Carbonyl cyanide phenylhydrazone → 1-methyl-4-phenylazo-1H-pyrazole-3,5-diamine
Reaction equation
[C:1]1([NH:7][N:8]=[C:9]([C:12]#[N:13])[C:10]#[N:11])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.S(O)(O)(=O)=O.[CH3:19][NH:20][NH2:21]>>[CH3:19][N:20]1[C:10]([NH2:11])=[C:9]([N:8]=[N:7][C:1]2[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=2)[C:12]([NH2:13])=[N:21]1Participants
3
Procedure
1-methyl-4-phenylazo-1H-pyrazole-3,5-diamine was prepared using 2-phenylhydrazonomalononitrile (425 mg) and methylhydrazine sulfate (720 mg). The compound was purified by column chromatography and afforded a yellow solid.
Workup
- customThe compound was purified by column chromatography
- customafforded a yellow solid
Sources & evidence
- ORD record
- ord-ef677bfe0df44b71a88d0a702ce1a17f
- Source dataset
- uspto-grants-2011_01
- Patent number
- US07875728B2
Reaction notes
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