HCID 10097475, compound → HCID 58905270, compound
Reaction equation
CS[CH2:3][CH2:4][NH:5][C:6]([C:8]1[C:17](=[O:18])[C:16]2[C:11](=[N:12][CH:13]=[CH:14][CH:15]=2)[N:10]([C:19]2[CH:20]=[C:21]([C:25]3[CH:30]=[CH:29][C:28]([C@@H:31]4[CH2:33][C@H:32]4[C:34]([OH:36])=[O:35])=[CH:27][CH:26]=3)[CH:22]=[CH:23][CH:24]=2)[CH:9]=1)=[O:7].O[O:38][S:39]([O-:41])=O.[K+].[CH2:43]1COCC1.CO.O>O>[CH3:43][S:39]([CH2:3][CH2:4][NH:5][C:6]([C:8]1[C:17](=[O:18])[C:16]2[C:11](=[N:12][CH:13]=[CH:14][CH:15]=2)[N:10]([C:19]2[CH:20]=[C:21]([C:25]3[CH:26]=[CH:27][C:28]([CH:31]4[CH2:33][CH:32]4[C:34]([OH:36])=[O:35])=[CH:29][CH:30]=3)[CH:22]=[CH:23][CH:24]=2)[CH:9]=1)=[O:7])(=[O:41])=[O:38]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
To a solution of EXAMPLE 22 (1 eq) in THF-MeOH—H2O (2:1:1, 0.1M) was added Oxone (2 eq). The mixture was stirred at rt for 18 h and diluted with water. The residue was isolated by filtration, washed with ether to afford the title compound as a solid.
Workup
- customThe residue was isolated by filtration
- washwashed with ether
Sources & evidence
- ORD record
- ord-c4817dd892fb43f19b6f2f53c2e757ab
- Source dataset
- uspto-grants-2007_07
- Patent number
- US07238706B2
Reaction notes
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