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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2108445Generated: October 29, 2026

1-(3,4-Dichlorophenyl)-4,4,4-trifluorobutane-1,3-dione → 5-(3,4-Dichloro-phenyl)-3-(2-methyl-pyridin-4-yl)-7-trifluoromethyl-pyrazolo[1,5-a]pyrimidine

https://huagongshe.com/reaction/2108445

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(3,4-Dichlorophenyl)-4,4,4-trifluorobutane-1,3-dioneHCID 12446255—
ReactantHCID 178422940HCID 178422940—
Product5-(3,4-Dichloro-phenyl)-3-(2-methyl-pyridin-4-yl)-7-trifluoromethyl-pyrazolo[1,5-a]pyrimidineHCID 1121239047.3%

Reaction Steps

Reaction of 1-(3,4-dichloro-phenyl)-4,4,4-trifluoro-butane-1,3-dione (143 mg, 0.5 mmol), prepared from commercially available 3,4-dichloro-acetophenone according to general procedure A, and 3-amino-4-(2-methyl-4-pyridinyl)-pyrazole [see part synthesis of amino-pyrazole derivatives] (87 mg, 0.5 mmol) according to general procedure B yielded the title compound as a yellow solid (100 mg, 47%). MS (ISP) 423.0 [(M+H)+]; mp 275° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07514443B2
Source datasetuspto-grants-2009_04
ORD IDord-55f3c830807f4f14abc8354c2dcb9e2e
Source noteuspto-grants-2009_04