brazil), A. brasilense strains Ab-V5 and Ab-V6 (e.g. in AzoMax from Novozymes BioAg Produtos para Agricultura Ltda., Quattro Barras, Brazil or Simbiose- Malz® from Simbiose-Agro, Brazil; Plant Soil 331, 413–425, 2010), Bacillus amyloliquefaciens strain AP-188 (NRRL B-50615 and B-50331; US8,445,255); B. amylo-liquefaciens ssp. plantarum strains formerly also sometimes referred to as B. subtilis, recently together with B. methylotrophicus, and B. velezensis classified as B. velezensis (Int. J. Syst. Evol. Microbiol. 66, 1212–1217, 2016): B. a. ssp. plantarum or B. velezensis D747 isolated from air in Kikugawashi, Japan (US 20130236522 A1; FERM BP 8234; e.g. Double Nickel™ 55 WDG from Certis LLC, USA), B. a. ssp. plantarum or B. velezensis FZB24 isolated from soil in Brandenburg, Germany (also called SB3615; DSM 96-2; J. Plant Dis. Prot. 105, 181–197, 1998; e.g. Taegro® from Novozyme Biologicals, Inc., USA), B. a. ssp. plantarum or B. velezensis FZB42 isolated from soil in Brandenburg, Germany (DSM 23117; J. Plant Dis. Prot. 105, 181–197, 1998; e.g. RhizoVital® 42 from AbiTEP GmbH, Germany), B. a. ssp. plantarum or B. vele-zensis MBI600 isolated from faba bean in Sutton Bonington, Nottinghamshire, U. K. at least before 1988 (also called 1430; NRRL B 50595; US 2012 / 0149571 A1; e.g. Integral® from BASF Corp., USA), B. a. ssp. plantarum or B. velezensis QST-713 isolated from peach orchard in 1995 in California, U. S. A. (NRRL B 21661; e.g. Serenade® MAX from Bayer Crop Science LP, USA), B. a. ssp. plantarum or B. velezensis TJ1000 isolated in 1992 in South Dakoda, U. S. A, (also called 1BE; ATCC BAA-390; CA 2471555 A1; e.g. QuickRoots™ from TJ Technologies, Watertown, SD, USA); B. firmus CNCM 1-1582, a variant of parental strain EIP-N1 (CNCM 1-1556) isolated from soil of central plain area of Israel (WO 2009 / 126473, US6,406,690; e.g. Votivo® from Bayer CropScience LP, USA), B. pumilus GHA 180 isolated from apple tree rhizo-sphere in Mexico (IDAC 260707-01; e.g. PROMIX® BX from Premier Horticulture, Quebec, Canada), B. pumilus INR-7 otherwise referred to as BU F22 and BU-F33 isolated at least be-fore 1993 from cucumber infested by Erwinia tracheiphila (NRRL B-50185, NRRL B-50153; US 8,445,255), B. pumilus KFP9F isolated from the rhizosphere of grasses in South Africa at least before 2008 (NRRL B-50754; WO 2014 / 029697; e.g. BAC-UP or FUSION-P from BASF Agricultural Specialities (Pty) Ltd., South Africa), B. pumilus QST 2808 was isolated from soil collected in Pohnpei, Federated States of Micronesia, in 1998 (NRRL B 30087; e.g. Sonata® or Ballad® Plus from Bayer Crop Science LP, USA), B. simplex ABU 288 (NRRL B-50304; US8,445,255), B. subtilis FB17 also called UD 1022 or UD10-22 isolated from red beet roots in North America (ATCC PTA-11857; System. Appl. Microbiol. 27, 372–379, 2004; US2010 / 0260735; WO 2011 / 109395); B. thuringiensis ssp. aizawai ABTS-1857 isolated from soil taken from a lawn in Ephraim, Wisconsin, U. S. A., in 1987 (also called ABG 6346; ATCC SD-1372; e.g. XenTari® from BioFa AG, Munsingen, Germany), B. t. ssp. kurstaki ABTS-351 identical to HD-1 isolated in 1967 from diseased Pink Bollworm black larvae in Brownsville, Texas, U. S. A. (ATCC SD-1275; e.g. Dipel® DF from Valent BioSciences, IL, USA), B. t. ssp. kurstaki SB4 isolated from E. saccharina larval cadavers (NRRL B-50753; e.g. Beta Pro® from BASF Agricultural Specialities (Pty) Ltd., South Africa), B. t. ssp. tenebrionis NB-176-1, a mutant of strain NB-125, a wild type strain isolated in 1982 from a dead pupa of the beetle Tenebrio molitor (DSM 5480; EP 585215 B1; e.g. Novodor® from Valent BioSciences, Switzerland), Beauveria bassiana GHA (ATCC 74250; e.g. BotaniGard® 22WGP from Laverlam Int. Corp., USA), B. bassiana JW-1 (ATCC 74040; e.g. Naturalis® from CBC (Europe) S.r.l., Italy), B. bassiana PPRI 5339 isolated from the larva of the tortoise beetle Conchyloctenia punctata (NRRL 50757; e.g. BroadBand® from BASF Agricultural Specialities (Pty) Ltd., South Africa), Bradyrhizobium elkanii strains SEMIA 5019 (also called 29W) isolated in Rio de Janeiro, Brazil and SEMIA 587 isolated in 1967 in the State of Rio Grande do Sul, from an area previously inoculated with a North American isolate, and used in commercial inoculants since 1968 (Appl. Environ. Microbiol. 73(8), 2635, 2007; e.g. GELFIX 5 from BASF Agricultural Specialties Ltd., Brazil), B. japonicum 532c isolated from Wisconsin field in U. S. A. (Nitragin 61A152; Can. J. Plant. Sci. 70, 661–666, 1990; e.g. in Rhizoflo®, Histick®, Hicoat® Super from BASF Agricultural Specialties Ltd., Canada), B. japonicum E-109 variant of strain USDA 138 (INTA E109, SEMIA 5085; Eur. J. Soil Biol. 45, 28–35, 2009; Biol. Fertil. Soils 47, 81–89, 2011); B. japonicum strains deposited at SEMIA known from Appl. Environ. Microbiol. 73(8), 2635, 2007: SEMIA 5079 isolated from soil in Cerrados region, Brazil by Embrapa-Cerrados used in commercial inoculants since 1992 (CPAC 15; e.g. GELFIX 5 or ADHERE 60 from BASF Agricultural Specialties Ltd., Brazil), B. japonicum SEMIA 5080 obtained under lab condtions by Embrapa-Cerrados in Brazil and used in commercial inoculants since 1992, being a natural variant of SEMIA 586 (CB1809) originally isolated in U. S. A. (CPAC 7; e.g. GELFIX 5 or ADHERE 60 from BASF Agricultural Specialties Ltd., Brazil); Burkholderia sp. A396 isolated from soil in Nikko, Japan, in 2008 (NRRL B-50319; WO 2013 / 032693; Marrone Bio Innovations, Inc., USA), Coniothyrium minitans CON / M / 91-08 isolated from oilseed rape (WO 1996 / 021358; DSM 9660; e.g. Contans® WG, Intercept® WG from Bayer CropScience AG, Germany), harpin (alpha-beta) protein (Science 257, 85-88, 1992; e.g. Messenger™ or HARP-N Tek from Plant Health Care pic, U. K.), Helicoverpa armigera nucleopolyhedrovirus (HearNPV) (J. Invertebrate Pathol. 107, 112–126, 2011; e.g. Helicovex® from Adermatt Biocontrol, Switzerland; Diplomata® from Koppert, Brazil; Vivus® Max from AgBiTech Pty Ltd., Queensland, Australia), Helicoverpa zea single capsid nucleopolyhedrovirus (HzSNPV) (e.g. Gemstar® from Certis LLC, USA), Helicoverpa zea nucleopolyhedrovirus ABA-NPV-U (e.g. Heligen® from AgBiTech Pty Ltd., Queensland, Australia), Heterorhabditis bacteriophora (e.g. Nemasys® G from BASF Agricultural Specialities Limited, UK), Isaria fumosorosea Apopka-97 isolated from mealy bug on gynura in Apopka, Florida, U. S. A. (ATCC 20874; Biocontrol Science Technol. 22(7), 747–761, 2012; e.g. PFR-97™ or PreFeRal® from Certis LLC, USA), Metarhizium anisopliae var. anisopliae F52 also called 275 or 275 isolated from codling moth in Austria (DSM 3884, ATCC 90448; e.g. Met52® Novozymes Biologicals BioAg Group, Canada), Metschnikowia fructicola 277 isolated from grapes in the central part of Israel (US 6,994,849; NRRL Y-30752; e.g. formerly Shemer® from Agrogreen, Israel), Paecilomyces lilacinus 251 isolated from infected nematode eggs in the Philippines (AGAL 89 / 030550; WO1991 / 02051; Crop Protection 27, 352–361, 2008; e.g. BioAct®from Bayer CropScience AG, Germany and MeloCon® from Certis, USA), Paenibacillus alvei NAS6G6 isolated from the rhizosphere of grasses in South Africa at least before 2008 (WO 2014 / 029697; NRRL B-50755; e.g. BAC-UP from BASF Agricultural Specialities (Pty) Ltd., South Africa), Paenibacillus strains isolated from soil samples from a variety of European locations including Germany: P. epiphyticus Lu17015 (WO 2016 / 020371; DSM 26971), P. polymyxa ssp. plantarum Lu16774 (WO 2016 / 020371; DSM 26969), P. p. ssp. plantarum strain Lu17007 (WO 2016 / 020371; DSM 26970); Pasteuria nishizawae Pn1 isolated from a soybean field in the mid-2000s in Illinois, U. S. A. (ATCC SD 5833; Federal Register 76(22), 5808, February 2, 2011; e.g. Clariva™ PN from Syngenta Crop Protection, LLC, USA), Penicillium bilaiae (also called P. bilaii) strains ATCC 18309 (= ATCC 74319), ATCC 20851 and / or ATCC 22348 (=ATCC 74318) originally isolated from soil in Alberta, Canada (Fertilizer Res. 39, 97-103, 1994; Can. J. Plant Sci.

[0566] 78(1), 91-102, 1998; US 5,026,417, WO 1995 / 017806; e.g. Jump Start®, Provide® from Novozymes Biologicals BioAg Group, Canada), Reynoutria sachalinensis extract (EP 0307510 B1; e.g. Regalia® SC from Marrone BioInnovations, Davis, CA, USA or Milsana® from BioFa AG, Germany), Steinernema carpocapsae (e.g. Millenium® from BASF Agricultural Specialities Limited, UK), S. feltiae (e.g. Nemashield® from BioWorks, Inc., USA; Nemasys® from BASF Agricultural Specialities Limited, UK), Streptomyces microflavus NRRL B-50550 (WO 2014 / 124369; Bayer CropScience, Germany), Trichoderma asperelloides JM41R isolated in South Africa (NRRL 50759; also referred to as T. fertile; e.g. Trichoplus® from BASF Agricultural Specialities (Pty) Ltd., South Africa), T. harzianum T-22 also called KRL-AG2 (ATCC 20847; BioControl 57, 687–696, 2012; e.g. Plantshield® from BioWorks Inc., USA or SabrEx™ from Advanced Biological Marketing Inc., Van Wert, OH, USA).

[0567] According to the invention, the solid material (dry matter) of the biopesticides (with the exception of oils e.g. Neem oil) are considered as active components (e.g. to be obtained after drying or evaporation of the extraction or suspension medium in case of liquid formulations of the microbial pesticides).

[0568] In accordance with the invention, the weight ratios and percentages used herein for a biological extract e.g. Quillay extract are based on the total weight of the dry content (solid material) of the respective extract(s).

[0569] The total weight ratios of compositions comprising at least one microbial pesticide in the form of viable microbial cells including dormant forms, can be determined using the amount of CFU of the respective microorganism to calculate the total weight of the respective active component with the following equation that 1x1010CFU equals one gram of total weight of the respective active component. Colony forming unit is measure of viable microbial cells, in particular fungal and bacterial cells. In addition, here “CFU” may also be understood as the number of (juvenile) individual nematodes in case of (entomopathogenic) nematode biopesticides, e.g. Steinernema feltiae.

[0570] When mixtures comprising microbial pesticides are employed in crop protection, the application rates range from 1x106to 5x1016(or more) CFU / ha, preferably from 1x108to 1x1013CFU / ha, and even more preferably from 1x109to 5x1015CFU / ha and in particular from 1x1012to 5x1014CFU / ha. In the case of nematodes as microbial pesticides (e.g. Steinernema feltiae), the application rates regularly range from 1x105to 1x1012(or more), preferably from 1x108to 1x1011, more preferably from 5x108to 1x1010individuals (e.g. in the form of eggs, juvenile or any other live stages, preferably in an infetive juvenile stage) per ha.

[0571] When mixtures comprising microbial pesticides are employed in seed treatment, the application rates generally range from 1x106to 1x1012(or more) CFU / seed, preferably from 1x106to 1x109CFU / seed. Furthermore, the application rates with respect to seed treatment generally range from 1x107to 1x1014(or more) CFU per 100 kg of seed, preferably from 1x109to 1x1012CFU per 100 kg of seed.

[0572] Formulations

[0573] The invention also relates to agrochemical compositions comprising an auxiliary and at least one compound of the invention or a mixture thereof.

[0574] An agrochemical composition comprises a pesticidally effective amount of a compound of the invention or a mixture thereof.

[0575] The compounds of the invention or the mixtures thereof can be converted into customary types of agro-chemical compositions, e.g. solutions, emulsions, suspensions, dusts, powders, pastes, granules, pressings, capsules, and mixtures thereof. Examples for composition types are suspensions (e.g. SC, OD, FS), emulsifiable concentrates (e.g. EC), emulsions (e.g. EW, EO, ES, ME), capsules (e.g. CS, ZC), pastes, pastilles, wettable powders or dusts (e.g. WP, SP, WS, DP, DS), pressings (e.g. BR, TB, DT), granules (e.g. WG, SG, GR, FG, GG, MG), insecticidal articles (e.g. LN), as well as gel formulations for the treatment of plant propagation materials e.g. seeds (e.g. GF). These and further compositions types are defined in the “Catalogue of pesticide formulation types and international coding system”, Technical Monograph No. 2, 6th Ed. May 2008, CropLife International.

[0576] The compositions are prepared in a known manner, e.g. described by Mollet and Grubemann, Formulation technology, Wiley VCH, Weinheim, 2001; or Knowles, New developments in crop protection product formulation, Agrow Reports DS243, T& F Informa, London, 2005.

[0577] Examples for suitable auxiliaries are solvents, liquid carriers, solid carriers or fillers, surfactants, dispersants, emulsifiers, wetters, adjuvants, solubilizers, penetration enhancers, protective colloids, adhesion agents, thickeners, humectants, repellents, attractants, feeding stimulants, compatibilizers, bactericides, anti-freezing agents, anti-foaming agents, colorants, tackifiers and binders.

[0578] Suitable solvents and liquid carriers are water and organic solvents, e.g. mineral oil fractions of medium to high boiling point, e.g. kerosene, diesel oil; oils of vegetable or animal origin; hydrocarbons, e.g. toluene, paraffin, tetrahydronaphthalene, alkylated naphthalenes; alcohols, e.g. ethanol, propanol, butanol, benzylalcohol, cyclohexanol; glycols; DMSO; ketones, e.g. cyclohexanone; esters, e.g. lactates, carbonates, fatty acid esters, gamma-butyrolactone; fatty acids; phosphonates; amines; amides, e.g. N-methylpyrrolidone, fatty acid dimethylamides; and mixtures thereof.

[0579] Suitable solid carriers or fillers are mineral earths, e.g. silicates, silica gels, talc, kaolins, limestone, lime, chalk, clays, dolomite, diatomaceous earth, bentonite, CaSO4, MgSO4, MgO; polysaccharide powders, e.g. cellulose, starch; fertilizers, e.g. (NH4)2SO4, (NH4)3PO4, NH4NO3, ureas; products of vegetable origin, e.g. cereal meal, tree bark meal, wood meal, nutshell meal, and mixtures thereof.

[0580] Suitable surfactants are surface-active compounds, e.g. anionic, cationic, nonionic and amphoteric surfactants, block polymers, polyelectrolytes, and mixtures thereof. Such surfactants can be used as emusifier, dispersant, solubilizer, wetter, penetration enhancer, protective col-loid, or adjuvant. Examples of surfactants are listed in McCutcheon’s, Vol.1: Emulsifiers & Detergents, McCutcheon’s Directories, Glen Rock, USA, 2008 (International or North American Ed.).

[0581] Suitable anionic surfactants are alkali, alkaline earth or ammonium salts of sulfonates, sulfates, phosphates, carboxylates, and mixtures thereof. Examples of sulfonates are alkylarylsulfonates, diphenylsulfonates, alpha-olefin sulfonates, lignine sulfonates, sulfonates of fatty acids and oils, sulfonates of ethoxylated alkylphenols, sulfonates of alkoxylated arylphenols, sulfonates of condensed naphthalenes, sulfonates of dodecyl- and tridecylbenzenes, sulfonates of naphthalenes and alkylnaphthalenes, sulfosuccinates or sulfosuccinamates. Examples of sulfates are sulfates of fatty acids and oils, of ethoxylated alkylphenols, of alcohols, of ethoxylated alcohols, or of fatty acid esters. Examples of phosphates are phosphate esters. Examples of carboxylates are alkyl carboxylates, and carboxylated alcohol or alkylphenol ethoxylates.

[0582] Suitable nonionic surfactants are alkoxylates, N-subsituted fatty acid amides, amine oxides, esters, sugar-based surfactants, polymeric surfactants, and mixtures thereof. Examples of alkoxylates are compounds e.g. alcohols, alkylphenols, amines, amides, arylphenols, fatty acids or fatty acid esters which have been alkoxylated with 1 to 50 equivalents. Ethylene oxide and / or propylene oxide may be employed for the alkoxylation, preferably ethylene oxide. Examples of N-subsititued fatty acid amides are fatty acid glucamides or fatty acid alkanola-mides. Examples of esters are fatty acid esters, glycerol esters or monoglycerides. Examples of sugar-based surfactants are sorbitans, ethoxylated sorbitans, sucrose and glucose esters or alkylpolyglucosides. Examples of polymeric surfactants are homo- or copolymers of vinylpyrrolidone, vinylalcohols, or vinylacetate.

[0583] Suitable cationic surfactants are quaternary surfactants, e.g. quaternary ammonium compounds with one or two hydrophobic groups, or salts of long-chain primary amines. Suitable amphoteric surfactants are alkylbetains and imidazolines. Suitable block polymers are block polymers of the A-B or A-B-A type comprising blocks of polyethylene oxide and polypropylene oxide, or of the A-B-C type comprising alkanol, polyethylene oxide and polypropylene oxide. Suitable polyelectrolytes are polyacids or polybases. Examples of polyacids are alkali salts of polyacrylic acid or polyacid comb polymers. Examples of polybases are polyvinylamines, or polyethyleneamines.

[0584] Suitable adjuvants are compounds, which have a neglectable or even no pesticidal activity themselves, and which improve the biological performance of the compounds of the invention on the target. Examples are surfactants, mineral or vegetable oils, and other auxilaries. Further examples are listed by Knowles, Adjuvants and additives, Agrow Reports DS256, T& F Informa UK, 2006, chapter 5.

[0585] Suitable thickeners are polysaccharides (e.g. xanthan gum, carboxymethylcellulose), anorganic clays (organically modified or unmodified), polycarboxylates, and silicates.

[0586] Suitable bactericides are bronopol and isothiazolinone derivatives e.g. alkylisothiazolinones and benzisothiazolinones.

[0587] Suitable anti-freezing agents are ethylene glycol, propylene glycol, urea, and glycerin.

[0588] Suitable anti-foaming agents are silicones, long chain alcohols, and salts of fatty acids.

[0589] Suitable colorants (e.g. in red, blue, or green) are pigments of low water solubility and water-soluble dyes. Examples are inorganic colorants (e.g. iron oxide, titan oxide, iron hexacyanoferrate) and organic colorants (e.g. alizarin-, azo-, and phthalocyanine colorants). Suitable tackifiers or binders are polyvinylpyrrolidons, polyvinylacetates, polyvinyl alcohols, polyacrylates, biological or synthetic waxes, and cellulose ethers.

[0590] Examples for composition types and their preparation are:

[0591] i) Water-soluble concentrates (SL, LS)

[0592] 10-60 wt% of a compound I according to the invention and 5-15 wt% wetting agent (e.g. alcohol alkoxylates) are dissolved in water and / or in a water-soluble solvent (e.g. alcohols) up to 100 wt%. The active substance dissolves upon dilution with water.

