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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 706592Generated: October 26, 2026

Oxalyl chloride → Methyl 7-bromoimidazo[1,2-a]pyridine-3-carboxylate

https://huagongshe.com/reaction/706592

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
Reactant7-Bromoimidazo[1,2-a]pyridine-3-carboxylic acidHCID 67261488—
CatalystDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
ProductMethyl 7-bromoimidazo[1,2-a]pyridine-3-carboxylateHCID 6725975289%

Reaction Steps

7-bromoimidazo[1,2-a]pyridine-3-carboxylic acid (4.93 g, 20.5 mmol) was dissolved in 80 mL of dry dichloromethane. To this solution was added oxalyl chloride (20.5 mL, 40.9 mmol, 2M in dichloromethane) followed by a few drops of DMF. The mixture was stirred at ambient temperature for 16 hours, then concentrated under reduced pressure. The resulting material was taken up in 100 mL of methanol and stirred at ambient temperature for 6 hours, then concentrated under reduced pressure. The resulting material was suspended in saturated aqueous sodium bicarbonate, extracted with dichloromethane and EtOAc. The organics were combined, dried over sodium sulfate and concentrated under reduced pressure to give 4.63 g (89%) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09174981B2
Source datasetuspto-grants-2015_11
ORD IDord-27e2f010cd3a4b9688a58513da1e1132
Source noteuspto-grants-2015_11