IP Library Granted Patent US 10,051,861
Granted Patent B2
US 10,051,861 · App. 15/349,297 · Granted Aug 21, 2018

N-arylamidine-substituted trifluoroethyl sulfide derivatives as acaricides and insecticides

Inventors: Adeline Koehler (Langenfeld, DE); Bernd Alig (Koenigswinter, DE); Angela Becker (Duesseldorf, DE); Arnd Voerste (Cologne, DE); Ulrich Goergens (Ratingen, DE); Reiner Fischer (Monheim, DE); Wahed Ahmed Moradi (Monheim, DE); Silvia Cerezo-Galvez (Langenfeld, DE); Julia Johanna Hahn (Duesseldorf, DE); Kerstin Ilg (Cologne, DE); Hans-Georg Schwarz (Dorsten, DE); Takuya Gomibuchi (Ibaraki, JP); Masahito Ito (Ibaraki, JP); Daiei Yamazaki (Yamaguchi, JP); Katsuhiko Shibuya (Tochigi, JP); Eiichi Shimojo (Osaka, JP)
Assignee: BAYER CROPSCIENCE AG
A01N41/10A01N41/12A01N43/08A01N43/10A01N43/36A01N43/40A01N43/60A01N43/84A01N43/86C07C315/02C07C317/34C07C317/40C07C319/14C07C319/20C07C323/36C07C323/41C07C323/44C07C323/45C07C335/16C07D207/22C07D207/34C07D211/38C07D211/72C07D211/98C07D213/61C07D213/78C07D239/28C07D241/24C07D263/28C07D277/16C07D277/18C07D277/38C07D277/54C07D279/06C07D285/08C07D295/125C07D295/13C07D305/08C07D307/24C07D307/68C07D331/04C07D333/38C07D333/48C07D401/06C07C2601/02C07C2601/04C07C2601/08C07C2601/14
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 10,051,861
App. No.
15/349,297
Granted
Aug 21, 2018
Kind
B2
Abstract

The present invention relates to novel N-arylamide-substituted trifluoroethyl sulfide derivatives of the formula (I) in which X 1 , X 2 , X 3 , X 4 , R 1 , R 2 , R 3 , n have the meanings given in the description—to their use as acaricides and insecticides for controlling animal pests and to processes and intermediates for their preparation.

Claims (40)

1. A process for preparing compounds of the formula (Ia-g)

in which

n represents the number 0 or 1,

A represents oxygen or sulfur,

X 1 , X 2 , X 3 , X 4 independently of one another represent hydrogen, halogen, hydroxy, amino, OCN, SCN, SF 5 , trialkylsilyl, alkyl, haloalkyl, cyanoalkyl, hydroxyalkyl, alkoxycarbonylalkyl, alkoxyalkyl, alkenyl, haloalkenyl, cyanoalkenyl, alkynyl, haloalkynyl, cyanoalkynyl, alkoxy, haloalkoxy, cyanoalkoxy, hydroxycarbonylalkoxy, alkoxycarbonylalkoxy, alkoxyalkoxy, alkylhydroxyimino, alkoxyimino, alkylalkoxyimino, haloalkylalkoxyimino, alkylthio, haloalkylthio, alkoxyalkylthio, alkylthioalkyl, alkylsulfinyl, haloalkylsulfinyl, alkoxyalkylsulfinyl, alkylsulfinylalkyl, alkylsulfonyl, haloalkylsulfonyl, alkoxyalkylsulfonyl, alkylsulfonylalkyl, alkylsulfonyloxy, alkylcarbonyl, haloalkylcarbonyl, carboxyl, alkylcarbonyloxy, alkoxycarbonyl, haloalkoxycarbonyl, alkoxycarbonylalkyl, aminocarbonyl, alkylaminocarbonyl, dialkylaminocarbonyl, alkenylaminocarbonyl, dialkenylaminocarbonyl, cycloalkylaminocarbonyl, alkylsulfonylamino, aminosulfonyl, alkylaminosulfonyl, dialkylaminosulfonyl, alkylsulfoximino, aminothiocarbonyl, alkylaminothiocarbonyl, dialkylaminothiocarbonyl,

or represent optionally substituted phenylalkyl, phenoxy, phenylalkyloxy, phenoxyalkyl, phenylthio, phenylthioalkyl, phenylsulfinyl, phenylsulfonyl, hetarylalkyl, hetaryloxy, hetarylalkyloxy, hetarylthio, hetarylsulfinyl, hetarylsulfonyl,

or represent optionally substituted saturated or unsaturated cycloalkylalkyl, cycloalkyloxy, cycloalkylalkoxy, cycloalkylthio, cycloalkylalkylthio, cycloalkylsulfinyl, cycloalkylalkylsulfinyl, cycloalkylsulfonyl, cycloalkylalkylsulfonyl,

