DOP2012000268A - Procedimiento para la preparacion de 4-{4-[({[4-cloro-3-(trifluorometil) fenil]animo}carbonil)amino]-3-fluorofenoxi}-n-metilpiridina-2-carboxamida, sus sales y su monohidrato - Google Patents
Procedimiento para la preparacion de 4-{4-[({[4-cloro-3-(trifluorometil) fenil]animo}carbonil)amino]-3-fluorofenoxi}-n-metilpiridina-2-carboxamida, sus sales y su monohidratoInfo
- Publication number
- DOP2012000268A DOP2012000268A DO2012000268A DO2012000268A DOP2012000268A DO P2012000268 A DOP2012000268 A DO P2012000268A DO 2012000268 A DO2012000268 A DO 2012000268A DO 2012000268 A DO2012000268 A DO 2012000268A DO P2012000268 A DOP2012000268 A DO P2012000268A
- Authority
- DO
- Dominican Republic
- Prior art keywords
- amino
- carboxamide
- salts
- preparation
- methylpiridine
- Prior art date
Links
- RZVAJINKPMORJF-UHFFFAOYSA-N Acetaminophen Chemical compound CC(=O)NC1=CC=C(O)C=C1 RZVAJINKPMORJF-UHFFFAOYSA-N 0.000 title 1
- 150000004682 monohydrates Chemical class 0.000 abstract 1
- FNHKPVJBJVTLMP-UHFFFAOYSA-N regorafenib Chemical compound C1=NC(C(=O)NC)=CC(OC=2C=C(F)C(NC(=O)NC=3C=C(C(Cl)=CC=3)C(F)(F)F)=CC=2)=C1 FNHKPVJBJVTLMP-UHFFFAOYSA-N 0.000 abstract 1
- 150000003839 salts Chemical class 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 presente invención se refiere a un procedimiento para la preparación de 4- {4-[({[4-cloro-3-(trifluorometil)fenil]amino}carbonil)amino]-3-fluorofenoxi}-N- metilpiridina-2-carboxamida, sus sales y su monohidrato.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP10004022 | 2010-04-15 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DOP2012000268A true DOP2012000268A (es) | 2012-12-15 |
Family
ID=44070712
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DO2012000268A DOP2012000268A (es) | 2010-04-15 | 2012-10-12 | Procedimiento para la preparacion de 4-{4-[({[4-cloro-3-(trifluorometil) fenil]animo}carbonil)amino]-3-fluorofenoxi}-n-metilpiridina-2-carboxamida, sus sales y su monohidrato |
| DO2016000285A DOP2016000285A (es) | 2010-04-15 | 2016-10-20 | Procedimiento para la preparación de 4-{4-[({[4-cloro-3-(trifluorometil)fenil]amino}carbonil)amino]-3-fluorofenoxi}-n-metilpiridina-2-carboxamida, sus sales y su monohidrato |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DO2016000285A DOP2016000285A (es) | 2010-04-15 | 2016-10-20 | Procedimiento para la preparación de 4-{4-[({[4-cloro-3-(trifluorometil)fenil]amino}carbonil)amino]-3-fluorofenoxi}-n-metilpiridina-2-carboxamida, sus sales y su monohidrato |
Country Status (40)
| Country | Link |
|---|---|
| US (5) | US8748622B2 (es) |
| EP (1) | EP2558448B1 (es) |
| JP (1) | JP5934182B2 (es) |
| KR (2) | KR20170129276A (es) |
| CN (2) | CN103980191A (es) |
| AR (2) | AR081060A1 (es) |
| AU (1) | AU2011240113B2 (es) |
| BR (1) | BR112012026117B1 (es) |
| CA (1) | CA2796238C (es) |
| CL (1) | CL2012002840A1 (es) |
| CO (1) | CO6630136A2 (es) |
| CR (1) | CR20120526A (es) |
| CU (2) | CU24123B1 (es) |
| DK (1) | DK2558448T3 (es) |
| DO (2) | DOP2012000268A (es) |
| EC (1) | ECSP12012234A (es) |
| ES (1) | ES2542610T3 (es) |
