Propylamine → HCID 178457528、化合物
反応式
[OH:1][C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([NH:8][CH:9]=[N:10][C:11]#N)[N:3]=1.[CH2:13](N)[CH2:14]C>O>[OH:1][C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([NH:8][CH:9]=[N:10][CH2:11][CH2:13][CH3:14])[N:3]=1参加物
4
実験手順
2.3 g (14 mmol) of N-(2-hydroxy-6-pyridyl)-N'-cyanoformamidine are added in portions at room temperature over a period of 20 minutes to a stirred solution of 8.3 ml (99 mmol) of n-propylamine in 8 ml of water The reaction mixture is stirred for 2 hours at room temperature It is then extracted three times with chloroform The combined organic phases are dried over MgSO4 and concentrated by evaporation. The resulting crude product is chromatographed on silica gel with methylene chloride and then crystallised from ether/n-hexane. N-(2-pyridon-6-yl)-N'-propylformamidine and N-(2-hydroxy-6-pyridyl)-N'-propylformamidine having a melting point of 178°-179° are obtained.
後処理
- extractionis then extracted three times with chloroform The combined organic phases
- dry with materialare dried over MgSO4
- concentrationconcentrated by evaporation
- customThe resulting crude product is chromatographed on silica gel with methylene chloride
- customcrystallised from ether/n-hexane
出典と根拠
- ORDレコード
- ord-aad0c63e0b1e42f486e5574c2ef82aa0
- 出典データセット
- uspto-grants-1989_09
- 特許番号
- US04863938
反応ノート
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