Hydrochloric Acid → 7-(2-Methoxyimino-3-oxo-4-chlorobutyramido)-3-cephem-4-carboxylic acid
Reaction equation
Cl.[CH3:2][O:3][N:4]=[C:5]([C:21](OCC)([O:24]CC)[CH2:22][Cl:23])[C:6]([NH:8][CH:9]1[C:19](=[O:20])[N:11]2[C:12]([C:16]([OH:18])=[O:17])=[CH:13][CH2:14][S:15][C@H:10]12)=[O:7]>C(Cl)Cl>[CH3:2][O:3][N:4]=[C:5]([C:21](=[O:24])[CH2:22][Cl:23])[C:6]([NH:8][CH:9]1[C:19](=[O:20])[N:11]2[C:12]([C:16]([OH:18])=[O:17])=[CH:13][CH2:14][S:15][C@H:10]12)=[O:7]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
6 N Hydrochloric acid (2.4 ml), 7-(2-methoxyimino-3,3-diethoxy-4-chlorobutyramido)-3-cephem-4-carboxylic acid (syn isomer, 301.5 mg) and methlene chloride (3 ml) were treated in a similar manner to that of Example 48 to give 7-(2-methoxyimino-3-oxo-4-chlorobutyramido)-3-cephem-4-carboxylic acid (syn isomer, 110.4 mg).
Sources & evidence
- ORD record
- ord-f7d403b10b2f438b98fcd14a6e232fa1
- Source dataset
- uspto-grants-1981_11
- Patent number
- US04298529
Reaction notes
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