[0593] ii) Dispersible concentrates (DC)

[0594] 5-25 wt% of a compound I according to the invention and 1-10 wt% dispersant (e.g. polyvinylpyrrolidone) are dissolved in up to 100 wt% organic solvent (e.g. cyclohexanone). Dilution with water gives a dispersion.

[0595] iii) Emulsifiable concentrates (EC)

[0596] 15-70 wt% of a compound I according to the invention and 5-10 wt% emulsifiers (e.g. calcium dodecylbenzenesulfonate and castor oil ethoxylate) are dissolved in up to 100 wt% waterinsoluble organic solvent (e.g. aromatic hydrocarbon). Dilution with water gives an emulsion. iv) Emulsions (EW, EO, ES)

[0597] 5-40 wt% of a compound I according to the invention and 1-10 wt% emulsifiers (e.g. calcium dodecylbenzenesulfonate and castor oil ethoxylate) are dissolved in 20-40 wt% water-insoluble organic solvent (e.g. aromatic hydrocarbon). This mixture is introduced into up to 100 wt% water by means of an emulsifying machine and made into a homogeneous emulsion. Dilution with water gives an emulsion.

[0598] v) Suspensions (SC, OD, FS)

[0599] In an agitated ball mill, 20-60 wt% of a compound I according to the invention are comminuted with addition of 2-10 wt% dispersants and wetting agents (e.g. sodium lignosulfonate and alcohol ethoxylate), 0,1-2 wt% thickener (e.g. xanthan gum) and up to 100 wt% water to give a fine active substance suspension. Dilution with water gives a stable suspension of the active sub-stance. For FS type composition up to 40 wt% binder (e.g. polyvinylalcohol) is added.

[0600] vi) Water-dispersible granules and water-soluble granules (WG, SG)

[0601] 50-80 wt% of a compound I according to the invention are ground finely with addition of up to 100 wt% dispersants and wetting agents (e.g. sodium lignosulfonate and alcohol ethoxylate) and prepared as water-dispersible or water-soluble granules by means of technical appliances (e.g. extrusion, spray tower, fluidized bed). Dilution with water gives a stable dispersion or solution of the active substance.

[0602] vii) Water-dispersible powders and water-soluble powders (WP, SP, WS)

[0603] 50-80 wt% of a compound I according to the invention are ground in a rotor-stator mill with addition of 1-5 wt% dispersants (e.g. sodium lignosulfonate), 1-3 wt% wetting agents (e.g. alcohol ethoxylate) and up to 100 wt% solid carrier, e.g. silica gel. Dilution with water gives a stable dispersion or solution of the active substance.

[0604] viii) Gel (GW, GF)

[0605] In an agitated ball mill, 5-25 wt% of a compound I according to the invention are comminuted with addition of 3-10 wt% dispersants (e.g. sodium lignosulfonate), 1-5 wt% thickener (e.g. carboxymethylcellulose) and up to 100 wt% water to give a fine suspension of the active substance. Dilution with water gives a stable suspension of the active substance.

[0606] ix) Microemulsion (ME)

[0607] 5-20 wt% of a compound I according to the invention are added to 5-30 wt% organic solvent blend (e.g. fatty acid dimethylamide and cyclohexanone), 10-25 wt% surfactant blend (e.g. alcohol ethoxylate and arylphenol ethoxylate), and water up to 100 %. This mixture is stirred for 1 h to produce spontaneously a thermodynamically stable microemulsion.

[0608] x) Microcapsules (CS)

[0609] An oil phase comprising 5-50 wt% of a compound I according to the invention, 0-40 wt% water insoluble organic solvent (e.g. aromatic hydrocarbon), 2-15 wt% acrylic monomers (e.g. methylmethacrylate, methacrylic acid and a di- or triacrylate) are dispersed into an aqueous solution of a protective colloid (e.g. polyvinyl alcohol). Radical polymerization initiated by a radical initiator results in the formation of poly(meth)acrylate microcapsules. Alternatively, an oil phase comprising 5-50 wt% of a compound I according to the invention, 0-40 wt% water insoluble organic solvent (e.g. aromatic hydrocarbon), and an isocyanate monomer (e.g. di-phenylme-thene-4,4’-diisocyanatae) are dispersed into an aqueous solution of a protective colloid (e.g. polyvinyl alcohol). The addition of a polyamine (e.g. hexamethylenediamine) results in the for-mation of a polyurea microcapsule. The monomers amount to 1-10 wt%. The wt% relate to the total CS composition.

[0610] xi) Dustable powders (DP, DS)

[0611] 1-10 wt% of a compound I according to the invention are ground finely and mixed intimately with up to 100 wt% solid carrier, e.g. finely divided kaolin.

[0612] xii) Granules (GR, FG) 0.5-30 wt% of a compound I according to the invention is ground finely and associated with up to 100 wt% solid carrier (e.g. silicate). Granulation is achieved by extrusion, spray-drying or the fluidized bed.

[0613] xiii) Ultra-low volume liquids (UL)

[0614] 1-50 wt% of a compound I according to the invention are dissolved in up to 100 wt% organic solvent, e.g. aromatic hydrocarbon.

[0615] The compositions types i) to xi) may optionally comprise further auxiliaries, e.g. 0.1-1 wt% bactericides, 5-15 wt% anti-freezing agents, 0.1-1 wt% anti-foaming agents, and 0.1-1 wt% colorants.

[0616] The agrochemical compositions generally comprise between 0.01 and 95%, preferably between 0.1 and 90%, and most preferably between 0.5 and 75%, by weight of active substance. The active substances are employed in a purity of from 90% to 100%, preferably from 95% to 100% (according to NMR spectrum).

[0617] Various types of oils, wetters, adjuvants, fertilizer, or micronutrients, and other pesticides (e.g. herbicides, insecticides, fungicides, growth regulators, safeners) may be added to the active substances or the compositions comprising them as premix or, if appropriate not until immediately prior to use (tank mix). These agents can be admixed with the compositions according to the invention in a weight ratio of 1: 100 to 100: 1, preferably 1: 10 to 10:1.

[0618] The user applies the composition according to the invention usually from a predosage device, a knapsack sprayer, a spray tank, a spray plane, or an irrigation system. Usually, the agro-chemical composition is made up with water, buffer, and / or further auxiliaries to the desired application concentration and the ready-to-use spray liquor or the agrochemical composition according to the invention is thus obtained. Usually, 20 to 2000 liters, preferably 50 to 400 liters, of the ready-to-use spray liquor are applied per hectare of agricultural useful area.

[0619] According to one embodiment, individual components of the composition of the invention e.g. parts of a kit or parts of a binary or ternary mixture may be mixed by the user himself in a spray tank and further auxiliaries may be added, if appropriate.

[0620] In a further embodiment, either individual components of the composition according to the invention or partially premixed components, e.g. components comprising compounds of the invention and / or mixing partners as defined above, may be mixed by the user in a spray tank and further auxiliaries and additives may be added.

[0621] In a further embodiment, either individual components of the composition according to the invention or partially premixed components, e.g. components comprising compounds of the invention and / or mixing partners as defined above, can be applied jointly (e.g. after tank mix) or consecutively.

[0622] Application methods

[0623] The compounds of the invention are suitable for use in protecting crops, plants, plant propagation materials, e.g. seeds, or soil or water, in which the plants are growing, from attack or infestation by animal pests. Therefore, the invention also relates to a plant protection method, which comprises contacting crops, plants, plant propagation materials, e.g. seeds, or soil or water, in which the plants are growing, to be protected from attack or infestation by animal pests, with a pesticidally effective amount of a compound of the invention.

[0624] The compounds of the invention are also suitable for use in combating or controlling animal pests. Therefore, the invention also relates to a method of combating or controlling animal pests, which comprises contacting the animal pests, their habitat, breeding ground, or food supply, or the crops, plants, plant propagation materials, e.g. seeds, or soil, or the area, material or environment in which the animal pests are growing or may grow, with a pesticidally effective amount of a compound of the invention.

[0625] The compounds of the invention are effective through both contact and ingestion. Further-more, the compounds of the invention can be applied to any and all developmental stages, e.g. egg, larva, pupa, and adult.

[0626] The compounds of the invention can be applied as such or in form of compositions comprising them as defined above. Furthermore, the compounds of the invention can be applied together with a mixing partner or in form of compositions comprising said mixtures. The components of said mixture can be applied simultaneously, jointly or separately, or in succession, that is immediately one after another and thereby creating the mixture “in situ” on the desired location, e.g. the plant, the sequence, in the case of separate application, generally not having any effect on the result of the control measures.

[0627] The application can be carried out both before and after the infestation of the crops, plants, plant propagation materials, e.g. seeds, soil, or the area, material or environment by the pests.

[0628] Suitable application methods include i.a. soil treatment, seed treatment, in furrow application, and foliar application. Soil treatment methods include drenching the soil, drip irrigation (drip application onto the soil), dipping roots, tubers or bulbs, or soil injection. Seed treatment techniques include seed dressing, seed coating, seed dusting, seed soaking, and seed pelleting. In furrow applications typically include the steps of making a furrow in cultivated land, seeding the furrow with seeds, applying the pesticidally active compound to the furrow, and closing the furrow. Foliar application refers to the application of the pesticidally active compound to plant foliage, e.g. through spray equipment. For foliar applications, it can be advantageous to modify the behavior of the pests by use of pheromones in combination with the compounds of the invention. Suitable pheromones for specific crops and pests are known and publicly available from databases of pheromones and semiochemicals, e.g. http: / / www.pherobase.com.

[0629] As used herein, the term "contacting" includes both direct contact (applying the com-pounds / compositions directly on the animal pest or plant - typically to the foliage, stem or roots of the plant) and indirect contact (applying the compounds / compositions to the locus, i.e. habitat, breeding ground, plant, seed, soil, area, material, or environment in which a pest is growing or may grow, of the animal pest or plant).

[0630] The term “animal pest” includes arthropods, gastropods, and nematodes. Preferred animal pests according to the invention are arthropods, preferably insects and arachnids, in particular insects. Insects, which are of particular relevance for crops, are typically referred to as crop insect pests. The term "crop" refers to both, growing and harvested crops.

[0631] The term “plant” includes cereals, e.g. durum and other wheat, rye, barley, triticale, oats, rice, or maize (fodder maize and sugar maize I sweet and field corn); beet, e.g. sugar beet, or fodder beet; fruits, e.g. pomes, stone fruits, or soft fruits, e.g. apples, pears, plums, peaches, nectarines, almonds, cherries, papayas, strawberries, raspberries, blackberries or gooseberries; leguminous plants, e.g. beans, lentils, peas, alfalfa, or soybeans; oil plants, e.g. rapeseed (oilseed rape), turnip rape, mustard, olives, sunflowers, coconut, cocoa beans, castor oil plants, oil palms, ground nuts, or soybeans; cucurbits, e.g. squashes, pumpkins, cucumber or melons; fiber plants, e.g. cotton, flax, hemp, or jute; citrus fruit, e.g. oranges, lemons, grapefruits or mandarins; vegetables, e.g. eggplant, spinach, lettuce (e.g. iceberg lettuce), chicory, cabbage, asparagus, cabbages, carrots, onions, garlic, leeks, tomatoes, potatoes, cucurbits or sweet peppers; lauraceous plants, e.g. avocados, cinnamon, or camphor; energy and raw material plants, e.g. corn, soybean, rapeseed, sugar cane or oil palm; tobacco; nuts, e.g. walnuts; pistachios; coffee; tea; bananas; vines; hop; sweet leaf (Stevia); natural rubber plants or ornamental and forestry plants, shrubs, broad-leaved trees or evergreens, eucalyptus; turf; lawn; grass. Preferred plants include potatoes sugar beets, tobacco, wheat, rye, barley, oats, rice, corn, cotton, soybeans, rapeseed, legumes, sunflowers, coffee, or sugar cane; fruits; vines; ornamentals; or vegetables, e.g. cucumbers, tomatoes, beans or squashes.

[0632] The term "cultivated plants" is to be understood as including plants which have been modified by mutagenesis or genetic engineering in order to provide a new trait to a plant or to modify an already present trait.

[0633] Mutagenesis includes techniques of random mutagenesis using X-rays or mutagenic chemicals, but also techniques of targeted mutagenesis, in order to create mutations at a specific locus of a plant genome. Targeted mutagenesis techniques frequently use oligonucleotides or proteins like CRISPR / Cas, zinc-finger nucleases, TALENs or meganucleases to achieve the targeting effect. Genetic engineering usually uses recombinant DNA techniques to create modifications in a plant genome which under natural circumstances cannot readily be obtained by cross breeding, mutagenesis or natural recombination. Typically, one or more genes are integrated into the genome of a plant in order to add a trait or improve a trait. These integrated genes are also referred to as transgenes in the art, while plant comprising such transgenes are referred to as transgenic plants. The process of plant transformation usually produces several transformation events, which differ in the genomic locus in which a transgene has been integrated. Plants comprising a specific transgene on a specific genomic locus are usually described as comprising a specific “event”, which is referred to by a specific event name. Traits which have been introduced in plants or have been modified include in particular herbicide tolerance, insect resistance, increased yield and tolerance to abiotic conditions, like drought.

[0634] Herbicide tolerance has been created by using mutagenesis as well as using genetic engineering. Plants which have been rendered tolerant to ALS inhibitor herbicides by conventional methods of mutagenesis and breeding comprise plant varieties commercially available under the name Clearfield®.

[0635] Herbicide tolerance has been created to glyphosate, glufosinate, 2,4-D, dicamba, oxynil herbicides, like bromoxynil and ioxynil, sulfonylurea herbicides, ALS inhibitor herbicides and HPPD inhibitors, like isoxaflutole and mesotrione.

[0636] Transgenes which have been used to provide herbicide tolerance traits comprise: for tolerance to glyphosate: cp4 epsps, epsps grg23ace5, mepsps, 2mepsps, gat4601, gat4621 and goxv247, for tolerance to glufosinate: pat and bar, for tolerance to 2,4-D: aad-1 and aad-12, for tolerance to dicamba: dmo, for tolerance to oxynil herbicies: bxn, for tolerance to sulfonylurea herbicides: zm-hra, csr1-2, gm-hra, S4-HrA, for tolerance to ALS inhibitor herbicides: csr1-2, for tolerance to HPPD inhibitor herbicides: hppdPF, W336 and avhppd-03.

[0637] Transgenic corn events comprising herbicide tolerance genes are e.g., but not excluding others, DAS40278, MON801, MON802, MON809, MON810, MON832, MON87411, MON87419, MON87427, MON88017, MON89034, NK603, GA21, MZHGOJG, HCEM485, VCO-Ø1981-5, 676, 678, 680, 33121, 4114, 59122, 98140, Bt10, Bt176, CBH-351, DBT418, DLL25, MS3, MS6, MZIR098, T25, TC1507 and TC6275. Transgenic soybean events comprising herbicide tolerance genes are e.g., but not excluding others, GTS 40-3-2, MON87705, MON87708, MON87712, MON87769, MON89788, A2704-12, A2704-21, A5547-127, A5547-35, DP356043, DAS44406-6, DAS68416-4, DAS-81419-2, GU262, SYHTØH2, W62, W98, FG72 and CV127.

[0638] Transgenic cotton events comprising herbicide tolerance genes are e.g., but not excluding others, 19-51a, 31707, 42317, 81910, 281-24-236, 3006-210-23, BXN10211, BXN10215, BXN10222, BXN10224, MON1445, MON1698, MON88701, MON88913, GHB119, GHB614, LLCotton25, T303-3 and T304-40.

[0639] Transgenic canola events comprising herbicide tolerance genes are e.g., but not excluding others, MON88302, HCR-1, HCN10, HCN28, HCN92, MS1, MS8, PHY14, PHY23, PHY35, PHY36, RF1, RF2 and RF3.

[0640] Insect resistance has mainly been created by transferring bacterial genes for insecticidal proteins to plants. Transgenes which have most frequently been used are toxin genes of Bacillus spec, and synthetic variants thereof, like cry1A, crylAb, cry1 Ab-Ac, crylAc, cry1A.1O5, cry1F, cry1Fa2, cry2Ab2, cry2Ae, mcry3A, ecry3.1Ab, cry3Bb1, cry34Ab1, cry35Ab1, cry9C, vip3A(a), vip3Aa20. However, also genes of plant origin have been transferred to other plants. In particular genes coding for protease inhibitors, like CpTI and pinll. A further approach uses transgenes in order to produce double stranded RNA in plants to target and downregulate in-sect genes. An example for such a transgene is dvsnf7.

[0641] Transgenic corn events comprising genes for insecticidal proteins or double stranded RNA are e.g., but not excluding others, Bt10, Bt11, Bt176, MON801, MON802, MON809, MON810, MON863, MON87411, MON88017, MON89034, 33121, 4114, 5307, 59122, TC1507, TC6275, CBH-351, MIR162, DBT418 and MZIR098.

[0642] Transgenic soybean events comprising genes for insecticidal proteins are e.g., but not excluding others, MON87701, MON87751 and DAS-81419.

[0643] Transgenic cotton events comprising genes for insecticidal proteins are e.g., but not excluding others, SGK321, MON531, MON757, MON1076, MON15985, 31707, 31803, 31807, 31808, 42317, BNLA-601, Eventl, COT67B, COT102, T303-3, T304-40, GFM Cry1A, GK12, MLS 9124, 281-24-236, 3006-210-23, GHB119 and SGK321.

[0644] Increased yield has been created by increasing ear biomass using the transgene athb17, being present in corn event MON87403, or by enhancing photosynthesis using the transgene bbx32, being present in the soybean event MON87712.

[0645] Cultivated plants comprising a modified oil content have been created by using the transgenes: gm-fad2-1, Pj. D6D, Nc. Fad3, fad2-1A and fatb1-A. Soybean events comprising at least one of these genes are: 260-05, MON87705 and MON87769.

[0646] Tolerance to abiotic conditions, in particular to tolerance to drought, has been created by using the transgene cspB, comprised by the corn event MON87460 and by using the transgene Hahb-4, comprised by soybean event IND-ØØ41Ø-5.

[0647] Traits are frequently combined by combining genes in a transformation event or by combining different events during the breeding process. Preferred combination of traits are herbicide tolerance to different groups of herbicides, insect tolerance to different kind of insects, in particular tolerance to lepidopteran and coleopteran insects, herbicide tolerance with one or several types of insect resistance, herbicide tolerance with increased yield as well as a combination of herbicide tolerance and tolerance to abiotic conditions. Plants comprising singular or stacked traits as well as the genes and events providing these traits are known (http: / / www.isaaa.org / gmapprovaldatabase) and (http: / / cera-gmc.org / GMCropDatabase).

[0648] Further information on specific events and methods to detect them can be found for canola events MS1, MS8, RF3, GT73, MON88302, KK179 in W001 / 031042, W001 / 041558, W001 / 041558, W002 / 036831, W011 / 153186, W013 / 003558, for cotton events MON1445, MON15985, MON531(MON15985), LLCotton25, MON88913, COT102, 281-24-236, 3006-210-23, COT67B, GHB614, T304-40, GHB119, MON88701, 81910 in WO02 / 034946, W002 / 100163, W002 / 100163, W003 / 013224, WO04 / 072235, WO04 / 039986, WO05 / 103266, WO05 / 103266, WO06 / 128573, W007 / 017186, W008 / 122406, W008 / 151780, WO12 / 134808, WO13 / 112527, for corn events GA21, MON810, DLL25, TC1507, MON863, MIR604, LY038, MON88017, 3272, 59122, NK603, MIR162, MON89034, 98140, 32138, MON87460, 5307, 4114, MON87427, DAS40278, MON87411, 33121, MON87403, MON87419 in W098 / 044140, US02 / 102582, US03 / 126634, WO04 / 099447, W004 / 011601, WO05 / 103301, W005 / 061720, W005 / 059103, WO06 / 098952, WO06 / 039376, US2007 / 292854, W007 / 142840, W007 / 140256, WO08 / 112019, W009 / 103049, WO09 / 111263, W010 / 077816, WO11 / 084621, WO11 / 062904, WO11 / 022469, WO13 / 169923, WO14 / 116854, WO15 / 053998, WO15 / 142571, for potato events E12, F10, J3, J55, V11, X17, Y9 in WO14 / 178910, WO14 / 178913, WO14 / 178941, WO14 / 179276, WO16 / 183445, WO17 / 062831, WO17 / 062825, for rice events LLRICE06, LLRICE601, LLRICE62 in WO00 / 026345, WO00 / 026356, WO00 / 026345 for soybean events H7-1, MON89788, A2704-12, A5547-127, DP305423, DP356043, MON87701, MON87769, CV127, MON87705, DAS68416-4, MON87708, MON87712, SYHTØH2, DAS81419, DAS81419 x DAS44406-6, MON87751 in WO04 / 074492, WO06 / 130436, WO06 / 108674, WO06 / 108675, WO08 / 054747, W008 / 002872, WO09 / 064652, W009 / 102873, W010 / 080829, W010 / 037016, W011 / 066384, W011 / 034704, W012 / 051199, W012 / 082548, W013 / 016527, WO13 / 016516, WO14 / 201235.

