PE20081466A1 - Procedimiento para la preparacion de pradofloxacina - Google Patents
Procedimiento para la preparacion de pradofloxacinaInfo
- Publication number
- PE20081466A1 PE20081466A1 PE2007001419A PE2007001419A PE20081466A1 PE 20081466 A1 PE20081466 A1 PE 20081466A1 PE 2007001419 A PE2007001419 A PE 2007001419A PE 2007001419 A PE2007001419 A PE 2007001419A PE 20081466 A1 PE20081466 A1 PE 20081466A1
- Authority
- PE
- Peru
- Prior art keywords
- pradofloxacin
- procedure
- preparation
- fluoro
- ethanol
- Prior art date
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
-
- 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)
- Chemical Kinetics & Catalysis (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Communicable Diseases (AREA)
- Pharmacology & Pharmacy (AREA)
- Oncology (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Abstract
SE REFIERE A UN PROCEDIMIENTO PARA LA PREPARACION DE PRADOFLOXACINA DE FORMULA (I) EN EL QUE SE INTRODUCE UN SUSTITUYENTE EN LA POSICION 7 MEDIANTE UNA SUSTITUCION NUCLEOFILICA; QUE COMPRENDE EN LA REACCION DE UN 7-HALOGENOCIANUROFLUOROQUINOLONICO, PARTICULARMENTE EL ACIDO 7-CLORO-8-CIANO-1-CICLOPROPIL-6-FLUORO-1,4-DIHIDRO-4-OXO-3-QUINOLINCARBOXILICO CON UN COMPUESTO (1S,6S)-2,8-DIAZABICICLO[4.3.0]NONANO (TAMBIEN DESIGNADO COMO S,S-PIRROLOPIPERIDINA); REALIZANDOSE EN UNA MEZCLA DE DISOLVENTES DE N-METILPIRROLIDONA Y ETANOL DONDE AL MENOS CONTIENE 50% EN PESO DE ETANOL, DONDE LA PROPORCION DE LOS REACTANTES ES DE 1:1,01 A 1: 1,30
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE102006049520A DE102006049520A1 (de) | 2006-10-20 | 2006-10-20 | Verfahren zur Herstellung von Pradofloxacin |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| PE20081466A1 true PE20081466A1 (es) | 2008-12-18 |
Family
ID=38982832
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PE2007001419A PE20081466A1 (es) | 2006-10-20 | 2007-10-19 | Procedimiento para la preparacion de pradofloxacina |
Country Status (22)
| Country | Link |
|---|---|
| US (1) | US8497377B2 (es) |
| EP (1) | EP2086976B1 (es) |
| JP (2) | JP5830221B2 (es) |
| AR (1) | AR063227A1 (es) |
| AT (1) | ATE509930T1 (es) |
| AU (1) | AU2007312599B2 (es) |
| BR (1) | BRPI0718480B8 (es) |
| CA (1) | CA2666932C (es) |
| CL (1) | CL2007003007A1 (es) |
| DE (1) | DE102006049520A1 (es) |
| DK (1) | DK2086976T3 (es) |
| ES (1) | ES2365637T3 (es) |
| MX (1) | MX2009003200A (es) |
| NZ (1) | NZ576333A (es) |
| PE (1) | PE20081466A1 (es) |
| PL (1) | PL2086976T3 (es) |
| PT (1) | PT2086976E (es) |
| SI (1) | SI2086976T1 (es) |
| TW (1) | TW200823210A (es) |
| UY (1) | UY30646A1 (es) |
| WO (1) | WO2008046532A1 (es) |
| ZA (1) | ZA200902530B (es) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE102006049520A1 (de) * | 2006-10-20 | 2008-04-24 | Bayer Healthcare Ag | Verfahren zur Herstellung von Pradofloxacin |
Family Cites Families (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NZ331468A (en) | 1996-02-23 | 2000-02-28 | Bayer Ag | Substituted 8-cyano-1-cyclopropyl-7-(2,8-diazabicyclo-[4,3.0]-nonan-8-yl)-6-fluoro-1, 4-dihydro-4-oxo-3-quinolin carboxylic acids and their derivatives |
| DE19717231A1 (de) | 1997-04-24 | 1998-10-29 | Bayer Ag | 3-Cyano-2,4,5-trifluor-benzoylfluorid |