or represent NR 4 R 5 , where R 4 and R 5 independently of one another represent hydrogen, cyano, alkyl, haloalkyl, cyanoalkyl, hydroxyalkyl, alkoxyalkyl, alkylthioalkyl, alkenyl, haloalkenyl, cyanoalkenyl, alkynyl, haloalkynyl, cyanoalkynyl, acyl, alkoxycarbonyl, or R 4 and R 5 together with the nitrogen atom to which they are attached may form an optionally substituted saturated or unsaturated five-to eight-membered ring which is optionally interrupted by heteroatoms from the group consisting of O, S and N,

or represent a 3- to 6-membered saturated, partially saturated or aromatic ring which may optionally contain one to three heteroatoms from the group consisting of O, S and N and which is optionally mono- or polysubstituted by identical or different substituents from the group consisting of halogen, cyano, nitro, hydroxy, amino, carboxy, alkyl, haloalkyl, alkenyl, haloalkenyl, alkynyl, alkoxy, haloalkoxy, alkylthio, alkylsulfinyl, alkylsulfonyl, alkylsulfonyloxy, haloalkylthio, haloalkylsulfinyl, haloalkylsulfonyl, alkylamino, dialkylamino, alkylcarbonylamino, alkoxycarbonyl, alkylcarbonyl, alkylcarbonyloxy, aminocarbonyl, alkylaminocarbonyl, dialkylaminocarbonyl, aminothiocarbonyl, alkylaminothiocarbonyl, dialkylaminothiocarbonyl, cycloalkylamino, alkylsulfonylamino, aminosulfonyl, alkylaminosulfonyl and dialkylaminosulfonyl, or by optionally substituted cycloalkyl, cycloalkoxy, cycloalkylalkyl or cycloalkylalkoxy which are optionally interrupted by heteroatoms from the group consisting of O, S and N,

or X 2 and X 3 or X 3 and X 4 , form, together with the carbon atoms to which they are attached, a 5- or 6-membered ring which is optionally substituted and optionally interrupted by heteroatoms from the group consisting of O, S, N and CO,

R 2 represents hydrogen, cyano, alkyl, haloalkyl, alkoxy, cyanoalkyl, hydroxyalkyl, alkoxyalkyl, alkylthioalkyl, alkenyl, haloalkenyl, cyanoalkenyl, alkynyl, haloalkynyl, cyanoalkynyl, represent optionally substituted alkylcarbonyl, alkoxycarbonyl, arylcarbonyl, hetarylcarbonyl, aryloxycarbonyl, hetaryloxycarbonyl, alkylsulfinyl, haloalkylsulfinyl, arylsulfinyl, arylalkylsulfinyl, hetarylsulfinyl, hetarylalkylsulfinyl, alkylsulfonyl, haloalkylsulfonyl, arylsulfonyl, arylalkylsulfonyl, hetarylsulfonyl, hetarylalkylsulfonyl,

or represents a 3- to 6-membered saturated, partially saturated or aromatic ring which may optionally contain one to three heteroatoms from the group consisting of O, S and N, which may optionally be interrupted once or twice by C═O, SO or SO 2 and which is optionally mono- or polysubstituted by identical or different substituents from the group consisting of halogen, cyano, nitro, hydroxy, amino, carboxy, alkyl, haloalkyl, alkenyl, haloalkenyl, alkynyl, alkoxy, haloalkoxy, alkylthio, alkylsulfinyl, alkylsulfonyl, alkylsulfonyloxy, haloalkylthio, haloalkylsulfinyl, haloalkylsulfonyl, alkylamino, dialkylamino, alkylcarbonylamino, alkoxycarbonyl, alkylcarbonyl, alkylcarbonyloxy, aminocarbonyl, alkylaminocarbonyl, dialkylaminocarbonyl, aminothiocarbonyl, alkylaminothiocarbonyl, dialkylaminothiocarbonyl, cycloalkylamino, alkylsulfonylamino, aminosulfonyl, alkylaminosulfonyl and dialkylaminosulfonyl, or by optionally substituted cycloalkyl, cycloalkoxy, cycloalkylalkyl or cycloalkylalkoxy which are optionally interrupted by heteroatoms from the group consisting of O, S and N,

or represents —(CH 2 ) m —R 6 , —O—(CH 2 ) m —R 6 , —(CH 2 ) m —O—R 6 , where R 6 represents a 3- to 6-membered saturated, partially saturated or aromatic ring which may optionally contain one to three heteroatoms from the group consisting of O, S and N, which may optionally be interrupted once or twice by C═O and which is optionally mono- or polysubstituted by identical or different substituents from the group consisting of halogen, cyano, nitro, hydroxy, amino, carboxy, alkyl, haloalkyl, alkenyl, haloalkenyl, alkynyl, alkoxy, haloalkoxy, alkylthio, alkylsulfinyl, alkylsulfonyl, alkylsulfonyloxy, haloalkylthio, haloalkylsulfinyl, haloalkylsulfonyl, alkylamino, dialkylamino, alkylcarbonylamino, alkoxycarbonyl, alkylcarbonyl, alkylcarbonyloxy, aminocarbonyl, alkylaminocarbonyl, dialkylaminocarbonyl, aminothiocarbonyl, alkylaminothiocarbonyl, dialkylaminothiocarbonyl, cycloalkylamino, alkylsulfonylamino, aminosulfonyl, alkylaminosulfonyl and dialkylaminosulfonyl, or by optionally substituted cycloalkyl, cycloalkoxy, cycloalkylalkyl or cycloalkylalkoxy which are optionally interrupted by heteroatoms from the group consisting of O, S and N, where m represents the number 1, 2, 3 or 4,

