IP Library Granted Patent US 11,339,155
Granted Patent B2
US 11,339,155 · App. 16/339,685 · Granted May 24, 2022

2-(het)aryl-substituted fused bicyclic heterocycle derivatives as pesticides

Inventors: Ruediger Fischer (Pulheim, DE); Dominik Hager (Monheim, DE); Laura Hoffmeister (Duesseldorf, DE); Nina Kausch-Busies (Bergisch Gladbach, DE); Marc Mosrin (Cologne, DE); David Wilcke (Duesseldorf, DE); Matthieu Willot (Duesseldorf, DE); Kerstin Ilg (Cologne, DE); Daniela Portz (Vettweiss, DE); Ulrich Goergens (Ratingen, DE); Andreas Turberg (Haan, DE)
Assignees: Bayer CropScience Aktiengesellschaft; Bayer Aktiengesellschaft
C07D471/04A01N43/90
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Quick Facts
Patent No.
US 11,339,155
App. No.
16/339,685
Granted
May 24, 2022
Kind
B2
Abstract

The invention relates to novel compounds of the formula (I) in which R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , R 7 , R 8 , A 1 , A 2 , A 3 and n each have the meanings given above, to their use as acaricides and/or insecticides for controlling animal pests and to processes and intermediates for their preparation.

Claims (113)

1. A compound of formula (I)

wherein

A 1 represents nitrogen, ═N + (O − )— or ═C(R 4 )—,

A 2 represents —N(R 5 )—, oxygen or sulfur,

A 3 represents oxygen or sulfur,

R 1 represents (C 1 -C 6 )-alkyl, (C 1 -C 6 )-haloalkyl, (C 1 -C 6 )-cyanoalkyl, (C 1 -C 6 )-hydroxyalkyl, (C 1 -C 6 )-alkoxy-(C 1 -C 6 )-alkyl, (C 1 -C 6 )-haloalkoxy-(C 1 -C 6 )-alkyl, (C 2 -C 6 )-alkenyl, (C 2 -C 6 )-alkenyloxy-(C 1 -C 6 )-alkyl, (C 2 -C 6 )-haloalkenyloxy-(C 1 -C 6 )-alkyl, (C 2 -C 6 )-haloalkenyl, (C 2 -C 6 )-cyanoalkenyl, (C 2 -C 6 )-alkynyl, (C 2 -C 6 )-alkynyloxy-(C 1 -C 6 )-alkyl, (C 2 -C 6 )-haloalkynyloxy-(C 1 -C 6 )-alkyl, (C 2 -C 6 )-haloalkynyl, (C 2 -C 6 )-cyanoalkynyl, (C 3 -C 8 )-cycloalkyl, (C 3 -C 8 )-cycloalkyl-(C 3 -C 8 )-cycloalkyl, (C 1 -C 6 )-alkyl-(C 3 -C 8 )-cycloalkyl, halo-(C 3 -C 8 )-cycloalkyl, amino, (C 1 -C 6 )-alkylamino, di-(C 1 -C 6 )-alkylamino, (C 3 -C 8 )-cycloalkylamino, (C 1 -C 6 )-alkylcarbonylamino, (C 1 -C 6 )-alkylthio-(C 1 -C 6 )-alkyl, (C 1 -C 6 )-haloalkylthio-(C 1 -C 6 )-alkyl, (C 1 -C 6 )-alkylsulfinyl-(C 1 -C 6 )-alkyl, (C 1 -C 6 )-haloalkylsulfinyl-(C 1 -C 6 )-alkyl, (C 1 -C 6 )-alkylsulfonyl-(C 1 -C 6 )-alkyl, (C 1 -C 6 )-haloalkylsulfonyl-(C 1 -C 6 )-alkyl, (C 1 -C 6 )-alkoxy-(C 1 -C 6 )-alkylthio-(C 1 -C 6 )-alkyl, (C 1 -C 6 )-alkoxy-(C 1 -C 6 )-alkylsulfinyl-(C 1 -C 6 )-alkyl, (C 1 -C 6 )-alkoxy-(C 1 -C 6 )-alkylsulfonyl-(C 1 -C 6 )-alkyl, (C 1 -C 6 )-alkylcarbonyl-(C 1 -C 6 )-alkyl, (C 1 -C 6 )-haloalkylcarbonyl-(C 1 -C 6 )alkyl, (C 1 -C 6 )-alkoxycarbonyl-(C 1 -C 6 )-alkyl, (C 1 -C 6 )-haloalkoxycarbonyl-(C 1 -C 6 )-alkyl, (C 1 -C 6 )-alkylsulfonylamino, aminosulfonyl-(C 1 -C 6 )-alkyl, (C 1 -C 6 )-alkylaminosulfonyl-(C 1 -C 6 )-alkyl, di-(C 1 -C 6 )-alkylaminosulfonyl-(C 1 -C 6 )-alkyl,

or represents (C 1 -C 6 )-alkyl, (C 1 -C 6 )-alkoxy, (C 2 -C 6 )-alkenyl, (C 2 -C 6 )-alkynyl, (C 3 -C 8 )-cycloalkyl, each of which is optionally mono- or polysubstituted by identical or different substituents from the group consisting of aryl, hetaryl and heterocyclyl, where aryl, hetaryl or heterocyclyl may each optionally be mono- or polysubstituted by identical or different substituents from the group consisting of halogen, cyano, nitro, hydroxy, amino, carboxy, carbamoyl, aminosulfonyl, (C 1 -C 6 )-alkyl, (C 3 -C 6 )-cycloalkyl, (C 1 -C 6 )-alkoxy, (C 1 -C 6 )-haloalkyl, (C 1 -C 6 )-haloalkoxy, (C 1 -C 6 )-alkylthio, (C 1 -C 6 )-alkylsulfinyl, (C 1 -C 6 )-alkylsulfonyl, (C 1 -C 6 )-alkylsulfimino, (C 1 -C 6 )-alkylsulfimino-(C 1 -C 6 )-alkyl, (C 1 -C 6 )-alkylsulfimino-(C 2 -C 6 )-alkylcarbonyl, (C 1 -C 6 )-alkylsulfoximino, (C 1 -C 6 )-alkylsulfoximino-(C 1 -C 6 )-alkyl, (C 1 -C 6 )-alkylsulfoximino-(C 2 -C 6 )-alkylcarbonyl, (C 1 -C 6 )-alkoxycarbonyl, (C 1 -C 6 )-alkylcarbonyl, (C 3 -C 6 )-trialkylsilyl and benzyl, or

R 1 represents aryl or hetaryl, each of which is optionally mono- or polysubstituted by identical or different substituents from the group consisting of halogen, cyano, nitro, hydroxy, amino, carboxyl, carbamoyl, (C 1 -C 6 )-alkyl, (C 3 -C 8 )-cycloalkyl, (C 1 -C 6 )-alkoxy, (C 1 -C 6 )-haloalkyl, (C 1 -C 6 )-haloalkoxy, (C 1 -C 6 )-alkylthio, (C 1 -C 6 )-alkylsulfinyl, (C 1 -C 6 )-alkylsulfonyl, (C 1 -C 6 )-alkylsulfimino, (C 1 -C 6 )-alkylsulfimino-(C 1 -C 6 )-alkyl, (C 1 -C 6 )-alkylsulfimino-(C 2 -C 6 )-alkylcarbonyl, (C 1 -C 6 )-alkylsulfoximino, (C 1 -C 6 )-alkylsulfoximino-(C 1 -C 6 )-alkyl, (C 1 -C 6 )-alkylsulfoximino-(C 2 -C 6 )-alkylcarbonyl, (C 1 -C 6 )-alkoxycarbonyl, (C 1 -C 6 )-alkylcarbonyl, and (C 3 -C 6 )-trialkylsilyl, or

