首页> 外国专利> PROCESSES FOR PREPARING N-HETEROARYL-N-ARYL-AMINE BY REACTING N-ARYL CARBAMIC ACID ESTER WITH HALO-HETEROARYL, AND ANALOGOUS PROCESSES

PROCESSES FOR PREPARING N-HETEROARYL-N-ARYL-AMINE BY REACTING N-ARYL CARBAMIC ACID ESTER WITH HALO-HETEROARYL, AND ANALOGOUS PROCESSES

机译:与卤代杂芳烃反应N-芳基氨基甲酸酯和类似物的方法制备N-杂芳基-N-芳基胺的方法

摘要

PROBLEM TO BE SOLVED: To provide processes for producing diaryl amine compounds or salts thereof.SOLUTION: The present invention relates to processes for producing diaryl amine compounds of the formula (I) or salts thereof. The processes comprise coupling a compound of the formula (II) with an amine of the formula (III) in the presence of a transition metal catalyst or an alkali metal salt. Ar1 and Ar2 are independently Q; each Q is an aryl or heteroaryl ring system optionally fused to a saturated or unsaturated 5-8 membered ring having 0-4 heteroatoms; and Q is optionally substituted as defined in the claim 1. X is a leaving group; Y is -C(O)-O-Z; and Z is selected from C-Caliphatic, benzyl, Fmoc, -SOR' and Q, provided that Q is not substituted with X or alkyne; where R' is as defined in the claim 1.
机译:解决的问题:提供制备二芳基胺化合物或其盐的方法。解决方案:本发明涉及制备式(I)的二芳基胺化合物或其盐的方法。该方法包括在过渡金属催化剂或碱金属盐的存在下,将式(II)的化合物与式(III)的胺偶联。 Ar1和Ar2独立地为Q;每个Q为任选地稠合到具有0-4个杂原子的饱和或不饱和5-8元环上的芳基或杂芳基环系统; Q为离去基团;和Q为如权利要求1所定义的取代基。 Y为-C(O)-O-Z; Z选自C-脂族基,苄基,Fmoc,-SOR′和Q,条件是Q不被X或炔取代。其中R'如权利要求1所定义。

著录项

  • 公开/公告号JP2014133745A

    专利类型

  • 公开/公告日2014-07-24

    原文格式PDF

  • 申请/专利权人 VERTEX PHARMACEUTICALS INC;

    申请/专利号JP20140009078

  • 申请日2014-01-22

  • 分类号C07D213/74;C07D213/82;C07D213/80;C07B61;

  • 国家 JP

  • 入库时间 2022-08-21 16:18:47

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