Hydrazine → HCID 85560040, compound
Reaction equation
[CH3:1][C:2]1[NH:6][C:5]([C:7]2[C:16]3[C:11](=[CH:12][CH:13]=[CH:14][CH:15]=3)[CH:10]=[CH:9][CH:8]=2)=[N:4][C:3]=1[C:17]([O:19]CC)=O.[NH2:22][NH2:23]>>[CH3:1][C:2]1[NH:6][C:5]([C:7]2[C:16]3[C:11](=[CH:12][CH:13]=[CH:14][CH:15]=3)[CH:10]=[CH:9][CH:8]=2)=[N:4][C:3]=1[C:17]([NH:22][NH2:23])=[O:19]Participants
3
Procedure
A mixture of 5.0 g of the above ester and 25 ml of hydrazine was refluxed overnight and then cooled. The solid was collected, stirred with water and cooled. The solid was collected, giving 4.5 g of 5-methyl-2-(1-naphthalenyl)-1H-imidazole-4-carboxylic acid, hydrazide.
Workup
- temperaturewas refluxed overnight
- temperaturecooled
- customThe solid was collected
- temperaturecooled
- customThe solid was collected
Sources & evidence
- ORD record
- ord-3ce6cf2706674dffa22d3ae111bf8bf4
- Source dataset
- uspto-grants-1988_05
- Patent number
- US04743586
Reaction notes
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