WO2015155129A1 - Composé de diaminotriazine - Google Patents

Composé de diaminotriazine Download PDF

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Publication number
WO2015155129A1
WO2015155129A1 PCT/EP2015/057370 EP2015057370W WO2015155129A1 WO 2015155129 A1 WO2015155129 A1 WO 2015155129A1 EP 2015057370 W EP2015057370 W EP 2015057370W WO 2015155129 A1 WO2015155129 A1 WO 2015155129A1
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alkyl
alkoxy
phenyl
carbonyl
formula
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PCT/EP2015/057370
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English (en)
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Julia Major
Florian Vogt
Frederick CALO
Thomas Seitz
Doreen Schachtschabel
Trevor William Newton
Kristin HANZLIK
Johannes Hutzler
Klaus Kreuz
Stefan Tresch
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Basf Se
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Publication of WO2015155129A1 publication Critical patent/WO2015155129A1/fr

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    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D251/00—Heterocyclic compounds containing 1,3,5-triazine rings
    • C07D251/02—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings
    • C07D251/12—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
    • C07D251/14—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members with hydrogen or carbon atoms directly attached to at least one ring carbon atom
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/64—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with three nitrogen atoms as the only ring hetero atoms
    • A01N43/66—1,3,5-Triazines, not hydrogenated and not substituted at the ring nitrogen atoms
    • A01N43/68—1,3,5-Triazines, not hydrogenated and not substituted at the ring nitrogen atoms with two or three nitrogen atoms directly attached to ring carbon atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D251/00—Heterocyclic compounds containing 1,3,5-triazine rings
    • C07D251/02—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings
    • C07D251/12—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
    • C07D251/14—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members with hydrogen or carbon atoms directly attached to at least one ring carbon atom
    • C07D251/16—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members with hydrogen or carbon atoms directly attached to at least one ring carbon atom to only one ring carbon atom
    • C07D251/18—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members with hydrogen or carbon atoms directly attached to at least one ring carbon atom to only one ring carbon atom with nitrogen atoms directly attached to the two other ring carbon atoms, e.g. guanamines

Definitions

  • the present invention relates to diaminotriazine compounds and to their use as herbicides.
  • the present invention also relates to agrochemical compositions for crop protection and to a method for controlling unwanted vegetation.
  • EP 0545 149 describes 6-trifluoromethyl-1 ,3,5-triazine compounds and their use as intermediates for crop protecting agents.
  • WO 01/17977 describes and US 6,069,1 14 describe 1 ,3,5-triazine derivatives, and thereof as herbicides.
  • the phenyl ring which is substituted by a fluorine atom in ortho position is the distinguishing feature of the compounds according to the invention over these two documents.
  • EP 12189762.3 describes 2-(o-fluorophenyl)amino-6-aminotriazine compounds having herbicide activity.
  • Compound 4-chloro-6-(2,5-dichlorophenyl)-1 ,3,5-triazin-2-amine, 4-chloro-6-(3,4- dichlorophenyl)-1 ,3,5-triazin-2-amine and 4-chloro-6-(4-chlorophenyl)-1 ,3,5-triazin-2- amine, known from EP 0066799, are used as starting material for the synthesis of nicotinoylbenzoguanamine derivatives, which nay useful in clinical field as remedies for rheumatism and for allergic nephritis.
  • Compound 4-chloro-6-phenyl-1 ,3,5-triazin-2-amine is known from Journal of the American Society, vol. 82m p. 3756.
  • diaminotriazine compounds of formula (I), defined below and by their agriculturally suitable salts.
  • the present invention relates to diaminotriazine compounds of formula (I)
  • R A selected from the group consisting of halogen, OH, CN, amino, NO2, C1-C6- alkyl, C2-C6-alkenyl, C2-C6-alkynyl, Ci-C6-alkoxy, C2-C6-alkenyloxy, C2-C6- alkynyloxy, (Ci-C6-alkoxy)-Ci-C6-alkyl, (Ci-C6-alkoxy)-Ci-C6-alkoxy, (C1-C6- alkoxy)-C2-C6-alkenyl, (Ci-C6-alkoxy)-C2-C6-alkynyl, Ci-C6-alkylthio, (C1-C6- alkyl)sulfinyl, (Ci-C6-alkyl)sulf
  • Ci-C6-alkyl is selected from the group consisting of H, OH, S(0)2NH2, CN, Ci-C6-alkyl, C2-C6-alkenyl, C2-C6-alkynyl, (C3-C6-cycloalkyl)-Ci-C4-alkyl, Ci-C6-alkoxy, (Ci-C6-alkoxy)-Ci-C6-alkyl, (Ci-C6-alkyl)-carbonyl, (Ci-C6-alkoxy)carbonyl, (Ci-C6-alkyl)sulfonyl, (Ci-C6-alkylamino)carbonyl, di(Ci-C6- alkyl)aminocarbonyl, (Ci-C6-alkylamino)sulfonyl, di(Ci-C6- alkyl)aminosulfonyl and (Ci-C6-alkoxy)sulfon
  • phenyl phenyl-Ci-C6-alkyl, phenylsulfonyl, phenylaminosulfonyl, phenylcarbonyl and phenoxycarbonyl,
  • phenyl in the last 6 mentioned radicals are unsubstituted or substituted by 1 , 2, 3, 4 or 5 identical or different substituents selected from the group consisting of halogen, CN, NO2, Ci-C6-alkyl, Ci-C6-haloalkyl, Ci- C6-alkoxy and Ci-C6-haloalkoxy;
  • Ci-C6-alkyl is selected from the group consisting of H, OH, S(0)2NH2, CN, Ci-C6-alkyl, C2-C6-alkenyl, C2-C6-alkynyl, (C3-C6-cycloalkyl)-Ci-C4-alkyl, Ci-C6-alkoxy, (Ci-C6-alkoxy)-Ci-C6-alkyl, (Ci-C6-alkyl)carbonyl, (Ci-C6-alkoxy)carbonyl, (Ci-C6-alkyl)sulfonyl, (Ci-C6-alkylamino)carbonyl, di(Ci-C6-alkyl)amino- carbonyl, (Ci-C6-alkylamino)sulfonyl, di(Ci-C6-alkyl)aminosulfonyl and (Ci- C6-alkoxy)sulfon
  • phenyl phenylsulfonyl, phenylaminosulfonyl, phenyl-Ci-C6 alkyl, phenoxy, phenylcarbonyl and phenoxycarbonyl,
  • phenyl in the last 6 mentioned radicals is unsubstituted or substituted by 1 , 2, 3, 4 or 5 identical or different substituents selected from the group consisting of halogen, CN, NO2, Ci-C6-alkyl, Ci-C6-haloalkyl, Ci- C6-alkoxy and Ci-C6-haloalkoxy;
  • R Ar is selected from the group consisting of halogen, OH, CN, amino, N0 2 , d-Ce-alkyl, C 2 -C 6 -alkenyl, C 2 -C 6 -alkynyl, Ci-C 6 -alkoxy, C 2 -C 6 - alkenyloxy, C2-C6-alkynyloxy, (Ci-C6-alkoxy)-Ci-C6-alkyl, (C1-C6- alkoxy)-Ci-C6-alkoxy, (Ci-C6-alkoxy)-C2-C6-alkenyl, (Ci-C6-alkoxy)-C2- C6-alkynyl, Ci-C6-alkylthio, (Ci-C6-alkyl)sulfinyl, (Ci-C6-alkyl)sulfonyl, (Ci-C6-alkyl)amino, di(C
  • Z is a chemical bond, O, S(0)m or NR B
  • R B is selected from the group consisting of H, CN, Ci-C6-alkyl, (C1-C6- alkoxy)-Ci-C6-alkyl, (Ci-C6-alkyl)-carbonyl, (Ci-C6-alkoxy)carbonyl, (Ci-C6-alkyl)sulfonyl, where the aliphatic parts of the 5 aforementioned radicals are unsubstituted, partly or completely halogenated, and
  • n 0, 1 , 2, and
  • Q is phenyl, phenyl-Ci-C6 alkyl, phenylcarbonyl and phenoxycarbonyl, wherein phenyl in the last 4 mentioned radicals is unsubstituted or substituted by 1 , 2, 3, 4 or 5 identical or different substituents selected from the group consisting of halogen, CN, NO2, Ci-C4-alkyl,
  • the present invention further relates to diaminotriazine compound of formula (I)
  • R A selected from the group consisting of halogen, OH, CN, amino, NO2, C1-C6- alkyl, C2-C6-alkenyl, C2-C6-alkynyl, Ci-C6-alkoxy, C2-C6-alkenyloxy, C2-C6- alkynyloxy, (Ci-C6-alkoxy)-Ci-C6-alkyl, (Ci-C6-alkoxy)-Ci-C6-alkoxy, (C1-C6- alkoxy)-C2-C6-alkenyl, (Ci-C6-alkoxy)-C2-C6-alkynyl, Ci-C6-alkylthio, (C1-C6- alkyl)sulfinyl, (Ci-C6-alkyl)s
  • Ci-C6-alkyl is selected from the group consisting of H, OH, S(0)2NH2, CN, Ci-C6-alkyl, C2-C6-alkenyl, C2-C6-alkynyl, (C3-C6-cycloalkyl)-Ci-C4-alkyl, Ci-C6-alkoxy, (Ci-C6-alkoxy)-Ci-C6-alkyl, (Ci-C6-alkyl)-carbonyl, (Ci-C6-alkoxy)carbonyl, (Ci-C6-alkyl)sulfonyl, (Ci-C6-alkylamino)carbonyl, di(Ci-C6- alkyl)aminocarbonyl, (Ci-C6-alkylamino)sulfonyl, di(Ci-C6- alkyl)aminosulfonyl and (Ci-C6-alkoxy)sulfon
  • phenyl phenyl-Ci-C6-alkyl, phenylsulfonyl, phenylaminosulfonyl, phenylcarbonyl and phenoxycarbonyl,
  • phenyl in the last 6 mentioned radicals are unsubstituted or substituted by 1 , 2, 3, 4 or 5 identical or different substituents selected from the group consisting of halogen, CN, NO2, Ci-C6-alkyl, Ci-C6-haloalkyl, Ci- C6-alkoxy and Ci-C6-haloalkoxy;
  • Ci-C6-alkyl is selected from the group consisting of H, OH, S(0)2NH2, CN, Ci-C6-alkyl, C2-C6-alkenyl, C2-C6-alkynyl, (C3-C6-cycloalkyl)-Ci-C4-alkyl, Ci-C6-alkoxy, (Ci-C6-alkoxy)-Ci-C6-alkyl, (Ci-C6-alkyl)carbonyl, (Ci-C6-alkoxy)carbonyl, (Ci-C6-alkyl)sulfonyl, (Ci-C6-alkylamino)carbonyl, di(Ci-C6-alkyl)amino- carbonyl, (Ci-C6-alkylamino)sulfonyl, di(Ci-C6-alkyl)aminosulfonyl and (Ci- C6-alkoxy)sulfon
  • phenyl phenylsulfonyl, phenylaminosulfonyl, phenyl-Ci-C6 alkyl, phenoxy, phenylcarbonyl and phenoxycarbonyl,
  • phenyl in the last 6 mentioned radicals is unsubstituted or substituted by 1 , 2, 3, 4 or 5 identical or different substituents selected from the group consisting of halogen, CN, NO2, Ci-C6-alkyl, Ci-C6-haloalkyl, Ci- C6-alkoxy and Ci-C6-haloalkoxy;
  • R Ar is selected from the group consisting of halogen, OH, CN, amino, N0 2 , d-Ce-alkyl, C 2 -C 6 -alkenyl, C 2 -C 6 -alkynyl, Ci-C 6 -alkoxy, C 2 -C 6 - alkenyloxy, C2-C6-alkynyloxy, (Ci-C6-alkoxy)-Ci-C6-alkyl, (C1-C6- alkoxy)-Ci-C6-alkoxy, (Ci-C6-alkoxy)-C2-C6-alkenyl, (Ci-C6-alkoxy)-C2 C6-alkynyl, Ci-C6-alkylthio, (Ci-C6-alkyl)sulfinyl, (Ci-C6-alkyl)sulfonyl, (Ci-C6-alkyl)amino, di(C
  • Z is a chemical bond, O, S(0)m or NR B
  • R B is selected from the group consisting of H, CN, Ci-C6-alkyl, (C1-C6- alkoxy)-Ci-C6-alkyl, (Ci-C6-alkyl)-carbonyl, (Ci-C6-alkoxy)carbonyl, (Ci-C6-alkyl)sulfonyl, where the aliphatic parts of the 6 aforementioned radicals are unsubstituted, partly or completely halogenated, and
  • n 0, 1 , 2, and
  • Q is phenyl, phenyl-Ci-C6 alkyl, phenylcarbonyl and phenoxycarbonyl, wherein phenyl in the last 4 mentioned radicals is unsubstituted or substituted by 1 , 2, 3, 4 or 5 identical or different substituents selected from the group consisting of halogen, CN, NO2, Ci-C 4 -alkyl, Ci-C 4 -alkoxy, (Ci-C 4 -alkyl)thio, (Ci-C 4 -alkyl)sulfonyl, (C1-C4- alkyl)amino, di(Ci-C 4 -alkyl)amino, (Ci-C 4 -alkyl)-carbonyl, (C1-C4- alkoxy)-carbonyl, where the last 8 mentioned radicals are
  • the present invention also relates to agrochemical compositions comprising at least one diaminotriazine compound of formula (I) and at least one auxiliary customary for formulating crop protection agents.
  • the present invention also relates to the use of diaminotriazine compound of formula (I) as herbicides, i.e. for controlling unwanted and/or harmful vegetation or plants.
  • the present invention furthermore provides a method for controlling unwanted plants.
  • the method includes allowing a herbicidally effective amount of at least one diaminotriazine compound of the formula (I) to act on the unwanted plants or vegetation, their seeds and/or their habitat.
  • Application can be done before, during and/or after, preferably during and/or after, the emergence of the unwanted plants.
  • the invention relates to processes for preparing diaminotriazine compound of formula (I) and to intermediates.
  • undesirable vegetation As used herein, the terms “undesirable vegetation”, “unwanted vegetation”, unwanted plants” and “harmful plants” are synonyms.
  • substitutents means that the number of substituents is e.g. from 1 to 10, in particular 1 , 2, 3, 4, 5, 6, 7 or 8.
  • the invention relates to both the pure isomers and mixtures thereof.
  • the invention relates to the use of the pure pure isomers and to the use of their mixtures and to compositions containing the pure isomers or mixtures thereof.
  • the invention relates to both the pure enantiomers or diastereomers, and mixtures thereof. Likeweise, the invention relates to the use of the pure enantiomers or diastereomers, and mixtures thereof. Likeweise, the invention relates to the use of the pure enantiomers or diastereomers, and mixtures thereof. Likeweise, the invention relates to the use of the pure enantiomers or diastereomers, and mixtures thereof. Likeweise, the invention relates to the use of the pure
  • compositions containing the pure enantiomers or diastereomers or mixtures thereof are provided.
  • diaminotriazine compounds of formula (I) as described herein have ionizable functional groups, they can also be employed in the form of their agriculturally acceptable salts. Suitable are, in general, the salts of those cations and the acid addition salts of those acids whose cations and anions, respectively, have no adverse effect on the activity of the active compounds.
  • Preferred cations are the ions of the alkali metals, preferably of lithium, sodium and potassium, of the alkaline earth metals, preferably of calcium and magnesium, and of the transition metals, preferably of manganese, copper, zinc and iron, further ammonium and substituted ammonium in which one to four hydrogen atoms are replaced by Ci-C4-alkyl, hydroxy-Ci-C4-alkyl, (Ci-C4-alkoxy)-Ci-C4-alkyl, hydroxy-(Ci- C4-alkoxy)-Ci-C4-alkyl, phenyl or benzyl, preferably ammonium, methylammonium, isopropylammonium, dimethylammonium, diisopropylammonium, trimethylammonium, heptylammonium, dodecylammonium, tetradecylammonium, tetramethylammonium, tetraethylammoni
  • Anions of useful acid addition salts are primarily chloride, bromide, fluoride, iodide, hydrogensulfate, methylsulfate, sulfate, dihydrogenphosphate, hydrogen- phosphate, nitrate, bicarbonate, carbonate, hexafluorosilicate, hexafluorophosphate, benzoate and also the anions of Ci-C4-alkanoic acids, preferably formate, acetate, propionate and butyrate.
  • organic moieties mentioned in the definition of the variables e.g. A, R A , R 1 , R 2 , X, R Ar , R B , Z, Q are - like the term halogen - collective terms for individual enumerations of the individual group members.
  • the term halogen denotes in each case fluorine, chlorine, bromine or iodine. All hydrocarbon chains, i.e.
  • alkyl all alkyl, haloalkyl, alkenyl, alkynyl, alkoxy, alkenyloxy, alkynyloxy, alkylthio, alkylsulfinyl, alkylsulfonyl, (alkyl)amino, di(alkyl)amino, alkoxyalkyl, alkoxyalkoxy, (alky)carbonyl, (alkoxy)carbonyl chains can be straight-chain or branched, the prefix C n -C m denoting in each case the possible number of carbon atoms in the group. The same applies to composed radicals, such as cycloalkylalkyl and phenylalkyl.
