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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1172943Generated: November 1, 2026

1,2-Dichloroethane → 4-(3-(3-Chloro-4-isopropoxyphenyl)-1,2,4-oxadiazol-5-yl)benzenesulfonamide

https://huagongshe.com/reaction/1172943

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
ReactantCarzenideHCID 8739—
Reactant1-Hydroxybenzotriazole hydrateHCID 2796029—
Reactant3-chloro-N'-hydroxy-4-propan-2-yloxybenzenecarboximidamideHCID 59556565—
SolventDimethylformamideHCID 6228—
Product4-(3-(3-Chloro-4-isopropoxyphenyl)-1,2,4-oxadiazol-5-yl)benzenesulfonamideHCID 5324766450%

Reaction Conditions

Temperature140 °C

Reaction Steps

To a slurry of 4-sulfamoylbenzoic acid (1.452 g, 7.22 mmol) in DMF (8.20 ml) was added EDC (1.383 g, 7.22 mmol) followed by HOBT hydrate (0.975 g, 7.22 mmol). After about 30 minutes a solution of (Z)-3-chloro-N′-hydroxy-4-isopropoxybenzimidamide in DMF (8.20 ml) was added. The reaction mixture was heated to about 140° C. for about 2 h. After cooling to room temperature the reaction mixture was concentrated in vacuo and purified by purified by chromatography on silica gel (eluting with EtOAc/Hep) to provide 4-(3-(3-chloro-4-isopropoxyphenyl)-1,2,4-oxadiazol-5-yl)benzenesulfonamide (1.28 g, 50%) as a colorless solid. LCMS (Table 1, Method c) Rt=2.74 min, m/z 392 (M−H)−.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07834039B2
Source datasetuspto-grants-2010_11
ORD IDord-0bfad23297c4436bbdaadc00bf90b0a9
Source noteuspto-grants-2010_11