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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1801792Generated: October 29, 2026

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

https://huagongshe.com/reaction/1801792

Reaction equation

Participants

RoleNameHCIDCharge
Reactant7-Trifluoromethyl-5-(3-trifluoromethyl-phenyl)-pyrazolo[1,5-a]pyrimidine-3-carboxylic acidHCID 86611627—
ReactantHCID 178513322HCID 178513322—
Product3-{5-[7-Trifluoromethyl-5-(3-trifluoromethyl-phenyl)-pyrazolo[1,5-a]pyrimidin-3-yl]-[1,2,4]oxadiazol-3-yl}-benzenesulfonamideHCID 16069085—

Reaction Steps

The title compound was prepared from 7-trifluoromethyl-5-(3-trifluoromethyl-phenyl)-pyrazolo[1,5-a]pyrimidine-3-carboxylic acid (example C.31) (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 flash chromatography (ethyl acetate/heptane) and crystallization (dichloromethane) as a light yellow solid (120 mg, 43%). MS (ISN) 552.9 [(M−H)−]; mp 251° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08349844B2
Source datasetuspto-grants-2013_01
ORD IDord-b002aa2ecc594ccf9f7835a9f65ac82b
Source noteuspto-grants-2013_01