HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
2-Cyano-4-methylpyridine → 2-(2-Furoyl)-4-methylpyridine
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | 2-Cyano-4-methylpyridine | HCID 88739 | — |
| Edukt | HCID 178506914 | HCID 178506914 | — |
| Produkt | 2-(2-Furoyl)-4-methylpyridine | HCID 20387572 | — |
Reaktionsschritte
2-Cyano-4-methylpyridine is reacted in an inert atmosphere with an ethereal solution of freshly prepared 2-furoyl-lithium followed by acid hydrolysis to form 2-(2-furoyl)-4-methylpyridine which is then reacted with methyl iodide to form 2-(2-furoyl)-1,4-dimethylpyridinium iodide. Both furoyl compounds exhibit thermal and chemical analgesic properties.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US04173705 |
| Quelldatensatz | uspto-grants-1979_11 |
| ORD ID | ord-6290a975a1e948968b6cee8acafe0858 |
| Quellennotiz | uspto-grants-1979_11 |