  • C2-C6-alkenyl and also the C2-C6-alkenyl moieties of (Ci-C6-alkoxy)-C2-C6- alkenyl: a linear or branched ethylenically unsaturated hydrocarbon group having 2 to 6 carbon atoms and a C C-double bond in any position, such as ethenyl, 1 -propenyl, 2- propenyl, 1 -methyl-ethenyl, 1 -butenyl, 2-butenyl, 3-butenyl, 1 -methyl-1 -propenyl, 2- methyl-1 -propenyl, 1 -methyl-2-propenyl, 2-methyl-2-propenyl, 1 -pentenyl, 2-pentenyl, 3-pentenyl, 4-pentenyl, 1 -methyl-1 -butenyl, 2-methyl-1 -butenyl, 3-methyl-1 -butenyl, 1 - methyl-2-butenyl,
  • Ci-C4-haloalkyl a Ci-C4-alkyl radical as mentioned above which is partially or fully substituted by fluorine, chlorine, bromine and/or iodine, for example, chloro- methyl, dichloromethyl, trichloromethyl, fluoromethyl, difluoromethyl, trifluoromethyl, chlorofluoromethyl, dichlorofluoromethyl, chlorodifluoromethyl, bromomethyl, iodomethyl, 2-fluoroethyl, 2-chloroethyl, 2-bromoethyl, 2-iodoethyl, 2,2-difluoroethyl, 2,2,2-trifluoroethyl, 2-chloro-2-fluoroethyl, 2-chloro-2,2-difluoroethyl, 2,2-dichloro- 2-fluoroethyl, 2,2,2-trichloroethyl, pentafluoroethyl,
  • Ci-C6-haloalkyl Ci-C4-haloalkyl as mentioned above, and also, for example, 5- fluoropentyl, 5-chloropentyl, 5-bromopentyl, 5-iodopentyl, undecafluoropentyl,
  • C3-C6-cycloalkyl monocyclic saturated hydrocarbons having 3 to 6 ring members, such as cyclopropyl, cyclobutyl, cyclopentyl and cyclohexyl;
  • Ci-C4-alkoxy for example methoxy, ethoxy, propoxy, 1 -methylethoxy butoxy, 1 - methylpropoxy, 2-methylpropoxy and 1 ,1 -dimethylethoxy;
  • Ci-C4-haloalkoxy a Ci-C4-alkoxy radical as mentioned above which is partially or fully substituted by fluorine, chlorine, bromine and/or iodine, for example, chloro- methoxy, dichloromethoxy, trichloromethoxy, fluoromethoxy, difluoromethoxy, trifluoromethoxy, chlorofluoromethoxy, dichlorofluoromethoxy, chlorodifluoromethoxy2- fluoroethoxy, 2-chloroethoxy, 2-bromoethxoy, 2,2-difluoroethoxy, 2,2,2-trifluoroethoxy, 2-chloro-2-fluoroethoxy, 2-chloro-2,2-difluoroethoxy, 2,2-dichloro-2-fluoroethoxy, 2,2,2- trichloroethoxy, pentafluoroethoxy, 2-fluoropropoxy, 3-fluoropropoxy, 2,2- difluoroprop
  • Ci-C6-haloalkoxy Ci-C4-alkoxy as mentioned above: Ci-C4-haloalkoxy as mentioned above, and also, for example, 5-fluoropentyl, 5-chloropentyl, 5-bromopentyl, 5-iodopentyl, undecafluoropentyl, 6-fluorohexyl, 6-chlorohexyl, 6-bromohexyl, 6- iodohexyl and dodecafluorohexyl;
  • C2-C6-alkenyloxy C2-C6-alkenyl as defined above, which is bound via an oxygen atom, such as ethenyloxy (vinyloxy), 1 -propenyloxy, 2-propenyloxy (allyloxy), 1 - butenyloxy, 2-butenyloxy, 3-butenyloxy 1 -methyl-2-propenyloxy and the like;
  • C2-C6-alkynyloxy C2-C6-alkynyl as defined above, which is bound via an oxygen atom, such as ethynyloxy, 1 -propynyl, 2-propynyloxy (propargyloxy), 1 -butynyloxy, 2- butynyloxy, 3-butynyloxy 1 -methyl-2-propynyloxy and the like;
  • Ci-C4-alkylthio for example methylthio, ethylthio, propylthio, 1 -methylethylthio, butylthio, 1 -methylpropylthio, 2-methylpropylthio and 1 ,1 -dimethylethylthio;
  • Ci-C6-alkylthio Ci-C4-alkylthio as mentioned above, and also, for example, pentylthio, 1 -methylbutylthio, 2-methylbutylthio, 3-methylbutylthio, 2,2- dimethylpropylthio, 1 -ethylpropylthio, hexylthio, 1 ,1 -dimethylpropylthio, 1 ,2- dimethylpropylthio, 1 -methylpentylthio, 2-methylpentylthio, 3-methylpentylthio, 4-methylpentylthio, 1 ,1 -dimethylbutylthio, 1 ,2-dimethylbutylthio, 1 ,3-dimethylbutylthio, 2,2-dimethylbutylthio, 2,3-dimethylbutylthio, 3,3-dimethylbutylthio, 1 -ethylbutylthio, 2- e
  • z.B methylsulfinyl, ethylsulfinyl, propylsulfinyl, 1 -methylethylsulfinyl, butylsulfinyl, 1-methylpropylsulfinyl, 2- methylpropylsulfinyl, 1 ,1 -dimethylethylsulfinyl, pentylsulfinyl, 1 -methylbutylsulfinyl, 2- methylbutylsulfinyl, 3-methylbutylsulfinyl, 2,2-dimethylpropylsulfinyl, 1 - ethylpropylsulfinyl, 1 ,1 -dimethylpropylsulfinyl, 1 ,2-dimethylpropyl
  • C3-C6-cyclolalkoxy a cycloaliphatic radical having 3 to 6 carbon atoms and bound via an oxygen atom, such as cyclopropyloxy, cyclobutyloxy, cyclopentyloxy and cyclohexyloxy;
  • Ci-C6-alkyl in particular Ci-C4-alkyl as defined above, such as methyl or ethyl, wherein 1 hydrogen atom is replaced by C3-C6- cyclolalkyl as defined above, examples including cyclopropyl methyl (Chb-cyclopropyl), cyclobutyl methyl, cyclopentylmethyl, cycloexylmethyl, 1 -cyclopropylethyl (CH(CH3)- cyclopropyl), 1 -cyclobutylethyl, 1 -cyclopentylethyl, 1 -cycloexylethyl, 2-cyclopropylethyl (ChbChb-cyclopropyl), 2-cyclobutylethyl, 2-cyclopentylethyl or 2-cycloexylethyl;
  • Ci-C6-alkoxy in particular Ci-C4-alkoxy as defined above, such as methoxy or ethoxy, wherein 1 hydrogen atom is replaced by C3-C6-cyclolalkyl as defined above, examples including cyclopropylmethoxy (OCH2- cyclopropyl), cyclobutyl methoxy, cyclopentylmethoxy, cycloexylmethoxy, 1 - cyclopropylethoxy (0-CH(CH3)-cyclopropyl), 1 -cyclobutylethoxy, 1 -cyclopentylethoxy, 1 -cycloexylethoxy, 2-cyclopropylethoxy (OChbChy-cyclopropyl), 2-cyclobutylethoxy, 2- cyclopentylethoxy and 2-cycloexylethoxy;
  • Ci-C6-alkoxy-Ci-C6-alkyl Ci-C6-alkyl, in particular Ci-C4-alkyl as defined above, such as methyl, ethyl or isopropyl, wherein 1 hydrogen atom is replaced by C1-C6- alkoxy as defined above, examples including methoxymethyl, ethoxymethyl, n- propoxymethyl, butoxymethyl, 1 -methoxyethyl, 1 -ethoxyethyl, 1 -(n-propoxy)ethyl, 1 - butoxyethyl, 2-methoxyethyl, 2-ethoxyethyl, 2-(n-propoxy)ethyl, 2-butoxyethyl, 2- methoxypropyl, 2-ethoxypropyl, 2-(n-propoxy)propyl, 2-butoxypropyl;
  • Ci-C6-alkoxy Ci-C6-alkoxy, in particular Ci-C4-alkoxy as defined above, such as methoxy or ethoxy, wherein 1 hydrogen atom is replaced by C1-C6- alkoxy as defined above, examples including methoxymethoxy, ethoxymethoxy, n- propoxymethoxy, butoxymethoxy, 2-methoxyethoxy, 2-ethoxyethoxy, 2-(n- propoxy)ethoxy and 2-butoxyethoxy;
  • (Ci-C6-alkoxy)-C2-C6-alkenyl C2-C6-alkenyl, in particular C2-C4-alkenyl as defined above, such as ethenyl, propenyl, 1 -butenyl or 2-butenyl, wherein 1 hydrogen atom is replaced by Ci-C6-alkoxy as defined above;
  • (Ci-C6-alkoxy)-C2-C6-alkynyl C2-C6-alkynyl, in particular C2-C4-alkynyl as defined above, such as ethynyl, propynyl or 2-butynyl, wherein 1 hydrogen atom is replaced by Ci-C6-alkoxy as defined above;
  • Ci-C6-alkyl as mentioned above, which is bound to the remainder of the molecule by a carbonyl group;
  • Ci-C6-alkoxycarbonyl Ci-C6-alkyloxy as mentioned above, which is bound to the remainder of the molecule by a carbonyl group;
  • di(Ci-C6-alkylamino)carbonyl di(Ci-C6-alkyl)amino as mentioned above, which is bound to the remainder of the molecule by a carbonyl group;
  • di(Ci-C6-alkylamino)sulfonyl di(Ci-C6-alkyl)amino as mentioned above, which is bound to the remainder of the molecule by a sulfonyl group;
  • Ci-C6-alkyl in particular Ci-C4-alkyl as defined above, such as methyl or ethyl, wherein 1 hydrogen atom is replaced by phenyl, examples including benzyl, 1 -phenylethyl, 2-phenylethyl, 1 -phenylpropyl, 2-phenylpropyl, 1 -phenyl-1 - methylethyl etc.;
  • Ci-C6-alkylamino sulfonyl: Ci-C6-alkyl, in particular Ci-C4-alkyl as defined above which is bound to the reminder molecule via a S(0)2-group;
  • Ci-C6-alkoxysulfonyl Ci-C6-alkixy, in particular Ci-C4-alkoxy as defined above which is bound to the reminder molecule via a S(0)2-group.
  • A is phenyl, which carries a fluorine atom in the 2-position of the phenyl ring and which additionally carries 1 , 2, 3 or 4, in particular 2, 3 or 4, substituents R A as defined above, which are
  • halogen in particular selected from the group consisting of halogen, CN, Ci-C6-alkyl, Ci- C6-alkoxy, Ci-C6-haloalkyl, C3-C6-cycloalkyl, C3-C6-cycloalkoxy, (C3-C6- cycloalkyl)methoxy, C2-C6-alkynyl, C2-C6-alkenyl, C2-C6-alkynyloxy, C2-C6- alkenyloxy and Ci-C6-haloalkoxy;
  • Ci-C4-alkyl Ci-C4-alkyl, C2-C4-alkynyl, C2-C4- alkynyloxy, Ci-C4-haloalkyl, Ci-C4-alkoxy, Ci-C4-haloalkoxy, C3-C6-cycloalkyl, C3- C6-cycloalkoxy, (C3-C6-cycloalkyl)methoxy and CN;
  • A is a moiety of the following formula, wherein # indicates the point of attachment to the nitrogen;
  • R A1 is hydrogen or halogen, in particular hydrogen or fluorine
  • R A2 is hydrogen or has one of the meanings given for R A , and is in particular selected from the group consisting of hydrogen, halogen, CN, Ci-C6-alkyl, Ci-C6-alkoxy, Ci-C6-haloalkyl, C3-C6-cycloalkyl, C3-C6-cycloalkoxy, (C3-C6- cycloalkyl)methoxy, C2-C6-alkynyl, C2-C6-alkenyl, C2-C6-alkynyloxy, C2-C6- alkenyloxy and Ci-C6-haloalkoxy;
  • R A3 is hydrogen or halogen, in particular hydrogen or fluorine
  • R M has one of the meanings given for R A , and is in particular selected from the group consisting of hydrogen, halogen, CN, Ci-C6-alkyl, Ci-C6-alkoxy, Ci- C6-haloalkyl, C3-C6-cycloalkyl, C3-C6-cycloalkoxy, (C3-C6- cycloalkyl)methoxy, C2-C6-alkynyl, C2-C6-alkenyl, C2-C6-alkynyloxy, C2-C6- alkenyloxy and Ci-C6-haloalkoxy;
  • A include 2,6-difluorophenyl, 2-chloro-6- fluorophenyl, 2-bromo-6-fluorophenyl, 2-fluoro-6-methylphenyl, 2-fluoro-6-cyanophenyl, 2,3,6-trifluorophenyl, 2,4,6-trifluorophenyl, 2-chloro-4,6-difluorophenyl, 2-chloro-5,6- difluorophenyl, 3-chloro-2,6-difluorophenyl, 2-chloro-3,6-difluorophenyl, 2,3-difluoro-6- cyanophenyl, 2,6-difluoro-3-cyanophenyl, 2,5-difluoro-6-cyanophenyl, 2,4-difluoro-6- cyanophenyl, 2,3,4,6-tetrafluorophenyl, 2,3,4,5-tetrafluorophenyl, 2,2,
  • R 1 is H, OH, S(0) 2 NH 2 , CN, Ci-C 6 -alkyl, C 2 -C 6 -alkenyl, C 2 -C 6 -alkynyl, (C 3 -C 6 - cycloalkyl)-Ci-C 4 -alkyl, Ci-C 6 -alkoxy, (Ci-C 6 -alkoxy)-Ci-C 6 -alkyl, (Ci-C 6 -alkyl)- carbonyl, (Ci-C6-alkoxy)carbonyl, (Ci-C6-alkyl)sulfonyl, (C1-C6- alkylamino)carbonyl, di(Ci-C6-alkyl)aminocarbonyl, (Ci-C6-alkylamino)sulfonyl, di(Ci-C
  • phenyl phenyl-Ci-C6-alkyl, phenylsulfonyl, phenylaminosulfonyl, phenylcarbonyl and phenoxycarbonyl,
  • phenyl in the last 6 mentioned radicals are unsubstituted or substituted by 1 , 2, 3, 4 or 5 identical or different substituents selected from the group consisting of halogen, CN, N0 2 , Ci-C6-alkyl, Ci-C6-haloalkyl, Ci-C6-alkoxy and Ci-C6-haloalkoxy;
  • H preferably, H, CN, Ci-C 6 -alkyl, (Ci-C 6 -alkoxy)-Ci-C 6 -alkyl, (Ci-C 6 -alkyl)carbonyl or (Ci-C6-alkyl)sulfonyl, where the aliphatic parts of the 4 aforementioned radicals unsubstituted partly or completely halogenated,
  • phenyl in the last 2 mentioned radical is unsubstituted or substituted by 1 , 2, 3, 4, or 5 identical or different substituents selected from the group consisting of halogen, CN, N0 2 , Ci-C6-alkyl, Ci-C6-haloalkyl, Ci-C6-alkoxy and Ci-C6-haloalkoxy;
  • Ci-C 6 -alkyl Ci-C 6 -haloalkyl, (Ci-C 6 -alkoxy)-Ci-C 6 -alkyl, Ci- C6-alkoxy, (Ci-C6-alkyl)carbonyl, (Ci-C6-haloalkyl)carbonyl, (Ci-C6-alkyl)sulfonyl or (Ci-C6-haloalkyl)sulfonyl;
  • H CN, Ci-C 4 -alkyl, (Ci-C 4 -alkoxy)-Ci-C 4 -alkyl, Ci-C 4 -alkoxy, (Ci-C 4 -alkyl)carbonyl or (Ci-C 4 -alkyl)sulfonyl;even more particularly H, CN, CH3, CH 2 OCH 3 , OCH3, C(0)CH 3 or S0 2 CH 3 ;
  • R 2 is H, OH, S(0) 2 NH 2 , CN, Ci-C 6 -alkyl, C 2 -C 6 -alkenyl, C 2 -C 6 -alkynyl, (C 3 -C 6 - cycloalkyl)-Ci-C 4 -alkyl, Ci-C 6 -alkoxy, (Ci-C 6 -alkoxy)-Ci-C 6 -alkyl, (Ci-C 6 - alkyl)carbonyl, (Ci-C6-alkoxy)carbonyl, (Ci-C6-alkyl)sulfonyl, (C1-C6- alkylamino)carbonyl, di(Ci-C6-alkyl)aminocarbonyl, (Ci-C6-alkylamino)sulfonyl, di(Ci-C6-alkyl)aminosulfonyl and (Ci-C6-alkoxy)
  • phenyl phenylsulfonyl, phenylaminosulfonyl, phenyl-Ci-C6 alkyl, phenoxy, phenylcarbonyl and phenoxycarbonyl,
  • phenyl in the last 6 mentioned radicals is unsubstituted or substituted by 1 , 2, 3, 4 or 5 identical or different substituents selected from the group consisting of halogen, CN, NO2, d-Ce-alkyl, d-Ce-haloalkyl, d-Ce-alkoxy and Ci-Ce- haloalkoxy;
  • H preferably, H, CN, Ci-C 6 -alkyl, (Ci-C 6 -alkoxy)-Ci-C 6 -alkyl, (Ci-C 6 -alkyl)carbonyl or (Ci-C6-alkyl)sulfonyl, where the aliphatic parts of the 4 aforementioned radicals unsubstituted partly or completely halogenated;
  • phenyl in the last 2 mentioned radical is unsubstituted or substituted by 1 , 2, 3, 4, or 5 identical or different substituents selected from the group consisting of halogen, CN, NO2, Ci-C6-alkyl, Ci-C6-haloalkyl, Ci-C6-alkoxy and Ci-C6-haloalkoxy;
  • Ci-C6-alkyl in particular H, CN, Ci-C6-alkyl, (Ci-C6-alkoxy)-Ci-C6-alkyl, (Ci-C6-alkyl)carbonyl or (Ci-C6-alkyl)sulfonyl;
  • H CN
  • Ci-C4-alkyl Ci-C4-alkyl, (Ci-C4-alkoxy)-Ci-C4-alkyl, (C1-C4- alkyl)carbonyl or (Ci-C4-alkyl)sulfonyl;
  • X is phenyl which is unsubstituted or may carry, 1 , 2, 3, 4 or 5 radicals R Ar as defined above, which are
  • Ci-C6-alkyl in particular selected from the group consisting of halogen, CN, Ci-C6-alkyl, Ci-
  • Q is phenyl, or benzyl, wherein the phenyl ring may additionally carry 1 , 2, 3, 4 or 5 substituents selected from the group consisting of F, CI, CN, CF3, methyl, vinyl, ethynyl, cyclopropyl, methoxy, ethoxy, isopropyloxy, allyloxy, propargyloxy, cyclopropyloxy, cyclobutyloxy, cyclopentyloxy,
  • R Ar is more particular selected from the group consisting of halogen, Ci- C4-alkyl, C2-C4-alkynyl, C2-C4-alkynyloxy, Ci-C4-haloalkyl, Ci-C4-alkoxy, C1-C4- haloalkoxy, C3-C6-cycloalkyl, C3-C6-cycloalkoxy, (C3-C6-cycloalkyl)methoxy, CN and where one of the radicals R Ar may also be Z-Q wherein
  • Q is phenyl, or benzyl, wherein the phenyl ring may additionally carry 1 , 2, 3, 4 or 5 substituents selected from the group consisting of F, CI, CN, CF3, methyl, vinyl, ethynyl, cyclopropyl, methoxy, ethoxy, isopropyloxy, allyloxy, propargyloxy, cyclopropyloxy, cyclobutyloxy, cyclopentyloxy, (cycloproyl)methoxy 2-butyloxy; even more particularly selected from the group consisting of F, CI, CN, CF3, methyl, vinyl, ethynyl, cyclopropyl, methoxy, ethoxy, isopropyloxy, allyloxy, propargyloxy, cyclopropyloxy, cyclobutyloxy, cyclopentyloxy, (cycloproyl)methoxy or 2-butyloxy;
  • R Ar is especially selected from the group consisting of F, CI, methoxy, ethoxy, CN, and where one of the radicals R Ar may also be Z-Q wherein
  • Q is phenyl, or benzyl
  • X is phenyl which carries 1 , 2, 3, 4 or 5 radicals R Ar as defined above.
