Sodium Iodide → Ethyl 8-(2,6-Dimethylbenzylamino)-3,6-dimethylimidazo[1,2-a]pyridin-2-carboxylate

HRID 1166171Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1166171
[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]=1

Komponenten

6

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

  1. temperaturerefluxed for 20 h
  2. customThe solvent was evaporated under reduced pressure
  3. dissolutionThe residue was dissolved in methylene chloride
  4. washwashed twice with water
  5. customthe organic layer was separated
  6. dry with materialdried (Na2SO4)
  7. customevaporated under reduced pressure
  8. 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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