[0649] The use of compositions according to the invention on cultivated plants may result in effects which are specific to a cultivated plant comprising a certain gene or event. These effects may comprise enhanced yield, enhanced resistance or tolerance to insects, nematodes, fungal, bacterial, mycoplasma, viral or viroid pathogens as well as early vigor, early or delayed ripening, cold or heat tolerance as well as changed amino acid or fatty acid spectrum or content.

[0650] It has been found that the pesticidal activity of the compounds of the invention may be enhanced by the insecticidal trait of a modified plant. Furthermore, it has been found that the compounds of the invention are suitable for preventing insects to become resistant to the insecticidal trait or for combating pests, which already have become resistant to the insecticidal trait of a modified plant. Moreover, the compounds of the invention are suitable for combating pests, against which the insecticidal trait is not effective, so that a complementary insecticidal activity can advantageously be used.

[0651] The term "plant propagation material" refers to all the generative parts of the plant e.g. seeds and vegetative plant material e.g. cuttings and tubers (e.g. potatoes), which can be used for the multiplication of the plant. This includes seeds, roots, fruits, tubers, bulbs, rhizomes, shoots, sprouts and other parts of plants. Seedlings and young plants, which are to be trans-planted after germination or after emergence from soil, may also be included. These plant propagation materials may be treated prophylactically with a plant protection compound either at or before planting or transplanting. The term “seed” embraces seeds and plant propagules of all kinds including but not limited to true seeds, seed pieces, suckers, corms, bulbs, fruit, tubers, grains, cuttings, cut shoots and the like, and means in a preferred embodiment true seeds.

[0652] In general, "pesticidally effective amount" means the amount of active ingredient needed to achieve an observable effect on growth, including the effects of necrosis, death, retardation, prevention, and removal, destruction, or otherwise diminishing the occurrence and activity of the target organism. The pesticidally effective amount can vary for the various compounds / compositions used in the invention. A pesticidally effective amount of the compositions will also vary according to the prevailing conditions e.g. desired pesticidal effect and duration, weather, target species, locus, mode of application.

[0653] In the case of soil treatment, in furrow application or of application to the pests dwelling place or nest, the quantity of active ingredient ranges from 0.0001 to 500 g per 100 m2, preferably from 0.001 to 20 g per 100 m2.

[0654] For use in treating crop plants, e.g. by foliar application, the rate of application of the active ingredients of this invention may be in the range of 0.0001 g to 4000 g per hectare, e.g. from 1 g to 2 kg per hectare or from 1 g to 750 g per hectare, desirably from 1 g to 100 g per hectare, more desirably from 10 g to 50 g per hectare, e.g., 10 to 20 g per hectare, 20 to 30 g per hec-tare, 30 to 40 g per hectare, or 40 to 50 g per hectare.

[0655] The compounds of the invention are particularly suitable for use in the treatment of seeds in order to protect the seeds from insect pests, in particular from soil-living insect pests, and the resulting seedling’s roots and shoots against soil pests and foliar insects. The invention therefore also relates to a method for the protection of seeds from insects, in particular from soil insects, and of the seedling's roots and shoots from insects, in particular from soil and foliar insects, said method comprising treating the seeds before sowing and / or after pregermination with a compound of the invention. The protection of the seedling's roots and shoots is preferred. More preferred is the protection of seedling’s shoots from piercing and sucking insects, chewing insects and nematodes.

[0656] The term “seed treatment” comprises e.g. seed dressing, seed coating, seed dusting, seed soaking, seed pelleting, and in-furrow application methods. Preferably, the seed treatment application of the active compound is carried out by spraying or by dusting the seeds before sowing of the plants and before emergence of the plants.

[0657] The invention also comprises seeds coated with or containing the active compound. The term "coated with and / or containing" generally signifies that the active ingredient is for the most part on the surface of the propagation product at the time of application, although a greater or lesser part of the ingredient may penetrate into the propagation product, depending on the method of application. When the said propagation product is (re)planted, it may absorb the active ingredient. Suitable seed is e.g. seed of cereals, root crops, oil crops, vegetables, spices, ornamentals, e.g. seed of durum and other wheat, barley, oats, rye, maize (fodder maize and sugar maize I sweet and field corn), soybeans, oil crops, crucifers, cotton, sunflowers, bananas, rice, oilseed rape, turnip rape, sugarbeet, fodder beet, eggplants, potatoes, grass, lawn, turf, fodder grass, tomatoes, leeks, pumpkin / squash, cabbage, iceberg lettuce, pepper, cucumbers, melons, Brassica species, melons, beans, peas, garlic, onions, carrots, tuberous plants e.g. potatoes, sugarcane, tobacco, grapes, petunias, geranium / pelargoniums, pansies and impatiens. In addition, the active compound may also be used for the treatment of seeds from plants, which have been modified by mutagenisis or genetic engineering, and which e.g. tolerate the action of herbicides or fungicides or insecticides.

[0658] Conventional seed treatment formulations include e.g. flowable concentrates FS, solutions LS, suspoemulsions (SE), powders for dry treatment DS, water dispersible powders for slurry treatment WS, water-soluble powders SS and emulsion ES and EC and gel formulation GF. These formulations can be applied to the seed diluted or undiluted. Application to the seeds is carried out before sowing, either directly on the seeds or after having pregerminated the latter. Preferably, the formulations are applied such that germination is not included.

[0659] The active substance concentrations in ready-to-use formulations, which may be obtained after two-to-tenfold dilution, are preferably from 0.01 to 60% by weight, more preferably from 0.1 to 40% by weight.

[0660] In a preferred embodiment a FS formulation is used for seed treatment. Typically, a FS formulation may comprise 1-800 g / l of active ingredient, 1-200 g / l Surfactant, 0 to 200 g / l antifreezing agent, 0 to 400 g / l of binder, 0 to 200 g / l of a pigment and up to 1 liter of a solvent, preferably water.

[0661] Especially preferred FS formulations of the compounds of the invention for seed treatment usually comprise from 0.1 to 80% by weight (1 to 800 g / l) of the active ingredient, from 0.1 to 20% by weight (1 to 200 g / l) of at least one surfactant, e.g. 0.05 to 5% by weight of a wetter and from 0.5 to 15% by weight of a dispersing agent, up to 20% by weight, e.g. from 5 to 20% of an antifreeze agent, from 0 to 15% by weight, e.g. 1 to 15% by weight of a pigment and / or a dye, from 0 to 40% by weight, e.g. 1 to 40% by weight of a binder (sticker / adhesion agent), optionally up to 5% by weight, e.g. from 0.1 to 5% by weight of a thickener, optionally from 0.1 to 2% of an antifoam agent, and optionally a preservative e.g. a biocide, antioxidant or the like, e.g. in an amount from 0.01 to 1% by weight and a filler / vehicle upto 100% by weight.

[0662] In the treatment of seed, the application rates of the compounds of the invention are generally from 0.1 g to 10 kg per 100 kg of seed, preferably from 1 g to 5 kg per 100 kg of seed, more preferably from 1 g to 1000 g per 100 kg of seed and in particular from 1 g to 200 g per 100 kg of seed, e.g. from 1 g to 100 g or from 5 g to 100 g per 100 kg of seed.

[0663] The invention therefore also relates to seed comprising a compound of the invention, or an agriculturally useful salt thereof, as defined herein. The amount of the compound of the invention or the agriculturally useful salt thereof will in general vary from 0.1 g to 10 kg per 100 kg of seed, preferably from 1 g to 5 kg per 100 kg of seed, in particular from 1 g to 1000 g per 100 kg of seed. For specific crops e.g. lettuce the rate can be higher.

[0664] The compounds of the invention may also be used for improving the health of a plant. Therefore, the invention also relates to a method for improving plant health by treating a plant, plant propagation material and / or the locus where the plant is growing or is to grow with an effective and non-phytotoxic amount of a compound of the invention.

[0665] As used herein “an effective and non-phytotoxic amount” means that the compound is used in a quantity which allows to obtain the desired effect but which does not give rise to any phytotoxic symptom on the treated plant or on the plant grown from the treated propagule or treated soil. " Plant health" is defined as a condition of the plant and / or its products which is determined by several aspects alone or in combination with each other e.g. yield (e.g. increased biomass and / or increased content of valuable ingredients), quality (e.g. improved content or composition of certain ingredients or shelf life), plant vigour (e.g. improved plant growth and / or greener leaves (“greening effect”), tolerance to abiotic (e.g. drought) and / or biotic stress (e.g. disease) and production efficiency (e.g., harvesting efficiency, processability).

[0666] The above identified indicators for the health condition of a plant may be interdependent and may result from each other. Each indicator is defined in the art and can be determined by methods known to a skilled person.

[0667] The compounds of the invention are also suitable for use against non-crop insect pests. For use against said non-crop pests, compounds of the invention can be used as bait composition, gel, general insect spray, aerosol, as ultra-low volume application and bed net (impregnated or surface applied). Furthermore, drenching and rodding methods can be used.

[0668] As used herein, the term “non-crop insect pest” refers to pests, which are particularly relevant for non-crop targets, e.g. ants, termites, wasps, flies, ticks, mosquitoes, bed bugs, crickets, or cockroaches.

[0669] The bait can be a liquid, a solid or a semisolid preparation (e.g. a gel). The bait employed in the composition is a product, which is sufficiently attractive to incite insects e.g. ants, termites, wasps, flies, mosquitoes, crickets etc. or cockroaches to eat it. The attractiveness can be manipulated by using feeding stimulants or sex pheromones. Food stimulants are preferably chosen from animal and / or plant proteins (meat-, fish- or blood meal, insect parts, egg yolk), from fats and oils of animal and / or plant origin, or mono-, oligo- or polyorganosaccharides, especially from sucrose, lactose, fructose, dextrose, glucose, starch, pectin or even molasses or honey. Fresh or decaying parts of fruits, crops, plants, animals, insects or specific parts thereof can also serve as a feeding stimulant. Sex pheromones are known to be more insect specific. Specific pheromones are known (http: / / www.pherobase.com).

[0670] For use in bait compositions, the typical content of active ingredient is from 0.001 wt% to 15 wt%, desirably from 0.001 wt% to 5 wt% of active compound.

[0671] Formulations of the compounds of the invention as aerosols (e.g in spray cans), oil sprays or pump sprays are highly suitable for professional or non-professional users for controlling pests e.g. flies, fleas, ticks, bed bugs, mosquitoes or cockroaches. Aerosol recipes are preferably composed of the active compound, solvents, furthermore auxiliaries e.g. emulsifiers, perfume oils, if appropriate stabilizers, and, if required, propellants.

[0672] The oil spray formulations differ from the aerosol recipes in that no propellants are used.

[0673] For use in spray compositions, the content of active ingredient is from 0.001 to 80 wt%, preferably from 0.01 to 50 wt% and most preferably from 0.01 to 15 wt%.

[0674] The compounds of the invention and its respective compositions can also be used in mosquito and fumigating coils, smoke cartridges, vaporizer plates or long-term vaporizers and also in moth papers, moth pads or other heat-independent vaporizer systems.

[0675] Methods to control infectious diseases transmitted by insects (e.g. malaria, dengue and yellow fever, lymphatic filariasis, and leishmaniasis) with compounds of the invention and its re-spective compositions also comprise treating surfaces of huts and houses, air spraying and impregnation of curtains, tents, clothing items, bed nets, tsetse-flytrap. Insecticidal compositions for application to fibers, fabric, knitgoods, nonwovens, netting material or foils and tarpaulins preferably comprise a mixture including the insecticide, optionally a repellent and at least one binder.

[0676] The compounds of the invention and its compositions can be used for protecting wooden materials e.g. trees, board fences, sleepers, frames, artistic artifacts, etc. and buildings, but also construction materials, furniture, leathers, fibers, vinyl articles, electric wires and cables etc. from ants, termites and / or wood or textile destroying beetles, and for controlling ants and termites from doing harm to crops or human beings (e.g. when the pests invade into houses and public facilities or nest in yards, orchards or parks).

[0677] Customary application rates in the protection of materials are, e.g., from 0.001 g to 2000 g or from 0.01 g to 1000 g of active compound per m2treated material, desirably from 0.1 g to 50 g per m2.

[0678] Insecticidal compositions for use in the impregnation of materials typically contain from 0.001 to 95 wt%, preferably from 0.1 to 45 wt%, and more preferably from 1 to 25 wt% of at least one repellent and / or insecticide.

[0679] Digital application

[0680] The compounds of the invention and the compositions containing them may be applied in combination with, or by utilizing smart agricultural technologies, such as precision agriculture, remote and proximate imaging and image recognition, or smart agricultural site management programs. These smart agricultural technologies typically include models, e.g. computer programs, that support the user by considering information from a wide variety of sources to increase the quality and yield of harvested material, reduce damage by pests including the prediction of pest pressure and smart application of crop protection products, secure environ-mental protection, support quick and reliable agronomic decision making, reduce usage of fertilizers and crop protection products, reduce product residues in consumables increase spatial and temporal precision of agronomical measures, automate processes, and enable traceability of measures. Commercially available systems which include agronomic models are e.g. FieldScripts™ from The Climate Corporation, Xarvio™ from BASF, AGLogic™ from John Deere, etc.

[0681] Information input for these models include but is not limited to soil data, information on the plants that are currently growing or that may grow at the area of interest including crop plants and / or unwanted vegetation, weather information, information on the location of the area and directly derivable information thereof, information on pest pressure, information on beneficial organisms, and I or historic information of any of the aforementioned.

[0682] The information usable for precision agriculture may be based on input by at least one user, be accessible from external data sources and databases, or be based on sensor data. Data sources typically includes proximate-detection systems like soil-borne sensors and remote sensing as may be achieved by imaging with unmanned airborne vehicles like drones, or satellites. Sensors may be included in an Internet-of-Things system and may be directly or indirectly connected to the processing unit, e.g. via a wireless network and / or cloud applications. The information is typically taken into account by at least one processing unit and used to provide recommendations and generate control signals.

[0683] Typical technologies that are used in smart agricultural technologies include self-steering robots (such as tractors, harvesters, drones), artificial intelligence (e.g. machine learning), imaging technologies (e.g. image segmentation technologies), big data analysis, and model generation, cloud computing, and machine-to-machine communication.

[0684] Precision agriculture such as precision farming is characterized by spatially and / or temporally resolved, targeted application of active ingredients like pesticides, plant-growth-regulators, fertilizers, and / or water including the variation of application rates over the agronomic site, zone or spot application, and of the spatially and / or temporally resolved, targeted planting or seeding of desired plant propagation material to a agronomic site. Precision farming typically includes the use of geo-positioning technologies like GPS for gaining information on the location and boundaries of the area of interest, the utilized application equipment, sensing equipment and recorded data, and to control the actions of farm vehicles such as spraying. By combining geopositioning data with (digital) maps, it is possible to (semi)-automate agricultural measures at the site of interest, e.g. by using (semi)-autonomous spraying or seeding equipment.

[0685] Precision farming may typically include the application of smart spraying equipment, e.g. spot spraying, and precision spraying at a farm, e.g. by irrigation systems, tractors, robots, helicopters, airplanes, unmanned aerial vehicles, such as drones. Such equipment usually includes input sensors (such as e.g. a camera) and a processing unit configured to analyze the input data and configured to provide a recommendation or decision based on the analysis of the input data to apply the compounds of the invention or compositions comprising them to the agronomic site, e.g. the soil, the crop plants, or to control pests in a specific and precise manner. For example, pests may be detected, identified, and / or classified from imagery acquired by a camera. Such identification and / classification can make use of image processing algorithms, which may utilize artificial intelligence (e.g. machine learning algorithms), or decision trees. In this manner, the compounds or compositions described herein can be applied only at the required location, point in time and dose rate.

[0686] Pests

[0687] The compounds of the invention are especially suitable for efficiently combating animal pests e.g. arthropods, gastropods and nematodes including:

