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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 989303Generated: October 25, 2026

Sodium Bicarbonate → 8-(2-Bromo-4-chloro-5-methoxy-phenylamino)imidazo[4,5-g]quinoline-7-carbonitrile

https://huagongshe.com/reaction/989303

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
ReactantPyridinium chlorideHCID 10176127—
Reactant2-Bromo-4-chloro-5-methoxyaniline hydrobromideHCID 21956421—
Reactant8-Chloroimidazo[4,5-g]quinoline-7-carbonitrileHCID 69372843—
SolventGlycol monoethyl etherHCID 8076—
Product8-(2-Bromo-4-chloro-5-methoxy-phenylamino)imidazo[4,5-g]quinoline-7-carbonitrileHCID 6937243044.9%

Reaction Steps

A mixture of 0.12 g (0.52 mmol) of 8-chloroimidazo[4,5-g]quinoline-7-carbonitrile, 0.2 g (0.63 mmol) of 2-bromo-4-chloro-5-methoxyaniline hydrobromide and 0.06 g (0.52 mmol) of pyridine hydrochloride in 5.0 mL of 2-ethoxyethanol is heated at reflux temperature for 1 hour, cooled to room temperature, poured into a saturated solution of sodium bicarbonate and stirred for 0.5 hour. The solid is collected by filtration, washed with water and dried. The solid is purified by silica gel chromatography utilizing a gradient of methylene chloride/methanol(97:3 to 90:10) to yield 0.1 g of 8-(2-bromo-4-chloro-5-methoxy-phenylamino)imidazo[4,5-g]quinoline-7-carbonitrile as a yellow solid, mp 257° C. (dec).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06638929B2
Source datasetuspto-grants-2003_10
ORD IDord-a6583902099247908369f0fca8949c46
Source noteuspto-grants-2003_10