Selenium Dioxide → 1-Methyl-1H-imidazo(4,5-c)pyridine-2-carboxaldehyde
Reaktionsgleichung
[CH3:1][N:2]1[C:10]2[CH:9]=[CH:8][N:7]=[CH:6][C:5]=2[N:4]=[C:3]1[CH3:11].[Se](=O)=[O:13]>O1CCOCC1>[CH3:1][N:2]1[C:10]2[CH:9]=[CH:8][N:7]=[CH:6][C:5]=2[N:4]=[C:3]1[CH:11]=[O:13]Komponenten
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Reaktionsbedingungen
- Temperatur
- 130 °C
Versuchsvorschrift
To a solution of 1,2-dimethyl-1H-imidazo[4,5-c]pyridine (500 mg, 3.40 mmol) in dry 1,4-dioxane (7.5 mL) was added http://newsearchch.chemexper.com/cheminfo/servlet/org.dbcreator.MainServlet?sort=%3E%7Eentry.int Value&query=structure._structureID%3D4635571 &target=entry&action=PowerSearch&onclick=1 &from=0 &history=off&forGroupNames=&style=&realQuery=rn.value%3D%22CF3 COOH%22+elsor+entry.catalogID%3D%22CF3 COOH%22+elsor+iupac.value%3D%22CF3 COOH%22+elsor+mf.value%3D%22CF3 COOH%22+elsor+%28iupac.value%3D%7E%22CF3 COOH%22+ or +catalog.description%3D%7E%22CF3 COOH%22%29&format=ccd&searchTemplate=rn.value%3D%3F+elsor+entry.catalogID%3D%3 selenium dioxide (665 mg, 5.10 mmol). The mixture heated by microwave at 130° C. for 5 min. Then the mixture was filtered and concentrated to give the crude product, which was purified by column chromatography (silica gel, petroleum ether:DCM 10:1 to 1:1) to give the title compound (400 mg, yield 28%). LC-MS (ESI) m/z: 162 (M+1)+. 1H-NMR (400 MHz, CD3OD) δ (ppm): 3.61 (s, 3H), 5.91 (s, 1H), 7.67-7.70 (d, J=5.6 Hz, 1H), 8.39-8.41 (d, J=5.6 Hz, 1H), 8.93 (s, 1H).
Aufarbeitung
- filtrationThen the mixture was filtered
- concentrationconcentrated
- customto give the crude product, which
- customwas purified by column chromatography (silica gel, petroleum ether:DCM 10:1 to 1:1)
Quellen und Nachweise
- ORD-Eintrag
- ord-20b4d9807cc84e2ea17adc5587d13356
- Quelldatensatz
- uspto-grants-2013_04
- Patentnummer
- US08420650B2
Notizen zur Reaktion
Wird geladen…