Reaktionsgleichung
[C:1]([C:4]1[CH:9]=[CH:8][N+:7]([O-])=[CH:6][CH:5]=1)(=[O:3])[CH3:2].[C:11]([NH:16][NH2:17])(=[O:15])[CH2:12][CH2:13][CH3:14].C([OH:20])C>>[OH2:3].[N:7]1[CH:8]=[CH:9][C:4]([C:1](=[N:17][NH+:16]([O-:20])[C:11](=[O:15])[CH2:12][CH2:13][CH3:14])[CH3:2])=[CH:5][CH:6]=1Komponenten
4
Versuchsvorschrift
A mixture of 5.48 gm (0.04 mole) of 4-acetylpyridine 1-oxide, 4.09 gm (0.04 mole) of butyric acid hydrazide and 100 ml of absolute ethanol is refluxed 6 hours. The reactions mixture is evaporated in vacuo to give a solid. The crude product is crystallized from ethyl acetate/ethanol to yield 7.41 gm (84%) of the title compound; mp 209.7°.
Aufarbeitung
- temperatureis refluxed 6 hours
- customThe reactions mixture is evaporated in vacuo
- customto give a solid
- customThe crude product is crystallized from ethyl acetate/ethanol
Quellen und Nachweise
- ORD-Eintrag
- ord-9651429d775a4dc4ab2fc6ea5dcd4e80
- Quelldatensatz
- uspto-grants-1991_04
- Patentnummer
- US05011932
Verknüpfte Notizen
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