Reacción #87364

ord-1014dd22256d4840b7f82a0e4d5823d7

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    workup.ADDITIONadded
  2. 2
    OtroThe solvent was evaporated
  3. 3
    OtroThe mixture was purified by preparative HPLC the title compound (194 mg, 73%)

Procedimiento

To a solution of 2,4-dichloro-6-((2,2,2-trifluoroethoxy)methyl)pyrimidine (200 mg, 0.77 mmol) in acetonitrile (3 mL) was benzylmethylamine (0.296 mL, 2.30 mmol) added. The reaction was stirred at ambient temperature for 30 minutes. The solvent was evaporated. The mixture was purified by preparative HPLC the title compound (194 mg, 73%).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US09439904B2uspto-grants-2016_09