Acetic Acid → 4-(Pyridin-3-yl)-1,2-oxazol-5-amine
Reaktionsgleichung
CN(C)[CH:3]([C:6]1[CH:7]=[N:8][CH:9]=[CH:10][CH:11]=1)[C:4]#[N:5].Cl.[NH2:14]O.[C:16]([OH:19])(=O)C>>[NH2:14][C:16]1[O:19][N:5]=[CH:4][C:3]=1[C:6]1[CH:7]=[N:8][CH:9]=[CH:10][CH:11]=1Komponenten
4
Reaktionsbedingungen
- Temperatur
- 100 °C
Versuchsvorschrift
To a solution of α-(dimethylamino)-α-(3-pyridyl)acetonitrile (5.19 g, 30 mmol) in acetic acid (40 ml) was added hydroxylamine hydrochloride (2.8 g, 40 mmol). The reaction mixture was stirred at 100° C. for 1 hour, cooled to room temperature and concentrated in vacuo. Water (50 ml) was added and the reaction mixture neutralized with solid potassium carbonate. The precipitated compound was filtered washed with water and dried giving the title compound in 4.2 g yield.
Aufarbeitung
- temperaturecooled to room temperature
- concentrationconcentrated in vacuo
- additionWater (50 ml) was added
- filtrationThe precipitated compound was filtered
- washwashed with water
- customdried
Quellen und Nachweise
- ORD-Eintrag
- ord-44726756555341708a135445766640bd
- Quelldatensatz
- uspto-grants-1999_11
- Patentnummer
- US05994373
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