  • diaminotriazine compounds of formula (I) Particularly preferred are the diaminotriazine compounds of formula (I), and likewise the diaminotriazine compounds of formula (I) according to embodiment groups, wherein
  • R 1 is hydrogen
  • R 2 is hydrogen
  • diaminotriazine compounds of formula (I) Particularly preferred are the diaminotriazine compounds of formula (I), and likewise the diaminotriazine compounds of formula (I) according to embodiment groups, wherein
  • R 1 is hydrogen
  • R 2 is hydrogen
  • A is phenyl, which carries a fluorine atom in the 2-position of the phenyl ring and which additionally carries 1 , 2, 3 or 4, in particular 2, 3 or 4, substituents R A as defined above, which are
  • halogen in particular selected from the group consisting of halogen, CN, Ci-C6-alkyl, Ci- C6-alkoxy, Ci-C6-haloalkyl, C3-C6-cycloalkyl, C3-C6-cycloalkoxy, (C3-C6- cycloalkyl)methoxy, C2-C6-alkynyl, C2-C6-alkenyl, C2-C6-alkynyloxy, C2-C6- alkenyloxy and Ci-C6-haloalkoxy;
  • Ci-C4-alkyl Ci-C4-alkyl, C2-C4-alkynyl, C2-C4- alkynyloxy, Ci-C4-haloalkyl, Ci-C4-alkoxy, Ci-C4-haloalkoxy, C3-C6-cycloalkyl, C3- C6-cycloalkoxy, (C3-C6-cycloalkyl)methoxy and CN;
  • diaminotriazine compounds of formula (I) Especially preferred are the diaminotriazine compounds of formula (I), and likewise the diaminotriazine compounds of formula (I) according to embodiment groups, wherein
  • R 1 is hydrogen
  • R 2 is hydrogen
  • A is a moiety of the following formula:
  • # indicates the point of attachment to the nitrogen
  • R A1 is hydrogen or halogen, in particular hydrogen or fluorine
  • R A2 is hydrogen or has one of the meanings given for R A , and is in particular selected from the group consisting of hydrogen, halogen, CN, Ci-C6-alkyl, Ci-C6-alkoxy, Ci-C6-haloalkyl, C3-C6-cycloalkyl, C3-C6-cycloalkoxy, (C3-C6- cycloalkyl)methoxy, C2-C6-alkynyl, C2-C6-alkenyl, C2-C6-alkynyloxy, C2-C6- alkenyloxy and Ci-C6-haloalkoxy;
  • R A3 is hydrogen or halogen, in particular hydrogen or fluorine
  • R M has one of the meanings given for R A , and is in particular selected from the group consisting of hydrogen, halogen, CN, Ci-C6-alkyl, Ci-C6-alkoxy, Ci- C6-haloalkyl, C3-C6-cycloalkyl, C3-C6-cycloalkoxy, (C3-C6- cycloalkyl)methoxy, C2-C6-alkynyl, C2-C6-alkenyl, C2-C6-alkynyloxy, C2-C6- alkenyloxy and Ci-C6-haloalkoxy;
  • A is especially selected from the group consisting of 2,6- difluorophenyl, 2-chloro-6-fluorophenyl, 2-bromo-6-fluorophenyl, 2-fluoro-6- methylphenyl, 2-fluoro-6-cyanophenyl, 2,3,6-trifluorophenyl, 2,4,6-trifluorophenyl, 2-chloro-4,6-difluorophenyl, 2-chloro-5,6-difluorophenyl, 3-chloro-2,6- difluorophenyl, 2-chloro-3,6-difluorophenyl, 2,3-difluoro-6-cyanophenyl, 2,6- difluoro-3-cyanophenyl, 2,5-difluoro-6-cyanophenyl, 2,4-difluoro-6-cyanophenyl, 2,3,4,6-tetrafluorophenyl, 2,3,4,5-tetrafluorophenyl
  • diaminotriazine compounds of formula (I) Especially preferred are the diaminotriazine compounds of formula (I), and likewise the diaminotriazine compounds of formula (I) according to embodiment groups, wherein
  • R 1 is hydrogen
  • R 2 is hydrogen
  • A is a moiety of the following formula: wherein # indicates the point of attachment to the nitrogen;
  • R A1 is hydrogen or halogen, in particular hydrogen or fluorine
  • R A2 is hydrogen or has one of the meanings given for R A , and is in particular selected from the group consisting of hydrogen, halogen, CN, Ci-C6-alkyl, Ci-C6-alkoxy, Ci-C6-haloalkyl, C3-C6-cycloalkyl, C3-C6-cycloalkoxy, (C3-C6- cycloalkyl)methoxy, C2-C6-alkynyl, C2-C6-alkenyl, C2-C6-alkynyloxy, C2-C6- alkenyloxy and Ci-C6-haloalkoxy;
  • R A3 is hydrogen or halogen, in particular hydrogen or fluorine
  • R M has one of the meanings given for R A , and is in particular selected from the group consisting of hydrogen, halogen, CN, Ci-C6-alkyl, Ci-C6-alkoxy, Ci- C6-haloalkyl, C3-C6-cycloalkyl, C3-C6-cycloalkoxy, (C3-C6- cycloalkyl)methoxy, C2-C6-alkynyl, C2-C6-alkenyl, C2-C6-alkynyloxy, C2-C6- alkenyloxy and Ci-C6-haloalkoxy;
  • A is especially selected from the group consisting of 2,6- difluorophenyl, 2-chloro-6-fluorophenyl, 2-bromo-6-fluorophenyl, 2-fluoro-6- methylphenyl, 2-fluoro-6-cyanophenyl, 2,3,6-trifluorophenyl, 2,4,6-trifluorophenyl, 2-chloro-4,6-difluorophenyl, 2-chloro-5,6-difluorophenyl, 3-chloro-2,6- difluorophenyl, 2-chloro-3,6-difluorophenyl, 2,3-difluoro-6-cyanophenyl, 2,6- difluoro-3-cyanophenyl, 2,5-difluoro-6-cyanophenyl, 2,4-difluoro-6-cyanophenyl, 2,3,4,6-tetrafluorophenyl, 2,3,4,5-tetrafluorophenyl
  • 6-(2-propoxy)phenyl 2,3,5-trifluoro-6-(2-propoxy)phenyl, 2,4,5-trifluoro-6-(2- propoxy) phenyl, 2,3,4,5-tetrafluoro-6-(2-propoxy)phenyl, 2-fluoro-6-(n- butoxy)phenyl, 2,3-difluoro-6-(n-butoxy)phenyl, 2,4-difluoro-6-(n-butoxy)phenyl,
  • X is phenyl which is unsubstituted or may carry, 1 , 2, 3, 4 or 5 radicals R Ar as defined above, which are in particular selected from the group consisting of halogen, CN, Ci-C6-alkyl, Ci- C6-alkoxy, Ci-C6-haloalkyl, C3-C6-cycloalkyl, C3-C6-cycloalkoxy, (C3-C6- cycloalkyl)methoxy, C2-C6-alkynyl, C2-C6-alkenyl, C2-C6-alkynyloxy, C2-C6- alkenyloxy, Ci-C6-haloalkoxy and where one of the radicals R Ar may also be Z-Q wherein
  • Q is phenyl, or benzyl, wherein the phenyl ring may additionally carry 1 , 2, 3, 4 or 5 substituents selected from the group consisting of F, CI, CN, CF3, methyl, vinyl, ethynyl, cyclopropyl, methoxy, ethoxy, isopropyloxy, allyloxy, propargyloxy, cyclopropyloxy, cyclobutyloxy, cyclopentyloxy,
  • R Ar is more particular selected from the group consisting of halogen, Ci- C4-alkyl, C2-C4-alkynyl, C2-C4-alkynyloxy, Ci-C4-haloalkyl, Ci-C4-alkoxy, C1-C4- haloalkoxy, C3-C6-cycloalkyl, C3-C6-cycloalkoxy, (C3-C6-cycloalkyl)methoxy, CN and where one of the radicals R Ar may also be Z-Q wherein
  • Q is phenyl, or benzyl, wherein the phenyl ring may additionally carry 1 , 2, 3, 4 or 5 substituents selected from the group consisting of F, CI, CN, CF3, methyl, vinyl, ethynyl, cyclopropyl, methoxy, ethoxy, isopropyloxy, allyloxy, propargyloxy, cyclopropyloxy, cyclobutyloxy, cyclopentyloxy, (cycloproyl)methoxy 2-butyloxy; even more particularly selected from the group consisting of F, CI, CN, CF3, methyl, vinyl, ethynyl, cyclopropyl, methoxy, ethoxy, isopropyloxy, allyloxy, propargyloxy, cyclopropyloxy, cyclobutyloxy, cyclopentyloxy, (cycloproyl)methoxy or 2-butyloxy;
  • R Ar is especially selected from the group consisting of F, CI, methoxy, ethoxy, CN, and where one of the radicals R Ar may also be Z-Q wherein
  • Q is phenyl, or benzyl.
  • diaminotriazine compounds of formula (la) which correspond to diaminotriazines of formula (I) wherin R 1 is hydrogen and where R 2 and X are as defined in the rows of the following table A and wherein A is as defined in the following tables A-1 to A-88:
  • Table A-1 Compounds of the formula I . a, where A is 2,6-difluorophenyl and R 2 and X are as defined in the rows of the following table A.
  • Table A-2 Compounds of the formula I. a, where A is 2-chloro-6-fluorophenyl and R 2 and X are as defined in the rows of the following table A.
  • Table A-3 Compounds of the formula I. a, where A is 2-bromo-6-fluorophenyl and R 2 and X are as defined in the rows of the following table A.
  • R 2 and X are as defined in the rows of the following table A.
  • Table A-5 Compounds of the formula I. a, where A is 2-fluoro-6-cyanophenyl and R 2 and X are as defined in the rows of the following table A.
  • Table A-6 Compounds of the formula I. a, where A is 2,3,6-trifluorophenyl and R 2 and X are as defined in the rows of the following table A.
  • Table A-7 Compounds of the formula I. a, where A is 2,4,6-trifluorophenyl and R 2 and X are as defined in the rows of the following table A.
  • Table A-8 Compounds of the formula I. a, where A is 2-chloro-4,6-difluorophenyl and R 2 and X are as defined in the rows of the following table A.
  • Table A-9 Compounds of the formula I. a, where A is 2-chloro-5,6-difluorophenyl and R 2 and X are as defined in the rows of the following table A.
  • Table A-10 Compounds of the formula I. a, where A is 3-chloro-2,6-difluorophenyl and R 2 and X are as defined in the rows of the following table A.
  • Table A-1 1 Compounds of the formula I. a, where A is 2-chloro-3,6-difluorophenyl and R 2 and X are as defined in the rows of the following table A.
  • Table A-12 Compounds of the formula I. a, where A is 2,3-difluoro-6-cyanophenyl and R 2 and X are as defined in the rows of the following table A.
  • Table A-13 Compounds of the formula I. a, where A is 2,6-difluoro-3-cyanophenyl and R 2 and X are as defined in the rows of the following table A.
  • Table A-14 Compounds of the formula I. a, where A is 2,5-difluoro-6-cyanophenyl and R 2 and X are as defined in the rows of the following table A.
  • Table A-15 Compounds of the formula I. a, where A is 2,3,4,6-tetrafluorophenyl and R 2 and X are as defined in the rows of the following table A.
  • Table A-16 Compounds of the formula I. a, where A is 2,3,4,5-tetrafluorophenyl and R 2 and X are as defined in the rows of the following table A.
  • Table A-17 Compounds of the formula I. a, where A is 2,3,5,6-tetrafluorophenyl and R 2 and X are as defined in the rows of the following table A.
  • Table A-18 Compounds of the formula I. a, where A is 2-chloro-3,4,6- trifluorophenyl and R 2 and X are as defined in the rows of the following table A.
  • Table A-19 Compounds of the formula I. a, where A is 2-chloro-3,5,6- trifluorophenyl and R 2 and X are as defined in the rows of the following table A.
  • Table A-20 Compounds of the formula I. a, where A is 3-chloro-2,4,6- trifluorophenyl and R 2 and X are as defined in the rows of the following table A.
  • Table A-21 Compounds of the formula I. a, where A is 3-chloro-2,5,6- trifluorophenyl and R 2 and X are as defined in the rows of the following table A.
  • Table A-22 Compounds of the formula I. a, where A is 6-cyano-2,4,5- trifluorophenyl and R 2 and X are as defined in the rows of the following table A.
  • Table A-23 Compounds of the formula I. a, where A is 3-cyano-2,4,6- trifluorophenyl and R 2 and X are as defined in the rows of the following table A.
  • Table A-24 Compounds of the formula I. a, where A is 6-cyano-2,3,4- trifluorophenyl and R 2 and X are as defined in the rows of the following table A.
  • Table A-25 Compounds of the formula I. a, where A is 6-cyano-2,3,5- trifluorophenyl and R 2 and X are as defined in the rows of the following table A.
  • Table A-26 Compounds of the formula I. a, where A is 3-cyano-2,5,6- trifluorophenyl and R 2 and X are as defined in the rows of the following table A.
  • Table A-27 Compounds of the formula I. a, where A is pentafluorophenyl and R 2 and X are as defined in the rows of the following table A.
  • Table A-28 Compounds of the formula I. a, where A is 2-chloro-3,4,5,6- tetrafluorophenyl and R 2 and X are as defined in the rows of the following table A.
  • Table A-29 Compounds of the formula I. a, where A is 3-chloro-2,4,5,6- tetrafluorophenyl and R 2 and X are as defined in the rows of the following table A.
  • Table A-30 Compounds of the formula I. a, where A is 6-cyano-2, 3,4,5- tetrafluorophenyl and R 2 and X are as defined in the rows of the following table A.
  • Table A-31 Compounds of the formula I. a, where A is 5-cyano-2, 3,4,6- tetrafluorophenyl and R 2 and X are as defined in the rows of the following table A.
  • Table A-32 Compounds of the formula I. a, where A is 4-bromo-2, 3,5,6- tetrafluorophenyl and R 2 and X are as defined in the rows of the following table A.
  • Table A-33 Compounds of the formula I. a, where A is 4-iodo-2, 3,5,6- tetrafluorophenyl and R 2 and X are as defined in the rows of the following table A.
  • Table A-34 Compounds of the formula I. a, where A is 4-ethynyl-2, 3,5,6- tetrafluorophenyl and R 2 and X are as defined in the rows of the following table A.
  • Table A-36 Compounds of the formula I. a, where A is 2-fluoro-6-methoxyphenyl and R 2 and X are as defined in the rows of the following table A.
  • Table A-37 Compounds of the formula I. a, where A is 2,3-difluoro-6- methoxyphenyl and R 2 and X are as defined in the rows of the following table A.
  • Table A-38 Compounds of the formula I. a, where A is 2,4-difluoro-6- methoxyphenyl and R 2 and X are as defined in the rows of the following table A.
  • Table A-39 Compounds of the formula I. a, where A is 2,5-difluoro-6- methoxyphenyl and R 2 and X are as defined in the rows of the following table A.
  • Table A-40 Compounds of the formula I. a, where A is 2,3,4-trifluoro-6- methoxyphenyl and R 2 and X are as defined in the rows of the following table A.
  • Table A-42 Compounds of the formula I. a, where A is 2,3,5-trifluoro-6- methoxyphenyl and R 2 and X are as defined in the rows of the following table A.
  • Table A-43 Compounds of the formula I. a, where A is 2,4,5-trifluoro-6- methoxyphenyl and R 2 and X are as defined in the rows of the following table A.
  • Table A-44 Compounds of the formula I. a, where A is 2,3,4,5-tetrafluoro-6- methoxyphenyl and R 2 and X are as defined in the rows of the following table A.
  • Table A-45 Compounds of the formula I. a, where A is 2-fluoro-6-ethoxyphenyl and R 2 and X are as defined in the rows of the following table A.
  • Table A-46 Compounds of the formula I. a, where A is 2,3-difluoro-6- ethoxyphenyl and R 2 and X are as defined in the rows of the following table A.
  • Table A-47 Compounds of the formula I. a, where A is 2,4-difluoro-6- ethoxyphenyl and R 2 and X are as defined in the rows of the following table A.
  • Table A-48 Compounds of the formula I. a, where A is 2,5-difluoro-6- ethoxyphenyl and R 2 and X are as defined in the rows of the following table A.
  • Table A-49 Compounds of the formula I. a, where A is 2,3,4-trifluoro-6- ethoxyphenyl and R 2 and X are as defined in the rows of the following table A.
  • Table A-50 Compounds of the formula I. a, where A is 2,3,5-trifluoro-6- ethoxyphenyl and R 2 and X are as defined in the rows of the following table A.
  • Table A-51 Compounds of the formula I. a, where A is 2,4,5-trifluoro-6- ethoxyphenyl and R 2 and X are as defined in the rows of the following table A.
  • Table A-52 Compounds of the formula I. a, where A is 2,3,4,5-tetrafluoro-6- ethoxyphenyl and R 2 and X are as defined in the rows of the following table A.
  • Table A-53 Compounds of the formula I. a, where A is 2,3-difluoro-6-(n- propoxy)phenyl and R 2 and X are as defined in the rows of the following table A.
  • Table A-54 Compounds of the formula I. a, where A is 2,4-difluoro-6-(n- propoxy)phenyl and R 2 and X are as defined in the rows of the following table A.
  • Table A-55 Compounds of the formula I. a, where A is 2,5-difluoro-6-(n- propoxy)phenyl and R 2 and X are as defined in the rows of the following table A.
  • Table A-56 Compounds of the formula I. a, where A is 2,3,4-trifluoro-6-(n- propoxy)phenyl and R 2 and X are as defined in the rows of the following table A.
  • Table A-57 Compounds of the formula I. a, where A is 2,3,5-trifluoro-6-(n- propoxy)phenyl and R 2 and X are as defined in the rows of the following table A.
  • Table A-58 Compounds of the formula I. a, where A is 2,4,5-trifluoro-6-(n- propoxy)phenyl and R 2 and X are as defined in the rows of the following table A.
  • Table A-59 Compounds of the formula I. a, where A is 2,3,4,5-tetrafluoro-6-(n- propoxy)phenyl and R 2 and X are as defined in the rows of the following table A.
  • Table A-60 Compounds of the formula I. a, where A is 2,3-difluoro-6-(2- propoxy)phenyl and R 2 and X are as defined in the rows of the following table A.
  • Table A-61 Compounds of the formula I. a, where A is 2,4-difluoro-6-(2- propoxy)phenyl and R 2 and X are as defined in the rows of the following table A.
  • Table A-62 Compounds of the formula I. a, where A is 2,5-difluoro-6-(2- propoxy)phenyl and R 2 and X are as defined in the rows of the following table A.
  • Table A-63 Compounds of the formula I. a, where A is 2,3,4-trifluoro-6-(2- propoxy)phenyl and R 2 and X are as defined in the rows of the following table A.
