SUBSTITUIERTE 2,4-DIAMINO-1,3,5-TRIAZINE ALS HERBIZIDE
    4.
    发明公开
    SUBSTITUIERTE 2,4-DIAMINO-1,3,5-TRIAZINE ALS HERBIZIDE 失效
    取代基2,4-二氨基-1,3,5-三嗪ALS HERBIDE

    公开(公告)号:EP0932605A1

    公开(公告)日:1999-08-04

    申请号:EP97910379.0

    申请日:1997-09-29

    摘要: The invention relates to a novel substituted 2,4-diamino-1,3,5-triazine of the general formula (I), in which R1 stands for hydrogen or for optionally substituting alkyl, R2 stands for formyl or for optionally substituting alkylcarbonyl, alkoxycarbonyl, alkylsulfonyl, arylcarbonyl or arysulfonyl respectively, R3 for optionally substituting alkyl or cycloalkyl respectively, R4 for hydrogen or alkyl, A for oxygen or methylene, Ar for optionally substituting aryl or heterocyclyl respectively and Z for hydrogen, hydroxy, cyano, nitro, halogen or for optionally substituted alkyl, alkoxy, alkylcarbonyl, alkoxycarbonyl, alkylthio, alkylsulfinyl, alkylsulfonyl, alkenyl or alkinyl respectively (in which three previously known combinations are excluded). The disclosure also relates to a method and to new intermediate products for producing the new compounds and their use as herbicides.

    摘要翻译: 本发明涉及通式(I)的新型取代的2,4-二氨基-1,3,5-三嗪,其中R1代表氢或任选地取代烷基,R2代表甲酰基或任选取代烷基羰基, 烷氧基羰基,烷基磺酰基,芳基羰基或芳基磺酰基,R3分别任选地取代烷基或环烷基,R4为氢或烷基,A为氧或亚甲基,Ar分别任选地分别取代芳基或杂环基,Z取代为氢,羟基,氰基,硝基,卤素 或分别用于任选取代的烷基,烷氧基,烷基羰基,烷氧基羰基,烷硫基,烷基亚磺酰基,烷基磺酰基,烯基或炔基(其中排除三种先前已知的组合)。 本公开还涉及用于生产新化合物及其作为除草剂的用途的新方法和新中间产物。

    VERFAHREN ZUR HERSTELLUNG VON HETEROCYCLISCHEN VERBINDUNGEN
    10.
    发明公开
    VERFAHREN ZUR HERSTELLUNG VON HETEROCYCLISCHEN VERBINDUNGEN 有权
    工艺制备杂环化合物

    公开(公告)号:EP1252159A1

    公开(公告)日:2002-10-30

    申请号:EP01900395.3

    申请日:2001-01-08

    IPC分类号: C07D417/06

    CPC分类号: C07D401/06 C07D417/06

    摘要: The invention relates to a method for producing compounds of formula (I), in which R1, A, D, X and Z are defined as per the description, by reacting compounds of formula (II), in which A, D and X are defined as above, with a base in the presence of a thinning agent. The reaction mixture is then reacted with the mixture of CCMP/CMP (2-chloro-5-chloromethylpyridine/2-chloro-5-methylpyridine) and the appropriate hydrochlorides.