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[C:1]([C:4]1[C:5](=[O:24])[NH:6][C:7]([C:17]2[CH:22]=[CH:21][CH:20]=[CH:19][C:18]=2[Cl:23])=[C:8]([C:10]2[CH:15]=[CH:14][C:13]([Cl:16])=[CH:12][CH:11]=2)[CH:9]=1)(=[O:3])[CH3:2].C(=O)([O-])[O-].[Cs+].[Cs+].Br[CH2:32][C:33](=[O:38])[C:34]([CH3:37])([CH3:36])[CH3:35]>CN(C=O)C>[C:1]([C:4]1[C:5]([O:24][CH2:32][C:33](=[O:38])[C:34]([CH3:37])([CH3:36])[CH3:35])=[N:6][C:7]([C:17]2[CH:22]=[CH:21][CH:20]=[CH:19][C:18]=2[Cl:23])=[C:8]([C:10]2[CH:15]=[CH:14][C:13]([Cl:16])=[CH:12][CH:11]=2)[CH:9]=1)(=[O:3])[CH3:2]참가 물질
5
실험 절차
To a 25 mL rb flask equipped with a magnetic stir bar was added 0.309 g(0.86 mmol) of the product of Step A, 0.422 g (1.29 mmol) of cesium carbonate, 3 mL DMF and finally 145 μL of 1-bromopinacolone was added. The reaction mixture was stirred at room temperature for 1.5 h then partitioned between EtOAc and water. The organic layer was separated, washed with 10% aq. NaHSO4, water, brine, dried (MgSO4), filtered and evaporated. The residue was purified on s silica gel flash chromatography column eluted with 0–10% EtOAc-hexane. Evaporation of the purified fractions and drying in vacuo afforded the title compound.
후처리
- customTo a 25 mL rb flask equipped with a magnetic stir bar
- additionwas added
- customthen partitioned between EtOAc and water
- customThe organic layer was separated
- washwashed with 10% aq. NaHSO4, water, brine
- dry with materialdried (MgSO4)
- filtrationfiltered
- customevaporated
- customThe residue was purified on s silica gel flash chromatography column
- washeluted with 0–10% EtOAc-hexane
- customEvaporation of the purified fractions
- customdrying in vacuo
출처 및 근거
- ORD 기록
- ord-ea6785e61a9d489682d374698133b827
- 출처 데이터셋
- uspto-grants-2006_08
- 특허 번호
- US07091216B2
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