Tetrahydrofuran → 8-Fluoro-6-nitro-1,2,3,4-tetrahydroquinoline

HRID 1922475노트

반응식

HRID 1922475 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.C1COCC1>>[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]2

참가 물질

3

반응 조건

온도
60 °C

실험 절차

8-Fluoro-6-nitro-3,4-dihydroquinolin-2(1H)-one (5.9 g, 28.1 mmol) was stirred in borane-THF complex, 1M in THF (140 ml, 140 mmol). The solution was heated to 60° C. and stirred overnight. The mixture was then cooled in an ice bath and quenched via addition of methanol (30 mL). The quenched solution was concentrated, then dissolved in methanol and refluxed for 1 h. The solution was then concentrated onto silica gel and chromatographed using 5-30% ethyl acetate in hexanes to give the desired 8-fluoro-6-nitro-1,2,3,4-tetrahydroquinoline (4.34 g, 22.12 mmol, 79% yield). 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

  1. temperatureThe mixture was then cooled in an ice bath
  2. customquenched via addition of methanol (30 mL)
  3. concentrationThe quenched solution was concentrated
  4. dissolutiondissolved in methanol
  5. temperaturerefluxed for 1 h
  6. concentrationThe solution was then concentrated onto silica gel
  7. customchromatographed

출처 및 근거

ORD 기록
ord-904c2d76e18c423cba4b819bd189807b
출처 데이터셋
uspto-grants-2012_05
특허 번호
US08173813B2

반응 노트

불러오는 중…