Hydroxyamine hydrochloride → HCID 87971557, compound
Reaction equation
[Br:1][C:2]1[C:7]2[CH:8]([C:18]3[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=3)[O:9][C:10]3[C:15]([C:6]=2[CH:5]=[CH:4][C:3]=1[C:24](=O)[CH3:25])=[C:14]([O:16][CH3:17])[CH:13]=[CH:12][CH:11]=3.Cl.[NH2:28][OH:29]>CCO.N1C=CC=CC=1>[Br:1][C:2]1[C:7]2[CH:8]([C:18]3[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=3)[O:9][C:10]3[C:15]([C:6]=2[CH:5]=[CH:4][C:3]=1[C:24](=[N:28][OH:29])[CH3:25])=[C:14]([O:16][CH3:17])[CH:13]=[CH:12][CH:11]=3Participants
5
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Procedure
A solution of Example 357C (700 mg, 2.03 mmol) and hydroxylamine hydrochloride (2.45 g, 30.4 mmol) in a mixture of EtOH (70 mL) and pyridine (70 mL) was refluxed for 8 hours, cooled and concentrated. The residue was dissolved in EtOAc, washed with water, brine, dried (Na2SO4) and concentrated to provide the desired compound without purifiction.
Workup
- temperaturewas refluxed for 8 hours
- temperaturecooled
- concentrationconcentrated
- dissolutionThe residue was dissolved in EtOAc
- washwashed with water, brine
- dry with materialdried (Na2SO4)
- concentrationconcentrated
Sources & evidence
- ORD record
- ord-061e0552205a42518d24f998ffc066f3
- Source dataset
- uspto-grants-2003_01
- Patent number
- US06506766B1
Reaction notes
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