首页> 外国专利> A procedure for preparing alkylated Derivatives of benzoic acid in Ortho position and the use of acid 4-chloro-2 - metilbenzoico, prepared according to the procedure,As an intermediate in the synthesis of N - diaminometilen - 2-methyl-4 - (1 - pirrolil) - 5 - metilsulfonilbenzamida and N - Day

A procedure for preparing alkylated Derivatives of benzoic acid in Ortho position and the use of acid 4-chloro-2 - metilbenzoico, prepared according to the procedure,As an intermediate in the synthesis of N - diaminometilen - 2-methyl-4 - (1 - pirrolil) - 5 - metilsulfonilbenzamida and N - Day

机译:一种制备邻位苯甲酸烷基化衍生物的方法,以及使用根据该方法制备的酸4-氯​​-2-甲基苯并甲酸酯作为合成N-二氨基Metilen-2-甲基-4-的中间体(1 -吡咯尔)-5-甲磺胺和氨氮-天

摘要

A procedure for preparing alkylated Derivatives of benzoic acid in Ortho position corresponding to formula (1) wherein a represents a rest dealquilo 1 to 4 c Atoms.Characterised by a reaction of aryl bromide Lafo, as indicated in formula (2) which have the meaning indicated for laformula (1) with a compound of organolithium Reagents and Secondary or TertiaryCO2.The use of acid - 2 - methyl 4-chloro benzoic acid, prepared under the procedimientodescripto,As productointermed Io in the synthesis of N - methyl - 2 - diaminometilen - (1 - pirrolil) - 5 -) - benzamide and N - diaminometilen - 2 - methyl - 5 - Di - (methylsulphonyl) - benzamide.
机译:一种制备对应于式(1)的邻位苯甲酸烷基化衍生物的方法,其中a代表1至4个c的剩余脱除原子。其特征在于如式(2)所示的芳基溴化物Lafo的反应指出在式(1)中与有机锂试剂和仲或叔CO 2的化合物一起使用。在过程亚甲基二茂铁上合成的过程中,使用酸-2-甲基4-氯苯甲酸作为产物中间体,用于合成N-甲基-2-二氨基甲酮-(1-吡咯尔)-5-)-苯甲酰胺和N-二氨基甲并基-2-甲基-5-二-(甲基磺酰基)-苯甲酰胺。

著录项

  • 公开/公告号AR020620A1

    专利类型

  • 公开/公告日2002-05-22

    原文格式PDF

  • 申请/专利号AR1999P103626

  • 发明设计人

    申请日1999-07-23

  • 分类号C07C63/04;C07D295/155;

  • 国家 AR

  • 入库时间 2022-08-22 00:46:28

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