반응식
FC(F)(F)S([O:6][CH2:7][CH:8]([F:10])[F:9])(=O)=O.[CH2:13]([O:20][C:21]1[CH:26]=[CH:25][C:24]([N:27]2[C:31]3=[N:32][CH:33]=[C:34](O)[CH:35]=[C:30]3[N:29]([CH2:37][CH3:38])[C:28]2=[O:39])=[CH:23][CH:22]=1)[C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1.C(=O)([O-])[O-].[K+].[K+].[Cl-].[Cl-].[Ca+2]>CN(C=O)C>[CH2:13]([O:20][C:21]1[CH:22]=[CH:23][C:24]([N:27]2[C:31]3=[N:32][CH:33]=[C:34]([O:6][CH2:7][CH:8]([F:10])[F:9])[CH:35]=[C:30]3[N:29]([CH2:37][CH3:38])[C:28]2=[O:39])=[CH:25][CH:26]=1)[C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1참가 물질
반응물 4
생성물 1
시약·촉매·용매 1
실험 절차
2,2-Difluoroethyl trifluoromethanesulfonate (213 mg) was added to a solution of 3-[4-(benzyloxy)phenyl]-1-ethyl-6-hydroxy-1,3-dihydro-2H-imidazo[4,5-b]pyridin-2-one (300 mg) and potassium carbonate (229 mg) in DMF (5 ml) at room temperature. The mixture was stirred at ambient temperature under a dry atmosphere (CaCl2 tube) for 3 h. The mixture was quenched with water at room temperature and extracted with AcOEt. The organic layer was separated, washed with water and brine, dried over MgSO4 and concentrated in vacuo. The residue was purified by column chromatography (silica gel, eluted with 15%-50% AcOEt in hexane) to give 3-[4-(benzyloxy)phenyl]-6-(2,2-difluoroethoxy)-1-ethyl-1,3-dihydro-2H-imidazo[4,5-b]pyridin-2-one (301 mg) as colorless oil.
후처리
- customThe mixture was quenched with water at room temperature
- extractionextracted with AcOEt
- customThe organic layer was separated
- washwashed with water and brine
- dry with materialdried over MgSO4
- concentrationconcentrated in vacuo
- customThe residue was purified by column chromatography (silica gel, eluted with 15%-50% AcOEt in hexane)
출처 및 근거
- ORD 기록
- ord-2a0c4da4549f412b9b3b8956645e66fe
- 출처 데이터셋
- uspto-grants-2014_09
- 특허 번호
- US08846713B2
연결된 노트
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