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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 415458Generated: October 28, 2026

Pyridine → HCID 178490872, compound

https://huagongshe.com/reaction/415458

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 numberUS08088790B2
Source datasetuspto-grants-2012_01
ORD IDord-73431f133e6549e5a1a9736b2706a6be
Source noteuspto-grants-2012_01