Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 356276Generated: October 29, 2026

2-Aminopyridine → Ethyl 2-{imidazo[1,2-a]pyridin-2-yl}acetate

https://huagongshe.com/reaction/356276

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-AminopyridineHCID 10439—
ReactantPotassium CarbonateHCID 11430—
ReactantEthyl 4-chloroacetoacetateHCID 69484—
SolventAcetonitrileHCID 6342—
ProductEthyl 2-{imidazo[1,2-a]pyridin-2-yl}acetateHCID 108220548.4%

Reaction Steps

A solution of 14.6 g of 2-aminopyridine and 25.5 g of ethyl 4-chloroacetoacetate in 200 ml of acetonitrile was heated under reflux for 14.5 hours. At the end of this time, the reaction mixture was freed from the solvent by distillation under reduced pressure. The residue thus obtained was mixed with an aqueous solution of potassium carbonate, after which it was extracted with ethyl acetate. The extract was washed with an aqueous solution of sodium chloride and dried over anhydrous sodium sulfate, after which the solvent was removed by distillation under reduced pressure. The residue was purified by column chromatography through silica gel, using ethyl acetate as the eluent, to give 2.65 g of the title compound having Rf=0.33 (on silica gel thin layer chromatography using ethyl acetate as the developing solvent).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05834501
Source datasetuspto-grants-1998_11
ORD IDord-608034d9cb5f444baafef4e88430ceba
Source noteuspto-grants-1998_11