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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1293879Generated: October 25, 2026

4-bromo-N-methylbenzene-1-sulfonamide → 4-[7-difluoromethyl-5-(4-trifluoromethyl-phenyl)-pyrazolo[1,5-a]pyrimidin-3-ylethynyl]-N-methyl-benzenesulfonamide

https://huagongshe.com/reaction/1293879

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-bromo-N-methylbenzene-1-sulfonamideHCID 101215—
Reactant3-Ethynyl-7-difluoromethyl-5-(4-trifluoromethyl-phenyl)-pyrazolo[1,5-a]pyrimidineHCID 86608034—
Product4-[7-difluoromethyl-5-(4-trifluoromethyl-phenyl)-pyrazolo[1,5-a]pyrimidin-3-ylethynyl]-N-methyl-benzenesulfonamideHCID 67000893—

Reaction Steps

The title compound was prepared from 7-difluoromethyl-3-ethynyl-5-(4-trifluoromethyl-phenyl)-pyrazolo[1,5-a]pyrimidine (example C.2) (340 mg, 1.0 mmol) and 4-bromo-N-methyl-benzenesulfonamide (example B.27) (276 mg, 1.0 mmol) according to general procedure II. Obtained as a yellow solid (300 mg, 58%). MS (ISP) 508.3 [(M+H)+]; mp 202–203° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07238808B2
Source datasetuspto-grants-2007_07
ORD IDord-cf0ba3a4c98b440bb343db662cbf8c09
Source noteuspto-grants-2007_07