Derivatives of Thiazolo [3,2-α] benzimidazole (Studies on Heterocyclic Compounds. II)
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概要
- 論文の詳細を見る
Depending upon reaction conditions, 2-mercaptobenzimidazole (I) treated with α-chloroacetaldehyde dimethylacetal under acidic or with ethylene dichloride under alkaline conditions undergo cyclization (V and VIII). Thioethers (IX and XI) are treated with acetic anhydride in pyridine to yield 2-alkyl-3-oxothiazolidino [3,2-α] benzimidazoles (X) and p-substituted 3-phenylthiazolo [3,2-α] benzimidazoles (XII).
- 社団法人日本薬学会の論文
- 1968-11-25
著者
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島田 靖子
College Of Pharmaceutical Sciences Kitasato University
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小倉 治夫
College of Pharmaceutical Sciences, Kitasato University
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伊東 常男
College of Pharmaceutical Sciences, Kitasato University
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伊東 常男
School Of Pharmaceutical Sciences Kitasato University
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