Reacción #50145

ord-922ecb3170614f658349b850a7ad2d53

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    LavadoThe reaction mixture is washed with a saturated sodium hydrogen carbonate solution and brine
  2. 2
    Otrodried
  3. 3
    Otroevaporated
  4. 4
    OtroThe crude product is purified by silica gel column chromatography (solvent; chloroform/methanol)

Procedimiento

The mixture of ethyl 2-n-propyl-3-[2'-(t-butoxycarbonyl)biphenyl-4-yl]methyl-5-ethoxycarbonylacetyl-4,5,6,7-tetrahydroimidazo[4,5-c]pyridine-4-carboxylate (657 mg), trifluoroacetic acid (3 ml) and methylene chloride (10 ml) is stirred overnight at room temperature. The reaction mixture is washed with a saturated sodium hydrogen carbonate solution and brine, dried, and evaporated. The crude product is purified by silica gel column chromatography (solvent; chloroform/methanol) to give ethyl 2-n-propyl-3-(2'-carboxybiphenyl-4-yl)methyl-5-ethoxycarbonylacetyl-4,5,6,7-tetrahydroimidazo[4,5-c]pyridine-4-carboxylate (516 mg).

Fuente

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