Triethylamine → 5-Chloro-N-(2-ethyl-1-{1-[(4-methylphenyl)sulfonyl]-1H-pyrazol-5-yl}butyl)thiophene-2-sulfonamide
반응식
[CH2:1]([CH:3]([CH2:21][CH3:22])[CH:4]([NH2:20])[C:5]1[N:9]([S:10]([C:13]2[CH:18]=[CH:17][C:16]([CH3:19])=[CH:15][CH:14]=2)(=[O:12])=[O:11])[N:8]=[CH:7][CH:6]=1)[CH3:2].C(N(CC)CC)C.[Cl:30][C:31]1[S:35][C:34]([S:36](Cl)(=[O:38])=[O:37])=[CH:33][CH:32]=1>C(Cl)Cl.C(Cl)(Cl)Cl>[Cl:30][C:31]1[S:35][C:34]([S:36]([NH:20][CH:4]([C:5]2[N:9]([S:10]([C:13]3[CH:14]=[CH:15][C:16]([CH3:19])=[CH:17][CH:18]=3)(=[O:12])=[O:11])[N:8]=[CH:7][CH:6]=2)[CH:3]([CH2:1][CH3:2])[CH2:21][CH3:22])(=[O:38])=[O:37])=[CH:33][CH:32]=1참가 물질
6
반응물 3
생성물 1
시약·촉매·용매 2
실험 절차
To (2-ethyl-1-{1-[(4-methylphenyl)sulfonyl]-1H-pyrazol-5-yl}butyl)amine (0.200 g, 0.630 mmol) in CH2Cl2 (10 mL) was added triethylamine (0.18 mL, 1.3 mmol) and 5-chlorothiophene-2-sulfonyl chloride (0.14, 0.76 mmol) After 1 day the reaction mixture was diluted with chloroform (30 mL), washed with H2O (2×30 mL), dried (Na2SO4) and concentrated. Column chromatography (EtOAc/hexane, 3:7) provided 5-chloro-N-(2-ethyl-1-{1-[(4-methylphenyl)sulfonyl]-1H-pyrazol-5-yl}butyl)thiophene-2-sulfonamide (0.104 g, 33%) as a white solid (mp=146-148° C.).
후처리
- washwashed with H2O (2×30 mL)
- dry with materialdried (Na2SO4)
- concentrationconcentrated
출처 및 근거
- ORD 기록
- ord-fe5fd333aae843498f7e3c5583719d99
- 출처 데이터셋
- uspto-grants-2008_07
- 특허 번호
- US07399778B2
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