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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 268980Generated: October 25, 2026

4,4,4-Trifluoro-1-(4-trifluoromethylphenyl)-1,3-butanedione → 7-(Trifluoromethyl)-5-(4-(trifluoromethyl)phenyl)pyrazolo[1,5-a]pyrimidine

https://huagongshe.com/reaction/268980

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4,4,4-Trifluoro-1-(4-trifluoromethylphenyl)-1,3-butanedioneHCID 10859020—
ReactantHCID 178418806HCID 178418806—
SolventAcetic AcidHCID 176—
Product7-(Trifluoromethyl)-5-(4-(trifluoromethyl)phenyl)pyrazolo[1,5-a]pyrimidineHCID 7153973199%

Reaction Steps

A mixture of 4,4,4-trifluoro-1-(4-trifluoromethyl-phenyl)-butane-1,3-dione (Example C.1, method 1, step 1) (2.84 g, 10 mmol) and 3-aminopyrazole (0.83 g, 10 mmol) in acetic acid (20 mL) were refluxed for 4 h. The reaction mixture was cooled to rt and poured into ice water (200 mL), extracted with EtOAc, dried over MgSO4, filtered and concentrated, and triturated with toluene, and dried to give 7-trifluoromethyl-5-(4-trifluoromethyl-phenyl)-pyrazolo[1,5-a]pyrimidine (3.28 g, 99%) as a yellow solid. MS (ISP) 332.1 [(M+H)+]; mp 110-111° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07446113B2
Source datasetuspto-grants-2008_11
ORD IDord-8e0f9f7d6cb24203af5c698fa1c48bcd
Source noteuspto-grants-2008_11