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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 719303Generated: October 31, 2026

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

https://huagongshe.com/reaction/719303

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 (WO 89/01488 pg33, 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 numberUS07132435B2
Source datasetuspto-grants-2006_11
ORD IDord-3337f86a728a4829ae44fa2f0b72f691
Source noteuspto-grants-2006_11