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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1055156Generated: November 2, 2026

Hydrochloric Acid → Ethyl 5,6,7,8-tetrahydroimidazo[1,2-a]pyridine-6-carboxylate hydrochloride

https://huagongshe.com/reaction/1055156

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantEthanolHCID 702—
ReactantMethyl imidazo(1,2-a)pyridine-6-carboxylateHCID 2764326—
CatalystPalladiumHCID 23938—
ProductEthyl 5,6,7,8-tetrahydroimidazo[1,2-a]pyridine-6-carboxylate hydrochlorideHCID 9042411588%

Reaction Conditions

Temperature60 °C

Reaction Steps

Add 5 N hydrochloric acid (100 mL; 500.00 mmoles) and ethanol (200 mL) to a flask containing methyl imidazo[1,2-a]pyridine-6-carboxylate (4.98 g; 1.0 equiv; 28.27 mmoles) and 10% palladium on carbon (3.01 g; 0.1 equiv; 2.83 mmoles). Evacuate and backfill the reaction vessel with nitrogen (3×), then re-evacuate and backfill the reaction with hydrogen (3×). Heat the reaction mixture to 60° C. and vigorously stir under a hydrogen atmosphere for 24 hours, then evacuate and backfill the reaction vessel with nitrogen (3×) and filter the reaction mixture through Celite™, rinsing the filter cake with ethanol (100 mL). Concentrate the filtrate, add toluene (200 mL), and concentrate to dryness (repeat 2 times) to afford ethyl 5,6,7,8-tetrahydroimidazo[1,2-a]pyridine-6-carboxylate hydrochloride (5.74 g; 88%) as a white solid. MS (m/z): 195(M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09394317B2
Source datasetuspto-grants-2016_07
ORD IDord-8b2081836c9a4cf08e2a6fc0b5f7f259
Source noteuspto-grants-2016_07