Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 706756Generated: October 29, 2026

Hydrochloric Acid → 7-(2-Methoxyethoxy)imidazo[1,2-a]pyridine-3-carboxylic acid

https://huagongshe.com/reaction/706756

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTetrahydrofuranHCID 8028—
ReactantLithium hydroxide, monohydrateHCID 168937—
ReactantEthyl 7-(2-methoxyethoxy)imidazo[1,2-a]pyridine-3-carboxylateHCID 66782057—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Product7-(2-Methoxyethoxy)imidazo[1,2-a]pyridine-3-carboxylic acidHCID 6678202590.6%

Reaction Conditions

Temperature40 °C

Reaction Steps

Ethyl 7-(2-methoxyethoxy)imidazo[1,2-a]pyridine-3-carboxylate (6.06 g; 22.9 mmol) was mixed with tetrahydrofuran (225 mL), ethanol (110 mL) and water (55 mL). Lithium hydroxide monohydrate (0.962 g; 22.9 mmol) was added. The mixture was stirred under an atmosphere of nitrogen and heated at 40° C. for 22 hours. The mixture was allowed to cool and then concentrated under reduced pressure to give a yellow gum. Water (50 mL) was added and the mixture stirred to until homogeneous. Hydrochloric acid (2N) was added with stirring to adjust to pH 3. The mixture was cooled with an ice/water bath. The resulting precipitate was collected by filtration and washed with a small amount of water (10 mL). The material was dried under vacuum to give 7-(2-methoxyethoxy)imidazo[1,2-a]pyridine-3-carboxylic acid as a white solid (4.90 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09174981B2
Source datasetuspto-grants-2015_11
ORD IDord-b967e31ef11c4f2180cbe6e50e6a7c90
Source noteuspto-grants-2015_11