  • Table A-64 Compounds of the formula I. a, where A is 2,3,5-trifluoro-6-(2- propoxy)phenyl and R 2 and X are as defined in the rows of the following table A.
  • Table A-65 Compounds of the formula I. a, where A is 2,4,5-trifluoro-6-(2- propoxy)phenyl and R 2 and X are as defined in the rows of the following table A.
  • Table A-66 Compounds of the formula I. a, where A is 2,3,4,5-tetrafluoro-6-(2- propoxy)phenyl and R 2 and X are as defined in the rows of the following table A.
  • Table A-67 Compounds of the formula I. a, where A is 2,3-difluoro-6-(2- butoxy)phenyl and R 2 and X are as defined in the rows of the following table A.
  • Table A-68 Compounds of the formula I. a, where A is 2,4-difluoro-6-(2- butoxy)phenyl and R 2 and X are as defined in the rows of the following table A.
  • Table A-69 Compounds of the formula I. a, where A is 2,5-difluoro-6-(2- butoxy)phenyl and R 2 and X are as defined in the rows of the following table A.
  • Table A-70 Compounds of the formula I. a, where A is 2,3,4-trifluoro-6-(2- butoxy)phenyl and R 2 and X are as defined in the rows of the following table A.
  • Table A-71 Compounds of the formula I. a, where A is 2,3,5-trifluoro-6-(2- butpoxy)phenyl and R 2 and X are as defined in the rows of the following table A.
  • Table A-72 Compounds of the formula I. a, where A is 2,4,5-trifluoro-6-(2- butoxy)phenyl and R 2 and X are as defined in the rows of the following table A.
  • Table A-73 Compounds of the formula I. a, where A is 2,3,4,5-tetrafluoro-6-(2- butoxy)phenyl and R 2 and X are as defined in the rows of the following table A.
  • Table A-74 Compounds of the formula I. a, where A is 2,6-difluoro-4- methoxyphenyl and R 2 and X are as defined in the rows of the following table A.
  • Table A-75 Compounds of the formula I. a, where A is 2,3,6-trifluoro-4- methoxyphenyl and R 2 and X are as defined in the rows of the following table A.
  • Table A-76 Compounds of the formula I. a, where A is 2,3,5,6-tetrafluoro-4- methoxyphenyl and R 2 and X are as defined in the rows of the following table A.
  • Table A-77 Compounds of the formula I. a, where A is 2,6-difluoro-4- ethoxyphenyl and R 2 and X are as defined in the rows of the following table A.
  • Table A-78 Compounds of the formula I. a, where A is 2,3,6-trifluoro-4- ethoxyphenyl and R 2 and X are as defined in the rows of the following table A.
  • Table A-79 Compounds of the formula I. a, where A is 2,3,5,6-tetrafluoro-4- ethoxyphenyl and R 2 and X are as defined in the rows of the following table A.
  • Table A-80 Compounds of the formula I. a, where A is 2,6-difluoro-4-(n- propoxy) phenyl and R 2 and X are as defined in the rows of the following table A.
  • Table A-81 Compounds of the formula I. a, where A is 2,3,6-trifluoro-4-(n- propoxy) phenyl and R 2 and X are as defined in the rows of the following table A.
  • Table A-82 Compounds of the formula I. a, where A is 2,3,5,6-tetrafluoro-4-(n- propoxy) phenyl and R 2 and X are as defined in the rows of the following table A.
  • Table A-83 Compounds of the formula I. a, where A is 2,6-difluoro-4-(2- propoxy) phenyl and R 2 and X are as defined in the rows of the following table A.
  • Table A-84 Compounds of the formula I. a, where A is 2,3,6-trifluoro-4-(2- propoxy) phenyl and R 2 and X are as defined in the rows of the following table A.
  • Table A-85 Compounds of the formula I. a, where A is 2,3,5,6-tetrafluoro-4-(2- propoxy) phenyl and R 2 and X are as defined in the rows of the following table A.
  • Table A-86 Compounds of the formula I. a, where A is 2,6-difluoro-4-(2- butoxy)phenyl and R 2 and X are as defined in the rows of the following table A.
  • Table A-87 Compounds of the formula I. a, where A is 2,3,6-trifluoro-4-(2- butoxy)phenyl and R 2 and X are as defined in the rows of the following table A.
  • Table A-88 Compounds of the formula I. a, where A is 2,3,5,6-tetrafluoro-4-(2- butoxy)phenyl and R 2 and X are as defined in the rows of the following table A.
  • Especially preferred compounds are compounds of formula (lb), which corresponds to the diaminotriazines of formula (I), wherein R 1 and R 2 are hydrogen and R a , R b , R c , R d , R e and R' are defined in the following table B
  • diaminotriazine compounds of formula (I) according to the invention can be prepared by standard processes of organic chemistry, for example by the following processes:
  • diaminotriazine compounds of formula (I), wherein R 2 is as defined above and in particular H, Ci-C6-alkyl or (Ci-C6-alkoxy)-Ci-C6-alkyl can be prepared by reacting halotriazines of formula (II) with amines of formula (III) in the presence of a base and a catalyst as depicted in the following scheme 1 :
  • halotriazines of formual (II) relate to compounds, where the variables Hal, R 1 , R 2 and X have in particular the following meanings:
  • R 2 is in particular H, Ci-C6-alkyl, (Ci-C6-alkoxy)-Ci-C6-alkyl;
  • Ci-C4-alkoxy-Ci-C4-alkyl such as CH2OCH3;
  • X is as defined above and in particular as defined in embodiments groups.
  • R 1 is in particular H, Ci-C6-alkyl, (Ci-C6-alkoxy)-Ci-C6-alkyl;
  • H (Ci-C4-alkoxy)-Ci-C4-alkyl, such as CH2OCH3;
  • A is as defined above.
  • the reaction of the halotriazines of formula (II) with the amines of formula (III) is usually carried out at temperatures in the range from from 50°C to the boiling point of the reaction mixture, preferably from 50°C to 150°C, particularly preferably from 60°C to 100°C, in an inert organic solvent (e.g. P. Dao et al., Tetrahedron 2012, 68, 3856 - 3860).
  • an inert organic solvent e.g. P. Dao et al., Tetrahedron 2012, 68, 3856 - 3860.
  • the reaction can be carried out at atmospheric pressure or under elevated pressure, if appropriate, under an inert gas, continuously or batchwise.
  • the halotriazines of formula (II) and the amines of formula (III) are used in equimolar amounts.
  • the amines of formula (III) are used in excess with regard to the halotriazines of formula (II).
  • the molar ratio of the amines of formula (III) to the halotriazines of formula (II) is in the range from 2 : 1 to 1 : 1 , preferably 1.5 : 1 to 1 : 1 , especially preferred 1 .2 : 1 .
  • the reaction of the halotriazines of formula (II) with the amines of formula (III) is usually carried out in an organic solvent.
  • Suitable in principle are all solvents which are capable of dissolving the halotriazines of formula (II) and the amines of formula (II) at least partly and preferably fully under reaction conditions.
  • Suitable solvents are aliphatic hydrocarbons such as pentane, hexane, cyclohexane, nitromethane and mixtures of Cs-Cs- alkanes, aromatic hydrocarbons such as benzene, chlorobenzene, toluene, cresols, 0-, m- and p-xylene, halogenated hydrocarbons such as dichloromethane, 1 ,2-dichloroethane, chloroform, carbon tetrachloride and chlorobenzene, ethers such as diethyl ether, diisopropyl ether, tert- butyl methylether (TBME), dioxane, anisole and tetrahydrofuran (THF), esters such as ethyl acetate and butyl acetate; nitriles such as acetonitrile and propionitrile, as well as dipolar aprotic solvents such as sulfolane
  • Preferred solvents are ethers as defined above.
  • the term solvent as used herein also includes mixtures of two or more of the above compounds.
  • the reaction of the halotriazines of formula (II) with the amines of formula (III) is usually carried out in the presence of a base.
  • suitable bases include metal-containing bases and nitrogen-containing bases.
  • suitable metal-containing bases are inorganic compounds such as alkali metal and alkaline earth metal hydroxides, and other metal hydroxides, such as lithium hydroxide, sodium hydroxide, potassium hydroxide, magnesium hydroxide, calcium hydroxide and aluminum hydroxide; alkali metal and alkaline earth metal oxide, and other metal oxides, such as lithium oxide, sodium oxide, potassium oxide, magnesium oxide, calcium oxide and magnesium oxide, iron oxide, silver oxide; alkali metal and alkaline earth metal hydrides such as lithium hydride, sodium hydride, potassium hydride and calcium hydride, alkali metal and alkaline earth metal formates, acetates and other metal salts of carboxylic acids, such as sodium formate, sodium benzoate, lithium acetate, sodium acetate, potassium acetate, magnesium acetate, and calcium acetate; alkali metal and alkaline earth metal carbonates such as lithium carbonate, sodium carbonate, potassium carbonate, magnesium carbonate, and calcium carbonate, as well as alkali metal hydrogen carbon
  • bases are alkali metal and alkaline earth metal alkoxides as defined above.
  • the term base as used herein also includes mixtures of two or more, preferably two of the above compounds. Particular preference is given to the use of one base.
  • the bases can be used in excess, preferably from 1 to 10, especially preferred from 2 to 4 base equivalents based on the halotriazines of formula (II), and they may also be used as the solvent.
  • the reaction of the halotriazines of formula (II) with the amines of formula (III) may be carried out in the presence of a catalyst.
  • a catalyst include for example, palladium based catalysts like, for example, Palladium(ll)acetate,
  • phosphines like, for example, P(o- tolyl)3, triphenylphosphine or BINAP (2,2'-Bis(diphenylphospino)-1 ,1 '-binaphthyl.
  • the amount of catalyst is usually 10 to 20 mol % (0.1 to 0.2 equivalents) based on the halotriazines of formula (II).
  • the end of the reaction can easily be determined by the skilled worker by means of routine methods.
  • reaction mixtures are worked up in a customary manner, for example by mixing with water, separation of the phases and, if appropriate, chromatographic purification of the crude product.
  • the amines of formula (III) used for the preparation of diaminotriazine compounds of formula (I), wherein R 1 is H, Ci-C6-alkyl, (Ci-C6-alkoxy)-Ci-C6-alkyl or Ci-C6-alkoxy, are commercially available and/or can be prepared by analogy to known literature.
  • halotriazines of formula (II) required for the preparation of diaminotriazine compounds of formula (I), wherein R 2 is H, Ci-C6-alkyl, (Ci-C6-alkoxy)-Ci-C6-alkyl or Ci-C6-alkoxy, can be prepared by analogy (e.g. J. K.Chakrabarti et al., Tetrahedron 1975, 31 , 1879 - 1882) by reacting thiotriazines of formula (IV) with a halogen, as depicted in scheme 2:
  • variable X in formulae (II) and (VI) has the meanings, in particular the preferred meanings, as defined above in context of formula (I).
  • R * is Ci-C6-alkyl, C2-C6-haloalkyl or phenyl
  • Ci-C4-alkyl or C2-C4-haloalkyl in particular Ci-C4-alkyl or C2-C4-haloalkyl
  • Ci-C4-alkyl More particularly Ci-C4-alkyl
  • R * is Ci-C6-alkyl, C2-C6-haloalkyl or phenyl
  • Ci-C4-alkyl or C2-C4-haloalkyl in particular Ci-C4-alkyl or C2-C4-haloalkyl
  • Ci-C4-alkyl More particularly Ci-C4-alkyl
  • R 2 is in particular H, Ci-Ce-alkyI, (Ci-C 6 -alkoxy)-Ci-C 6 -alkyl;
  • H (Ci-C4-alkoxy)-Ci-C4-alkyl, such as CH2OCH3;
  • X is as defined above and in particular as defined in the embodiments groups.
  • Particular embodiments relate to the compounds of formula (IV.a), which correspond to the compounds of formula (IV) wherein R 2 is hydrogen and R * is CH3.
  • the reaction of the thiotriazines of formula (IV) with the halogen is usually carried out from 0°C to the boiling point of the reaction mixture, preferably from 15°C to the boiling point of the reaction mixture, particularly preferably from 15°C to 40°C, in an inert organic solvent (e.g. J. K. Chakrabarti et al., Tetrahedron 1975, 31 , 1879 - 1882).
  • an inert organic solvent e.g. J. K. Chakrabarti et al., Tetrahedron 1975, 31 , 1879 - 1882).
  • the reaction can be carried out at atmospheric pressure or under elevated pressure, if appropriate under an inert gas, continuously or batchwise.
  • halogen is generally used in excess with regard to the thiotriazines of formula (IV).
  • the reaction of the thiotriazines of formula (IV) with the halogen is usually carried out in an organic solvent.
  • Suitable in principle are all solvents which are capable of dissolving the thiotriazines of formula (IV) and the halogen at least partly and preferably fully under reaction conditions.
  • Suitable solvents are aliphatic hydrocarbons such as pentane, hexane, cyclohexane and mixtures of Cs-Cs-alkanes, halogenated hydrocarbons such as
  • ethers such as diethyl ether, diisopropyl ether, tert. -butyl methylether (TBME), dioxane, anisole and
  • tetrahydrofuran THF
  • alcohols such as methanol, ethanol, n-propanol, isopropanol, n-butanol and tert.-butanol, as well as organic acids like formic acid, acetic acid, propionic acid, oxalic acid, citric acid, trifluoroacetic acid.
  • Preferred solvents are halogenated hydrocarbons and organic acids as defined above.
  • solvent as used herein also includes mixtures of two or more of the above compounds.
  • the end of the reaction can easily be determined by the skilled worker by means of routine methods.
  • the reaction mixtures are worked up in a customary manner, for example by mixing with water, separation of the phases and, if appropriate, chromatographic purification of the crude product.
  • halotriazines of formula (II) required for the preparation of diaminotriazine compounds of formula (I), wherein R 2 is H, Ci-C6-alkyl, (Ci-C6-alkoxy)-Ci-C6-alkyl, can also be prepared by reacting 2,4-dichlorotriazines of formula (VII) with a an amine H2N-R 2 , in particular with ammonia, as depicted in scheme 3:
  • variable X in formulae (II) and (VII) has the meanings, in particular the preferred meanings, as defined above in context of formula (I).
  • Hal and Hal' are each, indepentently, halogen, in particular bromine or chlorine, especially chlorine.
  • the reaction depicted in scheme 3 can be performed by simply mixing the required amounts of the compound of formula (VII) with the amine H2N-R 2 or by analogy to the reaction depicted in step 1. Replacing the the amine H2N-R 2 by a mercaptan
  • the molar ratio of the amine to the halotriazines of formula (II) is in the range from 10 : 1 to 1 : 1 , preferably 5: 1 to 1 : 1 .
  • the reaction depicted in scheme 3 is preferably carried out in an inert solvent.
  • suitable solvents are nitromethane, aromatic hydrocarbons such as benzene, chlorobenzene, toluene, cresols, 0-, m- and p-xylene, halogenated hydrocarbons such as dichloromethane, 1 ,2- dichloroethane, chloroform, carbon tetrachloride and chlorobenzene, ethers such as diethyl ether, diisopropyl ether, tert.
  • TBME -butyl methylether
  • dioxane dioxane
  • anisole and tetrahydrofuran (THF) esters such as ethyl acetate and butyl acetate
  • nitriles such as acetonitrile and propionitrile, as well as dipolar aprotic solvents such as sulfolane, dimethylsulfoxide, N,N- dimethylformamide (DMF), ⁇ , ⁇ -dimethylacetamide (DMAC), 1 ,3-dimethyl-2-imidazolidinone (DMI), ⁇ , ⁇ '-dimethylpropylene urea (DMPU), dimethyl sulfoxide (DMSO) and 1 -methyl-2 pyrrolidinone (NMP) and mixtures thereof with with water or with aliphatic hydrocarbons such as pentane, hexane, cyclohexane or with mixtures of Cs-Cs-alkane.
  • the reaction depicted in scheme 1 may be performed in the presence of an auxiliary base. Suitable bases are those mentioned in context with the reaction depicted in scheme 1. However, the amine H2N-R 2 may itself serve as an auxiliary base. In this case, usually an excess of the amine H2N-R 2 is used.
  • R 2 is different from hydrogen, e.g. Ci-C6-alkyl, (Ci-C6-alkoxy)-Ci-C6-alkyl, CN, (C1-C6- alkyl)carbonyl, (Ci-C6-alkoxy)carbonyl, (Ci-C6-alkyl)sulfonyl, phenylsulfonyl, phenyl, phenyl-Ci-C6 alkyl, phenylcarbonyl or phenoxycarbonyl,
  • variables A, R 1 and X have the meanings, in particular the preferred meanings, as in formula (I) mentioned above,
  • R 2 is different from hydrogen, e.g. Ci-C6-alkyl, (Ci-C6-alkoxy)-Ci-C6-alkyl, CN, (C1-C6- alkyl)carbonyl, (Ci-C6-alkoxy)carbonyl, (Ci-C6-alkyl)sulfonyl, phenylsulfonyl, phenyl, phenyl-Ci-C6 alkyl, phenylcarbonyl or phenoxycarbonyl,
  • Ci-C4-alkyl CN, (Ci-C6-alkyl)carbonyl, (Ci-C6-alkoxy)carbonyl or (C1-C6- alkyl)sulfonyl;
  • Y is halogen or oxycarbonyl-Ci-C6-alkyl
  • R 1 is is different from hydrogen, e.g. Ci-C 6 -alkyl, (Ci-C 6 -alkoxy)-Ci-C 6 -alkyl, CN, (Ci-C 6 - alkyl)carbonyl, (Ci-C6-alkoxy)carbonyl, (Ci-C6-alkyl)sulfonyl, phenylsulfonyl, phenyl, phenyl-Ci-C6 alkyl, phenylcarbonyl or phenoxycarbonyl,
  • phenyl is unsubstituted or substituted by one to five substituents selected from the group consisting of halogen, CN, NO2, Ci-C6-alkyl, Ci-C6-haloalkyl and C1-C6- alkoxy;
  • variables A, R 2 and X have the meanings, in particular the preferred meanings, as in formula (I) mentioned above,
  • R 1 is different from hydrogen, e.g. Ci-C6-alkyl, (Ci-C6-alkoxy)-Ci-C6-alkyl, CN, (C1-C6- alkyl)carbonyl, (Ci-C6-alkoxy)carbonyl, (Ci-C6-alkyl)sulfonyl, phenylsulfonyl, phenyl, phenyl-Ci-C6 alkyl, phenylcarbonyl or phenoxycarbonyl,
  • Ci-C4-alkyl CN, (Ci-C6-alkyl)carbonyl, (Ci-C6-alkoxy)carbonyl or (C1-C6- alkyl)sulfonyl;
  • V is halogen or oxycarbonyl-Ci-C6-alkyl
  • Both processes B and C independently of one another usually carried out at from 0°C to the boiling point of the reaction mixture, preferably from 23°C to 130°C, particularly preferably from
  • Both processes B and C independently of one another can be carried out at atmospheric pressure or under elevated pressure, if appropriate under an inert gas, continuously or batchwise.