R 1 represents heterocyclyl, which is optionally mono- or polysubstituted by identical or different substituents from the group consisting of halogen, cyano, nitro, hydroxy, amino, carboxyl, carbamoyl, (C 1 -C 6 )-alkyl, (C 3 -C 8 )-cycloalkyl, (C 1 -C 6 )-alkoxy, (C 1 -C 6 )-haloalkyl, (C 1 -C 6 )-haloalkoxy, (C 1 -C 6 )-alkylthio, (C 1 -C 6 )-alkylsulfinyl, (C 1 -C 6 )-alkylsulfonyl, (C 1 -C 6 )-alkylsulfimino, (C 1 -C 6 )-alkylsulfimino-(C 1 -C 6 )-alkyl, (C 1 -C 6 )-alkylsulfimino-(C 2 -C 6 )-alkylcarbonyl, (C 1 -C 6 )-alkylsulfoximino, (C 1 -C 6 )-alkylsulfoximino-(C 1 -C 6 )-alkyl, (C 1 -C 6 )-alkylsulfoximino-(C 2 -C 6 )-alkylcarbonyl, (C 1 -C 6 )-alkoxycarbonyl, (C 1 -C 6 )-alkylcarbonyl, (C 3 -C 6 )-trialkylsilyl, (═O) and (═O) 2 ,

R 2 , R 3 , R 4 and R 6 independently of one another represent hydrogen, cyano, halogen, nitro, acetyl, hydroxy, amino, SCN, tri-(C 1 -C 6 )-alkylsilyl, (C 3 -C 8 )-cycloalkyl, (C 3 -C 8 )-cycloalkyl-(C 3 -C 8 )-cycloalkyl, (C 1 -C 6 )-alkyl-(C 3 -C 8 )-cycloalkyl, halo-(C 3 -C 8 )-cycloalkyl, (C 1 -C 6 )-alkyl, (C 1 -C 6 )-haloalkyl, (C 1 -C 6 )-cyanoalkyl, (C 1 -C 6 )-hydroxyalkyl, hydroxycarbonyl-(C 1 -C 6 )-alkoxy, (C 1 -C 6 )-alkoxycarbonyl-(C 1 -C 6 )-alkyl, (C 1 -C 6 )-alkoxy-(C 1 -C 6 )-alkyl, (C 2 -C 6 )-alkenyl, (C 2 -C 6 )-haloalkenyl, (C 2 -C 6 )-cyanoalkenyl, (C 2 -C 6 )-alkynyl, (C 2 -C 6 )-haloalkynyl, (C 2 -C 6 )-cyanoalkynyl, (C 1 -C 6 )-alkoxy, (C 1 -C 6 )-haloalkoxy, (C 1 -C 6 )-cyanoalkoxy, (C 1 -C 6 )-alkoxycarbonyl-(C 1 -C 6 )-alkoxy, (C 1 -C 6 )-alkoxy-(C 1 -C 6 )-alkoxy, (C 1 -C 6 )-alkylhydroxyimino, (C 1 -C 6 )-alkoxyimino, (C 1 -C 6 )-alkyl-(C 1 -C 6 )-alkoxyimino, (C 1 -C 6 )-haloalkyl-(C 1 -C 6 )-alkoxyimino, (C 1 -C 6 )-alkylthio, (C 1 -C 6 )-haloalkylthio, (C 1 -C 6 )-alkoxy-(C 1 -C 6 )-alkylthio, (C 1 -C 6 )-alkylthio-(C 1 -C 6 )-alkyl, (C 1 -C 6 )-alkylsulfinyl, (C 1 -C 6 )-haloalkylsulfinyl, (C 1 -C 6 )-alkoxy-(C 1 -C 6 )-alkylsulfinyl, (C 1 -C 6 )-alkylsulfinyl-(C 1 -C 6 )-alkyl, (C 1 -C 6 )-alkylsulfonyl, (C 1 -C 6 )-haloalkylsulfonyl, (C 1 -C 6 )-alkoxy-(C 1 -C 6 )-alkylsulfonyl, (C 1 -C 6 )-alkylsulfonyl-(C 1 -C 6 )-alkyl, (C 1 -C 6 )-alkylsulfonyloxy, (C 1 -C 6 )-alkylcarbonyl, (C 1 -C 6 )-alkylthiocarbonyl, (C 1 -C 6 )-haloalkylcarbonyl, (C 1 -C 6 )-alkylcarbonyloxy, (C 1 -C 6 )-alkoxycarbonyl, (C 1 -C 6 )-haloalkoxycarbonyl, aminocarbonyl, (C 1 -C 6 )-alkylaminocarbonyl, (C 1 -C 6 )-alkylaminothiocarbonyl, di-(C 1 -C 6 )-alkylaminocarbonyl, di-(C 1 -C 6 )-alkylaminothiocarbonyl, (C 2 -C 6 )-alkenylaminocarbonyl, di-(C 2 -C 6 )-alkenylaminocarbonyl, (C 3 -C 8 )-cycloalkylaminocarbonyl, (C 1 -C 6 )-alkylsulfonylamino, (C 1 -C 6 )-alkylamino, di-(C 1 -C 6 )-alkylamino, aminosulfonyl, (C 1 -C 6 )-alkylaminosulfonyl, di-(C 1 -C 6 )-alkylaminosulfonyl, (C 1 -C 6 )-alkylsulfoximino, aminothiocarbonyl, (C 1 -C 6 )-alkylaminothiocarbonyl, di-(C 1 -C 6 )-alkyl-aminothiocarbonyl, (C 3 -C 8 )-cycloalkylamino, NHCO—(C 1 -C 6 )-alkyl ((C 1 -C 6 )-alkylcarbonylamino), SF 5 or represent aryl or hetaryl, each of which is optionally mono- or polysubstituted by identical or different substituents, where in the case of hetaryl at least one carbonyl group may optionally be present and/or where optional substituents are in each case as follows: cyano, carboxyl, halogen, nitro, acetyl, hydroxy, amino, SCN, tri-(C 1 -C 6 )-alkylsilyl, (C 1 -C 6 )-alkyl, (C 1 -C 6 )-haloalkyl, (C 1 -C 6 )-cyanoalkyl, (C 1 -C 6 )-hydroxyalkyl, hydroxycarbonyl-(C 1 -C 6 )-alkoxy, (C 1 -C 6 )-alkoxycarbonyl-(C 1 -C 6 )-alkyl, (C 1 -C 6 )-alkoxy-(C 1 -C 6 )-alkyl, (C 2 -C 6 )-alkenyl, (C 2 -C 6 )-haloalkenyl, (C 2 -C 6 )-cyanoalkenyl, (C 2 -C 6 )-alkynyl, (C 2 -C 6 )-haloalkynyl, (C 2 -C 6 )-cyanoalkynyl, (C 1 -C 6 )-alkoxy, (C 1 -C 6 )-haloalkoxy, (C 1 -C 6 )-cyanoalkoxy, (C 1 -C 6 )-alkoxycarbonyl-(C 1 -C 6 )-alkoxy, (C 1 -C 6 )-alkoxy-(C 1 -C 6 )-alkoxy, (C 1 -C 6 )-alkylhydroxyimino, (C 1 -C 6 )-alkoxyimino, (C 1 -C 6 )-alkyl-(C 1 -C 6 )-alkoxyimino, (C 1 -C 6 )-haloalkyl-(C 1 -C 6 )-alkoxyimino, (C 1 -C 6 )-alkylthio, (C 1 -C 6 )-haloalkylthio, (C 1 -C 6 )-alkoxy-(C 1 -C 6 )-alkylthio, (C 1 -C 6 )-alkylthio-(C 1 -C 6 )-alkyl, (C 1 -C 6 )-alkylsulfinyl, (C 1 -C 6 )-haloalkylsulfinyl, (C 1 -C 6 )-alkoxy-(C 1 -C 6 )-alkylsulfinyl, (C 1 -C 6 )-alkylsulfinyl-(C 1 -C 6 )-alkyl, (C 1 -C 6 )-alkylsulfonyl, (C 1 -C 6 )-haloalkylsulfonyl, (C 1 -C 6 )-alkoxy-(C 1 -C 6 )-alkylsulfonyl, (C 1 -C 6 )-alkylsulfonyl-(C 1 -C 6 )-alkyl, (C 1 -C 6 )-alkylsulfonyloxy, (C 1 -C 6 )-alkylcarbonyl, (C 1 -C 6 )-haloalkylcarbonyl, (C 1 -C 6 )-alkylcarbonyloxy, (C 1 -C 6 )-alkoxycarbonyl, (C 1 -C 6 )-haloalkoxycarbonyl, aminocarbonyl, (C 1 -C 6 )-alkylaminocarbonyl, di-(C 1 -C 6 )-alkyl-aminocarbonyl, (C 2 -C 6 )-alkenylaminocarbonyl, di-(C 2 -C 6 )-alkenylaminocarbonyl, (C 3 -C 8 )-cycloalkylaminocarbonyl, (C 1 -C 6 )-alkylsulfonylamino, (C 1 -C 6 )-alkylamino, di-(C 1 -C 6 )-alkylamino, aminosulfonyl, (C 1 -C 6 )-alkylaminosulfonyl, di-(C 1 -C 6 )-alkylaminosulfonyl, (C 1 -C 6 )-alkylsulfoximino, aminothiocarbonyl, (C 1 -C 6 )-alkylaminothiocarbonyl, di-(C 1 -C 6 )-alkylaminothiocarbonyl, (C 3 -C 8 )-cycloalkylamino,

