首页> 外文期刊>Indian Journal of Chemistry, Section B. Organic Including Medicinal >Stereoselective synthesis of steroidal (3/R)-spiro-DELTA~2-1',3',4'-oxadiazoline
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Stereoselective synthesis of steroidal (3/R)-spiro-DELTA~2-1',3',4'-oxadiazoline

机译:甾体(3 / R)-螺-DELTA〜2-1',3',4'-恶二唑啉的立体选择性合成

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摘要

Heterocyclic system namely cholest-5-en-(3r)-spiro-DELTA~2 -1',3',4'-oxadiazoline 3 has been synthesized via the reaction of cholest-5-en-3-one semicarbazone 2 with acetic anhydride and pyridine at 80(deg C),in high yield. Cholest-5-en-3-one semicarbazone 2 is obtained by the condensation of cholest-5-en-3-one 1 with semicar-bazide hydrochloride. The products 2 and 3 are characterized by their physical,analytical and spectral(IR,~1H NMR)data.
机译:通过胆甾-5-烯-3-酮半脲酮2与乙酸的反应合成了杂环体系,即胆甾-5-烯-(3r)-螺-DELTA〜2 -1',3',4'-恶二唑啉3在80℃下以较高的产率得到酸酐和吡啶。 Cholest-5-en-3-one缩氨基脲2是通过cholest-5-en-3-one 1与半碳化肼盐酸盐的缩合反应制得的。产物2和3的特征在于其物理,分析和光谱(IR,〜1H NMR)数据。

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