  • diaminotriazine compounds of formula (I), wherein R 2 , or R 1 respectively, is hydrogen are used in excess with regard to the compound of formula (V), or (VI) respectively.
  • diaminotriazine compounds of formula (I), wherein R 2 , or R 1 respectively, is hydrogen and the compound of formula (V), or (VI) respectively are used in equimolar amounts.
  • the molar ratio of the diaminotriazine compounds of formula (I), wherein R 2 , or R 1 respectively, is hydrogen to the compound of formula (V), or (VI) respectively is in the range from 1 : 1 .5 to 1 : 1 , preferably 1 : 1 .2 to 1 : 1 , especially preferred 1 : 1.
  • Both processes B and C independently of one another are usually carried out in an organic solvent.
  • Suitable in principle are all solvents which are capable of dissolving the diaminotriazine compounds of formula (I), wherein R 2 , or R 1 respectively, is hydrogen and the compound of formula (V), or (VI) respectively, at least partly and preferably fully under reaction conditions.
  • suitable solvents are halogenated hydrocarbons such as dichloromethane, 1 ,2- dichloroethane, chloroform, carbon tetrachloride and chlorobenzene; ethers such as diethyl ether, diisopropyl ether, tert.
  • TBME -butyl methylether
  • DMF dioxane
  • nitriles such as acetonitrile and propionitrile
  • alcohols such as methanol, ethanol, n- propanol, isopropanol, n-butanol and tert.-butanol
  • organic acids like formic acid, acetic acid, propionic acid, oxalic acid, methylbenzenesulfonic acid, benzenesulfonic acid, camphorsulfonic acid, citric acid, trifluoroacetic acid as well as dipolar aprotic solvents such as sulfolane, dimethylsulfoxide, ⁇ , ⁇ -dimethylformamide (DMF), ⁇ , ⁇ -dimethylacetamide (DMAC), 1 ,3- dimethyl-2-imidazolidinone (DMI), ⁇ , ⁇ '-dimethylpropylene urea (
  • solvents hydrocarbons, ethers and dipolar aprotic solvents as mentioned above. More preferred solvents are dichloromethane or dioxane. It is also possible to use mixtures of the solvents mentioned.
  • solvent as used herein also includes mixtures of two or more of the above
  • Both processes B and C independently of one another are optionally carried out in the presence of a base.
  • suitable bases include metal-containing bases and nitrogen-containing bases.
  • suitable metal-containing bases are inorganic compounds such as alkali metal and alkaline earth metal hydrides such as lithium hydride, sodium hydride, potassium hydride and calcium hydride, alkali metal and alkaline earth metal carbonates such as lithium carbonate, sodium carbonate, potassium carbonate, magnesium carbonate, and calcium carbonate, as well as alkali metal hydrogen carbonates (bicarbonates) such as lithium hydrogen carbonate, sodium hydrogen carbonate, potassium hydrogen carbonate; alkali metal and alkaline earth metal phosphates such as sodium phosphate, potassium phosphate and calcium phosphate; and furthermore organic bases, such as tertiary amines such as tri-Ci-Ce- alkylamines, for example triethylamine, trimethylamine, N-ethyldiisopropylamine, and N- methylpiperidine,
  • Preferred bases are organic bases and alkali metal carbonates as mentioned above. Especially preferred bases are organic bases as mentioned above.
  • the term base as used herein also includes mixtures of two or more, preferably two of the above compounds.
  • the bases are generally employed in excess; however they can also be employed in equimolar amounts, or, if appropriate, can be used as solvent.
  • Preferably from 1 to 5 base equivalents, particularly preferred 3 base equivalents of base are used, based on the diaminotriazine compounds of formula (I).
  • the compounds of formula (V), or (VI) respectively, are known compounds. They are commercially available or can be prepared in analogy to known methods.
  • diaminotrazine compounds of formula (I), wherein R 1 and R 2 are defined above can be prepared by reacting biguanidines of formula (VII) with carbonyl compounds of formula (VIII) in the presence of a base:
  • variable A and X have the meanings, in particular the preferred meanings, as in formula (I) mentioned above, and
  • L 1 is a nucleophilically displaceable leaving group such as halogen, CN, Ci-C6-alkoxy, C1-C6- alkoxycarbonyl, Ci-C6-alkylcarbonyloxy or Ci-C6-alkoxycarbonyloxy;
  • the reaction of biguanidines of formula (VII) with carbonyl compounds of formula (VIII) is usually carried out at temperatures from 50°C to the boiling point of the reaction mixture, preferably from 50°C to 200°C (e.g. R. Sathunuru et al., J. Heterocycl. Chem. 2008, 45, 1673- 1678).
  • the reaction can be carried out at atmospheric pressure or under elevated pressure, if appropriate under an inert gas, continuously or batchwise.
  • the biguanidines of formula (VII) and the carbonyl compounds of formula (VIII) are used in equimolar amounts.
  • the carbonyl compounds of formula (VIII) are used in excess with regard to the biguanidines of formula (VII).
  • the molar ratio of the carbonyl compounds of formula (VIII) to the biguanidines of formula (VII) is in the range from 1.5 : 1 to 1 : 1 , preferably 1 .2 : 1 to 1 : 1 , especially preferred 1 .2 : 1 , also especially preferred 1 : 1.
  • reaction of the biguanidines of formula (VII) with the carbonyl compounds of formula (VIII) is carried out in an organic solvent.
  • Suitable in principle are all solvents which are capable of dissolving the biguanidines of formula (VII) and the carbonyl compounds of formula (VIII) at least partly and preferably fully under reaction conditions.
  • aliphatic hydrocarbons such as pentane, hexane, cyclohexane, nitromethane and mixtures of C5-C8-alkanes; romatic hydrocarbons such as benzene, chlorobenzene, toluene, cresols, 0-, m- and p-xylene; halogenated hydrocarbons such as dichloromethane, 1 ,2-dichloroethane, chloroform, carbon tetrachloride and chlorobenzene, ethers such as diethyl ether, diisopropyl ether, tert.
  • romatic hydrocarbons such as benzene, chlorobenzene, toluene, cresols, 0-, m- and p-xylene
  • halogenated hydrocarbons such as dichloromethane, 1 ,2-dichloroethane, chloroform, carbon tetrachloride and chlorobenzene
  • TBME -butyl methylether
  • dioxane dioxane
  • anisole and tetrahydrofuran THF
  • nitriles such as acetonitrile and propionitrile
  • dipolar aprotic solvents such as sulfolane, dimethylsulfoxide, ⁇ , ⁇ -dimethylformamide (DMF), ⁇ , ⁇ -dimethylacetamide (DMAC), 1 ,3- dimethyl-2-imidazolidinone (DMI), ⁇ , ⁇ '-dimethylpropylene urea (DMPU), dimethyl sulfoxide (DMSO) and 1 -methyl-2 pyrrolidinone (NMP).
  • Preferred solvents are ethers and dipolar aprotic solvents as defined above.
  • More preferred solvents are ethers as defined above.
  • solvent as used herein also includes mixtures of two or more of the above
  • suitable bases include metal-containing bases and nitrogen-containing bases.
  • suitable metal-containing bases are inorganic compounds such as alkali metal and alkaline earth metal oxide, and other metal oxides, such as lithium oxide, sodium oxide, potassium oxide, magnesium oxide, calcium oxide and magnesium oxide, iron oxide, silver oxide; alkali metal and alkaline earth metal hydrides such as lithium hydride, sodium hydride, potassium hydride and calcium hydride, alkali metal amides such as lithium amide, sodium amide and potassium amide, alkali metal and alkaline earth metal carbonates such as lithium carbonate, sodium carbonate, potassium carbonate, magnesium carbonate, and calcium carbonate, as well as alkali metal hydrogen carbonates (bicarbonates) such as lithium hydrogen carbonate, sodium hydrogen carbonate, potassium hydrogen carbonate; alkali metal and alkaline earth metal phosphates such as sodium phosphate, potassium phosphate and calcium phosphate; and furthermore organic bases, such as tertiary amines such as tri-Ci-Ce- al
  • base as used herein also includes mixtures of two or more, preferably two of the above compounds. Particular preference is given to the use of one base.
  • the bases are generally employed in excess; however they can also be employed in equimolar amounts, or, if appropriate, can be used as solvent. Preferably from 1 to 5 base equivalents, particularly preferred 3 base equivalents of base are used, based on the biguanidines of formula (VII).
  • the end of the reaction can easily be determined by the skilled worker by means of routine methods.
  • reaction mixtures are worked up in a customary manner, for example by mixing with water, separation of the phases and, if appropriate, chromatographic purification of the crude product.
  • Some of the intermediates and end products are obtained in the form of viscous oils, which can be purified or freed from volatile components under reduced pressure and at moderately elevated temperature.
  • purification can also be carried out by recrystallisation or digestion.
  • the biguanidines of formula (VII) required for the preparation of azines of formula (I), wherein R 1 and R 2 are defined above, can be prepared by reacting guanidines of formula (IX) with amines of formula (X) in the presence of an acid:
  • variable A has the meanings, in particular the preferred meanings, as in formula (I) mentioned above.
  • reaction of guanidines of formula (IX) with amines of formula (X) is usually carried out from 50°C to 150 °C, preferably from 80°C to 130°C.
  • Microwave-Technology was used where applicable (e.g. CO. Kappe, A. Stadler, Microwaves in Organic and Medicinal Chemistry, Weinheim 2012).
  • the reaction can be carried out at atmospheric pressure or under elevated pressure, if appropriate under an inert gas, continuously or batchwise.
  • the guanidines of formula (IX) and the amines of formula (X) are used in equimolar amounts.
  • the amines of formula (X) are used in excess with regard to the guanidines of formula (IX).
  • the molar ratio of the amines of formula (X) to the guanidines of formula (IX) is in the range from 2 : 1 to 1 : 1 , preferably 1.5 : 1 to 1 : 1 , especially preferred 1 : 1.
  • reaction of the guanidines of formula (IX) with the amines of formula (X) is carried out in an organic solvent.
  • Suitable in principle are all solvents which are capable of dissolving the guanidines of formula (IX) and the amines of formula (X) at least partly and preferably fully under reaction conditions.
  • Suitable solvents are aliphatic hydrocarbons such as pentane, hexane,
  • cyclohexane nitromethane and mixtures of Cs-Cs-alkanes
  • aromatic hydrocarbons such as benzene, chlorobenzene, toluene, cresols, o-, m- and p-xylene, halogenated hydrocarbons such as dichloromethane, 1 ,2-dichloroethane, chloroform, carbon tetrachloride and chlorobenzene
  • ethers such as diethyl ether, diisopropyl ether, tert.
  • TBME -butyl methylether
  • dioxane dioxane
  • anisole and tetrahydrofuran esters
  • esters such as ethyl acetate and butyl acetate
  • nitriles such as acetonitrile and propionitrile, as well as dipolar aprotic solvents such as sulfolane
  • dimethylsulfoxide ⁇ , ⁇ -dimethylformamide (DMF), ⁇ , ⁇ -dimethylacetamide (DMAC), 1 ,3- dimethyl-2-imidazolidinone (DMI), ⁇ , ⁇ '-dimethylpropylene urea (DMPU), dimethyl sulfoxide (DMSO) and 1 -methyl-2 pyrrolidinone (NMP).
  • Preferred solvents are ethers, nitriles and dipolar aprotic solvents as defined above.
  • More preferred solvents are nitriles as defined above.
  • solvent as used herein also includes mixtures of two or more of the above
  • the reaction of the guanidines of formula (IX) with the amines of formula (X) is carried out in the presence of an acid.
  • acids and acidic catalysts inorganic acids like hydrofluoric acid, hydrochloric acid, hydrobromic acid, hydroiodic acid, phosphoric acid, sulfuric acid; mineral acids like hydrochloric acid, sulfuric acid, phosphoric acid, Lewis acids like boron trifluoride, aluminium chloride, ferric- lll-chloride, tin-IV-chloride, titanium-IV-chloride and zinc-ll-chloride, as well as organic acids like formic acid, acetic acid, propionic acid, oxalic acid, methylbenzenesulfonic acid,
  • benzenesulfonic acid camphorsulfonic acid, citric acid, trifluoroacetic acid, can be used.
  • the acids are generally employed in excess or, if appropriate, can be used as solvent. Work up can be carried out in a known manner.
  • guanidines of formula (IX) required for the preparation of biguanidines of formula (VII) are commercially available or can be prepared in accordance with literature procedures (e.g. J.L. LaMattina et al., J. Med. Chem. 1990, 33, 543 - 552; A. Perez-Medrano et al., J. Med. Chem. 2009, 52, 3366 - 3376).
  • the compounds of formula (I) have herbicidal activity. Therefore, they can be used for controlling unwanted or undesired plants or vegetation. They can also be used in a method for controlling unwanted or undesired plants or vegetation, which method comprises allowing at least one compound of formula (I) or a salt thereof to act on plants, their environment or on seed. In order to allow the compound of formula (I) or a salt thereof to act on plants, their environment or on seed the compounds of the invention are applied to the plants, their environment or to the seed of said plants.
  • diaminotriazine compounds of formula (I) may be mixed with a large number of representatives of other herbicidal or growth-regulating active ingredient groups and then applied concomitantly.
  • Suitable components for mixtures are, for example, herbicides from the classes of the acetamides, amides, aryloxyphenoxypropionates, benzamides, benzofuran, benzoic acids, benzothiadiazinones, bipyridylium, carbamates, chloroacetamides, chlorocarboxylic acids, cyclohexanediones, dinitroanilines, dinitrophenol, diphenyl ether, glycines, imidazolinones, isoxazoles, isoxazolidinones, nitriles, N-phenylphthalimides, oxadiazoles, oxazolidinediones, oxyacetamides, phenoxycarboxylic acids, phenylcarbamates, phenylpyrazoles,
  • phenylpyrazolines phenylpyridazines, phosphinic acids, phosphoroamidates,
  • phosphorodithioates phthalamates, pyrazoles, pyridazinones, pyridines, pyridinecarboxylic acids, pyridinecarboxamides, pyrimidinediones, pyrimidinyl(thio)benzoates, quinolinecarboxylic acids, semicarbazones, sulfonylaminocarbonyltriazolinones, sulfonylureas, tetrazolinones, thiadiazoles, thiocarbamates, triazines, triazinones, triazoles, triazolinones,
  • triazolocarboxamides triazolopyrimidines, triketones, uracils, ureas.
  • the invention also relates to combinations of diaminotriazine compounds of formula (I) with at least one further herbicide B and/or at least one safener C).
  • the further herbicidal compound B (component B) is in particular selected from the herbicides of class b1 ) to b15):
  • ALS inhibitors acetolactate synthase inhibitors
  • DHP inhibitors 7,8-dihydropteroate synthase inhibitors
  • VLCFA inhibitors very long chain fatty acids
  • b1 1 cellulose biosynthesis inhibitors
  • herbicides selected from the group consisting of bromobutide, chlorflurenol, chlorflurenol-methyl, cinmethylin, cumyluron, dalapon, dazomet, difenzoquat, difenzoquat-metilsulfate, dimethipin, DSMA, dymron, endothal and its salts, etobenzanid, flamprop, flamprop-isopropyl, flamprop-methyl, flamprop-M-isopropyl, flamprop-M-methyl, flurenol, flurenol-butyl, flurprimidol, fosamine, fosamine-ammonium, indanofan, indaziflam, maleic hydrazide, mefluidide, metam, methiozolin (CAS 403640-27-7), methyl azide, methyl bromide, methyl-dymron, methyl iodide, MSMA,
  • compositions according to the present invention comprise at least one diaminotriazine compound of formula (I) and at least one further active compound B (herbicide B).
  • compositions contain at least one inhibitor of the lipid biosynthesis (herbicide b1 ).
  • ACC herbicides acetylCoA carboxylase
  • non-ACC herbicides acetylCoA carboxylase
  • the ACC herbicides belong to the group A of the HRAC classification system whereas the non-ACC herbicides belong to the group N of the HRAC classification.
  • compositions contain at least one ALS inhibitor (herbicide b2).
  • the herbicidal activity of these compounds is based on the inhibition of acetolactate synthase and thus on the inhibition of the branched chain amino acid biosynthesis.
  • These inhibitors belong to the group B of the HRAC classification system.
  • compositions contain at least one inhibitor of photosynthesis (herbicide b3).
  • the herbicidal activity of these compounds is based either on the inhibition of the photosystem II in plants (so-called PSII inhibitors, groups C1 , C2 and C3 of HRAC classification) or on diverting the electron transfer in photosystem I in plants (so-called PSI inhibitors, group D of HRAC classification) and thus on an inhibition of photosynthesis.
  • PSII inhibitors are preferred.
  • compositions contain at least one inhibitor of protoporphyrinogen-IX-oxidase (herbicide b4).
  • the herbicidal activity of these compounds is based on the inhibition of the protoporphyrinogen-IX-oxidase.
  • These inhibitors belong to the group E of the HRAC classification system.
  • compositions contain at least one bleacher-herbicide (herbicide b5). The herbicidal activity of these compounds is based on the inhibition of the carotenoid biosynthesis.
  • PDS inhibitors compounds which inhibit carotenoid biosynthesis by inhibition of phytoene desaturase
  • HPPD inhibitors compounds that inhibit the 4-hydroxyphenyl- pyruvate-dioxygenase
  • DOXsynthase group F4 of HRAC class
  • compounds which inhibit carotenoid biosynthesis by an unknown mode of action (bleacher - unknown target, group F3 of HRAC classification).
  • compositions contain at least one EPSP synthase inhibitor (herbicide b6).
  • EPSP synthase inhibitor herebicide b6
  • the herbicidal activity of these compounds is based on the inhibition of enolpyruvyl shikimate 3-phosphate synthase, and thus on the inhibition of the amino acid biosynthesis in plants.
  • These inhibitors belong to the group G of the HRAC classification system.
  • compositions contain at least one glutamine synthetase inhibitor (herbicide b7).
  • the herbicidal activity of these compounds is based on the inhibition of glutamine synthetase, and thus on the inhibition of the aminoacid biosynthesis in plants.
  • These inhibitors belong to the group H of the HRAC classification system.
  • compositions contain at least one DHP synthase inhibitor (herbicide b8).
  • DHP synthase inhibitor herebicide b8
  • the herbicidal activity of these compounds is based on the inhibition of 7,8-dihydropteroate synthase.
  • These inhibitors belong to the group I of the HRAC classification system.
  • compositions contain at least one mitosis inhibitor (herbicide b9).
  • the herbicidal activity of these compounds is based on the disturbance or inhibition of microtubule formation or organization, and thus on the inhibition of mitosis.
  • These inhibitors belong to the groups K1 and K2 of the HRAC classification system. Among these, compounds of the group K1 , in particular
  • dinitroanilines are preferred.
