Reacción #155332
ord-a6485173d4c742ca9980532f6bdcee22
Ecuación de reacción
Reactantes
Reactivos
Disolventes
Condiciones de reacción
Tratamiento posterior
- 1ConcentraciónThe resulting mixture was concentrated under reduced pressure
- 2workup.ADDITIONAfter adding an aqueous sodium bicarbonate solution to the residue
- 3Lavadothe residue was washed with ethyl acetate
- 4workup.ADDITIONA 2N aqueous sodium hydroxide solution was added to the water layer
- 5Extracciónfollowed by extraction
- 6LavadoThe thus-obtained organic layer was washed with an aqueous saturated sodium chloride solution
- 7Secadodried over anhydrous magnesium sulfate
- 8Concentraciónconcentrated under reduced pressure
- 9OtroThe residue was recrystallized from ethanol-ethyl acetate
Procedimiento
A 4N hydrochloric acid ethyl acetate solution (25 ml) was added to an ethanol solution (12 ml) of tert-butyl 4-{2-[5-fluoro-3-(4-methoxyphenyl)-4-oxo-8-propoxy-4H-quinolin-1-yl]acetylamino}piperidine-1-carboxylate (820 mg, 1.44 mmol), followed by stirring at room temperature for 28 hours. The resulting mixture was concentrated under reduced pressure. After adding an aqueous sodium bicarbonate solution to the residue to adjust the pH to 8, the residue was washed with ethyl acetate. A 2N aqueous sodium hydroxide solution was added to the water layer to adjust its pH to 11, followed by extraction using dichloromethane. The thus-obtained organic layer was washed with an aqueous saturated sodium chloride solution and dried over anhydrous magnesium sulfate, and then concentrated under reduced pressure. The residue was recrystallized from ethanol-ethyl acetate, giving a white powder of 2-[5-fluoro-3-(4-methoxyphenyl)-4-oxo-8-propoxy-4H-quinolin-1-yl]-N-piperidin-4-ylacetamide (185 mg, yield: 27%).