Dimethyl Sulfoxide → HCID 69032281, compound
Reaction equation
[N:1]1[CH:6]=[CH:5][CH:4]=[CH:3][C:2]=1[CH:7]([OH:32])[C@@H:8]1[CH2:12][CH2:11][CH2:10][N:9]1[C:13](=[O:31])[C@H:14]([CH:28]([CH3:30])[CH3:29])[NH:15][C:16](=[O:27])[C@H:17]([CH3:26])[NH:18][C:19]([O:21][C:22]([CH3:25])([CH3:24])[CH3:23])=[O:20].C(Cl)(=O)C(Cl)=O.CS(C)=O>>[N:1]1[CH:6]=[CH:5][CH:4]=[CH:3][C:2]=1[C:7]([C@@H:8]1[CH2:12][CH2:11][CH2:10][N:9]1[C:13](=[O:31])[C@H:14]([CH:28]([CH3:30])[CH3:29])[NH:15][C:16](=[O:27])[C@H:17]([CH3:26])[NH:18][C:19]([O:21][C:22]([CH3:24])([CH3:25])[CH3:23])=[O:20])=[O:32]Participants
4
Procedure
41 (0.29 g, 0.64 mmol), oxalylchloride (0.10 ml, 1.15 mmol), DMSO (0.11 ml, 1.59 mmol), TEA (0.36 ml, 2.55 mmol)
Sources & evidence
- ORD record
- ord-64c8a1f641eb42b0911fc5ae601cb92d
- Source dataset
- uspto-grants-2009_10
- Patent number
- US07608577B2
Reaction notes
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