ZA9610405B - New crystal modification of cdch a process for its preparation and pharmaceutical formulations comprising this modification - Google Patents

New crystal modification of cdch a process for its preparation and pharmaceutical formulations comprising this modification

Info

Publication number
ZA9610405B
ZA9610405B ZA9610405A ZA9610405A ZA9610405B ZA 9610405 B ZA9610405 B ZA 9610405B ZA 9610405 A ZA9610405 A ZA 9610405A ZA 9610405 A ZA9610405 A ZA 9610405A ZA 9610405 B ZA9610405 B ZA 9610405B
Authority
ZA
South Africa
Prior art keywords
modification
cdch
preparation
pharmaceutical formulations
new crystal
Prior art date
Application number
ZA9610405A
Other languages
English (en)
Inventor
Alfons Grunenberg
Patrick Bosche
Original Assignee
Bayer Ag
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=7779831&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=ZA9610405(B) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Bayer Ag filed Critical Bayer Ag
Publication of ZA9610405B publication Critical patent/ZA9610405B/xx

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D471/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
    • C07D471/04Ortho-condensed systems
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/04Antibacterial agents

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Oncology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Communicable Diseases (AREA)
  • Animal Behavior & Ethology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
ZA9610405A 1995-12-12 1996-12-11 New crystal modification of cdch a process for its preparation and pharmaceutical formulations comprising this modification ZA9610405B (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE19546249A DE19546249A1 (de) 1995-12-12 1995-12-12 Neue Kristallmodifikation des 1-Cyclopropyl-7-([S,S]-2,8-diazabicyclo[4,3,0]non-8-yl)-6-fluor-1,4-dihydro-8-methoxy-4-oxo-3-chinolincarbonsäure Hydrochlorid (CDCH), Verfahren zu dessen Herstellung und diese enthaltende pharmazeutische Zubereitungen

Publications (1)

Publication Number Publication Date
ZA9610405B true ZA9610405B (en) 1997-06-23

Family

ID=7779831

Family Applications (1)

Application Number Title Priority Date Filing Date
ZA9610405A ZA9610405B (en) 1995-12-12 1996-12-11 New crystal modification of cdch a process for its preparation and pharmaceutical formulations comprising this modification

Country Status (42)

Country Link
US (1) US5849752A (cs)
EP (1) EP0780390B1 (cs)
JP (1) JP4104687B2 (cs)
KR (1) KR100525146B1 (cs)
CN (1) CN1061348C (cs)
AR (1) AR005009A1 (cs)
AT (1) ATE221531T1 (cs)
AU (1) AU708006B2 (cs)
BG (1) BG62258B1 (cs)
BR (1) BR9605968A (cs)
CA (1) CA2192418C (cs)
CO (1) CO4480105A1 (cs)
CU (1) CU22774A3 (cs)
CZ (1) CZ288657B6 (cs)
DE (2) DE19546249A1 (cs)
DK (1) DK0780390T3 (cs)
EE (1) EE03474B1 (cs)
ES (1) ES2179910T3 (cs)
HR (1) HRP960558B1 (cs)
HU (1) HU226521B1 (cs)
ID (1) ID22625A (cs)
IL (1) IL119795A (cs)
IN (1) IN185805B (cs)
MA (1) MA24342A1 (cs)
MY (1) MY117492A (cs)
NL (1) NL300109I1 (cs)
NO (1) NO306725B1 (cs)
NZ (1) NZ299905A (cs)
PL (1) PL184885B1 (cs)
PT (1) PT780390E (cs)
RO (1) RO119782B1 (cs)
RU (1) RU2162468C2 (cs)
SA (1) SA96170492B1 (cs)
SG (1) SG47201A1 (cs)
SI (1) SI0780390T1 (cs)
SK (1) SK282805B6 (cs)
SV (1) SV1996000109A (cs)
TR (1) TR199600970A2 (cs)
TW (1) TW411340B (cs)
UA (1) UA35638C2 (cs)
YU (1) YU49485B (cs)
ZA (1) ZA9610405B (cs)

