Reacción #155332

ord-a6485173d4c742ca9980532f6bdcee22

Ecuación de reacción

CCOC(C)=O.Cl
hydrochloric acid ethyl acetate
CCCOc1ccc(F)c2c(=O)c(-c3ccc(OC)cc3)cn(CC(=O)NC3CCN(C(=O)OC(C)(C)C)CC3)c12
tert-butyl 4-{2-[5-fluoro-3-(4-methoxyphenyl)-4-oxo-8-propoxy-4H-quinolin-1-yl]acetylamino}piperidine-1-carboxylate
CCCOc1ccc(F)c2c(=O)c(-c3ccc(OC)cc3)cn(CC(=O)NC3CCNCC3)c12
2-[5-fluoro-3-(4-methoxyphenyl)-4-oxo-8-propoxy-4H-quinolin-1-yl]-N-piperidin-4-ylacetamide
Rendimiento 27.5%

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    ConcentraciónThe resulting mixture was concentrated under reduced pressure
  2. 2
    workup.ADDITIONAfter adding an aqueous sodium bicarbonate solution to the residue
  3. 3
    Lavadothe residue was washed with ethyl acetate
  4. 4
    workup.ADDITIONA 2N aqueous sodium hydroxide solution was added to the water layer
  5. 5
    Extracciónfollowed by extraction
  6. 6
    LavadoThe thus-obtained organic layer was washed with an aqueous saturated sodium chloride solution
  7. 7
    Secadodried over anhydrous magnesium sulfate
  8. 8
    Concentraciónconcentrated under reduced pressure
  9. 9
    OtroThe 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%).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: USRE045108E1uspto-grants-2014_09