Synthesis of 17α-Acetoxy-6-chloro-2α, 3β-dihydroxy-4,6-pregnadien-20-one, a Metabolite of Chlormadinone Acetate
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概要
- 論文の詳細を見る
For the purpose of identifying a urinary metabolite of 17α-acetoxy-6-chloro-4,6-pregnadiene-3,20-dione (I, chlormadinone acetate) in the rabbit, 17α-acetoxy-6-chloro-2α, 3β-dihydroxy-4,6-pregnadien-20-one (V), which was found to be identical with the metabolite, was synthesized from I. The starting material (I) was converted to the 2α-and 2β-acetoxy compounds (II and III) on heating with lead tetraacetate in acetic acid. When II and III were reduced with sodium borohydride in anhydrous isopropanol, two 2,3-dihydroxy compounds (V and VI) were produced. These two diols were found to be 2α, 3β-diol (V) and 2β, 3β-diol (VI), It was also found that both diols formed acetonides. 17β-acetoxy-4-androstene-2α, 3β-diol (XIII) could be also transformed into the acetonide.
- 公益社団法人日本薬学会の論文
- 1973-06-25
著者
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神戸川 明
Department Of Obstetrics And Gynecology School Of Medicine Teikyo University
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神戸川 明
Research Division, Teikoku Hormone Mfg. Co.
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阿部 達也
Research Division Teikoku Hormone Mfg. Co. Ltd.:(present Address)department Of Chemistry Faculty Of
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- Synthesis of 17α-Acetoxy-6-chloro-2α, 3β-dihydroxy-4,6-pregnadien-20-one, a Metabolite of Chlormadinone Acetate
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