1-Methylhydantoin → 3-[3-(3-methylimidazolidine-2,5-dione-1-ylmethyl)phenyl]-5-iso-butyl-N-tert-butylthiophene-2-sulfonamide
반응식
[CH3:1][N:2]1[CH2:8][C:6](=[O:7])[NH:5][C:3]1=[O:4].CC([O-])(C)C.[K+].Br[CH2:16][C:17]1[CH:18]=[C:19]([C:23]2[CH:27]=[C:26]([CH2:28][CH:29]([CH3:31])[CH3:30])[S:25][C:24]=2[S:32]([NH:35][C:36]([CH3:39])([CH3:38])[CH3:37])(=[O:34])=[O:33])[CH:20]=[CH:21][CH:22]=1>CS(C)=O.C(Cl)Cl>[CH3:1][N:2]1[CH2:8][C:6](=[O:7])[N:5]([CH2:16][C:17]2[CH:18]=[C:19]([C:23]3[CH:27]=[C:26]([CH2:28][CH:29]([CH3:31])[CH3:30])[S:25][C:24]=3[S:32]([NH:35][C:36]([CH3:38])([CH3:37])[CH3:39])(=[O:33])=[O:34])[CH:20]=[CH:21][CH:22]=2)[C:3]1=[O:4]참가 물질
6
반응물 3
생성물 1
시약·촉매·용매 2
실험 절차
To a solution of 1-methylhydantoin (33.9 mg, 0.297 mmol) in DMSO (1 mL) and t-BuOK (46.6 mg, 0.415 mmol), that had been stirred for 40 min at ambient temperature, was added a solution of 3-(3-bromomethylphenyl)-5-iso-butyl-N-tert-butylthiophene-2-sulfonamide (87.9 mg, 0.198 mmol; see Example 1(e)) in DMSO (1 mL) dropwise. The reaction mixture was stirred for 1 h at ambient temperature and then diluted with CH2Cl2 (15 mL). The organic layer was washed with water, dried (over anhydrous MgSO4), concentrated in vacuo, and the residue purified by flash chromatography using EtOAc:petroleum ether (35:65) as eluent to give the sub-title compound in 54% yield as a colourless syrup (51.5 mg, 0.107 mmol).
후처리
- washThe organic layer was washed with water
- dry with materialdried (over anhydrous MgSO4)
- concentrationconcentrated in vacuo
- customthe residue purified by flash chromatography
출처 및 근거
- ORD 기록
- ord-79c177a6e78a435cb97e1bc9b7208bb1
- 출처 데이터셋
- uspto-grants-2011_11
- 특허 번호
- US08067418B2
반응 노트
불러오는 중…