HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetohydrazide → HCID 23467590, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetohydrazide | HCID 14039 | — |
| Reactant | 3-Chloro-6-(2-furanyl)pyridazine | HCID 23467580 | — |
| Reactant | HCID 54470727 | HCID 54470727 | — |
| Solvent | 1-Butanol | HCID 263 | — |
| Product | HCID 23467590 | HCID 23467590 | — |
Reaction Steps
As for Example 5, 4,5-dihydro-6-(2-furyl)-3(2H)-pyridazinone is converted to 3-chloro-6-(2-furyl)pyridazine. A 1.5 g. sample of the preceding compound, 1.2 g. of acethydrazide in 50 ml. of n-butyl alcohol is refluxed for 48 hours. The solvent is removed under reduced pressure and the residue is partitioned between dichloromethane and dilute sodium hydroxide. The dichloromethane layer is washed with water, dried over magnesium sulfate, filtered and concentrated. The residue is purified by conventional means to give the product of the Example.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04260756 |
| Source dataset | uspto-grants-1981_04 |
| ORD ID | ord-9a4accac960040f7bcdc01000eb6a2ad |
| Source note | uspto-grants-1981_04 |