R 5 represents (C 1 -C 6 )-alkyl, (C 1 -C 6 )-haloalkyl, (C 1 -C 6 )-cyanoalkyl, (C 1 -C 6 )-hydroxyalkyl, (C 1 -C 6 )-alkoxy-(C 1 -C 6 )-alkyl, (C 1 -C 6 )-haloalkoxy-(C 1 -C 6 )-alkyl, (C 2 -C 6 )-alkenyl, (C 2 -C 6 )-alkenyloxy-(C 1 -C 6 )-alkyl, (C 2 -C 6 )-haloalkenyloxy-(C 1 -C 6 )-alkyl, (C 2 -C 6 )-haloalkenyl, (C 2 -C 6 )-cyanoalkenyl, (C 2 -C 6 )-alkynyl, (C 2 -C 6 )-alkynyloxy-(C 1 -C 6 )-alkyl, (C 2 -C 6 )-haloalkynyloxy-(C 1 -C 6 )-alkyl, (C 2 -C 6 )-haloalkynyl, (C 2 -C 6 )-cyanoalkynyl, (C 3 -C 8 )-cycloalkyl, (C 3 -C 8 )-cycloalkyl-(C 3 -C 8 )-cycloalkyl, (C 1 -C 6 )-alkyl-(C 3 -C 8 )-cycloalkyl, halo-(C 3 -C 8 )-cycloalkyl, (C 1 -C 6 )-alkylthio-(C 1 -C 6 )-alkyl, (C 1 -C 6 )-haloalkylthio-(C 1 -C 6 )-alkyl, (C 1 -C 6 )-alkylsulfinyl-(C 1 -C 6 )-alkyl, (C 1 -C 6 )-haloalkylsulfinyl-(C 1 -C 6 )-alkyl, (C 1 -C 6 )-alkylsulfonyl-(C 1 -C 6 )-alkyl, (C 1 -C 6 )-haloalkylsulfonyl-(C 1 -C 6 )-alkyl, (C 1 -C 6 )-alkoxy-(C 1 -C 6 )-alkylthio-(C 1 -C 6 )-alkyl, (C 1 -C 6 )-alkoxy-(C 1 -C 6 )-alkylsulfinyl-(C 1 -C 6 )-alkyl, (C 1 -C 6 )-alkoxy-(C 1 -C 6 )-alkylsulfonyl-(C 1 -C 6 )-alkyl, (C 1 -C 6 )-alkylcarbonyl-(C 1 -C 6 )-alkyl, (C 1 -C 6 )-haloalkylcarbonyl-(C 1 -C 6 )-alkyl, (C 1 -C 6 )-alkoxycarbonyl-(C 1 -C 6 )-alkyl, (C 1 -C 6 )-haloalkoxycarbonyl-(C 1 -C 6 )-alkyl, aminocarbonyl-(C 1 -C 6 )-alkyl, (C 1 -C 6 )-alkylamino-(C 1 -C 6 )-alkyl, di-(C 1 -C 6 )-alkylamino-(C 1 -C 6 )-alkyl or (C 3 -C 8 )-cycloalkylamino-(C 1 -C 6 )-alkyl,

R 7 represents hydrogen or represents (C 1 -C 6 )-alkyl, (C 1 -C 6 )-alkoxy-(C 1 -C 6 )-alkyl, (C 2 -C 6 )-alkenyl, (C 2 -C 6 )-alkynyl, (C 3 -C 6 )-cycloalkyl, (C 3 -C 12 )-cycloalkyl-(C 1 -C 6 )-alkyl or (C 4 -C 12 )-bicycloalkyl, each of which is optionally mono- or polysubstituted by identical or different substituents, where the substituents independently of one another may be selected from the group consisting of halogen, cyano, nitro, hydroxy, (C 1 -C 6 )-alkyl, (C 1 -C 4 )-haloalkyl, (C 3 -C 6 )-cycloalkyl, (C 1 -C 4 )-alkoxy, (C 1 -C 4 )-haloalkoxy, (C 1 -C 4 )-alkylthio, (C 1 -C 4 )-alkylsulfinyl, (C 1 -C 4 )-alkylsulfonyl, (C 2 -C 6 )-alkoxycarbonyl, (C 2 -C 6 )-alkylcarbonyl, amino, (C 1 -C 4 )-alkylamino, di-(C 1 -C 4 -alkyl)amino, (C 3 -C 6 )-cycloalkylamino, a phenyl ring or a 3- or 6-membered aromatic, partially saturated or saturated heterocycle, where the phenyl ring or heterocycle may in each case optionally be mono- or polysubstituted by identical or different substituents, and where the substituents independently of one another may be selected from the group consisting of (C 1 -C 6 )-alkyl, (C 2 -C 6 )-alkenyl, (C 2 -C 6 )-alkynyl, (C 3 -C 6 )-cycloalkyl, (C 1 -C 6 )-haloalkyl, (C 2 -C 6 )-haloalkenyl, (C 2 -C 6 )-haloalkynyl, (C 3 -C 6 )-halocycloalkyl, halogen, cyano, NO 2 , OH, (C 1 -C 4 )-alkoxy, (C 1 -C 4 )-haloalkoxy, (C 1 -C 4 )-alkylthio, (C 1 -C 4 )-alkylsulfinyl, (C 1 -C 4 )-alkylsulfonyl, (C 1 -C 4 )-haloalkylthio, (C 1 -C 4 )-haloalkylsulfinyl, (C 1 -C 4 )-haloalkylsulfonyl, (C 1 -C 4 )-alkylamino, di-(C 1 -C 4 -alkyl)amino, (C 3 -C 6 )-cycloalkylamino, (C 1 -C 6 -alkyl)carbonyl, (C 1 -C 6 -alkoxy)carbonyl, aminocarbonyl, (C 1 -C 6 -alkyl)aminocarbonyl, di-(C 1 -C 4 -alkyl)aminocarbonyl,

