Reaktion #528152
ord-a354ce187e3a42f8bd87e5e13956ecee
Reaktionsgleichung
Edukte
Reagenzien
Reaktionsbedingungen
Aufarbeitung
- 1Temperaturto cool to about 50° C.
- 2Temperaturwhile maintaining the reaction mixture temperature at about 50°-53° C
- 3workup.ADDITIONUpon completion of addition
- 4Temperaturwhile still maintaining the reaction mixture temperature at about 50° C
- 5TemperaturAfter this time, the reaction mixture was cooled
- 6workup.ADDITIONpoured into ice
- 7workup.STIRRINGwith stirring
- 8FiltrationA precipitate was collected by filtration
- 9Waschenrinsed with water
- 10Sonstigedried
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.