Reaktionsgleichung
[C:1]([NH:6][C:7]1[C:12]([N+:13]([O-])=O)=[C:11]([CH3:16])[CH:10]=[CH:9][N:8]=1)(=O)[CH2:2][CH2:3][CH3:4]>C(O)(=O)C.C(O)C.[Fe]>[CH3:16][C:11]1[CH:10]=[CH:9][N:8]=[C:7]2[NH:6][C:1]([CH2:2][CH2:3][CH3:4])=[N:13][C:12]=12Komponenten
Edukt 1
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 3
Reaktionsbedingungen
- Temperatur
- 90 °C
Versuchsvorschrift
A solution of 2-butyrylamino-4-methyl-3-nitropyridine (7.0 g) and iron powder (17.5 g) in a mixture of acetic acid (14 ml) and ethanol (100 ml) was stirred at 90° C. for 3 hours under nitrogen atmosphere. After being cooled to room temperature, the reaction mixture was filtered through Celite and the filtrate was evaporated in vacuo. Ethyl acetate and saturated aqueous sodium hydrogencarbonate were added to the residue until pH 7~8 and the resulting suspension was filtered through Celite. The organic layer of the filtrate was separated, washed with brine and dried over magnesium sulfate. The solvent was evaporated in vacuo and the residue was purified with silica gel column chromatography (eluent: ethyl acetate) to give 7-methyl-2-propyl-3H-imidazo[4,5-b]pyridine (3.6 g).
Aufarbeitung
- temperatureAfter being cooled to room temperature
- filtrationthe reaction mixture was filtered through Celite
- customthe filtrate was evaporated in vacuo
- additionEthyl acetate and saturated aqueous sodium hydrogencarbonate were added to the residue until pH 7~8
- filtrationthe resulting suspension was filtered through Celite
- customThe organic layer of the filtrate was separated
- washwashed with brine
- dry with materialdried over magnesium sulfate
- customThe solvent was evaporated in vacuo
- customthe residue was purified with silica gel column chromatography (eluent: ethyl acetate)
Quellen und Nachweise
- ORD-Eintrag
- ord-4ea7fbf12f5f465086af47a2d5d03b9e
- Quelldatensatz
- uspto-grants-1993_05
- Patentnummer
- US05210092
Verknüpfte Notizen
Wird geladen…