R 8 represents amino or (C 1 -C 6 )-alkylamino, di-(C 1 -C 4 )-alkylamino, (C 2 -C 6 )-alkenylamino, (C 2 -C 6 )-alkynylamino, (C 3 -C 12 )-cycloalkylamino, (C 3 -C 12 )-cycloalkyl-(C 1 -C 6 )-alkylamino, (C 4 -C 12 )-bicycloalkylamino or hydrazino, each of which is optionally mono- or polysubstituted by identical or different substituents, where the substituents independently of one another may be selected from the group consisting of halogen, cyano, amino, nitro, hydroxy, (C═O)OH, (C 1 -C 6 )-alkyl, (C 3 -C 6 )-cycloalkyl, (C 1 -C 4 )-alkoxy, (C 1 -C 4 )-haloalkoxy, (C 1 -C 4 )-alkylthio, (C 1 -C 4 )-haloalkylthio, (C 1 -C 4 )-alkylsulfinyl, (C 1 -C 4 )-haloalkylsulfinyl, (C 1 -C 4 )-alkylsulfonyl, (C 1 -C 4 )-haloalkylsulfonyl, (C 1 -C 4 )-alkylsulfimino, (C 1 -C 4 )-alkylsulfoximino, (C 2 -C 6 )-alkoxycarbonyl, (C 2 -C 6 )-alkylcarbonyl, (C 1 -C 6 )-alkylthiocarbonyl, (C 1 -C 6 )-haloalkylcarbonyl, (C 1 -C 6 )-haloalkylthiocarbonyl, (C 1 -C 6 )-alkylcarbonylamino, aminocarbonyl, (C 1 -C 6 )-alkylaminocarbonyl, di-(C 1 -C 6 )-alkylaminocarbonyl, aminothiocarbonyl, (C 1 -C 6 )-alkylaminothiocarbonyl, di-(C 1 -C 6 )-alkylaminothiocarbonyl, (C 3 -C 6 )-trialkylsilyl, (C 1 -C 4 )-alkylamino, di-(C 1 -C 4 )-alkylamino, (C 3 -C 6 )-cycloalkylamino, aminosulfonyl, (C 1 -C 6 )-alkylaminosulfonyl, di-(C 1 -C 6 )-alkylaminosulfonyl, sulfonylamino, (C 1 -C 6 )-alkylsulfonylamino, di-(C 1 -C 6 )-alkylsulfonylamino, a phenyl ring or a 3- to 6-membered aromatic, partially saturated or saturated heterocycle, where the phenyl ring or heterocycle may in each case optionally be mono- or polysubstituted by identical or different substituents, and where the substituents independently of one another may be selected from the group consisting of (C 1 -C 6 )-alkyl, (C 2 -C 6 )-alkenyl, (C 2 -C 6 )-alkynyl, (C 3 -C 6 )-cycloalkyl, (C 1 -C 6 )-haloalkyl, (C 2 -C 6 )-haloalkenyl, (C 2 -C 6 )-haloalkynyl, (C 3 -C 6 )-halocycloalkyl, halogen, CN, (C═O)OH, NO 2 , OH, (C 1 -C 4 )-alkoxy, (C 1 -C 4 )-haloalkoxy, (C 1 -C 4 )-alkylthio, (C 1 -C 4 )-alkylsulfinyl, (C 1 -C 4 )-alkylsulfonyl, (C 1 -C 4 )-haloalkylthio, (C 1 -C 4 )-haloalkylsulfinyl, (C 1 -C 4 )-haloalkylsulfonyl, aminosulfonyl, (C 1 -C 6 )-alkylaminosulfonyl, di-(C 1 -C 6 )-alkylaminosulfonyl, (C 1 -C 6 )-alkylcarbonyl, (C 1 -C 6 )-alkoxycarbonyl, aminocarbonyl, (C 1 -C 6 )-alkylaminocarbonyl, di-(C 1 -C 4 )-alkylaminocarbonyl, tri-(C 1 -C 2 )-alkylsilyl,

or

R 8 represents a 3- to 6-membered aromatic, partially saturated or saturated heterocycle which is attached via a nitrogen atom and where the heteroatoms are selected from the group consisting of N, S, O, where in each case at least one carbonyl group may be present and/or the heterocycle may in each case optionally be mono- or polysubstituted by identical or different substituents, where the substituents independently of one another may be selected from the group consisting of (C 1 -C 6 )-alkyl, (C 2 -C 6 )-alkenyl, (C 2 -C 6 )-alkynyl, (C 3 -C 6 )-cycloalkyl, (C 1 -C 6 )-haloalkyl, (C 2 -C 6 )-haloalkenyl, (C 2 -C 6 )-haloalkynyl, (C 3 -C 6 )-halocycloalkyl, halogen, CN, (C═O)OH, NO 2 , OH, (C 1 -C 4 )-alkoxy, (C 1 -C 4 )-haloalkoxy, (C 1 -C 4 )-alkylthio, (C 1 -C 4 )-alkylsulfinyl, (C 1 -C 4 )-alkylsulfonyl, (C 1 -C 4 )-haloalkylthio, (C 1 -C 4 )-haloalkylsulfinyl, (C 1 -C 4 )-haloalkylsulfonyl, aminosulfonyl, (C 1 -C 6 )-alkylaminosulfonyl, di-(C 1 -C 6 )-alkylaminosulfonyl, amino, (C 1 -C 4 )-alkylamino, di-(C 1 -C 4 )-alkylamino, (C 3 -C 6 )-cycloalkylamino, (C 1 -C 6 )-alkylcarbonyl, (C 1 -C 6 )-alkoxycarbonyl, aminocarbonyl, (C 1 -C 6 )-alkylaminocarbonyl, di-(C 1 -C 4 )-alkylaminocarbonyl, tri-(C 1 -C 2 )-alkylsilyl, SF 5 ,

n represents 0, 1 or 2.

2. The compound of formula (I) according to claim 1 , wherein

A 1 represents nitrogen, ═N + (O − )— or ═C(R 4 )—,

A 2 represents —N(R 5 )—, oxygen or sulfur,

A 3 represents oxygen or sulfur,

R 1 represents (C 1 -C 4 )-alkyl, (C 1 -C 4 )-hydroxyalkyl, (C 1 -C 4 )-haloalkyl, (C 1 -C 4 )-cyanoalkyl, (C 1 -C 4 )-alkoxy-(C 1 -C 4 )-alkyl, (C 1 -C 4 )-haloalkoxy-(C 1 -C 4 )-alkyl, (C 2 -C 4 )-alkenyl, (C 2 -C 4 )-alkenyloxy-(C 1 -C 4 )-alkyl, (C 2 -C 4 )-haloalkenyloxy-(C 1 -C 4 )-alkyl, (C 2 -C 4 )-haloalkenyl, (C 2 -C 4 )-cyanoalkenyl, (C 2 -C 4 )-alkynyl, (C 2 -C 4 )-alkynyloxy-(C 1 -C 4 )-alkyl, (C 2 -C 4 )-haloalkynyloxy-(C 1 -C 4 )-alkyl, (C 2 -C 4 )-haloalkynyl, (C 2 -C 4 )-cyanoalkynyl, (C 3 -C 6 )-cycloalkyl, (C 3 -C 6 )-cycloalkyl-(C 3 -C 6 )-cycloalkyl, (C 1 -C 4 )-alkyl-(C 3 -C 6 )-cycloalkyl, halo-(C 3 -C 6 )-cycloalkyl, (C 1 -C 4 )-alkylamino, di-(C 1 -C 4 )-alkylamino, (C 3 -C 6 )-cycloalkylamino, (C 1 -C 4 )-alkylcarbonylamino, (C 1 -C 4 )-alkylthio-(C 1 -C 4 )-alkyl, (C 1 -C 4 )-haloalkylthio-(C 1 -C 4 )-alkyl, (C 1 -C 4 )-alkylsulfinyl-(C 1 -C 4 )-alkyl, (C 1 -C 4 )-haloalkylsulfinyl-(C 1 -C 4 )-alkyl, (C 1 -C 4 )-alkylsulfonyl-(C 1 -C 4 )-alkyl, (C 1 -C 4 )-alkylcarbonyl-(C 1 -C 4 )-alkyl, (C 1 -C 4 )-haloalkylcarbonyl-(C 1 -C 4 )-alkyl, (C 1 -C 4 )-alkylsulfonylamino,

or represents (C 1 -C 4 )-alkyl, (C 1 -C 4 )-alkoxy, (C 2 -C 4 )-alkenyl, (C 2 -C 4 )-alkynyl, (C 3 -C 6 )-cycloalkyl, each of which is optionally mono- or disubstituted by identical or different substituents from the group consisting of aryl, hetaryl and heterocyclyl, where aryl, hetaryl and heterocyclyl may each optionally be mono- or disubstituted by identical or different substituents from the group consisting of halogen, cyano, carbamoyl, aminosulfonyl, (C 1 -C 4 )-alkyl, (C 3 -C 4 )-cycloalkyl, (C 1 -C 4 )-alkoxy, (C 1 -C 4 )-haloalkyl, (C 1 -C 4 )-haloalkoxy, (C 1 -C 4 )-alkylthio, (C 1 -C 4 )-alkylsulfinyl, (C 1 -C 4 )-alkylsulfonyl, (C 1 -C 4 )-alkylsulfimino, or

