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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 250766Generated: November 3, 2026

Cyanogen Bromide → HCID 66869562, compound

https://huagongshe.com/reaction/250766

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyanogen BromideHCID 10476—
ReactantHCID 66868837HCID 66868837—
SolventEthanolHCID 702—
ProductHCID 66869562HCID 6686956252%

Reaction Steps

Add cyanogen bromide (101 mg, 0.96 mmol) to a solution of 1-(cyclohexyl)-4-phenyl-5-(3-(isobutylamino)-4-aminophenyl)-1H-imidazole (250 mg, 0.64 mmol) in 6 mL ethanol. Stir over night at room temperature. Add saturated aqueous sodium carbonate and extract well with 9:1 ethyl acetate:methanol. Combine the organic phases, dry over magnesium sulfate, and concentrate under reduced pressure. Subject the residue to silica gel chromatography, eluting with a gradient of 5-8% methanol in dichloromethane to provide the title compound (52%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07863310B2
Source datasetuspto-grants-2011_01
ORD IDord-c9f809c6aad942f19aa9d0b07504c6a8
Source noteuspto-grants-2011_01