Reaktionsgleichung
[CH3:1][C:2]1[CH:7]=[CH:6][C:5]([C:8](=O)[CH3:9])=[CH:4][N:3]=1.[C:11]([NH:14][NH2:15])(=[O:13])[CH3:12].C(O)C>CCCCCC>[CH3:1][C:2]1[N:3]=[CH:4][C:5]([C:8](=[N:15][NH:14][C:11](=[O:13])[CH3:12])[CH3:9])=[CH:6][CH:7]=1Komponenten
5
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
A mixture of 6.76 gm (0.05 mole) of 2-methyl-5-acetylpyridine, 3.7 gm (0.05 mole) of acetic acid hydrazide and 100 ml of ethanol was refluxed 5 hr. The solution was diluted with Skellysolve B until cloudy. The mixture was cooled to room temperature and then chilled in the freezer. The product was collected, washed with Skellysolve B and dried to afford 7.93 gm (83%) of the title compound having a melting point of 178.5° C.
Aufarbeitung
- temperaturewas refluxed 5 hr
- temperaturechilled in the freezer
- customThe product was collected
- washwashed with Skellysolve B
- customdried
Quellen und Nachweise
- ORD-Eintrag
- ord-948ebe38f64748edb27c9769bb893aaa
- Quelldatensatz
- uspto-grants-1991_04
- Patentnummer
- US05011932
Verknüpfte Notizen
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