  • compositions contain at least one VLCFA inhibitor (herbicide b10).
  • VLCFA inhibitor hereinafter b10
  • the herbicidal activity of these compounds is based on the inhibition of the synthesis of very long chain fatty acids and thus on the disturbance or inhibition of cell division in plants.
  • These inhibitors belong to the group K3 of the HRAC classification system.
  • compositions contain at least one cellulose biosynthesis inhibitor (herbicide b1 1 ).
  • the herbicidal activity of these compounds is based on the inhibition of the biosynthesis of cellulose and thus on the inhibition of the synthesis of cell walls in plants.
  • These inhibitors belong to the group L of the HRAC classification system.
  • compositions contain at least one decoupler herbicide (herbicide b12).
  • the herbicidal activity of these compounds is based on the disruption of the cell membrane.
  • These inhibitors belong to the group M of the HRAC classification system.
  • compositions contain at least one auxinic herbicide (herbicide b13).
  • auxinic herbicide include compounds that mimic auxins, i.e. plant hormones, and affect the growth of the plants. These compounds belong to the group O of the HRAC classification system.
  • compositions contain at least one auxin transport inhibitor (herbicide b14).
  • auxin transport inhibitor herein b14.
  • the herbicidal activity of these compounds is based on the inhibition of the auxin transport in plants.
  • These compounds belong to the group P of the HRAC classification system.
  • compositions according to the present invention comprisingst one herbicide B selected from herbicides of class b1 , b6, b9, b10 and b1 1.
  • compositions according to the present invention comprising at least one herbicide B selected from herbicides of class b2, b3, b4, b5, b6, b9 and b10.
  • compositions according to the present invention which comprise at least one herbicide B selected from the herbicides of class b4, b6 b9 and b10.
  • compositions according to the present invention which comprise at least one herbicide B selected from the herbicides of class b4, b6 and b10.
  • herbicides B which can be used in combination with the diaminitriazine compounds of formula (I) according to the present invention are:
  • ACC-herbicides such as alloxydim, alloxydim-sodium, butroxydim, clethodim, clodinafop, clodinafop-propargyl, cycloxydim, cyhalofop, cyhalofop-butyl, diclofop, diclofop-methyl, fenoxaprop, fenoxaprop-ethyl, fenoxaprop-P, fenoxaprop-P-ethyl, fluazifop, fluazifop-butyl, fluazifop-P, fluazifop-P-butyl, haloxyfop, haloxyfop-methyl, haloxyfop-P, haloxyfop-P-methyl, metamifop, pinoxaden, profoxydim, propaquizafop, quizalofop, quizalofop-ethy
  • sulfonylureas such as amidosulfuron, azimsulfuron, bensulfuron, bensulfuron- methyl, chlorimuron, chlorimuron-ethyl, chlorsulfuron, cinosulfuron, cyclosulfamuron, ethametsulfuron, ethametsulfuron-methyl, ethoxysulfuron, flazasulfuron, flucetosulfuron, flupyrsulfuron, flupyrsulfuron-methyl-sodium, foramsulfuron, halosulfuron, halosulfuron- methyl, imazosulfuron, iodosulfuron, iodosulfuron-methyl-sodium, iofensulfuron, iofensulfuron-sodium, mesosulfuron, metazosulfuron, metsulfuron, metsulfuron-methyl, nic
  • sulfometuron sulfometuron-methyl, sulfosulfuron, thifensulfuron, thifensulfuron-methyl, triasulfuron, tribenuron, tribenuron-methyl, trifloxysulfuron, triflusulfuron, triflusulfuron- methyl and tritosulfuron,
  • imidazolinones such as imazamethabenz, imazamethabenz-methyl, imazamox, imazapic, imazapyr, imazaquin and imazethapyr, triazolopyrimidine herbicides and sulfonamides such as cloransulam, cloransulam-methyl, diclosulam, flumetsulam, florasulam, metosulam, penoxsulam, pyrimisulfan and pyroxsulam,
  • pyrimidinylbenzoates such as bispyribac, bispyribac-sodium, pyribenzoxim, pyriftalid, pyriminobac, pyriminobac-methyl, pyrithiobac, pyrithiobac-sodium, 4-[[[2-[(4,6- dimethoxy-2-pyrimidinyl)oxy]phenyl]methyl]amino]-benzoic acid-1 -methylethyl ester (CAS 420138-41 -6), 4-[[[2-[(4,6-dimethoxy-2-pyrimidinyl)oxy]phenyl]methyl]amino]-benzoic acid propyl ester (CAS 420138-40-5), N-(4-bromophenyl)-2-[(4,6-dimethoxy-2- pyrimidinyl)oxy]benzenemethanamine (CAS 420138-01 -8),
  • sulfonylaminocarbonyl-triazolinone herbicides such as flucarbazone, flucarbazone- sodium, propoxycarbazone, propoxycarbazone-sodium, thiencarbazone and
  • compositions comprising at least one imidazolinone herbicide
  • inhibitors of the photosystem II e.g. triazine herbicides, including of chlorotriazine, triazinones, triazindiones, methylthiotriazines and pyridazinones such as ametryn, atrazine, chloridazone, cyanazine, desmetryn, dimethametryn,hexazinone, metribuzin, prometon, prometryn, propazine, simazine, simetryn, terbumeton,
  • triazine herbicides including of chlorotriazine, triazinones, triazindiones, methylthiotriazines and pyridazinones such as ametryn, atrazine, chloridazone, cyanazine, desmetryn, dimethametryn,hexazinone, metribuzin, prometon, prometryn, propazine, simazine, simetryn, terbumeton,
  • aryl urea such as chlorobromuron, chlorotoluron, chloroxuron, dimefuron, diuron, fluometuron, isoproturon, isouron, linuron, metamitron, methabenzthiazuron, metobenzuron, metoxuron, monolinuron, neburon, siduron, tebuthiuron and thiadiazuron, phenyl carbamates such as desmedipham, karbutilat, phenmedipham, phenmedipham-ethyl, nitrile herbicides such as bromofenoxim, bromoxynil and its salts and esters, ioxynil and its salts and esters, uraciles such as bromacil, lenacil and terbacil, and bentazon and bentazon-sodium, pyridate, pyridafo
  • a preferred embodiment of the invention relates to those compositions comprising at least one aryl urea herbicide. Among these, likewise a preferred embodiment of the invention relates to those compositions comprising at least one triazine herbicide. Among these, likewise a preferred embodiment of the invention relates to those compositions comprising at least one nitrile herbicide;
  • acifluorfen acifluorfen-sodium, azafenidin, bencarbazone, benzfendizone, bifenox, butafenacil, carfentrazone, carfentrazone-ethyl, chlomethoxyfen, cinidon-ethyl, fluazolate, flufenpyr, flufenpyr-ethyl, flumiclorac, flumiclorac-pentyl, flumioxazin, fluoroglycofen, fluoroglycofen-ethyl, fluthiacet, fluthiacet-methyl, fomesafen, halosafen, lactofen, oxadiargyl, oxadiazon, oxyfluorfen, pentoxazone, profluazol, pyraclonil, pyraflufen, pyraflufen-ethyl, saflufenacil, sulfentrazone,
  • PDS inhibitors beflubutamid, diflufenican, fluridone, flurochloridone, flurtamone, norflurazon, picolinafen, and 4-(3-trifluoromethylphenoxy)-2-(4- trifluoromethylphenyl)pyrimidine (CAS 180608-33-7), HPPD inhibitors: benzobicyclon, benzofenap, bicyclopyrone, clomazone, fenquintrione, isoxaflutole, mesotrione, pyrasulfotole, pyrazolynate, pyrazoxyfen, sulcotrione, tefuryltrione, tembotrione, tolpyralate, topramezone, bleacher, unknown target: aclonifen, amitrole and flumeturon; b6) from the group of the EPSP synthase inhibitors:
  • glyphosate glyphosate, glyphosate-isopropylammonium, glyposate-potassium and glyphosate- trimesium (sulfosate);
  • bilanaphos (bialaphos), bilanaphos-sodium, glufosinate, glufosinate-P and glufosinate-ammonium;
  • compounds of group K1 dinitroanilines such as benfluralin, butralin, dinitramine, ethalfluralin, fluchloralin, oryzalin, pendimethalin, prodiamine and trifluralin,
  • phosphoramidates such as amiprophos, amiprophos-methyl, and butamiphos
  • benzoic acid herbicides such as chlorthal, chlorthal-dimethyl, pyridines such as dithiopyr and thiazopyr, benzamides such as propyzamide and tebutam
  • compounds of group K2 carbetamide, chlorpropham, flamprop, flamprop-isopropyl, flamprop-methyl, flamprop-M- isopropyl, flamprop-M-methyl and propham ; among these, compounds of group K1 , in particular dinitroanilines are preferred;
  • chloroacetamides such as acetochlor, alachlor, butachlor, dimethachlor,
  • isoxazoline compounds of the formula (1)1 are known in the art, e.g. from WO
  • VLCFA inhibitors preference is given to chloroacetamides and oxyacetamides;
  • 2,4-D and its salts and esters such as clacyfos, 2,4-DB and its salts and esters, aminocyclopyrachlor and its salts and esters, aminopyralid and its salts such as aminopyralid-dimethylammonium, aminopyralid-tris(2-hydroxypropyl)ammonium and its esters, benazolin, benazolin-ethyl, chloramben and its salts and esters, clomeprop, clopyralid and its salts and esters, dicamba and its salts and esters, dichlorprop and its salts and esters, dichlorprop-P and its salts and esters, fluroxypyr, fluroxypyr-butometyl, fluroxypyr-meptyl, halauxifen and its salts and esters (CAS 943832-60-8 DOW, LS 566509); MCPA and its salts and esters, MCPA-thioethyl, MCPB and
  • auxin transport inhibitors diflufenzopyr, diflufenzopyr- sodium, naptalam and naptalam-sodium;
  • Preferred herbicides B that can be used in combination with the diaminotriazine compounds of the formula (I) according to the present invention are:
  • acifluorfen-sodium bencarbazone, benzfendizone, butafenacil, carfentrazone-ethyl, cinidon-ethyl, flufenpyr-ethyl, flumiclorac-pentyl, flumioxazin, fluoroglycofen-ethyl, fomesafen, lactofen, oxadiargyl, oxadiazon, oxyfluorfen, pentoxazone, pyraflufen, pyraflufen-ethyl, saflufenacil, sulfentrazone, tiafenacil, trifludimoxazin (BAS 850 H), ethyl [3-[2-chloro-4-fluoro-5-(1 -methyl-6-trifluoromethyl-2,4-dioxo-1 ,2,3,4-tetrahydropyrimidin-3- yl)phenoxy
  • glyphosate glyphosate, glyphosate-isopropylammonium, glyphosate-potassium and glyphosate- trimesium (sulfosate);
  • glufosinate glufosinate-P, glufosinate-ammonium
  • acetochlor alachlor, anilofos, butachlor, cafenstrole, dimethenamid, dimethenamid- P, fentrazamide, flufenacet, mefenacet, metazachlor, metolachlor, S-metolachlor, naproanilide, napropamide, napropamide-M, pretilachlor, fenoxasulfone, ipfencarbazone, pyroxasulfone thenylchlor and isoxazoline-compounds of the formulae 11.1 , II.2, II.3, II.4, II.5, II.6, II.7, II.8 and II.9 as mentioned above;
  • b1 1 from the group of the cellulose biosynthesis inhibitors: dichlobenil, flupoxam, indaziflam, isoxaben, triaziflam and 1 -cyclohexyl-5-pentafluorphenyloxy-1 4 -
  • 2,4-D and its salts and esters aminocyclopyrachlor and its salts and esters, aminopyralid and its salts such as aminopyralid-dimethylammonium, aminopyralid-tris(2- hydroxypropyl)ammonium and its esters, clopyralid and its salts and esters, dicamba and its salts and esters, dichlorprop-P and its salts and esters, fluroxypyr-meptyl, halauxifen and its salts and esters (CAS 943832-60-8 DOW, LS 566509), MCPA and its salts and esters, MCPB and its salts and esters, mecoprop-P and its salts and esters, picloram and its salts and esters, quinclorac, quinmerac, triclopyr and its salts and esters, 4-amino-3- chloro-6-(4-chloro-2-fluoro-3-methoxyphenyl)-5-fluoropyridine-2-carbox
  • auxin transport inhibitors diflufenzopyr and diflufenzopyr- sodium;
  • herbicides B that can be used in combination with the diaminotriazine compounds of the formula (I) according to the present invention are: b1 ) from the group of the lipid biosynthesis inhibitors: clodinafop-propargyl, cycloxydim, cyhalofop-butyl, fenoxaprop-P-ethyl, pinoxaden, profoxydim, tepraloxydim, tralkoxydim, 4-(4'-Chloro-4-cyclopropyl-2'-fluoro[1 ,1 '-biphenyl]-3-yl)-5-hydroxy-2,2,6,6- tetramethyl-2H-pyran-3(6H)-one (CAS 1312337-72-6); 4-(2',4'-Dichloro-4-cyclopropyl[1 ,1 '- biphenyl]-3-yl)-5-hydroxy-2,2,6,6-tetramethyl-2H-pyran
  • ALS inhibitors from the group of the ALS inhibitors: bensulfuron-methyl, bispyribac-sodium, cyclosulfamuron, diclosulam, flumetsulam, flupyrsulfuron-methyl-sodium, foramsulfuron, imazamox, imazapic, imazapyr, imazaquin, imazethapyr, imazosulfuron, iodosulfuron, iodosulfuron-methyl-sodium, iofensulfuron, iofensulfuron-sodium, mesosulfuron, metazosulfuron, nicosulfuron, penoxsulam, propoxycarbazon-sodium, propyrisulfuron, pyrazosulfuron-ethyl, pyroxsulam, rimsulfuron, sulfosulfuron, thiencarbazon-methyl, tritosulfuron
  • b3 from the group of the photosynthesis inhibitors: ametryn, atrazine, diuron, fluometuron, hexazinone, isoproturon, linuron, metribuzin, paraquat, paraquat-dichloride, propanil, terbutryn and terbuthylazine;
  • glufosinate from the group of the glutamine synthase inhibitors: glufosinate, glufosinate-P and glufosinate-ammonium;
  • auxinic herbicides 2,4-D and its salts and esters such as clacyfos, and aminocyclopyrachlor and its salts and esters, aminopyralid and its salts and its esters, clopyralid and its salts and esters, dicamba and its salts and esters, fluroxypyr- meptyl, halauxifen, halauxifen-methyl, quinclorac, quinmerac, 4-amino-3-chloro-6-(4- chloro-2-fluoro-3-methoxyphenyl)-5-fluoropyridine-2-carboxylic acid (DOW, "Rinskor-acid”) and benzyl 4-amino-3-chloro-6-(4-chloro-2-fluoro-3-methoxyphenyl)-5-fluoropyridine-2-carboxylic acid (DOW, "Rinskor-acid”) and benzyl 4-amino-3-chloro-6-(4-ch
  • auxin transport inhibitors diflufenzopyr and diflufenzopyr- sodium
  • herbicides B are the herbicides B as defined above; in particular the herbicides B.1 - B.196 listed below in table B:
  • Herbicide B Herbicide B
  • compositions according to the present invention comprise at least one diaminotriazine compound of formula (I) and at least one safener C.
  • Safeners are chemical compounds which prevent or reduce damage on useful plants without having a major impact on the herbicidal action of the herbicidal active components of the present compositions towards unwanted plants. They can be applied either before sowings (e.g. on seed treatments, shoots or seedlings) or in the pre-emergence application or post-emergence application of the useful plant.
  • the safeners and the diaminotriazine compound of formula (I) and/or the herbicides B can be applied simultaneously or in succession.
  • Suitable safeners are e.g. (quinolin-8-oxy)acetic acids, 1 -phenyl-5-haloalkyl-1 H- 1 ,2,4-triazol-3-carboxylic acids, 1 -phenyl-4,5-dihydro-5-alkyl-1 H-pyrazol-3,5- dicarboxylic acids, 4,5-dihydro-5,5-diaryl-3-isoxazol carboxylic acids,
  • dichloroacetamides alpha-oximinophenylacetonitriles, acetophenonoximes, 4,6-dihalo- 2-phenylpyrimidines, N-[[4-(aminocarbonyl)phenyl]sulfonyl]-2-benzoic amides, 1 ,8- naphthalic anhydride, 2-halo-4-(haloalkyl)-5-thiazol carboxylic acids, phosphorthiolates and N-alkyl-O-phenylcarbamates and their agriculturally acceptable salts and their agriculturally acceptable derivatives such amides, esters, and thioesters, provided they have an acid group.
  • Examples of preferred safeners C are benoxacor, cloquintocet, cyometrinil, cyprosulfamide, dichlormid, dicyclonon, dietholate, fenchlorazole, fenclorim, flurazole, fluxofenim, furilazole, isoxadifen, mefenpyr, mephenate, naphthalic anhydride, oxabetrinil, 4-(dichloroacetyl)-1 -oxa-4-azaspiro[4.5]decane (MON4660, CAS 71526-07- 3), 2,2,5-trimethyl-3-(dichloroacetyl)-1 ,3-oxazolidine (R-29148, CAS 52836-31 -4) and N-(2-Methoxybenzoyl)-4-[(methylaminocarbonyl)amino]benzenesulfonamide (CAS 129531 -12-0).
  • Especially preferred safeners C are benoxacor, cloquintocet, cyprosulfamide, dichlormid, fenchlorazole, fenclorim, flurazole, fluxofenim, furilazole, isoxadifen, mefenpyr, naphthalic anhydride, oxabetrinil, 4-(dichloroacetyl)-1 -oxa-4-azaspiro- [4.5]decane (MON4660, CAS 71526-07-3), 2,2,5-trimethyl-3-(dichloroacetyl)-1 ,3- oxazolidine (R-29148, CAS 52836-31 -4) and N-(2-Methoxybenzoyl)-4- [(methylaminocarbonyl)amino]benzenesulfonamide (CAS 129531 -12-0).
  • Particularly preferred safeners C are benoxacor, cloquintocet, cyprosulfamide, dichlormid, fenchlorazole, fenclorim, furilazole, isoxadifen, mefenpyr, naphtalic anhydride, 4-(dichloroacetyl)-1 -oxa-4-azaspiro[4.5]decane (MON4660, CAS 71526-07- 3), 2,2,5-trimethyl-3-(dichloroacetyl)-1 ,3-oxazolidine (R-29148, CAS 52836-31 -4) and N-(2-Methoxybenzoyl)-4-[(methylaminocarbonyl)amino]benzenesulfonamide (CAS 129531 -12-0).
