Hydrochloric Acid → HCID 131718938, compound
Reaction equation
C([NH:3][C:4]1[S:5][CH:6]=[C:7]([C:9](=[N:38][O:39][CH2:40][C:41]([O:43][C:44]([CH3:47])([CH3:46])[CH3:45])=[O:42])[C:10]([NH:12][C@@H:13]2[C:36](=[O:37])[N:15]3[C:16]([C:33]([O-:35])=[O:34])=[C:17]([CH2:20][N+:21]([CH3:32])([CH3:31])[CH2:22][C:23]4[NH:24][CH:25]=[C:26]([OH:30])[C:27](=[O:29])[CH:28]=4)[CH2:18][S:19][C@H:14]23)=[O:11])[N:8]=1)=O.Cl>CO.O>[NH2:3][C:4]1[S:5][CH:6]=[C:7]([C:9](=[N:38][O:39][CH2:40][C:41]([O:43][C:44]([CH3:47])([CH3:46])[CH3:45])=[O:42])[C:10]([NH:12][C@@H:13]2[C:36](=[O:37])[N:15]3[C:16]([C:33]([O-:35])=[O:34])=[C:17]([CH2:20][N+:21]([CH3:32])([CH3:31])[CH2:22][C:23]4[NH:24][CH:25]=[C:26]([OH:30])[C:27](=[O:29])[CH:28]=4)[CH2:18][S:19][C@H:14]23)=[O:11])[N:8]=1Participants
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Procedure
To a suspension of 7β-[2-(2-formamidothiazol-4-yl)- 2-tert-butoxycarbonylmethoxyiminoacetamido]-3-[N,N-dimethyl-N-{(5-hydroxy-4-oxo-1,4-dihydropyridin-2-yl)methyl}ammonio]methyl-3-cephem-4-carboxylate (syn isomer) (0.70 g) in methanol (35 ml) was added conc. hydrochloric acid (0.53 ml). After being stirred at ambient temperature, the reaction mixture was diluted with water (50 ml) and methanol was evaporated under reduced pressure. The resulting aqueous solution was adjusted to pH 1.0 and subjected to column chromatography on Diaion HP-20 (50 ml). The column was washed with water and the elution was carried out with 40% aqueous isopropanol. The fractions containing the object compound was lyophilized to give 7β-[2-(2-aminothiazol-4-yl)-2-tert-butoxycarbonylmethoxyiminoacetamido]-3-[N,N-dimethyl-N-{(5-hydroxy-4-oxo-1,4-dihydropyridin-2-yl)methyl}ammonio]methyl- 3-cephem-4-carboxylate (syn isomer) (0.53 g).
Workup
- customwas evaporated under reduced pressure
- washThe column was washed with water
- washthe elution
- additionThe fractions containing the object compound
Sources & evidence
- ORD record
- ord-0462d2f2ba44451b9173ee15ce7b51ed
- Source dataset
- uspto-grants-1995_03
- Patent number
- US05401734
Reaction notes
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