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KR100531065B1 (ko) * 1997-09-25 2005-11-28 바이엘 악티엔게젤샤프트 활성제 방출이 제어된 의약 제제
DE19751948A1 (de) 1997-11-24 1999-05-27 Bayer Ag Verfahren zur Herstellung von 8-Methoxy-Chinoloncarbonsäuren
US6509327B1 (en) 1998-09-30 2003-01-21 Alcon Manufacturing, Ltd. Compositions and methods for treating otic, ophthalmic and nasal infections
US6716830B2 (en) * 1998-09-30 2004-04-06 Alcon, Inc. Ophthalmic antibiotic compositions containing moxifloxacin
US6395746B1 (en) 1998-09-30 2002-05-28 Alcon Manufacturing, Ltd. Methods of treating ophthalmic, otic and nasal infections and attendant inflammation
HRP20010332B1 (hr) * 1998-11-10 2011-01-31 Bayer Schering Pharma Aktiengesellschaft Farmaceutski pripravak moksifloksacina
DE19854356A1 (de) * 1998-11-25 2000-05-31 Bayer Ag Kristallmodifikation A von 8-Cyan-1-cyclopropyl-7-(1S,6S-2,8-diazabicyclo-/4.3.0/nonan-8-yl)-6-fluor-1,4-dihydro-4-oxo-3-chinolincarbonsäure
DE19854357A1 (de) * 1998-11-25 2000-05-31 Bayer Ag Semi-Hydrochlorid von 8-Cyan-1-cyclopropyl-7-(1S,6S-2,8-diazabicyclo/4.3.0/ -nonan-8-yl)-6-fluor-1,4-dihydro-4-oxo-3-chinolincarbonsäure
DE19854355A1 (de) * 1998-11-25 2000-05-31 Bayer Ag Kristallmodifikation B von 8-Cyan-1-cyclopropyl-7-(1S, 6S-2,8-diazabicyclo-/4.3.O/nonan-8-yl)-6-fluor-1,4-dihydro-4-oxo-3-chinolincarbonsäure
DE19908449A1 (de) * 1999-02-26 2000-08-31 Bayer Ag Kristallmodifikation C von 8-Cyan-1-cyclopropyl-7-(1S,6S-2,8-diazabicylo-[4.3.0]nonan-8-yl)-6-fluor-1,4-dihydro-4-oxo-3-chino/incarbonsäure
EP1562942A1 (en) * 2002-10-31 2005-08-17 Ranbaxy Laboratories, Ltd. Amorphous moxifloxacin hydrochloride
US7230006B2 (en) * 2003-04-09 2007-06-12 Reddy's Laboratories Limited Crystalline form III of anhydrous moxifloxacin hydrochloride and a process for preparation thereof
US20060264635A1 (en) * 2003-08-05 2006-11-23 Chava Satyanarayana Process for the preparation of moxifloxacin hydrochloride
ITMI20032259A1 (it) 2003-11-20 2005-05-21 Chemi Spa Nuovo polimorfo dell'acido 1-ciclopropil-7-(s,s-2,8-diazabciclo-4.3.0-non-8-il)-6-fluoro-1,4-diidro-8-metossi-4-oxo-chinolin carbossilico cloridrato e metodi per la sua preparazione
ES2319125T3 (es) * 2003-11-20 2009-05-04 Chemi S.P.A. Polimorfos del clorhidrato del acido 1-ciclopropil-7-((s,s)-2,8-diazadiciclo(4.3.0)-non-8-il)-6-fluoro-1,4-dihidro-8-metoxi-4-oxo-3-quinolina carboxilico y metodos para la preparacion de los mismos.
US7491725B2 (en) 2004-02-06 2009-02-17 Bristol-Myers Squibb Company Process for preparing 2-aminothiazole-5-aromatic carboxamides as kinase inhibitors
DE102004015981A1 (de) * 2004-04-01 2005-10-20 Bayer Healthcare Ag Neue kirstalline Form von 8-Cyan-1-cyclopropyl-7-(1S,6S-2,8-diazabicyclo[4.3.0]nonan-8-yl)-6-fluor-1,4-dihydro-4-oxo-3-chinolincarbonsäure
DE102004063347A1 (de) * 2004-12-23 2006-07-13 Stada Arzneimittel Ag Gebrauchsfertige Gemcitabinlösungen und Gemcitabinlösungskonzentrate
WO2007033515A1 (fr) * 2005-09-21 2007-03-29 Shenzhen Tys R & D Co., Ltd. Formulation orale contenant de la moxifloxacine et son procédé de préparation
GB0612422D0 (en) * 2006-06-23 2006-08-02 Generics Uk Ltd Novel hydrate form
AU2007264030B2 (en) 2006-06-27 2012-04-05 Sandoz Ag New method for salt preparation
ES2303768B1 (es) * 2006-09-08 2009-06-05 Quimica Sintetica, S.A. Nueva forma cristalina de moxifloxacino clorhidrato.
WO2008059223A2 (en) * 2006-11-13 2008-05-22 Cipla Limited Process for the synthesis of moxifloxacin hydrochloride
EP1992626A1 (en) * 2007-05-10 2008-11-19 Sandoz AG Process for the preparation of moxifloxacin hydrochloride
EP2083010A1 (en) * 2008-01-08 2009-07-29 Chemo Ibérica, S.A. Polymorphic Forms of Moxifloxacin hydrochloride and processes for preparation thereof
EP2154137A1 (en) 2008-08-04 2010-02-17 Chemo Ibérica, S.A. Crystalline form of moxifloxacin base
PL2349220T3 (pl) * 2008-10-09 2012-12-31 Abdi Ibrahim Ilac Sanayi Ve Ticaret Anonim Sirketi Zastosowanie rozpuszczalników organicznych w granulacji na mokro moksyfloksacyny
US20110212990A1 (en) * 2008-11-06 2011-09-01 Hetero Research Foundation Novel polymorph of moxifloxacin hydrochloride
EA028676B1 (ru) 2008-12-08 2017-12-29 Рациофарм Гмбх Спрессованный моксифлоксацин
JP2012526793A (ja) 2009-05-15 2012-11-01 レッドエックス ファーマ リミテッド 酸化還元薬物誘導体
WO2011121596A2 (en) * 2010-04-01 2011-10-06 Neuland Laboratories Ltd. Crystal modification of moxifloxacin hydrochloride
BRPI1106900A2 (pt) 2011-12-26 2013-11-05 Ems Sa Composição farmacêutica sólida compreendendo antibótico da familia das quinolonas e processo de sua obtenção
FR2992218B1 (fr) 2012-06-22 2015-01-23 Rivopharm Sa Composition pharmaceutique de chlorhydrate de moxifloxacine et procede de preparation
CN102924449B (zh) * 2012-10-30 2015-08-12 重庆福安药业集团庆余堂制药有限公司 盐酸莫西沙星h晶型及其制备方法和药物组合物
WO2014087292A1 (en) 2012-12-04 2014-06-12 Mankind Research Centre An improved process for the preparation of moxifloxacin hydrochloride
RU2561037C2 (ru) * 2013-02-07 2015-08-20 Открытое акционерное общество "Химико-фармацевтический комбинат "АКРИХИН" (ОАО "АКРИХИН") Антибактериальная фармацевтическая композиция и способ ее получения
CA2904387C (en) 2013-03-15 2021-12-07 Melinta Therapeutics, Inc. Methods of treating infections in overweight and obese patients using antibiotics

