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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1352414Generated: November 3, 2026

1-(5-Trifluoromethyl-[1,3,4]thiadiazol-2-yl)-piperazine trifluoroacetate → 4-Cyclopentyloxy-N-methyl-3-[4-(5-trifluoromethyl-[1,3,4]thiadiazol-2-yl)-piperazine-1-carbonyl]-benzenesulfonamide

https://huagongshe.com/reaction/1352414

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(5-Trifluoromethyl-[1,3,4]thiadiazol-2-yl)-piperazine trifluoroacetateHCID 21100199—
ReactantHCID 21100227HCID 21100227—
Product4-Cyclopentyloxy-N-methyl-3-[4-(5-trifluoromethyl-[1,3,4]thiadiazol-2-yl)-piperazine-1-carbonyl]-benzenesulfonamideHCID 2110016446%

Reaction Steps

Prepared in analogy to example 1 (b) from 2-cyclopentyloxy-5-methylsulfamoyl-benzoic acid (Example A29) and 1-(5-trifluoromethyl-[1,3,4]thiadiazol-2-yl)-piperazine trifluoroacetate (Example 62(b)). The crude material was purified by chromatography (SiO2, ethyl acetate/heptane) to yield the title compound as a white solid (yield 46%). MS (m/e): 520.3 (M+H+, 100%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07220744B2
Source datasetuspto-grants-2007_05
ORD IDord-e91f1bcaf5804de68c563ca994cb95fb
Source noteuspto-grants-2007_05