IP Library Granted Patent US 10,986,840
Granted Patent B2
US 10,986,840 · App. 16/590,006 · Granted Apr 27, 2021

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

Inventors: Ruediger Fischer (Pulheim, DE); David Wilcke (Duesseldorf, DE); Nina Kausch-Busies (Bergisch Gladbach, DE); Dominik Hager (Monheim, DE); Kerstin Ilg (Cologne, DE); Laura Hoffmeister (Duesseldorf, DE); Matthieu Willot (Duesseldorf, DE); Daniela Portz (Vettweiss, DE); Ulrich Goergens (Ratingen, DE); Andreas Turberg (Haan, DE)
Assignee: BAYER CROPSCIENCE AKTIENGESELLSCHAFT
A01N43/90A01N43/52A01N43/54A01N43/56C07D235/18C07D401/04C07D401/12C07D401/14C07D403/10C07D409/10C07D409/14C07D471/04C07D487/04C07D491/056C07D498/04
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Quick Facts
Patent No.
US 10,986,840
App. No.
16/590,006
Granted
Apr 27, 2021
Kind
B2
Abstract

The invention relates to novel compounds of the formula (I) in welcher R 1 , R 2 , R 3 , A 1 , X and n 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 (81)

1. A compound of formula (I),

wherein

A 1 represents nitrogen,

R 1 represents methyl, ethyl, n-propyl, isopropyl or cyclopropyl,

R 2 represents a group selected from-NR 11 R 12 (G10), where R 11 is hydrogen and R 12 is hydrogen or oxetanyl

or —NR 11 —C(═O)—R 8 (G12), where R 11 represents hydrogen and R 8 represents hydrogen, methyl, ethyl, isopropyl, tert-butyl, trifluoromethyl, difluoromethyl, tetrafluoroethyl, pentafluoroethyl, cyclopropyl, cyclopropylmethyl, methylsulphanylmethyl

 methylsulphonylpropan-2-yl

 or 1-(methylsulphanyl)propan-2-yl

or —C(═O)—NR 11 R 12 (G3), where R 11 represents hydrogen and R 12 represents methyl, ethyl, isopropyl, cyclopropyl or tert-butyl,

R 3 represents hydrogen,

X represents a heteroaromatic 9-membered or 12-membered fused bicyclic or tricyclic ring system selected from the group consisting of H1, H2, H5, H15, H16, H17 and H19,

R 5 represents fluorine, chlorine, fluoromethyl, difluoromethyl, trifluoromethyl, fluoroethyl, difluoroethyl, trifluoroethyl, tetrafluoroethyl, pentafluoroethyl, trifluoromethoxy, difluorochloromethoxy, dichlorofluoromethoxy, trifluoromethylthio, trifluoromethylsulphonyl or trifluoromethylsulphinyl,

R 6 represents hydrogen,

R 7 represents methyl, ethyl, isopropyl, methoxymethyl or methoxyethyl,

n represents 0, 1 or 2,

where if R 2 represents G10 or G12, then X does not represent H1, H2, or H5.

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

A 1 represents nitrogen,

R 1 represents ethyl,

R 2 represents a group selected from G10, where R 11 represents hydrogen and R 12 represents hydrogen or oxetanyl,

G12, where R 11 represents hydrogen and R 8 represents methyl, trifluoromethyl, cyclopropyl,—CH 2 SCH 3 ,—CH(CH 3 )CH 2 SCH 3 or —CH(CH 3 )CH 2 SO 2 CH 3 ,

and G3, where R 11 represents hydrogen and R 12 represents methyl,

R 3 represents hydrogen,

X represents a heteroaromatic 9-membered or 12-membered fused bicyclic or tricyclic ring system selected from the group consisting of H1, H2, H5, H15, H16, H17 and H19,

R 5 represents trifluoromethyl

R 6 represents hydrogen,

R 7 represents methyl,

n represents 0, 1 or 2,

where if R 2 represents G10 or G12, then X does not represent H1, H2, or H5.

3. The compound of formula (I) according to claim 1 wherein A 1 , R 1 , R 3 , R 5 , R 6 , R 7 , X and n have the meanings given above and

R 2 represents a radical from the following series:

where if R 2 represents G10 or G12, then X does not represent H1, H2, or H5.

4. The compound of formula (I) according to claim 1 wherein A 1 , R 1 , R 2 , R 3 , R 5 , R 6 , R 7 and n have the meanings given above and

X represents a radical from the following series:

where if R 2 represents G10 or G12, then X does not represent H1, H2, or H5.

5. An agrochemical formulation comprising the compound of formula (I) according to claim 1 and one or more extenders and/or surfactants.

6. The agrochemical formulation according to claim 5 , additionally comprising a further agrochemically active compound.

7. A method for controlling one or more animal pests, comprising allowing the compound of formula (I) according to claim 1 or an agrochemical formulation thereof to act on the animal pests and/or a habitat thereof.

8. The compound of formula (I) according to claim 1 , where the substituents R 1 , R 2 , R 3 , A 1 , X and n have the meanings given in the table below and where the bond from X and R 2 to the remainder of the molecule is characterized by a wavy line:

Ex.

R 1

n

A 1

R 3

X

R 2

Ex. I-7 

—CH 2 CH 3

2

N

H

Ex. I-8 

—CH 2 CH 3

2

N

H

Ex. I-31

—CH 2 CH 3

2

N

H

Ex. I-32

—CH 2 CH 3

2

N

H

Bsp-I-34

—CH 2 CH 3

2

N

H

Ex. I-38

—CH 2 CH 3

2

N

H

Ex. I-39

—CH 2 CH 3

2

N

H

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 2, 2019
From: FISCHER, RUEDIGER; WILCKE, DAVID; KAUSCH-BUSIES, NINA; HAGER, DOMINIK; ILG, KERSTIN; HOFFMEISTER, LAURA; WILLOT, MATTHIEU; PORTZ, DANIELA; GOERGENS, ULRICH; TURBERG, ANDREAS
To: BAYER CROPSCIENCE AKTIENGESELLSCHAFT
Reel/Frame 050598/0744 →
Priority Claims (1)
EP 15180149 · Aug 7, 2015 · regional
Continuity (2)
Continuation 15750440
Related Publication 20200029567A1 · Jan 30, 2020
Cited By (1)
US 12,595,266