UA110613C2 - Спосіб одержання 4-{4-[({[4-хлор-3-(трифторметил)феніл]аміно}карбоніл)аміно]-3-фторфенокси}-n-метилпіридин-2-карбоксаміду, його солей і моногідрату - Google Patents

Спосіб одержання 4-{4-[({[4-хлор-3-(трифторметил)феніл]аміно}карбоніл)аміно]-3-фторфенокси}-n-метилпіридин-2-карбоксаміду, його солей і моногідрату

Info

Publication number
UA110613C2
UA110613C2 UAA201212983A UAA201212983A UA110613C2 UA 110613 C2 UA110613 C2 UA 110613C2 UA A201212983 A UAA201212983 A UA A201212983A UA A201212983 A UAA201212983 A UA A201212983A UA 110613 C2 UA110613 C2 UA 110613C2
Authority
UA
Ukraine
Prior art keywords
amino
fluorophenoxy
methylpyridine
monohydrate
trifluoromethyl
Prior art date
Application number
UAA201212983A
Other languages
English (en)
Inventor
Юрген Штіль
Вернер ХАЙЛЬМАНН
Міхаель Льогерс
Йоахім Резе
Міхаель Готтфрід
Саскіа Віхманн
Original Assignee
БАЄР ХЕЛСКЕР ЛЛСі
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=44070712&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=UA110613(C2) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by БАЄР ХЕЛСКЕР ЛЛСі filed Critical БАЄР ХЕЛСКЕР ЛЛСі
Publication of UA110613C2 publication Critical patent/UA110613C2/uk

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D213/00Heterocyclic 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
    • C07D213/02Heterocyclic 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
    • C07D213/04Heterocyclic 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
    • C07D213/60Heterocyclic 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
    • C07D213/78Carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen, e.g. ester or nitrile radicals
    • C07D213/81Amides; Imides
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435Heterocyclic 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
    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/4412Non condensed pyridines; Hydrogenated derivatives thereof having oxo groups directly attached to the heterocyclic ring
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • A61P35/02Antineoplastic agents specific for leukemia

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Epidemiology (AREA)
  • Hematology (AREA)
  • Oncology (AREA)
  • Pyridine Compounds (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
  • Containers And Plastic Fillers For Packaging (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

Представлений винахід стосується способу одержання 4-{4-[({[4-хлор-3-(трифторметил)феніл]аміно}карбоніл)аміно]-3-фторфенокси}-N-метилпіридин-2-карбоксаміду, його солі і моногідрату.
UAA201212983A 2010-04-15 2011-08-04 Спосіб одержання 4-{4-[({[4-хлор-3-(трифторметил)феніл]аміно}карбоніл)аміно]-3-фторфенокси}-n-метилпіридин-2-карбоксаміду, його солей і моногідрату UA110613C2 (uk)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
EP10004022 2010-04-15
PCT/EP2011/055508 WO2011128261A1 (en) 2010-04-15 2011-04-08 Process for the preparation of 4- {4-[({[4 -chloro-3 -(trifluoromethyl)-phenyl]amino}carbonyl)amino]-3-fluorophenoxy}-n-methylpyridine-2-carboxamide, its salts and monohydrate

Publications (1)

Publication Number Publication Date
UA110613C2 true UA110613C2 (uk) 2016-01-25

Family

ID=44070712

Family Applications (1)

Application Number Title Priority Date Filing Date
UAA201212983A UA110613C2 (uk) 2010-04-15 2011-08-04 Спосіб одержання 4-{4-[({[4-хлор-3-(трифторметил)феніл]аміно}карбоніл)аміно]-3-фторфенокси}-n-метилпіридин-2-карбоксаміду, його солей і моногідрату

Country Status (39)