[0688] insects from the order of Lepidoptera, e.g. Achroia grisella, Acleris spp. e.g. A. fimbriana, A. gloverana, A. variana; Acrolepiopsis assectella, Acronicta major, Adoxophyes spp. e.g. A. cyrtosema, A. orana; Aedia leucomelas, Agrotis spp. e.g. A. exclamationis, A. fucosa, A. ipsilon, A. orthogoma, A. segetum, A. subterranea; Alabama argillacea, Aleurodicus dispersus, Alsophila pometaria, Ampelophaga rubiginosa, Amyelois transitella, Anacampsis sarcitella, Anagasta kuehniella, Anarsia lineatella, Anisota senatoria, Antheraea pernyi, Anticarsia (=Thermesia) spp. e.g. A. gemmatalis; Apamea spp., Aproaerema modicella, Archips spp. e.g. A. argyrospila, A. fuscocupreanus, A. rosana, A. xyloseanus; Argyresthia conjugella, Argyroploce spp., Argyrotaenia spp. e.g. A. velutinana; Athetis mindara, Austroasca viridigrisea, Autographa gamma, Autographa nigrisigna, Barathra brassicae, Bedellia spp., Bonagota salubricola, Borbo cinnara, Bucculatrix thurberiella, Bupalus piniarius, Busseola spp., Cacoecia spp. e.g. C. murinana, C. podana; Cactoblastis cactorum, Cadra cautella, Calingo braziliensis, Caloptilis theivora, Capua reticulana, Carposina spp. e.g. C. niponensis, C. sasakii; Cephus spp., Chaetocnema aridula, Cheimatobia brumata, Chilo spp. e.g. C. Indicus, C. suppressalis, C. partellus; Choreutis pariana, Choristoneura spp. e.g. C. conflictana, C. fumiferana, C. longicellana, C. murinana, C. occidentalis, C. rosaceana; Chrysodeixis (=Pseudoplusia) spp., e.g. C. eriosoma, C. includens; Cirphis unipuncta, Clysia ambiguella, Cnaphalocerus spp., Cnaphalocrocis medinalis, Cnephasia spp., Cochylis hospes, Coleophora spp., Colias eurytheme, Conopomorpha spp., Conotrachelus spp., Copitarsia spp., Corcyra cephalonica, Crambus caliginosellus, Crambus teterrellus, Crocidosema (=Epinotia) aporema, Cydalima (=Diaphania) perspectalis, Cydia (=Carpocapsa) spp., e.g. C. pomonella, C. latiferreana; Dalaca noctuides, Datana integerrima, Dasychira pinicola, Dendrolimus spp., e.g. D. pini, D. spectabilis, D. sibiricus; Desmia funeralis, Diaphania spp., e.g. D. nitidalis, D. hyalinata; Diatraea grandiosella, Diatraea saccharalis, Diphthera festiva, Earias spp. e.g. E. insulana, E. vittella; Ecdytolopha aurantianu, Egira (=Xylomyges) curialis, Elasmopalpus lignosellus, Eldana saccharina, Endopiza viteana, Ennomos subsignaria, Eoreuma loftini, Ephestia spp., e.g. E. cautella, E. elutella, E. kuehniella; Epinotia aporema, Epiphyas postvittana, Erannis tiliaria, Erionota thrax, Etiella spp., Eulia spp., Eupoecilia ambiguella, Euproctis chrysorrhoea, Euxoa spp., Evetria bouliana, Faronta albilinea, Feltia spp. e.g. F. subterranean; Galleria mellonella, Gracillaria spp., Grapholita spp. e.g. G. funebrana, G. molesta, G. inopinata; Halysidota spp., Harrisina americana, Hedylepta spp., Helicoverpa spp. e.g. H. armigera (=Heliothis armigera), H. zea (=Heliothis zea); Heliothis spp. e.g. H. assulta, H. subflexa, H. virescens; Hellula spp. e.g. H. undalis, H. rogatalis; Helocoverpa gelotopoeon, Hemileuca oliviae, Herpetogramma licarsisalis, Hibernia defoliaria, Hofmannophila pseudospretella, Homoeosoma electellum, Homona magnanima, Hypena scabra, Hyphantria cunea, Hyponomeuta padella, Hyponomeuta malinellus, Kakivoria flavofasciata, Keiferia lycopersicella, Lambdina fiscellaria fiscellaria, Lambdina fiscellaria lugubrosa, Lamprosema indicata, Laspeyresia molesta, Leguminivora glycinivorella, Lerodea eufala, Leucinodes orbonalis, Leucoma salicis, Leucoptera spp. e.g. L. coffeella, L. scitella; Leuminivora lycinivorella, Lithocolletis blancardella, Lithophane antennata, Llattia octo (=Amyna axis), Lobesia botrana, Lophocampa spp., Loxagrotis albicosta, Loxostege spp. e.g. L. sticticalis, L. cereralis; Lymantria spp., e.g. L. dispar, L. monacha; Lyonetia clerkella, Lyonetia prunifoliella, Malacosoma spp., e.g. M. americanum, M. californicum, M. constrictum, M. neu-stria; Mamestra spp., e.g. M. brassicae, M. configurata; Mamstra brassicae, Manduca spp. e.g. M. quinquemaculata, M. sexta; Marasmia spp, Marmara spp., Maruca testulalis, Megalopyge lanata, Melanchra picta, Melanitis leda, Mocis spp., e.g. M. lapites, M. repanda; Mocis latipes, Monochroa fragariae, Mythimna separata, Nemapogon cloacella, Neoleucinodes elegantalis, Nepytia spp., Nymphula spp., Oiketicus spp., Omiodes indicata, Omphisa anastomosalis, Operophtera brumata, Orgyia pseudotsugata, Oria spp., Orthaga thyrisalis, Ostrinia spp. e.g. O. nubilalis; Oulema oryzae, Paleacrita vernata, Panolis flammea, Parnara spp., Papaipema nebris, Papilio cresphontes, Paramyelois transitella, Paranthrene regalis, Paysandisia archon, Pectinophora spp. e.g. P. gossypiella; Peridroma saucia, Perileucoptera spp., e.g. P. coffeella; Phalera bucephala, Phryganidia californica, Phthorimaea spp. e.g. P. operculella; Phyllocnistis citrella, Phyllonorycterspp. e.g. P. blancardella, P. crataegella, P. issikii, P. ringoniella; Pieris spp. e.g. P. brassicae, P. rapae, P. napi; Pilocrocis tripunctata, Plathypena scabra, Platynota spp. e.g. P. flavedana, P. idaeusalis, P. stultana; Platyptilia carduidactyla, Plebejus argus, Plo-dia interpunctella, Plusia spp, Plutella maculipennis, Plutella xylostella, Pontia protodica, Prays spp., Prodenia spp., Proxenus lepigone, Pseudaletia spp. e.g. P. sequax, P. unipuncta; Pyrausta nubilalis, Rachiplusia nu, Richia albicosta, Rhizobius ventralis, Rhyacionia frustrana, Sabulodes aegrotata, Schizura concinna, Schoenobius spp., Schreckensteinia festaliella, Scirpophaga spp. e.g. S. incertulas, S. innotata; Scotia segetum, Sesamia spp. e.g. S. inferens, Seudyra subflava, Sitotroga cerealella, Sparganothis pilleriana, Spilonota lechriaspis, S. ocelli-na, Spodoptera (=Lamphygma) spp. e.g. S. cosmoides, S. eridania, S. exigua, S. frugiperda, S. latisfascia, S. littoralis, S. litura, S. omithogalli; Stigmella spp., Stomopteryx subsecivella, Strymon bazochii, Sylepta derogata, Synanthedon spp. e.g. S. exitiosa, Tecia solanivora, Telehin licus, Thaumatopoea pityocampa, Thaumatotibia (=Cryptophlebia) leucotreta, Thaumetopoea pityocampa, Thecla spp., Theresimima ampelophaga, Thyrinteina spp, Tildenia inconspicuella, Tinea spp. e.g. T. cloacella, T. pellionella; Tineola bisselliella, Tortrix spp. e.g. T. viridana; Trichophaga tapetzella, Trichoplusia spp. e.g. T. ni; Tuta (=Scrobipalpula) absoluta, Udea spp. e.g. U. rubigalis, U. rubigalis; Virachola spp., Yponomeuta padella, and Zeiraphera canadensis; insects from the order of Coleoptera, e.g. Acalymma vittatum, Acanthoscehdes obtectus, Adoretus spp., Agelastica alni, Agrilus spp. e.g. A. anxius, A. planipennis, A. sinuatus; Agriotes spp. e.g. A. fuscicollis, A. lineatus, A. obscurus; Alphitobius diaperinus, Amphimallus solstitialis, Anisandrus dispar, Anisoplia austriaca, Anobium punctatum, Anomala corpulenta, Anomala rufocuprea, Anoplophora spp. e.g. A. glabripennis; Anthonomus spp. e.g. A. eugenii, A. grandis, A. pomorum; Anthrenus spp., Aphthona euphoridae, Apion spp., Apogonia spp., Athous haemorrhoidalis, Atomaria spp. e.g. A. linearis; Attagenus spp., Aulacophora femoralis, Blastophagus piniperda, Blitophaga undata, Bruchidius obtectus, Bruchus spp. e.g. B. lentis, B. pisorum, B. rufimanus; Byctiscus betulae, Callidiellum rufipenne, Callopistria floridensis, Callosobruchus chinensis, Cameraria ohridella, Cassida nebulosa, Cerotoma trifurcata, Cetonia aurata, Ceuthorhynchus spp. e.g. C. assimilis, C. napi; Chaetocnema tibialis, Cleonus mendicus, Conoderus spp. e.g. C. vespertinus; Conotrachelus nenuphar, Cosmopolites spp., Costelytra zealandica, Crioceris asparagi, Cryptolestes ferrugineus, Cryptorhynchus lapathi, Ctenicera spp. e.g. C. destructor; Curculio spp., Cylindrocopturus spp., Cyclocephala spp., Dac-tylispa balyi, Dectes texanus, Dermestes spp., Diabrotica spp. e.g. D. undecimpunctata, D. speciosa, D. longicornis, D. semipunctata, D. virgifera; Diaprepes abbreviates, Dichocrocis spp., Dicladispa armigera, Diloboderus abderus, Diocalandra frumenti (Diocalandra stigmaticollis), Enaphalodes rufulus, Epilachna spp. e.g. E. varivestis, E. vigintioctomaculata; Epitrix spp. e.g. E. hirtipennis, E. similaris; Eutheola humilis, Eutinobothrus brasiliensis, Faustinus cubae, Gibbium psylloides, Gnathocerus cornutus, Hellula undalis, Heteronychus arator, Hylamorpha elegans, Hylobius abietis, Hylotrupes bajulus, Hypera spp., e.g. H. brunneipennis, H. postica; Hypomeces squamosus, Hypothenemus spp., Ips typographus, Lachnosterna consanguinea, Lasioderma serricorne, Latheticus oryzae, Lathridius spp., Lerna spp. e.g. L. bilineata, L. melanopus; Leptinotarsa spp. e.g. L. decemlineata; Leptispa pygmaea, Limonius californi-cus, Lissorhoptrus oryzophilus, Lixus spp., Luperodes spp., Lyctus spp. e.g. L. bruneus; Liogenys fuscus, Macrodactylus spp. e.g. M. subspinosus; Maladera matrida, Megaplatypus mutates, Megascelis spp., Melanotus communis, Meligethes spp. e.g. M. aeneus; Melolontha spp. e.g. M. hippocastani, M. melolontha; Metamasius hemipterus, Microtheca spp., Migdolus spp. e.g. M. fryanus, Monochamus spp. e.g. M. alternatus; Naupactus xanthographus, Niptus hololeucus, Oberia brevis, Oemona hirta, Oryctes rhinoceros, Oryzaephilus surinamensis, Oryzaphagus oryzae, Otiorrhynchus sulcatus, Otiorrhynchus ovatus, Otiorrhynchus sulcatus, Oulema melanopus, Oulema oryzae, Oxycetonia jucunda, Phaedon spp. e.g. P. brassicae, P. cochleariae; Phoracantha recurva, Phyllobius pyri, Phyllopertha horticola, Phyllophaga spp. e.g. P. helleri; Phyllotreta spp. e.g. P. chrysocephala, P. nemorum, P. striolata, P. vittula; Phyllopertha horticola, Popillia japonica, Premnotrypes spp., Psacothea hilaris, Psylliodes chrysocephala, Prostephanus truncates, Psylliodes spp., Ptinus spp., Pulga saltona, Rhizopertha dominica, Rhynchophorus spp. e.g. R. billineatus, R. ferrugineus, R. palmarum, R. phoenicis, R. vulneratus; Saperda Candida, Scolytus schevyrewi, Scyphophorus acupunctatus, Sitona lineatus, Sitophilus spp. e.g. S. granaria, S. oryzae, S. zeamais; Sphenophorus spp. e.g. S. levis; Stegobium paniceum, Sternechus spp. e.g. S. subsignatus; Strophomorphus ctenotus, Symphyletes spp., Tanymecus spp., Tenebrio molitor, Tenebrioides mauretanicus, Tribolium spp. e.g. T. castaneum; Trogoderma spp., Tychius spp., Xylotrechus spp. e.g. X. pyrrhoderus; and, Zabrus spp. e.g. Z. tenebrioides; insects from the order of Diptera e.g. Aedes spp. e.g. A. aegypti, A. albopictus, A. vexans; Anastrepha ludens, Anopheles spp. e.g. A. albimanus, A. crucians, A. freeborni, A. gambiae, A. leucosphyrus, A. maculipennis, A. minimus, A. quadrimaculatus, A. sinensis; Bactrocera invadens, Bibio hortulanus, Calliphora erythrocephala, Calliphora vicina, Ceratitis capitata, Chrysomyia spp. e.g. C. bezziana, C. hominivorax, C. macellaria; Chrysops atlanticus, Chrysops discalis, Chrysops silacea, Cochliomyia spp. e.g. C. hominivorax; Contarinia spp. e.g. C. sorghicola; Cordylobia anthropophaga, Culex spp. e.g. C. nigripalpus, C. pipiens, C. quinquefasciatus, C. tarsalis, C. tritaeniorhynchus; Culicoides furens, Culiseta inornata, Culiseta melanura, Cuterebra spp., Dacus cucurbitae, Dacus oleae, Dasineura brassicae, Dasineura oxycoccana, Delia spp. e.g. D. antique, D. coarctata, D. platura, D. radicum; Dermatobia hominis, Drosophila spp. e.g. D. suzukii, Fannia spp. e.g. F. canicularis; Gastraphilus spp. e.g. G. intestinalis; Geomyza tipunctata, Glossina spp. e.g. G. fuscipes, G. morsitans, G. palpalis, G. tachinoides; Haematobia irritans, Haplodiplosis equestris, Hippelates spp., Hylemyia spp. e.g. H. platura; Hypoderma spp. e.g. H. lineata; Hyppobosca spp., Hydrellia philippina, Leptoconops torrens, Liriomyza spp. e.g. L. sativae, L. trifolii; Lucilia spp. e.g. L. caprina, L. cuprina, L. sericata; Lycoria pectoralis, Mansonia titillanus, Mayetiola spp. e.g. M. destructor; Musca spp. e.g. M. autumnalis, M. domestica; Muscina stabulans, Oestrus spp. e.g. O. ovis; Opomyza florum, Oscinella spp. e.g. O. frit; Orseolia oryzae, Pegomya hysocyami, Phlebotomus argentipes, Phorbia spp. e.g. P. antiqua, P. brassicae, P. coarctata; Phytomyza gymnostoma, Prosimulium mixtum, Psila rosae, Psorophora columbiae, Psorophora discolor, Rhagoletis spp. e.g. R. cerasi, R. cingulate, R. indifferens, R. mendax, R. pomonella; Rivellia quadrifasciata, Sarcophaga spp. e.g. S. haemorrhoidalis; Simulium vittatum, Sitodiplosis mosellana, Stomoxys spp. e.g. S. calcitrans; Tabanus spp. e.g. T. atratus, T. bovinus, T. lineola, T. similis; Tannia spp., Thecodiplo-sis japonensis, Tipula oleracea, Tipula paludosa, Wohlfahrtia spp, and Zaprionus indianus; insects from the order of Thysanoptera e.g., Baliothrips biformis, Dichromothrips corbetti, Dichromothrips ssp., Echinothrips americanus, Enneothrips flavens, Frankliniella spp. e.g. F. fusca, F. occidentalis, F. tritici; Heliothrips spp., Hercinothrips femoralis, Kakothrips spp., Microcephalothrips abdominalis, Neohydatothrips samayunkur, Pezothrips kellyanus, Rhipiphorothrips cruentatus, Scirtothrips spp. e.g. S. citri, S. dorsalis, S. perseae; Stenchaetothrips spp, Taeniothrips cardamoni, Taeniothrips inconsequens, Thrips spp. e.g. T. imagines, T. hawaiiensis, T. oryzae, T. palmi, T. parvispinus, T. tabaci;

[0689] insects from the order of Hemiptera e.g., Acizzia jamatonica, Acrosternum spp., e.g. A. hilare; Acyrthosipon spp., e.g. A. onobrychis, A. pisum; Adelges laricis, Adelges tsugae, Adelphocoris spp., e.g. A. rapidus, A. superbus; Aeneolamia spp., Agonoscena spp., Aulacorthum solani, Aleurocanthus woglumi, Aleurodes spp., Aleurodicus disperses, Aleurolobus barodensis, Aleurothrixus spp., Amrasca spp., Anasa tristis, Antestiopsis spp., Anuraphis cardui, Aonidiella spp., Aphanostigma piri, Aphidula nasturtii, Aphis spp. e.g. A. craccivora, A. fabae, A. forbesi, A. gossypii, A. grossulariae, A. maidiradicis, A. pomi, A. sambuci, A. schneideri, A. spiraecola; Arboridia apicalis, Arilus critatus, Aspidiella spp., Aspidiotus spp., Atanus spp., Aulacaspis yasumatsui, Aulacorthum solani, Bactericera cockerelli (Paratrioza cockerelli), Bemisia spp. e.g. B. argentifolii, B. tabaci (Aleurodes tabaci); Blissus spp. e.g. B. leucopterus; Brachycaudus spp. e.g. B. cardui, B. helichrysi, B. persicae, B. prunicola; Brachycolus spp., Brachycorynella as-paragi, Brevicoryne brassicae, Cacopsylla spp. e.g. C. fulguralis, C. pyricola (Psylla piri); Calligypona marginata, Calocoris spp., Campylomma livida, Capitophorus horni, Carneocephala fulgida, Cavelerius spp., Ceraplastes spp., Ceratovacuna lanigera, Ceroplastes ceriferus, Cerosipha gossypii, Chaetosiphon fragaefolii, Chionaspis tegalensis, Chlorita onukii, Chromaphis juglandicola, Chrysomphalus ficus, Cicadulina mbila, Cimex spp. e.g. C. hemipterus, C. lectularius; Circulifer tenellus, Coccomytilus halli, Coccus spp. e.g. C. hesperidum, C. pseudomagnoliarum; Corythucha arcuata, Creontiades dilutus, Cryptomyzus ribis, Chrysomphalus aonidum, Cryptomyzus ribis, Ctenarytaina spatulata, Cyrtopeltis notatus, Dalbulus spp., Dasynus piperis, Dialeurodes spp. e.g. D. citrifolii; Dalbulus maidis, Diaphorina spp. e.g. D. citri; Diaspis spp. e.g. D. bromeliae; Dichelops furcatus, Diconocoris hewetti, Doralis spp., Dreyfusia nordmannianae, Dreyfusia piceae, Drosicha spp., Dysaphis spp. e.g. D. plantaginea, D. pyri, D. radicola; Dysaulacorthum pseudosolani, Dysdercus spp. e.g. D. cingulatus, D. intermedius; Dysmicoccus spp., Edessa spp., Geocoris spp., Empoasca spp. e.g. E. fabae, E. solana; Epidiaspis leperii, Eriosoma spp. e.g. E. lanigerum, E. pyricola; Erythroneura spp., Eurygaster spp. e.g. E. integriceps; Euscelis bilobatus, Euschistus spp. e.g. E. heros, E. impictiventris, E. servus; Fiorinia theae, Geococcus coffeae, Glycaspis brimblecombei, Halyomorpha spp. e.g. H. halys; Heliopeltis spp., Homalodisca vitripennis (=H. coagulata), Horcias nobilellus, Hyalopterus pruni, Hyperomyzus lactucae, Icerya spp. e.g. I. purchase; Idiocerus spp., Idioscopus spp., Laodelphax striatellus, Lecanium spp., Lecanoideus floccissimus, Lepidosaphes spp. e.g. L. ulmi; Leptocorisa spp., Leptoglossus phyllopus, Lipaphis erysimi, Lygus spp. e.g. L. hesperus, L. lineolaris, L. praten-sis; Maconellicoccus hirsutus, Marchalina hellenica, Macropes excavatus, Macrosiphum spp. e.g. M. rosae, M. avenae, M. euphorbiae; Macrosteles quadrilineatus, Mahanarva fimbriolata, Megacopta cribraria, Megoura viciae, Melanaphis pyrarius, Melanaphis sacchari, Melanocallis (=Tinocallis) caryaefoliae, Metcafiella spp., Metopolophium dirhodum, Monellia costalis, Mo-nelliopsis pecanis, Myzocallis coryli, Murgantia spp., Myzus spp. e.g. M. ascalonicus, M. cerasi, M. nicotianae, M. persicae, M. varians; Nasonovia ribisnigri, Neotoxoptera formosana, Neomegalotomus spp, Nephotettix spp. e.g. N. malayanus, N. nigropictus, N. parvus, N. vires-cens; Nezara spp. e.g. N. viridula; Nilaparvata lugens, Nysius huttoni, Oebalus spp. e.g. O. pugnax; Oncometopia spp., Orthezia praelonga, Oxycaraenus hyalinipennis, Parabemisia myricae, Parlatoria spp., Parthenolecanium spp. e.g. P. corni, P. persicae; Pemphigus spp. e.g. P. bursarius, P. populivenae; Peregrinus maidis, Perkinsiella saccharicida, Phenacoccus spp. e.g. P. aceris, P. gossypii; Phloeomyzus passerinii, Phorodon humuli, Phylloxera spp. e.g. P. devastatrix, Piesma quadrata, Piezodorus spp. e.g. P. guildinii; Pinnaspis aspidistrae, Pianococcus spp. e.g. P. citri, P. ficus; Prosapia bicincta, Protopulvinaria pyriformis, Psallus seriatus, Pseudacysta persea, Pseudaulacaspis pentagona, Pseudococcus spp. e.g. P. comstocki; Psylla spp. e.g. P. mali; Pteromalus spp., Pulvinaria amygdali, Pyrilla spp., Quadraspidiotus spp., e.g. Q. perniciosus; Quesada gigas, Rastrococcus spp., Reduvius senilis, Rhizoecus americanus, Rhodnius spp., Rhopalomyzus ascalonicus, Rhopalosiphum spp. e.g. R. pseudobrassicas, R. insertum, R. maidis, R. padi; Sagatodes spp., Sahlbergella singulars, Saissetia spp., Sappaphis mala, Sappaphis mali, Scaptocoris spp., Scaphoideus titanus, Schizaphis graminum, Schizoneura lanuginosa, Scotinophora spp., Selenaspidus articulatus, Sitobion avenae, Sogata spp., Sogatella furcifera, Solubea insularis, Spissistilus festinus (=Stictocephala festina), Stephanitis nashi, Stephanitis pyrioides, Stephanitis takeyai, Tenalaphara malayensis, Tetraleurodes perseae, Therioaphis maculate, Thyanta spp. e.g. T. accerra, T. perditor; Tibraca spp., Tomaspis spp., Toxoptera spp. e.g. T. aurantii; Trialeurodes spp. e.g. T. abutilonea, T. ricini, T. vaporariorum; Triatoma spp., Trioza spp., Typhlocyba spp., Unaspis spp. e.g. U. citri, U. yanonensis; and Viteus vitifolii, Insects from the order Hymenoptera e.g. Acanthomyops interjectus, Athalia rosae, Atta spp. e.g. A. capiguara, A. cephalotes, A. cephalotes, A. laevigata, A. robusta, A. sexdens, A. texana, Bombus spp., Brachymyrmex spp., Camponotus spp. e.g. C. floridanus, C. pennsylvanicus, C. modoc; Cardiocondyla nuda, Chalibion sp, Crematogaster spp., Dasymutilla occidentalis, Diprion spp., Dolichovespula maculata, Dorymyrmex spp., Dryocosmus kuriphilus, Formica spp., Hoplocampa spp. e.g. H. minuta, H. testudinea; Iridomyrmex humilis, Lasius spp. e.g. L. niger, Linepithema humile, Liometopum spp., Leptocybe invasa, Monomorium spp. e.g. M. pharaonis, Monomorium, Nylandria fulva, Pachycondyla chinensis, Paratrechina longicornis, Paravespula spp., e.g. P. germanica, P. pennsylvanica, P. vulgaris; Pheidole spp. e.g. P. megacephala; Pogonomyrmex spp. e.g. P. barbatus, P. californicus, Polistes rubiginosa, Prenolepis impairs, Pseudomyrmex gracilis, Schelipron spp., Sirex cyaneus, Solenopsis spp. e.g. S. geminata, S. invicta, S. molesta, S. richteri, S. xyloni, Sphecius speciosus, Sphex spp., Tapinoma spp. e.g. T. melanocephalum, T. sessile; Tetramorium spp., e.g. T. caespitum, T. bicarinatum, Vespa spp., e.g. V. crabro; Vespula spp., e.g. V. squamosal; Wasmannia auropunctata, Xylocopa sp;

