Cesium carbonate → 2-(3-isopropyl-2-oxo-2,3-dihydro-benzoimidazol-1-ylmethyl)-1-(3-methyl-butyl)-1H-benzoimidazole-5-carbonitrile
반응식
[CH:1]([N:4]1[C:8]2[CH:9]=[CH:10][CH:11]=[CH:12][C:7]=2[NH:6][C:5]1=[O:13])([CH3:3])[CH3:2].C([O-])([O-])=O.[Cs+].[Cs+].Cl[CH2:21][C:22]1[N:26]([CH2:27][CH2:28][CH:29]([CH3:31])[CH3:30])[C:25]2[CH:32]=[CH:33][C:34]([C:36]#[N:37])=[CH:35][C:24]=2[N:23]=1>CN(C=O)C.CCOC(C)=O>[CH:1]([N:4]1[C:8]2[CH:9]=[CH:10][CH:11]=[CH:12][C:7]=2[N:6]([CH2:21][C:22]2[N:26]([CH2:27][CH2:28][CH:29]([CH3:31])[CH3:30])[C:25]3[CH:32]=[CH:33][C:34]([C:36]#[N:37])=[CH:35][C:24]=3[N:23]=2)[C:5]1=[O:13])([CH3:3])[CH3:2]참가 물질
반응물 3
생성물 1
시약·촉매·용매 2
실험 절차
A suspension of 1-isopropyl-1,3-dihydro-benzoimidazol-2-one (0.79 g, 4.5 mmol) and Cs2CO3 (4.40 g, 13.5 mmol) in DMF (50 mL) was stirred for 30 minutes then 2-chloromethyl-1-(3-methyl-butyl)-1H-benzoimidazole-5-carbonitrile (1.34 g, 4.5 mmol) was added and the mixture stirred for 5 h at ambient temperature. The reaction mixture was diluted with EtOAc (50 mL) and filtered. The filtrate was evaporated to dryness and the residue taken up in EtOAc (100 mL), washed with water and brine. The organic layer was dried over MgSO4 and evaporated. The residue was purified by flash chromatography (gradient, hexanes:EtOAc 3:1 to 1:1) to give 1.71 g (95%) of 2-(3-isopropyl-2-oxo-2,3-dihydro-benzoimidazol-1-ylmethyl)-1-(3-methyl-butyl)-1H-benzoimidazole-5-carbonitrile as a white solid.
후처리
- stirringthe mixture stirred for 5 h at ambient temperature
- filtrationfiltered
- customThe filtrate was evaporated to dryness
- washwashed with water and brine
- dry with materialThe organic layer was dried over MgSO4
- customevaporated
- customThe residue was purified by flash chromatography (gradient, hexanes:EtOAc 3:1 to 1:1)
출처 및 근거
- ORD 기록
- ord-2b292b75ad924b399e6d7d4241c56b9a
- 출처 데이터셋
- uspto-grants-2005_07
- 특허 번호
- US06919331B2
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