首页> 外国专利> PREPARATION PROCEDURE OF 4.10 BETA-DIACETOXI-2 ALFA-BENZOILOXI-5 BETA 20-EPOXI-1,13 ALFA-DIHIDROXI-9-OXO-19-NORCICLOPROPA (G) TAX-11-ENO.

PREPARATION PROCEDURE OF 4.10 BETA-DIACETOXI-2 ALFA-BENZOILOXI-5 BETA 20-EPOXI-1,13 ALFA-DIHIDROXI-9-OXO-19-NORCICLOPROPA (G) TAX-11-ENO.

机译:4.10 BETA-DIACETOXI-2 ALFA-BENZOILOXI-5 BETA 20-EPOXI-1,13 ALFA-DIHIDROXI-9-OXO-19-NORCICLOPROPA(G)TAX-11-ENO的制备程序。

摘要

Process for preparing the compound of formula (I) (See formula) in which: Ar represents an aryl radical, R represents a hydrogen atom or an acetyl, alkoxyacetyl or alkyl radical, R1 represents a benzoyl radical or an R2-O radical -CO- in which R2 represents a linear or branched alkyl radical containing from 1 to 8 carbon atoms. by a procedure that consists in contacting the compound of formula (II) (See formula) in which R '' is a protective group of the hydroxyl function when in formula (I) R represents hydrogen or one of the groups mentioned for R with a weak base chosen among the molecular sieves, then successively or previously condense a precursor of the side chain and finally protect the optionally protected hydroxyl functions, characterized in that the cyclopropaneation reaction takes place in the sulfolane.
机译:式(I)化合物的制备方法(参见式),其中:Ar表示芳基,R表示氢原子或乙酰基,烷氧基乙酰基或烷基,R1表示苯甲酰基或R2-O基-CO -其中R 2表示含有1至8个碳原子的直链或支链烷基。通过使式(II)的化合物(参见式)(其中R″是羟基官能团的保护基,当​​在式(I)中R代表氢或对于R提及的基团之一与式(II)的化合物接触时,从分子筛中选择弱碱,然后相继或预先缩合侧链的前体并最终保护任选保护的羟基官能团,其特征在于环丙烷化反应在环丁砜中进行。

著录项

  • 公开/公告号ES2302008T3

    专利类型

  • 公开/公告日2008-07-01

    原文格式PDF

  • 申请/专利权人 AVENTIS PHARMA S.A.;

    申请/专利号ES20040742484T

  • 发明设计人 DIDIER ERIC;AMOURET GUY;

    申请日2004-04-13

  • 分类号C07D305/14;

  • 国家 ES

  • 入库时间 2022-08-21 20:04:15

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