MA34156B1 - Procédédepréparationde 4-{4-[({[4-chloro-3-(trifluorométhyl)-phényl]amino}carbonyl)amino]-3-fluorophénoxy}-n-éthylpyridine - Google Patents
Procédédepréparationde 4-{4-[({[4-chloro-3-(trifluorométhyl)-phényl]amino}carbonyl)amino]-3-fluorophénoxy}-n-éthylpyridineInfo
- Publication number
- MA34156B1 MA34156B1 MA35304A MA35304A MA34156B1 MA 34156 B1 MA34156 B1 MA 34156B1 MA 35304 A MA35304 A MA 35304A MA 35304 A MA35304 A MA 35304A MA 34156 B1 MA34156 B1 MA 34156B1
- Authority
- MA
- Morocco
- Prior art keywords
- amino
- trifluoromethyl
- carbonyl
- chloro
- phenyl
- Prior art date
Links
- WZKSXHQDXQKIQJ-UHFFFAOYSA-N F[C](F)F Chemical class F[C](F)F WZKSXHQDXQKIQJ-UHFFFAOYSA-N 0.000 title 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 1
- -1 {[4-chloro-3- (trifluoromethyl) -phenyl] amino} carbonyl Chemical group 0.000 abstract 1
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
- A61K31/4412—Non condensed pyridines; Hydrogenated derivatives thereof having oxo groups directly attached to the heterocyclic ring
-
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Epidemiology (AREA)
- Oncology (AREA)
- Hematology (AREA)
- Pyridine Compounds (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Containers And Plastic Fillers For Packaging (AREA)
Abstract
La présente invention concerne un procédé de préparation de 4-{4-[({[4-chloro-3-(trifluorométhyl)-phényl]amino}carbonyl)amino]
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP10004022 | 2010-04-15 | ||
| PCT/EP2011/055508 WO2011128261A1 (fr) | 2010-04-15 | 2011-04-08 | Procédé de préparation de 4-{4-[({[4-chloro-3-(trifluorométhyl)-phényl]amino}carbonyl)amino]-3-fluorophénoxy}-n-méthylpyridine-2-carboxamide, ses sels et son monohydrate |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| MA34156B1 true MA34156B1 (fr) | 2013-04-03 |
Family
ID=44070712
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MA35304A MA34156B1 (fr) | 2010-04-15 | 2011-04-08 | Procédédepréparationde 4-{4-[({[4-chloro-3-(trifluorométhyl)-phényl]amino}carbonyl)amino]-3-fluorophénoxy}-n-éthylpyridine |
Country Status (40)
| Country | Link |
|---|---|
| US (5) | US8748622B2 (fr) |
| EP (1) | EP2558448B1 (fr) |
| JP (1) | JP5934182B2 (fr) |
| KR (2) | KR20170129276A (fr) |
| CN (2) | CN103980191A (fr) |
| AR (2) | AR081060A1 (fr) |
| AU (1) | AU2011240113B2 (fr) |
| BR (1) | BR112012026117B1 (fr) |
| CA (1) | CA2796238C (fr) |
| CL (1) | CL2012002840A1 (fr) |
| CO (1) | CO6630136A2 (fr) |
| CR (1) | CR20120526A (fr) |
| CU (2) | CU24123B1 (fr) |
| DK (1) | DK2558448T3 (fr) |
| DO (2) | DOP2012000268A (fr) |
| EC (1) | ECSP12012234A (fr) |
| ES (1) | ES2542610T3 (fr) |
| GT (1) | GT201200280A (fr) |
| HK (1) | HK1200831A1 (fr) |
| HR (1) | HRP20150885T1 (fr) |
| HU (1) | HUE026821T2 (fr) |
| IL (2) | IL222348B (fr) |
| JO (1) | JO3158B1 (fr) |
| MA (1) | MA34156B1 (fr) |
| MX (1) | MX2012011734A (fr) |
| MY (2) | MY177066A (fr) |
| NZ (1) | NZ602997A (fr) |
| PE (2) | PE20130181A1 (fr) |
| PH (1) | PH12012502060A1 (fr) |
| PL (1) | PL2558448T3 (fr) |
| PT (1) | PT2558448E (fr) |
| RS (1) | RS54219B1 (fr) |
| RU (1) | RU2581585C2 (fr) |
