HuagongsheHuagongshe Chemistry Print Report · For research reference only
4D-083 → HCID 14450229, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4D-083 | HCID 1475328 | — |
| Solvent | Acetic Anhydride | HCID 7918 | — |
| Product | HCID 14450229 | HCID 14450229 | — |
Reaction Steps
A mixture of 2,3-dihydro-3-oxo-6-phenyl-4-pyridazinecarboxamide (4.2 g) in 100 ml of acetic anhydride is heated under reflux for 6 hours. The acetic anhydride is removed by distillation and the residue is partitioned between ammonium hydroxide solution and dichloromethane. The dichloromethane layer is separated and concentrated on the rotary evaporator and the residue is recrystallized from ethanol to give 2,3-dihydro-3-oxo-6-phenyl-4-pyridazinecarbonitrile.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04404203 |
| Source dataset | uspto-grants-1983_09 |
| ORD ID | ord-7a7fc8ba17e14d108d5fe0783659d6cf |
| Source note | uspto-grants-1983_09 |