Chemical and Pharmaceutical Bulletin
Online ISSN : 1347-5223
Print ISSN : 0009-2363
ISSN-L : 0009-2363
Condensed Heteroaromatic Ring Systems. III. Synthesis of Naphthyridine Derivatives by Cyclization of Ethynylpyridinecarboxamides
坂本 尚夫根東 義則山中 宏
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キーワード: 1 (2H)-isoquinolone
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1985 年 33 巻 2 号 p. 626-633

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Four kinds of naphthyridinones, i.e. 1, 6-naphthyridin-5-one, 1, 7-naphthyridin-8-one, 2, 6-naphthyridin-2-one, and 2, 7-naphthyridin-1-one derivatives, were commonly synthesized by the intramolecular cyclization of pyridinecarboxamides having an ethynyl group or β, β-dimethoxyethyl group adjacent to the carbamoyl group. The syntheses of the starting pyridine derivatives were easily accomplished by cross-coupling of the corresponding halopyridines with acetylenes.

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© The Pharmaceutical Society of Japan
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