| DE19733243A1 (de) | 1997-08-01 | 1999-02-04 | Bayer Ag | Verfahren zur Herstellung von 3-Cyano-2,4-dihalogen-5-fluor-benzoesäure |
| 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 |
| DE10134719A1 (de) | 2001-07-17 | 2003-02-06 | Bayer Ag | Pharmazeutische Zubereitungen enthaltend wirkstoffbeladene Ionentauscherharze |
| DE10224086A1 (de) | 2002-05-31 | 2003-12-11 | Bayer Ag | Pharmazeutische Zubereitungen zur oralen Anwendung enthaltend wirkstoffbeladene Ionentauscherharze sowie strukturviskose Gelbildner als Verdicker |
| DE10312346A1 (de) | 2003-03-20 | 2004-09-30 | Bayer Healthcare Ag | Kontrolliertes Freisetzungssystem |
| DE10337191A1 (de) | 2003-08-13 | 2005-03-17 | Bayer Healthcare Ag | Neue Verwendung von Chinolon-Antibiotika |
| DE10351448A1 (de) | 2003-11-04 | 2005-06-09 | Bayer Healthcare Ag | Geschmackstoffhaltige Arzneimittelformulierungen mit verbesserten pharmazeutischen Eigenschaften |
| DE102005055385A1 (de) | 2004-12-09 | 2006-06-14 | Bayer Healthcare Ag | Arzneimittel zur hygienischen Applikation im Ohr |
| DE102006049520A1 (de) * | 2006-10-20 | 2008-04-24 | Bayer Healthcare Ag | Verfahren zur Herstellung von Pradofloxacin |
-
2006
- 2006-10-20 DE DE102006049520A patent/DE102006049520A1/de not_active Withdrawn
-
2007
- 2007-10-06 AU AU2007312599A patent/AU2007312599B2/en active Active
- 2007-10-06 PT PT07818763T patent/PT2086976E/pt unknown
- 2007-10-06 PL PL07818763T patent/PL2086976T3/pl unknown
- 2007-10-06 JP JP2009532704A patent/JP5830221B2/ja active Active
- 2007-10-06 ES ES07818763T patent/ES2365637T3/es active Active
- 2007-10-06 AT AT07818763T patent/ATE509930T1/de active
- 2007-10-06 MX MX2009003200A patent/MX2009003200A/es active IP Right Grant
- 2007-10-06 SI SI200730677T patent/SI2086976T1/sl unknown
- 2007-10-06 WO PCT/EP2007/008687 patent/WO2008046532A1/de not_active Ceased
- 2007-10-06 NZ NZ576333A patent/NZ576333A/en unknown
- 2007-10-06 EP EP07818763A patent/EP2086976B1/de active Active
- 2007-10-06 DK DK07818763.0T patent/DK2086976T3/da active
- 2007-10-06 BR BRPI0718480A patent/BRPI0718480B8/pt active IP Right Grant
- 2007-10-06 CA CA2666932A patent/CA2666932C/en active Active
- 2007-10-07 US US12/442,680 patent/US8497377B2/en active Active
- 2007-10-10 AR ARP070104475A patent/AR063227A1/es unknown
- 2007-10-16 UY UY30646A patent/UY30646A1/es not_active Application Discontinuation
- 2007-10-19 PE PE2007001419A patent/PE20081466A1/es not_active Application Discontinuation
- 2007-10-19 TW TW096139086A patent/TW200823210A/zh unknown
- 2007-10-19 CL CL200703007A patent/CL2007003007A1/es unknown
-
2009
- 2009-04-14 ZA ZA200902530A patent/ZA200902530B/xx unknown
-
2015
- 2015-09-01 JP JP2015171904A patent/JP2016028055A/ja active Pending
Also Published As
| Publication number | Publication date |
|---|---|
| DE102006049520A1 (de) | 2008-04-24 |
| CL2007003007A1 (es) | 2008-04-04 |
| CA2666932A1 (en) | 2008-04-24 |
| AU2007312599B2 (en) | 2013-11-14 |
| ATE509930T1 (de) | 2011-06-15 |
| JP2010506865A (ja) | 2010-03-04 |
| US20090318700A1 (en) | 2009-12-24 |
| DK2086976T3 (da) | 2011-09-05 |
| PL2086976T3 (pl) | 2011-10-31 |
| ZA200902530B (en) | 2010-07-28 |
| SI2086976T1 (sl) | 2011-09-30 |
