Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1784577Generated: October 29, 2026

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

https://huagongshe.com/reaction/1784577

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-(4-Chloro-phenyl)-7-trifluoromethyl-pyrazolo[1,5-a]pyrimidine-3-carboxylic acidHCID 53212223—
ReactantHCID 178513322HCID 178513322—
Product3-{5-[5-(4-Chloro-phenyl)-7-trifluoromethyl-pyrazolo[1,5-a]pyrimidin-3-yl]-[1,2,4]oxadiazol-3-yl}-benzenesulfonamideHCID 16068768—

Reaction Steps

The title compound was prepared from 5-(4-chloro-phenyl)-7-trifluoromethyl-pyrazolo[1,5-a]pyrimidine-3-carboxylic acid (example C.4) (171 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 (dichloromethane) as a light yellow solid (200 mg, 77%). MS (ISP) 521.2 [(M+H)+]; mp 247° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07504404B2
Source datasetuspto-grants-2009_03
ORD IDord-a4a0ddef59f748d7a8e6ef6c260d9afe
Source noteuspto-grants-2009_03