Studies on the Heterocyclic Compounds. XX. The Reaction of 4-Cyano-3,6-dichloropyridazine with Amines
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概要
- 論文の詳細を見る
4-Cyano-3,6-dichloropyridazine (II) was treated with primary amines in methanol under mild condition (stirring at 0-5°) to give neither the corresponding 3- nor 6-amino derivatives but the corresponding 5-amino derivatives (XVd-m) resulting from nuclear amination. However, when compound II was treated with secondary amines, the corresponding 3- or 6-amino derivatives were obtained.
- 公益社団法人日本薬学会の論文
- 1977-07-25
著者
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梁井 光二
Faculty Of Pharmaceutical Sciences Nagasaki University
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武田 成子
Faculty of Pharmaceutical Sciences, Nagasaki University
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光岡 玉雄
Faculty of Pharmaceutical Sciences, Nagasaki University
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光岡 玉雄
Faculty Of Pharmaceutical Sciences Nagasaki University
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武田 成子
Faculty Of Pharmaceutical Sciences Nagasaki University
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梁井 光二
Faculty of Pharmaceutical Sciences, Nagasaki University
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