Oxalic acid dihydrate → HCID 86658811, compound
Reaction equation
[CH:1]1([CH2:4][N:5]2[CH2:23][CH2:22][C@:12]34[C:13]5[C:14]6[O:21][C@H:11]3[C@H:10]([NH:24][C:25](=[O:33])/[CH:26]=[CH:27]/[C:28]3[CH:32]=[CH:31][O:30][CH:29]=3)[CH2:9][CH2:8][C@@:7]4([OH:34])[C@H:6]2[CH2:19][C:18]=5[CH:17]=[CH:16][C:15]=6[OH:20])[CH2:3][CH2:2]1.O.O.[C:37]([OH:42])(=[O:41])[C:38]([OH:40])=[O:39]>CO.O>[C:37]([OH:42])(=[O:41])[C:38]([OH:40])=[O:39].[CH:1]1([CH2:4][N:5]2[CH2:23][CH2:22][C@:12]34[C:13]5[C:14]6[O:21][C@H:11]3[C@H:10]([NH:24][C:25](=[O:33])/[CH:26]=[CH:27]/[C:28]3[CH:32]=[CH:31][O:30][CH:29]=3)[CH2:9][CH2:8][C@@:7]4([OH:34])[C@H:6]2[CH2:19][C:18]=5[CH:17]=[CH:16][C:15]=6[OH:20])[CH2:2][CH2:3]1Participants
5
Procedure
Compound 19b was converted to its oxalic salt using one equivalent of oxalic acid dihydrate in methanol. Solubility: 24.0 mg/mL in H2O.
Sources & evidence
- ORD record
- ord-01de910ffad14f3c80766be9c821c385
- Source dataset
- uspto-grants-2014_07
- Patent number
- US08778958B2
Reaction notes
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