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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1813884Generated: November 4, 2026

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

https://huagongshe.com/reaction/1813884

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-MethylpiperazineHCID 53167—
ReactantDi-p-tolylcarbodiimideHCID 69763—
SolventDimethylformamideHCID 6228—
Product1-[(N,N'-Di-p-tolyl)amidino]-4-methyl-piperizineHCID 988364278%

Reaction Steps

1.05 mmol of 1-methylpiperazine was dissolved in 10 ml of N,N′-dimethylformamide (DMF), and 1.0 mmol of 1,3-di-p-tolylcarbodiimide was added. After 0.5 h. of stirring at room temperature, a small precipitation was removed by filtration 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. An oil precipitated after 0.5 h which transformed into a solid. The solid residue was collected by filtration, washed twice with water and dissolved in 20 ml of methanol. 0.2 ml of conc. HCl was added was added to the methanol solution. After evaporation of the methanol, the residue was redissolved in methanol, and pure product was precipitated from the solution with ethyl ether. Yield=78%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06875759B1
Source datasetuspto-grants-2005_04
ORD IDord-9d916d402986456aaad4ee4eb054c539
Source noteuspto-grants-2005_04