Hydroxyamine hydrochloride → HCID 136166898, compound
Reaction equation
[CH3:1][N:2]([CH3:29])[C:3](=[O:28])[C:4]1[CH:9]=[CH:8][C:7]([C@H:10]([C:21]2[CH:26]=[CH:25][CH:24]=[CH:23][C:22]=2[CH3:27])[CH2:11][C:12]([C:14]2[CH:19]=[CH:18][N:17]=[C:16]([CH3:20])[CH:15]=2)=O)=[CH:6][CH:5]=1.Cl.[NH2:31][OH:32].C(=O)([O-])O.[Na+]>>[OH:32]/[N:31]=[C:12](/[C:14]1[CH:19]=[CH:18][N:17]=[C:16]([CH3:20])[CH:15]=1)\[CH2:11][C@H:10]([C:7]1[CH:8]=[CH:9][C:4]([C:3]([N:2]([CH3:29])[CH3:1])=[O:28])=[CH:5][CH:6]=1)[C:21]1[CH:26]=[CH:25][CH:24]=[CH:23][C:22]=1[CH3:27]Participants
4
Procedure
In analogy to example 132, step 6, from N,N-dimethyl-4-[(R)-3-(2-methyl-pyridin-4-yl)-3-oxo-1-o-tolyl-propyl]-benzamide and hydroxylamine hydrochloride in the presence of sodium hydrogencarbonate was prepared the title compound as a white foam, MS (ESI+): m/z=402.4 ([M+H]+).
Sources & evidence
- ORD record
- ord-7489a51d84104e41a628f77957120622
- Source dataset
- uspto-grants-2014_07
- Patent number
- US08765730B2
Reaction notes
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