Reacción #158342

ord-c8fce6d06f5245a9ba815595f6135105

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Extracciónthe mixture was extracted with ethyl acetate
  2. 2
    LavadoThe extract was washed with saturated brine
  3. 3
    Secadodried over anhydrous sodium sulfate
  4. 4
    Otrothe solvent was evaporated under reduced pressure
  5. 5
    OtroThe residue was purified by silica gel column chromatography (ethyl acetate/hexane)

Procedimiento

Ethyl 8-chloro-3-[3-methoxy-4-(2-methyl-1,3-oxazol-5-yl)phenyl]-5,6,7,8-tetrahydro[1,2,4]triazolo[4,3-a]pyridine-8-carboxylate (1.0 g) was added to a mixture of 3-(trifluoromethyl)phenol (408 mg), potassium carbonate (995 mg) and DMF (10 mL) at 90° C., and the mixture was stirred for 30 min. Saturated aqueous sodium hydrogen carbonate solution was added, and the mixture was extracted with ethyl acetate. The extract was washed with saturated brine, and dried over anhydrous sodium sulfate, and the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate/hexane) to give the title compound (663 mg).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US08822699B2uspto-grants-2014_09