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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 973492Generated: October 26, 2026

Hydrochloric Acid → Ethyl 2-(2-methylimidazo[4,5-c]pyrid-1-yl)pyrid-5-oylacetate

https://huagongshe.com/reaction/973492

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium BicarbonateHCID 516892—
Reactant6-(2-Methylimidazo[4,5-c]pyrid-1-yl)pyrid-3-oyl chlorideHCID 19877175—
ReactantHCID 178418918HCID 178418918—
ReactantHCID 178461627HCID 178461627—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 2-(2-methylimidazo[4,5-c]pyrid-1-yl)pyrid-5-oylacetateHCID 5424558263%

Reaction Steps

Ethyl potassium malonate (57 mg) was suspended in dry tetrahydrofuran (1 ml) and 2M isopropyl magnesium chloride in THF (170 μl) added. The suspension was sonicated for 1/2 hour giving a homogenous solution. This was added with stirring to the suspension of 6-(2-methylimidazo[4,5-c]pyrid-1-yl)pyrid-3-oyl chloride in dichloromethane. The mixture was stirred at room temperature for 1/2 hour. It was then poured into 1N hydrochloric acid, stirred for 15 minutes and adjusted to pH8 with saturated sodium bicarbonate. The aqueous phase was extracted with dichloromethane (2×10 ml), the extracts combined, dried over magnesium sulphate and the solvent removed under reduced pressure yielding the title compound as a pale red oil (40 mg, 63%) [as a 1:1 mixture of enol and keto tautomers].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05063237
Source datasetuspto-grants-1991_11
ORD IDord-7fd710a78dd048f29a3f57063702a122
Source noteuspto-grants-1991_11