Reaktionsgleichung
[CH3:1][O:2][C:3]1[CH:4]=[C:5]([CH:10]=[CH:11][C:12]=1[N+:13]([O-:15])=[O:14])[C:6]([NH:8][NH2:9])=O.[C:16]([NH2:19])(=S)[CH3:17]>N1C=CC=CC=1>[CH3:1][O:2][C:3]1[CH:4]=[C:5]([C:6]2[NH:19][C:16]([CH3:17])=[N:9][N:8]=2)[CH:10]=[CH:11][C:12]=1[N+:13]([O-:15])=[O:14]Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Reaktionsbedingungen
- Temperatur
- 95 °C
Versuchsvorschrift
The mixture consisting of 590 mg g of 3-methoxy-4-nitrobenzoic hydrazide, 6 ml of pyridine and 210 mg of thioacetamide was heated to 95° C. for 2 hours. After cooling, the volatile fractions were removed under reduced pressure at 40° C. and the residue was subjected to column chromatography purification (silica gel, solvent: 95:5 dichloromethane:methanol)
Aufarbeitung
- temperatureAfter cooling
- customthe volatile fractions were removed under reduced pressure at 40° C.
- customthe residue was subjected to column chromatography purification (silica gel, solvent: 95:5 dichloromethane:methanol)
Quellen und Nachweise
- ORD-Eintrag
- ord-1b016a8858ed40a18d46df865caf42b4
- Quelldatensatz
- uspto-grants-2006_11
- Patentnummer
- US07138414B2
Verknüpfte Notizen
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