Country Link
US (5) US8748622B2 (uk)
EP (1) EP2558448B1 (uk)
JP (1) JP5934182B2 (uk)
KR (2) KR20170129276A (uk)
CN (2) CN102947271B (uk)
AR (2) AR081060A1 (uk)
AU (1) AU2011240113B2 (uk)
BR (1) BR112012026117B1 (uk)
CA (1) CA2796238C (uk)
CL (1) CL2012002840A1 (uk)
CO (1) CO6630136A2 (uk)
CR (1) CR20120526A (uk)
CU (2) CU24123B1 (uk)
DK (1) DK2558448T3 (uk)
DO (2) DOP2012000268A (uk)
EC (1) ECSP12012234A (uk)
ES (1) ES2542610T3 (uk)
GT (1) GT201200280A (uk)
HK (1) HK1200831A1 (uk)
HR (1) HRP20150885T1 (uk)
HU (1) HUE026821T2 (uk)
IL (2) IL222348B (uk)
JO (1) JO3158B1 (uk)
MA (1) MA34156B1 (uk)
MX (1) MX2012011734A (uk)
MY (2) MY177066A (uk)
NZ (1) NZ602997A (uk)
PE (2) PE20160838A1 (uk)
PL (1) PL2558448T3 (uk)
PT (1) PT2558448E (uk)
RS (1) RS54219B1 (uk)
RU (1) RU2581585C2 (uk)
SG (2) SG184172A1 (uk)
SI (1) SI2558448T1 (uk)
TN (1) TN2012000492A1 (uk)
TW (2) TWI539951B (uk)
UA (1) UA110613C2 (uk)
UY (2) UY33290A (uk)
WO (1) WO2011128261A1 (uk)

Families Citing this family (21)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
BRPI0515946A (pt) * 2004-09-29 2008-08-12 Bayer Healthcare Ag sal de tosilato, sua preparação e uso, bem como composição farmacêutica compreendendo o mesmo
JP5304241B2 (ja) 2005-03-07 2013-10-02 バイエル・ヘルスケア・エルエルシー 癌の処置用のオメガ−カルボキシアリール置換ジフェニルウレアを含む医薬組成物
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
MX357035B (es) 2012-09-25 2018-06-25 Bayer Pharma AG Combinacion de regorafenib y acido acetilsalicilico para el tratamiento del 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
WO2015049698A2 (en) * 2013-10-04 2015-04-09 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
WO2017125941A1 (en) * 2016-01-18 2017-07-27 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
WO2018219807A1 (en) 2017-06-02 2018-12-06 Bayer Aktiengesellschaft 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 (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)

