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公开(公告)号:US3900464A
公开(公告)日:1975-08-19
申请号:US31872872
申请日:1972-12-27
Applicant: HOFFMANN LA ROCHE
Inventor: FURLENMEIER ANDRE , LANZ PAUL , QUITT PETER , VOGLER KARL , VOGLER HEIR BY FRANZISKA , VOGLER HEIR BY NIKLAUS E , VOGLER HEIR BY HEINRICH
IPC: C07D207/32 , C07D207/327 , C07D209/18 , C07D213/55 , C07D257/04 , C07D307/54 , C07D333/24 , C07D499/00 , C07D499/60 , C07D499/46
CPC classification number: C07D207/327 , C07D209/18 , C07D213/55 , C07D257/04 , C07D307/54 , C07D333/24 , C07D499/00 , Y02P20/55
Abstract: Novel antibiotic compounds represented by the formula
wherein R is a furyl, pyrrolyl, thienyl, oxazolyl, isoxazolyl, thiazolyl, pyridyl, pyrimidinyl, tetrazolyl or indolyl radical which can be substituted with halogen, C1-C3-alkyl, C1-C3alkoxy or C1-C3-alkylthio and T is a C2-C5-alkyl group, PHARMACEUTICALLY ACCEPTABLE SALTS THEREOF AND HYDRATES OF SUCH SALTS, A PROCESS FOR THEIR PREPARATION AND NOVEL INTERMEDIATES THEREOF ARE DISCLOSED.-
公开(公告)号:US3886142A
公开(公告)日:1975-05-27
申请号:US31873672
申请日:1972-12-27
Applicant: HOFFMANN LA ROCHE
Inventor: FURLENMEIER ANDRE , LANZ PAUL , VOGLER KARL , ZANETTI GUIDO
IPC: B25C5/02 , B25C5/06 , C07C51/60 , C07D499/00 , C07D499/60 , F16B15/04 , C07D99/16
CPC classification number: F16B15/04 , B25C5/0257 , B25C5/06 , C07C51/60 , C07D499/00 , Y10S411/92 , Y10S514/962 , Y10T29/49833 , C07C59/70
Abstract: WHEREIN R is halogen, lower alkyl, lower alkoxy, nitro, lower alkoxy-lower alkyl, dilower alkylamino, lower alkyl sulfonylamido, bis-lower alkylsulfonyl amido or lower alkanoyl amido, n is an integer of 0-2 and T is a C2-C5 alkyl group, PHARMACEUTICALLY ACCEPTABLE SALTS THEREOF AND HYDRATES OF SUCH SALTS, A PROCESS FOR THEIR PREPARATION AND NOVEL INTERMEDIATES THEREFOR ARE DISCLOSED.
Novel antibiotic compounds represented by the formula
D R A W I N GAbstract translation: 由式WHEREIN R表示的新型抗生素化合物是卤素,低级烷基,低级烷氧基,硝基,低级烷氧基 - 低级烷基,二元烷基氨基,低级烷基磺酰氨基,双 - 低级烷基磺酰基酰氨基或低级烷酰氨基,n是0〜 2和T是C 2 -C 5烷基,其药学上可接受的盐及其水合物,其制备和新型中间体的方法被公开。
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公开(公告)号:US3917584A
公开(公告)日:1975-11-04
申请号:US31873872
申请日:1972-12-27
Applicant: HOFFMANN LA ROCHE
Inventor: FURLENMEIER ANDRE , LANZ PAUL , VOGLER KARL , ZANETTI GUIDO
IPC: C07C51/60 , C07D499/00 , C07D499/60 , C07D499/44
CPC classification number: C07D499/00 , C07C51/60 , Y02P20/55 , C07C59/64
Abstract: Novel antibiotic compounds represented by the formula
wherein R is halogen, lower alkyl, lower alkoxy, lower alkylamino, di-lower alkylamino or lower alkanoylamino, n is an integer of 0-2 and T is a C2-C5 alkyl group, PHARMACEUTICALLY ACCEPTABLE SALTS THEREOF AND HYDRATES OF SUCH SALTS A PROCESS FOR THEIR PREPARATION AND NOVEL INTERMEDIATES THEREOF ARE DISCLOSED.Abstract translation: 由式-CH2-COO-CH-CO-NH- ||(R)nT S ANGLE CH3 CH-CHC ANGLE |||CH3 C --- N --- CH PARALLEL | OCOOH表示的新型抗生素化合物其中R 是卤素,低级烷基,低级烷氧基,低级烷基氨基,二低级烷基氨基或低级烷酰基氨基,n是0-2的整数,T是C2-C5烷基,其药学上可接受的盐及其等价物的方法 他们的准备和新闻中介被披露。
