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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1258622Generated: October 31, 2026

3,4-Dimethoxybenzenesulfonyl chloride → HCID 24994808, compound

https://huagongshe.com/reaction/1258622

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,4-Dimethoxybenzenesulfonyl chlorideHCID 2734183—
Reactant5-(4-chlorophenyl)-1,2,4-thiadiazol-3-amineHCID 2794757—
SolventPyridineHCID 1049—
ProductHCID 24994808HCID 2499480846.6%

Reaction Steps

To a solution of 5-(4-chlorophenyl)-1,2,4-thiadiazol-3-amine (423 mg, 2.0 mmol) in 10 mL of dry pyridine was added 529 mg (2.23 mmol) of 3,4-dimethoxybenzenesulfonyl chloride. The solution was stirred at room temperature under Argon. After 21 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. EtOH was used in the second extraction to assist solubilizing the sulfonamide. After drying over Na2SO4, solvent was removed in vacuo. The crude crystalline product weighed 0.45 g. The crude product was taken up in 13 mL of hot HOAc, diluted with 7 mL of H2O and seeded to give white needles (384 mg) after collection by filtration, washing with H2O, and drying in vacuo. The product had mp 220-221° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08466182B2
Source datasetuspto-grants-2013_06
ORD IDord-ae5eb72ab29043e99eaf62c31d0a8d33
Source noteuspto-grants-2013_06