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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1636283Generated: November 1, 2026

Piperazine → 1-(Thiazol-2-yl)piperazine

https://huagongshe.com/reaction/1636283

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperazineHCID 4837—
ReactantPotassium IodideHCID 4875—
ReactantPotassium CarbonateHCID 11430—
Reactant2-BromothiazoleHCID 76430—
SolventAcetonitrileHCID 6342—
ProductAmmoniaHCID 22228%
Product1-(Thiazol-2-yl)piperazineHCID 911806140.3%

Reaction Steps

In 50 ml of acetonitrile was dissolved 5.0 g (0.0305 mole) of 2-bromothiazole, then, 13.1 g (0.153 mole) of piperazine, 8.4 g (0.061 mole) of potassium carbonate and a catalytic amount of potassium iodide were added to the solution, and the mixture was refluxed under heating for 5 hours. After the mixture was cooled to room temperature and then filtered, the filtrate was concentrated under reduced pressure, and the residue was applied to silica gel column chromatography (eluent; a chloroform:methanol:28% aqueous ammonia=40:9:1 mixed solution) to obtain 3.62 g of 1-(2-thiazolyl)piperazine as a colorless liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06034086
Source datasetuspto-grants-2000_03
ORD IDord-5e6d32a15822492298e05cb8783b4137
Source noteuspto-grants-2000_03