HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Aminopyridine → 1-[(2-Pyridyl)thiocarbamoyl]imidazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Aminopyridine | HCID 10439 | — |
| Reactant | 1,1'-Thiocarbonyldiimidazole | HCID 80264 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 1-[(2-Pyridyl)thiocarbamoyl]imidazole | HCID 19704138 | 133.2% |
Reaction Steps
A solution of 1,1'-thiocarbonyldiimidazole (9.9 g, 50 mmol) and 2-aminopyridine (4.75 g, 50 mmol) in acetonitrile (50 mL) was stirred at room temperature for 72 h. The resulting solution was evaporated to a black oil and triturated with hexane. The remaining oily residue was placed under vacuum to provide 13.6 g of crude titled product as a black solid:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05714503 |
| Source dataset | uspto-grants-1998_02 |
| ORD ID | ord-f77799d54c6a4b718c44e9f555ce40c3 |
| Source note | uspto-grants-1998_02 |