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公开(公告)号:SE8306994D0
公开(公告)日:1983-12-16
申请号:SE8306994
申请日:1983-12-16
Applicant: HOECHST AG
Inventor: DURCKHEIMER W , BORMANN D , EHLERS E , SCHRINNER E , HAYMES R
IPC: A61K31/397 , A61K31/435 , A61K31/505 , A61K31/535 , A61K31/545 , A61K31/546 , A61P31/04 , B25J15/08 , C07D205/08 , C07D277/20 , C07D277/40 , C07D277/42 , C07D277/50 , C07D463/00 , C07D471/04 , C07D487/04 , C07D498/04 , C07D501/20 , C07D501/24 , C07D501/36 , C07D505/00 , C07D519/06 , C07F9/6561
Abstract: Cephem derivatives of the general formula in which the R2O group is in the syn-position, a process for their manufacture and pharmaceutical formulations which are active against bacterial infections and contain these compounds.
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公开(公告)号:SE426240B
公开(公告)日:1982-12-20
申请号:SE8202788
申请日:1982-05-04
Applicant: HOECHST AG
Inventor: MERKEL W , BORMANN D , MANIA D , MUSCHAWECK R
IPC: A61K31/40 , A61P7/10 , C07D207/32 , C07D207/327 , C07D295/155 , C07D317/64 , C07D401/12 , C07D403/12
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公开(公告)号:SE425487B
公开(公告)日:1982-10-04
申请号:SE7714648
申请日:1977-12-22
Applicant: HOECHST AG
Inventor: MERKEL W , BORMANN D , MANIA D , MUSCHAWECK R
IPC: A61K31/40 , A61P7/10 , C07D207/32 , C07D207/327 , C07D295/155 , C07D317/64 , C07D401/12 , C07D403/12
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公开(公告)号:AU519253B2
公开(公告)日:1981-11-19
申请号:AU3406478
申请日:1978-03-10
Applicant: HOECHST AG
Inventor: BORMANN D
IPC: A61K31/44 , A61K31/535 , A61K31/545 , A61K31/546 , A61P31/04 , C07D277/20 , C07D277/38 , C07D277/40 , C07D463/00 , C07D501/20 , C07D505/00 , C07D501/22 , C07D501/34 , C07D501/36 , C07D471/04 , C07D498/04 , C07D277/42 , C07D277/46 , C07D277/48
Abstract: Cephem derivatives of the formula in which R1 denotes hydrogen or low-molecular alkoxy, R2 denotes hydrogen, optionally substituted alkyl, phthalide or a cation, X denotes sulfur, oxygen or CH2 and A denotes hydrogen, alkoxy, halogen or a group -CH2Y, in which Y represents hydrogen, acyloxy, alkoxy, optionally substituted carbamoyloxy or a group -SR3, in which R3 can represent acyl, alkyl or an optionally substituted 5-membered or 6-membered heterocyclic structure are disclosed as valuable antibiotics which are well suited for combating Gram-positive and in particular Gram-negative infections and also have an unexpectedly good action against penicillinase-forming staphylococci.