R 1 represents aryl or hetaryl, each of which is optionally mono- or disubstituted by identical or different substituents from the group consisting of halogen, cyano, carbamoyl, (C 1 -C 4 )-alkyl, (C 3 -C 6 )-cycloalkyl, (C 1 -C 4 )-alkoxy, (C 1 -C 4 )-haloalkyl, (C 1 -C 4 )-haloalkoxy, (C 1 -C 4 )-alkylthio, (C 1 -C 4 )-alkylsulfinyl, (C 1 -C 4 )-alkylsulfonyl, (C 1 -C 4 )-alkylsulfimino, (C 1 -C 4 )-alkylsulfoximino, (C 1 -C 4 )-alkylcarbonyl, and (C 3 -C 4 )-trialkylsilyl,

or R 1 represents heterocyclyl, which is optionally mono- or disubstituted by identical or different substituents from the group consisting of halogen, cyano, carbamoyl, (C 1 -C 4 )-alkyl, (C 3 -C 6 )-cycloalkyl, (C 1 -C 4 )-alkoxy, (C 1 -C 4 )-haloalkyl, (C 1 -C 4 )-haloalkoxy, (C 1 -C 4 )-alkylthio, (C 1 -C 4 )-alkylsulfinyl, (C 1 -C 4 )-alkylsulfonyl, (C 1 -C 4 )-alkylsulfimino, (C 1 -C 4 )-alkylsulfoximino, (C 1 -C 4 )-alkylcarbonyl, (C 3 -C 4 )-trialkylsilyl, (═O) and (═O) 2 ,

R 2 , R 3 , R 4 and R 6 independently of one another represent hydrogen, cyano, halogen, nitro, acetyl, hydroxy, amino, SCN, tri-(C 1 -C 4 )-alkylsilyl, (C 3 -C 6 )-cycloalkyl, (C 3 -C 6 )-cycloalkyl-(C 3 -C 6 )-cycloalkyl, (C 1 -C 4 )-alkyl-(C 3 -C 6 )-cycloalkyl, halo-(C 3 -C 6 )-cycloalkyl, (C 1 -C 4 )-alkyl, (C 1 -C 4 )-haloalkyl, (C 1 -C 4 )-cyano alkyl, (C 1 -C 4 )-hydroxyalkyl, (C 1 -C 4 )-alkoxy-(C 1 -C 4 )-alkyl, (C 2 -C 4 )-alkenyl, (C 2 -C 4 )-haloalkenyl, (C 2 -C 4 )-cyanoalkenyl, (C 2 -C 4 )-alkynyl, (C 2 -C 4 )-haloalkynyl, (C 2 -C 4 )-cyanoalkynyl, (C 1 -C 4 )-alkoxy, (C 1 -C 4 )-haloalkoxy, (C 1 -C 4 )-cyanoalkoxy, (C 1 -C 4 )-alkoxy-(C 1 -C 4 )-alkoxy, (C 1 -C 4 )-alkylhydroxyimino, (C 1 -C 4 )-alkoxyimino, (C 1 -C 4 )-alkyl-(C 1 -C 4 )-alkoxyimino, (C 1 -C 4 )-haloalkyl-(C 1 -C 4 )-alkoxyimino, (C 1 -C 4 )-alkylthio, (C 1 -C 4 )-haloalkylthio, (C 1 -C 4 )-alkylthio-(C 1 -C 4 )-alkyl, (C 1 -C 4 )-alkylsulfinyl, (C 1 -C 4 )-haloalkylsulfinyl, (C 1 -C 4 )-alkylsulfinyl-(C 1 -C 4 )-alkyl, (C 1 -C 4 )-alkylsulfonyl, (C 1 -C 4 )-haloalkylsulfonyl, (C 1 -C 4 )-alkylsulfonyl-(C 1 -C 4 )-alkyl, (C 1 -C 4 )-alkylsulfonyloxy, (C 1 -C 4 )-alkylcarbonyl, (C 1 -C 4 )-haloalkylcarbonyl, aminocarbonyl, (C 1 -C 4 )-alkylaminocarbonyl, di-(C 1 -C 4 )-alkyl-aminocarbonyl, (C 1 -C 4 )-alkylsulfonylamino, (C 1 -C 4 )-alkylamino, di-(C 1 -C 4 )-alkylamino, aminosulfonyl, (C 1 -C 4 )-alkylaminosulfonyl, di-(C 1 -C 4 )-alkylaminosulfonyl, aminothiocarbonyl, NHCO—(C 1 -C 4 )-alkyl ((C 1 -C 4 )-alkylcarbonylamino), SF 5 or

represent phenyl or hetaryl, each of which is optionally mono- or disubstituted by identical or different substituents, where in the case of hetaryl at least one carbonyl group may optionally be present and/or where optional substituents are in each case as follows: cyano, halogen, nitro, acetyl, amino, (C 1 -C 4 )-alkyl, (C 1 -C 4 )-haloalkyl, (C 1 -C 4 )-cyanoalkyl, (C 1 -C 4 )-hydroxyalkyl, (C 1 -C 4 )-alkoxy-(C 1 -C 4 )-alkyl, (C 2 -C 4 )-alkenyl, (C 2 -C 4 )-haloalkenyl, (C 2 -C 4 )-cyanoalkenyl, (C 2 -C 4 )-alkynyl, (C 2 -C 4 )-haloalkynyl, (C 2 -C 4 )-cyanoalkynyl, (C 1 -C 4 )-alkoxy, (C 1 -C 4 )-haloalkoxy, (C 1 -C 4 )-cyanoalkoxy, (C 1 -C 4 )-alkoxy-(C 1 -C 4 )-alkoxy, (C 1 -C 4 )-alkylhydroxyimino, (C 1 -C 4 )-alkoxyimino, (C 1 -C 4 )-alkyl-(C 1 -C 4 )-alkoxyimino, (C 1 -C 4 )-haloalkyl-(C 1 -C 4 )-alkoxyimino, (C 1 -C 4 )-alkylthio, (C 1 -C 4 )-haloalkylthio, (C 1 -C 4 )-alkylthio-(C 1 -C 4 )-alkyl, (C 1 -C 4 )-alkylsulfinyl, (C 1 -C 4 )-haloalkylsulfinyl, (C 1 -C 4 )-alkylsulfinyl-(C 1 -C 4 )-alkyl, (C 1 -C 4 )-alkylsulfonyl, (C 1 -C 4 )-haloalkylsulfonyl, (C 1 -C 4 )-alkylsulfonyl-(C 1 -C 4 )-alkyl, (C 1 -C 4 )-alkylsulfonyloxy, (C 1 -C 4 )-alkylcarbonyl, (C 1 -C 4 )-haloalkylcarbonyl, aminocarbonyl, (C 1 -C 4 )-alkylaminocarbonyl, di-(C 1 -C 4 )-alkylpaminocarbonyl, (C 1 -C 4 )-alkylsulfonylamino, (C 1 -C 4 )-alkylamino, di-(C 1 -C 4 )-alkylamino, aminosulfonyl, (C 1 -C 4 )-alkylaminosulfonyl, di-(C 1 -C 4 )-alkylaminosulfonyl,

