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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1804120Generated: November 2, 2026

Methylboronic Acid → 4-(3,5,6-Trimethylpyridin-2-yl)piperazine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/1804120

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethylboronic AcidHCID 139377—
ReactantPotassium FluorideHCID 522689—
Reactant2-Dicyclohexylphosphino-2',6'-dimethoxybiphenylHCID 11269872—
Reactant4-(3,5,6-Trichloropyridin-2-yl)piperazine-1-carboxylic acid tert-butyl esterHCID 86658775—
Catalystpalladium(II) acetateHCID 167845—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
SolventSodium chloride; waterHCID 57417360—
Product4-(3,5,6-Trimethylpyridin-2-yl)piperazine-1-carboxylic acid tert-butyl esterHCID 67380981306%

Reaction Steps

To a mixture of 4-(3,5,6-trichloropyridin-2-yl)piperazine-1-carboxylic acid tert-butyl ester (9.27 g) described in Preparation Example 173, palladium (II) acetate (851 mg), 2-dicyclohexylphosphino-2′,6′-dimethoxybiphenyl (3.11 g), potassium fluoride (17.6 g) and methylboronic acid (9.08 g) was added tetrahydrofuran (190 mL), and the mixture was refluxed for 5.5 hr. After cooling, to the reaction mixture were added ethyl acetate and saturated brine and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine, and dried over sodium sulfate. The solvent was evaporated under reduced pressure and the residue was purified by column chromatography (hexane:ethyl acetate) to give the title compound (7.08 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08354401B2
Source datasetuspto-grants-2013_01
ORD IDord-95d28118eff74dcdb61b0292b103e3dd
Source noteuspto-grants-2013_01