O-Methylhydroxylamine → HCID 86760137, compound
Reaction equation
[C:1]([C:4]1[CH:31]=[CH:30][C:7]2[N:8]([CH2:12][CH2:13][O:14][C:15]3[CH:29]=[CH:28][C:18]([O:19][C:20]([CH3:27])([CH3:26])[C:21]([O:23][CH2:24][CH3:25])=[O:22])=[CH:17][CH:16]=3)[C:9](=[O:11])[S:10][C:6]=2[CH:5]=1)(=O)[CH3:2].[CH3:32][O:33][NH2:34]>>[CH3:32][O:33][N:34]=[C:1]([C:4]1[CH:31]=[CH:30][C:7]2[N:8]([CH2:12][CH2:13][O:14][C:15]3[CH:29]=[CH:28][C:18]([O:19][C:20]([CH3:27])([CH3:26])[C:21]([O:23][CH2:24][CH3:25])=[O:22])=[CH:17][CH:16]=3)[C:9](=[O:11])[S:10][C:6]=2[CH:5]=1)[CH3:2]Participants
3
Procedure
Starting from the compound obtained in Step A, the procedure is as in Step B of Example 2, replacing the hydroxylamine by O-methylhydroxylamine. The two (Z) and (E) compounds are not separated.
Workup
- customThe two (Z) and (E) compounds are not separated
Sources & evidence
- ORD record
- ord-26fc786b3d5346d4a077959ef5fcb4b9
- Source dataset
- uspto-grants-2006_07
- Patent number
- US07071221B2
Reaction notes
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