IP Library Granted Patent US 11,490,620
Granted Patent B2
US 11,490,620 · App. 16/632,180 · Granted Nov 8, 2022

Pesticidally active thiophene derivatives

Inventors: Denis Gribkov (Münchwilen, CH); Myriem El Qacemi (Stein, CH); André Stoller (Stein, CH); André Jeanguenat (Stein, CH); Aurelien Bigot (Stein, CH)
Assignee: SYNGENTA PARTICIPATIONS AG
A01N43/56A01N25/02A01N25/04A01N25/12A01N25/14A01N43/647C07D409/04
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Quick Facts
Patent No.
US 11,490,620
App. No.
16/632,180
Granted
Nov 8, 2022
Kind
B2
Abstract

Compounds of formula (I), as defined herein, to processes for preparing them, to pesticidal, in particular insecticidal, acaricidal, molluscicidal and nematicidal compositions comprising them and to methods of using them to combat and control pests such as insect, acarine, molluse and nematode pests.

Claims (45)

1. A compound of formula (I),

wherein

Y′ and Y 3 are independently selected from H, halogen, cyano, C 1 -C 6 -alkyl, C 1 -C 6 -haloalkyl, C 1 -C 6 -alkoxy, C 1 -C 6 -haloalkoxy, C 1 -C 6 -alkoxy-C 1 -C 6 -alkyl, C 1 -C 6 -alkylsulfanyl, C 1 -C 6 -haloalkylsulfanyl, C 1 -C 6 -alkylsulfinyl, C 1 -C 6 -haloalkylsulfinyl, C 1 -C 6 -alkylsulfonyl and C 1 -C 6 -haloalkyl sulfonyl;

Y 5 is -1-CF 3 -cyclopropyl;

A is CH or N;

R 1 is selected from H, C 1 -C 6 -alkyl, C 2 -C 6 alkenyl, C 2 -C 6 alkynyl, C 3 -C 1 cycloalkyl, C 3 -C 1 cycloalkyl, C 1 -C 3 -alkyl, —C(═O)H, C 1 -C 6 -alkylcarbonyl, C 3 -C 1 -cycloalkylcarbonyl, C 1 -C 6 -alkoxycarbonyl, aryl(C o -C 3 )-alkyl and heteroaryl(C o -C 3 )-alkyl, wherein each of C 1 -C 6 -alkyl, C 3 -C 6 alkenyl, C 3 -C 6 alkynyl, C 3 -C 1 cycloalkyl, C 3 -C 1 cycloalkyl-C 1 -C 3 -alkyl, C 1 -C 6 -alkylcarbonyl, C 1 -C 6 -alkoxycarbonyl, aryl(C 0 -C 3 )-alkyl and heteroaryl(C 0 -C 3 )-alkyl is unsubstituted or substituted with 1 to 5 substituents independently selected from halogen, cyano, C 1 -C 6 -alkoxy and C 1 -C 6 -alkoxycarbonyl;

R 2 is selected from chloro and cyano;

Q is H or cyano;

or an agrochemically acceptable salt or N-oxide thereof.

2. A compound of formula (I),

wherein

Y 1 and Y 3 are independently selected from H, halogen, cyano, C 1 -C 6 -haloalkyl, C 1 -C 6 -alkoxy, C 1 -C 6 -haloalkoxy, C 1 -C 6 -alkoxy-C 1 -C 6 -alkyl, C 1 -C 6 -alkylsulfanyl, C 1 -C 6 -haloalkylsulfanyl, C 1 -C 6 -alkylsulfinyl, C 1 -C 6 -haloalkylsulfinyl, C 1 -C 6 -alkylsulfonyl and C 1 -C 6 -haloalkyl sulfonyl;

Y 5 is selected from -i-CF(CF 3 )(CF 3 ) and - 1-CF 3 -cyclopropyl;

A is CH or N;

R 1 is selected from H, C 2 -C 6 alkenyl, C 2 -C 6 alkynyl, C 3 -C 1 cycloalkyl, C 3 -C 1 cycloalkyl- C 1 -C 3 -alkyl, —C(═O)H, C 1 -C 6 -alkylcarbonyl, C 3 -C 1 -cycloalkylcarbonyl, C1-C6-alkoxycarbonyl, aryl(C o -C 3 )-alkyl and heteroaryl(C o -C 3 )-alkyl, wherein each of C 1 -C 6 -alkyl, C 3 -C 6 alkenyl, C 3 -C 6 alkynyl, C 3 -C 1 cycloalkyl, C 3 -C 1 cycloalkyl- C1-C3-alkyl, C1-C6-alkylcarbonyl, C 1 -C 6 -alkoxycarbonyl, aryl(C 0 -C 3 )-alkyl and heteroaryl(C 0 -C 3 )-alkyl is unsubstituted or substituted with 1 to 5 substituents independently selected from halogen, cyano, C 1 -C 6 -alkoxy and C 1 -C 6 -alkoxycarbonyl;

R 2 is cyano;

Q is H or cyano;

or an agrochemically acceptable salt or N-oxide thereof.

