IP Library Granted Patent US 10,512,269
Granted Patent B2
US 10,512,269 · App. 15/569,885 · Granted Dec 24, 2019

Herbicidal compounds

Inventors: Stephen Edward Shanahan (Bracknell, GB); Timothy Jeremiah Cornelius O'Riordan (Bracknell, GB)
Assignee: SYNGENTA PARTICIPATIONS AG
A01N43/90A01N43/78C07D277/60C07D417/12C07D513/04
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Quick Facts
Patent No.
US 10,512,269
App. No.
15/569,885
Granted
Dec 24, 2019
Kind
B2
Abstract

The present invention relates to herbicidal heteroaryl-alkyl-oxy-substituted heteroaryl/phenyl derivatives of formula (I), as well as to processes and intermediates used for the preparation of such derivatives. The invention further extends to herbicidal compositions comprising such derivatives, as well as to the use of such compounds and compositions in controlling undesirable plant growth; in particular the use in controlling weeds in crops of useful plants.

Claims (51)

1. A compound of formula (I),

or a salt or N-oxide thereof, wherein,

A 2 is CR 10a R 10b or NR 11 ;

A 3 is C(O) or S(O) 2 ;

A 4 is CR 1 , N(R 13 ) n , O or S;

A 5 is CR 2 , N(R 14 ) n , O or S;

n is an integer of 0 or 1;

R 1 is independently hydrogen, halogen, nitro, cyano, or independently selected from the group consisting of: C 1 -C 6 alkyl, C 2 -C 6 alkenyl, C 1 -C 6 alkoxy C 1 -C 6 alkylthio, C 1 -C 6 alkylsulfinyl, C 1 -C 6 alkylsulfonyl, C 3 -C 6 cycloalkyl, C 1 -C 6 alkoxy-C 1 -C 6 alkyl-, C 1 -C 6 alkoxy-C 1 -C 6 alkoxy-, di-C 1 -C 6 alkoxy-C 1 -C 6 alkyl, and C 1 -C 6 alkylthio-C 1 -C 6 alkyl, each of which is optionally substituted by 1-3 halogen atoms;

R 2 is hydrogen, halogen, methyl or C 1 haloalkyl;

R 10a and R 10b are each independently hydrogen, halogen, cyano, C 1 -C 8 alkyl, C 1 -C 8 alkoxy-C 1 -C 4 alkyl-, 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, C 3 -C 10 cycloalkyl, C 3 -C 10 cycloalkyl-C 1 -C 4 alkyl-, heterocyclyl, heterocyclyl-C 1 -C 4 alkyl-, or C 1 -C 8 alkoxycarbonyl-; or R 10a and R 10b together with the carbon atom they are attached to join to form a 3- to 10-membered carbocyclic ring or a 4- to 1 0-membered heterocyclic ring;

R 11 is hydrogen, C 1 -C 10 alkyl, C 1 -C 4 haloalkyl, C 2 -C 10 alkenyl, C 2 -C 4 haloalkenyl, C 2 -C 10 alkynyl, C 2 -C 4 haloalkynyl, C 3 -C 10 cycloalkyl, C 3 -C 10 cycloalkyl-C 1 -C 6 alkyl-, C 1 -C 10 alkoxy-C 1 -C 6 alkyl-, C 1 -C 10 cyanoalkyl-, C 1 -C 10 alkoxycarbonyl-C 1 -C 6 alkyl-, N—C 1 -C 3 alkyl-aminocarbonyl-C 1 -C 6 alkyl-, N,N-di-(C 1 -C 3 alkyl)-aminocarbonyl-C 1 -C 6 alkyl-, aryl-C 1 -C 6 alkyl- or aryl-C 1 -C 6 alkyl- wherein the aryl moiety is substituted by one to three R 12 , or heterocyclyl-C 1 -C 6 alkyl- or heterocyclyl-C 1 -C 6 alkyl- wherein the heterocyclyl moiety is substituted by one to three R 12 ;

each R 12 is independently halogen, C 1 -C 4 alkyl, C 1 -C 4 haloalkyl, C 1 -C 4 alkoxy or C 1 -C 4 haloalkoxy;

R 13 is hydrogen, C 1 -C 3 alkyl, or C 1 -C 3 haloalkyl;

