Reacción #157899

ord-f6090705c34d44e294452ccad8fe1e87

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    ConcentraciónThe reaction solution was concentrated under reduced pressure
  2. 2
    OtroThe resulting residue was purified by silica gel column chromatography (hexane:ethyl acetate=88:12→0:100)

Procedimiento

Trifluoroacetic acid (50 mg) was added to a solution of 3-cyclopropyl-6-{[4-(cyclopropylsulfonyl)phenyl](2,4-difluorophenoxy)methyl}-2-[(4-methoxybenzyl)oxy]pyridine (90 mg) in chloroform (5 mL), and the mixture was stirred at room temperature for two hours. The reaction solution was concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography (hexane:ethyl acetate=88:12→0:100) to give the title compound as a yellow powder (53 mg, 74%).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US08822503B2uspto-grants-2014_09