反応式
[CH3:1][CH2:2][C@H:3]1[O:18][C:16](=[O:17])[C@H:15]([CH3:19])[C@@H:14]([O:20][C@@H:21]2[O:26][C@@H:25]([CH3:27])[C@H:24]([OH:28])[C@@:23]([O:30][CH3:31])([CH3:29])[CH2:22]2)[C@H:13]([CH3:32])[C@@H:12]([O:33][C@@H:34]2[O:39][C@H:38]([CH3:40])[CH2:37][C@H:36]([N:41]([CH3:43])[CH3:42])[C@H:35]2[OH:44])[C@@:11]([OH:46])([CH3:45])[CH2:10][C@@H:9]([CH3:47])[C:7](=[O:8])[C@H:6]([CH3:48])[C@@H:5]([OH:49])[C@@:4]1([OH:51])[CH3:50].[CH3:52][C:53](OC(C)=O)=[O:54]>C(Cl)Cl>[CH3:1][CH2:2][C@H:3]1[O:18][C:16](=[O:17])[C@H:15]([CH3:19])[C@@H:14]([O:20][C@@H:21]2[O:26][C@@H:25]([CH3:27])[C@H:24]([OH:28])[C@@:23]([O:30][CH3:31])([CH3:29])[CH2:22]2)[C@H:13]([CH3:32])[C@@H:12]([O:33][C@@H:34]2[O:39][C@H:38]([CH3:40])[CH2:37][C@H:36]([N:41]([CH3:42])[CH3:43])[C@H:35]2[O:44][C:53]([CH3:52])=[O:54])[C@@:11]([OH:46])([CH3:45])[CH2:10][C@@H:9]([CH3:47])[C:7](=[O:8])[C@H:6]([CH3:48])[C@@H:5]([OH:49])[C@@:4]1([OH:51])[CH3:50]参加物
4
反応条件
- 温度
- 0 °C
実験手順
To erythromycin A (2.674 mmol) dissolved in 100 mL of CH2Cl2 at ambient temperature and then cooled to 0° C. was added 1.1 equivalents of Ac2O (0.28 mL). The reaction mixture was allowed to warm to ambient temperature, stirred for 3 hours and extracted with CH2Cl2. The combined organic extracts were washed once with 8% sodium bicarbonate solution, tarice with water and once with brine, dried over Na2SO4 and concentrated in vacuo to afford the crude product as a white powder. Recrystallization from acetonitrile afforded the title compound.
後処理
- temperatureto warm to ambient temperature
- extractionextracted with CH2Cl2
- washThe combined organic extracts were washed once with 8% sodium bicarbonate solution, tarice with water and once with brine
- dry with materialdried over Na2SO4
- concentrationconcentrated in vacuo
- customto afford the crude product as a white powder
- customRecrystallization from acetonitrile
出典と根拠
- ORDレコード
- ord-27fb9f6ed5164e3fb2b31006a240004c
- 出典データセット
- uspto-grants-1995_02
- 特許番号
- US05393743
関連ノート
読み込み中…