| GT (1) | GT201200280A (es) |
| HK (1) | HK1200831A1 (es) |
| HR (1) | HRP20150885T1 (es) |
| HU (1) | HUE026821T2 (es) |
| IL (2) | IL222348B (es) |
| JO (1) | JO3158B1 (es) |
| MA (1) | MA34156B1 (es) |
| MX (1) | MX2012011734A (es) |
| MY (2) | MY162359A (es) |
| NZ (1) | NZ602997A (es) |
| PE (2) | PE20160838A1 (es) |
| PH (1) | PH12012502060A1 (es) |
| PL (1) | PL2558448T3 (es) |
| PT (1) | PT2558448E (es) |
| RS (1) | RS54219B1 (es) |
| RU (1) | RU2581585C2 (es) |
| SG (2) | SG10201501221UA (es) |
| SI (1) | SI2558448T1 (es) |
| TN (1) | TN2012000492A1 (es) |
| TW (2) | TWI475992B (es) |
| UA (1) | UA110613C2 (es) |
| UY (2) | UY33290A (es) |
| WO (1) | WO2011128261A1 (es) |
Families Citing this family (21)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR101381454B1 (ko) * | 2004-09-29 | 2014-04-04 | 바이엘 인텔렉쳐 프로퍼티 게엠베하 | 열역학적으로 안정한 형태의 bay 43-9006 토실레이트 |
| SG160364A1 (en) | 2005-03-07 | 2010-04-29 | Bayer Schering Pharma Ag | Pharmaceutical composition comprising an omega-carboxyaryl substituted diphenyl urea for the treatment of cancer |
| 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 |
| UY35006A (es) * | 2012-09-06 | 2014-03-31 | Bayer Healthcare Llc | Composición farmacéutica recubierta que contiene regorafenib |
| US10898500B2 (en) | 2012-09-25 | 2021-01-26 | Bayer Pharma Aktiengesellschaft | 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 |
| WO2016005874A1 (en) * | 2014-07-09 | 2016-01-14 | 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 |
| US20190300484A1 (en) * | 2016-01-18 | 2019-10-03 | 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 |
| PE20200859A1 (es) | 2017-06-02 | 2020-08-25 | Bayer Healthcare Llc | Combinacion farmaceutica que comprende regonafenib y nivolumab como anticancerigeno |
| 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 (en) | 2020-02-07 | 2021-08-11 | Bayer Aktiengesellschaft | Pharmaceutical composition containing regorafenib and a stabilizing agent |
| WO2021160708A1 (en) | 2020-02-14 | 2021-08-19 | Bayer Aktiengesellschaft | Combination of regorafenib and msln-ttc for treating 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 |
| US7517880B2 (en) | 1997-12-22 | 2009-04-14 | Bayer Pharmaceuticals Corporation | Inhibition of p38 kinase using symmetrical and unsymmetrical diphenyl ureas |
| US7329670B1 (en) | 1997-12-22 | 2008-02-12 | Bayer Pharmaceuticals Corporation | Inhibition of RAF kinase using aryl and heteroaryl substituted heterocyclic ureas |
| US20080269265A1 (en) | 1998-12-22 | 2008-10-30 | Scott Miller | Inhibition Of Raf Kinase Using Symmetrical And Unsymmetrical Substituted Diphenyl Ureas |
| WO2000042012A1 (en) | 1999-01-13 | 2000-07-20 | Bayer Corporation | φ-CARBOXYARYL SUBSTITUTED DIPHENYL UREAS AS RAF KINASE INHIBITORS |
| US8124630B2 (en) | 1999-01-13 | 2012-02-28 | Bayer Healthcare Llc | ω-carboxyaryl substituted diphenyl ureas as raf kinase inhibitors |
| US7351834B1 (en) | 1999-01-13 | 2008-04-01 | Bayer Pharmaceuticals Corporation | ω-Carboxyaryl substituted diphenyl ureas as raf kinase inhibitors |