  • safeners C which, as component C, are constituent of the composition according to the invention are the safeners C as defined above; in particular the safeners C.1 - C.17 listed below in table C:
  • the active compounds B of groups b1 ) to b15) and the active compounds C are known herbicides and safeners, see, for example, The Compendium of Pesticide Common Names (http://www.alanwood.net/pesticides/); Farm Chemicals Handbook 2000 volume 86, Meister Publishing Company, 2000; B. Hock, C. Fedtke,
  • the assignment of the active compounds to the respective mechanisms of action is based on current knowledge. If several mechanisms of action apply to one active compound, this substance was only assigned to one mechanism of action.
  • Active compounds B and C having a carboxyl group can be employed in the form of the acid, in the form of an agriculturally suitable salt as mentioned above or else in the form of an agriculturally acceptable derivative in the compositions according to the invention.
  • suitable salts include those, where the counterion is an agriculturally acceptable cation.
  • suitable salts of dicamba are dicamba- sodium, dicamba-potassium, dicamba-methylammonium, dicamba-dimethylammonium, dicamba-isopropylammonium, dicamba-diglycolamine, dicamba-olamine, dicamba- diolamine, dicamba-trolamine, dicamba-N,N-bis-(3-aminopropyl)methylamine and dicamba-diethylenetriamine.
  • a suitable ester are dicamba-methyl and dicamba-butotyl.
  • Suitable salts of 2,4-D are 2,4-D-ammonium, 2,4-D-dimethylammonium, 2,4-D- diethylammonium, 2,4-D-diethanolammonium (2,4-D-diolamine), 2,4-D-triethanol- ammonium, 2,4-D-isopropylammonium, 2,4-D-triisopropanolammonium, 2,4-D- heptylammonium, 2,4-D-dodecylammonium, 2,4-D-tetradecylammonium, 2,4-D- triethylammonium, 2,4-D-tris(2-hydroxypropyl)ammonium, 2,4-D-tris(isopropyl)- ammonium, 2,4-D-trolamine, 2,4-D-lithium, 2,4-D-sodium.
  • esters of 2,4-D are 2,4-D-butotyl, 2,4-D-2-butoxypropyl, 2,4-D-3-butoxypropyl, 2,4-D-butyl, 2,4-D-ethyl, 2,4-D-ethylhexyl, 2,4-D-isobutyl, 2,4-D-isooctyl, 2,4-D-isopropyl, 2,4-D- meptyl, 2,4-D-methyl, 2,4-D-octyl, 2,4-D-pentyl, 2,4-D-propyl, 2,4-D-tefuryl and clacyfos.
  • Suitable salts of 2,4-DB are for example 2,4-DB-sodium, 2,4-DB-potassium and 2,4-DB-dimethylammonium.
  • Suitable esters of 2,4-DB are for example 2,4-DB-butyl and 2,4-DB-isoctyl.
  • Suitable salts of dichlorprop are for example dichlorprop-sodium, dichlorprop- potassium and dichlorprop-dimethylammonium.
  • suitable esters of dichlorprop are dichlorprop-butotyl and dichlorprop-isoctyl.
  • Suitable salts and esters of MCPA include MCPA-butotyl, MCPA-butyl, MCPA- dimethylammonium, MCPA-diolamine, MCPA-ethyl, MCPA-thioethyl, MCPA-2- ethylhexyl, MCPA-isobutyl, MCPA-isoctyl, MCPA-isopropyl, MCPA- isopropylammonium, MCPA-methyl, MCPA-olamine, MCPA-potassium, MCPA-sodium and MCPA-trolamine.
  • a suitable salt of MCPB is MCPB sodium.
  • a suitable ester of MCPB is MCPB- ethyl.
  • Suitable salts of clopyralid are clopyralid-potassium, clopyralid-olamine and clopyralid-tris-(2-hydroxypropyl)ammonium.
  • Example of suitable esters of clopyralid is clopyralid-methyl.
  • Examples of a suitable ester of fluroxypyr are fluroxypyr-meptyl and fluroxypyr-2- butoxy-1 -methylethyl, wherein fluroxypyr-meptyl is preferred.
  • Suitable salts of picloram are picloram-dimethylammonium, picloram-potassium, picloram-triisopropanolammonium, picloram-triisopropylammonium and picloram- trolamine.
  • a suitable ester of picloram is picloram-isoctyl.
  • a suitable salt of triclopyr is triclopyr-triethylammonium.
  • Suitable esters of triclopyr are for example triclopyr-ethyl and triclopyr-butotyl.
  • Suitable salts and esters of chloramben include chloramben-ammonium, chloramben-diolamine, chloramben-methyl, chloramben-methylammonium and chloramben-sodium.
  • Suitable salts and esters of 2,3,6-TBA include 2,3,6-TBA- dimethylammonium, 2,3,6-TBA-lithium, 2,3,6-TBA-potassium and 2,3,6-TBA-sodium.
  • Suitable salts and esters of aminopyralid include aminopyralid-potassium, aminopyralid-dimethylammonium, and aminopyralid-tris(2-hydroxypropyl)ammonium.
  • Suitable salts of glyphosate are for example glyphosate-ammonium, glyphosate- diammonium, glyphoste-dimethylammonium, glyphosate-isopropylammonium, glyphosate-potassium, glyphosate-sodium, glyphosate-trimesium as well as the ethanolamine and diethanolamine salts, preferably glyphosate-diammonium, glyphosate-isopropylammonium and glyphosate-trimesium (sulfosate).
  • a suitable salt of glufosinate is for example glufosinate-ammonium.
  • a suitable salt of glufosinate-P is for example glufosinate-P-ammonium.
  • Suitable salts and esters of bromoxynil are for example bromoxynil-butyrate, bromoxynil-heptanoate, bromoxynil-octanoate, bromoxynil-potassium and bromoxynil- sodium.
  • Suitable salts and esters of ioxonil are for example ioxonil-octanoate, ioxonil- potassium and ioxonil-sodium.
  • Suitable salts and esters of mecoprop include mecoprop-butotyl, mecoprop- dimethylammonium, mecoprop-diolamine, mecoprop-ethadyl, mecoprop-2-ethylhexyl, mecoprop-isoctyl, mecoprop-methyl, mecoprop-potassium, mecoprop-sodium and mecoprop-trolamine.
  • Suitable salts of mecoprop-P are for example mecoprop-P-butotyl, mecoprop-P- dimethylammonium, mecoprop-P-2-ethylhexyl, mecoprop-P-isobutyl, mecoprop-P- potassium and mecoprop-P-sodium.
  • a suitable salt of diflufenzopyr is for example diflufenzopyr-sodium.
  • a suitable salt of naptalam is for example naptalam-sodium.
  • Suitable salts and esters of aminocyclopyrachlor are for example
  • aminocyclopyrachlor-dimethylammonium aminocyclopyrachlor-methyl
  • a suitable salt of quinclorac is for example quinclorac-dimethylammonium.
  • a suitable salt of quinmerac is for example quinmerac-dimethylammonium.
  • a suitable salt of imazamox is for example imazamox-ammonium.
  • Suitable salts of imazapic are for example imazapic-ammonium and imazapic- isopropylammonium.
  • Suitable salts of imazapyr are for example imazapyr-ammonium and imazapyr- isopropylammonium.
  • a suitable salt of imazaquin is for example imazaquin-ammonium.
  • Suitable salts of imazethapyr are for example imazethapyr-ammonium and imazethapyr-isopropylammonium.
  • a suitable salt of topramezone is for example topramezone-sodium.
  • the composition comprises as herbicidal active compound B or component B at least one, preferably exactly one herbicide B.
  • the composition comprises as herbicidal active compounds B or component B at least two, preferably exactly two herbicides B different from each other.
  • the composition comprises as herbicidal active compounds B or component B at least three, preferably exactly three herbicides B different from each other.
  • the composition comprises as safening component C or component C at least one, preferably exactly one safener C.
  • the composition comprises as component B at least one, preferably exactly one herbicide B, and as component C at least one, preferably exactly one, safener C.
  • the composition comprises at least two, preferably exactly two, herbicides B different from each other, and as component C at least one, preferably exactly one, safener C.
  • the composition comprises at least three, preferably exactly three, herbicides B different from each other, and as component C at least one, preferably exactly one, safener C.
  • the composition comprises at least one, preferably exactly one compound of formula (I) and as component B at least one, preferably exactly one, herbicide B.
  • the composition comprises at least one, preferably exactly one compound of formula (I) and at least two, preferably exactly two, herbicides B different from each other.
  • the composition comprises at least one, preferably exactly one compound of formula (I) and at least three, preferably exactly three, herbicides B different from each other.
  • the composition comprises at least one, preferably exactly one compound of formula (I) and as component C at least one, preferably exactly one, safener C.
  • the composition comprises at least one, preferably exactly one compound of formula (I) as component B at least one, preferably exactly one, herbicide B, and as component C at least one, preferably exactly one safener C.
  • the composition comprises at least one, preferably exactly one compound of formula (I), at least two, preferably exactly two herbicides B different from each other, and as component C at least one, preferably exactly one, safener C.
  • the composition comprises at least one, preferably exactly one compound of formula (I) at least three, preferably exactly three herbicides B different from each other, and as component C at least one, preferably exactly one, safener C.
  • the composition comprises, in addition to a compounds of formula (I), at least one and especially exactly one herbicidally active compound from group b1 ), in particular selected from the group consisting of clodinafop-propargyl, cycloxydim, cyhalofop-butyl, fenoxaprop-
  • the composition comprises, in addition to a compounds of formula (I), at least one and especially exactly one herbicidally active compound from group b2), in particular selected from the group consisting of bensulfuron-methyl, bispyribac-sodium, cyclosulfamuron, diclosulam, flumetsulam, flupyrsulfuron-methyl-sodium, foramsulfuron, imazamox, imazapic, imazapyr, imazaquin, imazethapyr, imazosulfuron, iodosulfuron,
  • iodosulfuron-methyl-sodium mesosulfuron, metazosulfuron, nicosulfuron, penoxsulam, propoxycarbazon-sodium, pyrazosulfuron-ethyl, pyroxsulam, rimsulfuron, sulfosulfuron, thiencarbazon-methyl and tritosulfuron.
  • the composition comprises, in addition to a compounds of formula (I), at least one and especially exactly one herbicidally active compound from group b3), in particular selected from the group consisting of ametryn, atrazine, diuron, fluometuron, hexazinone,
  • the composition comprises, in addition to a compounds of formula (I), at least one and especially exactly one herbicidally active compound from group b4), in particular selected from the group consisting of flumioxazin, oxyfluorfen, pyraflufen, pyraflufen-ethyl, saflufenacil, sulfentrazone, trifludimoxazin (BAS 850 H), ethyl [3-[2-chloro-4-fluoro-5-(1 - methyl-6-trifluoromethyl-2,4-dioxo-1 ,2,3,4-tetrahydropyrimidin-3-yl)phenoxy]-2- pyridyloxy]acetate (CAS 353292-31 -6; S-3100; Sumitomo; LS 5296489) , 3-[7-fluoro-3- oxo-4-(prop-2-ynyl)-3,4-dihydro
  • the composition comprises, in addition to a compounds of formula (I), at least one and especially exactly one herbicidally active compound from group b5), in particular selected from the group consisting of amitrole, bicyclopyrone, clomazone, diflufenican, flumeturon, flurochloridone, isoxaflutole, mesotrione, picolinafen, sulcotrione, tefuryltrione, tembotrione, tolpyralate and topramezone.
  • a compounds of formula (I) at least one and especially exactly one herbicidally active compound from group b5), in particular selected from the group consisting of amitrole, bicyclopyrone, clomazone, diflufenican, flumeturon, flurochloridone, isoxaflutole, mesotrione, picolinafen, sulcotrione, tefuryltrione, tembotrione, tolpyralate and topram
  • the composition comprises, in addition to a compounds of formula (I), at least one and especially exactly one herbicidally active compound from group b6), in particular selected from the group consisting of glyphosate, glyphosate-isopropylammonium and glyphosate- trimesium (sulfosate).
  • the composition comprises, in addition to a compounds of formula (I), at least one and especially exactly one herbicidally active compound from group b7), in particular selected from the group consisting of glufosinate, glufosinate-P and glufosinate-ammonium.
  • the composition comprises, in addition to a compounds of formula (I), at least one and especially exactly one herbicidally active compound from group b9), in particular selected from the group consisting of pendimethalin and trifluralin.
  • the composition comprises, in addition to a compounds of formula (I), at least one and especially exactly one herbicidally active compound from group b10), in particular selected from the group consisting of acetochlor, cafenstrole, dimethenamid-P, fentrazamide, flufenacet, mefenacet, metazachlor, metolachlor, S-metolachlor, fenoxasulfone and pyroxasulfone.
  • a compounds of formula (I) at least one and especially exactly one herbicidally active compound from group b10), in particular selected from the group consisting of acetochlor, cafenstrole, dimethenamid-P, fentrazamide, flufenacet, mefenacet, metazachlor, metolachlor, S-metolachlor, fenoxasulfone and pyroxasulfone.
  • compositions comprising in addition to a compounds of formula (I), at least one and especially exactly one herbicidally active compound from group b10), in particular selected from the group consisting of isoxazoline compounds of the formulae 11.1 , II.2, II.3, II.4, II.5, II.6, II.7, II.8 and II.9, as defined above.
  • the composition comprises, in addition to a compounds of formula (I), at least one and especially exactly one herbicidally active compound from group b1 1 ), in particular indaziflam, isoxaben and triaziflam.
  • the composition comprises, in addition to a compounds of formula (I), at least one and especially exactly one herbicidally active compound from group b13), in particular selected from the group consisting of 2,4-D and its salts and esters, aminocyclopyrachlor and its salts and esters, aminopyralid and its salts such as aminopyralid-dimethylammonium, aminopyralid-tris(2-hydroxypropyl)ammonium and its esters, clopyralid and its salts and esters, dicamba and its salts and esters, fluroxypyr-meptyl, halauxifen, halauxifen- methyl, quinclorac, quinmerac, 4-amino-3-chloro-6-(4-chloro-2-fluoro-3- methoxyphenyl)-5-fluoropyridine-2-carboxylic acid (DOW, "Rinskor-acid”) and benzyl 4- amino-3-chloro-6-(4-chloro-2-fluor
  • the composition comprises, in addition to a compounds of formula (I), at least one and especially exactly one herbicidally active compound from group b14), in particular selected from the group consisting of diflufenzopyr and diflufenzopyr-sodium.
  • the composition comprises, in addition to a compounds of formula (I), at least one and especially exactly one safener C, in particular selected from the group consisting of benoxacor, cloquintocet, cyprosulfamide, dichlormid, fenchlorazole, fenclorim, furilazole, isoxadifen, mefenpyr, 4-(dichloroacetyl)-1 -oxa-4-azaspiro[4.5]decane (MON4660, CAS 71526-07-3) and 2,2,5-trimethyl-3-(dichloroacetyl)-1 ,3-oxazolidine (R-29148, CAS 52836-31 -4).
  • safener C in particular selected from the group consisting of benoxacor, cloquintocet, cyprosulfamide, dichlormid, fenchlorazole, fenclorim, furilazole, isoxadifen, mefenpyr, 4-(dichlor
  • ternary compositions which correspond to the binary compositions mentioned above and additionally comprise a safener C, in particular selected from the group consisting of benoxacor, cloquintocet,
  • cyprosulfamide dichlormid, fenchlorazole, fenclorim, furilazole, isoxadifen, mefenpyr, 4-(dichloroacetyl)-1 -oxa-4-azaspiro[4.5]decane (MON4660, CAS 71526-07-3) and 2,2, 5-trimethyl-3-(dichloroacetyl)-1 ,3-oxazolidine (R-29148, CAS 52836-31 -4).
  • binary compositions includes compositions comprising one or more, for example 1 , 2 or 3, active compounds of the formula (I) and either one or more, for example 1 , 2 or 3, herbicides B or one or more safeners C.
  • ternary compositions includes compositions comprising one or more, for example 1 , 2 or 3, active compounds of the formula (I), one or more, for example 1 , 2 or 3, herbicides B and one or more, for example 1 , 2 or 3, safeners C.
  • the weight ratio of the active compounds A:B is generally in the range of from 1 :1000 to 1000:1 , preferably in the range of from 1 :500 to 500: 1 , in particular in the range of from 1 :250 to 250: 1 and particularly preferably in the range of from 1 :75 to 75:1 .
  • the weight ratio of the active compounds A:C is generally in the range of from 1 :1000 to 1000:1 , preferably in the range of from 1 :500 to 500:1 , in particular in the range of from 1 :250 to 250:1 and particularly preferably in the range of from 1 :75 to 75:1.
  • the relative proportions by weight of the components A:B are generally in the range of from 1 :1000 to 1000:1 , preferably in the range of from 1 :500 to 500:1 , in particular in the range of from 1 :250 to 250:1 and particularly preferably in the range of from 1 :75 to 75:1
  • the weight ratio of the components A:C is generally in the range of from 1 :1000 to 1000:1 , preferably in the range of from 1 :500 to 500:1 , in particular in the range of from 1 :250 to 250:1 and particularly preferably in the range of from 1 :75 to 75:1
  • the weight ratio of the components B:C is generally in the range of from 1 :1000 to 1000:1 , preferably in the range of from 1 :500 to 500:1 , in particular in the range of from 1 :250 to 250:1 and particularly preferably in the range of from 1 :75 to 75:1
  • the weight ratio of the components B:C is generally in the range of from 1 :1000
  • weight ratios of the individual components in the preferred mixtures mentioned below are within the limits given above, in particular within the preferred limits.
  • compositions mentioned below comprising the
  • compositions 1 .1 to 1.3545 comprising the compounds of formula (I) and the substance(s) as defined in the respective row of table 1 :
  • A-8.1 .1 to A-8.2252.3545 A-16.1.1 to A-16.2252.3545, A-17 1. 1 to A-17 2252 3545, A-54 1. 1 to A-54 2252 3545,
  • A-43 1. 1 to A-43 2252 3545, A-80 1. 1 to A-80 2252 3545,
  • A-X refers to the numbers of tables A-1 to A.88.
  • the integer Y refers to the row of table A, while the integer Z refers to the row of table 1 below.
  • the code A-1.1 .1 refers to the combination of the compound of formula I. a of table A-1 , wherein X and R 2 are as defined in row 1 of table A, with the combination of the herbicide B and and the safener C are as defined in combination no. 1 .1 of table 1 .
  • the code A-12.2.35 refers to the combination of the compound of formula I. a of table A-12, wherein X and R 2 are as defined in row 2 of table A, with the combination of the herbicide B and and the safener C are as defined in combination no. 1 .35 of table 1 .
  • the code A-35.2252.3545 refers to the combination of the compound of formula I. a of table A-35, wherein X and R 2 are as defined in row 2252 of table A, with the combination of the herbicide B and and the safener C are as defined in combination no. 1 .3545 of table 1.
