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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1391379Generated: November 3, 2026

Water → 2-(4-Methoxyphenyl)imidazo[1,2-a]pyridine

https://huagongshe.com/reaction/1391379

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantBromomethyl 4-methoxyphenyl ketoneHCID 4965—
Reactant2-AminopyridineHCID 10439—
ReactantSodium BicarbonateHCID 516892—
SolventEthanolHCID 702—
Product2-(4-Methoxyphenyl)imidazo[1,2-a]pyridineHCID 694963—

Reaction Steps

A mixture of 25.2 g. of sodium bicarbonate, 12.3 g. of 2-aminopyridine and 30 g. of α-bromo-p-methoxyacetophenone in 100 ml. of water and 550 ml. of absolute ethanol is heated at reflux temperatures for 1.5 hrs. The reaction mixture is concentrated under reduced pressure to a yellow solid, which is partitioned between chloroform and water. The organic layer is separated, dried over sodium sulfate. Removal of the chloroform in vacuo leaves the crude intermediate as a yellow solid. Recrystallization from ethanol-water give 15.2 g. of the desired material, m.p. 131°-134° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04141898
Source datasetuspto-grants-1979_02
ORD IDord-f2bc810db1f0406abf78ee59d82dac62
Source noteuspto-grants-1979_02