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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2054292Generated: October 31, 2026

1-(4-Bromophenyl)-4,4,4-trifluorobutane-1,3-dione → HCID 11464647, compound

https://huagongshe.com/reaction/2054292

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(4-Bromophenyl)-4,4,4-trifluorobutane-1,3-dioneHCID 2771477—
ReactantHCID 178422940HCID 178422940—
ProductHCID 11464647HCID 1146464743.4%

Reaction Steps

Reaction of 1-(4-bromo-phenyl)-4,4,4-trifluoro-butane-1,3-dione (148 mg, 0.5 mmol), prepared from commercially available 4-bromo-acetophenone according to general procedure A, and 3-amino-4-(2-methyl-4-pyridinyl)-pyrazole [prepared from 4-cyanomethyl-2-methyl-pyridine, as described in Bioorg. Med. Chem. Lett. 12 (2002) 3537-3541] (87 mg, 0.5 mmol) according to general procedure B yielded the title compound as a yellow solid (94 mg, 43%). MS (ISP) 433.3 [(M+H)+]; mp 226° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07329662B2
Source datasetuspto-grants-2008_02
ORD IDord-d6a5ec1737f84b1383217c9fb110367b
Source noteuspto-grants-2008_02