| ATE538794T1 (de) | 1999-01-13 | 2012-01-15 | Bayer Healthcare Llc | Gamma carboxyarylsubstituierte diphenylharnstoffverbindungen als p38 kinasehemmer |
| 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 |
| JP4982685B2 (ja) | 2001-12-03 | 2012-07-25 | バイエル、ファーマシューテイカルズ、コーポレイション | ヒトがんを処置するための他の細胞毒剤又は細胞増殖抑制剤と組合わせたアリール尿素化合物 |
| MXPA04007832A (es) | 2002-02-11 | 2005-09-08 | Bayer Pharmaceuticals Corp | Aril-ureas con actividad inhibitoria de angiogenesis. |
| US10653684B2 (en) | 2002-02-11 | 2020-05-19 | Bayer Healthcare Llc | Aryl ureas with angiogenisis inhibiting activity |
| WO2003068229A1 (en) | 2002-02-11 | 2003-08-21 | Bayer Pharmaceuticals Corporation | Pyridine, quinoline, and isoquinoline n-oxides as kinase inhibitors |
| MXPA04007830A (es) | 2002-02-11 | 2005-07-01 | Bayer Pharmaceuticals Corp | Arilureas como inhibidores de cinasa. |
| US7557129B2 (en) | 2003-02-28 | 2009-07-07 | Bayer Healthcare Llc | Cyanopyridine derivatives useful in the treatment of cancer and other disorders |
| WO2004113274A2 (en) | 2003-05-20 | 2004-12-29 | Bayer Pharmaceuticals Corporation | Diaryl ureas with kinase inhibiting activity |
| EA010485B1 (ru) * | 2003-07-23 | 2008-10-30 | Байер Фамэсьютиклс Копэрейшн | Производное n,n'-дифенилмочевины, фармацевтическая композиция (варианты) и способ лечения и предупреждения заболеваний и состояний с его использованием (варианты) |
| CN101010315A (zh) | 2004-04-30 | 2007-08-01 | 拜耳制药公司 | 用于治疗癌症的取代的吡唑基脲衍生物 |
| MY191349A (en) | 2004-08-27 | 2022-06-17 | Bayer Pharmaceuticals Corp | New pharmaceutical compositions for the treatment of hyper-proliferative disorders |
| WO2006026501A1 (en) | 2004-08-27 | 2006-03-09 | Bayer Pharmaceuticals Corporation | New pharmaceutical compositions for the treatment of cancer |
| KR101381454B1 (ko) | 2004-09-29 | 2014-04-04 | 바이엘 인텔렉쳐 프로퍼티 게엠베하 | 열역학적으로 안정한 형태의 bay 43-9006 토실레이트 |
| AU2005289099B2 (en) | 2004-09-29 | 2012-07-19 | Bayer Healthcare Llc | Process for the preparation of 4-{4-[({[4-chloro-3-(trifluoromethyl)phenyl]amino}carbonyl)amino]phenoxy}-N-methylpyridine-2-carboxamide |
| SG160364A1 (en) | 2005-03-07 | 2010-04-29 | Bayer Schering Pharma Ag | Pharmaceutical composition comprising an omega-carboxyaryl substituted diphenyl urea for the treatment of cancer |
| CA2627873A1 (en) | 2005-10-31 | 2007-05-10 | Scott Wilhelm | Treatment of cancer with sorafenib |
| WO2007059154A2 (en) | 2005-11-14 | 2007-05-24 | Bayer Healthcare Llc | Treatment of cancers with acquired resistance to kit inhibitors |
| 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 (en) * | 2006-11-09 | 2008-05-15 | Bayer Schering Pharma Aktiengesellschaft | Polymorph iii of 4-[4-({[4-chloro-3-(trifluoromethyl)phenyl]carbamoyl}amino)-3-fluorophenoxy]-n-methylpyridine-2-carboxamide |
| US20100113533A1 (en) * | 2006-11-14 | 2010-05-06 | Bayer Schering Pharma Aktiengesellschaft | Polymorph II of 4-[4-(Amino)-3- Fluorophenoxy]-N-Methylpyridine-2-Carboxamide |
| DK2111401T3 (da) | 2006-12-20 | 2011-05-30 | Bayer Healthcare Llc | 4-{4-[({3-tert-butyl-1-[3-(hydroxymethyl)phenyl]-1H-pyrazol-5-yl}carbamoyl)-amino]-3-fluorphenoxy}-N-methylpyridin-2-carboxamid samt prodrug og salte heraf til behandling af cancer |
