Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1368232Generated: October 27, 2026

Potassium Carbonate → methyl 3-(4-acetoxy-2-chlorobenzyl)-2,7-dimethyl-3H-imidazo[4,5-b]pyridine-5-carboxylate

https://huagongshe.com/reaction/1368232

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant4-Acetoxy-2-chlorobenzylbromideHCID 22387911—
Reactantmethyl 2,7-dimethyl-3H-imidazo[4,5-b]pyridine-5-carboxylateHCID 22388027—
SolventDimethylformamideHCID 6228—
Productmethyl 3-(4-acetoxy-2-chlorobenzyl)-2,7-dimethyl-3H-imidazo[4,5-b]pyridine-5-carboxylateHCID 22485009117.6%

Reaction Steps

A mixture of methyl 2,7-dimethyl-3H-imidazo[4,5-b]pyridine-5-carboxylate (2.70 g), 4-acetoxy-2-chlorobenzylbromide (4.85 g), potassium carbonate (2.73 g) and N,N-dimethylformamide (27 ml) was stirred at room temperature for 5 hr and left standing overnight. The reaction mixture was partitioned between ethyl acetate and saturated brine, and the resulting precipitate was collected by filtration and washed with water and ethyl acetate to give methyl 3-(4-acetoxy-2-chlorobenzyl)-2,7-dimethyl-3H-imidazo[4,5-b]pyridine-5-carboxylate (6.0 g) as a pale-brown powder. The mother liquor and washing were combined and the organic layer was separated, dried over magnesium sulfate and concentrated to dryness under reduced pressure. The residue was powdered from diethyl ether to give the second lot (680 mg) as a pale-brown powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06573274B1
Source datasetuspto-grants-2003_06
ORD IDord-e3540e440cdc4dc290f4b1389d90f646
Source noteuspto-grants-2003_06