US2004106518A1PendingUtilityA1

Herbicide-safener combination based on isoxozoline carboxylate safeners

Priority: Jan 31, 2001Filed: Jan 31, 2002Published: Jun 3, 2004
Est. expiryJan 31, 2021(expired)· nominal 20-yr term from priority
A01N 25/32A01N 43/80
51
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Claims

Abstract

Herbicide safener combiantions consisting of A) an effective amount of a compound of the formula (1) or a salt thereof, in which R 1 is phenyl which is unsubstituted or substituted, R 2 is (C 1 -C 6 )alkyl, (C 3 -C 6 )cycloalkyl or phenyl, each of the 3 last-mentioned radicals is unsubstituted or substituted, R 3 is hydrogen or a hydrocarbon radical having 1 to 18 C-atoms which is unsubstituted or substituted, and B) a herbicide selected form the group consisting of and florasulam, chloransulam, dicamba, diflufenzopyr; triclopyr, fluroxypyr, metribuzin, carfentrazone-ethyl, S.metolachlor, dimethenamide, dimethenamide-P or flufenacet and mixtures of the above herbicides, optionally in combination with toher herbicidal active ingredients can be used for effective selective cotrolling weeds in crop such as maize.

Claims

exact text as granted — not AI-modified
1 . herbicide safener combination consisting of 
 A) an effective amount of a compound of the formula (I) or a salt thereof,                           in which 
 R 1  is phenyl which is unsubstituted or substituted,  
 R 2  is (C 1 -C 6 )alkyl, (C 3 -C 6 )cycloalkyl or phenyl, each of the 3 last-mentioned radicals is unsubstituted or substituted,  
 R 3  is hydrogen or a hydrocarbon radical having 1 to 18 C-atoms which is unsubstituted or substituted,  
 and  
   B) a herbicide selected from the group consisting of 
 (B1) Triazolopyrimidine derivatives (B1-1) and (B1-2)  
 (B1-1) N-(2,6-difluorophenyl)-8-fluoro-5-methoxy-1,2,4-triazolo[1,5-c]pyrimidin-2-sulfonamide (florasulam),  
 (B-1-2) methyl 3-chloro-(5-ethoxy-7-fluoro[1,2,4]triazole-[1,5-c]pyrimidin-2-ylsulfonamido)-benzoate (chloransulam)  
 (B2) plant hormone-type herbicides (B2-1) to (B2-4)  
 (B2-1) 3,6-dichloro-2-methoxy-benzoic acid and salts and esters (e.g. methyl ester) thereof; (dicamba),  
 (B2-2) 2-{1-[4-(3,5-difluorophenyl)semicarbazono]ethyl}nicotinic acid and salts (e.g. sodium salt) thereof (diflufenzopyr);  
 (B2-3) 3,5,6-trichloro-2-pyridyloxyacetic acid (triclopyr);  
 (B2-4) 4-amino-3,5-dichloro-6-fluoro-2-pyridyloxyacetic acid and salts and esters thereof (fluroxypyr); and  
 (B3-1) 4-amino-6-tert-butyl-4,5-dihydro-3-methylthio-1,2,4-triazin-5-one (metribuzin);  
 (B4-1) ethyl (RS)-2-chloro-3-[2-chloro-5-(4-difluoromethyl-4,5-dihydro-3-methyl-5-oxo-1H-1,2,4-triazol-1-yl) 4 -fluorophenyl]propionate (carfentrazone-ethyl)  
 (B5) chloroacetanilides (B5-1) to (B5-4)  
 (B5-1) 2-chloro-N-(2-ethyl-6-methylphenyl)-N-[(1S)-2-methoxy-1-methylethyl)]-acetamide (S-metolachlor),  
 (B5-2) (RS)-2-chloro-N-(2,4-diethyl-3-thienyl)-N-(2-methoxy-1-methylethyl)acetamide (dimethenamide),  
 (B5-3) (S)-2-chloro-N-(2,4-diethyl-3-thienyl)-N-(2-methoxy-1-methylethyl)acetamide (dimethenamide-P), and  
 (B5-4) 4′-fluoro-N-isopropyl-2-[5-trifluoromethyl-1,3,4-thiadiazol-2-yloxy]acetanilide (flufenacet) and  
 mixtures of the above herbicides, optionally in combination with other herbicidal active ingredients.  
   
     
     
