Hydrazine → HCID 178424851, compound
Reaction equation
[CH3:1][C:2]1[CH:3]=[C:4]([C:9](=O)[CH2:10][C:11]#[N:12])[CH:5]=[C:6]([CH3:8])[CH:7]=1.[NH2:14][NH2:15]>CCO>[CH3:1][C:2]1[CH:3]=[C:4]([C:9]2[CH:10]=[C:11]([NH2:12])[NH:14][N:15]=2)[CH:5]=[C:6]([CH3:8])[CH:7]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
3-(3,5-Dimethyl-phenyl)-3-oxo-propionitrile (2.0175 gms.) is then suspended in 55 mL of anhydrous EtOH. This suspension is treated with 0.73 mL of anhydrous hydrazine and subsequently heated to refluxing temperature for 1 day. The reaction mixture is concentrated in vacuo. The residue is then triturated with isopropanol to precipitate out the 5-(3,5-dimethyl-phenyl)-2H-pyrazol-3-ylamine as a white solid.
Workup
- temperaturesubsequently heated
- temperatureto refluxing temperature for 1 day
- concentrationThe reaction mixture is concentrated in vacuo
- customThe residue is then triturated with isopropanol
- customto precipitate out the 5-(3,5-dimethyl-phenyl)-2H-pyrazol-3-ylamine as a white solid
Sources & evidence
- ORD record
- ord-d0d150858859474cb939e33b91fd7b93
- Source dataset
- uspto-grants-2006_02
- Patent number
- US07005444B2
Reaction notes
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