Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1901444Generated: November 1, 2026

Sodium Iodide → HCID 23368052, compound

https://huagongshe.com/reaction/1901444

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantPotassium CarbonateHCID 11430—
Reactant1-(2-Pyridyl)piperazineHCID 94459—
ReactantHCID 23368058HCID 23368058—
SolventAcetonitrileHCID 6342—
ProductHCID 23368052HCID 2336805279%

Reaction Steps

227 mg (1 mmol) of 2-(3-chloropropoxy)-5,6,7,8-tetrahydroquinoxaline was dissolved in 10 ml of acetonitrile. To the resultant solution were added 208 mg (1.5 mmol) of potassium carbonate, 196 mg (1.2 mmol) of 1-(2-pyridyl)piperazine and 149 mg (1 mmol) of sodium iodide, and the resultant mixture was heated under reflux for 15 hours. Then, the mixture was subjected to filtration to filter off insoluble substances, which were then washed with acetonitrile, to thereby obtain a filtrate. The solvent of the filtrate was distilled off in vacuo to thereby obtain a residue. The obtained residue was purified by silica gel column chromatography. That is, the residue was charged in a column of 20 g of silica gel (Art7734, manufactured and sold by E. Merck, Darmstadt) and eluted with chloroform-methanol (100:1), to thereby obtain 279 mg of 2-[3-{4-(2-pyridyl)-1-piperazinyl}propoxy]-5,6,7,8-tetrahydroquinoxaline (yield: 79%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05578596
Source datasetuspto-grants-1996_11
ORD IDord-55f230d3c27d400dae09670a891b20e5
Source noteuspto-grants-1996_11