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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 524873Generated: October 30, 2026

Piperazine → 1-(3-Chloro-5-fluoro-4-pyridyl)piperazine

https://huagongshe.com/reaction/524873

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperazineHCID 4837—
ReactantDiisopropylethylamineHCID 81531—
Reactant3-Chloro-5-fluoro-4-iodopyridineHCID 11032545—
SolventN-methyl-2-pyrrolidoneHCID 13387—
Product1-(3-Chloro-5-fluoro-4-pyridyl)piperazineHCID 86720930—

Reaction Conditions

Temperature120 °C

Reaction Steps

In a 100 mL sealed reaction vessel/bomb, 3-chloro-5-fluoro-4-iodo-pyridine (5600 mg, 21.75 mmol) was taken up in NMP (12 mL). To the resulting clear brown solution was added DIPEA (3.373 g, 4.546 mL, 26.10 mmol) followed by piperazine (2.810 g, 32.62 mmol). The vessel was sealed and heated thermally at 120° C. for 18 hrs. The mixture was allowed to cool to RT and was concentrated in vacuo to afford a brown gum which was purified by chromatography on silica, eluting with a gradient of DCM-DCM:MeOH:NH3(90: 10:1) 100-0 to 0:100. Fractions containing clean product were collected and concentrated in vacuo to afford 1-(3-chloro-5-fluoropyridin-4-yl)piperazine as a cream solid. (3.52 g, 75%). MS (ES+) 216.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09340546B2
Source datasetuspto-grants-2016_05
ORD IDord-0f87d594194e4f8cabd6539a6de738c8
Source noteuspto-grants-2016_05