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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1784569Generated: October 29, 2026

7-Trifluoromethyl-5-(4-trifluoromethyl-phenyl)-pyrazolo[1,5-a]pyrimidine-3-carboxylic acid → 3-{5-[7-Trifluoromethyl-5-(4-trifluoromethyl-phenyl)-pyrazolo[1,5-a]pyrimidin-3-yl]-[1,2,4]oxadiazol-3-yl}-benzenesulfonamide

https://huagongshe.com/reaction/1784569

Reaction equation

Participants

RoleNameHCIDCharge
Reactant7-Trifluoromethyl-5-(4-trifluoromethyl-phenyl)-pyrazolo[1,5-a]pyrimidine-3-carboxylic acidHCID 86607112—
ReactantHCID 178513322HCID 178513322—
Product3-{5-[7-Trifluoromethyl-5-(4-trifluoromethyl-phenyl)-pyrazolo[1,5-a]pyrimidin-3-yl]-[1,2,4]oxadiazol-3-yl}-benzenesulfonamideHCID 16068663—

Reaction Steps

The title compound was prepared from 7-trifluoromethyl-5-(4-trifluoromethyl-phenyl)-pyrazolo[1,5-a]pyrimidine-3-carboxylic acid (example C.2) (188 mg, 0.5 mmol) and N-hydroxy-3-sulfamoyl-benzamidine [CAS-No. 9000-88-7] (161 mg, 0.75 mmol) according to general procedure II. Obtained after purification by column chromatography (dichloromethane/MeOH/NH4OH) and crystallization (ethyl acetate/MeOH/hexane) as a yellow solid (175 mg, 63%). MS (ISN) 552.8 [(M−H)−]; mp 262° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07504404B2
Source datasetuspto-grants-2009_03
ORD IDord-d992d614470b43449d5b997f62f0c0bb
Source noteuspto-grants-2009_03