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公开(公告)号:DK375875A
公开(公告)日:1976-02-22
申请号:DK375875
申请日:1975-08-20
Applicant: HOFFMANN LA ROCHE
Inventor: FURLENMEIER A , QUITT P
IPC: A61K31/14 , A61K31/13 , C07D499/00 , C07D499/24 , C07D499/64 , C07D499/68 , C07D
Abstract: Choline and N-methyl-D-glucamine salts of amoxicillin, processes for their preparation and pharmaceutical compositions containing the salts as the active antibacterial component are disclosed.
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公开(公告)号:BR6681938D0
公开(公告)日:1973-12-26
申请号:BR18193866
申请日:1966-08-08
Applicant: HOFFMANN LA ROCHE
Inventor: FURST A , FURLENMEIER A , LANGEMANN A , WALDVOGEL G , HOCKS P , KERB U , WIECHERT R
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公开(公告)号:BR7200305D0
公开(公告)日:1973-12-18
申请号:BR30572
申请日:1972-01-19
Applicant: HOFFMANN LA ROCHE
Inventor: FURLENMEIER A , QUITT P , VOGLER K , LANZ P
IPC: C07D499/12 , A61K31/431 , A61P31/04 , C07D207/28 , C07D207/34 , C07D213/78 , C07D213/79 , C07D213/89 , C07D215/48 , C07D215/50 , C07D217/26 , C07D231/14 , C07D233/90 , C07D239/54 , C07D239/557 , C07D261/18 , C07D263/34 , C07D277/56 , C07D285/06 , C07D307/68 , C07D309/12 , C07D333/38 , C07D499/00 , C07D499/56 , C07D499/60
Abstract: Compounds represented by the following formula WHEREIN A is a substituted or unsubstituted heterocyclic radical and T is a C2-C5 alkyl, alkenyl, cycloproplymethyl, cyclobutylmethyl or cyclopentyl group A PROCESS FOR THEIR PREPARATION AND NOVEL INTERMEDIATES THEREFOR ARE DISCLOSED. These compounds are useful antibiotics.
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公开(公告)号:ZA7208924B
公开(公告)日:1973-09-26
申请号:ZA7208924
申请日:1972-12-18
Applicant: HOFFMANN LA ROCHE
Inventor: FURLENMEIER A , VOGLER K , LANZ P , QUITT P
IPC: C07D207/32 , C07D207/327 , C07D209/18 , C07D213/55 , C07D257/04 , C07D307/54 , C07D333/24 , C07D499/00 , C07D499/60 , C07D
CPC classification number: C07D207/327 , C07D209/18 , C07D213/55 , C07D257/04 , C07D307/54 , C07D333/24 , C07D499/00 , Y02P20/55
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公开(公告)号:ZA7208771B
公开(公告)日:1973-08-29
申请号:ZA7208771
申请日:1972-12-12
Applicant: HOFFMANN LA ROCHE
Inventor: FURLENMEIER A , VOGLER K , LANZ P , ZANETTI G
IPC: C07D499/60 , B25C5/02 , B25C5/06 , C07C51/60 , C07D499/00 , C07D
CPC classification number: C07D499/00 , B25C5/0257 , B25C5/06 , C07C51/60 , C07C59/70
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公开(公告)号:ZA718537B
公开(公告)日:1972-09-27
申请号:ZA718537
申请日:1971-12-21
Applicant: HOFFMANN LA ROCHE
Inventor: FURLENMEIER A , QUITT P , VOGLER K , LANZ P
IPC: C07D499/12 , A61K31/431 , A61P31/04 , C07D207/28 , C07D207/34 , C07D213/78 , C07D213/79 , C07D213/89 , C07D215/48 , C07D215/50 , C07D217/26 , C07D231/14 , C07D233/90 , C07D239/54 , C07D239/557 , C07D261/18 , C07D263/34 , C07D277/56 , C07D285/06 , C07D307/68 , C07D309/12 , C07D333/38 , C07D499/00 , C07D499/56 , C07D499/60 , C07D
Abstract: Compounds represented by the following formula WHEREIN A is a substituted or unsubstituted heterocyclic radical and T is a C2-C5 alkyl, alkenyl, cycloproplymethyl, cyclobutylmethyl or cyclopentyl group A PROCESS FOR THEIR PREPARATION AND NOVEL INTERMEDIATES THEREFOR ARE DISCLOSED. These compounds are useful antibiotics.
