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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 418202Generated: October 29, 2026

N-hydroxy-4-sulfamoylbenzene-1-carboximidamide → 4-{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/418202

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-hydroxy-4-sulfamoylbenzene-1-carboximidamideHCID 612025—
Reactant7-Trifluoromethyl-5-(3-trifluoromethyl-phenyl)-pyrazolo[1,5-a]pyrimidine-3-carboxylic acidHCID 86611627—
Product4-{5-[7-Trifluoromethyl-5-(3-trifluoromethyl-phenyl)-pyrazolo[1,5-a]pyrimidin-3-yl]-[1,2,4]oxadiazol-3-yl}-benzenesulfonamideHCID 16068988—

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-4-sulfamoyl-benzamidine [CAS-No. 4476-10-2] (161 mg, 0.75 mmol) according to general procedure II. Obtained after purification by flash chromatography (ethyl acetate/heptane) and crystallization (ethyl acetate/dichloromethane) as a yellow solid (220 mg, 79%). MS (ISP) 555.3 [(M+H)+]; mp 300° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08093263B2
Source datasetuspto-grants-2012_01
ORD IDord-75cba04168784ebeb91749866c6cf72c
Source noteuspto-grants-2012_01