CO4480105A1 - Nueva variante cristalina del cdch, procedimiento para su produccion y preparados farmaceuticos que la contienen - Google Patents

Nueva variante cristalina del cdch, procedimiento para su produccion y preparados farmaceuticos que la contienen

Info

Publication number
CO4480105A1
CO4480105A1 CO96064770A CO96064770A CO4480105A1 CO 4480105 A1 CO4480105 A1 CO 4480105A1 CO 96064770 A CO96064770 A CO 96064770A CO 96064770 A CO96064770 A CO 96064770A CO 4480105 A1 CO4480105 A1 CO 4480105A1
Authority
CO
Colombia
Prior art keywords
cdch
procedure
production
contain
pharmaceutical preparations
Prior art date
Application number
CO96064770A
Other languages
English (en)
Spanish (es)
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=CO4480105(A1) "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 CO4480105A1 publication Critical patent/CO4480105A1/es

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D471/00—Heterocyclic 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
    • C07D471/02—Heterocyclic 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
    • C07D471/04—Ortho-condensed systems
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/04—Antibacterial 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)
CO96064770A 1995-12-12 1996-12-10 Nueva variante cristalina del cdch, procedimiento para su produccion y preparados farmaceuticos que la contienen CO4480105A1 (es)

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
CO4480105A1 true CO4480105A1 (es) 1997-07-09

Family

ID=7779831

Family Applications (1)

Application Number Title Priority Date Filing Date
CO96064770A CO4480105A1 (es) 1995-12-12 1996-12-10 Nueva variante cristalina del cdch, procedimiento para su produccion y preparados farmaceuticos que la contienen

Country Status (42)

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

Families Citing this family (37)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2001517625A (ja) * 1997-09-25 2001-10-09 バイエル・アクチエンゲゼルシヤフト 活性成分放出制御薬物製剤
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
TR200101310T2 (tr) * 1998-11-10 2001-10-22 Bayer Aktiengesellschaft Farmasötik moksifloksasin preparatı.
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
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
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
US20060252789A1 (en) * 2002-10-31 2006-11-09 Sujay Biswas 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
WO2005012285A1 (en) * 2003-08-05 2005-02-10 Matrix Laboratories Ltd An improved 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
CN101484411A (zh) 2006-06-27 2009-07-15 桑多斯股份公司 盐的新制备方法
ES2303768B1 (es) * 2006-09-08 2009-06-05 Quimica Sintetica, S.A. Nueva forma cristalina de moxifloxacino clorhidrato.
JP2010509305A (ja) * 2006-11-13 2010-03-25 シプラ・リミテッド モキシフロキサシン塩酸塩の合成方法
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
ES2391132T3 (es) 2008-10-09 2012-11-21 Abdi Ibrahim Ilac Sanayi Ve Ticaret Anonim Sirketi Uso de disolventes orgánicos en la granulación húmeda de moxifloxacino
EP2342204A1 (en) * 2008-11-06 2011-07-13 Hetero Research Foundation Novel polymorph of moxifloxacin hydrochloride
WO2010066385A1 (de) 2008-12-08 2010-06-17 Ratiopharm Gmbh Kompaktiertes moxifloxacin
NZ610978A (en) 2009-05-15 2014-11-28 Redx Pharma Ltd Redox drug derivatives
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
EP2928892B1 (en) 2012-12-04 2018-03-21 Mankind Pharma Ltd. 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
KR102237887B1 (ko) 2013-03-15 2021-04-07 멜린타 서브시디어리 코프. 항생제를 사용하여 과체중 및 비만 환자에서 감염을 치료하는 방법

Family Cites Families (11)

* Cited by examiner, † Cited by third party
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
EP0241206A3 (en) * 1986-03-31 1989-05-10 Sankyo Company Limited Quinoline-3-carboxylic acid derivatives, their preparation and use
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 (https=) 1992-01-10 1993-07-21 Bayer Ag
CA2128601C (en) * 1992-01-31 2003-07-15 Hiroyuki Nagano Quinolone carboxylic acid derivatives in crystalline hydrate form
DE4234078A1 (de) 1992-10-09 1994-04-14 Bayer Ag Chinoloncarbonsäuren
CA2112165C (en) * 1992-12-25 2003-04-08 Makoto Takemura Bicyclic amine derivatives
ZA946853B (en) * 1993-09-10 1995-04-24 Daiichi Seiyaku Co Crystals of antimicrobial compound.
EP0676199B1 (en) * 1994-04-07 1998-09-02 Pfizer Inc. Use of trovafloxacin or derivatives thereof for the manufacture of a medicament for the treatment of H. pylori infections

