Réaction #67431

ord-7d217eca82a542c5b4d2f1a5e11e01ee

Solvants

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    FiltrationThe catalyst was filtered off
  2. 2
    Concentrationthe filtrate was concentrated to dryness

Mode opératoire

A suspension of (4′-cyano-biphenyl-3-yl)-carbamic acid tert-butyl ester (7.6 g, 26 mmol) and Raney Ni (1 g) in EtOH (500 mL) and NH3.H2O (10 mL) was hydrogenated under 50 psi of H2 at 50° C. for 6 h. The catalyst was filtered off and the filtrate was concentrated to dryness to give (4′-aminomethyl-biphenyl-3-yl)-carbamic acid tert-butyl ester, which was used directly in next step.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US08524767B2uspto-grants-2013_09