HuagongsheHuagongshe Chemistry Print Report · For research reference only
Piperazine → HCID 14459477, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Piperazine | HCID 4837 | — |
| Reactant | 6-(3,4-Difluorophenyl)-4,5-dihydro-5-methyl-3(2H)-pyridazinone | HCID 14459459 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 14459477 | HCID 14459477 | 54.1% |
Reaction Steps
5.0 g (22.3 mmol) of 6-(3,4-difluorophenyl)-4,5-dihydro-5-methyl-3(2H)-pyridazinone and 19.2 g (222 mmol) of piperazine are stirred at 160° C. for 15 hours. When the reaction mixture has cooled down, it is taken up with 200 ml of dichloromethane and washed with 3×30 ml of water. After drying, the organic phase is concentrated by evaporation and the residue is crystallized with methanol. The solid obtained is suction filtered and recrystallized from ethyl acetate. 3.5 g (54%) of colourless crystals, m.p. 172°-174° C., are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04954501 |
| Source dataset | uspto-grants-1990_09 |
| ORD ID | ord-98d6ad96491b45f4b45f99249944ed8f |
| Source note | uspto-grants-1990_09 |