Thionyl Chloride → 4-Chloroquinazoline-6-carbonitrile
反応式
O[C:2]1[C:11]2[C:6](=[CH:7][CH:8]=[C:9]([C:12](=O)[NH2:13])[CH:10]=2)[N:5]=[CH:4][N:3]=1.S(Cl)([Cl:17])=O>P(Cl)(Cl)(Cl)=O>[Cl:17][C:2]1[C:11]2[C:6](=[CH:7][CH:8]=[C:9]([C:12]#[N:13])[CH:10]=2)[N:5]=[CH:4][N:3]=1参加物
4
実験手順
A mixture comprising 2 g of 4-hydroxy-6-carbamoylquinazoline, 30 ml of thionyl chloride and 60 ml of phosphorus oxychloride was heated under reflux for 20 hours. The reaction mixture was concentrated under a reduced pressure and the obtained residue was dissolved in 100 ml of ethyl acetate. The obtained solution was washed with water (150 ml), dried over magnesium sulfate and concentrated under a reduced pressure. The obtained residue was introduced into a silica gel column, followed by eluting with ethyl acetate and acetone to give 800 mg of the title compound.
後処理
- temperaturewas heated
- temperatureunder reflux for 20 hours
- concentrationThe reaction mixture was concentrated under a reduced pressure
- dissolutionthe obtained residue was dissolved in 100 ml of ethyl acetate
- washThe obtained solution was washed with water (150 ml)
- dry with materialdried over magnesium sulfate
- concentrationconcentrated under a reduced pressure
- additionThe obtained residue was introduced into a silica gel column
- washby eluting with ethyl acetate and acetone
出典と根拠
- ORDレコード
- ord-6579ea8e0c0340f78ed6d1c313bc3504
- 出典データセット
- uspto-grants-1996_11
- 特許番号
- US05576322
反応ノート
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