Also Published As

Publication number Publication date
DE19546249A1 (de) 1997-06-19
HRP960558A2 (en) 1998-02-28
HUP9603428A3 (en) 1997-10-28
MY117492A (en) 2004-07-31
UA35638C2 (uk) 2001-04-16
BG101043A (en) 1998-04-30
KR970042550A (ko) 1997-07-24
RU2162468C2 (ru) 2001-01-27
BG62258B1 (bg) 1999-06-30
IL119795A0 (en) 1997-03-18
JP4104687B2 (ja) 2008-06-18
CZ288657B6 (cs) 2001-08-15
EE03474B1 (et) 2001-08-15
TR199600970A2 (tr) 1997-06-21
NZ299905A (en) 1998-09-24
ATE221531T1 (de) 2002-08-15
CU22774A3 (es) 2002-07-24
NL300109I1 (nl) 2003-02-03
SG47201A1 (en) 1998-03-20
IN185805B (https=) 2001-05-05
KR100525146B1 (ko) 2006-01-27
TW411340B (en) 2000-11-11
DK0780390T3 (da) 2002-11-11
CN1160052A (zh) 1997-09-24
AU708006B2 (en) 1999-07-29
SI0780390T1 (en) 2002-10-31
MA24342A1 (fr) 1998-07-01
CA2192418A1 (en) 1997-06-13
PL184885B1 (pl) 2003-01-31
EP0780390B1 (de) 2002-07-31
NO965298L (no) 1997-06-13
RO119782B1 (ro) 2005-03-30
BR9605968A (pt) 1998-08-18
HRP960558B1 (en) 2002-04-30
CA2192418C (en) 2001-06-12
PT780390E (pt) 2002-11-29
SK159196A3 (en) 1997-10-08
JPH09169757A (ja) 1997-06-30
YU49485B (sh) 2006-08-17
DE59609501D1 (de) 2002-09-05
HUP9603428A2 (en) 1997-08-28
PL317415A1 (en) 1997-06-23
US5849752A (en) 1998-12-15
NO306725B1 (no) 1999-12-13
SK282805B6 (sk) 2002-12-03
SA96170492B1 (ar) 2006-05-23
AU7421696A (en) 1997-06-19
ZA9610405B (en) 1997-06-23
IL119795A (en) 1998-12-27
AR005009A1 (es) 1999-04-07
MX9606325A (es) 1997-10-31
NO965298D0 (no) 1996-12-11
CN1061348C (zh) 2001-01-31
EP0780390A1 (de) 1997-06-25
ID22625A (id) 1999-12-02
SV1996000109A (es) 1997-10-23
YU65096A (sh) 1998-12-23
HU226521B1 (en) 2009-03-30
ES2179910T3 (es) 2003-02-01
CZ364696A3 (en) 1997-07-16
HU9603428D0 (en) 1997-01-28
EE9600201A (et) 1997-06-16

Similar Documents

Publication Publication Date Title
CO4480105A1 (es) Nueva variante cristalina del cdch, procedimiento para su produccion y preparados farmaceuticos que la contienen
OA09768A (en) Treatment of inflammation.
ES2005572A6 (es) Un procedimiento para la preparacion de nuevos derivados del tetrahidronaftaleno
ES2117034T3 (es) Composicion para la limpieza de vidrio.
FI882044A0 (fi) Orala doseringsformer med foerdroejd frigivning.
ES2009278A6 (es) Procedimiento para la preparacion de sulfato calcico alfa-hemidrato a partir de sulfato calcico dihidrato finamente dividido.
FR2353272A1 (fr) Dispositif accelerant la guerison des fractures osseuses
AR006401A1 (es) Compuestos de pirrolopirrolona, una composicion farmaceutica que los contiene, su uso en la fabricacion de un medicamento y en terapia, procesospara su preparación y compuestos intermediarios para dichos procesos.
ES2068705T3 (es) Tratamiento de la enfermedad neoplastica con interleuquina-10.
ES2129802T3 (es) Composicion para el tratamiento de agua y el saneamiento de suelos.
HU900669D0 (en) Process for the preparation of compounds useful as intermediates in the synthesis of tetrazole derivatives decreasing pathologically high cholestanol level of the blood
AR041865A1 (es) Derivados terapeuticos de prolina y su uso en el tratamiento de epilepsia y dolor
ES2134472T3 (es) Derivados de amida y su uso terapeutico.
ES2040201T3 (es) Acidos 3-piperidin- o 3-piridin-carboxilicos n-sustituidos y sus derivados.
AR240924A2 (es) "procedimiento para preparar derivados de 1,3-oxazolidin-2-ona y sus sales".
IT7852468A0 (it) Procedimento per produrre monocristalli purissimi di silicio
PE2591A1 (es) Composicion y metodo para reducir la afliccion gastrointestinal debido a azucares que contienen alfa-d-galactosidos
ES2064471T3 (es) Procedimiento para preparar cristales de sulfuro sodico anhidro.
ES8801173A1 (es) Procedimiento de producir agentes terapeuticos y profilacticos para ulceras pepticas
ES2127600T3 (es) Procedimiento para la purificacion de n-vinilpirrolidona mediante cristalizacion.
CA2225022A1 (en) New polymorphous form of doxazosine mesylate (form iii)
AR231796A1 (es) Mentonera miotatica con traccion anterior para el tratamiento del retrognatismo mandibular
HUT35519A (en) Process for producing of anelgetic medical preparatives
BE769392A (fr) Procede pour la preparation de charbon actif regenerable destine de preference a l'epuration des eaux
AR218690A1 (es) Procedimiento para producir dialquil(c1-c2)fosforocloridotionatos sustancialmente puros