Ring Transformation Reactions of 1-Substituted 2 (1H)-Pyrimidinones and Related Compounds with Active Methylene Compounds
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概要
- 論文の詳細を見る
1-Substituted 2 (1H)-pyrimidinones (I) underwent ring transformation with malononitrile and ethyl acetoacetate in the presence of sodium ethoxide to give 2-amino-3-pyridinecarbonitriles (II-VII) and N-(substituted) amino-3-pyridinecarboxylic acids (XIV and XV), respectively. Further, I reacted with ethyl cyanoacetate, dialkyl malonate, or ethyl benzoylacetate to give pyridine derivatives (VIII-XIII) bearing various functional groups at the C-3 position. The reaction of 1-substituted 2 (1H)-pyrimidinethiones and 4,6-dimethyl-1-phenyl-2-phenylimino-1,2-dihydropyrimidine with active methylene compounds is also discussed.
- 公益社団法人日本薬学会の論文
- 1984-08-25
著者
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鹿島 長次
Department of Chemistry, University of Tsukuba
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表 美守
Department of Chemistry, University of Tsukuba
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表 美守
Department Of Chemistry University Of Tsukuba
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鹿島 長次
筑波大学化学系
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鹿島 長次
Department Of Chemistry University Of Tsukuba
関連論文
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- Ring Transformation Reactions of 1-Substituted 2 (1H)-Pyrimidinones and Related Compounds with Active Methylene Compounds
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