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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 623092Generated: October 30, 2026

Ethanol → (S)-2-(4-Chlorophenyl)-alpha-methyl-3H-imidazo[4,5-b]pyridine-3-acetic acid ethyl ester

https://huagongshe.com/reaction/623092

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
Reactant(S)-2-(4-chlorophenyl)-alpha-methyl-3H-imidazo[4,5-b]pyridine-3-acetic acidHCID 14390427—
CatalystSulfuric AcidHCID 1118—
Product(S)-2-(4-Chlorophenyl)-alpha-methyl-3H-imidazo[4,5-b]pyridine-3-acetic acid ethyl esterHCID 1439041868%

Reaction Steps

A suspension of crude (S)-2-(4-chlorophenyl)-α-methyl-3H-imidazo[4,5-b]pyridine-3-acetic acid (2.0 g, 0.00663 mole) in absolute ethanol was stirred at room temperature while 4 drops of concentrated sulfuric acid was added. The reaction mixture was refluxed for three days. Approximately 1/2 to 2/3 of the solvent was removed under reduced pressure. Saturated sodium bicarbonate solution (20 ml) was added to the remaining solution. The product was extracted into two portions of ethyl acetate and the combined organic layers were washed twice with water, dried over sodium sulfate, filtered and evaporated to an oil which was dissolved in hot absolute ethanol. Water was added to the cloud point and upon cooling to room temperature, a solid precipitated. The solid was collected by filtration, rinsed with water and dried under high vacuum at 50° C. to give 1.48 g (68%) of title compound, mp 103°-106° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04772600
Source datasetuspto-grants-1988_09
ORD IDord-07d676cbd8f5404390d83179fd3e0851
Source noteuspto-grants-1988_09