O-Methylhydroxylamine → HCID 86760129, compound
Reaction equation
[C:1]([C:9]1[CH:42]=[CH:41][C:12]2[N:13]([CH2:17][CH2:18][O:19][C:20]3[CH:25]=[CH:24][C:23]([CH2:26][CH:27]([N:32]([C:34]([O:36][C:37]([CH3:40])([CH3:39])[CH3:38])=[O:35])[CH3:33])[C:28]([O:30][CH3:31])=[O:29])=[CH:22][CH:21]=3)[C:14](=[O:16])[S:15][C:11]=2[CH:10]=1)(=O)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[CH3:43][O:44][NH2:45]>>[C:37]([O:36][C:34]([N:32]([CH3:33])[CH:27]([CH2:26][C:23]1[CH:22]=[CH:21][C:20]([O:19][CH2:18][CH2:17][N:13]2[C:12]3[CH:41]=[CH:42][C:9]([C:1](=[N:45][O:44][CH3:43])[C:2]4[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=4)=[CH:10][C:11]=3[S:15][C:14]2=[O:16])=[CH:25][CH:24]=1)[C:28]([O:30][CH3:31])=[O:29])=[O:35])([CH3:40])([CH3:38])[CH3:39]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.
Sources & evidence
- ORD record
- ord-708b24f2e5e34bcf94303c04d4f13d44
- Source dataset
- uspto-grants-2006_07
- Patent number
- US07071221B2
Reaction notes
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