Reacción #1435735

ord-2414a0388fd14ddf837b721e2c92b3bc

Ecuación de reacción

Fc1cc(F)c(-c2c(Cl)nc3nccn3c2Cl)c(F)c1
5,7-dichloro-6-(2,4,6-trifluorophenyl)-imidazo[1,2-a]pyrimidine
CC1CCCCN1
2-methylpiperidine
CC1CCCCN1c1c(-c2c(F)cc(F)cc2F)c(Cl)nc2nccn12
5-(2-methylpiperidin-1-yl)-6-(2,4,6-trifluorophenyl)-7-chloroimidazo[1,2-a]pyrimidine
Rendimiento 39.8%

Disolventes

Condiciones de reacción

Temperatura
80°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Temperaturato cool

Procedimiento

A mixture of 0.63 g of 5,7-dichloro-6-(2,4,6-trifluorophenyl)-imidazo[1,2-a]pyrimidine, 0.79 g of 2-methylpiperidine and 2 ml of chloroform was heated at 80° C. for one hour. The reaction mixture was allowed to cool and subjected to silica gel column chromatography to give 0.30 g of 5-(2-methylpiperidin-1-yl)-6-(2,4,6-trifluorophenyl)-7-chloroimidazo[1,2-a]pyrimidine.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07211545B2uspto-grants-2007_05