Hydroxyamine hydrochloride → HCID 136167038, compound
Reaction equation
[Br:1][C:2]1[CH:3]=[C:4]([CH:8]([C:18]2[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=2)[CH2:9][C:10]([C:12]2[CH:17]=[CH:16][N:15]=[CH:14][CH:13]=2)=O)[CH:5]=[CH:6][CH:7]=1.Cl.[NH2:25][OH:26].C([O-])(O)=O.[Na+]>>[Br:1][C:2]1[CH:3]=[C:4]([CH:8]([C:18]2[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=2)[CH2:9]/[C:10](/[C:12]2[CH:17]=[CH:16][N:15]=[CH:14][CH:13]=2)=[N:25]\[OH:26])[CH:5]=[CH:6][CH:7]=1Participants
4
Procedure
In analogy to example 1, step 2, from 3-(3-bromo-phenyl)-3-phenyl-1-pyridin-4-yl-propan-1-one and hydroxylamine hydrochloride in the presence of NaHCO3 was prepared the title compound as a colorless oil, MS (ESI+): m/z=381.0 ([M+H]+, 1Br).
Sources & evidence
- ORD record
- ord-5cdfee02babf464e8d6041e0a2611b50
- Source dataset
- uspto-grants-2014_07
- Patent number
- US08765730B2
Reaction notes
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