Ethanol → HCID 178432286, Verbindung
Reaktionsgleichung
Cl.[NH2:2][C:3]1[N:4]=[CH:5][NH:6][C:7]=1[C:8](=[O:10])[NH2:9].[C:11]([O-:14])(=O)[CH3:12].[Na+].[C:16]1([CH3:22])C=CC=[CH:18][CH:17]=1.C([OH:25])C>>[C:8]([C:7]1[N:6]=[CH:5][N:4]2[C:18]([OH:25])=[C:17]([CH2:12][CH2:11][OH:14])[C:16]([CH3:22])=[N:2][C:3]=12)(=[O:10])[NH2:9]Komponenten
5
Versuchsvorschrift
3 g of 4-amino-5-carbamoylimidazole hydrochloride, 1.51 g of sodium acetate, 1.69 g of ethanol, 7 g of 3-acetyltetrahydro-3-furanone and 45 ml of toluene are introduced successively into a 3-necked flask. The mixture is heated to reflux for 90 h. After cooling, the precipitate formed is taken up with boiling ethanol. The mixture is filtered and the residue is taken up in boiling water, the mixture is filtered and the residue is washed with ethanol and then dried.
Aufarbeitung
- temperatureThe mixture is heated
- temperatureto reflux for 90 h
- temperatureAfter cooling
- customthe precipitate formed
- filtrationThe mixture is filtered
- filtrationthe mixture is filtered
- washthe residue is washed with ethanol
- customdried
Quellen und Nachweise
- ORD-Eintrag
- ord-52fe6cb195bc43c59c00d1ec4e1bcea4
- Quelldatensatz
- uspto-grants-1992_01
- Patentnummer
- US05079249
Notizen zur Reaktion
Wird geladen…