IMidazo[1,2-a]pyridine,6-Methoxy- Chemical Properties

Density 

1.18±0.1 g/cm3(Predicted)

storage temp. 

Sealed in dry,Room Temperature

pka

6.28±0.50(Predicted)

Safety Information

HS Code 

2933998090

IMidazo[1,2-a]pyridine,6-Methoxy- Usage And Synthesis

Uses

6-Methoxyimidazo[1,2-a]pyridine are?imidazopyridines. This class of compounds are suggested to?inhibit?interleukin-1 receptor-associated kinase 4 (IRAK-4), which is a protein kinase involved in the signalling of innate immune response from Toll-like receptors (TLR). It can also be used to synthesize c-Met Inhibitors that have potential therapeutic applications for cancer treatment.

Synthesis

General procedure for the synthesis of 6-methoxyimidazo[1,2-a]pyridine from methanol and 6-iodoimidazo[1,2-a]pyridine: In a solvent mixture of toluene (10 mL) and methanol (5 mL), 6-iodoimidazo[1,2-a]pyridine (1.0 g, 4.1 mmol) was added. After allowing to dissolve, copper(I) iodide (160 mg, 0.84 mmol), 1,10-phenanthroline (300 mg, 1.66 mmol) and cesium carbonate (3 g, 9 mmol) were added sequentially. The reaction mixture was stirred and reacted at 120 °C overnight. After completion of the reaction, it was cooled to room temperature and extracted by adding water and ethyl acetate. The organic layer was separated, washed sequentially with water and saturated saline and dried over anhydrous sodium sulfate. The solvent was removed by concentration under reduced pressure, and the resulting crude product was purified by silica gel column chromatography (eluent ratio: hexane:ethyl acetate:methanol, 50:50:0 → 0:100:0 → 0:95:5, v/v) to afford the target compound 6-methoxyimidazo[1,2-a]pyridine (360 mg, 59% yield).1H-NMR (CDCl3) δ: 3.82 (3H s), 6.96 (1H, dd, J = 9.6, 2.3 Hz), 7.50 (1H, d, J = 9.6 Hz), 7.52 (1H, s), 7.57 (1H, s), 7.66 (1H, d, J = 2.3 Hz).

References

[1] Patent: EP2565185, 2013, A1. Location in patent: Paragraph 0184

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