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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1534358Generated: November 4, 2026

Potassium Iodide → 1-(3-Pyridinyl)-4-[4-(2-pyridinyl)-1-piperazinyl]-1-butanone

https://huagongshe.com/reaction/1534358

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
Reactant1-(2-Pyridyl)piperazineHCID 94459—
Reactant4-Chloro-1-(pyridin-3-YL)butan-1-oneHCID 12471005—
SolventChloroformHCID 6212—
Product1-(3-Pyridinyl)-4-[4-(2-pyridinyl)-1-piperazinyl]-1-butanoneHCID 1990965044.1%

Reaction Steps

A solution of 4-chloro-1-(3-pyridinyl)-1-butanone (Example B) (9 g, 0.049 mol), 1-(2-pyridinyl)piperazine (24 g, 0.147 mol), and potassium iodide (0.8 g, 0.005 mol) is heated to 120° C. for 5 minutes. The residue is taken up in chloroform (40 mL) and the precipitate is filtered. The filtrate is evaporated in vacuo and purified by column chromatography (silica gel, 2% methanol/dichloromethane). The major product is crystallized from 2-propanol/diethyl ether to give 6.7 g 1-(3-pyridinyl)-4-[4-(2-pyridinyl)-1-piperazinyl]-1-butanone as a white solid; mp 89° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05089497
Source datasetuspto-grants-1992_02
ORD IDord-71340c46f9db4fc39852afb8f05d68a4
Source noteuspto-grants-1992_02