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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1624072Generated: October 30, 2026

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

https://huagongshe.com/reaction/1624072

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 2-chloroacetoacetateHCID 11858—
Reactant5-Chloro-3-[(2,6-difluorobenzyl)oxy]pyridine-2-amineHCID 86717877—
SolventEthanolHCID 702—
ProductEthyl 6-chloro-8-[(2,6-difluorobenzyl)oxy]-2-methylimidazo[1,2-a]pyridine-3-carboxylateHCID 86717878—

Reaction Steps

40 g of 5-chloro-3-[(2,6-difluorobenzyl)oxy]pyridine-2-amine (Example 17A; 147.8 mmol; 1 equivalent) were initially charged in 800 ml of ethanol, 30 g of powdered molecular sieve 3 Å and 128 g of ethyl 2-chloroacetoacetate (739 mmol, 5 equivalents) were added and the mixture was heated at reflux overnight. The reaction mixture was concentrated and the residue was taken up in ethyl acetate and filtered. The ethyl acetate phase was washed with water, dried, filtered and concentrated. This gave 44 g (78% of theory) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08778964B2
Source datasetuspto-grants-2014_07
ORD IDord-9310f17c3b6d414e97fb09ef67ab486e
Source noteuspto-grants-2014_07