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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

Reaction equation

Participants

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

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06355635B1
Source datasetuspto-grants-2002_03
ORD IDord-744f8038a3a9425696ce03a32d04e00f
Source noteuspto-grants-2002_03