Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2108434Generated: October 31, 2026

1-(3-Chloro-4-fluorophenyl)-4,4,4-trifluorobutane-1,3-dione → 5-(3-Chloro-4-fluoro-phenyl)-3-(2,6-dimethyl-pyridin-4-yl)-7-trifluoromethyl-pyrazolo[1,5-a]pyrimidine

https://huagongshe.com/reaction/2108434

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(3-Chloro-4-fluorophenyl)-4,4,4-trifluorobutane-1,3-dioneHCID 12921697—
ReactantHCID 178422939HCID 178422939—
Product5-(3-Chloro-4-fluoro-phenyl)-3-(2,6-dimethyl-pyridin-4-yl)-7-trifluoromethyl-pyrazolo[1,5-a]pyrimidineHCID 1145291146.1%

Reaction Steps

Reaction of 1-(3-chloro-4-fluoro-phenyl)-4,4,4-trifluoro-butane-1,3-dione (134 mg, 0.5 mmol), prepared from commercially available 3-chloro-4-fluoro-acetophenone according to general procedure A, and 3-amino-4-(2,6-dimethyl-4-pyridinyl)-pyrazole [prepared from 4-cyanomethyl-2,6-dimethyl-pyridine, CAS No. 130138-46-4, 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 (97 mg, 46%). MS (ISP) 421.1 [(M+H)+]; mp 271° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07514443B2
Source datasetuspto-grants-2009_04
ORD IDord-224c8ced3d7c453586353b05bc3d03f8
Source noteuspto-grants-2009_04