Reacción #92753

ord-ee6f02da9b1a4fd3a6a75201845dd495

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    FiltraciónThe reaction mixture was filtered over Celite
  2. 2
    Otrothe solvent was then evaporated under reduced pressure

Procedimiento

To a solution of 1.2 g of benzyl 4-({[8-(cyclohexylmethoxy)-2-methylimidazo[1,2-a]pyridin-3-yl]carbonyl}amino)-4-(2-methoxy-2-oxoethyl)piperidine-1-carboxylate in 30 ml of methanol was added 300 mg of 10% palladium-carbon, followed by stirring overnight under a hydrogen atmosphere. The reaction mixture was filtered over Celite and the solvent was then evaporated under reduced pressure to obtain 900 mg of methyl[4-({[8-(cyclohexylmethoxy)-2-methylimidazo[1,2-a]pyridin-3-yl]carbonyl}amino)piperidin-4-yl]acetate.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US09447090B2uspto-grants-2016_09