Acetic Acid → HCID 22449479, compound
Reaction equation
[C:1]([NH:4][C:5]1[CH:6]=[CH:7][C:8](Cl)=[C:9]2[C:14]=1[C:13](=O)[C:12](=CO)[CH2:11][CH2:10]2)(=[O:3])[CH3:2].[C:19](O)(=O)C.[ClH:23].[NH2:24][OH:25]>O>[C:1]([NH:4][C:5]1[CH:6]=[CH:7][C:8]([Cl:23])=[C:9]2[C:14]=1[C:13]1[CH:19]=[N:24][O:25][C:12]=1[CH2:11][CH2:10]2)(=[O:3])[CH3:2]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 120 °C
Procedure
1.29 gm of the compound prepared in (1) above was dissolved into 30 ml of acetic acid. After the addition of 339 mg of hydroxylamine hydrochloride, the mixture was heated for 10 minutes at 120° C. while stirring. After cooling, water was added to collect the precipitate by filtration. The precipitate was washed with water and hexane to obtain 1.1 gm of the title compound.
Workup
- temperatureAfter cooling
- customto collect the precipitate
- filtrationby filtration
- washThe precipitate was washed with water and hexane
Sources & evidence
- ORD record
- ord-a11f1dec819b44eab958c3208cca683d
- Source dataset
- uspto-grants-1997_08
- Patent number
- US05658920
Reaction notes
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