HCID 21877762, 화합물 → 8-Fluoro-6-nitro-1,2,3,4-tetrahydroquinoline
반응식
[F:1][C:2]1[CH:3]=[C:4]([N+:13]([O-:15])=[O:14])[CH:5]=[C:6]2[C:11]=1[NH:10][C:9](=O)[CH2:8][CH2:7]2>O1CCCC1>[F:1][C:2]1[CH:3]=[C:4]([N+:13]([O-:15])=[O:14])[CH:5]=[C:6]2[C:11]=1[NH:10][CH2:9][CH2:8][CH2:7]2참가 물질
3
반응 조건
- 온도
- 0 °C
실험 절차
To a stirred solution of 8-fluoro-6-nitro-3,4-dihydroquinolin-2(1H)-one (950 mg, 4.52 mmol) in tetrahydrofuran (5 ml) was added borane-tetrahydrofuran complex (45.2 ml, 45.2 mmol) as a solution in THF. The reaction mixture was then heated to reflux temperature overnight. The reaction mixture was then cooled to 0° C. and quenched with methanol. The quenched mixture was then concentrated in vacuo, redissolved in methanol and reconcentrated, then refluxed in methanol for 2 h. The mixture was then concentrated onto silica gel, and chromatographed using 0-20% ethyl acetate in hexanes. 1H NMR (DMSO-d6) δ 7.77-7.71 (m, 1H), 7.73 (m, 1H), 7.31 (brs, 1H), 3.35-3.28 (m, 2H), 2.77 (t, J=6.2 Hz, 2H), 1.85-1.77 (m, 2H).
후처리
- temperatureThe reaction mixture was then heated
- temperatureto reflux temperature overnight
- customquenched with methanol
- concentrationThe quenched mixture was then concentrated in vacuo
- dissolutionredissolved in methanol
- temperaturerefluxed in methanol for 2 h
- concentrationThe mixture was then concentrated onto silica gel
- customchromatographed
출처 및 근거
- ORD 기록
- ord-e0691f3898e14f7685bbbe9f125a64ad
- 출처 데이터셋
- uspto-grants-2012_05
- 특허 번호
- US08173813B2
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