반응식
[CH2:1]([C:5]1=[CH:6][N:7]([C:16]([CH3:19])([CH3:18])[CH3:17])[S:8]/[C:9]/1=[N:10]\C(=O)OCC)[CH2:2][CH2:3][CH3:4].I[Si](C)(C)C.C(=O)(O)[O-].[Na+]>C(Cl)(Cl)Cl>[C:16]([N:7]1[CH:6]=[C:5]([CH2:1][CH2:2][CH2:3][CH3:4])[C:9](=[NH:10])[S:8]1)([CH3:19])([CH3:18])[CH3:17]참가 물질
반응 조건
- 온도
- 60 °C
실험 절차
To a 250-mL, round-bottomed flask containing a magnetic stir bar were added the product from Example 92A (7.11 g, 25.0 mmol) and chloroform (100 mL). Neat iodotrimethylsilane (Aldrich, 6.25 g, 31.1 mmol) was added. A reflux condenser with nitrogen inlet was attached and a heating mantle was applied. The yellow reaction mixture was heated to 60° C. and stirred overnight. After cooling to room temperature, saturated aqueous sodium bicarbonate solution was added. The organic layer was separated and the aqueous layer was extracted with dichloromethane (2×50 mL). The combined organic layers were dried (MgSO4), filtered, and concentrated by rotary evaporator to give a yellow semi-solid. The product was purified by flash chromatography (silica gel: 30-90% ethyl acetate in hexanes) to afford the title compound. LC-MS (ESI+) m/z 213 (M+H)+.
후처리
- additionTo a 250-mL, round-bottomed flask containing a magnetic stir bar
- customA reflux condenser with nitrogen inlet was attached
- temperatureAfter cooling to room temperature
- customThe organic layer was separated
- extractionthe aqueous layer was extracted with dichloromethane (2×50 mL)
- dry with materialThe combined organic layers were dried (MgSO4)
- filtrationfiltered
- concentrationconcentrated by rotary evaporator
- customto give a yellow semi-solid
- customThe product was purified by flash chromatography (silica gel: 30-90% ethyl acetate in hexanes)
출처 및 근거
- ORD 기록
- ord-46403699378d4105b7ad9720346c5bf6
- 출처 데이터셋
- uspto-grants-2011_01
- 특허 번호
- US07872033B2
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