* Cited by examiner, † Cited by third party
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
ME00275B (me) 1999-01-13 2011-02-10 Bayer Corp ω-KARBOKSIARIL SUPSTITUISANI DIFENIL KARBAMIDI KAO INHIBITORI RAF KINAZE
EP1140840B1 (en) 1999-01-13 2006-03-22 Bayer Pharmaceuticals Corp. -g(v)-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
CA2359244C (en) 1999-01-13 2013-10-08 Bayer Corporation .omega.-carboxy aryl substituted diphenyl ureas as p38 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
ES2275931T5 (es) 2001-12-03 2018-10-23 Bayer Healthcare Llc Compuestos de aril-urea en combinación con otros agentes citostáticos o citotóxicos para tratamiento de cánceres humanos
US10653684B2 (en) 2002-02-11 2020-05-19 Bayer Healthcare Llc Aryl ureas with angiogenisis inhibiting activity
DK1478358T3 (da) 2002-02-11 2013-10-07 Bayer Healthcare Llc Sorafenibtosylat til behandling af sygdomme kendetegnet ved unormal angiogenese
WO2003068746A1 (en) 2002-02-11 2003-08-21 Bayer Pharmaceuticals Corporation Aryl ureas as kinase inhibitors
WO2003068229A1 (en) 2002-02-11 2003-08-21 Bayer Pharmaceuticals Corporation Pyridine, quinoline, and isoquinoline n-oxides as kinase inhibitors
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
ES2297490T3 (es) 2003-07-23 2008-05-01 Bayer Pharmaceuticals Corporation Omega-carboxiarildifenilurea fluoro sustituida para el tratamiento y prevencion de enfermadades y afecciones.
ATE517885T1 (de) 2004-04-30 2011-08-15 Bayer Healthcare Llc Substituierte pyrazolyl-harnstoff-derivate zur behandlung von krebs
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
WO2006034796A1 (en) 2004-09-29 2006-04-06 Bayer Healthcare Ag Process for the preparation of 4-{4-[({[4-chloro-3-(trifluoromethyl)phenyl]amino}carbonyl)amino]phenoxy}-n-methylpyridine-2-carboxamide
BRPI0515946A (pt) 2004-09-29 2008-08-12 Bayer Healthcare Ag sal de tosilato, sua preparação e uso, bem como composição farmacêutica compreendendo o mesmo
JP5304241B2 (ja) 2005-03-07 2013-10-02 バイエル・ヘルスケア・エルエルシー 癌の処置用のオメガ−カルボキシアリール置換ジフェニルウレアを含む医薬組成物
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
WO2008055629A1 (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
JP2010509382A (ja) * 2006-11-14 2010-03-25 バイエル・シェーリング・ファルマ・アクチェンゲゼルシャフト 4−[4−({[4−クロロ−3−(トリフルオロメチル)フェニル]カルバモイル}アミノ)−3−フルオロフェノキシ]−n−メチルピリジン−2−カルボキサミドの多形ii
JP2010514691A (ja) 2006-12-20 2010-05-06 バイエル ヘルスケア リミティド ライアビリティ カンパニー 4−{4−〔({3−tert−ブチル−1−〔3−(ヒドロキシメチル)フェニル〕−1H−ピラゾール−5−イル}カルバモイル)アミノ〕−3−フルオロフェノキシ}−N−メチルピリジン−2−カルボキサミド並びに癌の治療のためのそれのプロドラッグ及び塩
US8680124B2 (en) 2007-01-19 2014-03-25 Bayer Healthcare Llc Treatment of cancers with acquired resistance to kit inhibitors
US20100173954A1 (en) 2007-01-19 2010-07-08 Bayer Healthcare Llc Treatment of cancers having resistance to chemotherapeutic agents
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
WO2010048304A2 (en) 2008-10-21 2010-04-29 Bayer Healthcare Llc Identification of signature genes associated with hepatocellular carcinoma
BRPI1010979A2 (pt) 2009-05-15 2018-03-06 Novartis Ag "combinação de um inibidor de fosfoinositídeo 3- quinase e de uma composto antidiabético"
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
MX2013003695A (es) 2010-10-01 2013-05-20 Bayer Ip Gmbh Combinaciones que contienen n-(2-arilamino) arilsulfonamida sustituida.
PE20141031A1 (es) 2011-06-28 2014-08-21 Bayer Healthcare Llc Composicion farmaceutica oftalmologica topica que contiene regorafenib
WO2013000909A1 (en) 2011-06-28 2013-01-03 Bayer Intellectual Property Gmbh Topical ophthalmological pharmaceutical composition containing sorafenib
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

