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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 568360Generated: October 30, 2026

4-Bromobenzenesulfonamide → HCID 178514395, compound

https://huagongshe.com/reaction/568360

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-BromobenzenesulfonamideHCID 69696—
ReactantHCID 178468269HCID 178468269—
SolventMethanolHCID 887—
ProductHCID 178514395HCID 178514395—

Reaction Steps

To the crude product composed by ethyl N-[2-[[[2-[(aminoiminomethyl)amino]-4-thiazolyl]methyl]thio]ethyl]formimidate, 7.7 g of p-bromobenzenesulfonamide in 50 ml of methanol are dropwise added under stirring and at room temperature. The mixture is kept under stirring for 1 hour at room temperature, the solvent is removed by distillation under reduced pressure, and the obtained residue is purified by 60-silicagel column chromatography. 13.5 g of N-p-bromobenzene-sulphonyl-N'-[2-[[[2-[(aminoiminomethyl)amino]-4-thiazolyl]methyl]thio]ethyl]formamidine are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04728655
Source datasetuspto-grants-1988_03
ORD IDord-ce3df92d4c354d63a08a64d00ecdc2fe
Source noteuspto-grants-1988_03