| SG (2) | SG10201501221UA (fr) |
| SI (1) | SI2558448T1 (fr) |
| TN (1) | TN2012000492A1 (fr) |
| TW (2) | TWI539951B (fr) |
| UA (1) | UA110613C2 (fr) |
| UY (2) | UY33290A (fr) |
| WO (1) | WO2011128261A1 (fr) |
Families Citing this family (21)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DK1797038T3 (da) * | 2004-09-29 | 2012-09-03 | Bayer Pharma AG | Termodynamisk stabil form af bay 43-9006-tosylat |
| ATE482693T1 (de) | 2005-03-07 | 2010-10-15 | Bayer Schering Pharma Ag | Pharmazeutische zusammensetzung mit einem omega- carboxyaryl-substituierten diphenylharnstoff zur behandlung von krebs |
| 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 |
| AR092439A1 (es) | 2012-09-06 | 2015-04-22 | Bayer Healthcare Llc | Composicion farmaceutica recubierta que contiene regorafenib |
| EP2900269B1 (fr) | 2012-09-25 | 2018-08-01 | Bayer Pharma Aktiengesellschaft | Combinaison de régorafénib et d'acide acétylsalicylique destinée au traitement du cancer colorectal |
| CN104250227A (zh) * | 2013-06-29 | 2014-12-31 | 广东东阳光药业有限公司 | 瑞戈非尼新晶型及其制备方法 |
| WO2015049698A2 (fr) * | 2013-10-04 | 2015-04-09 | Hetero Research Foundation | Procédé pour le régorafénib |
| CN105218439B (zh) * | 2014-06-06 | 2018-11-20 | 连云港润众制药有限公司 | 一种瑞格非尼的晶体及其制备方法 |
| WO2016005874A1 (fr) * | 2014-07-09 | 2016-01-14 | Shilpa Medicare Limited | Procédé pour la préparation du régorafénib et ses formes cristallines |
| CN104557689B (zh) * | 2015-01-26 | 2016-06-29 | 重庆两江药物研发中心有限公司 | 制备4-[4-({[4-氯-3-(三氟甲基)苯基]氨基甲酰}氨基)-3-氟苯氧基]-n-甲基吡啶-2-甲酰胺及其一水合物的方法 |
| CN104592105B (zh) * | 2015-02-10 | 2017-01-18 | 杭州朱养心药业有限公司 | 瑞戈非尼及其制法 |
| CN105330600B (zh) * | 2015-11-30 | 2018-05-22 | 山东罗欣药业集团股份有限公司 | 一种瑞戈菲尼的制备方法 |
| SG11201806116SA (en) * | 2016-01-18 | 2018-08-30 | Natco Pharma Ltd | An improved process for the preparation of regorafenib |
| CN107118153A (zh) * | 2016-02-25 | 2017-09-01 | 石药集团中奇制药技术(石家庄)有限公司 | 一种瑞戈非尼一水合物晶型及其制备方法 |
| CN105879049B (zh) * | 2016-05-13 | 2019-03-26 | 浙江大学 | 一种瑞戈非尼与β-环糊精的包合物及其制备方法 |
| CA3244313A1 (en) | 2017-06-02 | 2025-06-13 | Bayer Healthcare Llc | Combination of regorafenib and pd-1/pd-l1(2) inhibitors for treating cancer |
| CN109438337B (zh) * | 2018-11-27 | 2019-08-09 | 广东安诺药业股份有限公司 | 一种瑞戈非尼中间体的制备工艺 |
| CN109438336B (zh) * | 2018-11-27 | 2019-11-22 | 广东安诺药业股份有限公司 | 一种瑞戈非尼水合物的制备方法 |
| EP3861989A1 (fr) | 2020-02-07 | 2021-08-11 | Bayer Aktiengesellschaft | Composition pharmaceutique contenant du régorafénib et un agent de stabilisation |
| WO2021160708A1 (fr) | 2020-02-14 | 2021-08-19 | Bayer Aktiengesellschaft | Combinaison de régorafenib et de msln-ttc pour traiter le cancer |
| CN114315710B (zh) * | 2022-01-07 | 2024-04-26 | 江苏豪森药业集团有限公司 | 一种制备或纯化瑞戈非尼的方法 |
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| US20080269265A1 (en) | 1998-12-22 | 2008-10-30 | Scott Miller | Inhibition Of Raf Kinase Using Symmetrical And Unsymmetrical Substituted Diphenyl Ureas |
| US8124630B2 (en) | 1999-01-13 | 2012-02-28 | Bayer Healthcare Llc | ω-carboxyaryl substituted diphenyl ureas as raf kinase inhibitors |
| ME00275B (fr) | 1999-01-13 | 2011-02-10 | Bayer Corp | DIPHENYLUREES A SUBSTITUANTS ω-CARBOXYARYLES, INHIBITRICES DE KINASE RAF |
