Sodium Methoxide → 2-(4-methoxycarbonylphenyl)-N-(3-methoxy-5-methylpyrazin-2-yl)pyridine-3-sulphonamide
반응식
C(OC([N:8]([C:28]1[C:33]([O:34][CH3:35])=[N:32][C:31]([CH3:36])=[CH:30][N:29]=1)[S:9]([C:12]1[C:13]([C:18]2[CH:23]=[CH:22][C:21]([C:24]([O:26][CH3:27])=[O:25])=[CH:20][CH:19]=2)=[N:14][CH:15]=[CH:16][CH:17]=1)(=[O:11])=[O:10])=O)C(C)C.C[O-].[Na+]>CO>[CH3:27][O:26][C:24]([C:21]1[CH:20]=[CH:19][C:18]([C:13]2[C:12]([S:9]([NH:8][C:28]3[C:33]([O:34][CH3:35])=[N:32][C:31]([CH3:36])=[CH:30][N:29]=3)(=[O:10])=[O:11])=[CH:17][CH:16]=[CH:15][N:14]=2)=[CH:23][CH:22]=1)=[O:25]참가 물질
실험 절차
A solution of N-(isobutoxycarbonyl)-2-(4-methoxycarbonylphenyl)-N-(3-methoxy-5-methylpyrazin-2-yl)pyridine-3-sulphonamide (830 mg) and sodium methoxide (433 mg) in methanol (25 ml) was heated under reflux for 1 hour. Volatile material was removed by evaporation and saturated ammonium chloride solution (20 ml) was added to the residue. The mixture was extracted with ethyl acetate (2×20 ml) and the extracts were washed with water (2×15 ml) and dried (MgSO4). The solvent was removed by evaporation and the residue was purified by flash chromatography, eluting with 25-50% ethyl acetate/hexane, to give 2-(4-methoxycarbonylphenyl)-N-(3-methoxy-5-methylpyrazin-2-yl)pyridine-3-sulphonamide (190 mg), m.p. 144-146° C.; microanalysis found: C, 55.2; H, 4.3; N, 13.3%; C23H24BrN4O4S requires: C, 55.1; H, 4.4; N, 13.5%.
후처리
- temperatureunder reflux for 1 hour
- customVolatile material was removed by evaporation and saturated ammonium chloride solution (20 ml)
- additionwas added to the residue
- extractionThe mixture was extracted with ethyl acetate (2×20 ml)
- washthe extracts were washed with water (2×15 ml)
- dry with materialdried (MgSO4)
- customThe solvent was removed by evaporation
- customthe residue was purified by flash chromatography
- washeluting with 25-50% ethyl acetate/hexane
출처 및 근거
- ORD 기록
- ord-beea5354b3554ea49b25e8a6f34be7ca
- 출처 데이터셋
- uspto-grants-2001_07
- 특허 번호
- US06258817B1
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