Diaminotriazine derivatives as herbicides

    公开(公告)号:US09822082B2

    公开(公告)日:2017-11-21

    申请号:US15302733

    申请日:2015-04-09

    Applicant: BASF SE

    CPC classification number: C07D251/18 A01N43/68 C07D251/48

    Abstract: The present invention relates to diaminotriazine compounds of the formula (I) 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. wherein A is phenyl, which is substituted by fluorine in the ortho-position and which may additionally carry 1, 2, 3 or 4 identical or different substituents RA; R1, R2 are inter alia H, OH, S(O)2NH2, CN, C1-C6-alkyl, C2-C6-alkenyl, etc. R3 is selected from the group consisting of C1-C6-alkyl, C2-C6-alkenyl, C2-C6-alkynyl, (C3-C6-cycloalkyl)-C1-C4-alkyl, (C1-C6-alkoxy)-C1-C6-alkyl, (C1-C6-alkyl)carbonyl, (C1-C6-alkoxy)carbonyl, (C1-C6-alkylamino)carbonyl and di(C1-C6-alkyl)aminocarbonyl, where the aliphatic and cycloaliphatic parts of the 9 aforementioned radicals are unsubstituted, partly or completely halogenated, R4 and R5, together with the carbon atom, to which they are bound form a saturated 3-, 4-, 5- or 6-membered carbocyclic radical or a saturated 3-, 4-, 5- or 6-membered heterocyclic radical, where the carbocyclic radical and the heterocyclic radical are unsubstituted, partly or completely halogenated or carry from 1 to 6 C1-C6-alkyl groups; including their agriculturally acceptable salts.

    Diaminotriazine derivatives as herbicides

    公开(公告)号:US10941122B2

    公开(公告)日:2021-03-09

    申请号:US15302681

    申请日:2015-04-09

    Applicant: BASF SE

    Abstract: The present invention relates to diaminotriazine compounds of the formula (I) 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. wherein q is 0, 1, 2 or 3 Ra is selected from the group consisting of C1-C6-haloalkoxy, C1-C6-haloalkylthio, (C1-C6-haloalkyl)sulfinyl, (C1-C6-haloalkyl)-carbonyl, etc.; Rb is selected from the group consisting of halogen, OH, CN, amino, NO2, C1-C6-alkyl, C2-C6-alkenyl, C2-C6-alkynyl, C1-C6-alkoxy, etc.; R1 is selected from the group consisting of H, OH, S(O)2NH2, CN, C1-C6-alkyl, C2-C6-alkenyl, C2-C6-alkynyl, (C3-C6-cycloalkyl)-C1-C4-alkyl, etc.; R2 is selected from the group consisting of H, OH, S(O)2NH2, CN, C1-C6-alkyl, C2-C6-alkenyl, C2-C6-alkynyl, (C3-C6-cycloalkyl)-C1-C4-alkyl, etc.; R3 is selected from the group consisting of H, halogen, OH, CN, C1-C6-alkyl, (C1-C6-alkoxy)-C1-C6-alkyl, C3-C6-cycloalkyl, etc.; R4 is H, halogen, CN, C1-C6-alkyl, C1-C6-haloalkyl, C3-C6-cycloalkyl, C3-C6-halocycloalkyl, C1-C6-alkoxy and C1-C6-haloalkoxy; R5 is selected from the group consisting of halogen, CN, C1-C6-alkyl, C2-C6-alkenyl, C3-C6-alkynyl, C3-C6-cycloalkyl, etc.; or R4 and R5 together with the carbon atom to which they are attached form a moiety selected from the group consisting of carbonyl, C3-C6-cycloalkan-1,1-diyl, ipso-C3-C6-cycloalkendiyl, three- to six-membered saturated or partially unsaturated ipso-heterocyclodiyl; including their agriculturally acceptable salts.

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