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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2054266Generated: October 27, 2026

1-(4-Methyl-3-trifluoromethyl-phenyl)-4,4,4-trifluoro-butane-1,3-dione → 5-(4-Methyl-3-trifluoromethyl-phenyl)-3-(2,6-dimethyl-pyridin-4-yl)-7-trifluoromethyl-pyrazolo[1,5-a]pyrimidine

https://huagongshe.com/reaction/2054266

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(4-Methyl-3-trifluoromethyl-phenyl)-4,4,4-trifluoro-butane-1,3-dioneHCID 86598665—
ReactantHCID 178422939HCID 178422939—
Product5-(4-Methyl-3-trifluoromethyl-phenyl)-3-(2,6-dimethyl-pyridin-4-yl)-7-trifluoromethyl-pyrazolo[1,5-a]pyrimidineHCID 1117844151%

Reaction Steps

Reaction of 1-(4-methyl-3-trifluoromethyl-phenyl)-4,4,4-trifluoro-butane-1,3-dione (149 mg, 0.5 mmol), prepared from 4-methyl-3-trifluoromethyl-acetophenone (synthesis: see part acetophenone derivatives) according to general procedure A, and 3-amino-4-(2,6-dimethyl-4-pyridinyl)-pyrazole [prepared from 4-cyanomethyl-2,6-dimethyl-pyridine, see part synthesis of amino-pyrazole derivatives] (94 mg, 0.5 mmol) according to general procedure B yielded the title compound as a yellow solid (114 mg, 51%). MS (ISP) 451.2 [(M+H)+]; mp 258° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07329662B2
Source datasetuspto-grants-2008_02
ORD IDord-041f5789a6da4c8bb869005fd52216aa
Source noteuspto-grants-2008_02