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)
- Containers And Plastic Fillers For Packaging (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (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) | CN102947271B (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) | PE20160838A1 (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 |
|---|---|---|---|---|
| UA91520C2 (en) * | 2004-09-29 | 2010-08-10 | Баер Шеринг Фарма Акциенгезельшафт | Thermodynamically stable form of tosylate |
| PT1868579E (pt) | 2005-03-07 | 2010-12-03 | Bayer Schering Pharma Ag | Composição farmacêutica que compreende uma difenil-ureia substituída com um omega-carboxiarilo para o tratamento do cancro |
| 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 |
| SG11201501963RA (en) | 2012-09-25 | 2015-04-29 | Bayer Pharma AG | Combination of regorafenib and acetylsalicylic acid for treating cancer |
| 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 |
| US9518020B2 (en) | 2013-10-04 | 2016-12-13 | Hetero Research Foundation | Process for Regorafenib |
| 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 |
| US9790185B2 (en) | 2014-07-09 | 2017-10-17 | Shilpa Medicare Limited | Process for the preparation of regorafenib and its crystalline forms |
| 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 |
| CA3011662A1 (fr) * | 2016-01-18 | 2017-07-27 | Natco Pharma Ltd | Procede ameliore pour la preparation de 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 |
| 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 |
| 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 |
| 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 |
Family Cites Families (43)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6187799B1 (en) | 1997-05-23 | 2001-02-13 | Onyx Pharmaceuticals | Inhibition of raf kinase activity using aryl ureas |
| US7329670B1 (en) | 1997-12-22 | 2008-02-12 | Bayer Pharmaceuticals Corporation | Inhibition of RAF kinase using aryl and heteroaryl substituted heterocyclic ureas |
| US7517880B2 (en) | 1997-12-22 | 2009-04-14 | Bayer Pharmaceuticals Corporation | Inhibition of p38 kinase using symmetrical and unsymmetrical diphenyl ureas |
| US20080269265A1 (en) | 1998-12-22 | 2008-10-30 | Scott Miller | Inhibition Of Raf Kinase Using Symmetrical And Unsymmetrical Substituted Diphenyl Ureas |
| JP2002534468A (ja) | 1999-01-13 | 2002-10-15 | バイエル コーポレイション | p38キナーゼ阻害剤としてのω−カルボキシアリール置換ジフェニル尿素 |
| ME00275B (fr) | 1999-01-13 | 2011-02-10 | Bayer Corp | DIPHENYLUREES A SUBSTITUANTS ω-CARBOXYARYLES, INHIBITRICES DE KINASE RAF |
| EP1140840B1 (fr) | 1999-01-13 | 2006-03-22 | Bayer Pharmaceuticals Corp. | Diphenylurees a substituants -g(v)-carboxyaryles, inhibitrices de kinase raf |
| US8124630B2 (en) | 1999-01-13 | 2012-02-28 | Bayer Healthcare Llc | ω-carboxyaryl substituted diphenyl ureas as raf kinase inhibitors |
| 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 |
| RU2316326C2 (ru) | 2001-12-03 | 2008-02-10 | Байер Фамэсьютиклс Копэрейшн | Способ и композиция для лечения ракового заболевания, тозилат и фармацевтически приемлемые соли n-(4-хлор-3-(трифторметил)фенил)-n'-(4-(2-(n-метилкарбамоил)-4-пиридилокси)фенил)мочевины |
| US20030216396A1 (en) | 2002-02-11 | 2003-11-20 | Bayer Corporation | Pyridine, quinoline, and isoquinoline N-oxides as kinase inhibitors |
| US10653684B2 (en) | 2002-02-11 | 2020-05-19 | Bayer Healthcare Llc | Aryl ureas with angiogenisis inhibiting activity |
| PT1580188E (pt) | 2002-02-11 | 2012-01-25 | Bayer Healthcare Llc | Aril-ureias como inibidores de cinases |
| PT1478358E (pt) | 2002-02-11 | 2013-09-11 | Bayer Healthcare Llc | Tosilato de sorafenib para o tratamento de doenças caracterizadas por angiogénese anormal |
| UY28213A1 (es) | 2003-02-28 | 2004-09-30 | Bayer Pharmaceuticals Corp | Nuevos derivados de cianopiridina útiles en el tratamiento de cáncer y otros trastornos. |
| DK1636585T3 (da) | 2003-05-20 | 2008-05-26 | Bayer Pharmaceuticals Corp | Diarylurinstoffer med kinasehæmmende aktivitet |
| PT1663978E (pt) | 2003-07-23 | 2008-02-15 | Bayer Pharmaceuticals Corp | Omega-carboxiaril difenil ureia substituída por flúor para o tratamento e a prevenção de doenças e estados patológicos |
| MXPA06012394A (es) | 2004-04-30 | 2007-01-31 | Bayer Pharmaceuticals Corp | Derivados de pirazolilurea sustituidos utiles en el tratamiento de cancer. |
