Reacción #54721
ord-aaf95424dd714d558075c4f775f387bd
Ecuación de reacción
Reactantes
Reactivos
Ninguno
Disolventes
Condiciones de reacción
Temperatura
5°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.
Tratamiento posterior
- 1workup.ADDITIONThe mixture is treated with 45 ml
- 2OtroThe mixture obtained
- 3Lavadois washed with water
- 4Extracciónextracted with methylene chloride
- 5Otroevaporated under reduced pressure
- 6OtroThe residue is recrystallized from ethanol, there
Procedimiento
20 G. of 2,4-diamino-6-[3,6-dihydro-1(2H)-pyridyl]pyrimidine-3-oxide are mixed with 250 ml. of methylene chloride and 35 ml. of triethylamine, stirred and cooled to 5° C. The mixture is treated with 45 ml. of chloroformic acid butyl ester and stirred at room temperature for 6 hours. The mixture obtained is washed with water, extracted with methylene chloride and evaporated under reduced pressure. The residue is recrystallized from ethanol, there being obtained dibutyl 6-[3,6-dihydro-1(2H)-pyridyl]-2,4-pyrimidine-dicarbamate-3-oxide, having a melting point of 131°-132° C.