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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1813886Generated: November 3, 2026

Piperazine → 1,4-Di-[(N,N'-di-p-tolyl)amidino]piperizine

https://huagongshe.com/reaction/1813886

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperazineHCID 4837—
ReactantDi-p-tolylcarbodiimideHCID 69763—
SolventDimethylformamideHCID 6228—
Product1,4-Di-[(N,N'-di-p-tolyl)amidino]piperizineHCID 982843576%

Reaction Steps

0.5 mmol of piperazine was dissolved in 10 ml of DMF and 1.05 mmol of 1,3 di-p-tolylcarbodiimide was added. After 0.5 h. 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. To the DMF solution, 50 ml of water was added. The precipitated solid was filtered and washed with water. The solid was dissolved in ethyl acetate (20 ml) and 0.2 ml of conc. HCl conc. was added. The product began to precipitate within 15 min. After 1 hour, the precipitate was filtered and washed with ethyl ether. Yield=76%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06875759B1
Source datasetuspto-grants-2005_04
ORD IDord-043855a5a4ea4824a411c7c077dd6982
Source noteuspto-grants-2005_04