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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1057312Generated: November 4, 2026

Piperazine → 2-(Piperazin-1-yl)pyridine-4-carbonitrile

https://huagongshe.com/reaction/1057312

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperazineHCID 4837—
Reactant2-Chloro-4-cyanopyridineHCID 568638—
Product2-(Piperazin-1-yl)pyridine-4-carbonitrileHCID 1622798628.4%

Reaction Conditions

Temperature70 °C

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° C. 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%). MS m/z 189 (M++1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06514966B2
Source datasetuspto-grants-2003_02
ORD IDord-9935f3d211f748f6845b79aebbe17961
Source noteuspto-grants-2003_02