Hydroxyamine hydrochloride → HCID 58043373, compound
Reaction equation
[Br:1][C:2]1[CH:7]=[CH:6][C:5]([CH:8]([CH2:20][CH2:21][CH3:22])[CH2:9][C:10]([C:12]2[CH:13]=[CH:14][C:15](=[O:19])[N:16]([CH3:18])[CH:17]=2)=O)=[C:4]([F:23])[CH:3]=1.Cl.[NH2:25][OH:26].C([O-])(O)=O.[Na+]>>[Br:1][C:2]1[CH:7]=[CH:6][C:5]([CH:8]([CH2:20][CH2:21][CH3:22])[CH2:9]/[C:10](/[C:12]2[CH:13]=[CH:14][C:15](=[O:19])[N:16]([CH3:18])[CH:17]=2)=[N:25]\[OH:26])=[C:4]([F:23])[CH:3]=1Participants
4
Procedure
In analogy to example 151, step 3, 5-[3-(4-bromo-2-fluoro-phenyl)-hexanoyl]-1-methyl-1H-pyridin-2-one was reacted with hydroxylamine hydrochloride in the presence of NaHCO3 to give the title compound as a colorless solid, MS (ESI+): m/z=395.1 [M+H]+.
Sources & evidence
- ORD record
- ord-f32238edccd34f0cb10f97f3e5e1e480
- Source dataset
- uspto-grants-2014_07
- Patent number
- US08765730B2
Reaction notes
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