IP Library › Granted Patent US 11,357,231
Granted Patent B2
US 11,357,231 · App. 17/000,978 · Granted Jun 14, 2022

Insecticidal compounds based on isoxazoline derivatives

Inventors: Jérôme Yves Cassayre (Stein, CH); Peter Renold (Stein, CH); Myriem El Qacemi (Stein, CH); Thomas Pitterna (Stein, CH); Julie Clementine Toueg (Stein, CH)
Assignee: SYNGENTA CROP PROTECTION LLC
A01N43/80C07D261/04C07D413/12C07D413/14C07D417/12C07D419/12
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Quick Facts
Patent No.
US 11,357,231
App. No.
17/000,978
Granted
Jun 14, 2022
Kind
B2
Abstract

Compounds of formula III wherein R 1 , R 2 , L, Y 1 , Y 2 , Y 3 , and Y 4 are defined in claim 1.

Claims (25)

1. A compound of formula III

wherein

L is a C 1 -C 8 alkylene;

R 1 is hydrogen, C 1 -C 8 alkyl, C 1 -C 8 alkylcarbonyl-, C 1 -C 8 alkoxy, C 1 -C 8 alkoxy-C 1 -C 8 alkyl or C 1 -C 8 alkoxycarbonyl-;

R 2 is hydrogen, C 1 -C 8 haloalkyl or C 1 -C 8 alkyl;

Y 1 is CR 7 R 8 or C═O; and

Y 2 , Y 3 and Y 4 are independently CR 7 R 8 , C═O, N—R 9 , O, S, SO or SO 2 ;

wherein at least two adjacent ring atoms in the ring formed by Y 1 , Y 2 , Y 3 and Y 4 are heteroatoms;

each R 7 and R 8 is independently hydrogen, halogen, C 1 -C 8 alkyl, or C 1 -C 8 haloalkyl;

each R 9 is independently hydrogen, cyano, cyano-C 1 -C 8 alkyl, C 1 -C 8 alkyl, C 1 -C 8 haloalkyl, C 3 -C 8 cycloalkyl, C 3 -C 8 cycloalkyl where one carbon atom is replaced by O, S, S(O) or SO 2 , or C 3 -C 8 cycloalkyl-C 1 -C 8 alkyl, C 3 -C 8 cycloalkyl-C 1 -C 8 alkyl where one carbon atom in the cycloalkyl group is replaced by O, S, S(O) or SO 2 , or C 3 -C 8 cycloalkyl-C 1 -C 8 haloalkyl, C 1 -C 8 hydroxyalkyl, C 1 -C 8 alkoxy-C 1 -C 8 alkyl, C 2 -C 8 alkenyl, C 2 -C 8 haloalkenyl, C 2 -C 8 alkynyl, C 2 -C 8 haloalkynyl, phenyl, phenyl substituted by one to three R 10 , phenyl-C 1 -C 4 alkyl, phenyl-C 1 -C 4 alkyl wherein the phenyl moiety is substituted by one to three R 10 , 5-6 membered heteroaryl-C 1 -C 4 alkyl or 5-6 membered heteroaryl-C 1 -C 4 alkyl wherein the heteroaryl moiety is substituted by one to three R 10 , or C 1 -C 4 alkyl-(C 1 -C 4 alkyl-O—N═)C—CH 2 —; and

each R 10 is independently halogen, cyano, nitro, C 1 -C 8 alkyl, C 1 -C 8 haloalkyl, C 1 -C 8 alkoxy, or C 1 -C 8 haloalkoxy;

or a salt or N-oxide thereof;

wherein the compound is not

2. The compound according to claim 1 , wherein L is C 1 -C 4 alkylene.

3. The compound according to claim 1 , wherein L is methylene.

4. The compound according to claim 3 , wherein Y 3 is N—R 9 and R 9 is cyano, cyano-C 1 -C 8 alkyl, C 1 -C 8 haloalkyl, C 3 -C 8 cycloalkyl, C 3 -C 8 cycloalkyl where one carbon atom is replaced by S, S(O) or SO 2 , or C 3 -C 8 cycloalkyl-C 1 -C 8 alkyl, C 3 -C 8 cycloalkyl-C 1 -C 8 alkyl where one carbon atom in the cycloalkyl group is replaced by S, S(O) or SO 2 , or C 3 -C 8 cycloalkyl-C 1 -C 8 haloalkyl, C 2 -C 8 alkenyl, C 2 -C 8 haloalkenyl, C 2 -C 8 alkynyl, C 2 -C 8 haloalkynyl, phenyl, phenyl substituted by one to three R 10 , phenyl-C 1 -C 4 alkyl, phenyl-C 1 -C 4 alkyl wherein the phenyl moiety is substituted by one to three R 10 , 5-6 membered heteroaryl-C 1 -C 4 alkyl or 5-6 membered heteroaryl-C 1 -C 4 alkyl wherein the heteroaryl moiety is substituted by one to three R 10 , C 1 -C 4 alkyl-(C 1 -C 4 alkyl-O—N═)C—CH 2 —, and wherein heteroaryl refers to pyridazinyl, pyrimidinyl, pyrazinyl, pyrazolyl, furanyl, thiophenyl, oxazolyl, isoxazolyl or thiazolyl.

