48.
    发明专利
    未知

    公开(公告)号:DE502004005772D1

    公开(公告)日:2008-01-31

    申请号:DE502004005772

    申请日:2004-12-01

    Applicant: BASF AG

    Abstract: A process is described for preparing 3-phenyl(thio)uracils or 3-phenyldithiouracils of the formula I, by reacting a phenyl iso(thio)cyanate of the formula II with an enamine of the formula III and, if appropriate, in a further step, the resulting 3-phenyl(thio)uracil or 3-phenyldithiouracil of the formula I where R1=R1a, when R1=hydrogen, is reacted with an aminating agent of the formula IV to give 3-phenyl(thio)uracils or 3-phenyldithiouracils of the formula I where R1=amino where the variables R1, R1a, R2, R3, R4, X1, X2, X3, Ar, A and L1 are each as defined in claim 1.

    49.
    发明专利
    未知

    公开(公告)号:BRPI0417052A

    公开(公告)日:2007-02-06

    申请号:BRPI0417052

    申请日:2004-12-01

    Applicant: BASF AG

    Abstract: A process is described for preparing 3-phenyl(thio)uracils or 3-phenyldithiouracils of the formula I, by reacting a phenyl iso(thio)cyanate of the formula II with an enamine of the formula III and, if appropriate, in a further step, the resulting 3-phenyl(thio)uracil or 3-phenyldithiouracil of the formula I where R1=R1a, when R1=hydrogen, is reacted with an aminating agent of the formula IV to give 3-phenyl(thio)uracils or 3-phenyldithiouracils of the formula I where R1=amino where the variables R1, R1a, R2, R3, R4, X1, X2, X3, Ar, A and L1 are each as defined in claim 1.

    50.
    发明专利
    未知

    公开(公告)号:BR0315932A

    公开(公告)日:2005-09-13

    申请号:BR0315932

    申请日:2003-10-29

    Applicant: BASF AG

    Abstract: Bifunctional phenyl iso(thio)cyanate derivatives (I) are new. Also new are aniline and nitrobenzene derivative intermediates (II) and (V). Bifunctional phenyl iso(thio)cyanate derivatives of formula W=C=N-Ar-CO-NH-SO 2-A (I) are new. W : O or S; Ar : phenylene (optionally substituted by one or more of halo, 1-4C haloalkyl and CN), and A : NH 2 or the residue of a primary or secondary amine. Independent claims are also included for: (a) preparation of (I); (b) new aniline and nitrobenzene derivative intermediates of formulae H 2N-Ar-CO-NH-SO 2-A (II) and O 2N-Ar-CO-NH-SO 2-A (V), and (c) preparation of 4-(sulfamidocarbonyl-phenyl)-1,2,4-triazolinedione derivatives of formula (VI) by reacting an ester of diaza-ester of formula R 4>-NH-NR 3>-C(W')OR' (VII) and cyclizing the obtained urea derivative of formula R'O-C(=W')-N(R 3>)-N(R 4>)-C(=W)-NH-Ar-CO-NH-SO 2-A (VIII). [Image] W' : O or S; R 3>, R 4> : H, CN, NH 2, 1-6C alkyl, 1-6C haloalkyl, 1-6C alkoxy, 1-6C haloalkoxy, 3-7C cycloalkyl, 2-6C alkenyl, 2-6C haloalkenyl, 3-6C alkynyl, benzyl, OR 5> or (1-3C) cyanoalkyl, or R 3> + R 4> : a group completing 4-7 membered heterocyclyl optionally interrupted by S, O, NR 6> or N and optionally substituted by one or more of halo or 1-4C alkyl; R 5> : H, 1-6C alkyl, 1-6C haloalkyl, 3-7C cycloalkyl, 2-6C alkenyl, 3-6C alkynyl, optionally substituted phenyl or optionally substituted benzyl; R 6> : H, 1-6C alkyl, 3-6C alkenyl or 3-6C alkynyl, and R' : 1-4C alkyl. ACTIVITY : Herbicide. MECHANISM OF ACTION : None given.

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