HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrazine hydrate (1:1) → 6-(p-Chloroacetylaminophenyl)-4,5-dihydropyridaz-3-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrazine hydrate (1:1) | HCID 24654 | — |
| Reactant | beta-(p-Chloroacetylaminobenzoyl)-propionic acid | HCID 20507196 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 6-(p-Chloroacetylaminophenyl)-4,5-dihydropyridaz-3-one | HCID 677107 | 84% |
Reaction Steps
4.0 g (14.8 millimoles) of β-(p-chloroacetylaminobenzoyl)-propionic acid are refluxed with 0.74 g (14.8 millimoles) of hydrazine hydrate and 70 ml of ethanol for 3 hours. After filtering off the product at 10° C. and drying it under reduced pressure at 50° C., 3.3 g (84% of theory) of 6-(p-chloroacetylaminophenyl)-4,5-dihydropyridaz-3-one are obtained as pale yellow crystals (identical with the compound from Example 1, according to its melting point and infrared and NMR spectra).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04376771 |
| Source dataset | uspto-grants-1983_03 |
| ORD ID | ord-e56cdb0533a047cd903e84995ef620f6 |
| Source note | uspto-grants-1983_03 |