反応式
[C:1](OC(=O)C)(=[O:3])[CH3:2].[O:8]=[C:9]1[N:13]2[C:14]3[CH:15]=[CH:16][CH:17]=[CH:18][C:19]=3[CH2:20][CH:12]2[CH:11]([CH2:21][NH:22][C:23](=[O:25])[CH3:24])[O:10]1.CS(OS(C)(=O)=O)(=O)=O>C(Cl)Cl.CS(O)(=O)=O>[C:1]([C:17]1[CH:16]=[CH:15][C:14]2[N:13]3[C:9](=[O:8])[O:10][CH:11]([CH2:21][NH:22][C:23](=[O:25])[CH3:24])[CH:12]3[CH2:20][C:19]=2[CH:18]=1)(=[O:3])[CH3:2]参加物
反応物 3
生成物 1
試薬・触媒・溶媒 2
実験手順
Acetic anhydride (53 μl) is slowly added to a mixture of (±) N-[(9,9a-dihydro-3-oxo-1H,3H-oxazolo[3,4-a]indol-1-yl)methyl]acetamide (X diastereomer A, EXAMPLE 18, 21 mg), methanesulfonic anhydride (33 mg) in methylene chloride (0.1 ml) and methane sulfonic acid (0.50 ml) at 0°. The temperature is kept below 15° for 3 hr, then allowed to warm slowly to 20°-25° overnight. Then the mixture is added to crushed ice (0.5 ml). After the ice has melted the mixture is extracted with ethyl acetate (4×3 ml). The combined organic layers are washed with saturated aqueous sodium bicarbonate (2 ml), saline (1 ml), dried over anhydrous potassium carbonate and concentrated to an oil. The oil is place on a silica prepratory plate (14 cm×17.5 cm, 250μ) and developed in methanol/methylene chloride (5/95, 3×). Extraction of the appropriate band and concentration give the title compound.
後処理
- temperatureto warm slowly to 20°-25° overnight
- additionThen the mixture is added
- extractionis extracted with ethyl acetate (4×3 ml)
- washThe combined organic layers are washed with saturated aqueous sodium bicarbonate (2 ml), saline (1 ml)
- dry with materialdried over anhydrous potassium carbonate
- concentrationconcentrated to an oil
- extractionExtraction of the appropriate band and concentration
出典と根拠
- ORDレコード
- ord-1b744634cec94374ac2598be1eb4e1c6
- 出典データセット
- uspto-grants-1993_09
- 特許番号
- US05247090
関連ノート
読み込み中…