P
USRE35754EExpiredUtilityPatentIndex 52

Cephem derivatives

Assignee: HOECHST AGPriority: Apr 2, 1977Filed: Jul 11, 1990Granted: Mar 24, 1998
Est. expiryApr 2, 1997(expired)· nominal 20-yr term from priority
Inventors:DUERCKHEIMER WALTERBORMANN DIETEREHLERS EBERHARDSCHRINNER ELMARHEYMES RENE
A61P 31/04C07D 505/00C07D 487/04A61K 31/505A61K 31/435C07D 498/04C07D 471/04A61K 31/545C07D 277/20C07D 277/40C07D 463/22C07D 277/50A61K 31/535C07D 277/587C07D 277/42
52
PatentIndex Score
0
Cited by
21
References
17
Claims

Abstract

Cephem derivatives of the general formula ##STR1## is which the R 2 O group is in the syn-position, a process for their manufacture and pharmaceutical formulations which are active against bacterial infections and contain these compounds.

Claims

exact text as granted — not AI-modified
What is claimed is: 
     
       1. A syn compound of the formula wherein in the above formula   R 3  is hydrogen, an alkali metal cation, or a carboxylic acid protecting group;   R 4  is hydrogen or methoxy;   R 1  is hydrogen or an amino protecting group; and   R 2  is hydrogen or C 1  -C 4  -alkyl.   
     
     
       2. A syn compound as in claim 1 which is ##STR1100## wherein R 3  is hydrogen or an alkali metal cation. 
     
     
       3. A syn compound of the formula ##STR1101## 
     
     
       4. A method for combating a bacterial infection in a patient suffering from such an infection, which method comprises administering to said patient a bactericidally effective amount of a compound as in claim 3. 
     
     
       5. A pharmaceutical composition for combating bacterial infections, acid composition comprising a bactericidally effective amount of a compound as in claim 3 and a pharmaceutically acceptable carrier therefor. 
     
     
       6. The compound of claim 1 wherein R 3  is a carboxylic acid protecting group. 
     
     
       7. The compound of claim 6 wherein R 3  is benzhydryl. 
     
     
       8. The compound of claim 1 wherein R 3  is hydrogen or an alkali metal cation. 
     
     
       9. The compound of claim 8 wherein R 4  is methoxy. 
     
     
       10. The compound of claim 8 wherein R 4  is hydrogen. 
     
     
       11. The compound of claim 10 wherein R 2  is C 1  -C 4  alkyl. 
     
     
       12. The compound of claim 11 wherein R 2  is methyl. 
     
     
       13. The compound of claim 12 wherein R 2  is hydrogen. 
     
     
       14. The compound or claim 2 said compound being 7- 2-(2-aminothiazol-4-yl)-2-methoxyiminoacetamido!-3-(4-methyl-5-oxo-6-hydroxy-4,5-dihydro-1,2,4-triazin-3-ylthio)methyl-3-cephem-4-carboxylic acid (syn isomer). 
     
     
       15. The compound of claim 3 wherein C 1  -C 4  -alkyl is methyl. 
     
     
       16. A method for combating a bacterial infection in a patient suffering from such an infection, which method comprises administering to said patient a bactericidally effective amount of a compound as in claim 1. 
     
     
       17. A pharmaceutical composition for combating bacterial infections, said composition comprising a bactericidally effective amount of a compound as in claim 1 and a pharmaceutically acceptable carrier therefor.

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