Reacción #84474

ord-d38557f23f964613bb73f2e16c57406a

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    FiltraciónThe mixture was then filtered
  2. 2
    Concentraciónthe filtrate was concentrated in vacuo
  3. 3
    OtroThe residue was purified by a silica gel column chromatography (PE/EtOAc (V/V)=1:1)

Procedimiento

To a suspension of 3-(3-fluoro-4-(piperazin-1-yl)phenyl)-2,6-dimethylpyrimidin-4(3H)-one (0.30 g, 1.00 mmol) and K2CO3 (0.69 g, 5.00 mmol) in CH3CN (15 mL) was added 3-bromoprop-1-yne (0.12 g, 1.01 mmol) and the mixture was stirred at rt for 36 h. The mixture was then filtered, and the filtrate was concentrated in vacuo. The residue was purified by a silica gel column chromatography (PE/EtOAc (V/V)=1:1) to give the title compound as a white solid (0.15 g, 44%). The compound was characterized by the following spectroscopic data:

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US09434695B2uspto-grants-2016_09