Reacción #50150

ord-2a44389fdbb44b129f553ffddd68fb85

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    OtroThe organic layer is separated
  2. 2
    Lavadowashed with brine
  3. 3
    Otrodried
  4. 4
    Otroevaporated
  5. 5
    OtroThe residue is purified by silica gel column chromatography (solvent; chloroform/methanol)

Procedimiento

A mixture of ethyl 2-ethyl-3-[2'-(t-butoxycarbonyl)biphenyl-4-yl]methyl-4,5,6,7-tetrahydroimidazo[4,5-c]pyridine-4-carboxylate (2.26 g), acetic anhydride (0.94 g), sodium hydrogen carbonate (2.33 g), chloroform (18 ml) and water (18 ml) is stirred overnight at room temperature. The organic layer is separated, washed with brine, dried, and evaporated. The residue is purified by silica gel column chromatography (solvent; chloroform/methanol) to give ethyl 2-ethyl-5-acetyl-3-[2'-(t-butoxycarbonyl)biphenyl-4-yl]methyl-4,5,6,7-tetrahydroimidazo[4,5-c]pyridine-4-carboxylate (2.10 g) as a white foam.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US05424316uspto-grants-1995_06