A Convenient Synthesis of Pyridoxine
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概要
- 論文の詳細を見る
A novel and convenient synthesis of pyridoxine starting from N-(1-cyanoethyl) formamide is described. The reaction of N-(1-cyanoethyl) acylamides with olefins in the presence of an acid catalyst gave 3-amino-2-methylpyridines. Similar reaction of N-(1-cyanoethyl) formamide with fumaronitrile in the presence of trifluoroacetic acid afforded 5-amino-6-methylpyridine-3,4-dicarbonitrile, which was easily converted to pyridoxine by reduction and diazotization.
- 公益社団法人日本薬学会の論文
- 1984-01-25
著者
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嶋田 定勝
Production Technology Research Laboratories Daiichi Seiyaku Co. Ltd.
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沖 正信
Production Technology Research Laboratories, Daiichi Seiyaku Co., Ltd.
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沖 正信
Research Laboratories of Production Technology, Daiichi Seiyaku Co., Ltd.
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沖 正信
Production Technology Research Laboratories Daiichi Seiyaku Co. Ltd.
関連論文
- Reaction of 1,2,4-Triazines with N-Phenylmaleimide(Organic,Chemical)
- A Convenient Synthesis of Pyridoxine
- Intramolecular Diels-Alder Reaction of Alkenyl Oxazole-5-carbamates and N-Alkenyl-oxazole-5-carboxamides
- A One-Pot Synthesis of 3-Aminopyridines