HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethyl Ether → HCID 178512294, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Aminoethylpiperazine | HCID 8795 | — |
| Reactant | HCID 2761294 | HCID 2761294 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 178512294 | HCID 178512294 | — |
Reaction Steps
S-methyl-N-cyano-N′-pyridylisothiourea (3.84 g, 20 mmol) and 1-(2-aminoethyl)piperazine (2.89 ml, 22 mmol) were suspended in pyridine (8 mL) in a reaction flask equipped with magnetic stirring under nitrogen. Triethylamine (2.8 mL, 20 mmol) was added followed by (4-dimethylamino)-pyridine (cat., 100 mg). The reaction mixture became clear. It was stirred at 50-60° C. for 12 hours and cooled to room temperature. Ether (100 mL) was then added and precipitate formed. The precipitate was collected to give crude N-cyano-N′-(2-piperazin-1-yl-ethyl)-N″-pyridin-4-yl-guanidine which was used without further purification. ESMS 274.2 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06255323B1 |
| Source dataset | uspto-grants-2001_07 |
| ORD ID | ord-e1418b90ec1249b49ba0959bb6a90164 |
| Source note | uspto-grants-2001_07 |