Heterocycle derivatives as pesticides

Patent metadata

Field	Value
Publication number	US-11083199-B2
Application number	US-201816476393-A
Country	US
Kind code	B2
Filing date	Jan 3, 2018
Priority date	Jan 10, 2017
Publication date	Aug 10, 2021
Grant date	Aug 10, 2021

Abstract

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

in which X, R 1 , R 2 , R 3 , and n have the meanings given above,

to the use thereof as acaricides and/or insecticides for controlling animal pests and to methods and intermediates for the preparation thereof.

First claim

The invention claimed is:

1. A compound of formula (I)

in which:
R 1 is (C 1 -C 6 )alkyl, (C 1 -C 6 )cyanoalkyl, (C 1 -C 6 )hydroxyalkyl, (C 1 -C 6 )alkoxy-(C 1 -C 6 )alkyl, (C 1 -C 6 )haloalkyl, (C 2 -C 6 )alkenyl, (C 2 -C 6 )haloalkenyl, (C 2 -C 6 )alkynyl, (C 2 -C 6 )haloalkynyl or (C 3 -C 8 )cycloalkyl,
R 2 is hydrogen, (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,
R 3 is hydrogen, halogen, cyano, nitro, (C 1 -C 6 )alkyl, (C 1 -C 6 )haloalkyl, (C 1 -C 6 )alkoxy, (C 1 -C 6 )haloalkoxy, (C 1 -C 6 )alkylthio, (C 1 -C 6 )haloalkylthio, (C 1 -C 6 )alkylsulfinyl, (C 1 -C 6 )haloalkylsulfinyl, (C 1 -C 6 )alkylsulfonyl, (C 1 -C 6 )haloalkylsulfonyl, SCN, (C 1 -C 6 )alkylcarbonyl, (C 1 -C 6 )haloalkylcarbonyl, (C 1 -C 6 )alkoxycarbonyl, (C 1 -C 6 )haloalkoxycarbonyl, aminocarbonyl, (C 1 -C 6 )alkylaminocarbonyl, di(C 1 -C 6 )alkylaminocarbonyl, (C 1 -C 6 )haloalkylaminocarbonyl, (C 3 -C 8 )cycloalkylaminocarbonyl, aminothiocarbonyl, (C 1 -C 6 )alkylaminothiocarbonyl, di(C 1 -C 6 )alkylaminothiocarbonyl, (C 1 -C 6 )haloalkylaminothiocarbonyl, (C 3 -C 8 )cycloalkylaminothiocarbonyl, amino, (C 1 -C 6 )alkylamino, (C 1 -C 6 )haloalkylamino, di(C 1 -C 6 )alkylamino, (C 3 -C 8 )cycloalkylamino, (C 1 -C 6 )alkylsulfonylamino, (C 1 -C 6 )alkylcarbonylamino, (C 1 -C 6 )haloalkylcarbonylamino, (C 1 -C 6 )alkylcarbonyl-(C 1 -C 6 )alkylamino, (C 1 -C 6 )haloalkylcarbonyl-(C 1 -C 6 )alkylamino, (C 3 -C 8 )cycloalkylcarbonylamino, (C 3 -C 8 )cycloalkylcarbonyl-(C 1 -C 6 )alkylamino, (C 1 -C 6 )alkylthiocarbonylamino, (C 1 -C 6 )haloalkylthiocarbonylamino, (C 1 -C 6 )alkylthiocarbonyl-(C 1 -C 6 )alkylamino, (C 1 -C 6 )haloalkylthiocarbonyl-(C 1 -C 6 )alkylamino, (C 3 -C 8 )cycloalkylthiocarbonylamino, (C 3 -C 8 )cycloalkylthiocarbonyl-(C 1 -C 6 )alkylamino, (C 2 -C 6 )alkenyl, (C 2 -C 6 )haloalkenyl, (C 2 -C 6 )cyanoalkenyl, (C 3 -C 8 )cycloalkyl-(C 2 )alkenyl, (C 2 -C 6 )alkynyl, (C 2 -C 6 )haloalkynyl, (C 3 -C 6 )cycloalkyl-(C 2 )alkynyl, (C 3 -C 6 )cycloalkyl-(C 1 -C 6 )alkyl, (C 1 -C 6 )alkylaminocarbonylamino, di(C 1 -C 6 )alkylaminocarbonylamino, (C 3 -C 6 )cycloalkylaminocarbonylamino, (C 1 -C 6 )haloalkylaminocarbonylamino, (C 1 -C 6 )alkylaminocarbonyl-(C 1 -C 6 )alkylamino, di(C 1 -C 6 )alkylaminocarbonyl-(C 1 -C 6 )alkylamino, (C 3 -C 6 )cycloalkylaminocarbonyl-(C 1 -C 6 )alkylamino or (C 1 -C 6 )haloalkylaminocarbonyl-(C 1 -C 6 )alkylamino,
or is aryl, hetaryl, cyclopentenyl or cyclohexenyl, each of which is optionally mono- or polysubstituted by identical or different substituents, wherein if R 3 is hetaryl at least one carbonyl group may optionally be present, and where optional substituents are as follows: cyano, carboxyl, halogen, nitro, acetyl, hydroxyl, amino, SCN, SF 5 , 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, (C 1 -C 6 )haloalkyl-(C 3 -C 8 )cycloalkyl, halo(C 3 -C 8 )cycloalkyl, cyano(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 3 -C 8 )cycloalkyl-(C 2 )alkenyl, (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 )alkoxyimino, (C 1 -C 6 )haloalkoxyimino, (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 )haloalkylsulfonyloxy, (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 1 -C 6 )haloalkylaminocarbonyl, (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, (C 1 -C 6 )haloalkylamino, (C 3 -C 8 )cycloalkylamino, 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 1 -C 6 )haloalkylaminothiocarbonyl, (C 3 -C 8 )cycloalkylaminothiocarbonyl, (C 1 -C 6 )alkylcarbonylamino, (C 1 -C 6 )haloalkylcarbonylamino, (C 1 -C 6 )alkylcarbonyl-(C 1 -C 6 )alkylamino, (C 1 -C 6 )haloalkylcarbonyl-(C 1 -C 6 )alkylamino, (C 3 -C 8 )cycloalkylcarbonylamino, (C 3 -C 8 )cycloalkylcarbonyl-(C 1 -C 6 )alkylamino, (C 1 -C 6 )alkylthiocarbonylamino, (C 1 -C 6 )haloalkylthiocarbonylamino, (C 1 -C 6 )alkylthiocarbonyl-(C 1 -C 6 )alkylamino, (C 1 -C 6 )haloalkylthiocarbonyl-(C 1 -C 6 )alkylamino, (C 3 -C 8 )cycloalkylthiocarbonylamino, (C 3 -C 8 )cycloalkylthiocarbonyl-(C 1 -C 6 )alkylamino, hetaryl, oxohetaryl, halohetaryl, halooxohetaryl, cyanohetaryl, cyanooxohetaryl, (C 1 -C 6 )haloalkylhetaryl or (C 1 -C 6 )haloalkyloxohetaryl,
X is a heteroaromatic 9-membered or 12-membered fused bicyclic or tricyclic ring system from the group of Q1 to Q12

