Reaktionsgleichung
Cl[C:2]1[N:7]=[CH:6][N:5]=[C:4]([N:8]2[CH2:13][CH2:12][O:11][CH2:10][CH2:9]2)[CH:3]=1.O.[NH2:15][NH2:16]>C(O)C>[NH:15]([C:2]1[N:7]=[CH:6][N:5]=[C:4]([N:8]2[CH2:13][CH2:12][O:11][CH2:10][CH2:9]2)[CH:3]=1)[NH2:16]Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
53.0 g (0.27 mol) of 4-(6-chloropyrimidin-4-yl)morpholine are initially charged in 260 ml of ethanol. 132.9 g (2.7 mol) of hydrazine hydrate are added, and the mixture is stirred under reflux for 16 h. The mixture is cooled to RT, and half of the solvent is removed by distillation. The mixture is then cooled to 0° C., and the solid formed is filtered off. The solid is washed with cold ethanol and initially air-dried and then dried under reduced pressure.
Aufarbeitung
- temperatureunder reflux for 16 h
- customhalf of the solvent is removed by distillation
- temperatureThe mixture is then cooled to 0° C.
- customthe solid formed
- filtrationis filtered off
- washThe solid is washed with cold ethanol
- custominitially air-dried
- customdried under reduced pressure
Quellen und Nachweise
- ORD-Eintrag
- ord-7c389d41bf3a4ef4b3baa8420d5e64df
- Quelldatensatz
- uspto-grants-2013_09
- Patentnummer
- US08524699B2
Verknüpfte Notizen
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