| EP1158985B1 (fr) | 1999-01-13 | 2011-12-28 | Bayer HealthCare LLC | DIPHENYLE UREES A SUBSTITUTION OMEGA-CARBOXY ARYLE EN TANT QU'INHIBITEURS DE LA KINASE p38 |
| EP1140840B1 (fr) | 1999-01-13 | 2006-03-22 | Bayer Pharmaceuticals Corp. | Diphenylurees a substituants -g(v)-carboxyaryles, inhibitrices de kinase raf |
| US7235576B1 (en) | 2001-01-12 | 2007-06-26 | Bayer Pharmaceuticals Corporation | Omega-carboxyaryl substituted diphenyl ureas as raf kinase inhibitors |
| US7371763B2 (en) | 2001-04-20 | 2008-05-13 | Bayer Pharmaceuticals Corporation | Inhibition of raf kinase using quinolyl, isoquinolyl or pyridyl ureas |
| WO2003047579A1 (fr) | 2001-12-03 | 2003-06-12 | Bayer Pharmaceuticals Corporation | Composes de type uree aryle combines a d'autres agents cytostatiques ou cytotoxiques et servant a traiter des cancers humains |
| WO2003068229A1 (fr) | 2002-02-11 | 2003-08-21 | Bayer Pharmaceuticals Corporation | N-oxydes de pyridine, de quinoline, et d'isoquinoline en tant qu'inhibiteurs de kinase |
| US10653684B2 (en) | 2002-02-11 | 2020-05-19 | Bayer Healthcare Llc | Aryl ureas with angiogenisis inhibiting activity |
| SI1478358T1 (sl) | 2002-02-11 | 2013-09-30 | Bayer Healthcare Llc | Sorafenib tozilat za zdravljenje bolezni, značilnih po abnormalni angiogenezi |
| ATE529406T1 (de) | 2002-02-11 | 2011-11-15 | Bayer Healthcare Llc | Aryl-harnstoffe als kinase inhibitoren |
| US7557129B2 (en) | 2003-02-28 | 2009-07-07 | Bayer Healthcare Llc | Cyanopyridine derivatives useful in the treatment of cancer and other disorders |
| EP1636585B2 (fr) | 2003-05-20 | 2012-06-13 | Bayer HealthCare LLC | Diaryl-urees presentant une activite d'inhibition des kinases |
| EP1663978B1 (fr) * | 2003-07-23 | 2007-11-28 | Bayer Pharmaceuticals Corporation | Omega-carboxyaryldiphenyluree fluoro-subtituee pour le traitement et la prevention de maladies et d'etats pathologiques |
| EP2295426A1 (fr) | 2004-04-30 | 2011-03-16 | Bayer HealthCare, LLC | Derives de pyrazolyl uree substitues utiles dans le traitement du cancer |
| MY191349A (en) * | 2004-08-27 | 2022-06-17 | Bayer Pharmaceuticals Corp | New pharmaceutical compositions for the treatment of hyper-proliferative disorders |
| ATE395905T1 (de) | 2004-08-27 | 2008-06-15 | Bayer Pharmaceuticals Corp | Pharmazeutische zusammensetzungen in form fester dispersionen zur behandlung von krebs |
| EP1797037B1 (fr) | 2004-09-29 | 2014-12-17 | Bayer HealthCare LLC | Procede de preparation de 4-{4-[({[4-chloro-3-(trifluoromethyl)phenyl]amino}carbonyl)amino]phenoxy}-n-methylpyridine-2-carboxamide |
| DK1797038T3 (da) | 2004-09-29 | 2012-09-03 | Bayer Pharma AG | Termodynamisk stabil form af bay 43-9006-tosylat |
| ATE482693T1 (de) | 2005-03-07 | 2010-10-15 | Bayer Schering Pharma Ag | Pharmazeutische zusammensetzung mit einem omega- carboxyaryl-substituierten diphenylharnstoff zur behandlung von krebs |
| US20090215835A1 (en) | 2005-10-31 | 2009-08-27 | Scott Wilhelm | Treatment of cancer with sorafenib |
| JP2009515978A (ja) | 2005-11-14 | 2009-04-16 | バイエル ヘルスケア エルエルシー | Kit阻害剤に対する獲得耐性を伴う癌の治療 |
| 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 |