| MX2007002398A (es) | 2004-08-27 | 2007-05-15 | Bayer Pharmaceuticals Corp | Nuevas composiciones farmaceuticas para el tratamiento de cancer. |
| MY191349A (en) * | 2004-08-27 | 2022-06-17 | Bayer Pharmaceuticals Corp | New pharmaceutical compositions for the treatment of hyper-proliferative disorders |
| ES2532377T3 (es) | 2004-09-29 | 2015-03-26 | Bayer Healthcare Llc | Procedimiento de preparación de 4-{4-[({[4-[cloro-3-(trifluorometil)fenil]amino}carbonil) amino]fenoxi}N-metilpiridina-2-carboxamida |
| UA91520C2 (en) | 2004-09-29 | 2010-08-10 | Баер Шеринг Фарма Акциенгезельшафт | Thermodynamically stable form of tosylate |
| PT1868579E (pt) | 2005-03-07 | 2010-12-03 | Bayer Schering Pharma Ag | Composição farmacêutica que compreende uma difenil-ureia substituída com um omega-carboxiarilo para o tratamento do cancro |
| US20090215835A1 (en) | 2005-10-31 | 2009-08-27 | Scott Wilhelm | Treatment of cancer with sorafenib |
| WO2007059154A2 (fr) | 2005-11-14 | 2007-05-24 | Bayer Healthcare Llc | Traitement de cancers a resistance acquise a des inhibiteurs de kit |
| 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 |
| CA2668748A1 (fr) * | 2006-11-09 | 2008-05-15 | Bayer Schering Pharma Aktiengesellschaft | Polymorphe iii de 4-[4-({[4-chloro-3-(trifluoromethyl)phenyl]carbamoyl}amino)-3-fluorophenoxy]-n-methylpyridine-2-carboxamide |
| WO2008058644A1 (fr) * | 2006-11-14 | 2008-05-22 | Bayer Schering Pharma Aktiengesellschaft | Polymorphe ii de 4-[4-({[4-chloro-3-(trifluorométhyl)phényl]carbamoyl}amino)-3-fluorophénoxy]-n-méthylpyridine-2-carboxamide |
| WO2008079968A1 (fr) | 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 ainsi que des promédicaments et des sels de ceux-ci utilisés pour traiter un cancer |
| EP2114403A2 (fr) | 2007-01-19 | 2009-11-11 | Bayer Healthcare, LLC | Traitement de cancers présentant une résistance à des agents chimiothérapeutiques |
| WO2008089389A2 (fr) | 2007-01-19 | 2008-07-24 | Bayer Healthcare Llc | Traitement de cancers à résistance acquise aux inhibiteurs 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 |
| RU2011150619A (ru) | 2009-05-15 | 2013-06-20 | Новартис Аг | Комбинация ингибитора фосфоинозитид-3-киназы и противодиабетического соединения |
| 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 |
| US20130183268A1 (en) | 2010-07-19 | 2013-07-18 | Bayer Healthcare Llc | Drug combinations with fluoro-substituted omega-carboxyaryl diphenyl urea for the treatment and prevention of diseases and conditions |
| PE20140165A1 (es) | 2010-10-01 | 2014-02-26 | Bayer Ip Gmbh | Combinaciones que contienen n-(2-arilamino)arilsulfonamida |
| 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 |
| AP2013007335A0 (en) | 2011-06-28 | 2013-12-31 | Bayer Healthcare Llc | Topical ophthalmological pharmaceutical composition containing regorafenib |
| 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 |
-
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 ES ES11712881.9T patent/ES2542610T3/es active Active
- 2011-04-08 JP JP2013504206A patent/JP5934182B2/ja active Active
- 2011-04-08 HU HUE11712881A patent/HUE026821T2/en unknown
- 2011-04-08 CN CN201180019150.1A patent/CN102947271B/zh active Active
- 2011-04-08 SG SG10201501221UA patent/SG10201501221UA/en unknown
- 2011-04-08 HR HRP20150885TT patent/HRP20150885T1/hr unknown
- 2011-04-08 AU AU2011240113A patent/AU2011240113B2/en active Active
- 2011-04-08 PL PL11712881T patent/PL2558448T3/pl unknown
- 2011-04-08 MA MA35304A patent/MA34156B1/fr unknown
- 2011-04-08 BR BR112012026117-7A patent/BR112012026117B1/pt active IP Right Grant
- 2011-04-08 PE PE2016000780A patent/PE20160838A1/es unknown
- 2011-04-08 DK DK11712881.9T patent/DK2558448T3/en active
- 2011-04-08 CA CA2796238A patent/CA2796238C/fr active Active
- 2011-04-08 PH PH1/2012/502060A patent/PH12012502060A1/en unknown
- 2011-04-08 WO PCT/EP2011/055508 patent/WO2011128261A1/fr not_active Ceased
- 2011-04-08 CN CN201410248545.4A patent/CN103980191A/zh active Pending
- 2011-04-08 SG SG2012069852A patent/SG184172A1/en unknown
- 2011-04-08 US US13/640,959 patent/US8748622B2/en active Active
- 2011-04-08 KR KR1020177032906A patent/KR20170129276A/ko not_active Ceased
- 2011-04-08 PT PT117128819T patent/PT2558448E/pt unknown
