Reacción #4436

ord-8713f1a083924a5fa46b8a31925ba557

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    LavadoThe reaction mixture was washed with water
  2. 2
    Secadodried over magnesium sulfate
  3. 3
    Otroevaporated
  4. 4
    OtroThe obtained mixture was chromatographed on silica gel eluting with chloroform-methanol mixture (49:1 v/v)

Procedimiento

To a solution of 6-(3,4-dimethoxyphenyl)-2-methyl-4-(1-piperazinyl)pyrimidine (0.8 g) in chloroform (10 ml) were added triethylamine (0.39 ml) and 2,4-dichloro-5-sulfamoylbenzoyl chloride (0.74 g), and the mixture was stirred at ambient temperature for 20 hours. The reaction mixture was washed with water, dried over magnesium sulfate, and evaporated. The obtained mixture was chromatographed on silica gel eluting with chloroform-methanol mixture (49:1 v/v), to give 4-[4-(2,4-dichloro-5-sulfamoylbenzoyl)piperazin-1-yl]-6-(3,4-dimethoxyphenyl)-2-methylpyrimidine (1.03 g).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US04725600uspto-grants-1988_02