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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1801846Generated: October 31, 2026

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

https://huagongshe.com/reaction/1801846

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-(3-Methyl-4-trifluoromethyl-phenyl)-7-trifluoromethyl-pyrazolo[1,5-a]pyrimidine-3-carboxylic acidHCID 86607114—
Reactant2-amino-N'-hydroxypyridine-4-carboximidamideHCID 178513375—
Product4-{5-[5-(3-Methyl-4-trifluoromethyl-phenyl)-7-trifluoromethyl-pyrazolo[1,5-a]pyrimidin-3-yl]-[1,2,4]oxadiazol-3-yl}-pyridine-2-ylamineHCID 16068133—

Reaction Steps

The title compound was prepared from 5-(3-methyl-4-trifluoromethyl-phenyl)-7-trifluoromethyl-pyrazolo[1,5-a]pyrimidine-3-carboxylic acid (example C.8) (195 mg, 0.5 mmol) and 2-amino-N-hydroxy-pyridine-4-carboxamidine (example B.6) (114 mg, 0.75 mmol) according to general procedure II. Obtained after trituration with water and further purification by crystallization (dichloromethane/hexane) as a yellow solid (167 mg, 66%). MS (EI) 505.2 [(M)+]; mp 245° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08349844B2
Source datasetuspto-grants-2013_01
ORD IDord-1a024b7165c0427a925dfd8485a8879b
Source noteuspto-grants-2013_01