5. The compound according to claim 4 , wherein Y 3 is N—R 9 and R 9 is cyclopropyl, cyclobutyl, oxetanyl, thietanyl, trifluoroethyl, difluoroethyl, allyl, propargyl, cyanomethyl, benzyl, benzyl substituted by one to three R 10 .

6. The compound according to claim 5 , wherein each R 10 and R 8 is independently hydrogen, halogen, C 1 -C 4 alkyl, or C 1 -C 4 haloalkyl.

7. The compound according to claim 6 , wherein each R 10 is independently halogen, cyano, nitro, C 1 -C 4 alkyl, C 1 -C 4 haloalkyl, C 1 -C 4 alkoxy, or C 1 -C 4 haloalkoxy.

8. The compound according to claim 7 , wherein R 2 is hydrogen, C 1 -C 4 haloalkyl or C 1 -C 4 alkyl.

9. The compound according to claim 8 , wherein R 1 is hydrogen, C 1 -C 4 alkyl, C 1 -C 4 alkylcarbonyl-, C 1 -C 4 alkoxy, C 1 -C 4 alkoxy-C 1 -C 4 alkyl or C 1 -C 4 alkoxycarbonyl-.

10. The compound according to claim 9 , wherein Y 4 is C═O.

11. The compound according to claim 10 , wherein Y 2 is O.

12. The compound according to claim 1 , wherein Y 3 is N—R 9 and R 9 is cyano, cyano-C 1 -C 8 alkyl, C 1 -C 8 haloalkyl, C 3 -C 8 cycloalkyl, C 3 -C 8 cycloalkyl where one carbon atom is replaced by S, S(O) or SO 2 , or C 3 -C 8 cycloalkyl-C 1 -C 8 alkyl, C 3 -C 8 cycloalkyl-C 1 -C 8 alkyl where one carbon atom in the cycloalkyl group is replaced by S, S(O) or SO 2 , or C 3 -C 8 cycloalkyl-C 1 -C 8 haloalkyl, C 2 -C 8 alkenyl, C 2 -C 8 haloalkenyl, C 2 -C 8 alkynyl, C 2 -C 8 haloalkynyl, phenyl, phenyl substituted by one to three R 10 , phenyl-C 1 -C 4 alkyl, phenyl-C 1 -C 4 alkyl wherein the phenyl moiety is substituted by one to three R 10 , 5-6 membered heteroaryl-C 1 -C 8 alkyl or 5-6 membered heteroaryl-C 1 -C 4 alkyl wherein the heteroaryl moiety is substituted by one to three R 10 , C 1 -C 4 alkyl-(C 1 -C 4 alkyl-O—N═)C—CH 2 —, and wherein heteroaryl refers to pyridazinyl, pyrimidinyl, pyrazinyl, pyrazoyl, furanyl, thiophenyl, oxazolyl, isoxazolyl or thiazolyl.

13. The compound according to claim 12 , wherein Y 3 is N—R 9 and R 9 is cyclopropyl, cyclobutyl, oxetanyl, thietanyl, trifluoroethyl, difluoroethyl, allyl, propargyl, cyanomethyl, benzyl, benzyl substituted by one to three R 10 .

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 30, 2020
From: CASSAYRE, JÉRÔME YVES; RENOLD, PETER; EL QACEMI, MYRIEM; PITTERNA, THOMAS; TOUEG, JULIE CLEMENTINE
To: SYNGENTA CROP PROTECTION LLC
Reel/Frame 054218/0906 →
Priority Claims (2)
EP 09177640 · Dec 1, 2009 · regional
EP 10186537 · Oct 5, 2010 · regional
Continuity (5)
Division 16267562 · Feb 5, 2019
Division 15429631 · Feb 10, 2017
Continuation 14258079 · Apr 22, 2014
Continuation 13512820
Related Publication 20200383330A1 · Dec 10, 2020
Cited By (3)
US 12,304,903 US 12,544,336 US 12,655,138