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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 415455Generated: October 29, 2026

Pyridine → HCID 178517323, compound

https://huagongshe.com/reaction/415455

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantDiethyl EtherHCID 3283—
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
ReactantHCID 86633712HCID 86633712—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178517323HCID 17851732375.5%

Reaction Conditions

Temperature80 °C

Reaction Steps

1,1′-Carbonyldiimidazole (3.20 g, 19.7 mmol) was added to 2-chloro-N4-(pyridin-3-ylmethyl)quinoline-3,4-diamine (5.09 g, 17.9 mmol) in THF (100 mL), and the resulting suspension was heated at 80° C. for three days. An analysis by LC/MS indicated the presence of starting material, and pyridine (100 mL) and additional 1,1′-carbonyldiimidazole (1 equivalent) were added. The reaction was stirred for two hours at 80° C., and additional 1,1′-carbonyldiimidazole (1 equivalent) was added. The reaction was stirred overnight at 80° C. and allowed to cool; a solid was present. Diethyl ether (50 mL) was added, and the solid was isolated by filtration and dried under vacuum to provide 4.2 g of 4-chloro-1-(pyridin-3-ylmethyl)-1H-imidazo[4,5-c]quinolin-2-ol as a gray solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08088790B2
Source datasetuspto-grants-2012_01
ORD IDord-22f22abd7e9542c1a0ad99a0d57f9a43
Source noteuspto-grants-2012_01