Cesium carbonate → HCID 9912941, 화합물
반응식
[O:1]1[C:5]2[CH:6]=[CH:7][CH:8]=[C:9]([C:10]([CH3:30])([CH3:29])[CH2:11][C:12](=[O:28])[C:13]([NH:15][C:16]3[CH:17]=[CH:18][C:19]4[C:24](=[O:25])[O:23][N:22]=[C:21]([CH3:26])[C:20]=4[CH:27]=3)=[O:14])[C:4]=2[O:3][CH2:2]1.[F:31][C:32]([Si](C)(C)C)([F:34])[F:33].C(=O)([O-])[O-].[Cs+].[Cs+].[F-].C([N+](CCCC)(CCCC)CCCC)CCC>CN(C)C=O.O>[O:1]1[C:5]2[CH:6]=[CH:7][CH:8]=[C:9]([C:10]([CH3:30])([CH3:29])[CH2:11][C:12]([OH:28])([C:32]([F:34])([F:33])[F:31])[C:13]([NH:15][C:16]3[CH:17]=[CH:18][C:19]4[C:24](=[O:25])[O:23][N:22]=[C:21]([CH3:26])[C:20]=4[CH:27]=3)=[O:14])[C:4]=2[O:3][CH2:2]1참가 물질
7
실험 절차
2.67 g of 6-[4-(benzo[1,3]dioxol-4-yl)-4-methyl-2-oxo-valeroyl-amino]-4-methyl-2,3-benzoxazin-1-one is dissolved under argon in 35 ml of dimethylformamide and mixed with 4.66 ml of trifluoromethyl-trimethylsilane and 2.6 g of cesium carbonate while being cooled with ice. After 18 hours of stirring at room temperature, a spatula tip full of tetrabutylammonium fluoride is added, and it is stirred for one hour at room temperature. After 300 ml of water is added, it is extracted with ethyl acetate, the organic phase is dried (Na2SO4) and concentrated by evaporation. The crude product is chromatographed on silica gel. With hexane/ethyl acetate (80:20), 1.33 g of the title compound is obtained in a pure state.
후처리
- temperaturewhile being cooled with ice
- stirringit is stirred for one hour at room temperature
- extractionit is extracted with ethyl acetate
- dry with materialthe organic phase is dried (Na2SO4)
- concentrationconcentrated by evaporation
- customThe crude product is chromatographed on silica gel
출처 및 근거
- ORD 기록
- ord-f80d09f83b1d4414a06ec8dd9f4fd148
- 출처 데이터셋
- uspto-grants-2006_09
- 특허 번호
- US07112584B2
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