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CARBOXAMIDE COMPOUNDS, METHOD OF SYNTHESIS OF CARBOXAMIDE COMPOUNDS, INTERMEDIATE COMPOUNDS AND METHODS OF THEIR SYNTHESIS

机译:羧酰胺化合物,羧酰胺化合物的合成方法,中间体化合物及其合成方法

摘要

FIELD: organic chemistry. SUBSTANCE: product: derivatives of indanylamine of the general formula (I) where R1 is optional substituted alkyl-group, and R2, R3 and R4 - independently hydrogen atom or optional substituted alkyl-group. Method involves stages of hydrogenation of compound of the general formula (II) where R1, R2, R3 and R4 - as indicated above, and R5 and R6 - independently halogen atom, hydroxyl, nitro- or cyano-group, or optional substituted alkyl, alkoxy, alkoxycarbonyl, alkylcarboxy or alkylamino-group at condition that R5 and R6 are different atoms and groups followed by their rearrangement and transformation. Compounds of the formula (I) can be used for synthesis of preferable stereoisomers of fungicide N-indanylcarboxamide compounds. EFFECT: improved method of synthesis.
机译:领域:有机化学。物质:产品:通式(I)的茚满胺的衍生物<图像文件=“ 00000001.GIF” he =“ 33” id =“ imag0.1” imgContent =“ undefined” imgFormat =“ GIF” wi =“ 30” />其中R 1 是可选的取代烷基,R 2 ,R 3 和R 4 -独立地为氢原子或任选取代的烷基。该方法涉及通式(II)化合物的氢化步骤。<图像文件=“ 00000002.GIF” he =“ 39” id =“ imag0.2” imgContent =“ undefined” imgFormat =“ GIF” wi =“ 28” />其中,R 1 ,R 2 ,R 3 和R 4 -如上所述,R < Sup> 5 和R 6 -独立地为卤素原子,羟基,硝基或氰基,或在R <=的情况下可选的取代的烷基,烷氧基,烷氧基羰基,烷基羧基或烷基氨基Sup> 5 和R 6 是不同的原子和基团,随后分别进行重排和转化。公式(I)的化合物可用于合成杀真菌剂N-茚满羧酰胺化合物的优选立体异构体的制备。效果:改进的合成方法。

著录项

  • 公开/公告号RU94037966A

    专利类型

  • 公开/公告日1996-08-10

    原文格式PDF

  • 申请/专利权人 SHELL INTERNEHSHNL RISERCH MAATSKHAPPIJ B.V.;

    申请/专利号RU19940037966

  • 发明设计人 POL GOVARD BRAJNER;

    申请日1994-10-21

  • 分类号C07D275/03;C07D277/56;C07D285/06;C07D307/68;

  • 国家 RU

  • 入库时间 2022-08-22 03:43:49

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