ES2563210T3 - Cristales multicomponentes constituidos por éster etílico del ácido ([2-amino-6-(4-fluoro-bencilamino)-piridin-3-il]-carbámico y ácido 2-[2-[(2,6-diclorofenil)-amino]-fenil]-acético - Google Patents
Cristales multicomponentes constituidos por éster etílico del ácido ([2-amino-6-(4-fluoro-bencilamino)-piridin-3-il]-carbámico y ácido 2-[2-[(2,6-diclorofenil)-amino]-fenil]-acético Download PDFInfo
- Publication number
- ES2563210T3 ES2563210T3 ES11805489.9T ES11805489T ES2563210T3 ES 2563210 T3 ES2563210 T3 ES 2563210T3 ES 11805489 T ES11805489 T ES 11805489T ES 2563210 T3 ES2563210 T3 ES 2563210T3
- Authority
- ES
- Spain
- Prior art keywords
- amino
- dichlorophenyl
- pyridin
- phenyl
- ethyl ester
- Prior art date
- Legal status (The legal status 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 status listed.)
- Active
Links
- -1 4-fluoro-benzylamino Chemical group 0.000 title abstract 3
- 239000013078 crystal Substances 0.000 title abstract 2
- 125000004494 ethyl ester group Chemical group 0.000 title abstract 2
- JUUFBMODXQKSTD-UHFFFAOYSA-N N-[2-amino-6-[(4-fluorophenyl)methylamino]-3-pyridinyl]carbamic acid ethyl ester Chemical compound N1=C(N)C(NC(=O)OCC)=CC=C1NCC1=CC=C(F)C=C1 JUUFBMODXQKSTD-UHFFFAOYSA-N 0.000 abstract 1
- DCOPUUMXTXDBNB-UHFFFAOYSA-N diclofenac Chemical compound OC(=O)CC1=CC=CC=C1NC1=C(Cl)C=CC=C1Cl DCOPUUMXTXDBNB-UHFFFAOYSA-N 0.000 abstract 1
- 229960003667 flupirtine Drugs 0.000 abstract 1
Classifications
-
- 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
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/185—Acids; Anhydrides, halides or salts thereof, e.g. sulfur acids, imidic, hydrazonic or hydroximic acids
- A61K31/19—Carboxylic acids, e.g. valproic acid
- A61K31/195—Carboxylic acids, e.g. valproic acid having an amino group
- A61K31/196—Carboxylic acids, e.g. valproic acid having an amino group the amino group being directly attached to a ring, e.g. anthranilic acid, mefenamic acid, diclofenac, chlorambucil
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/04—Centrally acting analgesics, e.g. opioids
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C229/00—Compounds containing amino and carboxyl groups bound to the same carbon skeleton
- C07C229/40—Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino groups bound to carbon atoms of at least one six-membered aromatic ring and carboxyl groups bound to acyclic carbon atoms of the same carbon skeleton
- C07C229/42—Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino groups bound to carbon atoms of at least one six-membered aromatic ring and carboxyl groups bound to acyclic carbon atoms of the same carbon skeleton with carboxyl groups linked to the six-membered aromatic ring, or to the condensed ring system containing that ring, by saturated carbon chains
-
- 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
- C07D213/72—Nitrogen atoms
- C07D213/75—Amino or imino radicals, acylated by carboxylic or carbonic acids, or by sulfur or nitrogen analogues thereof, e.g. carbamates
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Veterinary Medicine (AREA)
- Pharmacology & Pharmacy (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Medicinal Chemistry (AREA)
- Epidemiology (AREA)
- General Chemical & Material Sciences (AREA)
- Pain & Pain Management (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Biomedical Technology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Neurosurgery (AREA)
- Engineering & Computer Science (AREA)
- Rheumatology (AREA)
- Neurology (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicinal Preparation (AREA)
- Pyridine Compounds (AREA)
Abstract
Cristal multicomponentes, caracterizado por que consiste en éster etílico del ácido ([2-amino-6-(4-fluorobencilamino)- piridin-3-il]-carbámico (flupirtina) y ácido 2-[2-[(2,6-diclorofenil)-amino]-fenil]-acético (diclofenaco).
