Studies on 3,5-Dioxopiperidines and Related Compounds : Synthesis of 5-(3-tert-Butylamino-2-hydroxy) propoxy-1,2,3,4-tetrahydro-2-oxo-1,7-naphthyridine
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概要
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The 7-aza analog (1・HCl) of 5-(3-tert-butylamino-2-hydroxy) propoxy-3,4-dihydrocarbostyril・hydrochloride (2・HCl, carteolol・HCl) was prepared as part of a search for new adrenergic receptor antagonists. Thermal treatment of 1-acetyl-3-benzylamino-5-oxo-3,4-dehydropiperidine (3), derived from N-acetylpiperidine-3,5-dione (4a) by treatment with acryloyl chloride, gave 7-acetyl-1-benzyl-2,5-dioxo-1,2,3,4,5,6,7,8-octahydro-1,7-naphthyridine (7). Dehydrogenation of 7 on 5% palladium carbon, and subsequent reductive debenzylation with liquid ammonia and sodium gave 5-hydroxy-1,2,3,4-tetrahydro-2-oxo-1,7-naphthyridine (5). Alkylation of 5 with epichlorohydrin, treatment with alkali and amination with tert-butylamine gave 5-(3-tert-butylamino-2-hydroxy)-propoxy-1,2,3,4-tetrahydro-2-oxo-1,7-naphthyridine・hydrochloride (1・HCl) in 45% overall yield from 5.
- 公益社団法人日本薬学会の論文
- 1981-09-25
著者
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田村 恭光
Faculty Of Pharmaceutical Sciences Osaka University
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藤田 昌宣
Faculty Of Pharmaceutical Sciences Osaka University
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陳 麟慶
Faculty Of Pharmaceutical Sciences Osaka University
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北 泰行
Faculty Of Pharmaceutical Sciences Osaka University
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清川 博
Faculty Of Pharmaceutical Sciences Osaka University
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