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Abstract
Reactions of pyridine (I, IV, X, XIII) or condensed pyridine (VII, XVI, XVIII) N-oxides with formamide were described. Although pyrimidinyl cyclization of active methyl group was unsuccessful, introduction of carbamoyl group at pyridine ring carbon adjacent to nitrogen atom was successful, i. e., 6-methylpyridine-2-(II), 4-methylpyridine-2-(V), 4-methylquinoline-2-(VIII), 5-methylpyridine-2-(XI), pyridine-2-(XIV), quinoline-2-(XVII), and isoquinoline-1-(XIX) carboxyamides were obtained.
Journal
- Chemical & pharmaceutical bulletin [List of Volumes]
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Chemical & pharmaceutical bulletin 25(5), 964-967, 1977-05-25 [Table of Contents]
The Pharmaceutical Society of Japan
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