Hydroxyamine hydrochloride → HCID 136166853, compound
Reaction equation
[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]([C:9]2([CH2:15][C:16]([C:18]3[CH:23]=[CH:22][N:21]=[C:20]([CH3:24])[CH:19]=3)=O)[CH2:14][CH2:13][CH2:12][CH2:11][CH2:10]2)=[CH:5][CH:4]=1.Cl.[NH2:26][OH:27].C([O-])(O)=O.[Na+]>>[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]([C:9]2([CH2:15]/[C:16](/[C:18]3[CH:23]=[CH:22][N:21]=[C:20]([CH3:24])[CH:19]=3)=[N:26]\[OH:27])[CH2:14][CH2:13][CH2:12][CH2:11][CH2:10]2)=[CH:5][CH:4]=1Participants
4
Procedure
In analogy to example 151, step 3, 2-[1-(4-methoxy-phenyl)-cyclohexyl]-1-(2-methyl-pyridin-4-yl)-ethanone was reacted with hydroxylamine hydrochloride in the presence of NaHCO3 to give the title compound as a colorless solid, MS (ESI+): m/z=339.3 [M+H]+.
Sources & evidence
- ORD record
- ord-deb50aa12eb44b5a900efaf5671b2ef4
- Source dataset
- uspto-grants-2014_07
- Patent number
- US08765730B2
Reaction notes
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