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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 923503Generated: October 27, 2026

2,6-Lutidine → Ethyl 8-[(2,6-difluorobenzyl)oxy]-2-methylimidazo[1,2-a]pyridine-3-carboxylate

https://huagongshe.com/reaction/923503

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,6-LutidineHCID 7937—
ReactantEthyl 2-chloroacetoacetateHCID 11858—
Reactant3-(2,6-Difluoro-benzyloxy)-pyridin-2-ylamineHCID 10263498—
SolventTolueneHCID 1140—
ProductEthyl 8-[(2,6-difluorobenzyl)oxy]-2-methylimidazo[1,2-a]pyridine-3-carboxylateHCID 86717871—

Reaction Conditions

Temperature130 °C

Reaction Steps

Under a nitrogen atmosphere, a mixture of 5.0 g of 3-[(2,6-difluorobenzyl)oxy]pyridin-2-amine, 4.1 ml of ethyl 2-chloroacetoacetate, 3.5 ml of 2,6-dimethylpyridine, and 50 ml of toluene was stirred at 130° C. for 24 hours. After leaving to be cooled to room temperature, the reaction mixture was washed with water, a 1 M aqueous sodium hydroxide solution, a 10% aqueous citric acid solution, and a saturated aqueous sodium chloride solution. The organic layer was concentrated under reduced pressure to obtain 5.47 g of ethyl 8-[(2,6-difluorobenzyl)oxy]-2-methylimidazo[1,2-a]pyridine-3-carboxylate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09278968B2
Source datasetuspto-grants-2016_03
ORD IDord-049810546c274661a31b6b73477ade76
Source noteuspto-grants-2016_03