IP Library Granted Patent US 7,135,434
Granted Patent B2
US 7,135,434 · App. 10/265,925 · Granted Nov 14, 2006

Combinations of herbicides and safeners

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Quick Facts
Patent No.
US 7,135,434
App. No.
10/265,925
Granted
Nov 14, 2006
Kind
B2
Abstract

This invention provides for, inter alia, a herbicidal composition comprising a mixture of: A. a herbicidally effective amount of at least one compound of the formula where V and Z are defined in the specification; and B. an antidote.

Claims (34)

1. A herbicidally active composition comprising a mixture of:

A. a herbicidally active amount of one or more compounds of the formula (I)

in which

V is a radical of the formula,

where the symbols and indices have the following meanings:

R 2 is hydrogen, (C 1 –C 4 )alkyl, (C 1 –C 4 )alkoxy, (C 1 –C 4 )haloalkyl, halogen, (C 1 –C 4 )haloalkoxy, cyano, nitro;

R 3 is hydrogen or an optionally substituted (C 1 –C 4 )alkyl, (C 2 –C 4 )alkenyl, (C 2 –C 4 )alkynyl, (C 1 –C 4 )alkoxy-(C 1 –C 4 )alkyl, (C 1 –C 4 )alkylcarbonyl, (C 1 –C 4 )alkylsulfonyl, (C 1 –C 4 )haloalkylsulfonyl, arylsulfonyl, arylcarbonyl-(C 1 –C 4 )alkyl radical, or an aryl(C 1 –C 4 )alkyl radical;

R 4 is hydrogen or an optionally substituted (C 1 –C 7 )alkyl, (C 2 –C 7 )alkenyl, (C 2 –C 7 )alkynyl radical or aryl radical; and

Z is a radical (Z1)

where the symbols and indices have the following meanings:

R 9 is nitro, amino, cyano, halogen or an optionally substituted (C 1 –C 8 )alkyl, (C 2 –C 8 )alkenyl, (C 2 –C 8 )alkynyl, (C 1 –C 8 )alkoxycarbonyl, (C 1 –C 8 )alkylsulfonyl, (C 1 –C 8 )alkylsulfinyl, (C 1 –C 8 )alkylthio, aryl, arylsulfonyl, arylsulfinyl, arylthio, aryloxy, (C 1 –C 8 )alkoxy, (C 1 –C 8 )alkoxy-(C 1 –C 8 )alkoxy, (C 1 –C 8 )alkylcarbonyl, (C 1 –C 8 )alkylaminosulfonyl, (C 1 –C 8 )dialkylaminosulfonyl, (C 1 –C 8 )alkylcarbamoyl, (C 1 –C 8 )dialkylcarbamoyl, (C 1 –C 8 )alkoxy-(C 1 –C 8 )alkyl, (C 1 –C 8 )alkylamino, or (C 1 –C 8 )dialkylamino radical;

R 10 is a radical of formula

q is 0, 1, 2, 3, or 4;

and

B. an antidote-effective amount of one or more compounds selected from the groups consisting of a):

a) compounds of the formulae (II) and (III)

where the symbols and indices have the following meanings:

n′ is a natural number from 1 to 5,

T is a (C 1 or C 2 )-alkanediyl chain which is unsubstituted or substituted by one or two (C 1 –C 4 )alkyl radicals or by [(C 1 –C 3 )-alkoxy]carbonyl,

W is a radical of the formula

R 17 , R 19 are identical or different hydrogen, halogen, (C 1 –C 4 )alkyl, (C 1 –C 4 )alkoxy, nitro or (C 1 –C 4 )haloalkyl;

R 18 , R 20 are identical or different OR 24 , SR 24 or NR 24 R 25 or a saturated or unsaturated 3- to 7-membered heterocycle having at least one nitrogen atom and up to 3 hetero atoms which is linked to the carbonyl group in (II) or (III) via the nitrogen atom and which is unsubstituted or substituted by radicals from the group consisting of (C 1 –C 4 )alkyl, (C 1 –C 4 )alkoxy or optionally substituted phenyl;

R 24 is hydrogen or an unsubstituted or substituted aliphatic hydrocarbon radical;

R 25 is hydrogen, (C 1 –C 6 )alkyl, (C 1 –C 6 )alkoxy or substituted or unsubstituted phenyl;

R 26 is hydrogen, (C 1 –C 8 )alkyl, (C 1 –C 8 )haloalkyl, (C 1 –C 4 )alkoxy-(C 1 –C 4 )alkyl, (C 1 –C 6 )hydroxyalkyl, (C 3 –C 12 )cycloalkyl or tri-(C 1 –C 4 )-alkylsilyl;

R 27 , R 29 are identical or different hydrogen, (C 1 –C 8 )alkyl, (C 1 –C 6 )haloalkyl, (C 3 –C 7 )cycloalkyl or phenyl which is unsubstituted or substituted by one or more radicals selected from the group consisting of halogen, (C 1 –C 4 )alkyl, (C 1 –C 4 )alkoxy, nitro, (C 1 –C 4 )haloalkyl and (C 1 –C 4 )haloalkoxy; and

m′ is 0 or 1;

inclusive of the stereoisomers and of the salts conventionally used in agriculture.

2. The herbicidally active composition according to claim 1 wherein the compound of formula I is

and the antidote is

3. The herbicidally active compound according to claim 1 wherein the compound of formula I is

and the antidote is

4. The herbicidally active compound according to claim 1 wherein the compound of formula I is

and the antidote is

Assignments (4)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 6, 2015
From: BAYER CROPSCIENCE AG
To: BAYER INTELLECTUAL PROPERTY GMBH
Reel/Frame 034914/0354 →
CHANGE OF NAME Recorded Nov 12, 2008
From: HOECHST SCHERING AGREVO GMBH
To: AVENTIS CROPSCIENCE GMBH
Reel/Frame 021824/0729 →
CHANGE OF NAME Recorded Nov 12, 2008
From: BAYER CROPSCIENCE GMBH
To: BAYER CROPSCIENCE AG
Reel/Frame 021838/0869 →
CHANGE OF NAME Recorded Nov 12, 2008
From: AVENTIS CROPSCIENCE GMBH
To: BAYER CROPSCIENCE GMBH
Reel/Frame 021924/0762 →