- 2011-04-08 PE PE2012002008A patent/PE20130181A1/es active IP Right Grant
- 2011-04-08 NZ NZ602997A patent/NZ602997A/en unknown
- 2011-04-08 CU CU20120147A patent/CU24123B1/es active IP Right Grant
- 2011-04-08 EP EP20110712881 patent/EP2558448B1/fr active Active
- 2011-04-08 KR KR1020127026728A patent/KR101800041B1/ko active Active
- 2011-04-08 RS RS20150528A patent/RS54219B1/sr unknown
- 2011-04-08 MX MX2012011734A patent/MX2012011734A/es active IP Right Grant
- 2011-04-08 MY MYPI2016001879A patent/MY177066A/en unknown
- 2011-04-08 RU RU2012148386/04A patent/RU2581585C2/ru active
- 2011-04-08 MY MYPI2012004548A patent/MY162359A/en unknown
- 2011-04-08 SI SI201130559T patent/SI2558448T1/sl unknown
- 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
-
2012
- 2012-10-08 EC ECSP12012234 patent/ECSP12012234A/es unknown
- 2012-10-10 CL CL2012002840A patent/CL2012002840A1/es unknown
- 2012-10-11 GT GT201200280A patent/GT201200280A/es unknown
- 2012-10-11 IL IL222348A patent/IL222348B/en active IP Right Grant
- 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
-
2014
- 2014-04-15 US US14/252,850 patent/US9458107B2/en active Active
- 2014-05-26 CU CU2014000060A patent/CU20140060A7/es unknown
-
2015
- 2015-02-10 HK HK15101433.6A patent/HK1200831A1/xx unknown
-
2016
- 2016-09-08 US US15/259,576 patent/US20170057918A1/en not_active Abandoned
- 2016-10-20 DO DO2016000285A patent/DOP2016000285A/es unknown
-
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
-
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
Also Published As
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| MA34156B1 (fr) | Procédédepréparationde 4-{4-[({[4-chloro-3-(trifluorométhyl)-phényl]amino}carbonyl)amino]-3-fluorophénoxy}-n-éthylpyridine | |
| GT201300078A (es) | Proceso para la preparacion de inhibidores de pan-cdk de la formula ( i ), e intermediarios de la preparacion | |
| EA201300388A1 (ru) | Соединения замещенного бензамида | |
| SI2609071T1 (sl) | Novi postopek za pripravo intermediatov, uporabnih za izdelavo NEP inhibitorjev | |
| CL2009000503A1 (es) | Proceso de preparacion de compuestos derivados de acido 2-amino-5-cianobenzoico-3-sustituidos o 1h-pirazol-5-carboxamida. | |
| EP2590649A4 (fr) | Procédé de synthèse de morphinanes substitués | |
| CL2011000296A1 (es) | Proceso de preparación del ester metílico del ácido 4-oxo-octahidro-indol-1-carboxílico y compuestos intermediarios utilizados. | |
| MD20130094A2 (en) | Process for the preparation of a rivaroxaban and intermediates formed in said process | |
| NZ702935A (en) | Process for making hydroxylated cyclopentylpyrimidine compounds | |
| MX2014014138A (es) | Procedimiento nuevo para la preparacion de acido 2-ciclopentil-6-metoxi-isonicotinico. | |
| MY152980A (en) | Process for the preparation of derivatives of 1-(2-halobiphenyl-4-yl)-cyclopropanecarboxylic acid | |
| MY164880A (en) | Process for the preparation of isoxazolyl-methoxy-nicotinic acids | |
| EA201200498A1 (ru) | Новый способ синтеза ивабрадина и его фармацевтически приемлемых кислотно-аддитивных солей | |
| JOP20180012A1 (ar) | عملية السلفنة باستخدام نونافلوروبوتانيسولفونيل فلوريد | |
| EA201200123A1 (ru) | Новый способ синтеза ивабрадина и его фармацевтически приемлемых кислотно-аддитивных солей | |
| CR20120630A (es) | Nuevos procesos | |
| MX2012010443A (es) | Proceso para la preparacion de 1-alquiltetrazoles 5-sustituidos. | |
| MX2013004193A (es) | Procedimiento para la preparacion de derivados de acido 3-(6-amino-piridin-3-il)-2-acrilico. | |
| EA201100230A1 (ru) | Новый способ синтеза ивабрадина и его аддитивных солей с фармацевтически приемлемой кислотой | |
| PH12014501166A1 (en) | Novel process for racemization of an optically active (s)-3-carbamoylmethyl-5-methyl-hexanoic acid to corresponding 3-carbamoylmethyl-5-methyl-hexanoic acid racemate | |
| EA201201385A1 (ru) | Новый способ синтеза ивабрадина и его фармацевтически приемлемых кислотно-аддитивных солей | |
| MX2013006017A (es) | Separacion de enantiomeros derivados de triazina usando acido tartarico. | |
| JO3185B1 (ar) | طريقة لتحضير مشتقات استر متغايرة الحلقة | |
| MY161361A (en) | Substituted phenyl compounds | |
| EA201201571A1 (ru) | Новый способ синтеза ивабрадина и его фармацевтически приемлемых кислотно-аддитивных солей |