R 14 is hydrogen, methyl or C 1 haloalkyl;

G is hydrogen, or C(O)R 3 ;

R 3 is selected from the group consisting of C 1 -C 6 alkyl, C 1 -C 6 alkenyl, C 1 -C 6 alkynyl, C 1 -C 6 alkoxy, C 1 -C 6 alkyl-S—, —NR 4 R 5 and phenyl optionally substituted by one or more R 6 ;

R 4 and R 5 are independently selected from the group consisting of C 1 -C 6 alkyl and C 1 -C 6 alkoxy, or R 4 and R 5 together can form a morpholinyl ring;

R 6 is selected from the group consisting of halogen, cyano, nitro, C 1 -C 3 alkyl, C 1 -C 3 haloalkyl, C 1 -C 3 alkoxy and C 1 -C 3 haloalkoxy; and T is a 5- or 6-membered monocyclic heteroaryl ring system containing 1, 2, or 3 heteroatoms independently selected from nitrogen, oxygen and sulphur, said 5-membered ring system being substituted by one or more radicals selected from X, Y, and R 7 , and said 6-membered ring system being substituted by one or more radicals selected from X 1 , X 2 , X 3 , X 4 and R 7 , and wherein the oxy-alkyl-D moiety and the bi-cyclic moiety are linked via ring T such that they are situated ortho with respect to each other;

or T is a substituted phenyl ring of formula (Tp)

each X, X 3 , X 23 and each Y are independently hydrogen, C 1 -C 3 alkyl, C 1 -C 3 alkoxy, C 1 -C 3 haloalkyl, C 1 -C 3 haloalkoxy, or halogen;

X 1 is oxo, C 1 -C 3 alkyl, C 1 -C 3 alkoxy, C 1 -C 3 haloalkyl, C 1 -C 3 haloalkoxy, or halogen;

X 2 , and X 4 are independently hydrogen, C 1 -C 3 alkyl, C 1 -C 3 alkoxy, C 1 -C 3 haloalkyl, C 1 -C 3 haloalkoxy, oxo, or halogen;

X 21 is C 1 -C 3 alkyl, C 1 -C 3 alkoxy, C 1 -C 3 haloalkyl, C 1 -C 3 haloalkoxy, or halogen;

X 22 , and X 24 are independently hydrogen, C 1 -C 3 alkyl, C 1 -C 3 alkoxy, C 1 -C 3 haloalkyl, C 1 -C 3 haloalkoxy, or halogen;

R 7 is hydrogen, C 1 -C 3 alkyl, C 1 -C 3 alkoxy, C 1 -C 3 haloalkyl, C 1 -C 3 haloalkoxy;

A denotes the point of attachment to the oxy-alkyl-D moiety and B denotes the point of attachment to the bi-cyclic moiety; and

D is a substituted or unsubstituted monocyclic heteroaryl ring containing 1, 2, or 3 heteroatoms independently selected from oxygen, nitrogen and sulphur, and wherein when D is substituted it is substituted on at least one ring carbon atom with R 8 and/or on a ring nitrogen atom with R 9 ;

or D is the group (Dp)

each R 8 is independently oxygen, hydroxyl, halogen, cyano, C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, C 1 -C 6 haloalkoxy, C 1 -C 3 haloalkoxy-C 1 -C 3 alkyl-, C 1 -C 6 alkoxy, C 1 -C 3 alkoxy-C 1 -C 3 alkyl, C 1 -C 3 alkoxy-C 1 -C 3 alkoxy-C 1 -C 3 alkyl-, C 3 -C 6 cycloalkyl, C 2 -C 6 alkenyl, C 2 -C 6 haloalkenyl, C 2 -C 6 alkynyl, C 1 -C 6 hydroxyalkyl-, C 1 -C 6 alkylcarbonyl-, C 1 -C 6 alkyl-S(O) m —, amino, C 1 -C 6 alkylamino, C 1 -C 6 dialkylamino, —C(C 1 -C 3 alkyl)=N—O—C 1 -C 3 alkyl and C 2 -C 6 haloalkynyl;

m is an integer of 0, 1, or 2;

