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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1784635Generated: October 28, 2026

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

https://huagongshe.com/reaction/1784635

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-(3-Chloro-4-trifluoromethyl-phenyl)-7-trifluoromethyl-pyrazolo[1,5-a]pyrimidine-3-carboxylic acidHCID 86607116—
ReactantHCID 178513347HCID 178513347—
Product5-{5-[5-(3-Chloro-4-trifluoromethyl-phenyl)-7-trifluoromethyl-pyrazolo[1,5-a]pyrimidin-3-yl]-[1,2,4]oxadiazol-3-yl}-pyridin-2-ylamineHCID 16067909—

Reaction Steps

The title compound was prepared from 5-(3-chloro-4-trifluoromethyl-phenyl)-7-trifluoromethyl-pyrazolo[1,5-a]pyrimidine-3-carboxylic acid (example C.17) (205 mg, 0.5 mmol) and 6-amino-N-hydroxy-nicotinamidine (example B.4) (114 mg, 0.75 mmol) according to general procedure II. Obtained after flash chromatography on silica gel (ethyl acetate/heptane) and further purification by crystallization (dichloromethane/hexane) as a yellow solid (90 mg, 34%). MS (ISP) 526.1 [(M+H)+]; mp 234° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07504404B2
Source datasetuspto-grants-2009_03
ORD IDord-61ba1dd9c7eb4630ba781c489e5d2d4a
Source noteuspto-grants-2009_03