Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2278270Generated: October 30, 2026

Potassium Carbonate → HCID 89677105, compound

https://huagongshe.com/reaction/2278270

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant1,4-DioxaneHCID 31275—
Reactant3-Fluorophenylboronic acidHCID 2733986—
Reactant1,1-Dimethylethyl 4-[(5-bromo-2-pyridinyl)methyl]-1-piperazinecarboxylateHCID 58407727—
CatalystHCID 178418397HCID 178418397—
SolventWaterHCID 962—
ProductHCID 89677105HCID 8967710592%

Reaction Conditions

Temperature80 °C

Reaction Steps

A 100 mL round-bottom flask was purged with and maintained an inert atmosphere of nitrogen then charged with tert-butyl 4-[(5-bromopyridin-2-yl)methyl]piperazine-1-carboxylate (1.00 g, 2.81 mmol, 1.00 equiv), (3-fluorophenyl)boronic acid (0.790 g, 5.65 mmol, 2.00 equiv), Tetrakis(triphenylphosphine)palladium (0.325 g, 0.280 mmol, 0.10 equiv), potassium carbonate (1.17 g, 8.47 mmol, 3.00 equiv), dioxane (24 mL), and water (4 mL). The resulting solution was stirred overnight at 80° C. and then diluted with water (10 mL) and extracted with ethyl acetate (3×5 mL). The organic layers were combined, dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure. The residue was chromatographed on a silica gel column with ethyl acetate/petroleum ether (1/1) to provide 0.955 g (92% yield) of tert-butyl 4-[[5-(3-fluorophenyl)pyridin-2-yl]methyl]piperazine-1-carboxylate as yellow oil. LCMS (ESI, m/z): 372 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09133148B2
Source datasetuspto-grants-2015_09
ORD IDord-50122f1203a04f3392d098752e01519e
Source noteuspto-grants-2015_09