each R 9 is independently, C 1 -C 4 alkyl, C 3 -C 6 alkoxy, C 1 -C 2 alkoxy-C 1 -C 2 alkyl, C 2 -C 4 alkenyl, C 1 -C 4 haloalkyl, C 2 -C 4 haloalkenyl, C 2 -C 4 alkynyl or C 2 -C 4 haloalkynyl;

p denotes the point of attachment of (Dp) to the rest of the molecule; and

Z 1 , Z 2 , Z 3 , Z 4 , and Z 5 are each independently selected from hydrogen, C 1 -C 3 alkyl, C 1 -C 3 alkoxy, C 1 -C 3 haloalkyl, C 1 -C 3 haloalkoxy, or halogen;

provided that when A 4 is S, A 2 is NR 11 , and A 3 is C(O), then T is not (Tp) when D is (Dp).

2. The compound according to claim 1 , wherein G is hydrogen, or C(O)R 3 wherein R 3 is C 1 -C 4 alkyl, C 1 -C 4 alkoxy, C 2 -C 3 alkenyl, C 2 -C 3 alkynyl or —C 1 -C 3 alkoxy.

3. The compound according to claim 1 , wherein D is a substituted or unsubstituted furyl, thienyl, pyrrolyl, pyrazolyl, imidazolyl, 1,2,3-triazolyl, 1,2,4-triazolyl, oxazolyl, isoxazolyl, thiazolyl, isothiazolyl, 1,2,4-oxadiazolyl, 1,3,4-oxadiazolyl, 1,2,5-oxadiazolyl, 1,2,3-thiadiazolyl, 1,2,4-thiadiazolyl, 1,3,4-thiadiazolyl, 1,2,5-thiadiazolyl, pyridyl, pyridonyl, pyrimidinyl, pyridazinyl, pyrazinyl, 1,2,3-triazinyl, 1,2,4-triazinyl, or 1,3,5-triazinyl ring, wherein when D is substituted it is substituted on at least one ring carbon atom with R 8 and/or on a ring nitrogen atom with R 9 .

4. The compound according to claim 1 , wherein D is (Dp).

5. The compound according to claim 1 , wherein T is selected from the group consisting of (Tp) and (T1) to (T62):

wherein in X, X 1 , X 2 , X 3 , X 4 , Y, R 7 , A and B are as defined in claim 1 .

6. The compound according to claim 1 wherein T is (Tp) or an optionally substituted pyrazolyl ring selected from the group consisting of:

wherein,

X, Y, R 7 , A and B are as defined in claim 1 .

7. The compound of claim 1 , wherein T is selected from (T1), (T4), and (T5), and X is hydrogen or halogen.

8. The compound according to claim 6 , wherein T is selected from (T4) and (T5) and X is halogen.

9. The compound according to claim 6 , wherein T is selected from (T1), (T2), and (T3) and Y is hydrogen, C 1 -C 3 alkyl, C 1 -C 3 haloalkyl, or halogen.

10. The compound according to claim 6 , wherein T is selected from (T2), (T3), (T4), and (T5) wherein R 7 is C 1 -C 3 alkyl, or C 1 -C 3 haloalkyl.

11. The compound according to claim 1 , wherein T is (Tp) and X 21 is halogen, C 1 -C 3 alkyl, or C 1 -C 3 haloalkyl.

12. The compound according to claim 1 wherein T is (Tp) and X 24 is halogen, C 1 -C 3 alkyl, or C 1 -C 3 haloalkyl.

13. A herbicidal composition comprising a herbicidal compound according to claim 1 and an agriculturally acceptable formulation adjuvant.

14. A herbicidal composition according to claim 13 , further comprising at least one additional pesticide.

15. A method of controlling unwanted plant growth, comprising applying a compound of formula (I) as defined in claim 1 to the unwanted plants or to the locus thereof.

Assignments (2)
MERGER AND CHANGE OF NAME Recorded Mar 14, 2025
From: SYNGENTA PARTICIPATIONS AG; SYNGENTA PARTICIPATIONS AG
To: SYNGENTA CROP PROTECTION AG
Reel/Frame 070510/0501 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 21, 2018
From: SHANAHAN, STEPHEN EDWARD; O'RIORDAN, TIMOTHY JEREMIAH CORNELIUS
To: SYNGENTA PARTICIPATIONS AG
Reel/Frame 045864/0114 →