反応式
[NH2:1][C:2]1[N:10]=[CH:9][N:8]=[C:7]2[C:3]=1[N:4]=[CH:5][N:6]2[CH2:11][CH2:12][OH:13].[Br:14]Br>C(O[Na])(C)=O.CC(O)=O>[NH2:1][C:2]1[N:10]=[CH:9][N:8]=[C:7]2[C:3]=1[N:4]=[C:5]([Br:14])[N:6]2[CH2:11][CH2:12][OH:13]参加物
4
実験手順
To a solution of 10 g 2-(6-amino-purin-9-yl)ethanol in 200 ml 0.5M AcONa/AcOH buffer pH 4 were added 4 ml of Br2. The resulting mixture was stirred at room temperature for 8 hours. The precipitated product was isolated, washed with water and crystallized from ethanol to give 6.13 g (43%) of the desired compound.
後処理
- customThe precipitated product was isolated
- washwashed with water
- customcrystallized from ethanol
出典と根拠
- ORDレコード
- ord-7c2c581a412e4451ae310470494ed016
- 出典データセット
- uspto-grants-2012_05
- 特許番号
- US08173609B2
関連ノート
読み込み中…