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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 336388Generated: October 25, 2026

(4-Fluoro-3-methylphenyl)boronic acid → 2-(3-(4-Fluoro-3-methyl-phenyl)-5-phenyl-(1,2,4)triazol-1-yl)-1-(4-pyrimidin-2-yl-piperazin-1-yl)-ethanone

https://huagongshe.com/reaction/336388

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(4-Fluoro-3-methylphenyl)boronic acidHCID 2774580—
ReactantSodium dicarbonateHCID 22718997—
Reactant2-(3-Bromo-5-phenyl-(1,2,4)triazol-1-yl)-1-(4-pyrimidin-2-yl-piperazin-1-yl)-ethanoneHCID 86690171—
CatalystHCID 178418397HCID 178418397—
Solvent1,4-DioxaneHCID 31275—
Product2-(3-(4-Fluoro-3-methyl-phenyl)-5-phenyl-(1,2,4)triazol-1-yl)-1-(4-pyrimidin-2-yl-piperazin-1-yl)-ethanoneHCID 7161264930%

Reaction Conditions

Temperature120 °C

Reaction Steps

15 mg tetrakis(triphenylphosphine)palladium(0) was added to 100 mg 2-(3-bromo-5-phenyl-(1,2,4)triazol-1-yl)-1-(4-pyrimidin-2-yl-piperazin-1-yl)-ethanone, 500 μL 2 mol/L aqueous sodiumdicarbonate solution and 43 mg 4-fluoro-3-methylphenylboronic acid in 10 mL dioxane under nitrogen. The reaction was stirred over night at 120° C. The reaction was filltered and evaporated. The residue was purified by HPLC to give 32 mg of the desired product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08889677B2
Source datasetuspto-grants-2014_11
ORD IDord-84aea2a5210d410c990142fca04841a1
Source noteuspto-grants-2014_11