Triethylamine → tert-butyl 3-chloro-5-((3,5-dichloro-2-hydroxy-N-isobutylphenylsulfonamido)methyl)benzyl(isobutyl)carbamate
반응식
[Cl:1][C:2]1[CH:3]=[C:4]([CH:18]=[C:19]([CH2:21][NH:22][CH2:23][CH:24]([CH3:26])[CH3:25])[CH:20]=1)[CH2:5][N:6]([CH2:14][CH:15]([CH3:17])[CH3:16])[C:7](=[O:13])[O:8][C:9]([CH3:12])([CH3:11])[CH3:10].CCN(CC)CC.[Cl:34][C:35]1[C:36]([OH:46])=[C:37]([S:42](Cl)(=[O:44])=[O:43])[CH:38]=[C:39]([Cl:41])[CH:40]=1>C(Cl)Cl.O>[Cl:1][C:2]1[CH:3]=[C:4]([CH:18]=[C:19]([CH2:21][N:22]([CH2:23][CH:24]([CH3:26])[CH3:25])[S:42]([C:37]2[CH:38]=[C:39]([Cl:41])[CH:40]=[C:35]([Cl:34])[C:36]=2[OH:46])(=[O:43])=[O:44])[CH:20]=1)[CH2:5][N:6]([CH2:14][CH:15]([CH3:17])[CH3:16])[C:7](=[O:13])[O:8][C:9]([CH3:12])([CH3:11])[CH3:10]참가 물질
반응물 3
생성물 1
시약·촉매·용매 2
실험 절차
To a solution of tert-butyl 3-chloro-5-((isobutylamino)methyl)benzyl(isobutyl)carbamate (2.4 g, 6.27 mmol) in CH2Cl2 (30 mL) was added Et3N (1.3 mL, 9.40 mmol), followed by the addition of 3,5-dichloro-2-hydroxybenzenesulfonyl chloride (1.80 g, 6.89 mmol). The reaction mixture was stirred at rt for 2 h. The mixture was diluted with CH2Cl2 and water. The organic layer was washed with saturated NaHCO3 solution, NH4Cl solution, brine solution, and dried over MgSO4. The filtrate was concentrated and the residue was purified by silica gel flash chromatography. The column was eluted with hexane to 80% dichloromethane in hexane. The fractions containing the desired product were combined and concentrated to give colorless viscous solid (2.8 g, 72%).
후처리
- washThe organic layer was washed with saturated NaHCO3 solution, NH4Cl solution, brine solution
- dry with materialdried over MgSO4
- concentrationThe filtrate was concentrated
- customthe residue was purified by silica gel flash chromatography
- washThe column was eluted with hexane to 80% dichloromethane in hexane
- additionThe fractions containing the desired product
- concentrationconcentrated
출처 및 근거
- ORD 기록
- ord-8d8afe46468d4085b42d54342236d66c
- 출처 데이터셋
- uspto-grants-2013_08
- 특허 번호
- US08501992B2
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