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Publication number Priority date Publication date Assignee Title
DE3601567A1 (de) * 1986-01-21 1987-07-23 Bayer Ag 7-(azabicycloalkyl)-chinoloncarbonsaeure- und -naphthyridon-carbonsaeure-derivate
FI871419A7 (fi) * 1986-03-31 1987-10-01 Sankyo Co Kinoliini-3-karboksyylihappojohdannaiset, niiden valmistus ja käyttö
AU609974B2 (en) * 1988-05-18 1991-05-09 Warner-Lambert Company Improved process for the preparation of 5-amino-7- (substituted amino)-quinoline-3-carboxylic acids
DE3910663A1 (de) * 1989-04-03 1990-10-04 Bayer Ag 5-alkylchinoloncarbonsaeuren
RO108347B1 (ro) * 1989-10-30 1994-04-28 Bellon Labor Sa Roger DERIVATI DE BENZO-(b)-NAFTIRIDIN-1,8 SI PROCEDEU DE PREPARARE A ACESTORA
TW209865B (cs) 1992-01-10 1993-07-21 Bayer Ag
WO1993015070A1 (en) * 1992-01-31 1993-08-05 Chugai Seiyaku Kabushiki Kaisha Crystal of quinolonecarboxylic acid derivative hydrate
DE4234078A1 (de) * 1992-10-09 1994-04-14 Bayer Ag Chinoloncarbonsäuren
NO301165B1 (no) * 1992-12-25 1997-09-22 Daiichi Seiyaku Co Bicykliske aminderivater og antibakterielle midler inneholdende disse
ZA946853B (en) * 1993-09-10 1995-04-24 Daiichi Seiyaku Co Crystals of antimicrobial compound.
DK0676199T3 (da) * 1994-04-07 1999-02-08 Pfizer Anvendelse af trovafloxacin eller derivater deraf til fremstilling af et medikament til behandling af H. pylori-infektione

