Reacción #83638
ord-0a4079327cef4180b80bdeb70fb51037
Ecuación de reacción
Reactivos
Ninguno
Disolventes
Condiciones de reacción
Condiciones detalladas
See reaction.notes.procedure_details.
Tratamiento posterior
- 1Temperaturacooled in an ice bath
- 2Otrothe solvents are evaporated off under vacuum
- 3OtroThe white solid obtained
- 4Filtraciónis filtered off
- 5Lavadowashed with isopropyl ether
- 6Otrodried 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.