R 4 is hydrogen, (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 2 -C 6 )alkenyl, or (C 2 -C 6 )alkynyl,
R 5 is hydrogen, (C 1 -C 6 )alkyl, or (C 1 -C 6 )haloalkyl,
R 6 is hydrogen, and
n is 0, 1 or 2.

2. A compound of formula (I) according to claim 1 , in which
R 1 is (C 1 -C 4 )alkyl, (C 1 -C 4 )cyanoalkyl, (C 1 -C 4 )alkoxy-(C 1 -C 4 )alkyl, (C 1 -C 4 )haloalkyl, (C 2 -C 4 )alkenyl, or (C 2 -C 4 )alkynyl,
R 2 is hydrogen, (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, or (C 1 -C 4 )haloalkoxy-(C 1 -C 4 )alkyl,
R 3 is hydrogen, halogen, cyano, nitro, (C 1 -C 4 )alkyl, (C 1 -C 4 )haloalkyl, (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, SCN, (C 1 -C 4 )alkylcarbonyl, (C 1 -C 4 )haloalkylcarbonyl, (C 1 -C 4 )alkoxycarbonyl, (C 1 -C 4 )haloalkoxycarbonyl, aminocarbonyl, (C 1 -C 4 )alkylaminocarbonyl, di(C 1 -C 4 )alkylaminocarbonyl, (C 1 -C 4 )haloalkylaminocarbonyl, (C 3 -C 6 )cycloalkylaminocarbonyl, aminothiocarbonyl, (C 1 -C 4 )alkylaminothiocarbonyl, di(C 1 -C 4 )alkylaminothiocarbonyl, (C 1 -C 4 )haloalkylaminothiocarbonyl, (C 3 -C 6 )cycloalkylaminothiocarbonyl, amino, (C 1 -C 4 )alkylamino, (C 1 -C 4 )haloalkylamino, di(C 1 -C 4 )alkylamino, (C 3 -C 6 )cycloalkylamino, (C 1 -C 4 )alkylsulfonylamino, (C 1 -C 4 )alkylcarbonylamino, (C 1 -C 4 )haloalkylcarbonylamino, (C 1 -C 4 )alkylcarbonyl-(C 1 -C 4 )alkylamino, (C 1 -C 4 )haloalkylcarbonyl-(C 1 -C 4 )alkylamino, (C 3 -C 6 )cycloalkylcarbonylamino, (C 3 -C 6 )cycloalkylcarbonyl-(C 1 -C 4 )alkylamino, (C 1 -C 4 )alkylthiocarbonylamino, (C 1 -C 4 )haloalkylthiocarbonylamino, (C 1 -C 4 )alkylthio

Assignees

• Bayer Ag
• Bayer Cropscience Ag

Inventors

• Wilcke David
• Hager Dominik
• Hoffmeister Laura
• Kausch-Busies Nina
• Mosrin Marc
• Willot Matthieu
• Fischer Ruediger
• Ilg Kerstin
• 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

• C07D403/04

  directly linked by a ring-member-to-ring-member bond · CPC title

• C07D401/04

  directly linked by a ring-member-to-ring-member bond · CPC title

• C07D487/04

  Ortho-condensed systems · CPC title