R 5 represents (C 1 -C 4 )-alkyl, (C 1 -C 4 )-haloalkyl, (C 1 -C 4 )-cyanoalkyl, (C 1 -C 4 )-hydroxyalkyl, (C 1 -C 4 )-alkoxy-(C 1 -C 4 )-alkyl, (C 1 -C 4 )-haloalkoxy-(C 1 -C 4 )-alkyl, (C 2 -C 4 )-alkenyl, (C 2 -C 4 )-alkenyloxy-(C 1 -C 4 )-alkyl, (C 2 -C 4 )-haloalkenyloxy-(C 1 -C 4 )-alkyl, (C 2 -C 4 )-haloalkenyl, (C 2 -C 4 )-cyanoalkenyl, (C 2 -C 4 )-alkynyl, (C 2 -C 4 )-alkynyloxy-(C 1 -C 4 )-alkyl, (C 2 -C 4 )-haloalkynyl, (C 3 -C 6 )-cycloalkyl, (C 3 -C 6 )-cycloalkyl-(C 3 -C 6 )cycloalkyl, (C 1 -C 4 )-alkyl-(C 3 -C 6 )cycloalkyl, halo-(C 3 -C 6 )-cycloalkyl, (C 1 -C 4 )-alkylthio-(C 1 -C 4 )-alkyl, (C 1 -C 4 )-haloalkylthio-(C 1 -C 4 )-alkyl, (C 1 -C 4 )-alkylsulfinyl-(C 1 -C 4 )-alkyl, (C 1 -C 4 )-haloalkylsulfinyl-(C 1 -C 4 )-alkyl, (C 1 -C 4 )-alkylsulfonyl-(C 1 -C 4 )-alkyl, (C 1 -C 4 )-haloalkylsulfonyl-(C 1 -C 4 )-alkyl, (C 1 -C 4 )-alkoxy-(C 1 -C 4 )-alkylthio-(C 1 -C 4 )-alkyl or (C 1 -C 4 )-alkylcarbonyl-(C 1 -C 4 )-alkyl,

R 7 represents hydrogen or represents (C 1 -C 6 )-alkyl, (C 1 -C 6 )-alkoxy-(C 1 -C 6 )-alkyl, (C 2 -C 6 )-alkenyl, (C 2 -C 6 )-alkynyl, (C 3 -C 6 )-cycloalkyl, (C 3 -C 12 )-cycloalkyl-(C 1 -C 6 )-alkyl or (C 4 -C 12 )-bicycloalkyl, each of which is optionally mono- or polysubstituted by identical or different substituents, where the substituents independently of one another may be selected from the group consisting of halogen, cyano, (C 1 -C 6 )-alkyl, (C 1 -C 4 )-haloalkyl, (C 3 -C 6 )-cycloalkyl, (C 1 -C 4 )-alkoxy, (C 1 -C 4 )-haloalkoxy, (C 1 -C 4 )-alkylthio, (C 1 -C 4 )-alkylsulfinyl, (C 1 -C 4 )-alkylsulfonyl, (C 2 -C 6 )-alkoxycarbonyl, (C 2 -C 6 )-alkylcarbonyl, a phenyl ring or a 3- or 6-membered aromatic, partially saturated or saturated heterocycle, where the phenyl ring or heterocycle may in each case optionally be mono- or polysubstituted by identical or different substituents, and where the substituents independently of one another may be selected from the group consisting of (C 1 -C 6 )-alkyl, (C 2 -C 6 )-alkenyl, (C 2 -C 6 )-alkynyl, (C 3 -C 6 )-cycloalkyl, (C 1 -C 6 )-haloalkyl, (C 2 -C 6 )-haloalkenyl, (C 2 -C 6 )-haloalkynyl, (C 3 -C 6 )-halocycloalkyl, halogen, cyano, (C 1 -C 4 )-alkoxy, (C 1 -C 4 )-haloalkoxy, (C 1 -C 4 )-alkylthio, (C 1 -C 4 )-alkylsulfinyl, (C 1 -C 4 )-alkylsulfonyl, (C 1 -C 4 )-haloalkylthio, (C 1 -C 4 )-haloalkylsulfinyl, (C 1 -C 4 )-haloalkylsulfonyl, (C 1 -C 6 -alkyl)carbonyl, (C 1 -C 6 -alkoxy)carbonyl, aminocarbonyl, (C 1 -C 6 -alkyl)aminocarbonyl, di-(C 1 -C 4 -alkyl)aminocarbonyl,

R 8 represents amino or (C 1 -C 6 )-alkylamino, di-(C 1 -C 4 )-alkylamino, (C 2 -C 6 )-alkenylamino, (C 2 -C 6 )-alkynylamino, (C 3 -C 12 )-cycloalkylamino, (C 3 -C 12 )-cycloalkyl-(C 1 -C 6 )-alkylamino, (C 4 -C 12 )-bicycloalkylamino or hydrazino, each of which is optionally mono- or polysubstituted by identical or different substituents, where the substituents independently of one another may be selected from the group consisting of halogen, cyano, amino, nitro, hydroxy, (C═O)OH, (C 1 -C 6 )-alkyl, (C 3 -C 6 )-cycloalkyl, (C 1 -C 4 )-alkoxy, (C 1 -C 4 )-haloalkoxy, (C 1 -C 4 )-alkylthio, (C 1 -C 4 )-haloalkylthio, (C 1 -C 4 )-alkylsulfinyl, (C 1 -C 4 )-haloalkylsulfinyl, (C 1 -C 4 )-alkylsulfonyl, (C 1 -C 4 )-haloalkylsulfonyl, (C 2 -C 6 )-alkoxycarbonyl, (C 2 -C 6 )-alkylcarbonyl, (C 1 -C 6 )-haloalkylcarbonyl, (C 1 -C 6 )-alkylcarbonylamino, aminocarbonyl, (C 1 -C 6 )-alkylaminocarbonyl, di-(C 1 -C 6 )-alkylaminocarbonyl, (C 1 -C 4 )-alkylamino, di-(C 1 -C 4 )-alkylamino, (C 3 -C 6 )-cycloalkylamino, aminosulfonyl, (C 1 -C 6 )-alkylaminosulfonyl, di-(C 1 -C 6 )-alkylaminosulfonyl, sulfonylamino, (C 1 -C 6 )-alkylsulfonylamino, di-(C 1 -C 6 )-alkylsulfonylamino, a phenyl ring or a 3- to 6-membered aromatic, partially saturated or saturated heterocycle, where the phenyl ring or heterocycle may in each case optionally be mono- or polysubstituted by identical or different substituents, and where the substituents independently of one another may be selected from the group consisting of (C 1 -C 6 )-alkyl, (C 2 -C 6 )-alkenyl, (C 2 -C 6 )-alkynyl, (C 3 -C 6 )-cycloalkyl, (C 1 -C 6 )-haloalkyl, (C 2 -C 6 )-haloalkenyl, (C 2 -C 6 )-haloalkynyl, (C 3 -C 6 )-halocycloalkyl, halogen, cyano, (C═O)OH, NO 2 , OH, (C 1 -C 4 )-alkoxy, (C 1 -C 4 )-haloalkoxy, (C 1 -C 4 )-alkylthio, (C 1 -C 4 )-alkylsulfinyl, (C 1 -C 4 )-alkylsulfonyl, (C 1 -C 4 )-haloalkylthio, (C 1 -C 4 )-haloalkylsulfinyl, (C 1 -C 4 )-haloalkylsulfonyl, aminosulfonyl, (C 1 -C 6 )-alkylaminosulfonyl, di-(C 1 -C 6 )-alkylaminosulfonyl, (C 1 -C 6 )-alkylcarbonyl, (C 1 -C 6 )-alkoxycarbonyl, aminocarbonyl, (C 1 -C 6 )-alkylaminocarbonyl, di-(C 1 -C 4 )-alkylaminocarbonyl,

