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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2172832Generated: October 25, 2026

Hydrochloric Acid → 4-((4-Oxo-2-thioxothiazolidin-3-yl)methyl)benzenesulfonamide

https://huagongshe.com/reaction/2172832

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantMafenide HydrochlorideHCID 67313—
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
Reactant3,5-Dithia-4-thioxo-1,7-heptanedioic acidHCID 80618—
ReactantDiisopropylethylamineHCID 81531—
SolventTetrahydrofuranHCID 8028—
Product4-((4-Oxo-2-thioxothiazolidin-3-yl)methyl)benzenesulfonamideHCID 3367935970.7%

Reaction Steps

To a solution of bis(carboxymethyl)trithiocarbonate (200 mg) in tetrahydrofuran (10 ml) was added carbonyldiimidazole (291 mg), and the mixture was stirred at room temperature. After 2 hr, to the reaction mixture were added homosulfamine hydrochloride (200 mg) and N,N-diisopropylethylamine (155 mg), and the mixture was stirred overnight at 70° C. 2N Hydrochloric acid (10 ml) was added thereto under ice cooling, the mixture was extracted twice with ethyl acetate (40 ml), and the extract was dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (eluent: hexane/ethyl acetate=2:1) to give 3-(4-sulfamoylbenzyl)-2-thioxothiazolidin-4-one (189 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09056862B2
Source datasetuspto-grants-2015_06
ORD IDord-67e3bd37cd1e4a92ac033706125b7538
Source noteuspto-grants-2015_06