Reacción #356433

ord-4fdec7db3f724e3597768bfa9390a87b

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Procedimiento

The title compound was prepared from 5-(3-ethoxy-4-trifluoromethyl-phenyl)-3-ethynyl-7-trifluoromethyl-pyrazolo[1,5-a]pyrimidine (example C.3) (400 mg, 1 mmol) and commercially available 2-amino-5-bromopyridine (156 mg, 1 mmol) according to general procedure II. Obtained as a red solid (62 mg, 12%). MS (ISP) 492.2 [(M+H)+]; mp 218° C.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07446113B2uspto-grants-2008_11