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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 902418Generated: October 25, 2026

Pyridinium chloride → HCID 178486402, compound

https://huagongshe.com/reaction/902418

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridinium chlorideHCID 10176127—
Reactant3-chloro-4-(1-methyl-1H-imidazol-2-ylsulfanyl)phenylamineHCID 11459088—
ReactantHCID 178486400HCID 178486400—
SolventGlycol monoethyl etherHCID 8076—
SolventSodium CarbonateHCID 10340—
ProductHCID 178486402HCID 17848640265.6%

Reaction Conditions

Temperature120 °C

Reaction Steps

A mixture of 1.0 g (3.53 mmol) of 4-chloro-8-hydroxy-7-methoxybenzo[g]quinoline-3-carbonitrile, 0.93 g (3.88 mmol) of 3-chloro-4-(1-methyl-1H-imidazol-2-ylsulfanyl)phenylamine and 0.41 g (3.52 mmol) of pyridine hydrochloride in 20 mL of 2-ethoxyethanol is heated at 120° C. for 2 hours, then cooled to room temperature. The product mixture is diluted with a saturated solution of sodium carbonate, stirred for 15 minutes and the solid is collected by filtration. The solid is washed with water and dried in vacuo. The crude product is purified by silica gel chromatography, utilizing a 95:5 to 9:1 gradient of methylene chloride/methanol to give 1.13 g of 4-[3-chloro-4-(1-methyl-1H-imidazol-2-ylsulfanyl)phenylamino]-8-hydroxy-7-methoxybenzo[g]quinoline-3-carbonitrile as a yellow solid, mp>300° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07365197B2
Source datasetuspto-grants-2008_04
ORD IDord-59885a8480a1487a90ba476943dafbc9
Source noteuspto-grants-2008_04