Reacción #48816

ord-09e532e382744faebd128349e8aaedc0

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Otropurged with, Argon (×3)
  2. 2
    workup.ADDITIONPalladium on carbon (10% w/w, 400 mg) was added
  3. 3
    Otroreaction mixture
  4. 4
    Otrowas evacuated
  5. 5
    Otrofinally purged with hydrogen gas
  6. 6
    OtroReaction mixture
  7. 7
    workup.WAITwas left
  8. 8
    FiltraciónPd/C was filtered off
  9. 9
    Concentraciónconcentrated in vacuo

Procedimiento

A solution of 3-(benzyloxy)-5-((1S)-2-{[tert-butyl(dimethyl)silyl]oxy}-1-methylethoxy)-N-(1-isopropyl-1H-pyrazol-3-yl)benzamide (1.97 g, 3.77 mmol) and THF (70 mL) was evacuated and purged with, Argon (×3). Palladium on carbon (10% w/w, 400 mg) was added and reaction mixture was evacuated and finally purged with hydrogen gas. Reaction mixture was left to stir at ambient temperature under hydrogen for 16 hours. Pd/C was filtered off and concentrated in vacuo to give the product as a colourless oil (1.58 g, 97%).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07745475B2uspto-grants-2010_06