HuagongsheHuagongshe Chemistry Print Report · For research reference only
Piperazine → 1-[(N,N'-Di-p-tolyl)amidino]piperizine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Piperazine | HCID 4837 | — |
| Reactant | Di-p-tolylcarbodiimide | HCID 69763 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1-[(N,N'-Di-p-tolyl)amidino]piperizine | HCID 9948558 | 52% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06875759B1 |
| Source dataset | uspto-grants-2005_04 |
| ORD ID | ord-9d15c87cd55d4ee990477063cb17f854 |
| Source note | uspto-grants-2005_04 |