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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 440243Generated: October 29, 2026

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

https://huagongshe.com/reaction/440243

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, and 13.3 g (0.153 mole) of piperazine, 8.4 g (0.061 mole) of potassium carbonate and a catalytic amount of potassium iodide were added thereto. The mixture was refluxed by heating for 5 hours. 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 (the eluent used was a mixture of chloroform: methanol : 28% aqueous ammonia = 40 : 9 : 1) to obtain 3.62 g of 1-(2-thiazolyl)piperazine as colorless liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05519016
Source datasetuspto-grants-1996_05
ORD IDord-a2e35d4bbafe4ea5a1558451a6aebd19
Source noteuspto-grants-1996_05