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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1157278Generated: November 4, 2026

Methyl chloroglyoxylate → 2-(7-bromo-4-fluoro-1H-pyrrolo[2,3-c]pyridin-3-yl)-2-oxoacetic acid

https://huagongshe.com/reaction/1157278

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl chloroglyoxylateHCID 79846—
ReactantAluminum(III) ChlorideHCID 6451240—
Reactant7-Bromo-4-fluoro-1H-pyrrolo[2,3-C]pyridineHCID 15987021—
ReactantEthylmethylimidazolium chlorideHCID 17821953—
SolventWaterHCID 962—
Product2-(7-bromo-4-fluoro-1H-pyrrolo[2,3-c]pyridin-3-yl)-2-oxoacetic acidHCID 2079123992%

Reaction Steps

7-bromo-4-fluoro-1H-pyrrolo[2,3-c]pyridine (2.0 g, 9.3 mmol) was added to a mixture of AlCl3 (7.5 g, 55.8 mmol) and ethylmethylimidazolium chloride (2.7 g, 18.6 mmol). Methyl chlorooxoacetate (2.1 mL, 18.6 mmol) was added slowly to the above solution and the mixture was stirred at room temperature for 3 h. Reaction flask was placed in an ice bath and water was slowly added until a white precipitate formed. The solid was collected by filtration and washed with water to afford 2-(7-bromo-4-fluoro-1H-pyrrolo[2,3-c]pyridin-3-yl)-2-oxoacetic acid (2.4g, 92%). LCMS: m/e 287 (M+H)+, ret time 0.91 min (method 1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07807671B2
Source datasetuspto-grants-2010_10
ORD IDord-08bd52ab71f946a78ea08fbf315b7119
Source noteuspto-grants-2010_10