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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1804002Generated: October 25, 2026

Toluene → 4-(5-Cyclobutyl-3-methylpyridin-2-yl)piperazine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/1804002

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantPotassium Phosphate, TribasicHCID 62657—
ReactantCyclobutylboronic acidHCID 16217845—
Reactanttert-Butyl 4-(5-bromo-3-methylpyridin-2-yl)piperazine-1-carboxylateHCID 46739269—
CatalystBis(tricyclohexylphosphine)palladium(II) DichlorideHCID 11556747—
SolventWaterHCID 962—
Product4-(5-Cyclobutyl-3-methylpyridin-2-yl)piperazine-1-carboxylic acid tert-butyl esterHCID 6738097012.5%

Reaction Steps

To a mixture of 4-(5-bromo-3-methylpyridin-2-yl)piperazine-1-carboxylic acid tert-butyl ester (4.8 g), bis(tricyclohexylphosphine)palladium (II) dichloride (515 mg), tripotassium phosphate (16 g) and cyclobutylboronic acid (2.6 g) were added toluene (39 mL) and water (2 mL), and the mixture was refluxed for 8 hr. After cooling, the mixture was extracted with ethyl acetate, washed with saturated brine, and the solvent was evaporated. The residue was purified by column chromatography (hexane:ethyl acetate) to give 4-(5-cyclobutyl-3-methylpyridin-2-yl)piperazine-1-carboxylic acid tert-butyl ester (560 mg). 4-(5-cyclobutyl-3-methylpyridin-2-yl)piperazine-1-carboxylic acid tert-butyl ester (560 mg) was dissolved in chloroform (1.5 mL), 4N hydrogen chloride/ethyl acetate (1.5 mL) was added, and the mixture was stirred at room temperature overnight. To the reaction mixture was added 1N aqueous sodium hydroxide solution (8 mL), and the mixture was extracted with chloroform. The organic layer was washed with saturated brine, and the solvent was evaporated to give the title compound (350 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08354401B2
Source datasetuspto-grants-2013_01
ORD IDord-7ce875a981d945d4af3c13d85682da8d
Source noteuspto-grants-2013_01