| US20100063112A1 (en) * | 2006-11-09 | 2010-03-11 | Bayer Schering Pharma Aktiengesellschaft | Polymorph iii of 4-[4-(amino)-3-fluorophenoxy]-n-methylpyridine-2-carboxamide |
| EP2089363A1 (fr) * | 2006-11-14 | 2009-08-19 | Bayer Schering Pharma Aktiengesellschaft | Polymorphe ii de 4-[4-({[4-chloro-3-(trifluorométhyl)phényl]carbamoyl}amino)-3-fluorophénoxy]-n-méthylpyridine-2-carboxamide |
| AU2007336873A1 (en) | 2006-12-20 | 2008-07-03 | Bayer Healthcare Llc | 4-{4-[({3-tert-Butyl-1-[3-(hydroxymethyl) phenyl]-1H-pyrazol-5-yl } carbamoyl)-amino] -3-fluorophenoxy} -N-methylpyridine-2-carboxamide as well as prodrugs and salts thereof for the treatment of cancer |
| JP2010516692A (ja) | 2007-01-19 | 2010-05-20 | バイエル・ヘルスケア・エルエルシー | 化学療法剤に対し抵抗性を有する癌の処置 |
| CA2675980C (fr) | 2007-01-19 | 2016-06-21 | Bayer Healthcare Llc | Utilisation de dast dans le traitement des cancers a resistance acquise a des inhibiteurs de kit |
| EP2156834A1 (fr) * | 2008-08-08 | 2010-02-24 | S.I.F.I - Società Industria Farmaceutica Italiana - S.P.A. | Compositions pharmaceutiques ophtalmiques comprenant du Sorafenib pour le traitement de pathologies néoangiogéniques de l'ýil |
| JP5439494B2 (ja) | 2008-10-21 | 2014-03-12 | バイエル ヘルスケア エルエルシー | 肝細胞癌と関連するシグネチャ遺伝子の同定 |
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| 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 |
| CA2805874A1 (fr) | 2010-07-19 | 2012-01-26 | Bayer Healthcare Llc | Associations medicamenteuses contenant une omega-carboxyaryl diphenyluree fluorosubstituee utilisees pour le traitement et la prevention de maladies et d'affections |
| US9381177B2 (en) | 2010-10-01 | 2016-07-05 | Bayer Intellectual Property Gmbh | Substituted N-(2-arylamino)aryl sulfonamide-containing combinations |
| CN103764118A (zh) | 2011-06-28 | 2014-04-30 | 拜尔健康护理有限责任公司 | 含有索拉非尼的局部眼用药用组合物 |
| KR20140048218A (ko) | 2011-06-28 | 2014-04-23 | 바이엘 헬스케어 엘엘씨 | 레고라페닙을 함유하는 국소 안과용 약학 조성물 |
| US8841500B2 (en) | 2011-11-08 | 2014-09-23 | Chevron U.S.A. Inc. | Preparation of alkyl aromatic compounds |
| JP2014032346A (ja) | 2012-08-06 | 2014-02-20 | Japan Display Inc | 液晶表示パネル |
| AR092439A1 (es) | 2012-09-06 | 2015-04-22 | Bayer Healthcare Llc | Composicion farmaceutica recubierta que contiene regorafenib |
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2011
- 2011-03-23 AR ARP110100982A patent/AR081060A1/es not_active Application Discontinuation
- 2011-03-24 UY UY0001033290A patent/UY33290A/es active IP Right Grant
- 2011-04-08 EP EP20110712881 patent/EP2558448B1/fr active Active
- 2011-04-08 AU AU2011240113A patent/AU2011240113B2/en active Active
- 2011-04-08 MA MA35304A patent/MA34156B1/fr unknown
- 2011-04-08 JP JP2013504206A patent/JP5934182B2/ja active Active
- 2011-04-08 KR KR1020177032906A patent/KR20170129276A/ko not_active Ceased
- 2011-04-08 WO PCT/EP2011/055508 patent/WO2011128261A1/fr not_active Ceased
- 2011-04-08 NZ NZ602997A patent/NZ602997A/en unknown
- 2011-04-08 PL PL11712881T patent/PL2558448T3/pl unknown
- 2011-04-08 HU HUE11712881A patent/HUE026821T2/en unknown
- 2011-04-08 ES ES11712881.9T patent/ES2542610T3/es active Active
- 2011-04-08 SI SI201130559T patent/SI2558448T1/sl unknown
