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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 130466Generated: October 31, 2026

5-(5-chloro-1,2,4-thiadiazol-3-yl)thiophene-2-sulfonyl Chloride → 5-(5-Chloro-1,2,4-thiadiazol-3-yl)-N-[5-(cis-3,5-dimethyl-1-piperazinyl)-2-(methyloxy)phenyl]-2-thiophenesulfonamide

https://huagongshe.com/reaction/130466

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-(5-chloro-1,2,4-thiadiazol-3-yl)thiophene-2-sulfonyl ChlorideHCID 2735820—
Reactant5-(cis-3,5-Dimethyl-1-piperazinyl)-2-(methyloxy)anilineHCID 59007063—
SolventPyridineHCID 1049—
SolventDichloromethaneHCID 6344—
Product5-(5-Chloro-1,2,4-thiadiazol-3-yl)-N-[5-(cis-3,5-dimethyl-1-piperazinyl)-2-(methyloxy)phenyl]-2-thiophenesulfonamideHCID 11684751—

Reaction Steps

A solution of 5-(cis-3,5-dimethyl-1-piperazinyl)-2-(methyloxy)aniline (D4) (33 mg, 0.14 mmol) in dichloromethane (2 ml) and pyridine (0.5 ml) was treated with 5-(5-chloro-1,2,4-thiadiazol-3-yl)-2-thiophenesulfonyl chloride (50 mg, 0.17 mmol) and the resulting mixture stirred at room temperature overnight. The mixture was then concentrated in vacuo, co-evaporated with toluene and the crude product purified by mass directed autoprep HPLC to afford the desired product which was characterized as the hydrochloride salt. MS (ES+) m/e 500/502 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07381728B2
Source datasetuspto-grants-2008_06
ORD IDord-f2673600998b4da0b7abb280b675e6f3
Source noteuspto-grants-2008_06