[0690] Insects from the order Orthoptera e.g. Acheta domesticus, Calliptamus italicus, Chortoicetes terminifera, Ceuthophilus spp., Diastrammena asynamora, Dociostaurus maroccanus, Gryllotalpa spp. e.g. G. africana, G. gryllotalpa; Gryllus spp., Hieroglyphus daganensis, Kraussaria angulifera, Locusta spp. e.g. L. migratoria, L. pardalina; Melanoplus spp. e.g. M. bivittatus, M. femurrubrum, M. mexicanus, M. sanguinipes, M. spretus; Nomadacris septemfasciata, Oedaleus senegalensis, Scapteriscus spp., Schistocerca spp. e.g. S. americana, S. gregaria, Stemopelmatus spp., Tachycines asynamorus, and Zonozerus variegatus;

[0691] Pests from the Class Arachnida e.g. Acari.e.g. of the families Argasidae, Ixodidae and Sar-coptidae, e.g. Amblyomma spp. (e.g. A. americanum, A. variegatum, A. maculatum), Argas spp. e.g. A. persicu), Boophilus spp. e.g. B. annulatus, B. decoloratus, B. microplus, Dermacentor spp. e.g. D.silvarum, D. andersoni, D. variabilis, Hyalomma spp. e.g. H. truncatum, Ixodes spp. e.g. I. ricinus, I. rubicundus, I. scapularis, I. holocyclus, I. pacificus, Rhipicephalus sanguineus, Ornithodorus spp. e.g. O. moubata, O. hermsi, O. turicata, Ornithonyssus bacoti, Otobius megnini, Dermanyssus gallinae, Psoroptes spp. e.g. P. ovis, Rhipicephalus spp. e.g. R. sanguineus, R. appendiculatus, Rhipicephalus evertsi, Rhizoglyphus spp., Sarcoptes spp. e.g. S. Scabiei; and Family Eriophyidae including Aceria spp. e.g. A. sheldoni, A. anthocoptes, Acallitus spp., Aculops spp. e.g. A. lycopersici, A. pelekassi; Aculus spp. e.g. A. schlechtendali; Colomerus vitis, Epitrimerus pyri, Phyllocoptruta oleivora; Eriophytes ribis and Eriophyes spp. e.g. Eriophyes sheldoni; Family Tarsonemidae including Hemitarsonemus spp., Phytonemus pallidus and Polyphagotarsonemus latus, Stenotarsonemus spp. Steneotarsonemus spinki; Family Tenuipalpidae including Brevipalpus spp. e.g. B. phoenicis; Family Tetranychidae including Eotetranychus spp., Eutetranychus spp., Oligonychus spp., Petrobia latens, Tetranychus spp. e.g. T. cinnabarinus, T. evansi, T. kanzawai, T, pacificus, T. phaseulus, T. telarius and T. urticae; Bryobia praetiosa; Panonychus spp. e.g. P. ulmi, P. citri; Metatetranychus spp. and Oligonychus spp. e.g. O. pratensis, O. perseae, Vasates lycopersici; Raoiella indica, Family Carpoglyphidae including Carpoglyphus spp.; Penthaleidae spp. e.g. Halotydeus destructor; Family Demodicidae with species e.g. Demodex spp.; Family Trombicidea including Trombicula spp.; Family Macronyssidae including Ornothonyssus spp.; Family Pyemotidae including Pyemotes tritici; Tyrophagus putrescentiae; Family Acaridae includ-ing Acarus siro; Family Araneida including Latrodectus mactans, Eratigena agrestis, Cheiracanthium sp, Lycosa sp Achaearanea tepidariorum and Loxosceles reclusa; Pests from the Phylum Nematoda, e.g. plant parasitic nematodes e.g. root-knot nematodes, Meloidogyne spp. e.g. M. hapla, M. incognita, M. javanica; cyst-forming nematodes, Globodera spp. e.g. G. rostochiensis; Heterodera spp. e.g. H. avenae, H. glycines, H. schachtii, H. trifolii; Seed gall nematodes, Anguina spp.; Stem and foliar nematodes, Aphelenchoides spp. e.g. A. besseyi; Sting nematodes, Belonolaimus spp. e.g. B. longicaudatus; Pine nematodes, Bursaphelenchus spp. e.g. B. lignicolus, B. xylophilus; Ring nematodes, Criconema spp., Criconemella spp. e.g. C. xenoplax and C. ornata; and, Criconemoides spp. e.g. Criconemoides informis; Mesocriconema spp.; Stem and bulb nematodes, Ditylenchus spp. e.g. D. destructor, D. dipsaci; Awl nematodes, Dolichodorus spp.; Spiral nematodes, Heliocotylenchus multicinctus; Sheath and sheathoid nematodes, Hemicycliophora spp. and Hemicriconemoides spp.; Hirshmanniella spp.; Lance nematodes, Hoploaimus spp.; False rootknot nematodes, Nacobbus spp.; Needle nematodes, Longidorus spp. e.g. L. elongatus; Lesion nematodes, Pratylenchus spp. e.g. P. brachyurus, P. neglectus, P. penetrans, P. curvitatus, P. goodeyi; Burrowing nematodes, Radopholus spp. e.g. R. similis; Rhadopholus spp.; Rhodopholus spp.; Reniform nematodes, Rotylenchus spp. e.g. R. robustus, R. reniformis; Scutellonema spp.; Stubby-root nematode, Trichodorus spp. e.g. T. obtusus, T. primitivus; Paratrichodorus spp. e.g. P. minor; Stunt nematodes, Tylenchorhynchus spp. e.g. T. claytoni, T. dubius; Citrus nematodes, Tylenchulus spp. e.g. T. semipenetrans; Dagger nematodes, Xiphinema spp.; and other plant parasitic nematode species;

[0692] Insects from the order Blattodea e.g. Macrotermes spp. e.g. M. natalensis; Cornitermes cu-mulans, Procornitermes spp., Globitermes sulfureus, Neocapritermes spp. e.g. N. opacus, N. parvus; Odontotermes spp., Nasutitermes spp. e.g. N. corniger; Coptotermes spp. e.g. C. for-mosanus, C. gestroi, C. acinaciformis; Reticulitermes spp. e.g. R. hesperus, R. tibialis, R. speratus, R. flavipes, R. grassei, R. lucifugus, R. virginicus; Heterotermes spp. e.g. H. aureus, H. longiceps, H. tenuis; Cryptotermes spp. e.g. C. brevis, C. cavifrons; Incisitermes spp. e.g. I. minor, I. snyderi; Marginitermes hubbardi, Kalotermes flavicollis, Neotermes spp. e.g. N. cas-taneus, Zootermopsis spp. e.g. Z. angusticollis, Z. nevadensis, Mastotermes spp. e.g. M. dar-winiensis; Blatta spp. e.g. B. orientalis, B. lateralis; Blattella spp. e.g. B. asahinae, B. germanica; Rhyparobia maderae, Panchlora nivea, Periplaneta spp. e.g. P. americana, P. australasiae, P. brunnea, P. fuliginosa, P. japonica; Supella longipalpa, Parcoblatta pennsylvanica, Eurycotis floridana, Pycnoscelus surinamensis,

[0693] Insects from the order Siphonoptera e.g. Cediopsylla simples, Ceratophyllus spp., Ctenoce-phalides spp. e.g. C. felis, C. canis, Xenopsylla cheopis, Pulex irritans, Trichodectes canis, Tunga penetrans, and Nosopsyllus fasciatus,

[0694] Insects from the order Thysanura e.g. Lepisma saccharina, Ctenolepisma urbana, and Thermobia domestica,

[0695] Pests from the class Chilopoda e.g. Geophilus spp., Scutigera spp. e.g. Scutigera coleoptrata; Pests from the class Diplopoda e.g. Blaniulus guttulatus, Julus spp., Narceus spp.,

[0696] Pests from the class Symphyla e.g. Scutigerella immaculata,

[0697] Insects from the order Dermaptera, e.g. Forficula auricularia,

[0698] Insects from the order Collembola, e.g. Onychiurus spp., e.g. Onychiurus armatus,

[0699] Pests from the order Isopoda, e.g. Armadillidium vulgare, Oniscus asellus, Porcellio scaber, Insects from the order Phthiraptera, e.g. Damalinia spp., Pediculus spp. e.g. Pediculus humanus capitis, Pediculus humanus corporis, Pediculus humanus humanus; Pthirus pubis, Haematopinus spp. e.g. Haematopinus eurysternus, Haematopinus suis; Linognathus spp. e.g. Linognathus vituli; Bovicola bovis, Menopon gallinae, Menacanthus stramineus and Solenopotes capillatus, Trichodectes spp.,

[0700] Further pest species which may be controlled by compounds I include: from the Phylum Mollusca, class Bivalvia, e.g., Dreissena spp.; class Gastropoda, e.g., Arion spp., Biomphalaria spp., Bulinus spp., Deroceras spp., Galba spp., Lymnaea spp., Oncomelania spp., Pomacea canaliclata, Succinea spp.; from the class of the helminths, e.g., Ancylostoma duodenale, Ancylostoma ceylanicum, Acylostoma braziliensis, Ancylostoma spp., Ascaris lubricoides, Ascaris spp., Brugia malayi, Brugia timori, Bunostomum spp., Chabertia spp., Clonorchis spp., Cooperia spp., Dicrocoelium spp., Dictyocaulus filaria, Diphyllobothrium latum, Dracunculus medinensis, Echinococcus granulosus, Echinococcus multilocularis, Enterobius vermicularis, Faciola spp., Haemonchus spp. e.g. Haemonchus contortus; Heterakis spp., Hymenolepis nana, Hyostrongulus spp., Loa Loa, Nematodirus spp., Oesophagostomum spp., Opisthorchis spp., Onchocerca volvulus, Ostertagia spp., Paragonimus spp., Schistosomen spp., Strongyloides fuel-leborni, Strongyloides stercora lis, Stronyloides spp., Taenia saginata, Taenia solium, Trichinella spiralis, Trichinella nativa, Trichinella britovi, Trichinella nelsoni, Trichinella pseudopsiralis, Trichostrongulus spp., Trichuris trichuria, Wuchereria bancrofti.

[0701] The compounds of the invention are particularly suitable for efficiently combating

[0702] insects from the sub-order of Auchenorrhyncha, e.g. Amrasca biguttula, Empoasca spp., Nephotettix virescens, Sogatella furcifera, Mahanarva spp., Laodelphax striatellus, Nilapar-vata lugens, Diaphorina citri, Lycorma delicatula, Pentastiridus leporinus;

[0703] Lepidoptera, e.g. Helicoverpa spp., Heliothis virescens, Lobesia botrana, Ostrinia nubilalis, Plutella xylostella, Pseudoplusia includens, Scirpophaga incertulas, Spodoptera spp., Trichoplusia ni, Tuta absoluta, Cnaphalocrocis medialis, Cydia pomonella, Chilo suppressalis, Anticarsia gemmatalis, Agrotis ipsilon, Chrysodeixis includens;

[0704] True bugs, e.g. Lygus spp., Stink bugs such as Euschistus spp., Halyomorpha halys, Nezara viridula, Piezodorus guildinii, Dichelops furcatus;

[0705] Thrips, e.g. Frankliniella spp., Thrips spp., Dichromothrips corbettii;

[0706] Aphids, e.g. Acyrthosiphon pisum, Aphis spp., Myzus persicae, Rhopalosiphum spp., Schi-zaphis graminum, Megoura viciae;

[0707] Whiteflies, e.g. Trialeurodes vaporariorum, Bemisia spp.;

[0708] Coleoptera, e.g. Phyllotreta spp., Melanotus spp., Meligethes aeneus, Leptinotarsa decimlineata, Ceutorhynchus spp., Diabrotica spp., Anthonomus grandis, Atomaria linearia, Agriotes spp., Epilachna spp.;

[0709] Flies, e.g. Delia spp., Ceratitis capitate, Bactrocera spp., Liriomyza spp.;

[0710] Coccoidea, e.g. Aonidiella aurantia, Ferrisia virgate;

[0711] Anthropods of class Arachnida (Mites), e.g. Penthaleus major, Tetranychus spp.;

[0712] Nematodes, e.g. Heterodera glycines, Meloidogyne sp., Pratylenchus spp., Caenorhabditis elegans.

[0713] Animal health

[0714] The compounds of the invention are suitable for use in treating or protecting animals against infestation or infection by parasites. Therefore, the invention also relates to the use of a compound of the invention for the manufacture of a medicament for the treatment or protection of animals against infestation or infection by parasites. Furthermore, the invention relates to a method of treating or protecting animals against infestation and infection by parasites, which comprises orally, topically or parenterally administering or applying to the animals a parasiticidally effective amount of a compound of the invention.

[0715] The invention also relates to the non-therapeutic use of compounds of the invention for treating or protecting animals against infestation and infection by parasites. Moreover, the invention relates to a non-therapeutic method of treating or protecting animals against infestation and infection by parasites, which comprises applying to a locus a parasiticidally effective amount of a compound of the invention.

[0716] The compounds of the invention are further suitable for use in combating or controlling parasites in and on animals. Furthermore, the invention relates to a method of combating or con-trolling parasites in and on animals, which comprises contacting the parasites with a parasitical ly effective amount of a compound of the invention.

[0717] The invention also relates to the non-therapeutic use of compounds of the invention for controlling or combating parasites. Moreover, the invention relates to a non-therapeutic method of combating or controlling parasites, which comprises applying to a locus a parasiticidally effective amount of a compound of the invention.

[0718] The compounds of the invention can be effective through both contact (via soil, glass, wall, bed net, carpet, blankets or animal parts) and ingestion (e.g. baits). Furthermore, the compounds of the invention can be applied to any and all developmental stages.

[0719] The compounds of the invention can be applied as such or in form of compositions comprising the compounds of the invention.

[0720] The compounds of the invention can also be applied together with a mixing partner, which acts against pathogenic parasites, e.g. with synthetic coccidiosis compounds, polyetherantibiotics e.g. Amprolium, Robenidin, Toltrazuril, Monensin, Salinomycin, Maduramicin, Lasalocid, Narasin or Semduramicin, or with other mixing partners as defined above, or in form of compositions comprising said mixtures.

[0721] The compounds of the invention and compositions comprising them can be applied orally, parenterally or topically, e.g. dermally. The compounds of the invention can be systemically or non-systemically effective.

[0722] The application can be carried out prophylactically, therapeutically or non-therapeutically. Furthermore, the application can be carried out preventively to places at which occurrence of the parasites is expected.

[0723] As used herein, the term "contacting" includes both direct contact (applying the com-pounds / compositions directly on the parasite, including the application directly on the animal or excluding the application directly on the animal, e.g. at its locus for the latter) and indirect contact (applying the compounds / compositions to the locus of the parasite). The contact of the parasite through application to its locus is an example of a non-therapeutic use of the compounds of the invention.

[0724] The term "locus" means the habitat, food supply, breeding ground, area, material or environment in which a parasite is growing or may grow outside of the animal.

[0725] As used herein, the term “parasites” includes endo- and ectoparasites. In some embodiments of the invention, endoparasites can be preferred. In other embodiments, ectoparasites can be preferred. Infestations in warm-blooded animals and fish include lice, biting lice, ticks, nasal bots, keds, biting flies, muscoid flies, flies, myiasitic fly larvae, chiggers, gnats, mosquitoes and fleas. The compounds of the invention are especially useful for combating parasites of the following orders and species, respectively: fleas (Siphonaptera), e.g. Ctenocephalides felis, C. canis, Xenopsylla cheopis, Pulex irri-tans, Tunga penetrans, and Nosopsyllus fasciatus; cockroaches (Blattaria - Blattodea), e.g. Blattella germanica, B. asahinae, Periplaneta americana, P. japonica, P. brunnea, P. fuligginosa, P. australasiae, and Blatta orientalis; flies, mosquitoes (Diptera), e.g. Aedes aegypti, A. albopictus, A. vexans, Anastrepha ludens, Anopheles maculipennis, A. crucians, A. albimanus, A. gambiae, A. freeborni, A. leucosphyrus, A. minimus, A. quadrimaculatus, Calliphora vicina, Chrysomya bezziana, C. hominivorax, C. macellaria, Chrysops discalis, C. silacea, C. atlanticus, Cochliomyia hominivorax, Cordylobia anthropophaga, Culicoides furens, Culex pipiens, C. nigripalpus, C. quinquefasciatus, C. tarsalis, Culiseta inornata, C. melanura, Dermatobia hominis, Fannia canicularis, Gasterophilus intestinalis, Glossina morsitans, G. palpalis, G. fuscipes, G. tachinoides, Haematobia irritans, Haplodiplosis equestris, Hippelates spp., Hypoderma line-ata, Leptoconops torrens, Lucilia caprina, L. cuprina, L. sericata, Lycoria pectoralis, Mansonia spp., Musca domestica, M. stabulans, Oestrus ovis, Phlebotomus argentipes, Psorophora columbiae, P. discolor, Prosimulium mixtum, Sarcophaga spp., S. haemorrhoidalis, Simulium vittatum, Stomoxys calcitrans, Tabanus bovinus, T. atratus, T. lineola, and T. similis; lice (Phthiraptera), e.g. Pediculus humanus capitis, P. humanus humanus, Pthirus pubis, Haematopinus eurysternus, H. suis, Linognathus vituli, Bovicola bovis, Menopon gallinae, Menacanthus stramineus, and Solenopotes capillatus; ticks and parasitic mites (Parasitiformes): ticks (Ixodida), e.g. Ixodes scapularis, I. holocyclus, I. pacificus, Rhiphicephalus sanguineus, Dermacentor andersoni, D. variabilis, Amblyomma americanum, A. maculatum, Ornithodorus hermsi, O. turicata and parasitic mites (Mesostigmata), e.g. Ornithonyssus bacoti, Dermanyssus gallinae; Actinedida (Prostigmata) and Acaridida (Astigmata), e.g. Acarapis spp., Cheyletiella spp., Ornithocheyletia spp., Myobia spp., Psorergates spp., Demo-dex spp., Trombicula spp., Listrophorus spp., Acarus spp., Tyrophagus spp., Caloglyphus spp., Hypodectes spp., Pterolichus spp., Psoroptes spp., Chorioptes spp., Otodectes spp., Sarcoptes spp., Notoedres spp., Knemidocoptes spp., Cytodites spp., and Laminosioptes spp; Bugs (Het-eropterida): Cimex lectularius, C. hemipterus, Reduvius senilis, Triatoma spp., Rhodnius ssp., Panstrongylus ssp., and Arilus critatus; Anoplurida, e.g. Haematopinus spp., Linognathus spp., Pediculus spp., Phtirus spp., and Solenopotes spp.; Mallophagida (suborders Arnblycerina and Ischnocerina), e.g. Trimenopon spp., Menopon spp., Trinoton spp., Bovicola spp., Werneckiella spp., Lepikentron spp., Trichodectes spp., and Felicola spp.; Roundworms Nematoda: Wipeworms and Trichinosis (Trichosyringida), e.g. Trichinellidae (Trichinella spp.), (Trichuridae) Trichuris spp., Capillaria spp.; Rhabditida, e.g. Rhabditis spp., Strongyloides spp., Helicephalobus spp.; Strongylida, e.g. Strongylus spp., Ancylostoma spp., Necator americanus, Bunostomum spp. (Hookworm), Trichostrongylus spp., Haemonchus contortus, Ostertagia spp., Cooperia spp., Nematodirus spp., Dictyocaulus spp., Cyathostoma spp., Oesophagostomum spp., Stephanurus dentatus, Ollulanus spp., Chabertia spp., Stephanurus dentatus, Syngamus trachea, Ancylostoma spp., Uncinaria spp., Globocephalus spp., Necator spp., Metastrongylus spp., Muellerius capillaris, Protostrongylus spp., Angiostrongylus spp., Parelaphostrongylus spp., Aleurostrongylus abstrusus, and Dioctophyma renale; Intestinal roundworms (Ascaridida), e.g. Ascaris lumbricoides, Ascaris suum, Ascaridia galli, Parascaris equorum, Enterobius vermicularis (Threadworm), Toxocara canis, Toxascaris leonine, Skrjabinema spp., and Oxyuris equi; Camallanida, e.g. Dracunculus medinensis (guinea worm); Spirurida, e.g. Thelazia spp., Wuchereria spp., Brugia spp., Onchocerca spp., Dirofilari spp. a, Dipetalonema spp., Setaria spp., Elaeophora spp., Spirocerca lupi, and Habronema spp.; Thorny headed worms (Acanthocephala), e.g. Acanthocephalus spp., Macracanthorhynchus hirudinaceus and Oncicola spp.; Planarians (Plathelminthes): Flukes (Trematoda), e.g. Faciola spp., Fascioloides magna, Paragonimus spp., Dicrocoelium spp., Fasciolopsis buski, Clonorchis sinensis, Schistosoma spp., Trichobilharzia spp., Alaria alata, Paragonimus spp., and Nanocyetes spp.; Cercomeromorpha, in particular Cestoda (Tapeworms), e.g. Diphyllo-bothrium spp., Tenia spp., Echinococcus spp., Dipylidium caninum, Multiceps spp., Hymenolepis spp., Mesocestoides spp., Vampirolepis spp., Moniezia spp., Anoplocephala spp., Sirometra spp., Anoplocephala spp., and Hymenolepis spp..