Also Published As

Publication number Publication date
CZ288657B6 (cs) 2001-08-15
YU49485B (sh) 2006-08-17
HUP9603428A2 (en) 1997-08-28
AR005009A1 (es) 1999-04-07
SK282805B6 (sk) 2002-12-03
BR9605968A (pt) 1998-08-18
DE19546249A1 (de) 1997-06-19
SI0780390T1 (en) 2002-10-31
BG101043A (en) 1998-04-30
CO4480105A1 (es) 1997-07-09
CZ364696A3 (en) 1997-07-16
TR199600970A2 (tr) 1997-06-21
PL317415A1 (en) 1997-06-23
SK159196A3 (en) 1997-10-08
UA35638C2 (uk) 2001-04-16
YU65096A (sh) 1998-12-23
HRP960558B1 (en) 2002-04-30
ES2179910T3 (es) 2003-02-01
JP4104687B2 (ja) 2008-06-18
JPH09169757A (ja) 1997-06-30
NZ299905A (en) 1998-09-24
ATE221531T1 (de) 2002-08-15
AU7421696A (en) 1997-06-19
NO965298D0 (no) 1996-12-11
SV1996000109A (es) 1997-10-23
HUP9603428A3 (en) 1997-10-28
BG62258B1 (bg) 1999-06-30
KR970042550A (ko) 1997-07-24
HU226521B1 (en) 2009-03-30
EP0780390A1 (de) 1997-06-25
CU22774A3 (es) 2002-07-24
KR100525146B1 (ko) 2006-01-27
HU9603428D0 (en) 1997-01-28
CN1160052A (zh) 1997-09-24
NL300109I1 (nl) 2003-02-03
CA2192418C (en) 2001-06-12
SA96170492B1 (ar) 2006-05-23
MY117492A (en) 2004-07-31
ID22625A (id) 1999-12-02
DE59609501D1 (de) 2002-09-05
NO306725B1 (no) 1999-12-13
NO965298L (no) 1997-06-13
TW411340B (en) 2000-11-11
US5849752A (en) 1998-12-15
IN185805B (cs) 2001-05-05
RO119782B1 (ro) 2005-03-30
CA2192418A1 (en) 1997-06-13
MX9606325A (es) 1997-10-31
EP0780390B1 (de) 2002-07-31
EE03474B1 (et) 2001-08-15
IL119795A0 (en) 1997-03-18
AU708006B2 (en) 1999-07-29
CN1061348C (zh) 2001-01-31
IL119795A (en) 1998-12-27
SG47201A1 (en) 1998-03-20
PL184885B1 (pl) 2003-01-31
MA24342A1 (fr) 1998-07-01
RU2162468C2 (ru) 2001-01-27
PT780390E (pt) 2002-11-29
DK0780390T3 (da) 2002-11-11
EE9600201A (et) 1997-06-16
HRP960558A2 (en) 1998-02-28

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