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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1179426Generated: November 4, 2026

Piperazine → 1-(3-Chloropyridin-2-yl)piperazine

https://huagongshe.com/reaction/1179426

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperazineHCID 4837—
ReactantTriethylamineHCID 8471—
Reactant2,3-DichloropyridineHCID 16988—
SolventDimethyl SulfoxideHCID 679—
Product1-(3-Chloropyridin-2-yl)piperazineHCID 11412944—

Reaction Conditions

Temperature80 °C

Reaction Steps

2,3-Dichloropyridine (15.0 g, 101.6 mmol), piperazine(9.78 g, 113.70 mmol), and triethylamine (14.36 g, 141.95 mmol) were dissolved in 300 mL of DMSO and the resulting mixture was heated at about 80° C. for about 24 h. The reaction mixture was then cooled to room temperature and extracted with a saturated aqueous sodium bicarbonate solution. The organic layer was dried, concentrated, and purified using a silica gel column eluted with a gradient elution from ethyl acetate to 2:1 ethyl acetate:methanol to provide N-(3-chloropyridin-2-yl)-piperazine (compound 1) as a yellow liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07279493B2
Source datasetuspto-grants-2007_10
ORD IDord-bde381ca299a47819fd5623d1756365a
Source noteuspto-grants-2007_10