HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrazinecarboxaldehyde → 6-Phenyl[1,2,4]triazolo[4,3-b]pyridazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrazinecarboxaldehyde | HCID 12229 | — |
| Reactant | 3-Chloro-6-phenylpyridazine | HCID 88515 | — |
| Solvent | 1-Butanol | HCID 263 | — |
| Product | 6-Phenyl[1,2,4]triazolo[4,3-b]pyridazine | HCID 12726813 | — |
Reaction Steps
A 10 g. portion of 3-chloro-6-phenylpyridazine (Chem. Abs., 44, 5616i), 6.6 g. of formylhydrazine and 100 ml. of n-butanol are refluxed for 48 hours. The reaction mixture is cooled in an ice bath. The resulting solid is filtered, washed with petroleum ether and water and air dried giving 6-phenyl-1,2,4-triazolo[4,3-b]pyridazine as tan crystals, m.p. 138°-139° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04230705 |
| Source dataset | uspto-grants-1980_10 |
| ORD ID | ord-56247874ef1f48d3821bfb9fed27d10a |
| Source note | uspto-grants-1980_10 |