Benzoyl chloride → 2-Chloro-5-benzoylaminopyridine
反応式
[Cl:1][C:2]1[CH:7]=[CH:6][C:5](CN)=[CH:4][N:3]=1.C([N:12](CC)CC)C.[C:17](Cl)(=[O:24])[C:18]1[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=1>C(Cl)Cl>[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([NH:12][C:17](=[O:24])[C:18]2[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=2)=[CH:4][N:3]=1参加物
5
実験手順
14.25 g (0.1 mol) of 2-chloro-5-aminomethylpyridine and 11.1 g (0.11 mol) of triethylamine are dissolved in 150 ml of methylene chloride. 14.8 g (0.105 mol) of benzoyl chloride are then added dropwise at about 20° C. and the reaction mixture is subsequently stirred overnight at room temperature. It is washed three times with water and the organic phase is dried and concentrated. 24.6 g (99.8% of theory) of 2-chloro-5-benzoylaminopyridine are obtained as white crystals of melting point 118°-120° C.
後処理
- washIt is washed three times with water
- customthe organic phase is dried
- concentrationconcentrated
出典と根拠
- ORDレコード
- ord-f2161ce8085e4e71a9a2e8a6ca6c75aa
- 出典データセット
- uspto-grants-1997_04
- 特許番号
- US05623076
反応ノート
読み込み中…