CN106146503A — 一种Idelalisib的制备方法
Assigned to Shanghai Institute of Pharmaceutical Industry · Expires 2016-11-23 · 9y expired
What this patent protects
本发明公开了一种新的Idelalisib制备方法,该方法包括1)6-氯-9-(四氢-2-吡喃基)-嘌呤和(S)-2-(1-氨基-丙基)-5-氟-3-苯基-3H-喹唑啉-4-酮发生亲核取代反应得到(S)-5-氟-3-苯基-2-{1-[(9-四氢-2H-吡喃-2-基)-9H-嘌呤-6-基氨基]丙基}-3H-喹唑啉-4-酮;2)将第一步产物在盐酸乙醇中脱保护得到Idelalisib。本发明方法收率远高于现有技术,且后处理简单,只需要萃取和重结晶即可得到纯的Idelalisib,适于工业化生产。
USPTO Abstract
本发明公开了一种新的Idelalisib制备方法,该方法包括1)6-氯-9-(四氢-2-吡喃基)-嘌呤和(S)-2-(1-氨基-丙基)-5-氟-3-苯基-3H-喹唑啉-4-酮发生亲核取代反应得到(S)-5-氟-3-苯基-2-{1-[(9-四氢-2H-吡喃-2-基)-9H-嘌呤-6-基氨基]丙基}-3H-喹唑啉-4-酮;2)将第一步产物在盐酸乙醇中脱保护得到Idelalisib。本发明方法收率远高于现有技术,且后处理简单,只需要萃取和重结晶即可得到纯的Idelalisib,适于工业化生产。
Drugs covered by this patent
Bibliographic data sourced from FDA Orange Book + USPTO public records. Plain-English summary generated by AI grounded in source text. Patent term extensions (PTR, SPC, pediatric) may shift the effective expiry. Not legal advice.
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