Reacción #162817

ord-5bc2ea202f5a4324ab8f4d8de557b541

Reactivos

Ninguno

Disolventes

Condiciones de reacción

Temperatura
90°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    workup.ADDITIONwas added under a nitrogen atmosphere
  2. 2
    workup.STIRRINGThe mixture was stirred at 100° C. for 1.5 hrs
  3. 3
    Temperaturato cool to room temperature
  4. 4
    ConcentraciónThe reaction mixture was concentrated under reduced pressure
  5. 5
    workup.ADDITIONEthanol (500 ml) was added to the residue
  6. 6
    workup.STIRRINGthe mixture was stirred at 90° C
  7. 7
    TemperaturaWhen the mixture was cooled to 40° C.
  8. 8
    Filtraciónthe crystals were collected by filtration
  9. 9
    Lavadowashed with ethanol
  10. 10
    Otrodried

Procedimiento

Acetic anhydride (290 ml) was added to 1,3-diphenylurea 18 (148 g), malonic acid 4 (81.6 g) was added under a nitrogen atmosphere, and the mixture was stirred at 90° C. for 3 hrs. The mixture was stirred at 100° C. for 1.5 hrs and allowed to cool to room temperature. The reaction mixture was concentrated under reduced pressure. Ethanol (500 ml) was added to the residue, and the mixture was stirred at 90° C. When the mixture was cooled to 40° C., the crystals were collected by filtration, washed with ethanol and dried to give 1,3-diphenyl-pyrimidine-2,4,6-trione 19 (78.0 g, yield 40%).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US08835443B2uspto-grants-2014_09