반응식
[H-].[Na+].[C:3]([N:11]([CH2:13][CH2:14][OH:15])[CH3:12])(=[O:10])[C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1.F[C:17]1[CH:24]=[CH:23][C:20]([CH:21]=[O:22])=[CH:19][CH:18]=1>CN(C)C=O>[C:3]([N:11]([CH2:13][CH2:14][O:15][C:17]1[CH:24]=[CH:23][C:20]([CH:21]=[O:22])=[CH:19][CH:18]=1)[CH3:12])(=[O:10])[C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1참가 물질
실험 절차
Sodium hydride (60% dispersion in oil, 1.30 g) was added portionwise to a solution of 2-(N-benzoyl-N-methylamino)ethanol (5.0 g) in dry dimethylformamide (100 ml) at room temperature under a nitrogen atmosphere. The mixture was stirred at room temperature for 1 hour prior to the addition of 4-fluorobenzaldehyde (5.09 g, 4.4 ml), and the mixture then heated at 80° C. for 15 hours. The solvent was evaporated and the residue dissolved in water (500 ml) and extracted with ethyl acetate (3×500 ml). The combined ethyl acetate layers were washed with water (2×300 ml), brine (300 ml), dried (MgSO4) and evaporated to yield an oil. The oil was triturated with hexane, and the residue chromatographed on silica gel with 1.5% methanol in dichloromethane to afford the title compound as an oil.
후처리
- temperaturethe mixture then heated at 80° C. for 15 hours
- customThe solvent was evaporated
- dissolutionthe residue dissolved in water (500 ml)
- extractionextracted with ethyl acetate (3×500 ml)
- washThe combined ethyl acetate layers were washed with water (2×300 ml), brine (300 ml)
- dry with materialdried (MgSO4)
- customevaporated
- customto yield an oil
- customThe oil was triturated with hexane
- customthe residue chromatographed on silica gel with 1.5% methanol in dichloromethane
출처 및 근거
- ORD 기록
- ord-db686fe8ffe24339a2419a14a7183478
- 출처 데이터셋
- uspto-grants-1995_12
- 특허 번호
- US05478851
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