Description
Claims (1)
-
imagen1 imagen2
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE102010063612 | 2010-12-20 | ||
| DE102010063612A DE102010063612A1 (de) | 2010-12-20 | 2010-12-20 | Neue Multikomponentenkristalle aus ([2-Amino-6-(4-fluoro-benzylamino)-pyridin-3-yl]-carbamidsäureethylester und 2-[2-[(2,6-Dichlorphenyl)-amino]-phenyl]-essigsäure |
| PCT/EP2011/073441 WO2012084975A1 (de) | 2010-12-20 | 2011-12-20 | Neue multikomponentenkristalle aus ([2-amino-6-(4-fluoro-benzylamino)-pyridin-3-yl]-carbamidsäureethylester und 2-[2-[(2,6-dichlorphenyl)-amino]-phenyl]-essigsäure |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ES2563210T3 true ES2563210T3 (es) | 2016-03-11 |
Family
ID=45463576
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES11805489.9T Active ES2563210T3 (es) | 2010-12-20 | 2011-12-20 | Cristales multicomponentes constituidos por éster etílico del ácido ([2-amino-6-(4-fluoro-bencilamino)-piridin-3-il]-carbámico y ácido 2-[2-[(2,6-diclorofenil)-amino]-fenil]-acético |
Country Status (9)
| Country | Link |
|---|---|
| US (1) | US9149468B2 (es) |
| EP (2) | EP3020705A1 (es) |
| CN (1) | CN103261162B (es) |
| CA (1) | CA2821311A1 (es) |
| DE (1) | DE102010063612A1 (es) |
| EA (1) | EA022016B1 (es) |
| ES (1) | ES2563210T3 (es) |
| PL (1) | PL2655328T3 (es) |
| WO (1) | WO2012084975A1 (es) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE102010063609A1 (de) * | 2010-12-20 | 2012-06-21 | Awd.Pharma Gmbh & Co. Kg | Neue Multikomponentenkristalle aus ([2-Amino-6-(4-fluoro-benzylamino)-pyridin-3yl)-carbamidsäureethylester und einer Arylpropionsäure |
Family Cites Families (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3601195A1 (de) * | 1985-01-23 | 1986-07-24 | Degussa Ag, 6000 Frankfurt | Synergistische kombination von flupirtin und nicht-steroidalen antiphlogistika |
| DE3665538D1 (en) * | 1985-01-23 | 1989-10-19 | Asta Pharma Ag | Synergistic combination of flupirtin and non-steroidal anti-phlogistics |
| FI855016A7 (fi) | 1985-06-28 | 1986-12-29 | Degussa | Flupirtiinin ja 4-asetamido-fenolin synergistinen yhdistelmä. |
| DE19705555A1 (de) | 1997-02-13 | 1998-08-20 | Ulrich Dr Posanski | Pharmazeutische Präparate der Thioctsäure zur oralen Anwendung |
| DE19716984A1 (de) | 1997-04-23 | 1998-10-29 | Asta Medica Ag | Verfahren zur Herstellung von reinem Flupirtin-Maleat und dessen Modifikation A |
| EP1701725B1 (en) | 2003-12-16 | 2013-07-31 | Relevare Aust. Pty Ltd | Compositions comprising flupirtine and an opioid for use in the treatment of neuropathic pain |
| US7553858B2 (en) | 2003-12-17 | 2009-06-30 | Meda Pharma Gmbh & Co. Kg | Combination of flupirtine and tramadol |
| US20090285862A1 (en) | 2006-05-03 | 2009-11-19 | Cnsbio Pty Ltd. | Methods and composition for treatment of inflammatory pain |
| EP2123626A1 (en) * | 2008-05-21 | 2009-11-25 | Laboratorios del Dr. Esteve S.A. | Co-crystals of duloxetine and co-crystal formers for the treatment of pain |
| US8222282B2 (en) * | 2008-06-09 | 2012-07-17 | Teva Pharmaceuticals Usa, Inc. | Sulfonate salts of 2-amino-3-carbethoxyamino-6-(4-fluoro-benzylamino)-pyridine |
| US8183267B2 (en) * | 2008-06-09 | 2012-05-22 | Awd. Pharma Gmbh & Co. Kg | Carboxylic acid salts of 2-amino-3-carbethoxyamino-6-(4-fluoro-benzylamino)-pyridine |
-
2010
- 2010-12-20 DE DE102010063612A patent/DE102010063612A1/de not_active Withdrawn
-
2011
- 2011-12-20 EP EP15194938.5A patent/EP3020705A1/de not_active Withdrawn
- 2011-12-20 EP EP11805489.9A patent/EP2655328B1/de not_active Not-in-force
- 2011-12-20 PL PL11805489T patent/PL2655328T3/pl unknown
- 2011-12-20 EA EA201300601A patent/EA022016B1/ru not_active IP Right Cessation
- 2011-12-20 ES ES11805489.9T patent/ES2563210T3/es active Active
- 2011-12-20 CN CN201180061511.9A patent/CN103261162B/zh not_active Expired - Fee Related
- 2011-12-20 WO PCT/EP2011/073441 patent/WO2012084975A1/de not_active Ceased
- 2011-12-20 US US13/992,247 patent/US9149468B2/en not_active Expired - Fee Related
