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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 334942Generated: October 26, 2026

Potassium Carbonate → 4-{4-[2-(2,4-bis-benzyloxy-5-isopropenyl-benzoyl)-2,3-dihydro-1H-isoindol-5-yl]phenyl}piperazine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/334942

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant4-(4-tert-Butoxycarbonylpiperazinyl)phenylboronic acid, pinacol esterHCID 2795514—
Reactant(2,4-Bis-benzyloxy-5-isopropenyl-phenyl)-(5-bromo-1,3-dihydro-isoindol-2-yl)-methanoneHCID 46915776—
CatalystHCID 178418851HCID 178418851—
SolventEthyl AcetateHCID 8857—
SolventEthanol toluene waterHCID 86587398—
Product4-{4-[2-(2,4-bis-benzyloxy-5-isopropenyl-benzoyl)-2,3-dihydro-1H-isoindol-5-yl]phenyl}piperazine-1-carboxylic acid tert-butyl esterHCID 6667256226.9%

Reaction Conditions

Temperature135 °C

Reaction Steps

A mixture of (2,4-bis-benzyloxy-5-isopropenyl-phenyl)-(5-bromo-1,3-dihydro-isoindol-2-yl)-methanone (240 mg, 0.43 mmol), t-butyl-4-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]piperazine carboxylate (210 mg, 1.25 equiv.), bis(tri-t-butylphosphine)palladium(0) (12.5 mg, 2.5 mol %) and potassium carbonate (350 mg, 6 equiv.) in toluene/water/ethanol (1 ml: 1 ml: 4 ml) was heated at 135° C. for 30 minutes in a CEM explorer microwave synthesiser. The reaction mixture was diluted with EtOAc, washed with saturated NaHCO3, dried (MgSO4) and evaporated. Purification by flash column chromatography (Biotage SP4-25S, 25 ml/min) eluting with 1:3 then 1:1 EtOAc/P.E. Evaporation of product containing fractions gave 85 mg of 4-{4-[2-(2,4-bis-benzyloxy-5-isopropenyl-benzoyl)-2,3-dihydro-1H-isoindol-5-yl}phenyl]piperazine-1-carboxylic acid tert-butyl ester. MS: [M+H]+ 736.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08883790B2
Source datasetuspto-grants-2014_11
ORD IDord-c7efd8d4fe6541c6813de380eb406aea
Source noteuspto-grants-2014_11