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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2054228Generated: October 25, 2026

1-(3,4-Dichlorophenyl)-4,4,4-trifluorobutane-1,3-dione → 5-(3,4-Dichlorophenyl)-7-(trifluoromethyl)pyrazolo[1,5-a]pyrimidine-3-carbonitrile

https://huagongshe.com/reaction/2054228

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(3,4-Dichlorophenyl)-4,4,4-trifluorobutane-1,3-dioneHCID 12446255—
ReactantHCID 178510443HCID 178510443—
Product5-(3,4-Dichlorophenyl)-7-(trifluoromethyl)pyrazolo[1,5-a]pyrimidine-3-carbonitrileHCID 476748539.2%

Reaction Steps

Reaction of 1-(3,4-dichloro-phenyl)-4,4,4-trifluoro-butane-1,3-dione (285 mg, 1.0 mmol), prepared from commercially available 3,4-dichloro-acetophenone according to general procedure A, and 3-amino-4-cyano-pyrazole (108 mg, 1.0 mmol) according to general procedure B yielded the title compound as a yellow solid (140 mg, 39%). MS (ISP) 356.9 [(M+H)+]; mp 206° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07329662B2
Source datasetuspto-grants-2008_02
ORD IDord-50ab6cfe40da4356899c6e0696a26a31
Source noteuspto-grants-2008_02