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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1097560Generated: November 1, 2026

Cyanogen Bromide → HCID 86626282, compound

https://huagongshe.com/reaction/1097560

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyanogen BromideHCID 10476—
ReactantHCID 46830486HCID 46830486—
SolventEthanolHCID 702—
ProductHCID 86626282HCID 86626282103.3%

Reaction Conditions

Temperature90 °C

Reaction Steps

Cyanogen bromide (2.2 g, 21 mmol) was added to a solution of N4-benzyl-2-chloroquinoline-3,4-diamine (5.0 g, 17 mmol) in ethanol (50 mL), and the solution was heated at 90° C. for two hours. An analysis by liquid chromatography/mass spectrometry (LC/MS) indicated the presence of starting material. Additional cyanogen bromide (2.2 g, 21 mmol) was added, and the reaction was stirred for one hour at 90° C., stirred for three days at 50° C., and allowed to cool to ambient temperature. The solvent was removed under reduced pressure, and the resulting solid was washed with diethyl ether (1 L) to provide 6.84 g of 1-benzyl-4-chloro-1H-imidazo[4,5-c]quinoline-2-amine hydrobromide as a dark gray powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08143270B2
Source datasetuspto-grants-2012_03
ORD IDord-fd3a8ae96b3b4182826a910a96d2a1c3
Source noteuspto-grants-2012_03