Reacción #159015

ord-d7ce7cf331b84e96a50a523c59f59f68

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Otroevaporated under vacuum
  2. 2
    workup.DISSOLUTIONSolid was dissolved in dichloromethane (50 mL)
  3. 3
    Extracciónextracted with saturated NaHCO3 solution (50 mL)
  4. 4
    FiltraciónSolid was collected by vacuum filtration
  5. 5
    Lavadowashed with dichloromethane
  6. 6
    Otrodried under vacuum

Procedimiento

2-[5-(6-Bromonaphthalen-2-yl)-1H-imidazol-2-yl]-pyrrolidine-1-carboxylic acid tert-butyl ester (5.03 g) was dissolved in dichloromethane (75 mL), and trifluoroacetic acid (25 mL) was added. The reaction mixture was stirred at ambient temperature for 5 hours and evaporated under vacuum. Solid was dissolved in dichloromethane (50 mL) and extracted with saturated NaHCO3 solution (50 mL). Solid was collected by vacuum filtration, washed with dichloromethane, and dried under vacuum, giving 5-(6-Bromo-naphthalen-2-yl)-2-pyrrolidin-2-yl-1H-imidazole (98%) as an off-white solid.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US08822430B2uspto-grants-2014_09