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Halopredone acetate, Haloart

醋酸卤泼尼松 卤泼尼松 Chemical Name: 17,21-Bis(acetyloxy)-2-bromo-6beta,9-difluoro-11beta-hydroxypregna-1,4-diene-3,20-dione; 2-Bromo-6beta,9-difluoro-11beta,17,21-trihydroxypregna-1,4-diene-3,20-dione 17,21-diacetate
CAS No. 57781-14-3, 57781-15-4 (free acid)
项目整合开发状态: Launched-1988
项目研究机构: Taiho (Originator)
合成路线:The starting product being 21-acetoxy-11alpha,17alpha-dihydroxy-pregn-4-ene-3,20-dione (I).The first step is the ketalization of (I) giving the ethylenedioxy derivative (II),which is epoxidized with monoperphthalic acid (B) to the epoxide (III),then the epoxide ring is opened with HF giving the fluoro derivative (IV); its bromination in dioxane affords (V),which by reaction with methanesulfonyl chloride gives the mesyl ester (VI).This compound is acetylated with acetic anhydride to the triacetoxy derivative (VII),which by treatment first with sodium acetate and then with bromine gives the mono unsaturated dibromo compound (VIII).This product by treatment with lithium carbonate and lithium bromide is converted into the triene derivative (IX); this product by treatment with 1,3-dibromo-5,5-dimethylhydantoine (C) adds BrOH giving (X),which is epoxidized by treatment with potassium carbonate yielding (Xl).This epoxide ring is finally opened with HF.
📌 参考资料/链接:
参考文献标题:Halopredone diacetate
文献作者:Castar,J.; de Angelis,L.
参考来源:Drugs Fut 1976,1(11),526

📄 详细内容


合成路线:The starting product being 21-acetoxy-11alpha,17alpha-dihydroxy-pregn-4-ene-3,20-dione (I).The first step is the ketalization of (I) giving the ethylenedioxy derivative (II),which is epoxidized with monoperphthalic acid (B) to the epoxide (III),then the epoxide ring is opened with HF giving the fluoro derivative (IV); its bromination in dioxane affords (V),which by reaction with methanesulfonyl chloride gives the mesyl ester (VI).This compound is acetylated with acetic anhydride to the triacetoxy derivative (VII),which by treatment first with sodium acetate and then with bromine gives the mono unsaturated dibromo compound (VIII).This product by treatment with lithium carbonate and lithium bromide is converted into the triene derivative (IX); this product by treatment with 1,3-dibromo-5,5-dimethylhydantoine (C) adds BrOH giving (X),which is epoxidized by treatment with potassium carbonate yielding (Xl).This epoxide ring is finally opened with HF.
参考文献标题:2-Bromo-6beta-fluoropregna-1,4-3,20-diones
文献作者:Riva,M.; Toscano,L.
参考来源:BE 0826030; DE 2533377; ES 455934; FR 2261776; GB 1499822


产品链接: CAS No. 57781-14-3››

产品链接: CAS No.57781-15-4››