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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1097549Generated: October 29, 2026

Cyanogen Bromide → HCID 86626274, compound

https://huagongshe.com/reaction/1097549

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyanogen BromideHCID 10476—
Reactant2-Chloro-N~4~-(2-methylpropyl)quinoline-3,4-diamineHCID 11747039—
SolventEthanolHCID 702—
ProductHCID 86626274HCID 86626274—

Reaction Steps

A solution of 2-chloro-N4-(2-methylpropyl)-3,4-quinolinediamine (André et al, U.S. Pat. No. 4,988,815, Example 6, 8.92 g, 35.7 mmol) in ethanol (50 mL) was stirred at 100° C.; cyanogen bromide (5.67 g, 53.5 mmol) was added in one portion. The red solution was stirred overnight, washed three times with water, and washed once with brine. A precipitate formed in the aqueous washings and was isolated by filtration. The organic fraction was dried over magnesium sulfate, filtered through a layer of CELITE filer agent, concentrated under reduced pressure, further dried under high vacuum, and combined with the isolated precipitate to provide 9.81 g of 4-chloro-1-(2-methylpropyl)-1H-imidazo[4,5-c]quinoline-2-amine hydrobromide as a dark red solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08143270B2
Source datasetuspto-grants-2012_03
ORD IDord-a198fe4280b4467b9588fb7e93c36643
Source noteuspto-grants-2012_03