Reacción #83638

ord-0a4079327cef4180b80bdeb70fb51037

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Temperaturacooled in an ice bath
  2. 2
    Otrothe solvents are evaporated off under vacuum
  3. 3
    OtroThe white solid obtained
  4. 4
    Filtraciónis filtered off
  5. 5
    Lavadowashed with isopropyl ether
  6. 6
    Otrodried under vacuum

Procedimiento

0.50 g of 1-(2,4-dichlorophenyl)-5-(4-chlorophenyl)-1H-pyrazol-3-ylamine, obtained in the previous Example, is added in small portions to a mixture of 4 ml of formic acid and 0.5 ml of acetic anhydride, cooled in an ice bath. After stirring for 30 min, the solvents are evaporated off under vacuum and the residue is taken up in isopropyl ether. The white solid obtained is filtered off, washed with isopropyl ether and dried under vacuum to give 0.49 g of the expected formamide.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US05624941uspto-grants-1997_04