or

R 8 represents a 3- to 6-membered aromatic, partially saturated or saturated heterocycle which is attached via a nitrogen atom and where the heteroatoms are selected from the group consisting of N, S, O, where in each case at least one carbonyl group may be present and/or the heterocycle may in each case optionally be mono- or polysubstituted by identical or different substituents, where the substituents independently of one another may be selected from the group consisting of (C 1 -C 6 )-alkyl, (C 2 -C 6 )-alkenyl, (C 2 -C 6 )-alkynyl, (C 3 -C 6 )-cycloalkyl, (C 1 -C 6 )-haloalkyl, (C 2 -C 6 )-haloalkenyl, (C 2 -C 6 )-haloalkynyl, (C 3 -C 6 )-halocycloalkyl, halogen, cyano, (C═O)OH, NO 2 , OH, (C 1 -C 4 )-alkoxy, (C 1 -C 4 )-haloalkoxy, (C 1 -C 4 )-alkylthio, (C 1 -C 4 )-alkylsulfinyl, (C 1 -C 4 )-alkylsulfonyl, (C 1 -C 4 )-haloalkylthio, (C 1 -C 4 )-haloalkylsulfinyl, (C 1 -C 4 )-haloalkylsulfonyl, aminosulfonyl, (C 1 -C 6 )-alkylaminosulfonyl, di-(C 1 -C 6 )-alkylaminosulfonyl, amino, (C 1 -C 4 )-alkylamino, di-(C 1 -C 4 )-alkylamino, (C 3 -C 6 )-cycloalkylamino, (C 1 -C 6 )-alkylcarbonyl, (C 1 -C 6 )-alkoxycarbonyl, aminocarbonyl, (C 1 -C 6 )-alkylaminocarbony or di-(C 1 -C 4 )-alkylaminocarbonyl,

n represents 0, 1 or 2.

3. The compound of formula (I) according to claim 1 wherein

A 1 represents nitrogen or ═C(R 4 )—,

A 2 represents —N(R 5 )— or oxygen,

A 3 represents oxygen or sulfur,

R 1 represents (C 1 -C 4 )-alkyl, (C 1 -C 4 )-hydroxyalkyl, (C 1 -C 4 )-haloalkyl, (C 2 -C 4 )-alkenyl, (C 2 -C 4 )-haloalkenyl, (C 2 -C 4 )-alkynyl, (C 2 -C 4 )-haloalkynyl, (C 3 -C 6 )-cycloalkyl, (C 1 -C 4 )-alkylthio-(C 1 -C 4 )-alkyl, (C 1 -C 4 )-alkylsulfinyl-(C 1 -C 4 )-alkyl or (C 1 -C 4 )-alkylsulfonyl-(C 1 -C 4 )-alkyl,

R 2 represents hydrogen, cyano, halogen, (C 1 -C 4 )-alkyl, (C 1 -C 4 )-haloalkyl, (C 1 -C 4 )-haloalkoxy, (C 1 -C 4 )-alkylthio, (C 1 -C 4 )-alkylsulfinyl, (C 1 -C 4 )-alkylsulfonyl, (C 1 -C 4 )-haloalkylthio, (C 1 -C 4 )-haloalkylsulfinyl or (C 1 -C 4 )-haloalkylsulfonyl,

R 3 represents hydrogen, halogen, (C 1 -C 4 )-alkyl, (C 1 -C 4 )-haloalkyl, (C 1 -C 4 )-haloalkoxy, (C 1 -C 4 )-alkylthio, (C 1 -C 4 )-alkylsulfinyl, (C 1 -C 4 )-alkylsulfonyl, (C 1 -C 4 )-haloalkylthio, (C 1 -C 4 )-haloalkylsulfinyl or (C 1 -C 4 )-haloalkylsulfonyl,

R 4 represents hydrogen, halogen, cyano or (C 1 -C 4 )-alkyl,

R 5 represents (C 1 -C 4 )-alkyl or (C 1 -C 4 )-alkoxy-(C 1 -C 4 )-alkyl,

R 6 represents hydrogen, cyano, halogen, (C 1 -C 4 )-alkyl, (C 2 -C 4 )-alkenyl, (C 2 -C 4 )-alkynyl, (C 1 -C 4 )-haloalkyl, (C 3 -C 6 )-cycloalkyl, (C 1 -C 4 )-alkyl-(C 3 -C 6 )-cycloalkyl, (C 1 -C 4 )-alkoxy, (C 1 -C 4 )-haloalkoxy, (C 1 -C 4 )-alkylthio, (C 1 -C 4 )-haloalkylthio, (C 1 -C 4 )-alkylsulfinyl, (C 1 -C 4 )-haloalkylsulfinyl, (C 1 -C 4 )-alkylsulfonyl, (C 1 -C 4 )-haloalkylsulfonyl or (C 1 -C 4 )-alkylcarbonyl,

R 7 represents hydrogen or represents (C 1 -C 4 )-alkyl or (C 1 -C 4 )-alkoxy-(C 1 -C 4 )-alkyl, each of which is optionally mono- or polysubstituted by identical or different substituents from the group consisting of halogen, (C 1 -C 2 )-haloalkyl, cyano, phenyl and pyridyl, where phenyl and pyridyl may each optionally be mono- or disubstituted by identical or different substituents from the group consisting of (C 1 -C 4 )-alkyl, halogen and cyano,

R 8 represents amino or (C 1 -C 4 )-alkylamino, di-(C 1 -C 4 )-alkylamino, (C 2 -C 6 )-alkenylamino, (C 2 -C 4 )-alkynylamino, (C 3 -C 6 )-cycloalkylamino or hydrazino, each of which is optionally mono- or polysubstituted by identical or different substituents, where the substituents independently of one another may be selected from the group consisting of halogen, cyano, (C 1 -C 4 )-alkyl, (C 3 -C 6 )-cycloalkyl, (C 1 -C 4 )-alkoxy, (C 1 -C 4 )-haloalkoxy, (C 1 -C 4 )-alkylthio, (C 1 -C 4 )-haloalkylthio, (C 1 -C 4 )-alkylsulfinyl, (C 1 -C 4 )-haloalkylsulfinyl, (C 1 -C 4 )-alkylsulfonyl, (C 1 -C 4 )-haloalkylsulfonyl, (C 1 -C 4 )-alkoxycarbonyl, (C 1 -C 4 )-alkylcarbonyl, (C 1 -C 6 )-haloalkylcarbonyl, (C 1 -C 4 )-alkylcarbonylamino, aminocarbonyl, (C 1 -C 6 )-alkylaminocarbonyl, di-(C 1 -C 6 )-alkylaminocarbonyl, a phenyl ring or a 3- to 6-membered aromatic, partially saturated or saturated heterocycle, where the phenyl ring or heterocycle may in each case optionally be mono- or polysubstituted by identical or different substituents, and where the substituents independently of one another may be selected from the group consisting of (C 1 -C 4 )-alkyl, (C 3 -C 6 )-cycloalkyl, (C 1 -C 4 )-haloalkyl, halogen, cyano, (C 1 -C 4 )-alkoxy, (C 1 -C 4 )-haloalkoxy, (C 1 -C 4 )-alkylthio, (C 1 -C 4 )-alkylsulfinyl, (C 1 -C 4 )-alkylsulfonyl, (C 1 -C 4 )-haloalkylthio, (C 1 -C 4 )-haloalkylsulfinyl, (C 1 -C 4 )-haloalkylsulfonyl,

or

R 8 represents a 3- to 6-membered aromatic, partially saturated or saturated heterocycle which is attached via a nitrogen atom and where the heteroatoms are selected from the group consisting of N, S, O, where in each case at least one carbonyl group may be present and/or the heterocycle may in each case optionally be mono- or polysubstituted by identical or different substituents, where the substituents independently of one another may be selected from the group consisting of (C 1 -C 4 )-alkyl, (C 3 -C 6 )-cycloalkyl, (C 1 -C 6 )-haloalkyl, halogen, cyano, (C 1 -C 4 )-alkoxy, (C 1 -C 4 )-haloalkoxy, (C 1 -C 4 )-alkylthio, (C 1 -C 4 )-alkylsulfinyl, (C 1 -C 4 )-alkylsulfonyl, (C 1 -C 4 )-haloalkylthio, (C 1 -C 4 )-haloalkylsulfinyl, (C 1 -C 4 )-haloalkylsulfonyl,

n represents 0, 1 or 2.

