3-Oxoandrost-4-Ene-17β-Carboxylic Acid Chloride置于乙酸铵,Potassium Permanganate,Sodium Periodate,Sodium Carbonate体系中,用 水,溶剂黄146,叔丁醇 用作溶剂,化学反应 5.0H,反应生成N-叔丁基-3-酮-4-氮杂-5A-雄甾烯-17B-酰胺
参考文献:Synthesis Of N-Substituted 3-Oxo-17B-Carboxamide-4-Aza-5A-Androstanes And The Tautomerism Of 3-Oxo-4-Aza-5-Androstenes
标题:Synthesis Of N-Substituted 3-Oxo-17B-Carboxamide-4-Aza-5A-Androstanes And The Tautomerism Of 3-Oxo-4-Aza-5-Androstenes
摘要:An N-Aryl-3-Oxo-4-Aza-5 Alpha-Androst-1-Ene-17 Beta-Carboxamide And Three N-Aryl Or Alkyl Substituted 17 Alpha-Hydroxy-3-Oxo-4-Aza-5 Alpha-Androstane-17 Beta-Carboxamides Were Synthesized As Antiandrogen Candidates From 3-Oxoandrost-4-Ene-17 Beta-Carboxylic Acid And Androst-4-Ene-3,17-Dione Respectively. The Chemo-And Stereoselective Reduction Of 3-Oxo-4-Aza-5-Ene Intermediates With Formic Acid And Their Tautomerism In A Solution Of Chloroform And Methanol Were Described.
Doi:10.3987/com-97-S(N)35