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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 908220Generated: October 30, 2026

Hydrochloric Acid → 6-Bromo-2-phenylimidazo[1,2-a]pyridine-7-carboxylic acid

https://huagongshe.com/reaction/908220

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
ReactantMethyl 6-bromo-2-phenylimidazo[1,2-a]pyridine-7-carboxylateHCID 67041599—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Product6-Bromo-2-phenylimidazo[1,2-a]pyridine-7-carboxylic acidHCID 6704185098%

Reaction Steps

NaOH (1N, 61 ml) was added to a suspension of 6-bromo-2-phenyl-imidazo[1,2-a]pyridine-7-carboxylic acid methyl ester (10.11 g, 31 mmol) in a mixture of water (30 ml) and ethanol (60 ml), and the mixture was heated to reflux (2 h). The mixture was cooled (0° C.) and HCl (conc., ˜10 ml) was slowly added. The dark brown suspension was filtered, washed with a small amount of ethanol, and dried under vacuum. The obtained title compound (9.47 g, 98%) was used in the next step without further purification. MS (m/e)=318.9 [M+H+].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08017604B2
Source datasetuspto-grants-2011_09
ORD IDord-0e5ef9135e194e00b387ff9a5d7509ef
Source noteuspto-grants-2011_09