IP Library › Granted Patent US 12,302,900
Granted Patent B2
US 12,302,900 · App. 18/393,184 · Granted May 20, 2025

Protoporphyrinogen oxidase inhibitors

Inventors: Neville John Anthony (Northborough, MA); Paul Galatsis (Newton, MA); David Jeffrey Lauffer (Stow, MA); Peter Stchur, III (Waterford, CT)
Assignee: Enko Chem, Inc.
A01N41/06A01P13/00C07C311/51
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Quick Facts
Patent No.
US 12,302,900
App. No.
18/393,184
Granted
May 20, 2025
Kind
B2
Abstract

The present invention relates to protoporphyrinogen IX oxidase (PPO) inhibitors of the general formula (I) where the variables are defined herein. The invention features processes and intermediates for preparing the compounds of formula (I), compositions comprising them, and their use as herbicides—e.g., for controlling harmful plants. The invention also features methods for controlling unwanted vegetation comprising allowing an herbicidal effective amount of at least one PPO inhibitor of formula (I) to act on plants, their seed, and/or their habitat.

Claims (53)

1. A compound of formula (I):

or suitable salt thereof, wherein:

X is —CH or —N;

R 1 is —SR 1a or —S(O) 2 R 1b ;

R 1a is C 1-4 alkyl optionally substituted with phenyl, C(O)OR 1c , or C(O)N(R 1c ) 2 ;

each R 1c is independently, H, CH 2 CH 2 OC(O)R 1d , or optionally substituted C 1-4 alkyl, wherein the optional substituents are C 3-6 cycloalkyl, C(O)OC 1-4 alkyl, or up to 3 F atoms, or two R 1c with an intervening nitrogen atom form a 5-6 membered ring optionally substituted with C(O)OH or C(O)OC 1-4 alkyl;

R 1d is C 1-4 alkyl or C 1-4 alkenyl;

R 1b is CH 2 C(O)C 1-4 alkyl or N(R 1e )R 1f ;

R 1e is H, C 1-4 alkyl, C 1-4 alkenyl, C 1-4 alkynyl, C(O)C 1-2 alkyl, or OC 1-4 alkyl;

R 1f is H, C 1-6 alkyl, C(O)C(O)C 1-4 alkyl, C(O)R 1g , or S(O) 2 R 1g , or R 1e and R 1f together with the intervening nitrogen atom form a 5-6 membered ring, optionally containing up to two C(O) ring members;

R 1g is C 1-4 alkyl, C 1-4 alkenyl, phenyl, Het, N(R h ) 2 , OC 1-4 alkyl, C 3-6 cycloalkyl, or CH 2 (OCH 2 CH 2 ) 4 CH 3 , wherein each alkyl group is optionally substituted with up to 3 F atoms, phenyl, C 3-6 cycloalkyl, OH, OC 1-4 alkyl, wherein each cycloalkyl group is optionally substituted with OH or OC 1-4 alkyl, wherein each phenyl is optionally substituted with up to 3 Cl or F atoms, and wherein Het is a 5-6 membered heterocyclic ring containing up to two ring members selected from O, N, S, or S(O) 2 and optionally substituted with OH or OC 1-4 alkyl;

each R h is, independently H, C 1-4 alkyl, benzyl, or phenyl;

each of R 2 and R 3 is Cl or F; and

each of R 4 , R 5 , and R 6 is F or H, wherein Ring A comprises at least 4 F atoms.

2. The compound according to claim 1 , or a salt thereof, wherein R 1 is —SR 1a , and wherein R 1a is C 1-4 alkyl substituted with phenyl, C(O)OR 1c , or C(O)N(R 1c ) 2 .

3. The compound according to claim 1 , or a salt thereof, wherein R 1 is —S(O) 2 R 1b , and wherein R 1b is CH 2 C(O)C 1-4 alkyl.

4. The compound according to claim 1 , or a salt thereof, wherein R 1 is —S(O) 2 R 1b , and wherein R 1b is N(R 1e )R 1f .

5. The compound according to claim 1 having formula (II):

or a salt thereof.

