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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 418196Generated: October 29, 2026

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

https://huagongshe.com/reaction/418196

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-(4-Chloro-phenyl)-7-difluoromethyl-pyrazolo[1,5-a]pyrimidine-3-carboxylic acidHCID 66650326—
ReactantHCID 178513322HCID 178513322—
Product3-{5-[5-(4-Chloro-phenyl)-7-difluoromethyl-pyrazolo[1,5-a]pyrimidin-3-yl]-[1,2,4]oxadiazol-3-yl}-benzenesulfonamideHCID 16068882—

Reaction Steps

The title compound was prepared from 5-(4-chloro-phenyl)-7-difluoromethyl-pyrazolo[1,5-a]pyrimidine-3-carboxylic acid (example C.3) (162 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 trituration with water and further purification by crystallization (dichloromethane) as a light yellow solid (170 mg, 68%). MS (ISN) 501.1 [(M−H)−]; mp 231° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08093263B2
Source datasetuspto-grants-2012_01
ORD IDord-2dc0036290364ad897719126c25582ab
Source noteuspto-grants-2012_01