         2 . A combination as claimed in  claim 1  wherein in formula (I) 
 R 1  is phenyl which is unsubstituted or substituted by one or more radicals selected from the group consisting of halogen, cyano, nitro, amino, (C 1 -C 4 )haloalkyl, (C 1 -C 4 )haloalkoxy, (C 1 -C 4 )alkyl, (C 1 -C 4 )alkoxy, mono(C 1 -C 4 )alkyl-amino, di(C 1 -C 4 )alkyl-amino, (C 1 -C 4 )alkylthio and (C 1 -C 4 )alkylsulfonyl,  
 R 2  is (C 1 -C 6 )alkyl, (C 3 -C 6 )cycloalkyl or phenyl, each of the 3 last-mentioned radicals is unsubstituted or substituted by one or more radicals selected from the group consisting of halogen, cyano, nitro, amino, (C 1 -C 4 )haloalkyl, (C 1 -C 4 )haloalkoxy, (C 1 -C 4 )alkyl, (C 1 -C 4 )alkoxy, mono(C 1 -C 4 )alkyl-amino, di(C 1 -C 4 )alkyl-amino, (C 1 -C 4 )alkylthio and (C 1 -C 4 )alkylsulfonyl,  
 R 3  is hydrogen or a hydrocarbon radical having 1 to 18 C-atoms which is unsubstituted or substituted by one or more radicals selected from the group consisting of 
 halogen, cyano, thio, nitro, hydroxyl, (C 1 -C 6 )alkyl, (C 1 -C 6 )haloalkyl, the 2 last-mentioned radicals as substituents of cyclic radicals only, (C 1 -C 6 )alkoxy, (C 2 -C 6 )alkenyloxy, (C 2 -C 6 )alkinyloxy, (C 1 -C 6 )haloalkoxy, (C 2 -C 6 )alkylthio, (C 3 -C 6 )cycloalkyl, (C 3 -C 6 )cycloalkoxy, (C 1 -C 8 )alkoxy-carbonyl, (C 2 -C 6 )alkenyloxy-carbonyl, (C 2 -C 6 )alkinyloxy-carbonyl, (C 1 -C 8 )alkyl-carbonyl, (C 1 -C 6 )alkyl-carbonyloxy, phenyl, phenyl-(C 1 -C 6 )alkoxy, phenyl-(C 1 -C 6 )alkoxy-carbonyl, phenoxy, phenoxy-(C 1 -C 6 )alkoxy, phenoxy-(C 1 -C 6 )alkoxy-carbonyl, phenoxycarbonyl, phenylcarbonyloxy and phenyl-(C 1 -C 6 )alkyl-carbonyloxy,  
 wherein the 9 last-mentioned radicals are unsubstituted or substituted in the phenyl ring by one or more radicals selected from the group consisting of halogen, (C 1 -C 4 )alkyl, (C 1 -C 4 )alkoxy, (C 1 -C 4 )haloalkyl, (C 1 -C 4 )haloalkoxy and nitro,  
 
 and radicals of the formula —O—N═CR′ 2 , —N═CR′ 2 . 
 wherein the R′ in the formulae independently of one another are hydrogen, (C 1 -C 4 )alkyl 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, (C 1 -C 4 )haloalkyl, (C 1 -C 4 )haloalkoxy and nitro, or together are a (C 2 -C 6 )alkylene chain.  
 
 
     
     
         3 . combination claimed in  claim 1  or  2  wherein in formula (I) 
 R 1  and R 2  both are phenyl and R 3  is hydrogen or (C 1 -C 6 )alkyl which is unsubstituted or substituted by one or more radicals selected from the group consisting of halogen, cyano, (C 1 -C 4 )alkoxy, (C 2 -C 4 )alkenyloxy, (C 2 -C 4 )alkinyloxy, (C 1 -C 4 )haloalkoxy, (C 2 -C 4 )alkylthio, (C 3 -C 6 )cycloalkyl, (C 3 -C 6 )cycloalkoxy, (C 1 -C 4 )alkoxy-carbonyl, (C 2 -C 4 )alkenyloxy-carbonyl, (C 2 -C 4 )alkinyloxy-carbonyl, (C 1 -C 4 )alkyl-carbonyl, (C 1 -C 4 )alkyl-carbonyloxy, phenyl which is unsubstituted or substituted in the phenyl ring by one or more radicals selected from the group consisting of halogen, (C 1 -C 4 )alkyl, (C 1 -C 4 )alkoxy, (C 1 -C 4 )haloalkyl and (C 1 -C 4 )haloalkoxy.  
 
     
     
         4 . A combination as claimed in any of  claims 1  to  3  wherein in formula (I) R 3  is H or (C 1 -C 4 )alkyl.  
     
     
         5 . A combination as claimed in  claim 1  wherein the safener of formula (I) is 5,5-diphenyl-2-isoxazoline-3-carboxylic acid.  
     
     
         6 . A combination as claimed in  claim 1  wherein the safener of formula (I) is ethyl 5,5-diphenyl-2-isoxazoline-3-carboxylate.  
     
     
         7 . A combination as claimed in any of  claims 1  to  5  which is a co-formulation additionally containing formulation auxiliaries.  
     
     
         8 . A method of combatting weed plants in a crop of useful plants wherein a safener A) is applied to the plants, seed of the plants or the area under cultivation before, simultaneously or after a herbicide A) pre-emergent and/or post-emergent related to the crop and wherein the safener A) and the herbicide B) are as defined in any of  claims 1  to  7 .  
     
     
         9 . A method of reducing the phytotoxicity of a herbicide B) to a crop plant wherein a safener A) is applied to the plants, seed of the plants or the area under cultivation before, simultaneously or after a herbicide A) pre-emergent and/or post-emergent related to the crop and wherein the safener A) and the herbicide B) are as defined in any of  claims 1  to  7 .

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