Hydroxyamine hydrochloride → HCID 58043163, compound
Reaction equation
[C:1]1([CH:7]([C:19]2[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=2)[CH2:8][C:9]([C:11]2[CH:12]=[CH:13][C:14](=[O:18])[N:15]([CH3:17])[CH:16]=2)=O)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.Cl.[NH2:26][OH:27].C([O-])(O)=O.[Na+]>>[OH:27]/[N:26]=[C:9](/[C:11]1[CH:12]=[CH:13][C:14](=[O:18])[N:15]([CH3:17])[CH:16]=1)\[CH2:8][CH:7]([C:19]1[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=1)[C:1]1[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1Participants
4
Procedure
In analogy to example 151, step 3, 5-(3,3-diphenyl-propionyl)-1-methyl-1H-pyridin-2-one was reacted with hydroxylamine hydrochloride in the presence of NaHCO3 to give the title compound containing less than 10% of the corresponding Z isomer as a colorless solid, MS (ESI+): m/z=333.3 [M+H]+.
Sources & evidence
- ORD record
- ord-a413b5b2f7444cf497a133b9f276a773
- Source dataset
- uspto-grants-2014_07
- Patent number
- US08765730B2
Reaction notes
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