[0726] The term “animal” includes warm-blooded animals (including humans) and fish. Preferred are mammals, e.g. cattle, sheep, swine, camels, deer, horses, pigs, poultry, rabbits, goats, dogs and cats, water buffalo, donkeys, fallow deer and reindeer, and also in fur-bearing animals e.g. mink, chinchilla and raccoon, birds e.g. hens, geese, turkeys and ducks and fish e.g. fresh- and saltwater fish e.g. trout, carp and eels. Particularly preferred are domestic animals, e.g. dogs or cats. Generally, "parasiticidally effective amount" means the amount of active ingredient needed to achieve an observable effect on growth, including the effects of necrosis, death, retardation, prevention, and removal, destruction, or otherwise diminishing the occurrence and activity of the target organism. The parasiticidally effective amount can vary for the various compounds / compositions used in the invention. A parasiticidally effective amount of the compositions will also vary according to the prevailing conditions e.g. desired parasiticidal effect and duration, target species, mode of application.

[0727] Generally, it is favorable to apply the compounds of the invention in total amounts of 0.5 mg / kg to 100 mg / kg per day, preferably 1 mg / kg to 50 mg / kg per day.

[0728] For oral administration to warm-blooded animals, the compounds I may be formulated as animal feeds, animal feed premixes, animal feed concentrates, pills, solutions, pastes, suspensions, drenches, gels, tablets, boluses and capsules. In addition, the compounds I may be ad-ministered to the animals in their drinking water. For oral administration, the dosage form chosen should provide the animal with 0.01 mg / kg to 100 mg / kg of animal body weight per day of the compounds I, preferably with 0.5 mg / kg to 100 mg / kg of animal body weight per day.

[0729] Alternatively, the compounds I may be administered to animals parenterally, e.g., by intraruminal, intramuscular, intravenous or subcutaneous injection. The compounds I may be dispersed or dissolved in a physiologically acceptable carrier for subcutaneous injection. Alternatively, the compounds I may be formulated into an implant for subcutaneous administration. In addition the compounds I may be transdermally administered to animals. For parenteral administration, the dosage form chosen should provide the animal with 0.01 mg / kg to 100 mg / kg of animal body weight per day of the compounds I.

[0730] The compounds I may also be applied topically to the animals in the form of dips, dusts, powders, collars, medallions, sprays, shampoos, spot-on and pour-on formulations and in ointments or oil-in-water or water-in-oil emulsions. For topical application, dips and sprays usually contain 0.5 ppm to 5,000 ppm and preferably 1 ppm to 3,000 ppm of the compounds I. In addition, the compounds I may be formulated as ear tags for animals, particularly quadrupeds e.g. cattle and sheep.

[0731] Suitable preparations are:

[0732] - Solutions e.g. oral solutions, concentrates for oral administration after dilution, solutions for use on the skin or in body cavities, pouring-on formulations, gels;

[0733] - Emulsions and suspensions for oral or dermal administration; semi-solid preparations; - Formulations in which the active compound is processed in an ointment base or in an oil-in-water or water-in-oil emulsion base;

[0734] - Solid preparations e.g. powders, premixes or concentrates, granules, pellets, tablets, boluses, capsules; aerosols and inhalants, and active compound-containing shaped articles.

[0735] Compositions suitable for injection are prepared by dissolving the active ingredient in a suit-able solvent and optionally adding further auxiliaries e.g. acids, bases, buffer salts, preservatives, and solubilizers. Suitable auxiliaries for injection solutions are known in the art. The solutions are filtered and filled sterile.

[0736] Oral solutions are administered directly. Concentrates are administered orally after prior dilution to the use concentration. Oral solutions and concentrates are prepared according to the state of the art and as described above for injection solutions, sterile procedures not being necessary. Solutions for use on the skin are trickled on, spread on, rubbed in, sprinkled on or sprayed on. Solutions for use on the skin are prepared according to the state of the art and according to what is described above for injection solutions, sterile procedures not being necessary.

[0737] Gels are applied to or spread on the skin or introduced into body cavities. Gels are prepared by treating solutions which have been prepared as described in the case of the injection solutions with sufficient thickener that a clear material having an ointment-like consistency results. Suitable thickeners are known in the art.

[0738] Pour-on formulations are poured or sprayed onto limited areas of the skin, the active compound penetrating the skin and acting systemically. Pour-on formulations are prepared by dis-solving, suspending or emulsifying the active compound in suitable skin-compatible solvents or solvent mixtures. If appropriate, other auxiliaries e.g. colorants, bioabsorption-promoting substances, antioxidants, light stabilizers, adhesives are added. Suitable such auxiliaries are known in the art. Emulsions can be administered orally, dermally or as injections. Emulsions are either of the water-in-oil type or of the oil-in-water type. They are prepared by dissolving the active com-pound either in the hydrophobic or in the hydrophilic phase and homogenizing this with the solvent of the other phase with the aid of suitable emulsifiers and, if appropriate, other auxiliaries e.g. colorants, absorption-promoting substances, preservatives, antioxidants, light stabilizers, viscosity-enhancing substances. Suitable hydrophobic phases (oils), suitable hydrophilic phases, suitable emulsifiers, and suitable further auxiliaries for emulsions are known in the art.

[0739] Suspensions can be administered orally or topically / dermally. They are prepared by suspending the active compound in a suspending agent, if appropriate with addition of other auxiliaries e.g. wetting agents, colorants, bioabsorption-promoting substances, preservatives, antioxidants, light stabilizers. Suitable suspending agents, and suitable other auxiliaries for suspensions including wetting agents are known in the art.

[0740] Semi-solid preparations can be administered orally or topically / dermally. They differ from the suspensions and emulsions described above only by their higher viscosity.

[0741] For the production of solid preparations, the active compound is mixed with suitable excipients, if appropriate with addition of auxiliaries, and brought into the desired form. Suitable auxiliaries for this purpose are known in the art.

[0742] The compositions which can be used in the invention can comprise generally from about 0.001 to 95% of the compound of the invention.

[0743] Ready-to-use preparations contain the compounds acting against parasites, preferably ectoparasites, in concentrations of 10 ppm to 80% by weight, preferably from 0.1 to 65% by weight, more preferably from 1 to 50% by weight, most preferably from 5 to 40% by weight. Preparations which are diluted before use contain the compounds acting against ectoparasites in concentrations of 0.5 to 90% by weight, preferably of 1 to 50% by weight.

[0744] Furthermore, the preparations comprise the compounds of formula I against endoparasites in concentrations of 10 ppm to 2% by weight, preferably of 0.05 to 0.9% by weight, very particularly preferably of 0.005 to 0.25% by weight.

[0745] Topical application may be conducted with compound-containing shaped articles e.g. collars, medallions, ear tags, bands for fixing at body parts, and adhesive strips and foils.

[0746] Generally it is favorable to apply solid formulations which release compounds of the invention in total amounts of 10 mg / kg to 300 mg / kg, preferably 20 mg / kg to 200 mg / kg, most preferably 25 mg / kg to 160 mg / kg body weight of the treated animal in the course of three weeks.

[0747] A. Preparation Examples

[0748] The compounds were characterized by melting point determination, by NMR spectroscopy or by the mass-to-charge ratio ([m / z]) and retention time (RT; [min.]), as determined by mass spectrometry (MS) coupled with HPLC analysis (HPLC-MS = high performance liquid chromatography-coupled mass spectrometry), LC analysis (LC-MS = liquid chromatography-coupled mass spectrometry) or chiral SFC (SFC = supercritical fluid chromatography).

[0749] Method D: Column: X-Bridge C18, 5u (4.6mmX100mm) Mobile Phase A: 10 mM Ammonium Bicarbonate in Water, B: 100% ACN, Gradient (T%B): 0 / 10, 8 / 95, 11 / 95, 13 / 10,15 / 10, Flow Rate: 1.0 ml / min Column Temp: 40°C, Sample Diluent: ACN+WATER

[0750] Method E: Acquity UPLC BEH C18, 1.7pm (50mmX2.1mm), Mobile Phase A: 0.1% Formic Acid in Water, B: 0.1% Formic Acid in ACN, Gradient (T%B): 0 / 3, 1.0 / 3, 7.0 / 95, 7.5 / 95, 9.0 / 3, 10.0 / 3, Flow Rate: 0.5ml / min, Column Temp: 40°C Mass range (m / z): 100-700

[0751] Method F: Shimadzu Nexera UHPLC + Shimadzu LCMS 20-20, ESI, Column: C-18, 50 mm, 4.6 mm, 5 micron, Mobile Phase: A: 10mM ammonium Formate + B: ACN, Column Oven Temperature: 40°C, Gradient: 10% B to 100% B in 1,50min; 100% B 1.0 min, Flow: 1.2 ml / min, MS method: ESI Positive - Negative (Dual Ionisation), mass range (m / z): 100-700

[0752] Method G: Analytical SFC Condition: Column / dimensions: DCPAK P4VP (4.6x250)mm, 5p % CO2:70%, % Co solvent:30% (0.5% DEA in MeOH), Flow: 3mL / min Back Pressure:1500 psi; Temperature: 30°C

[0753] Method H: Shimadzu Nexera UHPLC + Shimadzu LCMS 20-20, ESI Column: Phenomenex Kinetex 1,7pm XB-C18 100A, 50 x 2,1mm. Mobile Phase: A: water + 0,1% TFA; B: ACN Temperature: 60°C, Gradient:5% B to 100% B in 1,50min; 100% B 0,25min Flow: 0,8ml / min to 1,0ml / min in 1,51 min, MS method: ESI positive Mass range (m / z): 100-700 Example 1: Synthesis of 2-((6-(1-(4-chlorobenzoyl) piperidin-4-yl) pyridin-3-yl) methylene)-N-(2-isopropyl-5-methylphenyl) hydrazine-1 -carbothioamide (compound I-2)

[0754] c

[0755]

[0756] arboxylate (A3): To a stirred solution of 2-bromo-5-(dimethoxymethyl)pyridine (A1) (4.8 g, 20.683 mmol, 1 equiv.), tert-butyl 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3,6-dihydropyridine-1 (2H)-carboxylate (A2) (7.035 g, 22.751 mmol, 1.1 equiv.) and sodium carbonate (5.480 g, 51.707 mmol, 2.5 equiv.) in mixture of 1,4-dioxane (38.400 mL) and water (9.600 mL), was degassed with nitrogen for 5 min. After that, Pd(PPh3)4 (1.195 g, 1.034 mmol, 0.05 equiv.) was added and the resulting mixture was again degassed with N2for 5 minutes and stirred at 100 °C for 16 h. After completion of the reaction, the reaction mass was quenched with water (100 mL) and extracted with ethyl acetate (3 x 100 mL). The combined organic layer was washed with brine (100 mL), dried over sodium sulphate, filtered and concentrated under reduced pressure to get the crude product. The crude product was purified by silica gel (100~200 mesh) column chromatography using 50% ethyl acetate in pet ether as an eluent to afford tert-butyl 5-(dimethoxymethyl)-3',6'-dihydro-[2,4'-bipyridine]-1'(2'H)-carboxylate (A3) (4 g, 57%). LC-MS (m / z): 335.32 [M+H] + ion present

[0757] Step 2: Synthesis of tert-butyl 4-(5-(dimethoxy methyl) pyridin-2-yl) piperidine- 1 -carboxylate (A4):

[0758] To a stirred solution of tert-butyl 5-(dimethoxymethyl)-3',6'-dihydro-[2,4'-bipyridine]-1'(2'H)-carboxylate (A3) (4 g, 11.961 mmol, 1 equiv.) in ethyl acetate (80 mL) was added 10% Pd / C (1.2 g, 0.3 w / w) under H2(60 Psi) atmosphere at room temperature and continued the stirring for 16 h (the progress of the reaction was monitored by TLC). After completion of the reaction, the reaction mass was diluted with ethyl acetate (100 mL), filtered through celite bed and the filtrate was concentrated under reduced pressure to afford tert-butyl 4-(5-(dimethoxy methyl) pyridin-2-yl) piperidine-1 -carboxylate (A4) (4 g crude). The crude product was used in the next step without further purification. LC-MS (m / z): 337.33 [M+H] + ion present Step 3: Synthesis of 6-(piperidin-4-yl)nicotinaldehyde hydrochloride (A5):

[0759] To a stirred solution of tert-butyl 4-(5-(dimethoxy methyl) pyridin-2-yl) piperidine-1 -carboxylate (A4) (4 g, 11.889 mmol, 1 equiv.) in DCM (40 mL) was added 4M HCI in 1,4-dioxane (40 mL) dropwise at room temperature. The resulting mixture was stirred for 4 hours under same condition. After completion of the reaction, reaction mass was concentrated under reduced pressure to get 6-(piperidin-4-yl)nicotinaldehyde hydrochloride (A5) (3 g crude). The crude product was used in the next step without further purification. LC-MS (m / z): 191.10 [M+H] + ion present

[0760] Step 4: Synthesis of 6-(1-(4-chlorobenzoyl) piperidin-4-yl) nicotinaldehyde (A7):

[0761] To a stirred solution of 6-(piperidin-4-yl)nicotinaldehyde hydrochloride (A5) (3 g, 13.233 mmol, 1 equiv.) and DIPEA (9.245 mL, 52.932 mmol, 4 equiv.) in THF (60 mL) was added 4-chlorobenzoyl chloride (A6) (2.316 g, 13.233 mmol, 1 equiv.) at room temperature. The resulting mixture was stirred for 16 h under same condition. After completion of the reaction, the reaction mass was quenched with water (100 mL) and extracted with ethyl acetate (3 x 100 mL). The combined organic layer was washed with brine (50 mL), dried over sodium sulphate, filtered and concentrated under reduced pressure to get the crude product. The crude product was purified by silica gel (100~200 mesh) column chromatography using 60% ethyl acetate in pet ether as an eluent to afford 6-(1-(4-chlorobenzoyl) piperidin-4-yl) nicotinaldehyde (A7) (2 g, 46%). LC-MS (m / z): 329.25 [M+H] + ion present

[0762] Step 5: Synthesis of 2-((6-(1-(4-chlorobenzoyl) piperidin-4-yl) pyridin-3-yl) methylene)-N-(2-isopropyl-5-methylphenyl) hydrazine-1 -carbothioamide (compound I-2):

[0763] To a stirred solution of 6-(1-(4-chlorobenzoyl)piperidin-4-yl)nicotinaldehyde (A7) (2 g, 6.083 mmol, 1 equiv.) and N-(2-isopropyl-5-methylphenyl)hydrazinecarbothioamide (E6) (1.359 g, 6.083 mmol, 1 equiv.) in methanol (20 mL) was added acetic acid (1.0 mL, 0.5 V) at room temperature. The resulting mixture was stirred for 16 h under same condition (progress of the reaction was monitored TLC and LCMS). After completion of the reaction, the precipitated solid was filtered and dried to afford 2-((6-(1-(4-chlorobenzoyl) piperidin-4-yl) pyridin-3-yl) methylene)-N-(2-isopropyl-5-methylphenyl) hydrazine-1 -carbothioamide (1.7 g) as a white solid. 0.8 g (HPLC purity: 89%) of compound was purified by reverse phase preparative HPLC and lyophilized to afford 2-((6-(1-(4-chlorobenzoyl) piperidin-4-yl) pyridin-3-yl) methylene)-N-(2-isopropyl-5-methylphenyl) hydrazine- 1 -carbothioamide (compound I-2) (0.54 g). LC-MS (m / z): 534.32 [M+H] + ion present.1H NMR (400 MHz, DMSO-d6): δ 11.86 (s, 1H), 9.98 (s, 1H), 8.85 (d, J = 1.6 Hz, 1H), 8.36 (dd, J = 8.4 & 2.0 Hz, 1H), 8.13 (s, 1H), 7.52 (d, J = 8.4 Hz, 2H), 7.45 (d, J = 8.8 Hz, 2H), 7.38 (d, J= 8.4 Hz, 1H), 7.23 (d, J= 8.0 Hz, 1H), 7.11 (d, J= 7.6 Hz, 1H), 7.00 (s, 1H), 4.70-4.50 (m, 1H), 3.81-3.50 (m, 1H), 3.25-3.10 (m, 1H), 3.09-3.01 (m, 2H), 2.98-2.80 (s, 1H), 2.28 (s, 3H), 1.98 -1.62 (m, 4H), 1.15 (d, J = 6.8 Hz, 6H). Example 2: Synthesis of compound (E / Z)-2-(((E)-(6-(1-(4-chlorobenzoyl)piperidin-4-yl)pyridin-3-yl)methylene)hydrazineylidene)-3-(2-isopropyl-5-methyl phenyl)thiazolidin-4-one (compound 1-1)

[0764]

[0765] To a stirred solution of (E)-2-((6-(1-(4-chlorobenzoyl)piperidin-4-yl)pyridin-3-yl)methylene)-N-(2-isopropyl-5-methylphenyl)hydrazine-1-carbothioamide (compound I-2) (0.8 g, 1.498 mmol, 1 equiv.) and sodium acetate (0.491 g, 5.991 mmol, 4 equiv.) in ethanol (16.0 mL) was added methyl 2-bromoacetate (0.344 g, 2.247 mmol, 1.5 equiv.) at rt. The resulting mixture was stirred at 70 °C for 16 hours. After completion of the reaction, the reaction mass was diluted with water (100 mL) and extracted with ethyl acetate (2 X 100 mL). The combined organic layer was washed with brine (50 mL), dried over sodium sulfate, filtered and concentrated under reduced pressure to get the crude compound. The crude compound was purified by silica gel (100-200 mesh) column chromatography using 60% ethyl acetate in pet ether as an eluent to afford (E / Z)-2-(((E)-(6-(1-(4-chlorobenzoyl)piperidin-4-yl)pyridin-3-yl)methylene)hydrazineylidene)-3-(2-isopropyl-5-methyl phenyl)thiazolidin-4-one (compound 1-1) (0.62 g, 72%). LC-MS (m / z): 574.30 [M+H]+ion present.1H-NMR (400 MHz, DMSO-d6): δ 8.77 (d, J = 1.6 Hz, 1 H), 8.36 (s, 1 H), 8.04-8.06 (dd, J = 8.4 & 2.4 Hz, 1 H), 7.52 (d, J = 8.4 Hz, 2H), 7.46-7.37 (m, 4H), 7.27 (d, J= 8.4 Hz, 1H), 7.06 (s, 1H), 4.62-4.54 (m, 1H), 4.24 (d, J= 17.2 Hz, 1H), 4.12 (d, J= 17.2 Hz, 1H), 3.66-3.58 (m, 1H), 3.22-3.14 (m, 1H), 3.07-3.01 (m, 1H), 2.96-2.84 (m, 1H), 2.76-2.71 (m, 1H), 2.31 (s, 3H), 1.93-1.68 (m, 4H), 1.13-1.09 (m, 6H).

