PE20142042A1 - Forma termodinamicamente estable de una sal tosilato de sorafenib - Google Patents
Forma termodinamicamente estable de una sal tosilato de sorafenibInfo
- Publication number
- PE20142042A1 PE20142042A1 PE2014000731A PE2014000731A PE20142042A1 PE 20142042 A1 PE20142042 A1 PE 20142042A1 PE 2014000731 A PE2014000731 A PE 2014000731A PE 2014000731 A PE2014000731 A PE 2014000731A PE 20142042 A1 PE20142042 A1 PE 20142042A1
- Authority
- PE
- Peru
- Prior art keywords
- salt
- thermodynamically stable
- stable form
- tosilate
- amino
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D213/78—Carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen, e.g. ester or nitrile radicals
- C07D213/81—Amides; Imides
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
- A61P35/02—Antineoplastic agents specific for leukemia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P7/00—Drugs for disorders of the blood or the extracellular fluid
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Hematology (AREA)
- Oncology (AREA)
- Diabetes (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Pyridine Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Medicinal Preparation (AREA)
- Paper (AREA)
- Catalysts (AREA)
- Glass Compositions (AREA)
- Analysing Materials By The Use Of Radiation (AREA)
Abstract
REFERIDO A UN COMPUESTO TERMODINAMICAMENTE ESTABLE A TEMPERATURA AMBIENTE, DE LA SAL TOSILATO DE 4-{4-[({[4-CLORO-3-(TRIFLUOROMETIL) FENIL]AMINO}CARBONIL)AMINO]FENOXI}-N-METILPIRIDIN-2-CARBOXAMIDA. DICHO COMPUESTO MUESTRA EN LA DIFRACTOMETRIA DE RAYOS X EL PICO MAXIMO DE 2 THETA ANGULO DE 4.4, 10.7, 11.1, 11.4 ENTRE OTROS. SE REFIERE TAMBIEN A UNA COMPOSICION FARMACEUTICA, SIENDO UTIL EN EL TRATAMIENTO DE RETINOPATIA, ARTRITIS REUMATOIDEA, ENTRE OTRAS.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP04023130 | 2004-09-29 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| PE20142042A1 true PE20142042A1 (es) | 2014-12-03 |
Family
ID=35482258
Family Applications (3)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PE2009001132A PE20100445A1 (es) | 2004-09-29 | 2005-09-28 | Forma termodinamicamente estable de una sal tosilato de sorafenib |
| PE2014000731A PE20142042A1 (es) | 2004-09-29 | 2005-09-28 | Forma termodinamicamente estable de una sal tosilato de sorafenib |
| PE2005001145A PE20060699A1 (es) | 2004-09-29 | 2005-09-28 | Forma termodinamicamente estable de una sal tosilato |
Family Applications Before (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PE2009001132A PE20100445A1 (es) | 2004-09-29 | 2005-09-28 | Forma termodinamicamente estable de una sal tosilato de sorafenib |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PE2005001145A PE20060699A1 (es) | 2004-09-29 | 2005-09-28 | Forma termodinamicamente estable de una sal tosilato |
Country Status (32)
| Country | Link |
|---|---|
| US (1) | US8877933B2 (es) |
| EP (1) | EP1797038B1 (es) |
| JP (2) | JP5215666B2 (es) |
| KR (4) | KR20070058537A (es) |
| CN (1) | CN101065360B (es) |
| AR (1) | AR051301A1 (es) |
| AU (1) | AU2005289100B2 (es) |
| BR (1) | BRPI0515946A (es) |
| CA (1) | CA2581843C (es) |
| CU (1) | CU20070068A7 (es) |
| CY (1) | CY1113598T1 (es) |
| DK (1) | DK1797038T3 (es) |
| EC (1) | ECSP077356A (es) |
| ES (1) | ES2387812T3 (es) |
| GT (1) | GT200500270A (es) |
| HN (1) | HN2005000722A (es) |
| HR (1) | HRP20120662T1 (es) |
| IL (1) | IL181734A (es) |
| MA (1) | MA28880B1 (es) |
| MY (1) | MY176929A (es) |
| NO (1) | NO344272B1 (es) |
| NZ (1) | NZ553804A (es) |
| PE (3) | PE20100445A1 (es) |
| PL (1) | PL1797038T3 (es) |
| PT (1) | PT1797038E (es) |
| SG (1) | SG155996A1 (es) |
| SI (1) | SI1797038T1 (es) |
| TW (1) | TWI382016B (es) |
| UA (1) | UA91520C2 (es) |
| UY (1) | UY29144A1 (es) |
| WO (1) | WO2006034797A1 (es) |
| ZA (1) | ZA200702510B (es) |
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| HK1042251B (en) | 1999-01-13 | 2012-07-20 | Bayer Healthcare Llc | Omega-carboxy aryl substituted diphenyl ureas as p38 kinase inhibitors |
| US8124630B2 (en) | 1999-01-13 | 2012-02-28 | Bayer Healthcare Llc | ω-carboxyaryl substituted diphenyl ureas as raf kinase inhibitors |