  • mixtures A-1 .2.1 to A-1.2.3545 i.e. the mixtures of the compound of table A-1 , where R 2 and X are as defined in row 2 of table A and where the herbicide or herbicide safener combination is as defined in one of the rows 1.1 to 1 .3545 of table 1 ;
  • mixtures A-1 .52.1 to A-1 .52.3545 i.e. the mixtures of the compound of table A-1 , where R 2 and X are as defined in row 52 of table A and where the herbicide or herbicide safener combination is as defined in one of the rows 1.1 to 1 .3545 of table 1 ;
  • mixtures A-1 .565.1 to A-1.565.3545 i.e. the mixtures of the compound of table A- 1 , where R 2 and X are as defined in row 565 of table A and where the herbicide or herbicide safener combination is as defined in one of the rows 1 .1 to 1.3545 of table 1 ;
  • mixtures A-1 .615.1 to A-1.615.3545 i.e. the mixtures of the compound of table A- 1 , where R 2 and X are as defined in row 615 of table A and where the herbicide or herbicide safener combination is as defined in one of the rows 1 .1 to 1.3545 of table 1 ;
  • mixtures A-1 .838.1 to A-1. 838.3545 i.e. the mixtures of the compound of table A-1 , where R 2 and X are as defined in row 838of table A and where the herbicide or herbicide safener combination is as defined in one of the rows 1 .1 to 1.3545 of table 1 ;
  • mixtures A-1 .1 128.1 to A-1 . 1 128.3545 i.e. the mixtures of the compound of table A-1 , where R 2 and X are as defined in row 1 128 of table A and where the herbicide or herbicide safener combination is as defined in one of the rows 1 .1 to 1 .3545 of table 1 ;
  • mixtures A-1 .1401 .1 to A-1 . 1401 .3545 i.e. the mixtures of the compound of table A-1 , where R 2 and X are as defined in row 1401 of table A and where the herbicide or herbicide safener combination is as defined in one of the rows 1 .1 to
  • mixtures A-1 .1691 .1 to A-1 . 1691 .3545 i.e. the mixtures of the compound of table A-1 , where R 2 and X are as defined in row 1691 of table A and where the herbicide or herbicide safener combination is as defined in one of the rows 1 .1 to 1 .3545 of table 1 ;
  • mixtures A-1 .1741 .1 to A-1 . 1741 .3545 i.e. the mixtures of the compound of table A-1 , where R 2 and X are as defined in row 1741 of table A and where the herbicide or herbicide safener combination is as defined in one of the rows 1 .1 to 1 .3545 of table 1 ;
  • mixtures A-6.2.1 to A-6.2.3545 i.e. the mixtures of the compound of table A-6, where R 2 and X are as defined in row 2 of table A and where the herbicide or herbicide safener combination is as defined in one of the rows 1.1 to 1 .3545 of table 1 ;
  • mixtures A-6.52.1 to A-6.52.3545 i.e. the mixtures of the compound of table A-6, where R 2 and X are as defined in row 52 of table A and where the herbicide or herbicide safener combination is as defined in one of the rows 1.1 to 1 .3545 of table 1 ;
  • mixtures A-6.275.1 to A-6.275.3545 i.e. the mixtures of the compound of table A- 6, where R 2 and X are as defined in row 275 of table A and where the herbicide or herbicide safener combination is as defined in one of the rows 1 .1 to 1.3545 of table 1 ;
  • mixtures A-6.565.1 to A-6.565.3545 i.e. the mixtures of the compound of table A- 6, where R 2 and X are as defined in row 565 of table A and where the herbicide or herbicide safener combination is as defined in one of the rows 1 .1 to 1.3545 of table 1 ;
  • mixtures A-6.615.1 to A-6.615.3545 i.e. the mixtures of the compound of table A- 6, where R 2 and X are as defined in row 615 of table A and where the herbicide or herbicide safener combination is as defined in one of the rows 1 .1 to 1.3545 of table 1 ;
  • mixtures A-6.838.1 to A-6.838.3545 i.e. the mixtures of the compound of table A- 6, where R 2 and X are as defined in row 838 of table A and where the herbicide or herbicide safener combination is as defined in one of the rows 1 .1 to 1.3545 of table 1 ; mixtures A-6.1 128.1 to A-6.1 128.3545, i.e. the mixtures of the compound of table A-6, where R 2 and X are as defined in row 1 128 of table A and where the herbicide or herbicide safener combination is as defined in one of the rows 1 .1 to 1 .3545 of table 1 ;
  • mixtures A-6.1401 .1 to A-6.1401 .3545 i.e. the mixtures of the compound of table A-6, where R 2 and X are as defined in row 1401 of table A and where the herbicide or herbicide safener combination is as defined in one of the rows 1 .1 to 1 .3545 of table 1 ;
  • mixtures A-9.2.1 to A-9.2.3545 i.e. the mixtures of the compound of table A-9, where R 2 and X are as defined in row 2 of table A and where the herbicide or herbicide safener combination is as defined in one of the rows 1.1 to 1 .3545 of table 1 ;
  • mixtures A-9.52.1 to A-1 .52.3545 i.e. the mixtures of the compound of table A-9, where R 2 and X are as defined in row 52 of table A and where the herbicide or herbicide safener combination is as defined in one of the rows 1.1 to 1 .3545 of table 1 ;
  • mixtures A-9.275.1 to A-9.275.3545 i.e. the mixtures of the compound of table A- 9, where R 2 and X are as defined in row 275 of table A and where the herbicide or herbicide safener combination is as defined in one of the rows 1 .1 to 1.3545 of table 1 ;
  • mixtures A-9.565.1 to A-9.565.3545 i.e. the mixtures of the compound of table A- 9, where R 2 and X are as defined in row 565 of table A and where the herbicide or herbicide safener combination is as defined in one of the rows 1 .1 to 1.3545 of table 1 ;
  • mixtures A-9.615.1 to A-9.615.3545 i.e. the mixtures of the compound of table A- 9, where R 2 and X are as defined in row 615 of table A and where the herbicide or herbicide safener combination is as defined in one of the rows 1 .1 to 1.3545 of table 1 ;
  • mixtures A-9.838.1 to A-9.838.3545 i.e. the mixtures of the compound of table A- 9, where R 2 and X are as defined in row 838 of table A and where the herbicide or herbicide safener combination is as defined in one of the rows 1 .1 to 1.3545 of table 1 ;
  • mixtures A-9.1 128.1 to A-9.1 128.3545 i.e. the mixtures of the compound of table A-9, where R 2 and X are as defined in row 1 128 of table A and where the herbicide or herbicide safener combination is as defined in one of the rows 1 .1 to 1 .3545 of table 1 ;
  • mixtures A-9.1 178.1 to A-9.1 178.3545 i.e. the mixtures of the compound of table A-9, where R 2 and X are as defined in row 1 178 of table A and where the herbicide or herbicide safener combination is as defined in one of the rows 1 .1 to 1 .3545 of table 1 ;
  • mixtures A-17.2.1 to A-17.2.3545 i.e. the mixtures of the compound of table A- 17, where R 2 and X are as defined in row 2 of table A and where the herbicide or herbicide safener combination is as defined in one of the rows 1.1 to 1 .3545 of table 1 ;
  • mixtures A-17.275.1 to A-17.275.3545 i.e. the mixtures of the compound of table A-17, where R 2 and X are as defined in row 275 of table A and where the herbicide or herbicide safener combination is as defined in one of the rows 1 .1 to 1 .3545 of table 1 ; mixtures A-17.565.1 to A-17.565.3545, i.e. the mixtures of the compound of table A-17, where R 2 and X are as defined in row 565 of table A and where the herbicide or herbicide safener combination is as defined in one of the rows 1 .1 to 1 .3545 of table 1 ;
  • mixtures A-17.615.1 to A-17.615.3545 i.e. the mixtures of the compound of table A-17, where R 2 and X are as defined in row 615 of table A and where the herbicide or herbicide safener combination is as defined in one of the rows 1 .1 to 1 .3545 of table 1 ;
  • mixtures A-17.838.1 to A-17.838.3545 i.e. the mixtures of the compound of table A-17, where R 2 and X are as defined in row 838 of table A and where the herbicide or herbicide safener combination is as defined in one of the rows 1 .1 to 1 .3545 of table 1 ;
  • mixtures A-17.1 128.1 to A-17.1 128.3545 i.e. the mixtures of the compound of table A-17, where R 2 and X are as defined in row 1 128 of table A and where the herbicide or herbicide safener combination is as defined in one of the rows 1 .1 to
  • mixtures A-17.1 178.1 to A-17.1 178.3545 i.e. the mixtures of the compound of table A-17, where R 2 and X are as defined in row 1 178 of table A and where the herbicide or herbicide safener combination is as defined in one of the rows 1 .1 to 1 .3545 of table 1 ;
  • mixtures A-17.1401 .1 to A-17.1401 .3545 i.e. the mixtures of the compound of table A-17, where R 2 and X are as defined in row 34 of table A and where the herbicide or herbicide safener combination is as defined in one of the rows 1 .1 to 1 .3545 of table 1 ;
  • mixtures A-27.2.1 to A-27.2.3545 i.e. the mixtures of the compound of table A- 27, where R 2 and X are as defined in row 2 of table A and where the herbicide or herbicide safener combination is as defined in one of the rows 1.1 to 1 .3545 of table 1 ;
  • mixtures A-27.52.1 to A-27.52.3545 i.e. the mixtures of the compound of table A- 27, where R 2 and X are as defined in row 14 of table A and where the herbicide or herbicide safener combination is as defined in one of the rows 1 .1 to 1.3545 of table 1 ;
  • mixtures A-27.275.1 to A-27.275.3545 i.e. the mixtures of the compound of table A-27, where R 2 and X are as defined in row 275 of table A and where the herbicide or herbicide safener combination is as defined in one of the rows 1 .1 to
  • mixtures A-27.565.1 to A-27.565.3545 i.e. the mixtures of the compound of table A-27, where R 2 and X are as defined in row 565 of table A and where the herbicide or herbicide safener combination is as defined in one of the rows 1 .1 to 1 .3545 of table 1 ;
  • mixtures A-27.615.1 to A-27.615.3545 i.e. the mixtures of the compound of table A-27, where R 2 and X are as defined in row 615 of table A and where the herbicide or herbicide safener combination is as defined in one of the rows 1 .1 to 1 .3545 of table 1 ;
  • mixtures A-27.1 128.1 to A-27.1 128.3545 i.e. the mixtures of the compound of table A-27, where R 2 and X are as defined in row 1 128 of table A and where the herbicide or herbicide safener combination is as defined in one of the rows 1 .1 to 1 .3545 of table 1 ;
  • mixtures A-27.1 178.1 to A-27.1 178.3545 i.e. the mixtures of the compound of table A-27, where R 2 and X are as defined in row 1 178 of table A and where the herbicide or herbicide safener combination is as defined in one of the rows 1 .1 to
  • mixtures A-27.1401 .1 to A-27.1401 .3545 i.e. the mixtures of the compound of table A-27, where R 2 and X are as defined in row 1401 of table A and where the herbicide or herbicide safener combination is as defined in one of the rows 1 .1 to 1 .3545 of table 1 ;
  • mixtures A-32.275.1 to A-32.275.3545 i.e. the mixtures of the compound of table A-32, where R 2 and X are as defined in row 275 of table A and where the herbicide or herbicide safener combination is as defined in one of the rows 1 .1 to 1 .3545 of table 1 ;
  • mixtures A-32.565.1 to A-32.565.3545 i.e. the mixtures of the compound of table A-32, where R 2 and X are as defined in row 565 of table A and where the herbicide or herbicide safener combination is as defined in one of the rows 1 .1 to
  • mixtures A-32.615.1 to A-32.615.3545 i.e. the mixtures of the compound of table A-32, where R 2 and X are as defined in row 615 of table A and where the herbicide or herbicide safener combination is as defined in one of the rows 1 .1 to 1 .3545 of table 1 ;
  • mixtures A-32.838.1 to A-32.838.3545 i.e. the mixtures of the compound of table A-32, where R 2 and X are as defined in row 838 of table A and where the herbicide or herbicide safener combination is as defined in one of the rows 1 .1 to 1 .3545 of table 1 ;
  • mixtures A-32.1 178.1 to A-32.1 178.3545 i.e. the mixtures of the compound of table A-32, where R 2 and X are as defined in row 1 178 of table A and where the herbicide or herbicide safener combination is as defined in one of the rows 1 .1 to 1 .3545 of table 1 ;
  • mixtures A-32.1401 .1 to A-32.1401 .3545 i.e. the mixtures of the compound of table A-32, where R 2 and X are as defined in row 1401 of table A and where the herbicide or herbicide safener combination is as defined in one of the rows 1 .1 to
  • mixtures A-33.2.1 to A-33.2.3545 i.e. the mixtures of the compound of table A- 33, where R 2 and X are as defined in row 2 of table A and where the herbicide or herbicide safener combination is as defined in one of the rows 1.1 to 1 .3545 of table 1 ;
  • mixtures A-33.52.1 to A-33.52.3545 i.e. the mixtures of the compound of table A- 33, where R 2 and X are as defined in row 14 of table A and where the herbicide or herbicide safener combination is as defined in one of the rows 1 .1 to 1.3545 of table 1 ;
  • mixtures A-33.565.1 to A-33.565.3545 i.e. the mixtures of the compound of table A-33, where R 2 and X are as defined in row 565 of table A and where the herbicide or herbicide safener combination is as defined in one of the rows 1 .1 to 1 .3545 of table 1 ;
  • mixtures A-33.615.1 to A-33.615.3545 i.e. the mixtures of the compound of table A-33, where R 2 and X are as defined in row 615 of table A and where the herbicide or herbicide safener combination is as defined in one of the rows 1 .1 to
  • mixtures A-33.838.1 to A-33.838.3545 i.e. the mixtures of the compound of table A-33, where R 2 and X are as defined in row 838 of table A and where the herbicide or herbicide safener combination is as defined in one of the rows 1 .1 to 1 .3545 of table 1 ;
  • mixtures A-33.1 128.1 to A-33.1 128.3545 i.e. the mixtures of the compound of table A-33, where R 2 and X are as defined in row 1 128 of table A and where the herbicide or herbicide safener combination is as defined in one of the rows 1 .1 to 1 .3545 of table 1 ;
  • mixtures A-33.1401 .1 to A-33.1401 .3545 i.e. the mixtures of the compound of table A-33, where R 2 and X are as defined in row 1401 of table A and where the herbicide or herbicide safener combination is as defined in one of the rows 1 .1 to 1 .3545 of table 1 ; mixtures A-33.1691.1 to A-33.1691.3545, i.e. the mixtures of the compound of table A-33, where R 2 and X are as defined in row 1691 of table A and where the herbicide or herbicide safener combination is as defined in one of the rows 1.1 to 1.3545 of table 1;

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Agronomy & Crop Science (AREA)
  • Pest Control & Pesticides (AREA)
  • Plant Pathology (AREA)
  • Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Dentistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Wood Science & Technology (AREA)
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  • Agricultural Chemicals And Associated Chemicals (AREA)
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Abstract

La présente invention concerne des composés de diaminotriazine de formule (I) et leur utilisation comme herbicides. La présente invention concerne également des compositions agrochimiques pour la protection phytosanitaire et un procédé pour lutter contre toute végétation parasite.
PCT/EP2015/057370 2014-04-07 2015-04-02 Composé de diaminotriazine WO2015155129A1 (fr)

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Cited By (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN105820133A (zh) * 2016-03-25 2016-08-03 浙江工业大学 多取代均三嗪类化合物及其制备方法和应用
US9822105B2 (en) 2014-04-23 2017-11-21 Basf Se Diaminotriazine compounds as herbicides
US9822082B2 (en) 2014-04-11 2017-11-21 Basf Se Diaminotriazine derivatives as herbicides
US9999222B2 (en) 2014-04-23 2018-06-19 Basf Se Herbicidal combination comprising azines
US10023590B2 (en) 2014-04-17 2018-07-17 Basf Se Substituted pyridine compounds having herbicidal activity
US10029992B2 (en) 2014-04-23 2018-07-24 Basf Se Diaminotriazine compounds and their use as herbicides
US10167297B2 (en) 2014-10-24 2019-01-01 Basf Se Substituted pyridine compounds having herbicidal activity
US10479777B2 (en) 2013-07-16 2019-11-19 Basf Se Herbicidal azines
US10538782B2 (en) 2015-01-21 2020-01-21 Basf Se Plants having increased tolerance to herbicides
US10941122B2 (en) 2014-04-11 2021-03-09 Basf Se Diaminotriazine derivatives as herbicides
US11499162B2 (en) 2016-07-15 2022-11-15 Basf Se Plants having increased tolerance to herbicides
US11939587B2 (en) 2018-01-17 2024-03-26 Basf Se Plants having increased tolerance to herbicides

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US6069114A (en) * 1996-02-28 2000-05-30 Hoechst Schering Agrevo Gmbh 2-amino-4-bicycloamino-1,3,5-Triazines, their preparation, and their use as herbicide and plant growth regulators
WO2001017977A1 (fr) * 1999-09-09 2001-03-15 Nihon Bayer Agrochem K.K. 1,3,5-triazines utilises comme herbicides
WO2009049157A1 (fr) * 2007-10-11 2009-04-16 Smithkline Beecham Corporation Nouveaux inhibiteurs de seh et leur utilisation
WO2013102431A1 (fr) * 2012-01-06 2013-07-11 Agios Pharmaceuticals, Inc. Composés thérapeutiquement actifs et leurs procédés d'utilisation

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Cited By (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US10479777B2 (en) 2013-07-16 2019-11-19 Basf Se Herbicidal azines
US9822082B2 (en) 2014-04-11 2017-11-21 Basf Se Diaminotriazine derivatives as herbicides
US10941122B2 (en) 2014-04-11 2021-03-09 Basf Se Diaminotriazine derivatives as herbicides
US10023590B2 (en) 2014-04-17 2018-07-17 Basf Se Substituted pyridine compounds having herbicidal activity
US9822105B2 (en) 2014-04-23 2017-11-21 Basf Se Diaminotriazine compounds as herbicides
US9999222B2 (en) 2014-04-23 2018-06-19 Basf Se Herbicidal combination comprising azines
US10029992B2 (en) 2014-04-23 2018-07-24 Basf Se Diaminotriazine compounds and their use as herbicides
US10167297B2 (en) 2014-10-24 2019-01-01 Basf Se Substituted pyridine compounds having herbicidal activity
US10538782B2 (en) 2015-01-21 2020-01-21 Basf Se Plants having increased tolerance to herbicides
CN105820133A (zh) * 2016-03-25 2016-08-03 浙江工业大学 多取代均三嗪类化合物及其制备方法和应用
CN105820133B (zh) * 2016-03-25 2018-06-05 浙江工业大学 多取代均三嗪类化合物及其制备方法和应用
US11499162B2 (en) 2016-07-15 2022-11-15 Basf Se Plants having increased tolerance to herbicides
US11939587B2 (en) 2018-01-17 2024-03-26 Basf Se Plants having increased tolerance to herbicides

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