反応式
[F:1][C@@H:2]1[C@H:6]([OH:7])[C@@H:5]([CH2:8][OH:9])[O:4][C@H:3]1[N:10]1[CH:18]=[N:17][C:16]2[C:11]1=[N:12][CH:13]=[N:14][C:15]=2[NH2:19].C(O)(C)C.[ClH:24]>CO.O>[ClH:24].[F:1][C@@H:2]1[C@H:6]([OH:7])[C@@H:5]([CH2:8][OH:9])[O:4][C@H:3]1[N:10]1[CH:18]=[N:17][C:16]2[C:11]1=[N:12][CH:13]=[N:14][C:15]=2[NH2:19]参加物
6
実験手順
To a solution of 9-(2-deoxy-2-fluoro-β-D-ribofuranosyl)adenine (500 mg. 1.86 mmol) in MeOH (40 ml) and water (10 ml) was added a solution of isopropanol (15 ml) previously saturated with HCl gas. The solution was evaporated under vacuum at room temperature, and triturated with EtOH (25 ml) to afford the title compound as a white solid.
後処理
- customThe solution was evaporated under vacuum at room temperature
- customtriturated with EtOH (25 ml)
出典と根拠
- ORDレコード
- ord-6f3bdcf96f5c441380f7fe1672130045
- 出典データセット
- uspto-grants-1995_05
- 特許番号
- US05420115
関連ノート
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