| BRPI0718480A2 (pt) | 2014-02-18 |
| CA2666932C (en) | 2015-03-10 |
| JP2016028055A (ja) | 2016-02-25 |
| ES2365637T3 (es) | 2011-10-07 |
| UY30646A1 (es) | 2008-05-31 |
| EP2086976A1 (de) | 2009-08-12 |
| MX2009003200A (es) | 2009-04-07 |
| NZ576333A (en) | 2011-12-22 |
| AR063227A1 (es) | 2009-01-14 |
| BRPI0718480B1 (pt) | 2021-04-13 |
| WO2008046532A1 (de) | 2008-04-24 |
| JP5830221B2 (ja) | 2015-12-09 |
| PT2086976E (pt) | 2011-07-27 |
| EP2086976B1 (de) | 2011-05-18 |
| BRPI0718480B8 (pt) | 2022-09-20 |
| TW200823210A (en) | 2008-06-01 |
| US8497377B2 (en) | 2013-07-30 |
| AU2007312599A1 (en) | 2008-04-24 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| EA201270550A1 (ru) | Процесс получения соединений для применения в качестве ингибиторов sglt2 | |
| UY31832A (es) | Derivados de indazol sustituidos con fenilo y benzodioxinilo | |
| ECSP11011181A (es) | Compuestos orgánicos | |
| ECSP099044A (es) | Compuestos de pirimido fusionados | |
| PH12014500855A1 (en) | Novel substituted imidazopyrimidines as gpbar1 receptor modulators | |
| ECSP066856A (es) | Compuestos novedosos como moduladores del receptor opioide | |
| UY30824A1 (es) | Nuevos derivados de idazolil éster o amida, composiciones farmacéuticas conteniéndolas, procesos de preparacion y aplicaciones. | |
| UY33337A (es) | DERIVADOS SUSTITUIDOS DE 1H-PIRAZOL[ 3,4-d]PIRIMIDINA COMO INHIBIDORES DE LAS FOSFOINOSITIDA 3-QUINASAS | |
| CR20110313A (es) | Compuestos orgánicos | |
| UY29886A1 (es) | Derivados de pirazol novedosos, composiciones farmaccuticas que los contienen, procedimientos para la preparacinn de los mismos y aplicaciones | |
| PE20120495A1 (es) | 3-ciclopentilamino-2,2-difluor-propanoato de etilo como intermediario en la preparacion de pirimidodiazepinas | |
| CO6311106A2 (es) | Derivados novedosos del acido oleanólico con saturacion del anillo c | |
| PE20070845A1 (es) | Derivados de pirazolo[1,5-alfa]pirimidin utiles como receptores antagonistas del factor de liberacion de corticotropina (crf) | |
| CO6351723A2 (es) | Derivados de pirazolo-[5,1-b]-oxazol como antagonistas de crf1 | |
| AR073304A1 (es) | Moduladores del receptor de bradiquinina b2 de molecula pequena | |
| MX2013000773A (es) | Procedimiento de preparacion de derivados de amino-benzoil-benzofu rano. | |
| NI201000089A (es) | Derivados de pirazol como inhibidores de 5-lo. | |
| UY29798A1 (es) | Derivados de carboxamida como antagonistas del receptor muscarínico | |
| SV2011003808A (es) | Compuestos novedosos activos como antagonistas de receptor muscarinico | |
| UY30356A1 (es) | Derivados de 3-halo-n-(2.(4-fluorofenil)-4-oxobutil)-n-metil-5-(trifluorometil)benzamida y composiciones de los mismos. | |
| TW200714587A (en) | Biphenyl compounds useful as muscarinic receptor antagonists | |
| CR9595A (es) | Derivados de benzofurarona como moduladores no esteroides de receptores de progesterona | |
| UY31338A1 (es) | Compuestos novedosos activos como antagonistas de receptores muscarinicos | |
| PE20081466A1 (es) | Procedimiento para la preparacion de pradofloxacina | |
| UY29221A1 (es) | Derivados de octahidropirrolo(3,4-c)pirrol |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FD | Application declared void or lapsed |