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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 51919Generated: October 25, 2026

Pyridine → 7-(2-Bromobenzoylamino)quinoline-3-carboxylic acid ethyl ester

https://huagongshe.com/reaction/51919

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant2-Bromobenzoyl chlorideHCID 23542—
ReactantEthyl 7-aminoquinoline-3-carboxylateHCID 9877801—
SolventChloroformHCID 6212—
Product7-(2-Bromobenzoylamino)quinoline-3-carboxylic acid ethyl esterHCID 6989115850%

Reaction Steps

A solution of 2-Bromobenzoyl chloride (5.38 g, 24.5 mmol) in 100 ml chloroform was added dropwise at room temperature to a solution of ethyl 7-aminoquinoline-3-carboxylate (2.65 g, 12.25 mmol), 4-N,N-dimethylaminopyridine (150 mg, 1.23 mmol) and pyridine (3.96 ml, 49 mmol) in 100 ml chloroform. The resulting solution was heated under reflux for 4 hr, then cooled to room temperature. The chloroform solution was then washed sequentially with dilute aqueous hydrochloric acid solution, water and brine, dried over anhydrous sodium sulfate and concentrated to dryness in vacuo. The residue was chromatographed on silica gel, eluting with 60:40 hexane/ethyl acetate to yield the title product as a solid foam (2.45 g 50% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06713489B2
Source datasetuspto-grants-2004_03
ORD IDord-515124e287874ebd87ffdaa652a8f319
Source noteuspto-grants-2004_03