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公开(公告)号:RO70672A
公开(公告)日:1982-08-17
申请号:RO6939572
申请日:1972-01-14
Applicant: HOFFMANN LA ROCHE
Inventor: FURLENMEIER ANDRE , QUITT PETER , VOGLER KARL , LANZ PAUL
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 , C07D499/52
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:HU170008B
公开(公告)日:1977-03-28
申请号:HUHO001538
申请日:1973-01-03
Applicant: HOFFMANN LA ROCHE
Inventor: LANZ PAUL , REINER ROLAND , VOGLER KARL
IPC: C07D499/00 , C07D499/60 , C07D501/20 , C07D501/28 , C07D499/48 , C07D207/08 , C07D499/58
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公开(公告)号:CA1177823A
公开(公告)日:1984-11-13
申请号:CA373267
申请日:1981-03-18
Applicant: HOFFMANN LA ROCHE
Inventor: FURLENMEIER ANDRE , LANZ PAUL
IPC: A61K31/545 , A61K31/546 , A61P31/04 , C07D253/075 , C07D501/36
Abstract: RAN 4410/144 A cephalosporin derivative of the formula as well as readily hydrolysable esters and salts of this compound and hydrates of the compound of formula I or of esters and salts thereof. Further, also corresponding preparations, the use of these products in the treatment of illnesses, the manufacture of the active substances as well as intermediates thereby occurring.
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公开(公告)号:AU4949272A
公开(公告)日:1974-05-30
申请号:AU4949272
申请日:1972-11-30
Applicant: HOFFMANN LA ROCHE
Inventor: LANZ PAUL , REINER ROLAND , VOGLER KARL
IPC: C07D499/00 , C07D499/60 , C07D501/20 , C07D501/28 , C07D99/16 , C07D99/24
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公开(公告)号:DE2301543A1
公开(公告)日:1973-07-19
申请号:DE2301543
申请日:1973-01-12
Applicant: HOFFMANN LA ROCHE
Inventor: FURLENMEIER ANDRE DR , LANZ PAUL , ZANETTI GUIDO DR , VOGLER KARL DR
IPC: C07C51/60 , C07D499/00 , C07D499/60 , C07D99/22
Abstract: Novel antibiotic compounds represented by the formula -CH2-COO-CH-CO-NH- ¦¦ (R)nT S ANGLE CH3 CH--CHC ANGLE ¦¦¦CH3 C---N---CH PARALLEL ¦ OCOOH wherein R is halogen, lower alkyl, lower alkoxy, lower alkylamino, di-lower alkylamino or lower alkanoylamino, n is an integer of 0-2 and T is a C2-C5 alkyl group, PHARMACEUTICALLY ACCEPTABLE SALTS THEREOF AND HYDRATES OF SUCH SALTS A PROCESS FOR THEIR PREPARATION AND NOVEL INTERMEDIATES THEREOF ARE DISCLOSED.
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公开(公告)号:AU3735371A
公开(公告)日:1973-06-28
申请号:AU3735371
申请日:1971-12-24
Applicant: HOFFMANN LA ROCHE
Inventor: FURLENMEIER ANDRE , QUITT PETER , VOGLER KARL , LANZ PAUL
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 , A61K21/00 , C07D99/16
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:DK141966B
公开(公告)日:1980-07-28
申请号:DK27072
申请日:1972-01-19
Applicant: HOFFMANN LA ROCHE
Inventor: FURLENMEIER ANDRE , QUITT PETER , VOGLER KARL , LANZ PAUL
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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