Sodium Iodide → Ethyl 8-(2,6-Dimethylbenzylamino)-3,6-dimethylimidazo[1,2-a]pyridin-2-carboxylate
Reaktionsgleichung
[NH2:1][C:2]1[C:3]2[N:4]([C:9]([CH3:17])=[C:10]([C:12]([O:14][CH2:15][CH3:16])=[O:13])[N:11]=2)[CH:5]=[C:6]([CH3:8])[CH:7]=1.[CH3:18][C:19]1[CH:26]=[CH:25][CH:24]=[C:23]([CH3:27])[C:20]=1[CH2:21]Cl.C(=O)([O-])[O-].[K+].[K+].[I-].[Na+]>C(#N)C>[CH3:18][C:19]1[CH:26]=[CH:25][CH:24]=[C:23]([CH3:27])[C:20]=1[CH2:21][NH:1][C:2]1[C:3]2[N:4]([C:9]([CH3:17])=[C:10]([C:12]([O:14][CH2:15][CH3:16])=[O:13])[N:11]=2)[CH:5]=[C:6]([CH3:8])[CH:7]=1Komponenten
6
Edukt 4
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
Ethyl 8-amino-3,6-dimethylimidazo[1,2-a]pyridin-2-carboxylate (1.3 g, 5.6 mmol), 2,6-dimethylbenzyl chloride (0.9 g, 6.2 mmol), potassium carbonate (1.5 g, 11 mmol) and sodium iodide (0.1 g, 0.6 mmol) were added to acetonitrile (15 ml) and refluxed for 20 h. The solvent was evaporated under reduced pressure. The residue was dissolved in methylene chloride , washed twice with water and the organic layer was separated dried (Na2SO4) and evaporated under reduced pressure. Purification of the residue by column chromatography on silica gel using heptane:ethyl acetate (2:1) as eluent gave 0.9 g (47%) of the title compound as an oil.
Aufarbeitung
- temperaturerefluxed for 20 h
- customThe solvent was evaporated under reduced pressure
- dissolutionThe residue was dissolved in methylene chloride
- washwashed twice with water
- customthe organic layer was separated
- dry with materialdried (Na2SO4)
- customevaporated under reduced pressure
- customPurification of the residue by column chromatography on silica gel
Quellen und Nachweise
- ORD-Eintrag
- ord-8532f34b556b4cfda8b41e11893ad865
- Quelldatensatz
- uspto-grants-2003_09
- Patentnummer
- US06613775B1
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