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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1258618Generated: October 31, 2026

3,4-Dimethoxybenzenesulfonyl chloride → 3,4-Dimethoxy-N-(1-methyl-3-phenyl-1,2,4-triazol-5-yl)benzenesulfonamide

https://huagongshe.com/reaction/1258618

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,4-Dimethoxybenzenesulfonyl chlorideHCID 2734183—
Reactant1-methyl-3-phenyl-1H-1,2,4-triazol-5-amineHCID 12581307—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
SolventPyridineHCID 1049—
Product3,4-Dimethoxy-N-(1-methyl-3-phenyl-1,2,4-triazol-5-yl)benzenesulfonamideHCID 2499450619.1%

Reaction Steps

To a solution of 1-methyl-3-phenyl-1,2,4-triazol-5-amine (320 mg, 2 mmol) in 10 mL 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 salt was partitioned between EtOAc and water. The EtOAc phase was extracted alternately with 1M NaOH and H2O. The basic phase was made acid (pH˜3) with 1M HCl and extracted with EtOAc. The organic phase was evaporated in vacuo, toluene was added and was again evaporated in vacuo to give a white solid. The product was taken up in hot HOAc (16 mL), diluted with H2O (10 mL) and seeded to give 143 mg of white needles with mp 279-280° C. after drying in vacuo.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08466182B2
Source datasetuspto-grants-2013_06
ORD IDord-f4d2cd777fc14e0680f73f22b9f2ff69
Source noteuspto-grants-2013_06