[0766] Example 3: Synthesis of 1-(4-(4-(4-chlorobenzoyl)-2-oxopiperazin-1-yl)phenyl)-3-(3-(2-

[0767]

[0768] Step-1: Synthesis of tert-butyl 4-(4-nitrophenyl)-3-oxopiperazine-1 -carboxylate (B3):

[0769] A solution of 1-bromo-4-nitrobenzene (B1) (5 g, 24.751 mmol) and tert-butyl 3-oxopiperazine-1-carboxylate (B2) (5.947 g, 29.702 mmol) and cesium carbonate (16.129 g, 49.502 mmol) in 1,4-dioxane was degassed with nitrogen for 10 minutes followed by addition of palladium (II) acetate (1.667 g, 2.475 mmol) and xantphos (1.432 g, 2.475 mmol). The resulting mixture was degassed again for 5 min. The resulting mixture heated at 80 °C for 6 h. After completion, water (200 mL) was added and extracted with ethyl acetate (3 x 200 mL). The combined organic layers and washed with brine (200 mL), dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure. The crude product was adsorbed on a plug of silica gel and purified by flash column chromatography using 50-70% ethyl acetate in pet ether as an eluent to afford tert-butyl 4-(4-nitrophenyl)-3-oxopiperazine-1 -carboxylate (B3) (4 g, 50%).

[0770] LC-MS (m / z): 322.28 [M+H]+ion present

[0771] Step-2: Synthesis of 1-(4-nitrophenyl)piperazin-2-one trifluoroacetic acid salt (B4):

[0772] To a stirred solution of tert-butyl 4-(4-nitrophenyl)-3-oxopiperazine-1 -carboxylate (B3) (4 g, 12.448 mmol) in dichloromethane (40 mL) was added trifluoroacetic acid (14.193 g, 124.481 mmol) at RT. The resulting mixture was stirred at RT for 3 h. After completion of the reaction, concentrated the reaction mixture under reduced pressure. The crude product thus obtained was triturated in diethyl ether (2 x 5 mL) to afford 1-(4-nitrophenyl)piperazin-2-one trifluoroacetic acid salt (B4) (2.5 g). LC-MS (m / z): 222.12 [M-TFA+H] + ion present

[0773] Step-3: Synthesis of 4-(4-chlorobenzoyl)-1-(4-nitrophenyl)piperazin-2-one (B6):

[0774] To a stirred solution of 1-(4-nitrophenyl)piperazin-2-one trifluoroacetic acid salt (B4) (2.5 g, 7.831 mmol) and triethylamine (1.189 g, 11.447 mmol) in THF (25 mL) was added 4-chlorobenzoyl chloride (B5) (1.371 g, 7.831 mmol) dropwise at 0 °C. The resulting mixture was stirred at RT for 2 h. After completion, the reaction mass was quenched with water (100 mL) and extracted with ethyl acetate (3 x 100 mL). The combined organic layer was washed with brine (100 mL), dried over sodium sulfate, filtered and concentrated under reduced pressure. The crude product thus obtained was triturated in diethyl ether (2 x 25 mL) to afford 4-(4-chlorobenzoyl)-1-(4-nitrophenyl)piperazin-2-one (B6) (3 g).

[0775] LC-MS (m / z): 360.20 [M+H]+ion present

[0776] Step-4: Synthesis of 1-(4-aminophenyl)-4-(4-chlorobenzoyl)piperazin-2-one (B7):

[0777] To a stirred solution of 4-(4-chlorobenzoyl)-1-(4-nitrophenyl)piperazin-2-one (B6) (3 g, 8.339 mmol) in mixture of THF: water (30 mL, 10V, 7:3 ratio) was added sodium dithionite (7.259 g, 41.694 mmol) at RT. The resulting mixture was stirred at 55 °C for 3 h. After completion, the reaction mass was diluted with water (100 mL) and extracted with ethyl acetate (2 x 100 mL). The combined organic layer was washed with brine (100 mL), dried over sodium sulfate, filtered and concentrated under reduced pressure. The crude product thus obtained was triturated in diethyl ether (2 x 10 mL) to afford 1-(4-aminophenyl)-4-(4-chlorobenzoyl)piperazin-2-one (B7) (1.2 g, 44%). LC-MS (m / z): 330.23 [M+H]+ion present Step-5: Synthesis of 1-(4-(4-(4-chlorobenzoyl)-2-oxopiperazin-1-yl)phenyl)-3-(3-(2-isopropyl-5-methylphenyl)-4-oxothiazolidin-2-ylidene)urea (compound I-3):

[0778] To a stirred solution of 1-(4-aminophenyl)-4-(4-chlorobenzoyl) piperazin-2-one (7) (1.2 g, 3.639 mmol) and N, N'-disuccinimidyl carbonate (1.119 g, 4.366 mmol) in acetonitrile (12 mL) was added N, N-diisopropylethylamine (0.941 g, 7.277 mmol) at rt. The resulting reaction mixture stirred for 30 min at room temperature. After that, 2-imino-3-(2-isopropyl-5-methylphenyl) thiazolidin-4-one (B8) (0.904 g, 3.639 mmol) was added at room temperature and continue the reaction at same temperature for 4 h. After completion, the reaction mass was quenched with water (100 mL) and extracted with ethyl acetate (3 x 100 mL). The combined organic layer was washed with brine (50 mL), dried over sodium sulfate, filtered and concentrated under reduced pressure. The crude product was purified by a SFC purification to afford 1- (4- (4- (4-chlorobenzoyl)-2-oxopiperazin-1-yl)phenyl)-3-(3-(2-isopropyl-5-methyl phenyl)-4-oxothiazolidin-2-ylidene)urea (compound I-3) (0.312 g, 14%). LC-MS (m / z): 604.33 [M+H]+ion present.1H NMR (400 MHz, DMSO-d6): δ 9.82 (s, 1H), 7.64 (d, J= 8.8 Hz, 2H), 7.60-7.52 (m, 4H), 7.39 (d, J= 8.0 Hz, 1H), 7.27-7.22 (m, 3H), 7.05 (s, 1H), 4.28-4.04 (m, 4H), 3.93-3.70 (m, 4H), 2.69-2.62 (m, 1H), 2.31 (s, 3H), 1.15 (d, J = 6.8 Hz, 3H), 1.08 (d, J= 6.8 Hz, 3H).

[0779] Example 4: Synthesis of (E / Z)-1-(4-(1-(4-chlorobenzoyl)-1,2,3,6-tetrahydropyridin-4-yl)-2-fluorophenyl)-3-(3-(2-isopropyl-5-methylphenyl)-4-oxothiazolidin-2-ylidene)urea (compound 1-15)

[0780]

[0781] Step 1: Synthesis of 3

[0782] To a stirred solution of 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1,2,3,6-tetrahydropyridine hydrochloride (C1) (8 g, 32.579 mmol, 1 equiv.) in dichloromethane (80 mL) was added triethylamine (9.89 g, 97.738 mmol, 3 equiv.) followed by 4-chlorobenzoyl chloride (C2) (6.84 g, 39.095 mmol, 1.2 equiv.) at 0°C, and the reaction mixture was stirred at room temperature for 16 hours. After completion of reaction, the reaction mixture was quenched with water (300 mL) and extracted with DCM (2 x 300 mL). The organic layer was washed with brine (200 mL) and dried over anhydrous sodium sulfate, filtered, and concentrated under reduced pressure to get the crude product. The crude product was triturated with diethyl ether (30 mL), filtered and dried to afford (4-chlorophenyl)(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3,6-dihydropyridin-1(2H)-yl)methanone (C3) (9.5 g, 83.8%). LC-MS (m / z): 348.69 [M+H]+ion present Step 2: Synthesis of (4-(4-amino-3-fluorophenyl)-3,6-dihydropyridin-1(2H)-yl)(4-chlorophenyl)methanone (C5)

[0783] To a stirred solution of (4-chlorophenyl)(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3,6-dihydropyridin-1(2H)-yl)methanone (C3) (2 g, 5.753 mmol, 1 equiv.) in 1,4-dioxane (17 mL) and water (3 mL) were added 4-bromo-2-fluoroaniline (C4) (1.202 g, 6.328 mmol, 1.1 equiv.) and potassium carbonate (1.988 g, 14.382 mmol, 2.5 equiv.) at room temperature and degassed with nitrogen for 10 minutes. Then was added tetrakis(triphenylphosphine)-palladium(0), (0.5 g, 0.575 mmol, 0.1 equiv.) at same temperature and again degassed with nitrogen for 10 minutes. The resultant reaction mixture was heated to 100 °C and stirred for 16 hours. After completion of the reaction, the reaction mass was concentrated under reduced pressure. To the obtained crude mass, water (200 mL) was added and extracted with ethyl acetate (2 x 200 mL). The combined organic layer was washed with saturated brine solution (200 mL), dried over anhydrous sodium sulphate and concentrated to get the crude product. The crude product was purified by column chromatography using silica gel (230-400 mesh) and 25% ethyl acetate in petroleum ether to get (4-(4-amino-3-fluorophenyl)-3,6-dihydropyridin-1(2H)-yl)(4-chlorophenyl)methanone (C5) (1.2 g, 63%). LC-MS (m / z): 331.63 [M+H]+ion present

[0784] Step 3: Synthesis of phenyl (4-(1-(4-chlorobenzoyl)- 1,2,3, 6-tetrahydropyridin-4-yl)-2-fluorophenyl)carbamate (C7)

[0785] To a stirred solution of (4-(4-amino-3-fluorophenyl)-3,6-dihydropyridin-1(2H)-yl)(4-chloro phenyl)methanone (C5) (1.2 g, 3.628 mmol, 1 equiv.) in dichloromethane (18 mL) was added pyridine (0.439 mL, 5.442 mmol, 1.5 equiv.) at room temperature. The resultant reaction mixture was cooled to 0 °C, then was added phenyl carbonochloridate (C6) (0.625 g, 3.990 mmol, 1.1 equiv.) in dichloromethane (6 mL). The resultant reaction mixture was warm to room temperature and stirred for 2 hours (reaction followed by TLC). After completion of reaction, reaction mass was concentrated. To the obtained crude product was dissolved in ethyl acetate (200 mL) and the organic layer was washed with 1N hydrochloric acid (50 mL), saturated sodium bicarbonate (30 mL) and saturated brine solution (50 mL). Then the organic layer was dried over anhydrous sodium sulphate and concentrated to get the crude product. To the obtained crude product was added diethyl ether (5 mL) and stirred for 5 minutes at room temperature. After filtration, the solid was dried for 30 minutes to obtain phenyl (4-(1-(4-chlorobenzoyl)-1,2,3,6-tetrahydropyridin-4-yl)-2-fluorophenyl)carbamate (C7) (0.6 g, 37%), which was used directly for next step without purification.

[0786] Step 4: Synthesis of (Z)-1-(4-(1-(4-chlorobenzoyl)-1,2,3,6-tetrahydropyridin-4-yl)-2-fluoro phenyl)-3-(3-(2-isopropyl-5-methylphenyl)-4-oxothiazolidin-2-ylidene)urea (compound 1-15) To a stirred solution of phenyl (4-(1-(4-chlorobenzoyl)-1,2,3,6-tetrahydropyridin-4-yl)-2-fluorophenyl)carbamate (C7) (0.6 g, 1.331 mmol, 1 equiv.) in dry tetrahydrofuran (12 mL) were added 2-imino-3-(2-isopropyl-5-methylphenyl)thiazolidin-4-one (B8) (0.330 g, 1.331 mmol, 1 equiv.) and N, N-diisopropylethylamine (0.695 mL, 3.992 mmol, 3 equiv.) at room temperature. The reaction mixture was heated to 80 °C and stirred at same temperature for 24 hours. After completion of the reaction, the mass was concentrated. To the obtained crude product was added water (100 mL) and extracted the compound with ethyl acetate (2 x 50 mL). Combined organic layer was washed with saturated brine solution (100 mL) then dried over anhydrous sodium sulphate and concentrated to get the crude product. The crude product was purified by silica gel (230-400 mesh) column chromatography using 30% ethyl acetate in petroleum ether and further purified with reverse phase preparative HPLC to get (E / Z)-1-(4-(1-(4-chlorobenzoyl)-1, 2,3,6-tetrahydropyridin-4-yl)-2-fluorophenyl)-3-(3-(2-isopropyl-5-methylphenyl)-4-oxothiazolidin-2-ylidene)urea (compound 1-15) (0.13 g, 16%). LC-MS (m / z): 605.30 [M+H]+ion present;1H NMR (400 MHz, DMSO-d6): δ 9.34 (s, 1H), 7.59-7.45 (m, 5H), 7.41-7.36 (m, 1H), 7.31-7.18 (m, 3H), 7.05 (s, 1H), 6.32-6.08 (m, 1H), 4.35-3.98 (m, 4H), 3.91-3.48 (m, 2H), 2.67-2.61 (m, 1H), 2.57-2.52 (m, 2H), 2.30 (s, 3H), 1.21-1.04 (m, 6H).

[0787] Example 5: Synthesis of (E / Z)-1-(5-(1-(4-chlorobenzoyl)-1,2,3,6-tetrahydropyridin-4-yl)pyrazin-2-yl)-3-(3-(2-isopropyl-5-methylphenyl)-4-oxothiazolidin-2-ylidene)urea (compound 1-12)

[0788] ci C3

[0789]

[0790] Step 1: Synthesis of (4-(5-aminopyrazin-2-yl)-3,6-dihydropyridin-1(2H)-yl)(4-chlorophenyl) methanone (D2)

[0791] To a stirred solution of (4-chlorophenyl)(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3,6-dihydropyridin-1(2H)-yl)methanone (C3) (1.5 g, 4.315 mmol, 1.0 equiv.) in 1,4-dioxane (12.75 mL, 8.5 V) and water (2.25 mL, 1.5 V) were added 5-bromopyrazin-2-amine (D1) (0.826 g, 4.746 mmol, 1.1 equiv.) and potassium carbonate (1.491 g, 10.787 mmol, 2.5 equiv.) at room temperature. The reaction mass was purged with nitrogen for 10 minutes. Then was added Tetrakis(triphenylphosphine)palladium(0), (0.5 g, 0.431 mmol, 0.1 equiv.) at same temperature and again purged the reaction mass with nitrogen for 10 minutes. Resultant reaction mixture was heated to 100°C and stirred for 4 hours. After completion of the reaction, the reaction mass was concentrated under reduced pressure. To the obtained crude mass, water (20 mL) was added and extracted with ethyl acetate (2x 30 mL). The combined organic layer was washed with saturated brine solution (30 mL). Then the organic layer was dried over anhydrous sodium sulphate and concentrated to get the crude product. Obtained crude product was purified by column chromatography using silica gel (230-400 mesh) and 90% ethyl acetate in petroleum ether to get (4-(5-aminopyrazin-2-yl)-3,6-dihydropyridin-1(2H)-yl)(4-chloro phenyl)methanone (D2) (0.80 g, 59%). LC-MS (m / z): 315.11 [M+H]+ion present.

[0792] Step 2: Synthesis of phenyl (5-(1-(4-chlorobenzoyl)-1,2,3,6-tetrahydropyridin-4-yl)pyrazin-2-yl)carbamate (D4) To a stirred solution of (4-(5-aminopyrazin-2-yl)-3,6-dihydropyridin-1(2H)-yl)(4-chlorophenyl) methanone (D2) (0.8 g, 2.542 mmol, 1.0 equiv.) in dichloromethane (8 mL) was added pyridine (0.308 mL, 3.812 mmol, 1.5 equiv.) at room temperature. Resultant reaction mixture was cooled to 0°C, then was added phenyl carbonochloridate (3) (0.438 g, 2.796 mmol, 1.1equiv.) in dichloromethane (4 mL). The resultant reaction mixture was warmed to room temperature and stirred for 1 hour. After completion of reaction, reaction mass was concentrated to get crude reaction mass. The obtained crude mass was dissolved in ethyl acetate (20 mL) then the organic layer washed with 1N hydrochloric acid (20 mL), saturated sodium bicarbonate (20 mL) and saturated brine solution (10 mL). Then the organic layer was separated, dried over anhydrous sodium sulphate and concentrated to get the crude product. To the obtained crude product was added diethyl ether (10 mL) and stirred for 5 minutes at room temperature. After filtration, the obtained solid was dried for 30 minutes under vacuum to get phenyl (5-(1-(4-chlorobenzoyl)- 1.2.3.6-tetrahydropyridin-4-yl)pyrazin-2-yl)carbamate (4) (0.8 g, 72%). LC-MS (m / z): 435.14 [M+H]+ion present.

[0793] Step 3: Synthesis of (E / Z)-1 -(5-(1 -(4-chlorobenzoyl)- 1,2,3,6-tetrahydropyridin-4-yl)pyrazin-2-yl)-3-(3-(2-isopropyl-5-methylphenyl)-4-oxothiazolidin-2-ylidene)urea (compound 1-12)

[0794] To a stirred solution of phenyl (5-(1-(4-chlorobenzoyl)-1,2,3,6-tetrahydropyridin-4...

