IP Library Granted Patent US 11,006,631
Granted Patent B2
US 11,006,631 · App. 15/551,656 · Granted May 18, 2021

Substituted pyrimidinyloxy pyridine derivatives as herbicides

Inventors: Ravisekhara Pochimireddy Reddy (Secunderabad, IN); Nicholas Ryan Deprez (East Windsor, NJ); Yuzhong Chen (Wilmington, DE)
Assignee: FMC Corporation
A01N43/54A01N43/56A01N43/647A01N43/653A01N43/76A01N43/78A01N43/80A01N43/82C07D401/12C07D401/14C07D413/14C07D417/14
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Quick Facts
Patent No.
US 11,006,631
App. No.
15/551,656
Granted
May 18, 2021
Kind
B2
Abstract

Disclosed are compounds of Formula 1, including all stereoisomers, N-oxides, and salts thereof, wherein Q, Z, R 2 , R 3 and m are as defined in the disclosure. Also disclosed are compositions containing the compounds of Formula 1 and methods for controlling undesired vegetation comprising contacting the undesired vegetation or its environment with an effective amount of a compound or a composition of the invention.

Claims (31)

1. A compound selected from Formula 1, N-oxides and salts thereof,

wherein

Q is selected from

Z is O;

m is 0 or 1;

r is 1;

each R 1 is independently halogen, cyano, C 1 -C 4 alkyl, C 1 -C 4 haloalkyl, C 1 -C 4 alkoxy, C 1 -C 4 haloalkoxy or SO n R 1A ;

n is 0, 1 or 2;

R 2 is halogen or C 1 -C 4 alkyl;

each R 3 is independently halogen, cyano, C 1 -C 4 alkyl, C 2 -C 4 alkenyl, C 2 -C 4 alkynyl, C 1 -C 4 haloalkyl, C 2 -C 6 alkylcarbonyl, C 2 -C 6 haloalkylcarbonyl, C 2 -C 6 alkoxycarbonyl, C 1 -C 4 alkoxy, C 1 -C 4 haloalkoxy, C 2 -C 6 alkoxyalkyl or C 2 -C 6 haloalkoxyalkyl; and

each R 1A is independently C 1 -C 4 alkyl or C 1 -C 4 haloalkyl.

2. The compound of claim 1 wherein

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

R 2 is halogen or CH 3 ; and

each R 3 is independently halogen, cyano, C 1 -C 4 alkyl or C 1 -C 4 haloalkyl.

3. The compound of claim 1 selected from the group consisting of

2-[[2-(4-bromo-1H-pyrazol-1-yl)-3-pyridinyl]oxyl]-5-chloropyrimidine,

5-chloro-2-[[2-(4-chloro-1H-pyrazol-1-yl)-3-pyridinyl]oxy]pyrimidine,

5-chloro-2-[[2-[3-(difluoromethyl)-5-isoxazolyl]-3-pyridinyl]oxy]pyrimidine and

5-chloro-2-[[2-[5-(difluoromethyl)-3-isoxazolyl]-3-pyridinyl]oxy]pyrimidine.

4. A herbicidal composition comprising a compound of claim 1 and at least one component selected from the group consisting of surfactants, solid diluents and liquid diluents.

5. A herbicidal composition comprising a compound of claim 1 , at least one additional active ingredient selected from the group consisting of other herbicides and herbicide safeners, and at least one component selected from the group consisting of surfactants, solid diluents and liquid diluents.

6. A herbicidal mixture comprising (a) a compound of claim 1 , and (b) at least one additional active ingredient selected from (b1) photosystem II inhibitors, (b2) acetohydroxy acid synthase (AHAS) inhibitors, (b3) acetyl-CoA carboxylase (ACCase) inhibitors, (b4) auxin mimics, (b5) 5-enol-pyruvylshikimate-3-phosphate (EPSP) synthase inhibitors, (b6) photosystem I electron diverters, (b7) protoporphyrinogen oxidase (PPO) inhibitors, (b8) glutamine synthetase (GS) inhibitors, (b9) very long chain fatty acid (VLCFA) elongase inhibitors, (b10) auxin transport inhibitors, (b11) phytoene desaturase (PDS) inhibitors, (b12) 4-hydroxyphenyl-pyruvate dioxygenase (HPPD) inhibitors, (b13) homogentisate solanesyltransferase (HST) inhibitors, (b14) cellulose biosynthesis inhibitors, (b15) other herbicides including mitotic disruptors, organic arsenicals, asulam, bromobutide, cinmethylin, cumyluron, dazomet, difenzoquat, dymron, etobenzanid, flurenol, fosamine, fosamine-ammonium, hydantocidin, metam, methyldymron, oleic acid, oxaziclomefone, pelargonic acid and pyributicarb, (b16) herbicide safeners, and salts of compounds of (b1) through (b16).

7. A method for controlling the growth of undesired vegetation comprising contacting the vegetation or its environment with a herbicidally effective amount of a compound of claim 1 .

8. The compound of claim 1 wherein

Q is

9. The compound of claim 8 wherein

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

R 2 is halogen or CH 3 ; and

each R 3 is independently halogen, cyano, C 1 -C 4 alkyl or C 1 -C 4 haloalkyl.

10. The compound of claim 1 that is 5-chloro-2-[[2-[5-(difluoromethyl)-3-isoxazolyl]-3-pyridinyl]oxy]pyrimidine.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 17, 2018
From: E.I. DU PONT DE NEMOURS AND COMPANY
To: FMC CORPORATION
Reel/Frame 046732/0016 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 25, 2017
From: REDDY, RAVISEKHARA POCHIMIREDDY; DEPREZ, NICHOLAS RYAN; CHEN, YUZHONG
To: E. I. DU PONT DE NEMOURS AND COMPANY
Reel/Frame 043681/0811 →
Continuity (2)
Provisional Application 62134665 · Mar 18, 2015
Related Publication 20180020664A1 · Jan 25, 2018