HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1006690Generated: October 26, 2026
Potassium Iodide → Ethyl 8-(2,6-dimethylbenzylamino)-3-methylimidazo[1,2-a]pyridine-2-carboxylate
https://huagongshe.com/reaction/1006690
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 2,6-Dimethylbenzyl Chloride | HCID 221154 | — |
| Reactant | Ethyl 8-amino-3-methylimidazo[1,2-a]pyridine-2-carboxylate | HCID 22672637 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | Ethyl 8-(2,6-dimethylbenzylamino)-3-methylimidazo[1,2-a]pyridine-2-carboxylate | HCID 22672581 | 56.5% |
Reaction Steps
Ethyl 8-amino-3-methylimidazo[1,2-a]pyridine-2-carboxylate (4.6 g, 21 mmol), 2,6-dimethylbenzyl chloride (3.2 g, 21 mmol), sodium carbonate (4.4 g, 42 mmol) and a cat. amount of potassium iodide were added to acetonitrile (50 ml) and refluxed for 3 h., stirred for 20 h. at room temperature and refluxed for 1 h. The solids were removed by filtration and the solvents were evaporated under reduced pressure. The residue was dissolved in methylene chloride and washed with water. The organic layer was separated, dried (Na2SO4) and evaporated under reduced pressure. Purification of the residue by column chromatography on silica gel using methylene chloride:methanol (10:1) as eluent and crystallization from ethyl acetate gave 4.0 g (56%) of the desired product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06790960B2 |
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| Source dataset | uspto-grants-2004_09 |
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| ORD ID | ord-a24f2177ff374f62bb0d8aa718521ae8 |
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| Source note | uspto-grants-2004_09 |
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