Claims

ClaimswhereinB1is N orCRB1;B2is N or CRB2;B3is N or CRB3;B4is N or CRB4;with the proviso that not more than two of B1, B2, B3, or B4are N;W is O, S, or N-RN;RNis H, or Ci-C4-alkyl, wherein the alkyl moiety is unsubstituted or substituted with one or more halogen;Q is a group Q1, Q2, Q3, Q4, or Q5#-N / \l— §Q50wherein # is the bond to the -C(W)- spacer, and § is the bond to the 6-membered ring;RB1, RB2, RB3, and RB4independently of each other are H, halogen, N3, OH, CN, NO2, - SCN, -SF5, C1-C6-alkyl, C1-C6-alkoxy, C2-C6-alkenyl, tri-C1-C6-alkylsilyl, C2-C6- alkynyl, C1-C6-alkoxy-C1-C4-alkyl, C1-C6-alkoxy-C1-C4-alkoxy, C3-C6-cycloalkyl, C3-C6-cycloalkoxy, C3-C6-cycloalkyl-C1-C4-alkyl, C1-C4-alkyl-C3-C6-cycloalkoxy, wherein the alkyl, alkoxy, alkenyl, alkynyl, cycloalkyl and cycloalkoxy moieties are unsubstituted or substituted with one or more halogen; C(=O)-ORa, NRbRc, C1-C6-alkylene-NRbRc, O-C1-C6-alkylene-NRbRc, C1-C6-alkylene-CN, NH-C1-C6- alkylene-NRbRc, C(=O)-NRbRc, C(=O)-Rd, SO2NRbRc, or S(=O)mRe, phenyl, phenoxy, phenylcarbonyl, phenylthio, or -CH2-phenyl, wherein the phenyl rings are unsubstituted or substituted with one or more Rf;R1a, R1b, and R1cindependently of each other are H, halogen, N3, OH, CN, NO2, - SCN, -SF5, C1-C6-alkyl, C1-C6-alkoxy, C2-C6-alkenyl, tri-C1-C6-alkylsilyl, C2-C6- alkynyl, C1-C6-alkoxy-C1-C4-alkyl, C1-C6-alkoxy-C1-C4-alkoxy, C3-C6-cycloalkyl, C3-C6-cycloalkoxy, C3-C6-cycloalkyl-C1-C4-alkyl, C3-C6-cycloalkoxy-C1-C4-alkyl, wherein the alkyl, alkoxy, alkenyl, alkynyl, cycloalkyl and cycloalkoxy moieties are unsubstituted or substituted with one or more halogen; C(=O)-ORa, NRbRc, Ci-C6-alkylene-NRbRc, O-Ci-C6-alkylene-NRbRc, Ci-C6-alkylene-CN, NH-CI-C6-alkylene-NRbRc, C(=O)-NRbRc, C(=O)-Rd, SO2NRbRc, or S(=O)mRe, phenyl, phenoxy, phenylcarbonyl, phenylthio or-CH2-phenyl, wherein phenyl rings are unsubstituted or substituted with one or more Rf; orR1aand R1b, or R1band R1c, form together with the carbon atoms to which they are bonded a 5- or 6-membered partially unsaturated heterocyclic ring, which is unsubstituted or substituted with one or more halogen, CN, Ci-C4-alkyl, or Ci- C4-haloalkyl;m is 0, 1, or 2;R2is a moiety of formula X-Y-Z-T-R3; whereinX is a single bond;-(C(Rxa)2)p-, wherein p is an integer of 1 to 3, preferably 1 or 2; -(C(Rxa)2)0-NRxc-, wherein o is an integer of 1 or 2 and N is bound to Y; or -NRXC-;Y is -CRya=N-, wherein the N is bound to Z;-NRyc-C(=O)-, wherein C(=O) is bound to Z; or-NRyc-C(=S)-, wherein C(=S) is bound to Z;Z is -NRZC-C(=O)-, wherein C(=O) is bound to T;-NRZC-C(=S)-, wherein C(=S) is bound to T;-N=C(S-Rza)-, wherein T is bound to the carbon atom; or-NRzc-C(S-Rza)=, wherein T is bound to the carbon atom;T is O, N or N-RT;R3is aryl, aryl-Ci-C4-alkyl, hetaryl, or hetaryl-Ci-C4-alkyl, wherein the aryl or hetaryl rings are unsubstituted or substituted with one or more Rs and wherein the hetaryl is a 5- or 6-membered monocyclic hetaryl or a 8-, 9- or 10-membered bicyclic hetaryl;and whereinRxa, Ryaare, identical or different, H, halogen, Ci-C6-alkyl, Ci-C6-alkoxy, C2-C6- alkenyl, C2-C6-alkynyl, Ci-C6-alkoxy-Ci-C4-alkyl, C3-C6-cycloalkyl, Ci-C4- alkyl-C3-C6-cycloalkyl, Ci-C4-alkyl-C3-C6-cycloalkoxy, wherein the alkyl, alkoxy, alkenyl, alkynyl, cycloalkyl and cycloalkoxy moieties are unsubstituted or substituted with one or more halogen;Rxc, Ryc, Rzcare, identical or different, H, Ci-C6-alkyl, C2-C6-alkenyl, C2-C6- alkynyl, Ci-C4-alkyl-Ci-C6-alkoxy, C3-C6-cycloalkyl, Ci-C4-alkyl-C3-C6- cycloalkyl, Ci-C4-alkyl-C3-C6-cycloalkoxy, or -NRbRc, wherein the alkyl, alkoxy, alkenyl, alkynyl, cycloalkyl and cycloalkoxy moieties are unsubstituted or substituted with one or more halogen;RTis H, Ci-C6-alkyl, C2-C6-alkenyl, C2-C6-alkynyl, Ci-C4-alkyl-Ci-C6-alkoxy, C3- C6-cycloalkyl, C3-C6-cycloalkyl-Ci-C4-alkyl, C3-C6-cycloalkoxy-Ci-C4-alkyl, wherein the alkyl, alkoxy, alkenyl, alkynyl, cycloalkyl and cycloalkoxy moieties are unsubstituted or substituted with one or more halogen;Rzais H, Ci-C6-alkyl, Ci-C6-alkoxy, C2-C6-alkenyl, tri-Ci-C6-alkylsilyl, C2-C6- alkynyl, Ci-C4-alkyl-Ci-C6-alkoxy, C3-C6-cycloalkyl, Ci-C4-alkyl-C3-C6- cycloalkoxy, Ci-C4-alkyl-C3-C6-cycloalkyl, wherein the alkyl, alkoxy, alkenyl, alkynyl, cycloalkyl and cycloalkoxy moieties are unsubstituted or substitutedwith one or more halogen; Ci-C6-alkylene-NRbRc, Ci-C6-alkylene-CN, C(=O)- NRbRc, C(=O)-Rd, phenyl, phenylcarbonyl, or -CH2-phenyl, wherein the phenyl rings are unsubstituted or substituted with one or more Rf;Rzatogether with RTor Rzcif present, may form a linear Ci-C6-alkylene or a linear C2-C6-alkenylene group, where in the linear Ci-C6-alkylene and the linear C2- C6-alkenylene a CH2moiety is optionally replaced by a carbonyl and / or wherein 1 or 2 CH2moieties are optionally replaced by O or S and / or wherein the linear Ci-C6-alkylene and the linear C2-C6-alkenylene are unsubstituted or substituted with one or more Rh;Ra, Rband Rcare, identical or different, H, Ci-C6-alkyl, C2-C6-alkenyl, C2-C6- alkynyl, Ci-C6-alkoxy-Ci-C4-alkyl, C3-C6-cycloalkyl, C3-C6-cycloalkyl-Ci-C4- alkyl, C3-C6-cycloalkoxy-Ci-C4-alkyl, wherein the alkyl, alkoxy, alkenyl, alkynyl, cycloalkyl and cycloalkoxy moieties are unsubstituted or substituted with one or more halogen, Ci-C6-alkylene-CN, phenyl, or -CH2-phenyl, wherein the phenyl rings are unsubstituted or substituted with one or more Rf;Rdis H, Ci-C6-alkyl, C2-C6-alkenyl, C2-C6-alkynyl, Ci-C6-alkoxy-Ci-C4-alkyl, C3- C6-cycloalkyl, C3-C6-cycloalkyl-Ci-C4-alkyl, C3-C6-cycloalkoxy-Ci-C4-alkyl, wherein the alkyl, alkoxy, alkenyl, alkynyl, cycloalkyl and cycloalkoxy moieties are unsubstituted or substituted with one or more halogen; phenyl, or -CH2-phenyl, wherein the phenyl rings are unsubstituted or substituted with one or more Rf;Reis Ci-C6-alkyl, C3-C6-cycloalkyl, C3-C6-cycloalkyl-Ci-C4-alkyl, wherein the alkyl, cycloalkyl moieties are unsubstituted or substituted with one or more halogen; phenyl or-CH2-phenyl, wherein the phenyl rings are unsubstituted or substituted with one or more Rf;Rfis halogen, N3, OH, CN, NO2, -SON, -SF5, Ci-C6-alkyl, Ci-C6-alkoxy, C2-C6- alkenyl, tri-Ci-C6-alkylsilyl, C2-C6-alkynyl, Ci-C6-alkoxy-Ci-C4-alkyl, Ci-C6- alkoxy-Ci-C4-alkoxy, C3-C6-cycloalkyl, C3-C6-cycloalkoxy, C3-C6-cycloalkyl- Ci-C4-alkyl, C3-C6-cycloalkoxyx-Ci-C4-alkyl, wherein the alkyl, alkoxy, alkenyl, alkynyl, cycloalkyl and cycloalkoxy moieties are unsubstituted or substituted with one or more halogen;Rs is halogen, N3, OH, CN, NO2, -SON, -SF5, Ci-C6-alkyl, Ci-C6-alkoxy, C2-C6- alkenyl, tri-Ci-C6-alkylsilyl, C2-C6-alkynyl, Ci-C6-alkoxy-Ci-C4-alkyl, Ci-C4- alkyl-Ci-C6-alkoxy, Ci-C6-alkoxy-Ci-C4-alkoxy, C3-C6-cycloalkyl, C3-C6- cycloalkoxy, C3-C6-cycloalkyl-Ci-C4-alkyl, C3-C6-cycloalkoxy-Ci-C4-alkyl, wherein the alkyl, alkoxy, alkenyl, alkynyl, cycloalkyl and cycloalkoxy moieties are unsubstituted or substituted with one or more halogen; C(=O)- ORa, NRbRc, Ci-C6-alkylene-NRbRc, O-Ci-C6-alkylene-NRbRc, Ci-C6- alkylene-CN, NH-Ci-C6-alkylene-NRbRc, C(=O)-NRbRc, C(=O)-Rd, SO2NRbRc, or S(=O)mRe;Rhis halogen, OH, Ci-C6-alkyl, C3-C6-cycloalkyl, or CN;and the N-oxides, stereoisomers, tautomers, and agriculturally or veterinarily acceptable salts thereof.

2. The compounds of formula I according to claim 1, whereina) B1is CRB1, B2is CRB2, B3is CRB3, and B4is CRB4; orb) B1is N, B2is CRB2, B3is CRB3, and B4is CRB4; orc) B1is CRB1, B2is N, B3is CRB3, and B4is CRB4; ord) B1is N, B2is CRB2, B3is CRB3, and B4is N; ore) B1is N, B2is CRB2, B3is N, and B4is CRB4; orf) B1is CRB1, B2is N, B3is N, and B4is CRB4.

3. The compounds of formula I according to any of claims 1 or 2, wherein(1) X is a single bond, Y is -CRya=N-, wherein the N is bound to Z, Z is -N=C(S- Rza)-, wherein T is bound to the carbon atom, and T is N-RT, wherein Rzatogether with RTforms a linear Ci-C6-alkylene group, preferably C2alkylene group, where in the linear Ci-C6-alkylene a CH2moiety is replaced by a carbonyl and wherein the linear Ci-C6-alkylene is unsubstituted or substituted with one or more Rh, and Ryais preferably H; or(2) X is a single bond, Y is -NRyc-C(=O)-, wherein C(=O) is bound to Z, Z is - N=C(S-Rza)-, wherein T is bound to the carbon atom, and T is N-RT, wherein Rzatogether with RTforms a linear Ci-C6-alkylene group, preferably C2alkylene group, where in the linear Ci-C6-alkylene a CH2moiety is replaced by a carbonyl and wherein the linear Ci-C6-alkylene is unsubstituted or substituted with one or more Rh, and Rycis preferably H; or(3) X is -(C(Rxa)2)p-, wherein p is 2, Y is -NRyc-C(=O)-, wherein C(=O) is bound to Z, Z is -N=C(S-Rza)-, wherein T is bound to the carbon atom, and T is N-RT, wherein Rzatogether with RTforms a linear Ci-C6-alkylene group, preferably C2alkylene group, where in the linear Ci-C6-alkylene a CH2moiety is replaced by a carbonyl and wherein the linear Ci-C6-alkylene is unsubstituted or substituted with one or more Rh, and all Rxaand Rycare preferably H; or(4) X is -(C(Rxa)2)0-NRxc-, wherein o is 1 and N is bound to Y, Y is -NRyc-C(=O)-, wherein C(=O) is bound to Z, Z is -N=C(S-Rza)-, wherein T is bound to the carbon atom, and T is N-RT, wherein Rzatogether with RTforms a linear Ci-C6-alkylene group, preferably C2alkylene group, where in the linear Ci-C6-alkylene a CH2moiety is replaced by a carbonyl and wherein the linear Ci-C6-alkylene is unsubstituted or substituted with one or more Rh, wherein one Rxa, Rxcand Rycare preferably H and the other Rxais preferably methyl, or wherein one Rxaand Rycare preferably H and the other Rxaand Rxcare preferably methyl; or (5) X is -(C(Rxa)2)0-NRxc-, wherein o is 1 and N is bound to Y, Y is -NRyc-C(=O)-, wherein C(=O) is bound to Z, Z is -NRZC-C(=S)-, wherein C(=S) is bound to T, and T is N-RT, wherein one Rxa, Rxc, Ryc, Rzcand RTare preferably H and the other Rxais preferably methyl, or wherein one Rxa, Ryc, Rzcand RTare preferably H and the other Rxaand Rxcare preferably methyl; or(6) X is -(C(Rxa)2)p-, wherein p is 1, Y is -NRyc-C(=O)-, wherein C(=O) is bound to Z, Z is -NRzc-C(=S)-, wherein C(=S) is bound to T, and T is N-RT, wherein oneRxa, Rzcand RTare preferably H, the other Rxais preferably methyl, and Rycis preferably -NH2; or(7) X is -(C(Rxa)2)0-NRxc-, wherein o is 1 and N is bound to Y, Y is -NRyc-C(=O)-, wherein C(=O) is bound to Z, Z is -NRZC-C(=S)-, wherein C(=S) is bound to T, and T is N-RT, wherein one Rxa, Ryc, Rzcand RTare preferably H and the other Rxaand Rxcare preferably methyl; or(8) X is -(C(Rxa)2)0-NRxc-, wherein o is 1 and N is bound to Y, Y is -NRyc-C(=O)-, wherein C(=O) is bound to Z, Z is -N=C(S-Rza)-, wherein T is bound to the carbon atom, and T is N-RT, wherein Rzatogether with RTforms a linear Ci-C6-alkylene group, preferably C2alkylene group, where in the linear Ci-C6-alkylene a CH2moiety is replaced by a carbonyl and wherein the linear Ci-C6-alkylene is unsubstituted or substituted with one or more Rh, and one Rxaand Rycare preferably H and the other Rxaand Rxcare preferably methyl;(9) X is a single bond, Y is -CRya=N-, wherein the N is bound to Z, Z is -NRZC- C(=S)-, wherein C(=S) is bound to T and T is N-RT, wherein Rya, Rzc, and RTare preferably H; or(10) X is a single bond, Y is -NRyc-C(=O)-, wherein C(=O) is bound to Z, Z is -NRZC- C(=S)-, wherein C(=S) is bound to T and T is N-RT, wherein Ryc, Rzc, and RTare preferably H.

4. The compounds of formula I according to any of claims 1 to 3, whereinR3is monocyclic or bicyclic aryl substituted with one or more R9, preferably phenyl, naphthyl, or pyridinyl substituted with one or more R9.

5. The compounds of formula I according to any of claims 1 to 4, whereinR1a, R1b, and R1cindependently of each other are halogen, OH, Ci-C6-alkyl, Ci-C6- haloalkyl, Ci-C6-alkoxy, Ci-C6-haloalkoxy, or S-Re;Reis Ci-C6-alkyl, C3-C6-cycloalkyl, C3-C6-cycloalkyl-Ci-C4-alkyl, wherein the alkyl, cycloalkyl moieties are unsubstituted or substituted with one or more halogen; and RB1, RB2, RB3, and RB4independently of each other are H, halogen, Ci-C6-alkyl, Ci-C6- alkoxy, C2-C6-alkenyl, C2-C6-alkynyl, wherein the alkyl, alkoxy, alkenyl, alkynyl, moieties are unsubstituted or substituted with one or more halogen.

6. The compounds of formula I according to any of claims 1 to 5, wherein R2is selected from the following groups:O sR2-3,R2-5, R2-6,R2-9, or R2-10.

7. The compounds of formula I according to any of claims 1 to 6, wherein R3is selectedR3-8,R3-12,R3-19, R3-20,R3-21, R3-22, R3-23, R3-24,preferably, wherein R3is R3-1, R3-29, R3-30, or R3-31.

8. The compounds of formula I according to any of claims 1 to 7, wherein the compounds are selected from the following compounds:No. R1aR1bw Q B1B2B3B4R2R31-1 H Cl 0 Q1CH CH CH N R2-1 R3-29 I-2 H Cl 0 Q1CH CH CH N R2-4 R3-29 I-3 H Cl 0 Q5CH CH CH CH R2-2 R3-29 I-4 H Cl 0 Q3CH CH CH N R2-2 R3-29 I-5 H Cl 0 Q3CH CH CH N R2-4 R3-29 I-6 H Cl 0 Q3CH CH CH N R2-1 R3-29 I-7 H Cl 0 Q3CH CCl CH CH R2-2 R3-29 I-8 H OCF30 Q3CH CCl CH CH R2-2 R3-29 I-9 H Cl 0 Q3CCl CH CH CH R2-1 R3-29 1-10 H OCF30 Q3CH CH CH N R2-1 R3-29 1-11 H Cl 0 Q3CH N CH N R2-1 R3-29 1-12 H Cl 0 Q3CH N CH N R2-2 R3-29 1-13 H Cl 0 Q4CH CCI CH CH R2-2 R3-29 1-14 H Cl 0 Q3CCl CH CH CH R2-4 R3-29 1-15 H Cl 0 Q3CH CF CH CH R2-2 R3-29 1-16 H OCF30 Q3CH CH CH N R2-4 R3-29 1-17 H OCF30 Q2CH CCl CH CH R2-2 R3-29 1-18 H Cl 0 Q2CH CCl CH CH R2-2 R3-29 1-19 H OCF30 Q2CH CF CH CH R2-3 R3-29 I-20 H OCF30 Q2CH CF CH CH R2-2 R3-29 1-21 H Cl 0 Q2CH CF CH CH R2-2 R3-29 I-22 Cl F 0 Q2CH CF CH CH R2-2 R3-29 I-23 Cl F 0 Q2CH CCI CH CH R2-2 R3-29I-24 H OCF30 Q2CH CF CH CH R2-2 R3-31No. R1aR1bW Q B1B2B3B4R2R3I-25 OCF3H 0 Q2CH CCI CH CH R2-2 R3-29 I-26 OCF3Cl 0 Q2CH CCI CH CH R2-2 R3-29 I-27 OCF3F 0 Q2CH CCI CH CH R2-2 R3-29 I-28 H OCF30 Q2CH CCI CH CH R2-7 R3-29 I-29 Cl F 0 Q2CH CCI CH CH R2-7 R3-29 I-30 H Cl 0 Q2CH CCI CH CH R2-7 R3-29 I-31 Cl F 0 Q2CH N CH N R2-2 R3-29 I-32 H OCF30 Q2CH CCI CH CH R2-9 R3-29 I-33 Cl F 0 Q2CH CCI CH CH R2-9 R3-29 I-34 H OCF30 Q2CH CF CH CH R2-7 R3-29 I-35 Cl Cl 0 Q2CH CCI CH CH R2-2 R3-30 I-36 H OCH20 Q2CH CH CH CH R2-2 R3-29CH3I-37 Cl F 0 Q2CH CF CH CH R2-7 R3-29 I-38 H OCF30 Q2CH CH CH CH R2-1 R3-29 I-39 H OCF30 Q2CCI CH CH CH R2-1 R3-29 I-40 H OCF30 Q2CH CF CH CH R2-9 R3-29 I-41 H Br 0 Q2N CH CH CH R2-1 R3-1 I-42 H Cl 0 Q2CH CCI CH CH R2-7 R3-29 I-43 H Cl 0 Q2CCI CH CH CH R2-1 R3-30 I-44 Cl F 0 Q2CH CF CH CH R2-9 R3-29 I-45 H CN 0 Q2CH CBr CH CH R2-2 R3-29 I-46 H OCF30 Q2CCI CH CH CH R2-4 R3-29 I-47 H OCF30 Q2CH CH CH CH R2-2 R3-29 I-48 H 2,2- 0 Q2CH CBr CH CH R2-2 R3-1Cl2- cyclo- propylI-49 H OCF30 Q2CH CCI CH CH R2-3 R3-29 I-50 Cl Cl 0 Q2CCI CH CH CH R2-1 R3-7 I-51 -OCF2-O- 0 Q2CH CF CH CH R2-2 R3-29 I-52 H OCF3NH Q2CH CCI CH CH R2-2 R3-29 I-53 H OCF30 Q2N CH CH N R2-2 R3-29 I-54 H OCF30 Q2N CH CH N R2-7 R3-29 I-55 H OCF30 Q2CH CH CH N R2-7 R3-29 I-56 H OCF3S Q2CH CCI CH CH R2-2 R3-29 I-57 H OCF30 Q2CH N CH CH R2-2 R3-29 I-58 H OCF30 Q2CH CH CH N R2-2 R3-29I-59 F OCF30 Q2CH CCI CH CH R2-2 R3-29 wherein R1cis H.

9. An agricultural or veterinary composition comprising at least one compound according to any one of claims 1 to 8 and / or at least one agriculturally or veterinarily acceptable salt thereof, and at least one inert liquid and / or solid agriculturally or veterinarily acceptable carrier.

10. An agricultural composition for combating animal pests comprising at least one compound as defined in any of claims 1 to 8 and at least one inert liquid and / or solid acceptable carrier and, if desired, at least one surfactant.

11. A method for combating or controlling invertebrate pests, which method comprises contacting said pest or its food supply, habitat or breeding grounds with a pesticidally effective amount of at least one compound as defined in any one of claims 1 to 8.

12. A method for protecting growing plants from attack or infestation by invertebrate pests, which method comprises contacting a plant, or soil or water in which the plant is growing, with a pesticidally effective amount of at least one compound as defined in any of claims 1 to 8.

13. Seed comprising a compound as defined in any of claims 1 to 8, or the enantiomers, diastereomers or salts thereof, in an amount of from 0.1 g to 10 kg per 100 kg of seed.

14. A method for treating or protecting an animal from infestation or infection by invertebrate pests which comprises bringing the animal in contact with a pesticidally effective amount of at least one compound of the formula I as defined in any of claims 1 to 8, a stereoisomer thereof and / or at least one veterinarily acceptable salt thereof.

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