반응식
[NH:1]1[CH:5]=[C:4]([CH:6]=[O:7])[N:3]=[CH:2]1.[H-].[Na+].Br[CH2:11][CH2:12][C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1>O1CCCC1>[C:13]1([CH2:12][CH2:11][N:1]2[CH:5]=[C:4]([CH:6]=[O:7])[N:3]=[CH:2]2)[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1참가 물질
실험 절차
Imidazole-4-carboxaldehyde (6.73 g, 70 mmol) was added portionwise to a suspension of sodium hydride (1.68 g, 60% dispersion in mineral oil, 70 mmol) in tetrahydrofuran (280 ml), and the mixture was then stirred at room temperature for 30 minutes. (2-Bromoethyl)benzene (9.56 ml, 70 mmol) was added, and the mixture was stirred at room temperature for 72 hours. The mixture was evaporated under reduced pressure and the residue was partitioned between water (300 ml) and dichloromethane (500 ml), and the layers were separated. The organic phase was dried (MgSO4) and evaporated under reduced pressure. The crude product was pre-adsorbed onto silica gel, and purified by column chromatography on silica gel using an elution gradient of ethyl acetate:pentane (50:50 to 100:0) to afford the title compound, 1.44 g. 1H-NMR (CDCl3, 400 MHz) δ: 3.16 (t, 2H), 4.23 (t, 2H), 7.02 (d, 2H), 7.28 (m, 3H), 7.36 (s, 1H), 7.50 (s, 1H), 9.83 (s, 1H). LRMS: m/z (ES+) 223 [MNa+].
후처리
- stirringthe mixture was stirred at room temperature for 72 hours
- customThe mixture was evaporated under reduced pressure
- customthe residue was partitioned between water (300 ml) and dichloromethane (500 ml)
- customthe layers were separated
- dry with materialThe organic phase was dried (MgSO4)
- customevaporated under reduced pressure
- custompurified by column chromatography on silica gel using an elution gradient of ethyl acetate:pentane (50:50 to 100:0)
출처 및 근거
- ORD 기록
- ord-31441750fe72498fa9d8520b043eb1a1
- 출처 데이터셋
- uspto-grants-2004_03
- 특허 번호
- US06713496B2
연결된 노트
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