Ammonia → 4(3H)-Quinazolinone, 3-amino-2-hydrazino-
Reaction equation
Cl[C:2]1[N:11]=[C:10]([OH:12])[C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[N:3]=1.O.[NH2:14][NH2:15].[NH3:16]>O>[NH2:16][N:11]1[C:10](=[O:12])[C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[N:3]=[C:2]1[NH:14][NH2:15]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
A mixture of 134 g of the product of Step B and 670 ml of hydrazine hydrate was refluxed with stirring for about 5 hours until evolution of ammonia ceased and the mixture was cooled slightly and was diluted with 670 ml of water. The mixture was cooled to room temperature and was filtered and the product was rinsed with water and methanol and dried to obtain 101.5 of 3-amino-2-hydrazino-quinazolin-4(3H)-one.
Workup
- temperaturewas refluxed
- temperaturethe mixture was cooled slightly
- filtrationwas filtered
- washthe product was rinsed with water and methanol
- customdried
Sources & evidence
- ORD record
- ord-021658b6ce544c0c8061a5e51f515619
- Source dataset
- uspto-grants-1982_09
- Patent number
- US04350695
Reaction notes
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