Ammonia → 2-Chloro-5-methoxypyrimidin-4-amine
反応式
[Cl:1][C:2]1[N:7]=[C:6](Cl)[C:5]([O:9][CH3:10])=[CH:4][N:3]=1.[NH3:11]>CO>[Cl:1][C:2]1[N:7]=[C:6]([NH2:11])[C:5]([O:9][CH3:10])=[CH:4][N:3]=1参加物
4
実験手順
A mixture of 2,4 dichloro-5-methoxypyrimidine (0.45 g, 2.5 mmol) and ammonia in methanol (2N, 20 ml) was stirred at room temperature overnight. The mixture was then concentrated in vacuo and washed with water. The residue was purified by column chromatography (20-60% ethyl acetate/petroleum ether) to furnish the title compound as a white solid (211 mg). MS: [M+H]+=160
後処理
- concentrationThe mixture was then concentrated in vacuo
- washwashed with water
- customThe residue was purified by column chromatography (20-60% ethyl acetate/petroleum ether)
出典と根拠
- ORDレコード
- ord-e3a34c5197bd42178377e0d632b1b333
- 出典データセット
- uspto-grants-2014_08
- 特許番号
- US08796244B2
反応ノート
読み込み中…