Hydrazine → HCID 178434371, compound
Reaction equation
[C:1]([C:4]1[C:5](=[O:14])[N:6]([CH3:13])[N:7]=[CH:8][C:9]=1[N:10](C)C)(=O)[CH3:2].[NH2:15]N>C(O)C>[CH3:2][C:1]1[C:4]2[C:5](=[O:14])[N:6]([CH3:13])[N:7]=[CH:8][C:9]=2[NH:10][N:15]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
4-Acetyl-5-dimethylamino-2-methyl-3(2H)-pyridazinone (137 mg) was added to hydrazine (224 mg)/ethanol (5 ml) and the mixture was refluxed with stirring for 6 hours. After the ethanol-hydrazine was distilled off, the residue was washed with diethyl ether and dried. White powder, 114 g. 1H-NMR (CDCl3) 8: 2.57(3H,s), 3.64(3H,s), 8.30(1H,s).
Workup
- temperaturethe mixture was refluxed
- distillationAfter the ethanol-hydrazine was distilled off
- washthe residue was washed with diethyl ether
- customdried
Sources & evidence
- ORD record
- ord-780ebb2529f14e6dbc87b95d17a7162c
- Source dataset
- uspto-grants-1998_05
- Patent number
- US05753664
Reaction notes
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