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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2050682Generated: October 30, 2026

Potassium Iodide → HCID 19837167, compound

https://huagongshe.com/reaction/2050682

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantSodium CarbonateHCID 10340—
Reactant1-(2-Pyridyl)piperazineHCID 94459—
ReactantHCID 54368735HCID 54368735—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 19837167HCID 19837167—

Reaction Steps

0.2 g of 3',4',5'-trimethoxy-3-(2-bromoethylamino-carbonyl) flavone were dissolved in 10 ml dichloromethane, and the solution was reacted with a spatula tip full of potassium iodide and 0.5 ml 1-(2-pyridyl)-piperazine. The reaction mixture was heated at reflux temperature for one hour. After cooling, the reaction mixture was worked up by adding further dichloromethane and shaking with saturated sodium carbonate solution and water. Then the organic phase was dried over sodium sulfate, concentrated, and the residue was purified by column chromatography on silica gel under slightly elevated pressure (flash chromatography) using tetrahydrofuran/ethylacetate 1:1 as the eluent. In this way 3',4',5'-trimethoxy-3-{2-[4-(2-pyridyl)-piperazin-1-yl]-ethylamino-carbonyl) flavone was obtained in pure amorphous form.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05013852
Source datasetuspto-grants-1991_05
ORD IDord-cf6d6098519949f2873081360d2e1c93
Source noteuspto-grants-1991_05