O-Benzylhydroxylamine → 5-(5-Ethyl-2-methyl-6-oxo-1,6-dihydro-pyridin-3-yl)-furan-2-carbaldehyde-O-benzyl-oxime
Reaction equation
[CH2:1]([C:3]1[C:8](=[O:9])[NH:7][C:6]([CH3:10])=[C:5]([C:11]2[O:15][C:14]([CH:16]=O)=[CH:13][CH:12]=2)[CH:4]=1)[CH3:2].[CH2:18]([O:25][NH2:26])[C:19]1[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=1>>[CH2:18]([O:25][N:26]=[CH:16][C:14]1[O:15][C:11]([C:5]2[CH:4]=[C:3]([CH2:1][CH3:2])[C:8](=[O:9])[NH:7][C:6]=2[CH3:10])=[CH:12][CH:13]=1)[C:19]1[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=1Participants
3
Procedure
Example 198 is substantially repeated except for utilizing 5-(5-ethyl-2-methyl-6-oxo-1,6-dihydropyridin-3-yl]furan-2-carbaldehyde and benzyloxyamine to afford the title compound. MS: m/e=337 (M+H).
Sources & evidence
- ORD record
- ord-0d2a1dfea5b440c28e150e7a2e70805e
- Source dataset
- uspto-grants-2012_05
- Patent number
- US08173682B2
Reaction notes
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