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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2293988Generated: November 1, 2026

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

https://huagongshe.com/reaction/2293988

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 numberUS05688791
Source datasetuspto-grants-1997_11
ORD IDord-067cdc9de95049fcb135b8e79e54e589
Source noteuspto-grants-1997_11