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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 388588Generated: October 29, 2026

Pyridine → HCID 178490872, compound

https://huagongshe.com/reaction/388588

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantAcetonitrileHCID 6342—
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
ReactantHCID 86633716HCID 86633716—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178490872HCID 17849087241.8%

Reaction Conditions

Temperature80 °C

Reaction Steps

1,1′-Carbonyldiimidazole (6.53 g, 40.3 mmol) was added to a solution of 2-chloro-N4-(4-methoxybenzyl)quinoline-3,4-diamine (11.49 g, 36.62 mmol) and pyridine (75 mL) in THF (75 mL), and the reaction was heated at 80° C. overnight. An analysis by LC/MS indicated the presence of starting material, and additional 1,1′-carbonyldiimidazole (1 equivalent) was added. The reaction was stirred overnight at 80° C., and additional 1,1′-carbonyldiimidazole (1 equivalent) was added. The reaction was stirred overnight at 80° C. and allowed to cool, and the solvent was removed under reduced pressure. The residue was dissolved in dichloromethane (500 mL), and the resulting solution was washed sequentially with brine and water, dried over magnesium sulfate, filtered, and concentrated under reduced pressure to provide a solid. The solid was mixed with acetonitrile and isolated by filtration to provide 5.2 g of 4-chloro-1-(4-methoxybenzyl)-1H-imidazo[4,5-c]quinolin-2-ol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08377957B2
Source datasetuspto-grants-2013_02
ORD IDord-f57afb5205d64210b909d7b6c61d145b
Source noteuspto-grants-2013_02