Piperidine → HCID 69181070, Verbindung
Reaktionsgleichung
[N+:1]([N:4]1[C:9](=[O:10])[CH:8]=[CH:7][NH:6][C:5]1=[O:11])([O-:3])=[O:2].N1CCC[CH2:14][CH2:13]1>C(O)C>[CH:13]([C:8]1[C:9](=[O:10])[N:4]([N+:1]([O-:3])=[O:2])[C:5](=[O:11])[NH:6][CH:7]=1)=[CH2:14]Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
As shown in Scheme 1, a suitable nitro-uracil precursor, (1), is mixed with an appropriate aldehyde, (2), and piperidine, in a suitable solvent such as ethanol. The solution is heated to reflux for approximately 10-20 hours. After reflux, the mixture is concentrated and purified using conventional methods, such as thin layer chromatography, to produce the vinyl-nitro-uracil (3).
Aufarbeitung
- temperatureThe solution is heated
- temperatureto reflux for approximately 10-20 hours
- temperatureAfter reflux
- concentrationthe mixture is concentrated
- custompurified
Quellen und Nachweise
- ORD-Eintrag
- ord-8c6aeed16de9417a8f4b15f68c80124a
- Quelldatensatz
- uspto-grants-2008_11
- Patentnummer
- US07449473B2
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