http://rdf.ncbi.nlm.nih.gov/pubchem/patent/AR-100318-A1

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_8e0bf0928b608797b70bbc2b91c7e52e
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N43-68
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N25-08
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N25-02
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N25-32
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N43-68
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D401-12
filingDate 2015-04-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 2016-09-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber AR-100318-A1
titleOfInvention HERBICIDE COMBINATION UNDERSTANDING AZINAS
abstract Claim 1: A herbicidal combination comprising: a) at least one compound a) of the formula (1) wherein Rᵃ, Rᵇ, Rᶜ, Rᵈ are, independently of each other, H, halogen, CN, NO₂, C₁₋₆- alkyl, C₁₋₆-haloalkyl, OH, C₁₋₆-alkoxy, C₁₋₆-alkylthio, (C₁₋₆-alkyl) sulfinyl, (C₁₋₆-alkyl) sulfonyl, amino, (C₁₋₆-alkyl) amino , di (C₁₋₆-alkyl) amino, (C₁₋₆-alkyl) -carbonyl, (C₁₋₆-alkoxy) -carbonyl and (C₁₋₆-alkyl) C₃₋₆-cycloalkyl; R¹ is selected from the group consisting of H, OH, S (O) ₂NH₂, CN, C₁₋₆-alkyl, C₂₋₆-alkenyl, C₂₋₆-alkynyl, (C₃₋₆-cycloalkyl) -C₁₋₄- alkyl, C₁₋₆-alkoxy, (C₁₋₆-alkoxy) -C₁₋₆-alkyl, (C₁₋₆-alkyl) -carbonyl, (C₁₋₆-alkoxy) carbonyl, (C₁₋₆-alkyl) sulfonyl, (C₁₋₆-alkylamino) carbonyl, di (C₁₋₆-alkyl) aminocarbonyl, (C₁₋₆-alkylamino) sulfonyl, di (C₁₋₆-alkyl) aminosulfonyl and (C₁₋₆-alkoxy) sulfonyl, wherein aliphatic and cycloaliphatic parts of the aforementioned 14 radicals are unsubstituted, partially or completely halogenated, phenyl, phenyl-C₁₋₆-alkyl, phenylsulfonyl, phenylaminosulfonyl, phenylcarbonyl and phenoxycarbonyl, wherein the phenyl in the last 6 radicals mentioned is unsubstituted or substituted with 1, 2, 3, 4 or 5 identical or different substituents selected from the group consisting of halogen, CN, NO₂, C₁₋₆-alkyl, C₁₋₆-haloal chyl, C₁₋₆-alkoxy and C₁₋₆-haloalkoxy; R² is selected from the group consisting of H, halogen, CN, C₁₋₆-alkyl, C₁₋₆-haloalkyl, C₂₋₆-alkenyl, C₃₋₆-alkynyl, C₃₋₆-cycloalkyl, (C₁₋₆-alkyl ) C₃₋₆-cycloalkyl, C₃₋₆-cycloalkenyl, OH, C₁₋₆-alkoxy or C₁₋₆-alkoxy-C₁₋₆-alkyl; R³ is H, halogen, CN, C₁₋₆-alkyl, C₁₋₆-haloalkyl or C₁₋₆-alkoxy; R⁴ is H, halogen, CN, C₁₋₆-alkyl or C₁₋₆-haloalkyl; or R³ and R⁴, together with the carbon atom to which they are attached, form a portion selected from the group consisting of carbonyl, C₂₋₆-alkenyl, C₃₋₆-cycloalkyl, C₃₋₆-cycloalkenyl and heterocyclyl of 3 to 6 members, wherein C₃₋₆-cycloalkyl, C₃₋₆-cycloalkenyl or heterocyclyl 3 to 6 members is unsubstituted or substituted with 1 to 3 substituents selected from halogen, CN, C₁₋₆-alkyl and C₁₋₆-alkoxy; R⁵ is selected from the group consisting of H, OH, S (O) ₂NH₂, CN, C₁₋₆-alkyl, C₂₋₆-alkenyl, C₂₋₆-alkynyl, (C₃₋₆-cycloalkyl) -C₁₋₄- alkyl, C₁₋₆-alkoxy, (C₁₋₆-alkoxy) -C₁₋₆-alkyl, (C₁₋₆-alkyl) -carbonyl, (C₁₋₆-alkoxy) carbonyl, (C₁₋₆-alkyl) sulfonyl, (C₁₋₆-alkylamino) carbonyl, di (C₁₋₆-alkyl) aminocarbonyl, (C₁₋₆-alkylamino) sulfonyl, di (C₁₋₆-alkyl) aminosulfonyl and (C₁₋₆-alkoxy) sulfonyl, wherein aliphatic and cycloaliphatic parts of the aforementioned 14 radicals are unsubstituted, partially or completely halogenated, phenyl, phenyl-C₁₋₆-alkyl, phenylsulfonyl, phenylaminosulfonyl, phenylcarbonyl and phenoxycarbonyl, wherein the phenyl in the last 6 