Hydroxyamine hydrochloride → HCID 87098080, compound
Reaction equation
[Cl:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[CH:8]([C:20]1[CH:31]=[CH:30][C:23]([C:24]([NH:26][CH:27]2[CH2:29][CH2:28]2)=[O:25])=[C:22]([F:32])[CH:21]=1)[CH2:9][C:10]([C:12]1[CH:17]=[CH:16][C:15](=[O:18])[N:14]([CH3:19])[CH:13]=1)=O.Cl.[NH2:34][OH:35].C([O-])(O)=O.[Na+]>>[Cl:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[CH:8]([C:20]1[CH:31]=[CH:30][C:23]([C:24]([NH:26][CH:27]2[CH2:29][CH2:28]2)=[O:25])=[C:22]([F:32])[CH:21]=1)[CH2:9]/[C:10](=[N:34]\[OH:35])/[C:12]1[CH:17]=[CH:16][C:15](=[O:18])[N:14]([CH3:19])[CH:13]=1Participants
4
Procedure
In analogy to example 151, step 3, 4-(1-(2-chlorophenyl)-3-(1-methyl-6-oxo-1,6-dihydropyridin-3-yl)-3-oxopropyl)-N-cyclopropyl-2-fluorobenzamide was reacted with hydroxylamine hydrochloride in the presence of NaHCO3 to give the title compound containing 4% of the corresponding Z isomer as a colorless waxy solid, MS (ESI+): m/z=468.2 [M+H]+.
Sources & evidence
- ORD record
- ord-435045bf88b040818522997bf7177195
- Source dataset
- uspto-grants-2014_07
- Patent number
- US08765730B2
Reaction notes
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