Réaction #68393

ord-32ae3754bca94027a12c29c136f4dd5a

Solvants

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    Lavagewashed with H2O and brine
  2. 2
    Séchagedried over Na2SO4
  3. 3
    Concentrationconcentrated in vacuo
  4. 4
    AutreThe residue was purified by chromatography on silica gel (0→30% EtOAc-hexanes)

Mode opératoire

To a solution of ethyl2-tert-butyl-3-(3,4-difluorobenzylcarbamoyl)-1H-indole-6-carboxylate (Compound 115, 33 mg, 0.080 mmol) in DMF (1 ml) was added benzyl bromide (47 μl, 0.40 mmol) and K2CO3 (33 mg, 0.24 mmol). The mixture was stirred at room temperature for 24 h, diluted with EtOAc, washed with H2O and brine, dried over Na2SO4, and concentrated in vacuo. The residue was purified by chromatography on silica gel (0→30% EtOAc-hexanes) followed by PTLC (5% MeOH—CH2Cl2) to yield the title compound.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US08524917B2uspto-grants-2013_09