반응식
Cl.[CH3:2][C:3]1([CH3:14])[C:12]2[C:7](=[CH:8][CH:9]=[CH:10][CH:11]=2)[N:6](N)[CH2:5][CH2:4]1.O=[C:16]([CH2:20][CH2:21]C(O)=O)[C:17]([OH:19])=[O:18]>C(O)(=O)C>[CH3:2][C:3]1([CH3:14])[C:12]2[C:7]3=[C:8]([C:20]([CH2:16][C:17]([OH:19])=[O:18])=[CH:21][N:6]3[CH2:5][CH2:4]1)[CH:9]=[CH:10][CH:11]=2참가 물질
실험 절차
To a solution of glacial acetic acid (80 mL) and concentrated hydrochloric acid (9 mL) was added 3,4-dihydro-4,4-dimethyl-1-(2H)-quinolinamine (9.5 g, 53.9 mmol) and 2-ketoglutaric acid (9.7 g, 65.1 mmol) and the suspension heated at reflux for 3 hours. After cooling the solvents were removed under reduced pressure and the residue dissolved in 500 mL of ethyl acetate. The ethyl acetate solution was washed with water (3×150 mL) and saturated aqueous sodium chloride (1×50 mL), dried over sodium sulfate,-filtered and concentrated under reduced pressure. The residue was subjected to silica gel chromatography, eluting with 1-4% methanol in dichloromethane. Fractions containing product were combined and concentrated under reduced pressure to provide 4.45 g (34%) of the desired compound as a tan foam. An impure fraction was extracted with 1N sodium hydroxice (2×50 mL) and the combined aqueous layers washed with diethyl ether (20 mL) and made acidic with concentrated hydrochloric acid (8 mL). This aqueous mixture was extracted with dichloromethane (2×100 mL), followed by drying (Na2SO4) to provide an additional 2.55 g (19%) of desired product
후처리
- temperaturethe suspension heated
- temperatureat reflux for 3 hours
- temperatureAfter cooling the solvents
- customwere removed under reduced pressure
- dissolutionthe residue dissolved in 500 mL of ethyl acetate
- washThe ethyl acetate solution was washed with water (3×150 mL) and saturated aqueous sodium chloride (1×50 mL)
- dry with materialdried over sodium sulfate
- concentration-filtered and concentrated under reduced pressure
- washeluting with 1-4% methanol in dichloromethane
- additionFractions containing product
- concentrationconcentrated under reduced pressure
출처 및 근거
- ORD 기록
- ord-810a0b9bc06a41b2be897756a6f3c268
- 출처 데이터셋
- uspto-grants-2004_06
- 특허 번호
- US06743785B2
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