HCID 20430445, compound → HCID 20430412, compound
Reaction equation
C([O:14][C:15]([C:17]1[N:18]2[CH:21]([S:22][CH2:23][C:24]=1[C:25]1[S:29][C:28]([N:30]([CH3:32])[CH3:31])=[N:27][CH:26]=1)[CH:20]([NH:33][C:34](=[O:41])[CH2:35][C:36]1[S:37][CH:38]=[CH:39][CH:40]=1)[C:19]2=[O:42])=[O:16])(C1C=CC=CC=1)C1C=CC=CC=1>C(O)=O>[C:15]([C:17]1[N:18]2[CH:21]([S:22][CH2:23][C:24]=1[C:25]1[S:29][C:28]([N:30]([CH3:31])[CH3:32])=[N:27][CH:26]=1)[CH:20]([NH:33][C:34](=[O:41])[CH2:35][C:36]1[S:37][CH:38]=[CH:39][CH:40]=1)[C:19]2=[O:42])([OH:16])=[O:14]Participants
3
Reactant 1
Product 1
Reagents, catalysts & solvents 1
Procedure
2-Benzhydryloxycarbonyl-3-(2-dimethylamino-thiazol-5-yl)-8-oxo-7-(thien-2-yl-acetamido)-5-thia-1-azabicyclo[4.2.0]oct-2-ene (2.4 g) is treated with formic acid (25 cc) in accordance with the working method described in Example 17, and 2-carboxy-3-(2-dimethylamino-thiazol-5-yl)-8-oxo-7-(thien-2-yl-acetamido)-5-thia-1-azabicyclo[4.2.0]oct-2-ene (1.05 g) is obtained, as the inner salt, in the form of a yellow solid.
Sources & evidence
- ORD record
- ord-5a3c0f05a9994d3c9ba0fe342031cf04
- Source dataset
- uspto-grants-1985_01
- Patent number
- US04496560
Reaction notes
Loading…