Reacción #8718

ord-6f110095d41b437f9aec3433c29d3d1d

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    workup.ADDITIONpoured onto ice water
  2. 2
    OtroThe organic phase is separated off
  3. 3
    ExtracciónThe aqueous phase is extracted once again with dichloromethane
  4. 4
    Otrodried
  5. 5
    Otroevaporated

Procedimiento

372.3 mg (1.1 mmol) of 8-cyclopentyl-2-(2-ethoxy-phenyl)-6-methyl-3H-imidazo[1,5-a][1,3,5]triazin-4-one (example IX) are added in portions to 0.66 ml (9.9 mmol) of ice-cooled chlorosulfonic acid. The mixture is subsequently stirred overnight at room temperature before being diluted with dichloromethane and poured onto ice water. The organic phase is separated off. The aqueous phase is extracted once again with dichloromethane and the organic phases are combined, dried and evaporated.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07091203B2uspto-grants-2006_08