HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → HCID 178485028, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Ici 109,081 | HCID 161928 | — |
| Reactant | HCID 12295279 | HCID 12295279 | — |
| Product | HCID 178485028 | HCID 178485028 | — |
Reaction Steps
To a solution of N-cyano-N1 -methyl-O-phenylisourea (0.175 g) in anhydrous pyridine (3 ml) was added 6-(4-aminophenyl)-5-methyl-4,5-dihydro-3(2H)-pyridazinone (0.2 g). The mixture was stirred at room temperature for 3 hours, stirred under reflux for 4 hours and allowed to cool overnight. This mixture was evaporated under reduced pressure to give a solid which was triturated with diethyl ether to remove phenol. Thin layer chromatography indicated the presence of unreacted starting-material and the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04654342 |
| Source dataset | uspto-grants-1987_03 |
| ORD ID | ord-4890a8b411b3493abd3b50f131b6a305 |
| Source note | uspto-grants-1987_03 |