HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Methylmorpholine → N-[2-(Dimethylamino)-3-pyridyl]-N"-cyano-N'-(1-phenylcyclobutyl)guanidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Methylmorpholine | HCID 7972 | — |
| Reactant | 1-Phenylcyclobutylamine | HCID 152214 | — |
| Reactant | N'-Cyano-N-(2-dimethylamino-3-pyridyl)-O-phenylisourea | HCID 178483039 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | N-[2-(Dimethylamino)-3-pyridyl]-N"-cyano-N'-(1-phenylcyclobutyl)guanidine | HCID 178483038 | 44.2% |
Reaction Steps
A stirred mixture of the product from Step 1 (3.23 g, 0.0115 mol), 1-phenylcyclobutylamine (1.73 g, 0.0126 mol) (A. Kalir and Z. Pelah, Israel J. Chem. 5:223 (1967)), N-methylmorpholine (2.74 ml, 0.0249 mol) and dioxane (40 ml) was refluxed, under nitrogen for 18 hours and concentrated in vacuo. The residue was mixed with EtOAc and concentrated to give a solid which was recrystallized from EtOAc-hexane to give 1.7 g, mp 204°-205° C. of the titled product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05668157 |
| Source dataset | uspto-grants-1997_09 |
| ORD ID | ord-1f76135a2898439a9a2c7271201578d9 |
| Source note | uspto-grants-1997_09 |