O-Methylhydroxylamine → HCID 86760127, compound

HRID 1790251Notes

Reaction equation

[C:1]([NH:4][CH:5]([CH2:10][C:11]1[CH:16]=[CH:15][C:14]([O:17][CH2:18][CH2:19][N:20]2[C:24]3[CH:25]=[CH:26][C:27]([C:29](=O)[C:30]4[CH:35]=[CH:34][CH:33]=[CH:32][CH:31]=4)=[CH:28][C:23]=3[S:22][C:21]2=[O:37])=[CH:13][CH:12]=1)[C:6]([O:8][CH3:9])=[O:7])(=[O:3])[CH3:2].[CH3:38][O:39][NH2:40]>>[C:1]([NH:4][CH:5]([CH2:10][C:11]1[CH:16]=[CH:15][C:14]([O:17][CH2:18][CH2:19][N:20]2[C:24]3[CH:25]=[CH:26][C:27]([C:29](=[N:40][O:39][CH3:38])[C:30]4[CH:31]=[CH:32][CH:33]=[CH:34][CH:35]=4)=[CH:28][C:23]=3[S:22][C:21]2=[O:37])=[CH:13][CH:12]=1)[C:6]([O:8][CH3:9])=[O:7])(=[O:3])[CH3:2]

Participants

Reactant 2

HCID 4113O-Methylhydroxylamine

HCID 22041586HCID 22041586, compound

Product 1

HCID 86760127HCID 86760127, compound

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-fc6f7c8c4ba2404bbed671328fca3321
Source dataset: uspto-grants-2006_07
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US07071221B2

Reaction notes

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