Sodium Bicarbonate → HCID 131717276, compound
Reaction equation
S(O)([O-])(=O)=O.[NH2:6][C:7]1[S:11][N:10]=[C:9]([C:12](=[N:35][O:36][CH2:37][CH:38]=[CH2:39])[C:13]([NH:15][CH:16]2[C:33](=[O:34])[N:18]3[C:19]([C:30]([OH:32])=[O:31])=[C:20]([CH2:23][N+:24]4[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=4)[CH2:21][S:22][C@H:17]23)=[O:14])[N:8]=1.[C:40](=O)([O-:42])[OH:41].[Na+:44]>>[C:40]([NH:6][C:7]1[S:11][N:10]=[C:9]([C:12](=[N:35][O:36][CH2:37][CH:38]=[CH2:39])[C:13]([NH:15][CH:16]2[C:33](=[O:34])[N:18]3[C:19]([C:30]([O-:32])=[O:31])=[C:20]([CH2:23][N+:24]4[CH:25]=[CH:26][CH:27]=[CH:28][CH:29]=4)[CH2:21][S:22][C@H:17]23)=[O:14])[N:8]=1)([O-:42])=[O:41].[Na+:44]Participants
3
Procedure
Sodium 7-[2-(5-carboxylatoamino-1,2,4-thiadiazol-3-yl)-2-allyloxyiminoacetamido]-3-(1-pyridinio)methyl-3-cephem-4-carboxylate (syn isomer) was prepared by reacting 7-[2-(5-amino-1,2,4-thiadiazol-3yl)-2-allyloxyiminoacetamido]-3-(1-pyridinio)methyl-3-cephem-4-carboxylate sulfate (syn isomer) (50 mg) and sodium hydrogencarbonate (21 mg) and detected according to a similar manner to that of Example 17.
Sources & evidence
- ORD record
- ord-aa2ffcc073bd43358a18f9dc3cf955a6
- Source dataset
- uspto-grants-1992_04
- Patent number
- US05104866
Reaction notes
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