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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1293772Generated: October 30, 2026

5-Bromo-2,4-difluorobenzenesulfonamide → 2,4-Difluoro-5-[7-trifluoromethyl-5-(4-trifluoromethyl-phenyl)-pyrazolo[1,5-a]pyrimidin-3-ylethynyl]-benzenesulfonamide

https://huagongshe.com/reaction/1293772

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Bromo-2,4-difluorobenzenesulfonamideHCID 2773295—
Reactant3-Ethynyl-7-trifluoromethyl-5-(4-trifluoromethyl-phenyl)-pyrazolo[1,5-a]pyrimidineHCID 71539732—
Product2,4-Difluoro-5-[7-trifluoromethyl-5-(4-trifluoromethyl-phenyl)-pyrazolo[1,5-a]pyrimidin-3-ylethynyl]-benzenesulfonamideHCID 11853036—

Reaction Steps

The title compound was prepared from 3-ethynyl-7-trifluoromethyl-5-(4-trifluoromethyl-phenyl)-pyrazolo[1,5-a]pyrimidine (example C.1) (355 mg, 1.0 mmol) and commercially available 5-bromo-2,4-difluorobenzenesulphonamide (245 mg, 0.9 mmol) according to general procedure II. Obtained as a yellow solid (230 mg, 42%). MS (ISP) 614.3 [(M+H)+]; mp 281–284° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07238808B2
Source datasetuspto-grants-2007_07
ORD IDord-5c43aa7c9cb6416ea4b95eb893250745
Source noteuspto-grants-2007_07