Reaktionsgleichung
[O-]CC.[Na+].[C:5]([O:14][CH2:15][CH3:16])(=[O:13])/[CH:6]=[CH:7]\[C:8]([O:10]CC)=O.[NH:17]([C:19]1[CH:20]=[N:21][CH:22]=[CH:23][CH:24]=1)[NH2:18]>C(O)C>[O:10]=[C:8]1[NH:18][N:17]([C:19]2[CH:20]=[N:21][CH:22]=[CH:23][CH:24]=2)[CH:6]([C:5]([O:14][CH2:15][CH3:16])=[O:13])[CH2:7]1Komponenten
5
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
In a preferred reaction, sodium ethoxide in an anhydrous ethanol are introduced into a reaction vessel and 3-hydrazinopyridine•dihydrochloride is added. The mixture is stirred and diethyl maleate is added. The mixture is heated at about 60° C. until most of the 3-hydrazinopyridine has reacted. The mixture is allowed to cool and the excess base is neutralized with acid. The crude ethyl 5-oxo-2-(pyridin-3-yl)pyrazolidine-3-carboxylate (10a) is conveniently isolated and purified by standard techniques.
Aufarbeitung
- additionare introduced into a reaction vessel
- customhas reacted
- temperatureto cool
Quellen und Nachweise
- ORD-Eintrag
- ord-42d8946a0a5a4bf3931940a96bca62d0
- Quelldatensatz
- uspto-grants-2015_08
- Patentnummer
- US09115115B1
Verknüpfte Notizen
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