HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 253055Generated: October 25, 2026
Piperazine → 1-(5-Chloropyridin-2-yl)piperazine
https://huagongshe.com/reaction/253055
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Piperazine | HCID 4837 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2,5-Dichloropyridine | HCID 27685 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1-(5-Chloropyridin-2-yl)piperazine | HCID 3805301 | 10.5% |
Reaction Steps
To a solution of 2,5-dichloropyridine (2 g) in dimethylformamide (30 mL) was added potassium carbonate (3.73 g) and piperazine (1.16 g) and the mixture was stirred at 110° C. for 4 hours. After cooling the reaction mixture, thereto was added ethyl acetate and an aqueous saturated sodium hydrogencarbonate solution and the mixture was extracted with ethyl acetate. The organic layer was washed with water, dried over magnesium sulfate and filtered. The filtrate was concentrated in vacuo and the resultant crude product was purified by column chromatography on NH-silica gel (Chromatorex NH-silica gel, solvent: chloroform/methanol=100/0 to 99/1) to obtain 5-chloro-2-(1-piperazinyl)pyridine (0.28 g, Yield: 10%) as a pale yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07872006B2 |
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| Source dataset | uspto-grants-2011_01 |
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| ORD ID | ord-8a7a5ce49bf646938a9726503156bb7d |
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| Source note | uspto-grants-2011_01 |
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