Diisopropylethylamine → 7-Fluoro-2-methyl-5-{4-[2-(3-nitrophenyl)ethyl]-1-piperazinyl}quinoline
반응식
C(N(CC)C(C)C)(C)C.[CH3:10][C:11]1[CH:20]=[CH:19][C:18]2[C:13](=[CH:14][C:15]([F:27])=[CH:16][C:17]=2[N:21]2[CH2:26][CH2:25][NH:24][CH2:23][CH2:22]2)[N:12]=1.CS(O[CH2:33][CH2:34][C:35]1[CH:40]=[CH:39][CH:38]=[C:37]([N+:41]([O-:43])=[O:42])[CH:36]=1)(=O)=O>CN(C)C=O>[F:27][C:15]1[CH:14]=[C:13]2[C:18]([CH:19]=[CH:20][C:11]([CH3:10])=[N:12]2)=[C:17]([N:21]2[CH2:26][CH2:25][N:24]([CH2:33][CH2:34][C:35]3[CH:40]=[CH:39][CH:38]=[C:37]([N+:41]([O-:43])=[O:42])[CH:36]=3)[CH2:23][CH2:22]2)[CH:16]=1참가 물질
반응 조건
- 온도
- 90 °C
실험 절차
N,N-Diisopropylethylamine (0.07 mL; 3 eq) was added to a solution of 2-methyl-5-(1-piperazinyl)-7-fluoro quinoline (0.03 g; 1 eq) and 2-(3-nitrophenyl)ethyl methanesulfonate (D4) (0.033 g; 1.1 eq) in dimethylformamide (1.0 mL). The reaction mixture was heated to 90° C. for 10 hours. The dark solution was cooled to room temperature and concentrated under reduced pressure, diluted with water (3 mL) and brine (1 mL) and extracted into ethyl acetate (3×3 mL). The organic layers were combined, dried over sodium sulfate and concentrated under reduced pressure. The crude was purified by flash chromatography on silica, eluting with a gradient from dichloromethane to dichloromethane-MeOH (98:2) affording the title compound in 88% yield (0.04 g).
후처리
- temperatureThe dark solution was cooled to room temperature
- concentrationconcentrated under reduced pressure
- additiondiluted with water (3 mL) and brine (1 mL)
- extractionextracted into ethyl acetate (3×3 mL)
- dry with materialdried over sodium sulfate
- concentrationconcentrated under reduced pressure
- customThe crude was purified by flash chromatography on silica
- washeluting with a gradient from dichloromethane to dichloromethane-MeOH (98:2)
출처 및 근거
- ORD 기록
- ord-9b7d567bdd9f4a2f8c41e6a41934d698
- 출처 데이터셋
- uspto-grants-2010_06
- 특허 번호
- US07732600B2
반응 노트
불러오는 중…