3. The compound according to claim 1 wherein Q is cyano.

4. The compound according to claim 1 wherein R 1 is selected from H, methyl, ethyl, —CH 2 CH═CH 2 , isobutyl, isopropyl, 2,2,2-trifluoroethyl, cyclopropylmethyl, —C(═O)CH 3 , —C(═O)CH 2 CH 3 , —C(═O)cyclopropyl, —C(═O)OCH 3 , —C(═O)OCH 2 CH 3 , —C(═O)CH(CH 3 )(CH 3 ), —CH 2 C═CH, —CH 2 CN, —CH 2 —O—CH 3 , —CH 2 —O—CH 2 —CH 3 and —CH 2 -cyclopropyl.

5. The compound according to claim 1 wherein R 1 is selected from H, isobutyl, 2,2,2-trifluoroethyl, cyclopropylmethyl, —C(═O)CH 3 , —C(═O)OCH 3 ,—C(═O)OCH 2 CH 3 , —C(═O)CH(CH 3 )(CH 3 ), —CH 2 —C—CH, —CH 2 CN and —CH 2 —O—CH 3 .

6. The compound according to claim 1 wherein Y 1 and Y 3 are independently selected from chloro, bromo, —CF 3 , —CHF 2 , —OCF 3 , —OCHF 2 , methyl, ethyl —SCH 3 , —SOCH 3 , —S(O) 2 CH 3 and CN.

7. The compound according to claim 1 wherein Y 1 and Y 3 are independently selected from chloro, bromo, —CF 3 , —OCHF 2 and methyl.

8. A compound selected from

2-cyano-N-cyclopropyl-5-[1-[2,6-dichloro-4-[1,2,2,2-tetrafluoro-1-(trifluoromethyl)ethyl]phenyl]pyrazol-4-yl]thiophene-3-carboxamide;

2 chloro N (1 cyanocyclopropyl) 5 [1 [2,6 dichloro 11 [1,2,2,2 tetrafluoro 1 (trifluoromethyl) ethyl]phenyl]pyrazol yl]thiophene 3 carboxamide;

2-cyano-N-cyclopropyl-5-[1-[2,6-dimethyl-4-[1,2,2,2-tetrafluoro-1-(trifluoromethyl)ethyl]phenyl]pyrazol-4-yl]thiophene-3-carboxamide;

2-chloro-5-[1-[2-chloro-4-[1,2,2,2-tetrafluoro-1-(trifluoromethyl)ethyl]phenyl]pyrazol-4-yl]-N-(1-cyanocyclopropyl)thiophene-3-carboxamide;

5- [1- [2-b rom o-6-chloro-4-[1,2,2,2-tetrafluoro-1-(trifluoromethyl)ethyl] phenyl] pyrazo1-4-yl]-2-chloro-N-(1-cyanocyclopropyl)thiophene-3-carboxamide;

5- [1- [2-chloro-4-[1,2,2,2-tetrafluoro-1-(trifluoromethyl)ethyl] phenyl]pyrazol-4-yl]-2-cyano-N-cyclopropyl-thiophene-3-carboxamide;

5- [1- [2-bromo-6-chloro-4-[1,2,2,2-tetrafluoro-1-(trifluoromethyl)ethyl] phenyl]pyrazol-4-yl]-2-chloro-N-cyclopropyl -thiophene-3-carboxamide;

2-chloro-N-(1-cyanocyclopropyl)-5-[1-[2,6-dimethyl-4-[1,2,2,2-tetrafluoro-1-(trifluoromethyl)ethyl]phenyl]pyrazol-4-yl]thiophene-3-carboxamide;

