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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 390215Generated: October 29, 2026

Cyanogen Bromide → HCID 58625163, compound

https://huagongshe.com/reaction/390215

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyanogen BromideHCID 10476—
ReactantHCID 58625066HCID 58625066—
SolventEthanolHCID 702—
ProductHCID 58625163HCID 58625163—

Reaction Steps

A mixture of N-[3-(4-amino-3-propylaminomethyl-phenoxy)-phenyl]-benzenesulfonamide (0.0044 mol) in ethanol (50 mL) was stirred at room temperature and cyanogen bromide (0.0064 mol) was added, then the reaction mixture was stirred and refluxed for 4 hours. After cooling, the precipitate was filtered off and was stirred in boiling CH3CN with CH3OH. The resulting solids were filtered off, washed with diisopropyl ether and dried to yield the title compound as a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08383637B2
Source datasetuspto-grants-2013_02
ORD IDord-0c8ad2e30e9a41f8ae624719e98d474e
Source noteuspto-grants-2013_02