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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1813885Generated: November 3, 2026

Piperazine → 1-[(N,N'-Di-p-tolyl)amidino]piperizine

https://huagongshe.com/reaction/1813885

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperazineHCID 4837—
ReactantDi-p-tolylcarbodiimideHCID 69763—
SolventDimethylformamideHCID 6228—
Product1-[(N,N'-Di-p-tolyl)amidino]piperizineHCID 994855852%

Reaction Steps

1.2 mmol of piperazine was dissolved in 10 ml of DMF and 1.0 mmol of 1,3-di-p-tolylcarbodiimide was added. After 0.5 hour of stirring at room temperature, a small precipitation was filtered off, and washed twice with 1 ml of DMF. The filtrates were collected and kept at room temperature overnight. 50 ml of water was added to the solution. A precipitated oil was separated by centrifugation. The residual oil was dissolved in 10 ml of methanol and 0.2 ml of conc. HCl was added. The methanol solution was concentrated to 2 ml and purified by gel filtration on Sephadex LH-20 in methanol. Yield=52%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06875759B1
Source datasetuspto-grants-2005_04
ORD IDord-9d15c87cd55d4ee990477063cb17f854
Source noteuspto-grants-2005_04