| US20100173954A1 (en) | 2007-01-19 | 2010-07-08 | Bayer Healthcare Llc | Treatment of cancers having resistance to chemotherapeutic agents |
| JP5885012B2 (ja) | 2007-01-19 | 2016-03-15 | バイエル・ヘルスケア・エルエルシーBayer HealthCareLLC | Kit阻害剤に対して獲得した抵抗性を有する癌の処置 |
| EP2156834A1 (en) * | 2008-08-08 | 2010-02-24 | S.I.F.I - Società Industria Farmaceutica Italiana - S.P.A. | Ophthalmic pharmaceutical compositions comprising Sorafenib for the treatment of neoangiogenic pathologies of the eye |
| 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 |
| CN102958518A (zh) | 2009-05-15 | 2013-03-06 | 诺瓦提斯公司 | 磷脂酰肌醇3-激酶抑制剂和抗糖尿病化合物的组合 |
| 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 (en) | 2010-07-19 | 2012-01-26 | Bayer Healthcare Llc | Drug combinations with fluoro-substituted omega-carboxyaryl diphenyl urea for the treatment and prevention of diseases and conditions |
| MA34553B1 (fr) | 2010-10-01 | 2013-09-02 | Bayer Ip Gmbh | Combinaisons contenant du n-(2-arylamino)arylsulfonamide substitué |
| WO2013000909A1 (en) | 2011-06-28 | 2013-01-03 | Bayer Intellectual Property Gmbh | Topical ophthalmological pharmaceutical composition containing sorafenib |
| 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 |
| UY35006A (es) | 2012-09-06 | 2014-03-31 | Bayer Healthcare Llc | Composición farmacéutica 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 KR KR1020177032906A patent/KR20170129276A/ko not_active Ceased
- 2011-04-08 HR HRP20150885TT patent/HRP20150885T1/hr unknown
- 2011-04-08 MY MYPI2012004548A patent/MY162359A/en unknown
- 2011-04-08 CA CA2796238A patent/CA2796238C/en active Active
- 2011-04-08 MA MA35304A patent/MA34156B1/fr unknown
- 2011-04-08 PL PL11712881T patent/PL2558448T3/pl unknown
- 2011-04-08 DK DK11712881.9T patent/DK2558448T3/en active
- 2011-04-08 EP EP20110712881 patent/EP2558448B1/en 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 MY MYPI2016001879A patent/MY177066A/en unknown
- 2011-04-08 SI SI201130559T patent/SI2558448T1/sl unknown
- 2011-04-08 HU HUE11712881A patent/HUE026821T2/en unknown
- 2011-04-08 KR KR1020127026728A patent/KR101800041B1/ko active Active
- 2011-04-08 CN CN201410248545.4A patent/CN103980191A/zh active Pending
- 2011-04-08 PT PT117128819T patent/PT2558448E/pt unknown
- 2011-04-08 SG SG10201501221UA patent/SG10201501221UA/en unknown
- 2011-04-08 PE PE2016000780A patent/PE20160838A1/es unknown
- 2011-04-08 AU AU2011240113A patent/AU2011240113B2/en active Active
- 2011-04-08 RS RS20150528A patent/RS54219B1/sr unknown
- 2011-04-08 ES ES11712881.9T patent/ES2542610T3/es active Active
- 2011-04-08 JP JP2013504206A patent/JP5934182B2/ja active Active
- 2011-04-08 WO PCT/EP2011/055508 patent/WO2011128261A1/en not_active Ceased
- 2011-04-08 US US13/640,959 patent/US8748622B2/en active Active
- 2011-04-08 PH PH1/2012/502060A patent/PH12012502060A1/en unknown
- 2011-04-08 SG SG2012069852A patent/SG184172A1/en unknown
- 2011-04-08 BR BR112012026117-7A patent/BR112012026117B1/pt active IP Right Grant
