반응식
[C:1]1([NH:7][C:8](=[O:15])[C:9]2[CH:14]=[CH:13][N:12]=[CH:11][CH:10]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.C([Li])CCC.[CH2:21]1[O:23][CH2:22]1.O1CCOCC1>O1CCCC1>[OH:23][CH2:22][CH2:21][C:14]1[CH:13]=[N:12][CH:11]=[CH:10][C:9]=1[C:8]([NH:7][C:1]1[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1)=[O:15]참가 물질
실험 절차
To a solution of N-phenylisonicotinamide (1.98 g, 10 mmol) in tetrahydrofuran (40 ml) at -78° C. was added a solution of n-butyllithium (1.6M in hexanes; 13.5 ml, 21.6 mmol) and the resulting red solution stirrred for 40 minutes before addition of a solution of ethylene oxide in dioxane (3.56M; 3.0 ml, 11 mmol). After allowing the mixture to warm to room temperature over 21/2 hours, the reaction was quenched by addition of methanol (8 ml). The solvent was evaporated and the residue partitioned between ethyl acetate (70 ml) and water (25 ml). The organic layer was washed with saturated brine (25 ml), dried (MgSO4) and evaporated. The residue was chromatographed on silica eluting with 10% methanol/dichloromethane to afford the title compound as a solid (1.05 g, 43%); δH (CDCl3) 3.07 (2H, t, J 5.6 Hz, ArCH2 CH2OH), 3.70 (1H, br s, OH), 4.10 (2H, t, J 5.6 Hz, ArCH2 CH2OH), 7.15-7.19 (1H, m, ArH), 7.35-7.39 (2H, m, ArH), 7.49 (1H, d, J 5.2 Hz, ArH), 7.69-7.71 (2H, m, ArH), 8.44-8.48 (2H, m, ArH), 9.77 (1H, s, NH).
후처리
- customthe reaction was quenched by addition of methanol (8 ml)
- customThe solvent was evaporated
- customthe residue partitioned between ethyl acetate (70 ml) and water (25 ml)
- washThe organic layer was washed with saturated brine (25 ml)
- dry with materialdried (MgSO4)
- customevaporated
- customThe residue was chromatographed on silica eluting with 10% methanol/dichloromethane
출처 및 근거
- ORD 기록
- ord-0430b92b9d694fa9a72bd1392d6bf059
- 출처 데이터셋
- uspto-grants-1997_12
- 특허 번호
- US05700941
연결된 노트
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