Tetrahydrofuran → 7-(4-Fluorophenyl)-4-methyl-5,6,7,8-tetrahydroquinolin-5-one
Reaktionsgleichung
[F:1][C:2]1[CH:7]=[CH:6][C:5]([CH:8]2[CH2:13][C:12](=[O:14])[CH2:11][C:10](=O)[CH2:9]2)=[CH:4][CH:3]=1.Cl.[NH2:17][CH2:18][C:19]#[C:20][CH3:21].O1CCCC1>C(N(CC)CC)C>[F:1][C:2]1[CH:3]=[CH:4][C:5]([CH:8]2[CH2:9][C:10]3[N:17]=[CH:18][CH:19]=[C:20]([CH3:21])[C:11]=3[C:12](=[O:14])[CH2:13]2)=[CH:6][CH:7]=1Komponenten
Reaktionsbedingungen
- Temperatur
- 220 °C
Versuchsvorschrift
To a mixture of 5-(4-fluorophenyl)cyclohexane-1, 3-dione (0.98 g), 1-amino-2-butyne hydrochloride (0.5 g), molecular sieves 4A (2 g) and tetrahydrofuran (20 ml) was added triethylamine (0.48 g), and the mixture was refluxed for 14 hours and cooled. Insoluble materials were filtered off. Under reduced pressure, the solvent was evaporated, and the residue was stirred for 6 hours at 220° C. and cooled, 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) to give oil of 7-(4-fluorophenyl)-4methyl-5,6,7,8-tetrahydroquinolin-5-one (0.35 g).
Aufarbeitung
- temperaturethe mixture was refluxed for 14 hours
- temperaturecooled
- filtrationInsoluble materials were filtered off
- customUnder reduced pressure, the solvent was evaporated
- temperaturecooled, to which
- additionwere added ethyl acetate and sodium hydrogen carbonate solution
- washThe organic layer was washed with water and saturated brine
- dry with materialdried with magnesium sulfate
- concentrationconcentrated under reduced pressure
- customthe residue was purified with silica gel column chromatography (EtoAc/hexane)
Quellen und Nachweise
- ORD-Eintrag
- ord-7b1d9882db1e45fab35f7d280fdeb31f
- Quelldatensatz
- uspto-grants-2002_02
- Patentnummer
- US06350749B1
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