- 2011-04-08 CN CN201180019150.1A patent/CN102947271B/zh active Active
- 2011-04-08 PE PE2012002008A patent/PE20130181A1/es active IP Right Grant
- 2011-04-08 NZ NZ602997A patent/NZ602997A/en 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 TW100112905A patent/TWI475992B/zh active
- 2011-04-14 TW TW103141317A patent/TWI539951B/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 |
|---|---|---|
| DOP2012000268A (es) | Procedimiento para la preparacion de 4-{4-[({[4-cloro-3-(trifluorometil) fenil]animo}carbonil)amino]-3-fluorofenoxi}-n-metilpiridina-2-carboxamida, sus sales y su monohidrato | |
| DK2760444T3 (da) | Cannabinoidcarboxylsyrer, salte af cannabinoidcarboxylsyrer, fremstilling og anvendelse deraf | |
| BR112013020611A2 (pt) | método para produção de compostos quelato de aminoácido, compostos quelato de aminoácido e uso de compostos quelato de aminoácido | |
| LT3034497T (lt) | 3,5-diamino-6-chlor-n-(n-(4-(4-(2-(heksil(2,3,4,5,6-penta-hidroksiheksil)amino)etoksi)fenil)butil)karbamimidoil)pirazin-2-karboksamidas | |
| HUE049168T2 (hu) | L-aminosav elõállítására képes mikroorganizmus és eljárás L-aminosav elõállítására annak alkalmazásával | |
| BR112015023453A2 (pt) | composição de acil aminoácidos, método para sua produção, célula manipulada e método de preparação de um produto | |
| CO7081156A2 (es) | Sales de 5-[(1r)-2-({2-[4-(2,2-difluoro-2-feniletoxi)fenil] etil}amino)-1-hidroxietil]-8-hidroxiquinolin-2(1h)-ona | |
| UA111333C2 (uk) | Спосіб одержання l-аргінінової солі периндроприлу | |
| UY34386A (es) | Método para la producción de ácido láctico | |
| EA201200123A1 (ru) | Новый способ синтеза ивабрадина и его фармацевтически приемлемых кислотно-аддитивных солей | |
| EA201100230A1 (ru) | Новый способ синтеза ивабрадина и его аддитивных солей с фармацевтически приемлемой кислотой | |
| UA111329C2 (uk) | Спосіб синтезу івабрадину і його адитивних солей з фармацевтично прийнятною кислотою | |
| UA118008C2 (uk) | Спосіб синтезу (2е)-3-(3,4-диметоксифеніл)проп-2-еннітрилу та застосування в синтезі івабрадину та його адитивних солей з фармацевтично прийнятною кислотою | |
| UA117900C2 (uk) | Спосіб синтезу 3-(2-бром-4,5-диметоксифеніл)пропаннітрилу та застосування в синтезі івабрадину та його адитивних солей з фармацевтично прийнятною кислотою | |
| BR112017002922A2 (pt) | ?processo para a produção em grande escala de dihidrocloreto de n-[4-(1-ciclobutil piperidin-4-iloxi) fenil]-2-(morfolin-4-il) acetamida? | |
| UA111156C2 (uk) | Спосіб синтезу івабрадину і його адитивних солей з фармацевтично прийнятною кислотою | |
| EA201300281A2 (ru) | Новый способ синтеза ивабрадина и его аддитивных солей с фармацевтически приемлемой кислотой | |
| EA201301020A1 (ru) | Новый способ синтеза 3-(2-бром-4,5-диметоксифенил)пропаннитрила и применение в синтезе ивабрадина и его фармацевтически приемлемых кислотно-аддитивных солей | |
| UY34626A (es) | Proceso para la preparación estereoselectiva de pirazol carboxamida y compuestos intermediarios | |
| CY1116366T1 (el) | Νεα μεθοδος για τη συνθεση αγομελατινης |