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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Piperazine | HCID 4837 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 3-Chloro-5-fluoro-4-iodopyridine | HCID 11032545 | — |
| Solvent | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Product | 1-(3-Chloro-5-fluoro-4-pyridyl)piperazine | HCID 86720930 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09340546B2 |
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| Source dataset | uspto-grants-2016_05 |
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| ORD ID | ord-0f87d594194e4f8cabd6539a6de738c8 |
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| Source note | uspto-grants-2016_05 |
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