Hydroxyamine hydrochloride → HCID 58043463, compound
Reaction equation
[CH3:1][N:2]([CH2:30][C:31]([OH:33])=[O:32])[C:3](=[O:29])[C:4]1[CH:9]=[CH:8][C:7]([CH:10]([C:22]2[CH:27]=[CH:26][CH:25]=[CH:24][C:23]=2[CH3:28])[CH2:11][C:12]([C:14]2[CH:19]=[CH:18][C:17](=[O:20])[N:16]([CH3:21])[CH:15]=2)=O)=[CH:6][CH:5]=1.Cl.[NH2:35][OH:36].C([O-])(O)=O.[Na+]>>[OH:36]/[N:35]=[C:12](/[C:14]1[CH:19]=[CH:18][C:17](=[O:20])[N:16]([CH3:21])[CH:15]=1)\[CH2:11][CH:10]([C:7]1[CH:8]=[CH:9][C:4]([C:3]([N:2]([CH2:30][C:31]([OH:33])=[O:32])[CH3:1])=[O:29])=[CH:5][CH:6]=1)[C:22]1[CH:27]=[CH:26][CH:25]=[CH:24][C:23]=1[CH3:28]Participants
4
Procedure
In analogy to example 151, step 3, (methyl-{4-[3-(1-methyl-6-oxo-1,6-dihydro-pyridin-3-yl)-3-oxo-1-o-tolyl-propyl]-benzoyl}-amino)-acetic acid was reacted with hydroxylamine hydrochloride in the presence of NaHCO3 to give the title compound as a colorless solid, MS (ESI−): m/z=460.3 [M−H]−.
Sources & evidence
- ORD record
- ord-59f03d20e3604472886a10c7ad4eb804
- Source dataset
- uspto-grants-2014_07
- Patent number
- US08765730B2
Reaction notes
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