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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1097606Generated: October 31, 2026

Cyanogen Bromide → HCID 86626306, compound

https://huagongshe.com/reaction/1097606

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyanogen BromideHCID 10476—
ReactantHCID 86626305HCID 86626305—
SolventEthanolHCID 702—
ProductHCID 86626306HCID 86626306136.7%

Reaction Conditions

Temperature80 °C

Reaction Steps

A suspension of 1-[(3-amino-7-bromo-2-chloroquinolin-4-yl)amino]-2-methylpropan-2-ol (1.5 g, 4.35 mmol) in ethanol (25 mL) was heated to 80° C. Cyanogen bromide (0.50 g, 4.8 mmol) was added to the resulting solution, and the reaction was heated at 80° C. overnight and allowed to cool. A precipitate was present and was isolated by filtration, washed with diethyl ether, and dried under vacuum for one hour to provide 1.34 g of 1-(2-amino-7-bromo-4-chloro-1H-imidazo[4,5-c]quinolin-1-yl)-2-methylpropan-2-ol hydrobromide as a pinkish-white solid, mp >260° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08143270B2
Source datasetuspto-grants-2012_03
ORD IDord-158c9454a670476789a4e81a29cc0a64
Source noteuspto-grants-2012_03