Also Published As

Publication number Publication date
MY177066A (en) 2020-09-03
PL2558448T3 (pl) 2015-10-30
TWI539951B (zh) 2016-07-01
BR112012026117B1 (pt) 2022-08-30
CO6630136A2 (es) 2013-03-01
US8748622B2 (en) 2014-06-10
EP2558448B1 (en) 2015-05-20
US20170057918A1 (en) 2017-03-02
CN102947271A (zh) 2013-02-27
KR101800041B1 (ko) 2017-11-21
UY39590A (es) 2022-01-31
PE20160838A1 (es) 2016-09-24
IL222348B (en) 2018-08-30
ES2542610T3 (es) 2015-08-07
TW201509415A (zh) 2015-03-16
BR112012026117A2 (pt) 2015-09-08
GT201200280A (es) 2014-07-23
RU2581585C2 (ru) 2016-04-20
SG184172A1 (en) 2012-11-29
WO2011128261A1 (en) 2011-10-20
HRP20150885T1 (hr) 2015-10-09
AU2011240113B2 (en) 2014-12-18
IL222348A0 (en) 2012-12-31
RU2012148386A (ru) 2014-05-20
CU20120147A7 (es) 2013-01-30
MA34156B1 (fr) 2013-04-03
BR112012026117A8 (pt) 2017-12-19
CN102947271B (zh) 2016-11-09
HUE026821T2 (en) 2016-07-28
JP2013523851A (ja) 2013-06-17
CU20140060A7 (es) 2014-10-02
HK1200831A1 (en) 2015-08-14
TWI475992B (zh) 2015-03-11
US10822305B2 (en) 2020-11-03
DOP2016000285A (es) 2016-11-30
CR20120526A (es) 2013-03-11
PE20130181A1 (es) 2013-02-23
UY33290A (es) 2011-12-01
MX2012011734A (es) 2012-12-17
AU2011240113A1 (en) 2012-10-11
KR20170129276A (ko) 2017-11-24
MY162359A (en) 2017-06-15
CL2012002840A1 (es) 2013-01-18
DOP2012000268A (es) 2012-12-15
TW201204356A (en) 2012-02-01
US20190144391A1 (en) 2019-05-16
ECSP12012234A (es) 2012-11-30
CA2796238C (en) 2019-12-31
US20130116442A1 (en) 2013-05-09
CN103980191A (zh) 2014-08-13
JO3158B1 (ar) 2017-09-20
CU24123B1 (es) 2015-08-27
RS54219B1 (en) 2015-12-31
US20170334857A1 (en) 2017-11-23
US9458107B2 (en) 2016-10-04
IL253119B (en) 2018-03-29
SG10201501221UA (en) 2015-04-29
AR116395A2 (es) 2021-05-05
DK2558448T3 (en) 2015-08-24
PT2558448E (pt) 2015-09-01
SI2558448T1 (sl) 2015-11-30
NZ602997A (en) 2014-10-31
IL253119A0 (en) 2017-08-31
JP5934182B2 (ja) 2016-06-15
TN2012000492A1 (en) 2014-04-01
EP2558448A1 (en) 2013-02-20
AR081060A1 (es) 2012-06-06
US20140221661A1 (en) 2014-08-07
KR20130061670A (ko) 2013-06-11
CA2796238A1 (en) 2011-10-20

Similar Documents

Publication Publication Date Title
UA110613C2 (uk) Спосіб одержання 4-{4-[({[4-хлор-3-(трифторметил)феніл]аміно}карбоніл)аміно]-3-фторфенокси}-n-метилпіридин-2-карбоксаміду, його солей і моногідрату
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
EA201301235A1 (ru) Новый способ синтеза 3-(2-бром-4,5-диметоксифенил)пропаннитрила и применение в синтезе ивабрадина и его фармацевтически приемлемых кислотно-аддитивных солей
EA201301020A1 (ru) Новый способ синтеза 3-(2-бром-4,5-диметоксифенил)пропаннитрила и применение в синтезе ивабрадина и его фармацевтически приемлемых кислотно-аддитивных солей
UA111156C2 (uk) Спосіб синтезу івабрадину і його адитивних солей з фармацевтично прийнятною кислотою
EA201300281A3 (ru) Новый способ синтеза ивабрадина и его аддиктивных солей с фармацевтически приемлемой кислотой
WO2011076711A3 (en) Polymorphs of salts of 4- [4- [ [4-chloro-3- (trifluoromethyl) phenyl] carbamoylamino] phenoxy] -n-methylpyridine - 2 - carboxamide
PL399095A1 (pl) Sposób wytwarzania nilotinibu