4. The compound of formula (I) according to claim 1 , wherein

A 1 represents nitrogen or ═C(R 4 )—,

A 2 represents —N(R 5 )— or oxygen,

A 3 represents oxygen or sulfur,

R 1 represents methyl, ethyl, n-propyl, isopropyl, cyclopropyl, n-butyl, isobutyl, tert-butyl, cyclobutyl, fluoromethyl, difluoromethyl, trifluoromethyl, fluoroethyl, difluoroethyl, trifluoroethyl, tetrafluoroethyl or pentafluoroethyl,

R 2 represents hydrogen, methyl, ethyl, fluorine, chlorine, bromine, cyano, fluoromethyl, difluoromethyl, trifluoromethyl, fluoroethyl, difluoroethyl, trifluoroethyl, tetrafluoroethyl, pentafluoroethyl, trifluoromethoxy, difluorochloromethoxy, dichlorofluoromethoxy, trifluoromethylthio, trifluoromethylsulfinyl or trifluoromethylsulfonyl,

R 3 represents fluorine, chlorine, fluoromethyl, difluoromethyl, trifluoromethyl, fluoroethyl, difluoroethyl, trifluoroethyl, tetrafluoroethyl, pentafluoroethyl, trifluoromethoxy, difluorochloromethoxy, dichlorofluoromethoxy, trifluoromethylthio, trifluoromethylsulfinyl or trifluoromethylsulfonyl,

R 4 represents hydrogen, fluorine, chlorine, bromine or cyano,

R 5 represents methyl, ethyl, isopropyl, methoxymethyl or methoxyethyl,

R 6 represents hydrogen,

R 7 represents hydrogen, methyl, ethyl, isopropyl, tert-butyl, methoxymethyl or methoxyethyl,

R 8 represents amino or represents methylamino, dimethylamino, ethylamino, isopropylamino, diethylamino, methylethylamino, propylamino, methylpropylamino, ethylpropylamino, methoxyethylamino, cyanoethylamino, methylthioethylamino, methylsulfinylethylamino, methylsulfonylethylamino, cyclopropylamino, cyclobutylamino, methylcyclopropylamino, methylcyclobutylamino, methylhydrazino, dimethylhydrazino, trimethylhydrazino or phenylhydrazino,

or

R 8 represents aziridinyl, azetidinyl, pyrrolidinyl, pyrazolidinyl, imidazolidinyl, thiazolidinyl, oxazolidinyl, piperidinyl, piperazinyl, morpholinyl, thiomorpholinyl, pyrrolidonyl, imidazolidonyl, triazolinonyl, tetrazolinonyl, piperidonyl, pyrrolyl, pyrazolyl, triazolyl, imidazolyl or oxazolyl, attached via a nitrogen atom, in each case optionally mono- or polysubstituted by identical or different substituents from the group consisting of methyl, ethyl, trifluoromethyl, fluorine, chlorine, bromine and cyano,

n represents 0, 1 or 2.

5. The compound of formula (I) according to claim 1 , wherein

A 1 represents nitrogen,

A 2 represents —N(R 5 )—,

A 3 represents oxygen,

R 1 represents ethyl,

R 2 represents hydrogen, methyl or trifluoromethyl,

R 3 represents trifluoromethyl, pentafluoroethyl, trifluoromethylthio, trifluoromethylsulfinyl or trifluoromethylsulfonyl,

R 5 represents methyl,

R 6 represents hydrogen,

R 7 represents hydrogen or methyl,

R 8 represents amino, methylamino, dimethylamino, ethylamino, isopropylamino, cyclopropylamino, methoxyethylamino, cyanoethylamino, methylthioethylamino, methylsulfinylethylamino or methylsulfonylethylamino,

or

R 8 represents pyrrolidinyl, attached via a nitrogen atom, or represents pyrazolyl, attached via a nitrogen atom and optionally monosubstituted by bromine,

n represents 0, 1 or 2.

6. The compound of formula (I) according to claim 1 , wherein

A 1 represents nitrogen,

A 2 represents —N—(R 5 )—,

A 3 represents oxygen,

R 1 represents ethyl,

R 2 represents hydrogen or methyl,

R 3 represents trifluoromethyl,

R 5 represents methyl,

R 6 represents hydrogen,

R 7 represents hydrogen or methyl,

R 8 represents methylamino (—NHCH 3 ), ethylamino (—NHCH 2 CH 3 ), isopropylamino (—NHiC 3 H 7 ), methoxyethylamino (—NHCH 2 CH 2 OCH 3 , cyanoethylamino (—NHCH 2 CH 2 CN), methylthioethylamino (—NHCH 2 CH 2 SCH 3 ), methylsulfinylethylamino (—NHCH 2 CH 2 SOCH 3 ), methylsulfonylethylamino (—NHCH 2 CH 2 SO 2 CH 3 ) or dimethylamino (—N(CH 3 ) 2 ),

or

R 8 represents pyrrolidinyl, attached via a nitrogen atom, or represents pyrazolyl, attached via a nitrogen atom and optionally monosubstituted by bromine,

n represents 2.

7. The compound of formula (I) according to claim 1 , wherein

A 1 represents nitrogen,

A 2 represents —N—(R 5 )—,

A 3 represents oxygen,

R 1 represents ethyl,

R 2 represents hydrogen or methyl,

R 3 represents trifluoromethyl,

R 5 represents methyl,

R 6 represents hydrogen,

R 7 represents hydrogen or methyl,

R 8 represents methylamino (—NHCH 3 ), ethylamino (—NHCH 2 CH 3 ), isopropylamino (—NHiC 3 H 7 ), methoxyethylamino (—NHCH 2 CH 2 OCH 3 ), cyanoethylamino (—NHCH 2 CH 2 CN), methylthioethylamino (—NHCH 2 CH 2 SCH 3 ), methylsulfinylethylamino (—NHCH 2 CH 2 SOCH 3 ), methylsulfonylethylamino (—NHCH 2 CH 2 SO 2 CH 3 ) or dimethylamino (—N(CH 3 ) 2 ),

or

R 8 represents pyrrolidinyl, attached via a nitrogen atom, of the formula

below:

or represents pyrazolyl, attached via a nitrogen atom and monosubstituted

by bromine, of the formula:

n represents 2.

8. Agrochemical formulation comprising the compound of formula (I) according to claim 1 and also one or more extenders and/or surfactants.

9. Agrochemical formulation according to claim 8 , further comprising an additional agrochemically active compound.

10. A method for controlling one or more arthropod pests, comprising applying the compound of formula (I) according to claim 1 to the arthropod pests and/or a habitat thereof.

11. A product comprising the compound of formula (I) according to claim 1 for controlling one or more arthropod pests.

12. A method for controlling one or more arthropod pests, comprising applying the agrochemical formulation according to claim 8 to the arthropod pests and/or a habitat thereof.

13. A product comprising the agrochemical formulation according to claim 8 for controlling one or more arthropod pests.

Assignments (3)
SECURITY INTEREST Recorded Mar 24, 2026
From: AMVAC CHEMICAL CORPORATION; TYRATECH, INC.
To: BMO BANK N.A., AS ADMINISTRATIVE AGENT
Reel/Frame 075188/0405 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 12, 2021
From: BAYER CROPSCIENCE AKTIENGESELLSCHAFT
To: BAYER CROPSCIENCE AKTIENGESELLSCHAFT; BAYER AKTIENGESELLSCHAFT
Reel/Frame 056827/0489 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 8, 2019
From: FISCHER, RUEDIGER; HAGER, DOMINIK; HOFFMEISTER, LAURA; KAUSCH-BUSIES, NINA; MOSRIN, MARC; WILCKE, DAVID; WILLOT, MATTHIEU; ILG, KERSTIN; PORTZ, DANIELA; GOERGENS, ULRICH; TURBERG, ANDREAS
To: BAYER CROPSCIENCE AKTIENGESELLSCHAFT
Reel/Frame 049119/0876 →
Priority Claims (1)
EP 16192636 · Oct 6, 2016 · regional
Continuity (1)
Related Publication 20200048246A1 · Feb 13, 2020