Reaktion #1168824

ord-ce40fc01ef884b5ab53584cc160ea270

Reaktionsbedingungen

Temperatur
65°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturto cool to about 50° C.
  2. 2
    Temperaturwhile maintaining the reaction mixture temperature at about 50°-53° C
  3. 3
    workup.ADDITIONUpon completion of addition
  4. 4
    Temperaturwhile still maintaining the reaction mixture temperature at about 50° C
  5. 5
    TemperaturAfter this time, the reaction mixture was cooled
  6. 6
    workup.ADDITIONpoured into ice
  7. 7
    workup.STIRRINGwith stirring
  8. 8
    FiltrationA precipitate was collected by filtration
  9. 9
    Waschenrinsed with water
  10. 10
    Sonstigedried

Vorschrift

Concentrated sulfuric acid, 90 mL, and 70% nitric acid, 90 mL, were stirred together during which time the mixture warmed to about 65° C. The mixture was allowed to cool to about 50° C., and 30.0 grams (0.12 mole) of 2,4-diamino-6-ethyl-5-(4-chlorophenyl)pyrimidine (commercially available) was added portionwise during a 45 minute period, while maintaining the reaction mixture temperature at about 50°-53° C. Upon completion of addition, the reaction mixture was stirred for one hour, while still maintaining the reaction mixture temperature at about 50° C. After this time, the reaction mixture was cooled and poured into ice. The resultant mixture was cooled further and, with stirring, was made basic with concentrated ammonium hydroxide. A precipitate was collected by filtration, rinsed with water and dried, yielding 35.4 grams of 2,4-diamino-6-ethyl-5-(4-chloro-3-nitrophenyl)pyrimidine, mp 220°-223° C., dec. The NMR spectrum was consistent with the proposed structure.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05587379uspto-grants-1996_12