반응식
[C:1]([NH:11][C:12]1[CH:17]=[CH:16][CH:15]=[C:14]([F:18])[CH:13]=1)(OCC1C=CC=CC=1)=O.[C:19]([O:24][CH2:25][C@@H:26]1[O:28]C1)(=[O:23])CCC>O1CCCC1>[F:18][C:14]1[CH:13]=[C:12]([N:11]2[CH2:1][C@H:25]([CH2:26][OH:28])[O:24][C:19]2=[O:23])[CH:17]=[CH:16][CH:15]=1참가 물질
실험 절차
A mixture of N-(carbobenzyloxy)-3-fluoroaniline (1.000 g, 4.08 mmol) in dry tetrahydrofuran (10 ml) is cooled with a dry ice/acetone bath to about -78° and then nbutyllithium (1.87 ml of a 1.6M mixture in hexanes, 2.91 mmol) is added. (R)-glycidyl butyrate (0.420 g or 0.413 ml, 2.91 mmol) is then added via syringe and the cooling bath allowed to dissipate overnight, with the reaction mixture reaching 20°-25°. The reaction mixture is quenched by the careful addition of saturated aqueous ammonium chloride, the entire mixture transferred to a separatory funnel with dichloromethane washings, and the mixture extracted with dichloromethane. The combined organic extracts are dried over sodium sulfate, filtered and concentrated under reduced pressure to give a concentrate which is purified by chromatography over silica gel, eluting with acetonitrile/chloroform (10/90) containing 1% methanol, to give the title compound.
후처리
- temperatureis cooled with a dry ice/acetone bath to about -78°
- customreaching 20°-25°
- customThe reaction mixture is quenched by the careful addition of saturated aqueous ammonium chloride
- customthe entire mixture transferred to a separatory funnel with dichloromethane washings
- extractionthe mixture extracted with dichloromethane
- dry with materialThe combined organic extracts are dried over sodium sulfate
- filtrationfiltered
- concentrationconcentrated under reduced pressure
- customto give
- concentrationa concentrate which
- customis purified by chromatography over silica gel
- washeluting with acetonitrile/chloroform (10/90)
- additioncontaining 1% methanol
출처 및 근거
- ORD 기록
- ord-b6a38fab3b1a4dcfa3842487012f291e
- 출처 데이터셋
- uspto-grants-1996_10
- 특허 번호
- US05565571
연결된 노트
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