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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1258612Generated: October 25, 2026

1,2,4-Thiadiazol-5-amine, 3-phenyl- → 3,4-Dimethoxy-n-[3-(phenyl)-1,2,4-thiadiazol-5-yl]benzenesulfonamide

https://huagongshe.com/reaction/1258612

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2,4-Thiadiazol-5-amine, 3-phenyl-HCID 28561—
Reactant3,4-Dimethoxybenzenesulfonyl chlorideHCID 2734183—
SolventPyridineHCID 1049—
Product3,4-Dimethoxy-n-[3-(phenyl)-1,2,4-thiadiazol-5-yl]benzenesulfonamideHCID 2499388814.4%

Reaction Steps

3-Phenyl-1,2,4-thiadiazol-5-amine (326 mg, 1.84 mmol) was dissolved in dry pyridine (10 mL). Then 3,4-dimethoxybenzenesulfonyl chloride (529 mg, 2.23 mmol) was added. The solution was stirred at room temperature under Argon. After 46 h, the pyridine was removed in vacuo and flashed off with toluene. The residue was partitioned between EtOAc and 1M NaOH. The organic phase was washed with 1M NaOH until no turbidity was observed on rectification of a small sample. The alkaline phase was made acidic (˜pH 3) with 1M HCl and extracted with EtOAc. After drying over Na2SO4, the solvent was removed in vacuo to give a solid (100 mg) which was crystallized from EtOAc. Yield was 29.3 mg; mp 170-171° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08466182B2
Source datasetuspto-grants-2013_06
ORD IDord-f30479d44bf84d69896b857a12ee40c3
Source noteuspto-grants-2013_06