- 2011-12-20 CA CA2821311A patent/CA2821311A1/en not_active Abandoned
Also Published As
| Publication number | Publication date |
|---|---|
| EP3020705A1 (de) | 2016-05-18 |
| US9149468B2 (en) | 2015-10-06 |
| EP2655328B1 (de) | 2015-11-18 |
| PL2655328T3 (pl) | 2016-07-29 |
| WO2012084975A1 (de) | 2012-06-28 |
| EA201300601A1 (ru) | 2013-09-30 |
| CN103261162B (zh) | 2016-06-15 |
| DE102010063612A1 (de) | 2012-06-21 |
| US20130261157A1 (en) | 2013-10-03 |
| EA022016B1 (ru) | 2015-10-30 |
| CN103261162A (zh) | 2013-08-21 |
| EP2655328A1 (de) | 2013-10-30 |
| CA2821311A1 (en) | 2012-06-28 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| ES2525918T3 (es) | Proceso para la fabricación de Nicorandil | |
| CY1122951T1 (el) | Φαρμακευτικα σκευασματα ενος αναστολεα υδροξυλασης ηιf | |
| ES2661582T3 (es) | Efecto antiinflamatorio de la celulosa microfibrilada | |
| ES2487271T3 (es) | Formulaciones de dosificación sólidas inhibidoras de DPP-IV | |
| CY1120805T1 (el) | Κρυσταλλικες μορφες αναστολεα προλυλο υδροξυλασης | |
| BR112014013872A2 (pt) | amidas dos ácidos n-(1,2,5-oxadiazol-3-il) -, n-(1,3,4-oxadiazol-2-il)-, n-(tetrazol - 5 - il) - e n - (triazol -5-il) - aril-carboxílico e sua utilização enquanto herbicidas | |
| UA110642C2 (uk) | Композиція гербіциду і сафенеру | |
| CU20120147A7 (es) | Procedimiento para la preparación de 4-{ 4-[({[4-cloro-3-(trifluorometil)fenil]amino}carbonil)amino]-3-fluorofenixi}-n-metilpiridina-2-carboxamida y su monohidrato | |
| EP2685505A4 (en) | THIN FILM TRANSISTOR, MANUFACTURING METHOD AND DISPLAY DEVICE THEREFOR | |
| CY1121895T1 (el) | Σκευασματα διαλυματος κατασκευασμενων αντισωματων anti-il-23p19 | |
| ES2421956B1 (es) | Nueva forma cristalina de sulfato de sitagliptina | |
| ECSP078030A (es) | Formas cristalinas y otras formas de las sales de ácido láctico de 4-amino-5-fluoro-3-[6-(4-metilpiperazin -1-il)-1h-bencimidazol-2 -il]-1h-quinolin-2-ona | |
| MX377589B (es) | Composiciones sólidas que comprenden agonista de glp-1 y sal del ácido n-(8-(2-hidroxibenzoil)amino)caprílico. | |
| CL2008003088A1 (es) | Metodo de preparacion de la sal de de maleato de (e)-n-{4-[3-cloro-4-(2-piridinilmetoxi)anilino]-3-ciano-7-etoxi-6-quinolinil}-4-(dimetilanino)-2-butenamida; formas cristalinas anhidra y monohidrato de la sal maleato; metodo de preparacion; composicion farmaceutica; utiles en el tratamiento de cancer. | |
| EA201200728A1 (ru) | Новые сокристаллы агомелатина, способ их получения и фармацевтические композиции, которые их содержат | |
| BR112015005369A2 (pt) | inibidores de usp30 e métodos para sua utilização | |
| CL2007003389A1 (es) | Formas cristalinas de sales de acido zoledronico; composicion farmaceutica; y uso en el tratamiento del cancer. | |
| CL2013000488A1 (es) | Co-cristales de compuestos derivados de (2r)-5-oxo-1-(bencilpiperidin-4-il)-n-(piridin-2-il)pirrolidin-2-carboxamida y un agente de formacion de co-cristales; sales de los compuestos; compuestos intermediarios; composicion farmaceutica; y su uso para el tratamiento de enfermedades inflamatorias e infecciosas. | |
| CL2013003563A1 (es) | Compuestos derivados de amidas del ácido gambógico y sus sales; composición farmacéutica que los comprende, útil en el tratamiento del glioblastoma. | |
| AR083268A1 (es) | Conjugado de naloxol-peg cristalino | |
| SV2009003286A (es) | Sal de potasio cristalina de analogos de lipoxina a4 | |
| CR10052A (es) | Proceso para la preparación de aminas | |
| ECSP11011286A (es) | Formulaciones orales sólidas de una pirido-pirimidinona | |
| ECSP13012608A (es) | Nuevas formas cristalinas de la sal sódica del ácido (4-{4-[5-(6-trifluoro-metil-piridin-3-il-amino)-piridin-2-il]-fenil}-ciclohexil)-acético | |
| ES2563210T3 (es) | Cristales multicomponentes constituidos por éster etílico del ácido ([2-amino-6-(4-fluoro-bencilamino)-piridin-3-il]-carbámico y ácido 2-[2-[(2,6-diclorofenil)-amino]-fenil]-acético |