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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 860028Generated: October 30, 2026

Chloroacetaldehyde → Methyl imidazo[1,2-a]pyridine-8-carboxylate

https://huagongshe.com/reaction/860028

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroacetaldehydeHCID 33—
ReactantMethyl 2-aminopyridine-3-carboxylateHCID 351633—
SolventAmmoniaHCID 222—
SolventEthanolHCID 702—
SolventWaterHCID 962—
ProductMethyl imidazo[1,2-a]pyridine-8-carboxylateHCID 15098894—

Reaction Steps

A mixture of methyl 2-aminonicotinate (prepared according to the method of WO 89/01488 at page 33, prep 17) (1 g, 6.56 mmol), and chloroacetaldehyde (1.05 mL, 6.56 mmol) in ethanol (5 mL) was heated under reflux for 18 hours. The cooled mixture was diluted with water (10 mL), 0.88 ammonia (1 mL) added and the solution concentrated in vacuo. The residue was dissolved in methanol and the dark solution treated with charcoal, the mixture filtered and the filtrate concentrated in vacuo. The residue was purified by column chromatography on silica gel using dichloromethane:methanol:0.88 ammonia (97:2.5:0.5) as eluant, and the product triturated with ether, to afford the title compound, 768 mg.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07153870B2
Source datasetuspto-grants-2006_12
ORD IDord-6690819859614821b2b477e1c7692a54
Source noteuspto-grants-2006_12