Reacción #61527

ord-8b3cc6a0b9da435da253f01bb3052e09

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Otroto precipitate the pure product, which
  2. 2
    Filtraciónwas collected by filtration

Procedimiento

To a solution of 400 mg 1-[5-(5-Chloro-thiophen-2-yl)-isoxazol-3-ylmethyl]-5-furan-2-yl-1H-pyrazole-3-carboxylic acid ethyl ester in 5 ml THF and 1 ml water, 1 ml aqueous NaOH (1M) were added and the mixture was stirred for 16 h at RT. Then the solution was acidified to pH 3 with half concentrated hydrochloric acid to precipitate the pure product, which was collected by filtration. Yield: 360 mg.

Fuente

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