Reacción #1280636

ord-515d729af01a4916b94c28052f22c858

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    OtroAfter work up and evaporation of the methylene chloride solvent
  2. 2
    Otrothe residue was triturated with ethyl acetate

Procedimiento

By the procedure of Example 14, 2 g of 2-(1-methyl-1H-pyrazol-4-yl)benzenesulfonamide, prepared in Example 19, was reacted in 100 ml of methylene chloride with 0.7 g of trimethylaluminum (5 ml of 2M toluene solution) followed by 1.7 g of methyl (4-methoxy-6-methyl-1,3,5-triazin-2-yl)carbamate. After work up and evaporation of the methylene chloride solvent, the residue was triturated with ethyl acetate to yield 0.6 g of the title compound; m.p. 221°-224° C. The IR spectrum showed a carbonyl absorption at 1700 cm-1 indicative for a sulfonylurea.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US04810282uspto-grants-1989_03