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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1643953Generated: November 1, 2026

Carbonate Ion → 5-Chloro-1-{2-oxo-1-phenyl-2-[3-(4-propylpiperazin-1-yl)pyrrolidin-1-yl]-ethyl}-1,3-dihydrobenzimidazol-2-one

https://huagongshe.com/reaction/1643953

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbonate IonHCID 19660—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantCarbodiimideHCID 160435—
Reactant(5-Chloro-2-oxo-2,3-dihydrobenzimidazol-1-yl)phenyl-acetic acidHCID 24901021—
Reactant1-Propyl-4-pyrrolidin-3-ylpiperazineHCID 66754661—
SolventDichloromethaneHCID 6344—
Product5-Chloro-1-{2-oxo-1-phenyl-2-[3-(4-propylpiperazin-1-yl)pyrrolidin-1-yl]-ethyl}-1,3-dihydrobenzimidazol-2-oneHCID 66755062—

Reaction Steps

110 mg (0.36 mmol) of (5-chloro-2-oxo-2,3-dihydrobenzimidazol-1-yl)phenyl-acetic acid (VIIIe), 69.1 mg (0.51 mmol) of HOBt and 335 mg (0.44 mmol, 1.3 mmol/g) of solid phase-bound PS-carbodiimide were dissolved in 6 ml of dry dichloromethane in a screw-cap tube and shaken mechanically at room temperature for 10 min. 78.9 mg (0.40 mmol) of 1-propyl-4-pyrrolidin-3-ylpiperazine were added, and the mixture was then shaken mechanically overnight. Three equivalents of solid phase-bound MP-carbonate were then added to the reaction mixture, and shaking was continued for 2 h. The solid phase-bound reagents were filtered off and washed with dichloromethane. The filtrate was concentrated in vacuo and the residue was dried in vacuo. The reaction product was used without further purification for the next reaction step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08119676B2
Source datasetuspto-grants-2012_02
ORD IDord-285fa30fc11a478a94886c41dad10d94
Source noteuspto-grants-2012_02