반응식
[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]참가 물질
반응물 3
생성물 1
시약·촉매·용매 2
실험 절차
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.
후처리
- 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
출처 및 근거
- ORD 기록
- ord-1b744634cec94374ac2598be1eb4e1c6
- 출처 데이터셋
- uspto-grants-1993_09
- 특허 번호
- US05247090
연결된 노트
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