发明授权
EP0589034B1 METHOD FOR MAKING 3-ALPHA-HYDROXY,3-BETA-SUBSTITUTED-PREGNANES
失效
VERFARHREN为3-α-羟基的制剂,3-β取代的孕烷衍生物
- 专利标题: METHOD FOR MAKING 3-ALPHA-HYDROXY,3-BETA-SUBSTITUTED-PREGNANES
- 专利标题(中): VERFARHREN为3-α-羟基的制剂,3-β取代的孕烷衍生物
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申请号: EP93918762.1申请日: 1993-02-22
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公开(公告)号: EP0589034B1公开(公告)日: 1999-05-06
- 发明人: TAHIR, Syed, Hasan , BOLGER, Michael, Bruce , BUSWELL, Richard , GABRIEL, Richard , STEARNS, Jay
- 申请人: CoCensys, Inc.
- 申请人地址: 201 Technology Drive Irvine, CA 92618 US
- 专利权人: CoCensys, Inc.
- 当前专利权人: CoCensys, Inc.
- 当前专利权人地址: 201 Technology Drive Irvine, CA 92618 US
- 代理机构: Sexton, Jane Helen
- 优先权: US846193 19920304
- 国际公布: WO9318053 19930916
- 主分类号: C07J41/00
- IPC分类号: C07J41/00 ; C07J17/00 ; C07J43/00 ; C07J21/00 ; C07J7/00
摘要:
This invention provides a simplified method for converting pregnan-3,20-dione compounds to 3α-hydroxy,3β-substituted-pregnanes. By selective use of reagents the unprotected dione is converted chemoselectively and diastereoselectively into a 3(R)-pregnan-3-spiro-2'oxirane-20-one intermediate. This intermediate can then be converted regioselectively by a second set of reactions to the 3α-hydroxy,3β-substituted-20-one form, which can be further modified at the 20-keto position. Through this method, each ketone group is independently treated. By modifying the ketones one at a time, one can obtain the desired stereo-specificity at each site.
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