Reacción #61540

ord-10dda125a7034fc9b1c612e1464b988d

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Otroquenched with diluted HCl
  2. 2
    Filtraciónfiltered through a chem elut® cartridge by elution with ethyl acetate and DCM
  3. 3
    ConcentraciónAfter concentration under reduced pressure the crude residue
  4. 4
    Otrowas directly subjected to the next reaction step

Procedimiento

To a solution of 1 g 1-[5-(5-Chloro-thiophen-2-yl)-isoxazol-3-ylmethyl]-1H-pyrazole-3,5-dicarboxylic acid 3-ethyl ester in 15 ml THF 314 mg LiBH4 were added cautiously. Then the reaction mixture was stirred for 16 h, quenched with diluted HCl and filtered through a chem elut® cartridge by elution with ethyl acetate and DCM. After concentration under reduced pressure the crude residue was directly subjected to the next reaction step. Yield: 800 mg.

Fuente

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