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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantSodium CarbonateHCID 10340—
Reactant2,6-Dimethylbenzyl ChlorideHCID 221154—
ReactantEthyl 8-amino-3-methylimidazo[1,2-a]pyridine-2-carboxylateHCID 22672637—
SolventAcetonitrileHCID 6342—
ProductEthyl 8-(2,6-dimethylbenzylamino)-3-methylimidazo[1,2-a]pyridine-2-carboxylateHCID 2267258156.5%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06790960B2
Source datasetuspto-grants-2004_09
ORD IDord-a24f2177ff374f62bb0d8aa718521ae8
Source noteuspto-grants-2004_09