Reacción #87385

ord-bf500ce66b424f97b4f9bdfd3fce0bff

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Filtraciónthe suspension was filtered
  2. 2
    OtroThe mixture was purified by preparative HPLC

Procedimiento

1-Amino-2-methylpropan-2-ol hydrochloride (221 mg, 1.76 mmol) was suspended in MeOH (2 mL). Triethylamine (0.147 mL, 1.06 mmol) was added and the suspension was filtered. The filtrate was added to an ice-cold solution of 2,4-dichloro-6-((2,2,2-trifluoroethoxy)methyl)-pyrimidine (92 mg, 0.35 mmol) in acetonitrile (2 mL). The mixture was stirred for 1 h at rt. The mixture was purified by preparative HPLC to give the title compound (35 mg, 32%).

Fuente

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