| US10653684B2 (en) | 2002-02-11 | 2020-05-19 | Bayer Healthcare Llc | Aryl ureas with angiogenisis inhibiting activity |
| EP1478358B1 (en) | 2002-02-11 | 2013-07-03 | Bayer HealthCare LLC | Sorafenib tosylate for the treatment of diseases characterized by abnormal angiogenesis |
| UY28213A1 (es) | 2003-02-28 | 2004-09-30 | Bayer Pharmaceuticals Corp | Nuevos derivados de cianopiridina útiles en el tratamiento de cáncer y otros trastornos. |
| PT1626714E (pt) * | 2003-05-20 | 2007-08-24 | Bayer Pharmaceuticals Corp | Diarilureias para doenças mediadas por pdgfr |
| DE602004010407T2 (de) | 2003-07-23 | 2008-10-16 | Bayer Pharmaceuticals Corp., West Haven | Fluorsubstituierter omega-carboxyaryldiphenylharnstoff zur behandlung und prävention von krankheiten und leiden |
| PL1797038T3 (pl) | 2004-09-29 | 2012-11-30 | Bayer Healthcare Llc | Termodynamicznie trwała postać tosylanu bay 43-9006 |
| MX2007010856A (es) | 2005-03-07 | 2007-11-12 | Bayer Healthcare Ag | Composicion farmaceutica que comprende una difenilurea sustituida con omega-carboxiarilo para el tratamiento del cancer. |
| EP1968589A2 (en) | 2005-10-31 | 2008-09-17 | Bayer Pharmaceuticals Corporation | Combinations comprising sorafenib and interferon for the treatment of cancer |
| AR062927A1 (es) * | 2006-10-11 | 2008-12-17 | Bayer Healthcare Ag | 4- [4-( [ [ 4- cloro-3-( trifluorometil) fenil) carbamoil] amino] -3- fluorofenoxi) -n- metilpiridin-2- carboxamida monohidratada |
| WO2008058644A1 (en) * | 2006-11-14 | 2008-05-22 | Bayer Schering Pharma Aktiengesellschaft | Polymorph ii of 4-[4-({[4-chloro-3-(trifluoromethyl)phenyl]carbamoyl}amino)-3-fluorophenoxy]-n-methylpyridine-2-carboxamide |
| CN101220024A (zh) * | 2007-12-11 | 2008-07-16 | 杜晓敏 | 一组抑制激酶的抗癌化合物 |
| EP2231612A1 (en) * | 2008-01-17 | 2010-09-29 | Sicor, Inc. | Polymorph form iii of sorafenib tosylate, sorafenib tosylate methanol solvate and sorafenib tosylate ethanol solvate, and processes for preparation thereof |
| WO2009106825A1 (en) * | 2008-02-27 | 2009-09-03 | Cipla Limited | Polymorphs of sorafenib and salts thereof |
| WO2010079498A2 (en) * | 2009-01-12 | 2010-07-15 | Hetero Research Foundation | Novel polymorph of sorafenib tosylate |
| AU2009344660A1 (en) * | 2009-04-15 | 2011-11-17 | Fondazione Irccs Istituto Nazionale Dei Tumori | Use of multi-kinase inhibitors in the treatment of vascular hyperpermeability |
| WO2010142678A2 (en) * | 2009-06-12 | 2010-12-16 | Ratiopharm Gmbh | Polymorphs of 4-[4-[[4-chloro-3-(trifluoromethyl)phenyl]carbamoylamino]phenoxy]-n-methyl-pyridine-2-carboxamide |
| CA2775296A1 (en) | 2009-09-24 | 2011-03-31 | Ranbaxy Laboratories Limited | Polymorphs of sorafenib acid addition salts |
| EP2480534A1 (en) | 2009-09-24 | 2012-08-01 | Ranbaxy Laboratories Limited | Process for the preparation of sorafenib tosylate |
| EP2499116A1 (en) | 2009-11-12 | 2012-09-19 | Ranbaxy Laboratories Limited | Sorafenib ethylsulfonate salt, process for preparation and use |
| WO2011076711A2 (en) | 2009-12-23 | 2011-06-30 | Ratiopharm Gmbh | Polymorphs of 4-[4-[[4-chloro-3-(trifluoromethyl)phenyl]carbamoylamino]phenoxy]-n-methylpyridine-2-carboxamide |
| US8618305B2 (en) | 2010-01-29 | 2013-12-31 | Ranbaxy Laboratories Limited | Sorafenib dimethyl sulphoxide solvate |
| AR081060A1 (es) | 2010-04-15 | 2012-06-06 | Bayer Schering Pharma Ag | Procedimiento para preparar 4-{4-[({[4-cloro-3-(trifluorometil)fenil]amino}carbonil)amino]-3-fluorofenoxi}-n-metilpiridin-2-carboxamida |
| MX2013003695A (es) | 2010-10-01 | 2013-05-20 | Bayer Ip Gmbh | Combinaciones que contienen n-(2-arilamino) arilsulfonamida sustituida. |
| WO2012071425A1 (en) | 2010-11-22 | 2012-05-31 | Teva Pharmaceutical Industries Ltd. | Solid state forms of sorafenib besylate, and processes for preparations thereof |
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| EP2559431A1 (en) | 2011-08-17 | 2013-02-20 | Ratiopharm GmbH | Pharmaceutical composition comprising 4-[4-[[4-chloro-3-(trifluoromethyl)phenyl]carbamoylamino]phenoxy]-N-methyl-pyridine-2-carboxamide |
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