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製備4,10β-二乙醯氧基-2α-苄醯氧基-5β,20-基-1,13α-二羥基-9-酮基-19-去環丙〔g〕紫杉-11-烯之方法
专利权人:
AVENTIS PHARMA S. A.
发明人:
DIDIER, ERIC,狄瑞克,AMOURET, GUY,安盖伊,安蓋伊
申请号:
TW093110164
公开号:
TWI360545B
申请日:
2004.04.13
申请国别(地区):
TW
年份:
2012
代理人:
摘要:
Preparation of taxoid compounds (I) comprises reacting an optionally protected taxene compound (II) with a molecular sieve base in sulfolane, condensing with a side chain, and removing protecting groups. Preparation of taxoid compounds of formula (I) comprises reacting an optionally protected taxene compound of formula (II) with a basic molecular sieve in sulfolane to cyclize the 7 beta -trifluoromethyl sulfonyloxy group, condensing with a side chain, and removing protecting groups. [Image] Ar : aryl; R : H, acetyl, alkoxyacetyl or alkyl; R 1benzoyl or R 2-O-CO; R 21-8C alkyl; R' : a protecting group when R in (I) is H, or R. An independent claim is also included for the preparation of intermediate compounds of formula (III) which comprises reacting (II) with a molecular sieve base in sulfolane. [Image] ACTIVITY : None given. MECHANISM OF ACTION : None given.從4-乙醯氧基-2 α-苄醯氧基-5β,20-環氧基-1,13 α-二羥基-9-酮基-7β-(三氟甲加磺基氧基)紫杉-11-烯與分子篩在碸茂烷中反應,製備4-乙醯氧基-2 α-苄醯氧基-5β,20-環氧基-1,13 α-二羥基-9-酮基-19-去環丙[g]紫杉-11-烯。
来源网站:
中国工程科技知识中心
来源网址:
http://www.ckcest.cn/home/

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