Reacción #6792

ord-17ed47ef835b4d92b99869f4520b7108

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    OtroThis resulted in a precipitate
  2. 2
    Otrobeing formed
  3. 3
    Filtraciónwhich was collected by filtration
  4. 4
    Otrodried in vacuo (0.258 g)
  5. 5
    OtroThis material was then purified by autopurification

Procedimiento

To a solution of 2-(methylsulfonyl)-4-[4-(methylsulfonyl)phenyl]-6-(trifluoromethyl)pyrimidine (0.277 g, 0.73 mmol) in N-methylpyrrolidone (1.25 ml) was added tetrahydro-2H-pyran-4-amine (0.147 g, 2 eq.), the mixture was stirred for 1 hour and then water (1.25 ml) was added dropwise. This resulted in a precipitate being formed, which was collected by filtration, and dried in vacuo (0.258 g). This material was then purified by autopurification to give the title compound as a colourless solid (0.116 g, 40%).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07084148B2uspto-grants-2006_08