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

Patent metadata

Field	Value
Publication number	US-10772332-B2
Application number	US-201816483138-A
Country	US
Kind code	B2
Filing date	Feb 5, 2018
Priority date	Feb 6, 2017
Publication date	Sep 15, 2020
Grant date	Sep 15, 2020

Abstract

The invention relates to novel compounds of the formula (I)

in which R 1 , R 2 , R 3 , R 4 , A 1 , A 2 , X and n have the definitions given above,
to the use thereof as acaricides and/or insecticides for controlling animal pests and to processes and intermediates for preparation thereof.

First claim

The invention claimed is:

1. Compound of formula (I)

in which
A 1 is nitrogen, ═N + —O − or ═C—R 5 ,
A 2 is —N(R 6 )—, oxygen or sulfur,
R 1 is (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 6 )halocycloalkyl, (C 3 -C 6 )cyanocycloalkyl, (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 is in each case optionally singly or multiply, identically or differently aryl-, hetaryl- or heterocyclyl-substituted (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, where aryl, hetaryl or heterocyclyl may each optionally be mono- or polysubstituted identically or differently by halogen, cyano, nitro, hydroxyl, 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 or benzyl,

R 2 is an optionally singly or multiply, identically or differently substituted saturated heterocyclic, partly saturated heterocyclic or heteroaromatic ring in which at least one carbon atom is replaced by a heteroatom, where at least one carbonyl group may optionally be present in each case and where possible substituents in each case are as follows: cyano, carboxyl, halogen, nitro, acetyl, hydroxyl, 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 3 -C 6 )cycloalkyl, (C 3 -C 6 )halocycloalkyl, (C 3 -C 6 )cyanocycloalkyl, (C 3 -C 6 )cycloalkyl-(C 3 -C 6 )cycloalkyl, (C 1 -C 4 )alkyl-(C 3 -C 6 )cycloalkyl, (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 )alkoxyimino, —N═C(H)—O(C 1 -C 6 )alkyl, —C(H)═N—O(C 1 -C 6 )alkyl, (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 )alkylaminocarbonyl, (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, (C 1 -C 6 )alkylcarbamoyl (including —NHCOO(C 1 -C 6 )alkyl, —N(C 1 -C 6 )alkylCOO(C 1 -C 6 )alkyl, —OCONH(C 1 -C 6 )alkyl or —OCON(C 1 -C 6 )dialkyl), (C 1 -C 6 )alkylcarbonylamino ((C 1 -C 6 )alkylCONH), (C 1 -C 6 )alkylurea (including —NHCONH(C 1 -C 6 )alkyl, and —NHCON(C 1 -C 6 )dialkyl), an optionally singly or multiply, identically or differently substituted saturated, partly saturated or heteroaromatic ring in which at least one carbon atom is replaced by a heteroatom, or a singly or multiply, identically or differently substituted aromatic ring, where at least one carbonyl group may optionally be present in each case and where possible substituents in each case are as follows: cyano, carboxyl, halogen, nitro, acetyl, hydroxyl, 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 3 -C 6 )cycloalkyl, (C 3 -C 6 )halocycloalkyl, (C 3 -C 6 )cyanocycloalkyl, (C 3 -C 6 )cycloalkyl-(C 3 -C 6 )cycloalkyl, (C 1 -C 4 )alkyl-(C 3 -C 6 )cycloalkyl, (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 )alkoxyimino, —N═C(H)—O(C 1 -C 6 )alkyl, —C(H)═N—O(C 1 -C 6 )alkyl, (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 )alkylaminocarbonyl, (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 or (C 1 -C 6 )alkylcarbonylamino,
R 2 is optionally a group selected from —C(═O)—R 8 (G1), —C(═S)—R 8 (G2), —C(═O)—NR 11 R 12 (G3), —C(═S)—NR 11 R 12 (G4), —S(O) m —R 3 (G5), —S═O(═NH)—R 13 (G6), —S═O(═N—CN)—R 13 (G7), —S(═N—CN)—R 13 (G8), —S(O) 2 —NR 11 R 12

Assignees

• Bayer Ag
• Bayer Cropscience Ag

Inventors

• Mosrin Marc
• Fischer Ruediger
• Hager Dominik
• Hoffmeister Laura
• Ilg Kerstin
• Kausch-Busies Nina
• Wilcke David
• Willot Matthieu
• Eilmus Sascha
• Goergens Ulrich
• Turberg Andreas

Classifications

• C07D471/04 Primary

  Ortho-condensed systems · CPC title

• A01N43/90 Primary

  having two or more relevant hetero rings, condensed among themselves or with a common carbocyclic ring system · CPC title