反応式
[CH:1]1[N:5]=[CH:4][NH:3][C:2]=1[CH2:6][CH2:7][NH2:8].Cl[C:10]1[C:15]([N+:16]([O-:18])=[O:17])=[CH:14][CH:13]=[CH:12][N:11]=1>CC(O)C>[NH:5]1[CH:1]=[C:2]([CH2:6][CH2:7][NH:8][C:10]2[C:15]([N+:16]([O-:18])=[O:17])=[CH:14][CH:13]=[CH:12][N:11]=2)[N:3]=[CH:4]1参加物
4
実験手順
1.14 g (10.2 mmol) of histamine base and 1.62 g (10.2 mmol) of 2-chloro-3-nitropyridine are brought to reflux in 5 ml of 2-propanol for 3 h. Evaporation of the solvent under reduced pressure and purification of the solid residue by chromatography on a column of silica gel, eluted with chloroform containing increasing amounts of methanol (5, 10 and 20%), provide the title compound. M.p.: 178°-180° C. (yield 65%; ethanol:water).
後処理
- customEvaporation of the solvent
- customunder reduced pressure and purification of the solid residue by chromatography on a column of silica gel
- washeluted with chloroform containing
- temperatureincreasing amounts of methanol (5, 10 and 20%)
出典と根拠
- ORDレコード
- ord-82a4e4fab68b49b09087fd77473ed05a
- 出典データセット
- uspto-grants-1996_09
- 特許番号
- US05559113
関連ノート
読み込み中…