O-Methylhydroxylamine → HCID 86760132, compound

HRID 1790261Notes

Reaction equation

[C:1]([C:9]1[CH:40]=[CH:39][C:12]2[N:13]([CH2:17][CH2:18][O:19][C:20]3[CH:38]=[CH:37][C:23]([CH2:24][CH:25]([CH2:30][C:31]4[CH:36]=[CH:35][CH:34]=[CH:33][CH:32]=4)[C:26]([O:28][CH3:29])=[O:27])=[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.[CH3:41][O:42][NH2:43]>>[CH2:30]([CH:25]([CH2:24][C:23]1[CH:37]=[CH:38][C:20]([O:19][CH2:18][CH2:17][N:13]2[C:12]3[CH:39]=[CH:40][C:9]([C:1](=[N:43][O:42][CH3:41])[C:2]4[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=4)=[CH:10][C:11]=3[S:15][C:14]2=[O:16])=[CH:21][CH:22]=1)[C:26]([O:28][CH3:29])=[O:27])[C:31]1[CH:36]=[CH:35][CH:34]=[CH:33][CH:32]=1

Participants

Reactant 2

HCID 4113O-Methylhydroxylamine

HCID 22041487HCID 22041487, compound

Product 1

HCID 86760132HCID 86760132, 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-79a3ed52a681452f9e6408051ec6d478
Source dataset: uspto-grants-2006_07
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US07071221B2

Reaction notes

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