2-cyano-N-cyclopropyl-5- [1-[2,6-dichloro-4-[1,2,2,2-tetrafluoro-1-(trifluoromethyl)ethyl]phenyl]triazol-4-yl]-N-ethyl-thiophene-3-carboxamide; 2-cyano-N-cyclopropyl-5-[1- [2, 6-dichloro-4-[1,2,2,2-tetrafluoro-1-(trifluoromethyl)ethyl] phenyl]triaz01-4-yl]-N-methyl -thiophene-3-carboxamide; 2-cyano-N-cyclopropyl-5-[1- [2, 6-dichloro-4-[1,2,2,2-tetrafluoro-1-(trifluoromethyl)ethyl]phenyl]triazol -4-yl]thiophene-3-carboxamide;

2-chloro-N-(1-cyanocyclopropyl)-5-[1-[2,6-dichloro-4-[1,2,2,2-tetrafluoro-1-(trifluoromethyl)ethyl] phenyl]triazol-4-yl]-N-ethyl -thiophene-3-carb oxamide; 2-chloro-N-(1-cyanocyclopropyl)-5-[1-[2,6-dichloro-4-[1,2,2,2-tetrafluoro-1-(trifluoromethyl)ethyl] phenyl]triazol -4-yl]-N-methyl -thiophene-3-carboxamide; 2-chloro-N-(1-cyanocyclopropyl)-5-[1-[2,6-dichloro-4-[1,2,2,2-tetrafluoro-1-(trifluoromethyl)ethyl]phenyl]triazol-4-yl]thiophene-3-carboxamide; and

2-chloro-N-cyclopropyl-5- [1-[2,6-dichloro-4-[1,2,2,2-tetrafluoro-1-(trifluoromethyl)ethyl]phenyl]triazo11-4-yl]thiophene-3-carboxamide.

9. A pesticidal composition, which comprises at least one compound according to claim 1 , or an agrochemically acceptable salt or N-oxide thereof, as active ingredient and at least one auxiliary.

10. The composition according to claim 9 , which further comprises one or more other insecticidally, acaricidally, nematicidally and/or fungicidally active agents.

11. A method for controlling pests, which comprises applying a composition according to claim 9 to the pests or their environment.

12. A method for the protection of plant propagation material from the attack by pests, which comprises treating the propagation material or the site, where the propagation material is planted, with a composition according to claim 11 .

13. A coated plant propagation material, wherein the coating of the plant propagation material comprises a compound as defined in claim 1 .

14. The compound according to claim 2 , wherein Q is cyano.

15. The compound according to claim 2 , wherein R 1 is selected from H, methyl, ethyl, —CH 2 CH═CH 2 , isobutyl, isopropyl, 2,2,2-trifluoroethyl, cyclopropylmethyl, —C(═O)CH 3 , —C(═O)CH 2 CH 3 , —C(═O)cyclopropyl, —C(═O)OCH 3 , —C(═O)OCH 2 CH 3 , —C(═O)CH(CH 3 )(CH 3 ), —CH 2 C═CH, —CH 2 CN, —CH 2 —O—CH 3 , —CH 2 —O—CH 2 —CH 3 and —CH 2 -cyclopropyl.

16. The compound according to claim 2 , wherein R 1 is selected from H, isobutyl, 2,2,2-trifluoroethyl, cyclopropylmethyl, —C(═O)CH 3 , —C(═O)OCH 3 ,—C(═O)OCH 2 CH 3 —C(═O)CH(CH 3 )(CH 3 ), —CH 2 —C—CH, —CH 2 CN and —CH 2 —O—CH 3 .

17. The compound according to claim 2 , wherein Y 1 and Y 3 are independently selected from chloro, bromo, —CF 3 , —CHF 2 , —OCF 3 , —OCHF 2 , methyl, ethyl, —SCH 3 , —SOCH 3 , —S(O) 2 CH 3 and CN.

18. The compound according to claim 2 , wherein Y 1 and Y 3 are independently selected from chloro, bromo, —CF 3 , —OCHF 2 and methyl.

Assignments (2)
MERGER AND CHANGE OF NAME Recorded Feb 28, 2025
From: SYNGENTA PARTICIPATIONS AG; SYNGENTA PARTICIPATIONS AG
To: SYNGENTA CROP PROTECTION AG
Reel/Frame 070362/0665 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 23, 2020
From: GRIBKOV, DENIS; EL QACEMI, MYRIEM; STOLLER, ANDRÉ; JEANGUENAT, ANDRÉ; BIGOT, AURELIEN
To: SYNGENTA PARTICIPATIONS AG
Reel/Frame 051596/0201 →