Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1789197Generated: November 1, 2026

Imidazo[1,2-a]pyridin-8-ylmethanol → HCID 178488119, compound

https://huagongshe.com/reaction/1789197

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazo[1,2-a]pyridin-8-ylmethanolHCID 11029987—
ReactantHCID 178488032HCID 178488032—
SolventAcetic AcidHCID 176—
SolventHydrogen BromideHCID 260—
ProductHCID 178488119HCID 178488119—

Reaction Steps

A mixture of 2.92 g (23 mmole) of 3-hydroxymethyl-2-pyridinamine, 6.15 g (35 mmole) of chloroacetaldehyde, and 2.0 g (35 mmole) of sodium bicarbonate in 100 ml of ethanol was heated at reflux for 1.5 hours. The mixture was filtered and the filtrate was concentrated in vacuo to a solid. Recrystallization from diethyl ether yielded 4.4 g of 8-hydroxymethylimidazo[1,2-a]pyridine, as confirmed by the nmr and infrared spectra. A mixture of 683 mg (3.8 mmole) of 2-mercapto-5-methoxybenzimidazole and 700 mg (3.8 mmole) of 8-hydroxymethylimidazo[1,2-a]pyridine was dissolved in 3 ml of 30% hydrogen bromide in acetic acid and heated on a steam bath. After being cooled to room temperature, the mixture was partitioned between 5% aqueous sodium hydroxide and dichloromethane. The organic layer was dried over sodium sulfate, filtered, and concentrated to yield the title compound as an oil. Structure assignment was supported by the nmr and infrared spectra.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04687775
Source datasetuspto-grants-1987_08
ORD IDord-fa237b32af6b4b098a33a40beb816430
Source noteuspto-grants-1987_08