O-Methylhydroxylamine → HCID 85418942, compound
Reaction equation
[Cl:1][C:2]1[CH:3]=[C:4]([CH:35]=[CH:36][CH:37]=1)[C:5]([C:7]1[CH:34]=[CH:33][C:10]2[N:11]([CH2:15][CH2:16][O:17][C:18]3[CH:23]=[CH:22][C:21]([CH2:24][CH:25]([O:30][CH2:31][CH3:32])[C:26]([O:28][CH3:29])=[O:27])=[CH:20][CH:19]=3)[C:12](=[O:14])[S:13][C:9]=2[CH:8]=1)=O.[CH3:38][O:39][NH2:40]>>[Cl:1][C:2]1[CH:3]=[C:4]([C:5](=[N:40][O:39][CH3:38])[C:7]2[CH:34]=[CH:33][C:10]3[N:11]([CH2:15][CH2:16][O:17][C:18]4[CH:23]=[CH:22][C:21]([CH2:24][CH:25]([O:30][CH2:31][CH3:32])[C:26]([O:28][CH3:29])=[O:27])=[CH:20][CH:19]=4)[C:12](=[O:14])[S:13][C:9]=3[CH:8]=2)[CH:35]=[CH:36][CH:37]=1Participants
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-8806e84ee0fb48c0ae41a84d9c3dcbae
- Source dataset
- uspto-grants-2006_07
- Patent number
- US07071221B2
Reaction notes
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