Hydroxyamine hydrochloride → HCID 136167010, compound
Reaction equation
[O:1]=[S:2]1(=[O:32])[CH2:7][CH2:6][N:5]([C:8]2[CH:13]=[CH:12][C:11]([C@H:14]([C:25]3[CH:30]=[CH:29][CH:28]=[CH:27][C:26]=3[CH3:31])[CH2:15][C:16]([C:18]3[CH:23]=[CH:22][N:21]=[C:20]([CH3:24])[CH:19]=3)=O)=[CH:10][CH:9]=2)[CH2:4][CH2:3]1.Cl.[NH2:34][OH:35].C([O-])(O)=O.[Na+]>>[O:1]=[S:2]1(=[O:32])[CH2:7][CH2:6][N:5]([C:8]2[CH:13]=[CH:12][C:11]([C@H:14]([C:25]3[CH:30]=[CH:29][CH:28]=[CH:27][C:26]=3[CH3:31])[CH2:15]/[C:16](/[C:18]3[CH:23]=[CH:22][N:21]=[C:20]([CH3:24])[CH:19]=3)=[N:34]\[OH:35])=[CH:10][CH:9]=2)[CH2:4][CH2:3]1Participants
4
Procedure
In analogy to example 132, step 6, from (R)-3-[4-(1,1-dioxo-1lambda6-thiomorpholin-4-yl)-phenyl]-1-(2-methyl-pyridin-4-yl)-3-o-tolyl-propan-1-one and hydroxylamine hydrochloride in the presence of NaHCO3 was prepared the title compound as a light yellow foam, MS (ESI+): m/z=464.2 ([M+H]+).
Sources & evidence
- ORD record
- ord-e88c8449806c42cb8898c29bde1988e9
- Source dataset
- uspto-grants-2014_07
- Patent number
- US08765730B2
Reaction notes
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