Tetrahydrofuran → 4-Methyl-7-(2-methylphenyl)-5,6,7,8-tetrahydroquinolin-5-one

HRID 1700478

반응식

HRID 1700478 반응식
[CH3:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[CH:8]1[CH2:13][C:12](=O)[CH2:11][C:10](=[O:15])[CH2:9]1.Cl.[NH2:17][CH2:18][C:19]#[C:20][CH3:21].O1CCCC1>C(N(CC)CC)C>[CH3:21][C:20]1[C:11]2[C:10](=[O:15])[CH2:9][CH:8]([C:3]3[CH:4]=[CH:5][CH:6]=[CH:7][C:2]=3[CH3:1])[CH2:13][C:12]=2[N:17]=[CH:18][CH:19]=1

참가 물질

5

실험 절차

To a mixture of 5-(2-methylphenyl)cyclohexane-1,3-dione (1.5 g), 1-amino-2-butyne hydrochloride (0.86 g), molecular sieves 4A (2 g) and tetrahydrofuran (20 ml) was added triethylamine (0.74 g), and the mixture was stirred at room temperature for 1 hour and then refluxed for 17 hours and cooled. Insoluble materials were filtered off. Under reduced pressure, the solvent was evaporated, and the residue was stirred at 220° C. for 4 hours, to which were added ethyl acetate and sodium hydrogen carbonate solution. The organic layer was washed with water and saturated brine, dried with magnesium sulfate and concentrated under reduced pressure, and the residue was purified with silica gel column chromatography (EtOAc/hexane). The resulting crystals were recrystallized from ethyl acetate-hexane to give colorless crystals of 4-methyl-7-(2-methylphenyl)-5,6,7,8-tetrahydroquinolin-5-one (0.52 g).

후처리

  1. temperaturerefluxed for 17 hours
  2. temperaturecooled
  3. filtrationInsoluble materials were filtered off
  4. customUnder reduced pressure, the solvent was evaporated
  5. stirringthe residue was stirred at 220° C. for 4 hours, to which
  6. additionwere added ethyl acetate and sodium hydrogen carbonate solution
  7. washThe organic layer was washed with water and saturated brine
  8. dry with materialdried with magnesium sulfate
  9. concentrationconcentrated under reduced pressure
  10. customthe residue was purified with silica gel column chromatography (EtOAc/hexane)
  11. customThe resulting crystals were recrystallized from ethyl acetate-hexane

출처 및 근거

ORD 기록
ord-f83281d605a8455db1e59cf654f4f318
출처 데이터셋
uspto-grants-2002_02
특허 번호
US06350749B1

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