Reacción #1103

ord-13d9fefea0ad416fb3ed3b3104651c13

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Otroare deprotonated at 10° to 20° C.
  2. 2
    Extracciónextracted with methylene chloride
  3. 3
    OtroThe product is purified by column chromatography on silica gel (eluent: ethanol)

Procedimiento

7.8 g of benzyltriphenylphosphonium bromide in 50 ml of ethylene glycol dimethyl ether are deprotonated at 10° to 20° C. using 11 ml of 1.6 molar butyllithium solution in hexane. After 30 minutes 1.3 g of 4-(4-oxocyclohexylamino)-3-methoxy-2-methylpyridine are added dropwise in 10 ml of DMSO. After 5 hours at 40° to 50° C. the mixture is poured into water and extracted with methylene chloride. The product is purified by column chromatography on silica gel (eluent: ethanol). 0.6=41%; m.p.: 120° C.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US05723450uspto-grants-1998_03