;Also provided is a process for its preparation based on the stereoselective epoxidation of the corresponding olefin precursor and a process for the preparation of several pharmaceutically active ingredients comprising the preparation of the compound of formula (II)."/> PROCESS FOR THE PREPARATION OF AN INTERMEDIATE FOR THE SYNTHESIS OF I.A. CARFILZOMIB
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PROCESS FOR THE PREPARATION OF AN INTERMEDIATE FOR THE SYNTHESIS OF I.A. CARFILZOMIB

机译:I.A.合成中间体的制备方法卡非佐米

摘要

The present invention provides a compound which is the trichloroacetic acid salt of a compound of Formula (II) wherein R is selected from the group consisting of H, CH3-, (CH3)2CH-, (CH3)2CHCH2-, CH3CH2CH(CH3)-, and PhCH2-, and a process for its preparation.;Also provided is a process for its preparation based on the stereoselective epoxidation of the corresponding olefin precursor and a process for the preparation of several pharmaceutically active ingredients comprising the preparation of the compound of formula (II).
机译:本发明提供了一种化合物,该化合物是式(II)化合物的三氯乙酸盐,其中R选自H,CH 3 -Sub,-CH 3-。 Sub>) 2 CH-,(CH 3 2 CHCH 2 -,CH 3 < / Sub> CH 2 CH(CH 3 )-和PhCH 2 -及其制备方法。 <图像文件=“ IMGA0001.GIF” he =“ 28” imgContent =“ chem” imgFormat =“ GIF” wi =“ 30” /> ;还提供了用于其基于相应烯烃前体的立体选择性环氧化的制备,以及几种药物活性成分的制备方法,包括式(II)化合物的制备。

著录项

  • 公开/公告号EP3330260A1

    专利类型

  • 公开/公告日2018-06-06

    原文格式PDF

  • 申请/专利权人 ENANTIA S.L.;

    申请/专利号EP20160382582

  • 申请日2016-12-01

  • 分类号C07D303/12;

  • 国家 EP

  • 入库时间 2022-08-21 13:14:54

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