Reacción #61555

ord-57c29de120fb4baaaa05701015f191c3

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    FiltraciónThe precipitating product was collected by filtration
  2. 2
    Otrodried under reduced pressure

Procedimiento

To a solution of 400 mg 1-[(5-Chloro-pyridin-2-ylcarbamoyl)-methyl]-4-(2,2,2-trifluoro-ethoxy)-1H-pyrazole-3,5-dicarboxylic acid diethyl ester in 5 ml THF and 0.9 ml 1N NaOH were added. After standing for 16 h, the solution was acidified using 1 N HCl to pH 1. The precipitating product was collected by filtration and dried under reduced pressure. Yield: 142 mg.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07429581B2uspto-grants-2008_09