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公开(公告)号:ZA7103845B
公开(公告)日:1972-03-29
申请号:ZA7103845
申请日:1971-06-14
Applicant: HOFFMANN LA ROCHE
Inventor: FURLENMEIER A , VOGLER K , ZANETTI G , LANZ P
IPC: C07C229/38 , C07D207/32 , C07D207/327 , C07D207/46 , C07D309/12 , C07D499/00 , C07D499/60 , C07C
CPC classification number: C07D207/327 , C07C229/38 , C07C317/00 , C07C323/00 , C07D207/46 , C07D309/12 , C07D499/00 , Y02P20/55
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公开(公告)号:FI43596B
公开(公告)日:1971-02-01
申请号:FI212066
申请日:1966-08-12
Applicant: HOFFMANN LA ROCHE
Inventor: FUERST A , FURLENMEIER A , LANGEMANN A , KERB U , WIECHERT R , WALDVOGEL G , HOCKS P
IPC: C07J1/00 , C07J5/00 , C07J9/00 , C07J31/00 , C07J75/00 , C07C167/16 , C07C169/60
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公开(公告)号:SE305873B
公开(公告)日:1968-11-11
申请号:SE1011667
申请日:1967-06-30
Applicant: HOFFMANN LA ROCHE
Inventor: BATCHO A , BERGER J , SPIEGELBERG H , VATERLAUS B , PECHERER B , SCHOCHER A , FURLENMEIER A , KELLER O
IPC: C07D27/22
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公开(公告)号:YU216188A
公开(公告)日:1990-04-30
申请号:YU216188
申请日:1988-11-24
Applicant: HOFFMANN LA ROCHE
Inventor: FURLENMEIER A , HUBSCHWERLEN C , MONTAVON M
IPC: C07D499/897 , A61K31/397 , A61K31/40 , A61K31/435 , A61K31/47 , A61K31/545 , A61K31/546 , A61P31/04 , C07D463/00 , C07D477/00 , C07D477/08 , C07D499/00 , C07D499/32 , C07D499/893 , C07D501/04 , C07D501/06 , C07D501/16 , C07D501/18 , C07D501/20 , C07D501/22 , C07D501/24 , C07D501/34 , C07D501/36 , C07D501/46 , C07D505/00 , C07D513/04 , A61K31/43
Abstract: Novel esters of pharmacologically active carboxylic acids, which can be cleaved under physiological conditions, in particular of antibiotically active carboxylic acids from the beta -lactam antibiotic field, are described, which are characterised in that the alcohol component of the ester is a group of the general formula in which R denotes hydrogen or lower alkyl, R denotes hydrogen, lower alkyl, lower haloalkyl, lower alkenyl, lower alkoxycarbonyl, aryl or heteroaryl or, together with R denotes lower alkylene, R denotes hydrogen, lower alkyl or lower alkoxycarbonyl, R denotes the group -COOR , -COR , -SO2-R , -CONR R or -PO(OR )2, R denotes a saturated or unsaturated hydrocarbon radical having up to 12 carbon atoms, in which up to two methylene groups can be replaced by oxygen atoms, or denotes aryl or aryl-lower alkyl, R denotes lower alkyl or aryl, R and R each denotes hydrogen or lower alkyl or together denotes lower alkylene in which a methylene group can be replaced by an oxygen or sulphur atom or by an imino or lower alkylimino group, and R denotes lower alkyl. If a basic substituent is present, these esters can also be present in the form of pharmaceutically acceptable acid addition salts.
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