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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1473883Generated: October 30, 2026

Water → Imidazo[1,5-a]pyridin-8-ylmethanol

https://huagongshe.com/reaction/1473883

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTetrahydrofuranHCID 8028—
ReactantSodium HydroxideHCID 14798—
Reactantethyl 3H-imidazo[4,5-b]pyridine-2-carboxylateHCID 13353748—
ReactantAluminium lithium hydrideHCID 21226445—
SolventEthyl AcetateHCID 8857—
ProductImidazo[1,5-a]pyridin-8-ylmethanolHCID 10351843—

Reaction Steps

To a cold solution of lithium aluminum hydride (1.0 g, 26.3 mmol, 2.0 eq) in THF (40 mL) was added the crude ethyl imidazopyridine carboxylate (2.5 g, 13.2 mmol, 1.0 eq) and the reaction mixture was stirred at rt for 2 h. Reaction was cooled and water (1.7 mL), 15% NaOH (1.7 mL) and water (5.1 mL) were slowly added. Solution was next diluted with excess EtOAc and stirred at rt for 30 min. The solution was filtered and the solid was washed with ethyl acetate. Organic layers were combined, dried and solvent was removed to give crude imidazo[1,5-a]pyridine-8-methanol, which was purified by column chromatography (EtOAc/Hexane). MS: exact mass calculated for C8H8N2O, 148.06; m/z found, 149 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09018210B2
Source datasetuspto-grants-2015_04
ORD IDord-62aeadd3de064a23bf3ed4c459f1bd6c
Source noteuspto-grants-2015_04