- 2011-04-08 BR BR112012026117-7A patent/BR112012026117B1/pt active IP Right Grant
- 2011-04-08 PE PE2012002008A patent/PE20130181A1/es active IP Right Grant
- 2011-04-08 PT PT117128819T patent/PT2558448E/pt unknown
- 2011-04-08 CN CN201410248545.4A patent/CN103980191A/zh active Pending
- 2011-04-08 CA CA2796238A patent/CA2796238C/fr active Active
- 2011-04-08 MY MYPI2016001879A patent/MY177066A/en unknown
- 2011-04-08 KR KR1020127026728A patent/KR101800041B1/ko active Active
- 2011-04-08 RU RU2012148386/04A patent/RU2581585C2/ru active
- 2011-04-08 CU CU20120147A patent/CU24123B1/es active IP Right Grant
- 2011-04-08 SG SG10201501221UA patent/SG10201501221UA/en unknown
- 2011-04-08 US US13/640,959 patent/US8748622B2/en active Active
- 2011-04-08 DK DK11712881.9T patent/DK2558448T3/en active
- 2011-04-08 MY MYPI2012004548A patent/MY162359A/en unknown
- 2011-04-08 CN CN201180019150.1A patent/CN102947271B/zh active Active
- 2011-04-08 HR HRP20150885TT patent/HRP20150885T1/hr unknown
- 2011-04-08 SG SG2012069852A patent/SG184172A1/en unknown
- 2011-04-08 PH PH1/2012/502060A patent/PH12012502060A1/en unknown
- 2011-04-08 PE PE2016000780A patent/PE20160838A1/es unknown
- 2011-04-08 RS RS20150528A patent/RS54219B1/sr unknown
- 2011-04-08 MX MX2012011734A patent/MX2012011734A/es active IP Right Grant
- 2011-04-13 JO JOP/2011/0125A patent/JO3158B1/ar active
- 2011-04-14 TW TW103141317A patent/TWI539951B/zh active
- 2011-04-14 TW TW100112905A patent/TWI475992B/zh active
- 2011-08-04 UA UAA201212983A patent/UA110613C2/uk unknown
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2012
- 2012-10-08 EC ECSP12012234 patent/ECSP12012234A/es unknown
- 2012-10-10 CL CL2012002840A patent/CL2012002840A1/es unknown
- 2012-10-11 IL IL222348A patent/IL222348B/en active IP Right Grant
- 2012-10-11 GT GT201200280A patent/GT201200280A/es unknown
- 2012-10-12 DO DO2012000268A patent/DOP2012000268A/es unknown
- 2012-10-12 TN TNP2012000492A patent/TN2012000492A1/en unknown
- 2012-10-12 CO CO12180992A patent/CO6630136A2/es not_active Application Discontinuation
- 2012-10-16 CR CR20120526A patent/CR20120526A/es unknown
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2014
- 2014-04-15 US US14/252,850 patent/US9458107B2/en active Active
- 2014-05-26 CU CU2014000060A patent/CU20140060A7/es unknown
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2015
- 2015-02-10 HK HK15101433.6A patent/HK1200831A1/xx unknown
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2016
- 2016-09-08 US US15/259,576 patent/US20170057918A1/en not_active Abandoned
- 2016-10-20 DO DO2016000285A patent/DOP2016000285A/es unknown
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2017
- 2017-06-22 IL IL253119A patent/IL253119B/en active IP Right Grant
- 2017-08-03 US US15/668,178 patent/US20170334857A1/en not_active Abandoned
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2019
- 2019-01-09 US US16/243,284 patent/US10822305B2/en active Active
- 2019-09-13 AR ARP190102596A patent/AR116395A2/es unknown
-
2021
- 2021-12-23 UY UY0001039590A patent/UY39590A/es unknown
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