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

HRID 1922475ノート

反応式

HRID 1922475 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.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

参加物

3

反応条件

温度
60 °C

実験手順

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).

後処理

  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

出典と根拠

ORDレコード
ord-904c2d76e18c423cba4b819bd189807b
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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