Pyridine → HCID 57476240, 화합물
반응식
[NH2:1][C:2]1[CH:3]=[C:4]([O:16][CH3:17])[CH:5]=[C:6]2[C:10]=1[NH:9][C:8]([C:11]([O:13][CH2:14][CH3:15])=[O:12])=[CH:7]2.[N:18]1[CH:23]=[CH:22][CH:21]=[CH:20][C:19]=1[S:24](Cl)(=[O:26])=[O:25].N1C=CC=C[CH:29]=1>>[CH3:17][O:16][C:4]1[CH:5]=[C:6]2[C:10](=[C:2]([N:1]([CH3:29])[S:24]([C:19]3[CH:20]=[CH:21][CH:22]=[CH:23][N:18]=3)(=[O:26])=[O:25])[CH:3]=1)[NH:9][C:8]([C:11]([O:13][CH2:14][CH3:15])=[O:12])=[CH:7]2참가 물질
실험 절차
To a solution of ethyl 7-amino-5-methoxy-1H-indole-2-carboxylate (2.5 g) in pyridine (20 mL) was added 2-pyridinesulfonyl chloride (2.1 g) under ice-cooling, and the mixture was stirred for 2 hr. The reaction mixture was concentrated, water was added, and the mixture was extracted with ethyl acetate. The ethyl acetate layer was washed with saturated brine, dried (MgSO4), and concentrated. The obtained residue was dissolved in N,N-dimethylformamide (20 mL), methyl iodide (1.5 g) and potassium carbonate (2 g) were added, and the mixture was stirred at room temperature for 3 hr. Water was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The organic layer was washed with 1N hydrochloric acid and saturated brine, dried (MgSO4), and concentrated under reduced pressure. The obtained residue was subjected to silica gel column chromatography to give the title compound (2.7 g, yield 68%) as pale-yellow crystals from a fraction eluted with ethyl acetate-hexane (50:50, volume ratio). MS: 390 (MH+).
후처리
- temperaturecooling
- concentrationThe reaction mixture was concentrated
- additionwater was added
- extractionthe mixture was extracted with ethyl acetate
- washThe ethyl acetate layer was washed with saturated brine
- dry with materialdried (MgSO4)
- concentrationconcentrated
- dissolutionThe obtained residue was dissolved in N,N-dimethylformamide (20 mL)
- additionmethyl iodide (1.5 g) and potassium carbonate (2 g) were added
- stirringthe mixture was stirred at room temperature for 3 hr
- additionWater was added to the reaction mixture
- extractionthe mixture was extracted with ethyl acetate
- washThe organic layer was washed with 1N hydrochloric acid and saturated brine
- dry with materialdried (MgSO4)
- concentrationconcentrated under reduced pressure
출처 및 근거
- ORD 기록
- ord-025c0446c2734ad398df4bdea3b655a4
- 출처 데이터셋
- uspto-grants-2010_08
- 특허 번호
- US07777047B2
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