HuagongsheHuagongshe Chemistry Print Report · For research reference only
6-(4-Aminophenyl)-4,5-dihydropyridazin-3(2H)-one → HCID 13193380, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 6-(4-Aminophenyl)-4,5-dihydropyridazin-3(2H)-one | HCID 676750 | — |
| Reactant | 2-Cyanoacetyl chloride | HCID 11051594 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 13193380 | HCID 13193380 | 54.2% |
Reaction Steps
5.9 g (57.0 millimoles) of cyanoacetyl chloride were added dropwise to 6.0 g (31.7 millimoles) of 6-(p-aminophenyl)-4,5-dihydro-3(2H)-pyridazinone in 150 ml of absolute tetrahydrofuran at room temperature, while stirring. After the addition was complete, stirring was continued for a further 10 minutes at 50° C. The product was filtered off under suction at 10° C., washed first with tetrahydrofuran and then with water and recrystallized from dimethylformamide/water. 4.4 g (54%) of 6-[p-(cyanoacetylamino)-phenyl]-4.5,-dihydro-3(2H)-pyridazinone were obtained as pale beige crystals. Mp.: 270° C. (decomposition).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04544562 |
| Source dataset | uspto-grants-1985_10 |
| ORD ID | ord-94ed8b954ebf4babac871bcc0ed0f9f7 |
| Source note | uspto-grants-1985_10 |