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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1801807Generated: October 29, 2026

4-Trifluoromethyl-2-(4-trifluoromethyl-phenyl)-imidazo[1,5-a]pyrimidine-8-carboxylic acid → 5-{5-[4-Trifluoromethyl-2-(4-trifluoromethyl-phenyl)-imidazo[1,5-a]pyrimidin-8-yl]-[1,2,4]oxadiazol-3-yl}-thiophene-2-sulfonic acid amide

https://huagongshe.com/reaction/1801807

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Trifluoromethyl-2-(4-trifluoromethyl-phenyl)-imidazo[1,5-a]pyrimidine-8-carboxylic acidHCID 86608004—
ReactantHCID 178513361HCID 178513361—
Product5-{5-[4-Trifluoromethyl-2-(4-trifluoromethyl-phenyl)-imidazo[1,5-a]pyrimidin-8-yl]-[1,2,4]oxadiazol-3-yl}-thiophene-2-sulfonic acid amideHCID 16068463—

Reaction Steps

The title compound was prepared from 4-trifluoromethyl-2-(4-trifluoromethyl-phenyl)-imidazo[1,5-a]pyrimidine-8-carboxylic acid (example C.30) (188 mg, 0.5 mmol) and N-hydroxy-5-sulfamoyl-thiophene-2-carboxamidine (example B.2) (166 mg, 0.75 mmol) according to general procedure II. Obtained after purification by flash chromatography (ethyl acetate/heptane) and crystallization (dichloromethane/ethyl acetate) as a yellow solid (199 mg, 71%). MS (ISN) 559.1 [(M−H)−]; mp 295° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08349844B2
Source datasetuspto-grants-2013_01
ORD IDord-1d952837538a40ee91b9b6893d5248e1
Source noteuspto-grants-2013_01