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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1253564Generated: November 2, 2026

Hydrochloric Acid → 7-Iodo-5-methoxyimidazo[1,2-a]pyridine

https://huagongshe.com/reaction/1253564

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant2-Bromo-1,1-dimethoxyethaneHCID 81672—
ReactantSodium BicarbonateHCID 516892—
Reactant4-Iodo-6-methoxypyridin-2-amineHCID 67204680—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
Product7-Iodo-5-methoxyimidazo[1,2-a]pyridineHCID 67207747—

Reaction Conditions

Temperature80 °C

Reaction Steps

To a mixture of bromoacetaldehyde dimethylacetal (4.50 ml, 37.1 mmol) in water (126 ml) was added a 1M solution of hydrochloric acid (8.40 ml, 8.40 mmol). After 2.5 h the reaction mixture was heated to 80° C. resulting in a clear solution. After 40 minutes the reaction mixture was cooled to ambient temperature and sodium bicarbonate (3.83 g, 45.6 mmol) and 4-iodo-6-methoxypyridin-2-amine (5.25 g, 21.0 mmol) were added. After 16 hours the reaction mixture was diluted with ethyl acetate, washed with water, then dried over magnesium sulfate, filtered, and concentrated. The residue was purified by column chromatography on silica gel (methanol/dichloromethane gradient) to give 7-iodo-5-methoxyimidazo[1,2-a]pyridine. LRMS (ESI) calculated for C8H8IN2O [M+H]+, 275.0 found 274.9.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08455477B2
Source datasetuspto-grants-2013_06
ORD IDord-369cb5a8b09e495ea775380a7c6dfb85
Source noteuspto-grants-2013_06