radicals mentioned is unsubstituted or substituted with 1, 2, 3, 4 or 5 identical or different substituents selected from the group consisting of halogen, CN, NO₂, C₁₋₆-alkyl, C₁₋₆-haloa alkyl, C₁₋₆-alkoxy and C₁₋₆-haloalkoxy; which includes its salts or N-oxides acceptable in agriculture, and at least one other compound selected from herbicidal compounds b) and protectors c) and mixtures thereof; b) wherein the active compounds such as herbicides b) are selected from the compounds of the following classes b1) to b15): b1) lipid biosynthesis inhibitors; b2) acetolactate synthase inhibitors; b3) photosynthesis inhibitors; b4) protoporphyrinogen-IX oxidase inhibitors, b5) Lye herbicides; b6) enolpiruvil shiquimate 3-phosphate synthase inhibitors; b7) glutamine synthetase inhibitors; b8) 7,8-dihydropteroate synthase inhibitors; b9) mitosis inhibitors; b10) inhibitors of the synthesis of very long chain fatty acids; b11) cellulose biosynthesis inhibitors; b12) decoupling herbicides; b13) auxinic herbicides; b14) auxin transport inhibitors; and b15) other herbicides selected from the group consisting of bromobutide, chlorflurenol, chlorflurenol-methyl, cinmethylin, cumyluron, dalapon, dazomet, diphezoquat, diphezoquat-methyl sulfate, dimethipin, DSMA, dymron, endothal and their salts, etobenzanid, flamproprop- flamproprop isopropyl, flamprop-methyl, flamprop-M-isopropyl, flamprop-M-methyl, flurenol, flurenol-butyl, flurprimidol, fosamine, fosamine-ammonium, indanofan, indaziflam, maleic hydrazide, mefluidide, metam, methiozolin, bromide of methyl, methyl-dymron, methyl iodide, MSMA, oleic acid, oxaziclomefone, pelargonic acid, pyributicarb, quinoclamine, triaziflam, tridiphane and 6-chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinol and its salts and esters; including its derivatives or acceptable salts in agriculture. Claim 2: The combination according to claim 1, wherein the compound (1) comprises at least one compound (1), wherein R¹ is H, R² is H, halogen, C₁₋₆-alkyl, C₁₋₆- alkoxy, C₁₋₆-haloalkyl or C₁₋₆-haloalkoxy, R³ is H, halogen, CN, C₁₋₆-alkyl, C₁₋₆-haloalkyl or C₁₋₆-alkoxy, R⁴ is H, halogen, CN, C₁₋ ₆-alkyl or C₁₋₆-haloalkyl, R³ and R⁴, together with the carbon atom to which they are attached, form a C₃₋₆-cycloalkyl, R⁵ is H, Rᵃ is H, halogen, CN, Rᵇ is H, halogen , CN, Rᶜ is H, halogen, CN and Rᵈ is H, halogen, CN. Claim 15: The combination according to any of the preceding claims, wherein compound a) is selected from 6- (1-methylcyclobutyl) -N4- (2,3,5,6-tetrafluorophenyl) -1,3,5 -triazin-2,4-diamine, 6- (1-fluorocyclopentyl) -N4- (2,3,5,6-tetrafluorophenyl) -1,3,5-triazin-2,4-diamine, 6- (1- fluoro-1-methyl-ethyl) -N4- (2,3,5,6-tetrafluorophenyl) -1,3,5-triazin-2,4-diamine and N4- (2,6-difluorophenyl) -6- ( 1-fluoro-1-methyl-ethyl) -1,3,5-triazin-2,4-diamine. Claim 18: Use of the combination according to any of the preceding claims to control unwanted vegetation. Claim 21: The compounds of the formula (1) selected from the group consisting of 6- (1-methylbutyl) -N4- (2,3,5,6-tetrafluorophenyl) -1,3,5-triazine-2,4 -diamine, N4- (2,3,5,6-tetrafluorophenyl) -6- (1,2,2-trimethylpropyl) -1,3,5-triazin-2,4-diamine, 6- (cyclopropylmethyl) -N4 - (2,4,6-Trifluorophenyl) -1,3,5-triazin-2,4-diamine and its salts or N-oxides acceptable in agriculture.
priorityDate 2014-04-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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