HCID 13175960, compound → HCID 13175966, compound
Reaction equation
[NH:1]([C:8]1[S:9][C:10]([C:13]2[CH2:20][S:19][CH:18]3[N:15]([C:16](=[O:30])[CH:17]3[NH:21][C:22](=[O:29])[CH2:23][C:24]3[S:25][CH:26]=[CH:27][CH:28]=3)[C:14]=2[C:31]([O:33]C(C2C=CC=CC=2)C2C=CC=CC=2)=[O:32])=[CH:11][N:12]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1>C(O)=O>[NH:1]([C:8]1[S:9][C:10]([C:13]2[CH2:20][S:19][CH:18]3[N:15]([C:16](=[O:30])[CH:17]3[NH:21][C:22](=[O:29])[CH2:23][C:24]3[S:25][CH:26]=[CH:27][CH:28]=3)[C:14]=2[C:31]([OH:33])=[O:32])=[CH:11][N:12]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1Participants
3
Reactant 1
Product 1
Reagents, catalysts & solvents 1
Procedure
3-(2-Anilinothiazol-5-yl)-2-benzhydryloxycarbonyl-8-oxo-7-(thien-2-yl-acetamido)-5-thia-1-azabicyclo[4.2.0]oct-2-ene (0.9 g) is treated with formic acid (9 cc) by following the procedure described in Reference Example 1, and 3-(2-anilinothiazol-5-yl)-2-carboxy-8-oxo-7-(thien-2-yl-acetamido)-5-thia-1-azabicyclo[4.2.0]oct-2-ene (0.4 g) is obtained in the form of a yellow solid.
Sources & evidence
- ORD record
- ord-e045095416604cffaeaf441aa79c912e
- Source dataset
- uspto-grants-1985_07
- Patent number
- US04526962
Reaction notes
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