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公开(公告)号:PH14409A
公开(公告)日:1981-06-25
申请号:PH20590
申请日:1977-12-22
Applicant: HOECHST AG
Inventor: MANIA D , MERKEL W , MUSCHAWECK R , BORMANN D
IPC: A61K31/40 , A61P7/10 , C07D207/32 , C07D207/327 , C07D295/155 , C07D317/64 , A01N9/20 , A01N9/24 , C07C63/06
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公开(公告)号:AU4897279A
公开(公告)日:1981-01-22
申请号:AU4897279
申请日:1979-07-17
Applicant: HOECHST AG
Inventor: HITZEL V , LATTRELL R , BORMANN D
IPC: C07D501/04 , C07D501/06 , C07D501/20 , C07D501/22 , C07D501/24 , C07D501/32 , C07D501/34 , C07D501/36
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公开(公告)号:DK269679A
公开(公告)日:1980-12-27
申请号:DK269679
申请日:1979-06-26
Applicant: HOECHST AG
Inventor: HITZEL V , LATTRELL R , BORMANN D
IPC: C07D20060101 , C07D501/06 , C07D501/34 , C07D501/36 , C07D
Abstract: Cephem compounds of the general formula in which A denotes hydrogen, an equivalent of an alkali metal or alkaline earth metal or an organic nitrogen base, or the radical of an ester group, R1 denotes hydrogen, and optionally substituted alkyl, alkenyl, alkynyl, cycloalkyl, aralkyl, acyl, aryl, arylsulphonyl, alkylsulphonyl or heterocyclic group, R2 denotes a furyl, thiazolyl or phenyl group which is optionally substituted by alkyl, aryl or an optionally protected amino group, and B denotes alkoxy, methyl, acetoxymethyl, carbamoylmethyl, halogen or CH2S-Het, where Het can denote a 5- to 6-membered ring having 1-4 carbon atoms, and in which R1O groups are located in the syn position and n denotes 0, 1 or 2, are prepared by reacting a carboxylic acid of the general formula or a salt thereof, in the presence of approx. 0.1 to approx. 3.0 mol of a compound of the general formula in which R3, R4 and R5 can be identical or different, and denote alkyl, with R3 and R4 or R3 and R5 also together being able to form a ring which is optionally interrupted by a heteroatom, and R5 also being able to denote a dialkylamino group in which the alkyl groups in each case contain 1-6 carbon atoms and can, where appropriate, be closed to form a ring which is interrupted by a heteroatom, with an acid halide former and reacting the resulting complex with a cephemic acid of the general formula in the form of an amine salt or an ester which is optionally eliminable by acid hydrolysis or hydrogenolysis, or a silyl ester, and, if necessary, converting, in a manner known per se, any resulting carboxyl group into another of the groups specified under A. This process prevents isomerization, and homogeneous products in the syn form are obtained.
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公开(公告)号:ZA792571B
公开(公告)日:1980-06-25
申请号:ZA792571
申请日:1979-05-25
Applicant: HOECHST AG
Inventor: SCHRINNER E , DUERCHHEIMER W , BORMANN D
IPC: C07D501/22 , A61K31/545 , A61K31/546 , A61P31/04 , C07D277/24 , C07D277/28 , C07D277/32 , C07D501/20 , C07D501/34 , C07D
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公开(公告)号:NZ186094A
公开(公告)日:1979-10-25
申请号:NZ18609477
申请日:1977-12-22
Applicant: HOECHST AG
Inventor: MUSCHAWECK R , MERKEL W , BORMANN D , MANIA D
IPC: A61K31/40 , A61P7/10 , C07D207/32 , C07D207/327 , C07D295/155 , C07D317/64
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公开(公告)号:ZA781433B
公开(公告)日:1979-02-28
申请号:ZA781433
申请日:1978-03-10
Applicant: HOECHST AG
Inventor: SCHRINNER E , BORMANN D , KNABE B , WORM M
IPC: A61K31/44 , A61K31/535 , A61K31/545 , A61K31/546 , A61P31/04 , C07D277/20 , C07D277/38 , C07D277/40 , C07D463/00 , C07D501/20 , C07D505/00 , A61K31/00
Abstract: Cephem derivatives of the formula in which R1 denotes hydrogen or low-molecular alkoxy, R2 denotes hydrogen, optionally substituted alkyl, phthalide or a cation, X denotes sulfur, oxygen or CH2 and A denotes hydrogen, alkoxy, halogen or a group -CH2Y, in which Y represents hydrogen, acyloxy, alkoxy, optionally substituted carbamoyloxy or a group -SR3, in which R3 can represent acyl, alkyl or an optionally substituted 5-membered or 6-membered heterocyclic structure are disclosed as valuable antibiotics which are well suited for combating Gram-positive and in particular Gram-negative infections and also have an unexpectedly good action against penicillinase-forming staphylococci.
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