and/or diastereomers, enantiomers, rotamers, tautomers, and/or salts thereof,

wherein

(A) anilines of the formula (X)

are converted with isocyanates or isothiocyanates, optionally in the presence of a base and optionally in the presence of an organic solvent, into compounds of the formula (XXXVIII),

and

(B) compounds of the formula (XXXVIII) are converted by cycloacylation into compounds of the formula (Ia-g),

2. The process according to claim 1 , further comprising

(C) oxidizing the compound of formula (Ia-g)

to a compound of formula (Ib-g)

3. The process according to claim 2 , wherein the compound of formula (Ib-g) is

4. The process according to claim 1 , wherein A represents oxygen.

5. The process according to claim 1 , wherein A represents sulfur.

6. The process according to claim 1 , wherein n represents the number 0.

7. The process according to claim 1 , wherein n represents the number 1.

8. The process according to claim 1 , wherein anilines of the formula (X)

are converted with isocyanates or isothiocyanates, in the presence of a base, into compounds of the formula (XXXVIII),

9. The process according to claim 1 , wherein anilines of the formula (X)

are converted with isocyanates or isothiocyanates, in the presence of an organic solvent, into compounds of the formula (XXXVIII),

10. The process according to claim 1 , wherein anilines of the formula (X)

are converted with isocyanates or isothiocyanates, in the presence of pyridine, into compounds of the formula (XXXVIII),

11. The process according to claim 1 , wherein X 1 , X 2 , X 3 , X 4 independently of one another represent hydrogen, fluorine, chlorine, bromine, iodine, (C 1 -C 4 )-alkyl, (C 1 -C 4 )-haloalkyl, (C 2 -C 4 )-alkenyl, (C 2 -C 4 )-alkynyl, (C 1 -C 4 )-alkoxy, (C 1 -C 4 )-haloalkoxy, or aminothiocarbonyl.

12. The process according to claim 1 , wherein X 1 and X 3 represent hydrogen.

13. The process according to claim 1 , wherein X 2 and X 4 independently of one another represent hydrogen, fluorine, chlorine, bromine, methyl, ethyl, trifluoromethyl, difluoromethyl, difluoromethoxy, trifluoromethoxy, or OCH 2 CF 3 .

14. The process according to claim 1 , wherein X 2 and X 4 represent one of the combinations X 2 /X 4 : fluorine/fluorine, chlorine/chlorine, fluorine/chlorine, chlorine/fluorine, bromine/bromine, bromine/chlorine, chlorine/bromine, bromine/fluorine, fluorine/bromine, methyl/methyl, methyl/fluorine, fluorine/methyl, methyl/chlorine, chlorine/methyl, methyl/bromine, bromine/methyl, ethyl/ethyl, ethyl/fluorine, fluorine/ethyl, ethyl/chlorine, chlorine/ethyl, ethyl/bromine, bromine/ethyl.

15. The process according to claim 2 , wherein the compound of formula (Ib-g) is selected from the group consisting of:

16. The process according to claim 1 , wherein the compound of formula (Ia-g) is

17. The process according to claim 2 , wherein the compound of formula (Ib-g) is

Assignments (3)
NUNC PRO TUNC ASSIGNMENT Recorded Jul 4, 2023
From: BAYER INTELLECTUAL PROPERTY GMBH
To: BAYER CROPSCIENCE AKTIENGESELLSCHAFT
Reel/Frame 064198/0823 →
CHANGE OF ADDRESS Recorded Jun 12, 2023
From: BAYER INTELLECTUAL PROPERTY GMBH
To: BAYER INTELLECTUAL PROPERTY GMBH
Reel/Frame 064021/0344 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 9, 2017
From: KOEHLER, ADELINE; ALIG, BERND; BECKER, ANGELA; GOERGENS, ULRICH; FISCHER, REINER; MORADI, WAHED AHMED; HAHN, JULIA JOHANNA; ILG, KERSTIN; SCHWARZ, HANS-GEORG; GOMIBUCHI, TAKUYA; ITO, MASAHITO; YAMAZAKI, DAIEI; SHIBUYA, KATSUHIKO; SHIBUYA, EIICHI; VOERSTE, ARND; CEREZO-GALVEZ, SILVIA
To: BAYER CROPSCIENCE AG; BAYER INTELLECTUAL PROPERTY GMBH
Reel/Frame 042658/0713 →
Priority Claims (1)
EP 11194855 · Dec 21, 2011 · regional
Continuity (2)
Division 14366715
Related Publication 20170057914A1 · Mar 2, 2017