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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2054236Generated: October 26, 2026

3-amino-5-methyl-1H-pyrazole-4-carbonitrile → 5-(3-Chloro-4-fluoro-phenyl)-2-methyl-7-trifluoromethyl-pyrazolo[1,5-a]pyrimidine-3-carbonitrile

https://huagongshe.com/reaction/2054236

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-amino-5-methyl-1H-pyrazole-4-carbonitrileHCID 227460—
Reactant1-(3-Chloro-4-fluorophenyl)-4,4,4-trifluorobutane-1,3-dioneHCID 12921697—
Product5-(3-Chloro-4-fluoro-phenyl)-2-methyl-7-trifluoromethyl-pyrazolo[1,5-a]pyrimidine-3-carbonitrileHCID 6721324469%

Reaction Steps

Reaction of 1-(3-chloro-4-fluoro-phenyl)-4,4,4-trifluoro-butane-1,3-dione (269 mg, 1.0 mmol), prepared from commercially available 3-chloro-4-fluoro-acetophenone according to general procedure A, and commercially available 3-amino-4-cyano-5-methyl-pyrazole (122 mg, 1.0 mmol) according to general procedure B yielded the title compound as a light yellow solid (243 mg, 69%). MS (ISP) 355.0 [(M+H)+]; mp 196° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07329662B2
Source datasetuspto-grants-2008_02
ORD IDord-4bcb9b674ffc463f820022df92e9d2ed
Source noteuspto-grants-2008_02