HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetohydrazide → HCID 20310364, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetohydrazide | HCID 14039 | — |
| Reactant | HCID 20310394 | HCID 20310394 | — |
| Solvent | 1-Butanol | HCID 263 | — |
| Product | HCID 20310364 | HCID 20310364 | — |
Reaction Steps
As described in Example 35, 2-chloro-5-methylbenzaldehyde is reacted with morpholine and potassium cyanide to give γ-(2-chloro-5-methylphenyl)-4-morpholineacetonitrile. In a similar manner as described in Example 35, the preceding compound is converted to 3-chloro-6-(2-chloro-5-methylphenyl)pyridazine which is reacted with acetic acid hydrazide in refluxing n-butanol for 24 hours to give the product of the example.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04112095 |
| Source dataset | uspto-grants-1978_09 |
| ORD ID | ord-066dc6e9ed6245cfa7edc8abeb531c5b |
| Source note | uspto-grants-1978_09 |