反応式
O.[NH2:2][NH2:3].O.Cl[C:6]1[CH:11]=[CH:10][C:9]([N+:12]([O-:14])=[O:13])=[CH:8][N:7]=1>C(O)C>[NH:2]([C:6]1[CH:11]=[CH:10][C:9]([N+:12]([O-:14])=[O:13])=[CH:8][N:7]=1)[NH2:3]参加物
5
実験手順
To a stirred solution of hydrazine hydrate (30.0 equivalents), water (4 ml/gm of pyridine), and ethanol (2 ml/gm of pyridine) was added 2-chloro-5-nitropyridine (1 equivalent). The reaction mixture was stirred at 20° for 16 hours (a very thick green slurry forms). The precipitate was isolated by filtration and the solid was washed with methanol and then ether to give a green solid. The product was used without further purification; yield 77.3%; m.p. 205°-207°. IR {KBr): 3340, 3200, 2980, 1670, 1605, 1580, 1485, 1420, 1330, 1300, 1120, 980, 830, 770 cm-1.
後処理
- customThe precipitate was isolated by filtration
- washthe solid was washed with methanol
- customether to give a green solid
- customThe product was used without further purification
出典と根拠
- ORDレコード
- ord-4c57f95f2e1b4fcc8dd9b527d8bf30de
- 出典データセット
- uspto-grants-1995_05
- 特許番号
- US05420285
関連ノート
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