HCID 21877762, 화합물 → 8-Fluoro-6-nitro-1,2,3,4-tetrahydroquinoline

HRID 1922461노트

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HRID 1922461 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]2

참가 물질

3

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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

  1. temperatureThe reaction mixture was then heated
  2. temperatureto reflux temperature overnight
  3. customquenched with methanol
  4. concentrationThe quenched mixture was then concentrated in vacuo
  5. dissolutionredissolved in methanol
  6. temperaturerefluxed in methanol for 2 h
  7. concentrationThe mixture was then concentrated onto silica gel
  8. customchromatographed

출처 및 근거

ORD 기록
ord-e0691f3898e14f7685bbbe9f125a64ad
출처 데이터셋
uspto-grants-2012_05
특허 번호
US08173813B2

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