6. The compound according to claim 5 , or a salt thereof, wherein each of R 4 , R 5 , and R 6 is F.

7. The compound according to claim 5 , or a salt thereof, wherein each of R 4 and R 6 is F.

8. The compound according to claim 5 , or a salt thereof, wherein each of R 4 and R 5 is F.

9. The compound according to claim 5 , or a salt thereof, wherein R 1a is C 1-4 alkyl substituted with C(O)N(R 1c ) 2 ; one R 1c is H; and the other R 1c is C 1-4 alkyl substituted with C(O)OC 1-4 alkyl.

10. The compound according to claim 1 having formula (III):

or a salt thereof.

11. The compound according to claim 10 , or a salt thereof, wherein each of R 4 , R 5 , and R 6 is F.

12. The compound according to claim 10 , or a salt thereof, wherein each of R 4 and R 6 is F.

13. The compound according to claim 10 , or a salt thereof, wherein each of R 4 and R 5 is F.

14. The compound according to claim 10 , or a salt thereof, wherein R 1f is C(O)R 1g ; and R 1g is C 1-6 alkyl, C 3-6 cycloalkyl, or OC 1-4 alkyl.

15. A compound selected from the group consisting of:

or a salt thereof.

16. An agricultural composition comprising the compound of claim 1 , or a salt thereof, and at least one additional component that serves as a carrier.

17. The composition of claim 16 , wherein at least one additional component is a surfactant or a diluent.

18. The composition of claim 16 , wherein the composition is an herbicidal composition.

19. A method of controlling undesired vegetation, said method comprising contacting said vegetation or its environment with an herbicidally effective amount of the compound of claim 1 , or a salt thereof.

20. The method of claim 19 , wherein the undesired vegetation comprises weeds.

21. The method of claim 19 , wherein the undesired vegetation comprises protoporphyrinogen IX oxidase (PPO) inhibitor-resistant weeds.

22. The method of claim 21 , wherein the PPO inhibitor-resistant weeds have a dG210 mutation.

23. The method of claim 19 , wherein the compound or composition is applied at a rate of 1 to 100 g per 10,000 m 2 .

24. The method of claim 19 , wherein contacting the undesired vegetation or its environment with the compound or composition leads to postemergence control of the undesired vegetation.

25. The method of claim 19 , wherein contacting the undesired vegetation or its environment with the compound or composition leads to preemergence control of the undesired vegetation.

26. The method of claim 19 , wherein the undesired vegetation is at least 60% controlled.

27. An agricultural composition comprising the compound of claim 15 , or a salt thereof, and at least one additional component that serves as a carrier.

28. The composition of claim 27 , wherein at least one additional component is a surfactant or a diluent.

29. The composition of claim 27 , wherein the composition is an herbicidal composition.

30. A method of controlling undesired vegetation, said method comprising contacting said vegetation or its environment with an herbicidally effective amount of the compound of claim 15 , or a salt thereof.

31. The method of claim 30 , wherein the undesired vegetation comprises weeds.

32. The method of claim 30 , wherein the undesired vegetation comprises protoporphyrinogen IX oxidase (PPO) inhibitor-resistant weeds.

33. The method of claim 32 , wherein the PPO inhibitor-resistant weeds have a dG210 mutation.

34. The method of claim 32 , wherein the compound or composition is applied at a rate of 1 to 100 g per 10,000 m 2 .

35. The method of claim 32 , wherein contacting the undesired vegetation or its environment with the compound or composition leads to postemergence control of the undesired vegetation.

36. The method of claim 32 , wherein contacting the undesired vegetation or its environment with the compound or composition leads to preemergence control of the undesired vegetation.

37. The method of claim 32 , wherein the undesired vegetation is at least 60% controlled.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 14, 2024
From: ANTHONY, NEVILLE JOHN; GALATSIS, PAUL; LAUFFER, DAVID JEFFREY; STCHUR, PETER, III
To: ENKO CHEM, INC.
Reel/Frame 068890/0545 →
Continuity (4)
Continuation 18355800 · Jul 20, 2023
Continuation PCTUS2023060450 · Jan 11, 2023
Provisional Application 63299866 · Jan 14, 2022
Related Publication 20240130365A1 · Apr 25, 2024
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