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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1643952Generated: November 1, 2026

Potassium Carbonate → 1-[2-Oxo-1-phenyl-2-(4-pyridin-4-ylpiperazin-1-yl)ethyl]-1,3-dihydrobenzimidazol-2-one

https://huagongshe.com/reaction/1643952

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant1-(4-Pyridyl)piperazineHCID 70517—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantDiisopropylethylamineHCID 81531—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant(2-Oxo-2,3-dihydrobenzimidazol-1-yl)phenylacetic acidHCID 66754578—
SolventDichloromethaneHCID 6344—
Product1-[2-Oxo-1-phenyl-2-(4-pyridin-4-ylpiperazin-1-yl)ethyl]-1,3-dihydrobenzimidazol-2-oneHCID 24901169—

Reaction Steps

179 mg (0.94 mmol) of EDCl were added to a solution of 193 mg (0.72 mmol) of (2-oxo-2,3-dihydrobenzimidazol-1-yl)phenylacetic acid (VIIId), 106 mg (0.79 mmol) of HOBt, 117 mg (0.72 mmol) of 1-pyridin-4-ylpiperazine and 0.49 ml (2.87 mmol) of ethyldiisopropylamine in dichloromethane (8 ml) while stirring in an ice-water bath. The reaction solution was slowly warmed and stirred at room temperature for 16 h. Half-saturated aqueous potassium carbonate solution was added, and the organic phase was separated off. The aqueous phase was extracted with ethyl acetate (4×50 ml) and the combined organic phases were washed with sat. NaHCO3 solution, dried over magnesium sulfate and concentrated under reduced pressure. The reaction product was used without further purification for the next reaction step. Yield: 292 mg (98%) of yellow solid

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08119676B2
Source datasetuspto-grants-2012_02
ORD IDord-7a107e1d5fab4b2fad6d6a6daa41f6da
Source noteuspto-grants-2012_02