反応式
[NH2:1][C:2]1[CH:7]=[C:6]([CH3:8])[CH:5]=[CH:4][N:3]=1.[C:9](OC(=O)C)(=[O:11])[CH3:10]>C(O)(=O)C>[C:9]([NH:1][C:2]1[CH:7]=[C:6]([CH3:8])[CH:5]=[CH:4][N:3]=1)(=[O:11])[CH3:10]参加物
4
実験手順
To a solution of 2-amino-4-methylpyridine (20 g) in acetic acid (80 ml) was added acetic anhydride and the resulting solution was refluxed for 3 h. The solution was concentrated in vacuo and the solid obtained was triturated with about 50 ml of water and carefully neutralised with solid sodium bicarbonate. The solid was filtered, washed with water and dried under vacuum to give the crude title compound as a white solid (20 g).
後処理
- temperaturethe resulting solution was refluxed for 3 h
- concentrationThe solution was concentrated in vacuo
- customthe solid obtained
- customwas triturated with about 50 ml of water
- filtrationThe solid was filtered
- washwashed with water
- customdried under vacuum
出典と根拠
- ORDレコード
- ord-363bc9926a5c42c3a799942f32be0d9c
- 出典データセット
- uspto-grants-2003_03
- 特許番号
- US06531466B2
関連ノート
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