HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 276779Generated: October 30, 2026
Piperazine → 2-(Piperazin-1-yl)pyridine-4-carbonitrile
https://huagongshe.com/reaction/276779
Participants
| Role | Name | HCID | Charge |
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| Reactant | Piperazine | HCID 4837 | — |
| Reactant | 2-Chloro-4-cyanopyridine | HCID 568638 | — |
| Product | 2-(Piperazin-1-yl)pyridine-4-carbonitrile | HCID 16227986 | 28.4% |
Reaction Steps
2-Chloro-isonicotinonitrile (80 g, 0.58 mol) and piperazine (199 g, 2.32 mol, 5 equiv) were combined and heated at 70 DC for 2.5 hours. The resulting suspension was cooled to room temperature and partitioned between a solution of 50% ethyl acetate/dichloromethane and water. The organic phase was separated, and the aqueous phase was extracted with dichloromethane. The combined organic phases were concentrated in vacuo to about half the initial volume and ether was added. The suspension was stirred overnight, then filtered. The solid was dried under vacuum to give the desired product (31 g). The mother liquors were concentrated in vacuo and the residue was triturated with ether and filtered. The solid collected in this second batch was dried under vacuum and combined with the first batch to give the total amount of desired product (46 g, 42%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06355635B1 |
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| Source dataset | uspto-grants-2002_03 |
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| ORD ID | ord-744f8038a3a9425696ce03a32d04e00f |
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| Source note | uspto-grants-2002_03 |
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