Hydrochloric Acid → 7beta-Amino-3-[3-amino-2-(2-hydroxyethyl)-1-pyrazolio]methyl-3-cephem-4-carboxylate trihydrochloride
Reaction equation
[ClH:1].[NH2:2][C@@H:3]1[C:27](=[O:28])[N:5]2[C:6]([C:24]([O-:26])=[O:25])=[C:7]([CH2:10][N+:11]3[N:12]([CH2:19][CH2:20][O:21]C=O)[C:13]([NH:16]C=O)=[CH:14][CH:15]=3)[CH2:8][S:9][C@H:4]12.C(OCC)(=O)C>CO>[ClH:1].[ClH:1].[ClH:1].[NH2:2][C@@H:3]1[C:27](=[O:28])[N:5]2[C:6]([C:24]([O-:26])=[O:25])=[C:7]([CH2:10][N+:11]3[N:12]([CH2:19][CH2:20][OH:21])[C:13]([NH2:16])=[CH:14][CH:15]=3)[CH2:8][S:9][C@H:4]12Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
Concentrated hydrochloric acid (5.67 ml) was added to a mixture of di(trifluoroacetic acid) salt of 7β-amino-3-[3-formamido-2-(2-formyloxyethyl)-1-pyrazolio]methyl-3-cephem-4-carboxylate (10 g) in methanol (50 ml ) at ambient temperature. After being stirred at the same temperature for 3 hours, the mixture was added dropwise to ethyl acetate (500 ml). The resultant precipitate was collected by filtration to give 7β-amino-3-[3-amino-2-(2-hydroxyethyl)-1-pyrazolio]methyl-3-cephem-4-carboxylate trihydrochloride (6.1 g).
Workup
- filtrationThe resultant precipitate was collected by filtration
Sources & evidence
- ORD record
- ord-2766ea0e58cd4130b11f3ebcad3928e9
- Source dataset
- uspto-grants-1993_05
- Patent number
- US05210080
Reaction notes
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