HCID 21877762、化合物 → 8-Fluoro-6-nitro-1,2,3,4-tetrahydroquinoline

HRID 1922461ノート

反応式

HRID 1922461 の反応式
[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

参加物

3

反応条件

温度
0 °C

実験手順

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).

後処理

  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

出典と根拠

ORDレコード
ord-e0691f3898e14f7685bbbe9f125a64ad
出典データセット
uspto-grants-2012_05
特許番号
US08173813B2

反応ノート

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