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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1418319Generated: October 27, 2026

Water → 1-{3-[4-(5-Chloro-pyridin-2-yl)-piperazin-1-yl]-propyl}-1,3-dihydro-benzoimidazol-2-one

https://huagongshe.com/reaction/1418319

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantDiisopropylethylamineHCID 81531—
Reactant1-(3-chloropropyl)-1,3-dihydro-2H-benzimidazol-2-oneHCID 1810419—
Reactant1-(5-Chloropyridin-2-yl)piperazineHCID 3805301—
SolventTolueneHCID 1140—
SolventDimethylformamideHCID 6228—
Product1-{3-[4-(5-Chloro-pyridin-2-yl)-piperazin-1-yl]-propyl}-1,3-dihydro-benzoimidazol-2-oneHCID 9885785116.6%

Reaction Steps

A mixture of 1.14 gm of 2-piperazino 5-chloro pyridine, 1.35 gm of 1-(3-chloro propyl)-2,3-dihydro-1H-benzimidazol-2-one (available from Janssen) and 1.49 gm of diisopropylethylamine in 3 ml DMF and 30 ml toluene is kept for 12 hours at 110° C. Upon cooling to ambient temperature, 30 ml water is added and the mixture is extracted with chloroform (CHCl3) and the extract is collected, washed with 20 ml water and dried over sodium sulfate (Na2SO4). The crude product (2.5 gm) which is obtained after removing the solvents is purified using chromatography: solid phase (SiO2 ; 40 μm; Baker); eluant 2% methanol (CH3OH) in methylene chloride (CH2Cl2). A sample of this purified material (1.2 gm) was transferred into its hydrochloride (mp: 200° C.) by treating an ethanolic suspension of this material with a mixture of ethyl ether/HCl.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05883094
Source datasetuspto-grants-1999_03
ORD IDord-9a87f6a3a8764ef8a645bbcb9442a8c5
Source noteuspto-grants-1999_03