WO2006114415A3 - Physiologisch verträgliche salze von 3-[(2-{[4-(hexyloxycarbonylamino-imino-methyl)-phenylamino]-methyl}-1-methyl-1h-benzimidazol-5-carbonyl)-pyridin-2-yl-amino]-propionsäure-ethylester - Google Patents

Physiologisch verträgliche salze von 3-[(2-{[4-(hexyloxycarbonylamino-imino-methyl)-phenylamino]-methyl}-1-methyl-1h-benzimidazol-5-carbonyl)-pyridin-2-yl-amino]-propionsäure-ethylester Download PDF

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Publication number
WO2006114415A3
WO2006114415A3 PCT/EP2006/061820 EP2006061820W WO2006114415A3 WO 2006114415 A3 WO2006114415 A3 WO 2006114415A3 EP 2006061820 W EP2006061820 W EP 2006061820W WO 2006114415 A3 WO2006114415 A3 WO 2006114415A3
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WO
WIPO (PCT)
Prior art keywords
methyl
hexyloxycarbonylamino
phenylamino
benzimidazole
imino
Prior art date
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PCT/EP2006/061820
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English (en)
French (fr)
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WO2006114415A2 (de
Inventor
Peter Sieger
Norbert Hauel
Rolf Schmid
Original Assignee
Boehringer Ingelheim Int
Boehringer Ingelheim Pharma
Peter Sieger
Norbert Hauel
Rolf Schmid
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Application filed by Boehringer Ingelheim Int, Boehringer Ingelheim Pharma, Peter Sieger, Norbert Hauel, Rolf Schmid filed Critical Boehringer Ingelheim Int
Priority to JP2008508213A priority Critical patent/JP2008539199A/ja
Priority to EP06754844A priority patent/EP1877395A2/de
Priority to CA002606090A priority patent/CA2606090A1/en
Publication of WO2006114415A2 publication Critical patent/WO2006114415A2/de
Publication of WO2006114415A3 publication Critical patent/WO2006114415A3/de

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    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
    • C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P7/00—Drugs for disorders of the blood or the extracellular fluid
    • A61P7/02—Antithrombotic agents; Anticoagulants; Platelet aggregation inhibitors
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system

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  • Organic Chemistry (AREA)
  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Engineering & Computer Science (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Public Health (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Cardiology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Diabetes (AREA)
  • Hematology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)

Abstract

Die Erfindung betrifft physiologisch verträgliche Salze des Wirkstoffs 3- [(2-{ [4- (Hexyloxycarbonylamino-imino-methyl) -phenylamino] -methyl}-l-methyl-lH-benzimidazol-5-carbonyl ) -pyridin-2-yl-amino] -propionsäure-ethylester .
PCT/EP2006/061820 2005-04-27 2006-04-25 Physiologisch verträgliche salze von 3-[(2-{[4-(hexyloxycarbonylamino-imino-methyl)-phenylamino]-methyl}-1-methyl-1h-benzimidazol-5-carbonyl)-pyridin-2-yl-amino]-propionsäure-ethylester WO2006114415A2 (de)

Priority Applications (3)

Application Number Priority Date Filing Date Title
JP2008508213A JP2008539199A (ja) 2005-04-27 2006-04-25 ３−［（２−｛［４−（ヘキシルオキシカルボニルアミノ−イミノ−メチル）−フェニルアミノ］−メチル｝−１−メチル−１ｈ−ベンゾイミダゾール−５−カルボニル）−ピリジン−２−イル−アミノ］−プロピオン酸エチルエステルの生理的に許容される塩
EP06754844A EP1877395A2 (de) 2005-04-27 2006-04-25 Physiologisch verträgliche salze von 3-[(2-{[4-(hexyloxycarbonylamino-imino-methyl)-phenylamino]-methyl}-1-methyl-1h-benzimidazol-5-carbonyl)-pyridin-2-yl-amino]-propionsäure-ethylester
CA002606090A CA2606090A1 (en) 2005-04-27 2006-04-25 Physiologically acceptable salts of 3-[(2-{[4-(hexyloxycarbonylamino-imino-methyl)-phenylamino]-methyl}-1-methyl-1h-benzimidazole-5-carbonyl)-pyridin-2-yl-amino] propionic acid ethyl ester

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE102005020002A DE102005020002A1 (de) 2005-04-27 2005-04-27 Physiologisch verträgliche Salze von 3-[(2-{[4-(Hexyloxycarbonylamino-imino-methyl)-phenylamino]-methyl}-1-methyl-1H-benzimidazol-5-carbonyl)-pyridin-2-yl-amino]-propionsäure-ethylester
DE102005020002.8 2005-04-27

Publications (2)

Publication Number Publication Date
WO2006114415A2 WO2006114415A2 (de) 2006-11-02
WO2006114415A3 true WO2006114415A3 (de) 2007-01-25

Family

ID=36952435

Family Applications (1)

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PCT/EP2006/061820 WO2006114415A2 (de) 2005-04-27 2006-04-25 Physiologisch verträgliche salze von 3-[(2-{[4-(hexyloxycarbonylamino-imino-methyl)-phenylamino]-methyl}-1-methyl-1h-benzimidazol-5-carbonyl)-pyridin-2-yl-amino]-propionsäure-ethylester

Country Status (10)

Country Link
US (2) US20060247278A1 (de)
EP (1) EP1877395A2 (de)
JP (1) JP2008539199A (de)
AR (1) AR054261A1 (de)
CA (1) CA2606090A1 (de)
DE (1) DE102005020002A1 (de)
PE (1) PE20061321A1 (de)
TW (1) TW200716610A (de)
UY (1) UY29493A1 (de)
WO (1) WO2006114415A2 (de)

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US20030181488A1 (en) * 2002-03-07 2003-09-25 Boehringer Ingelheim Pharma Gmbh & Co. Kg Administration form for the oral application of 3-[(2-{[4-(hexyloxycarbonylamino-imino-methyl)-phenylamino]-methyl}-1-methyl-1H-benzimidazol-5-carbonyl)-pyridin-2-yl-amino]-propionic acid ethyl ester and the salts thereof
DE10339862A1 (de) * 2003-08-29 2005-03-24 Boehringer Ingelheim Pharma Gmbh & Co. Kg 3-[(2-{[4-(Hexyloxycarbonylamino-imino-methyl)- phenylamino]-methyl}-1-methyl-1H-benzimidazol-5-carbonyl)-pyridin-2-yl-amino]-propionsäure-ethylester-Methansulfonat und dessen Verwendung als Arzneimittel
EP2074112A1 (de) * 2006-10-10 2009-07-01 Boehringer Ingelheim International GmbH Physiologisch akzeptable salze aus 3-[(2-{[4-(hexyloxycarbonylamino-imino-methyl)-phenylamino]-methyl}-1-methyl-1h-benzimidazol-5-carbonyl)-pyridin-2-yl-amino]-propionsäureethylester
NZ586868A (en) * 2008-03-28 2012-02-24 Boehringer Ingelheim Int Process for preparing orally administered dabigatran formulations
TWI436994B (zh) * 2008-07-14 2014-05-11 Boehringer Ingelheim Int 製備含有達比加群（ｄａｂｉｇａｔｒａｎ）之藥物組合物的新穎方法
PE20110431A1 (es) 2008-11-11 2011-07-13 Boehringer Ingelheim Int Etexilato de dabigatran o una sal del mismo
KR101822368B1 (ko) * 2009-02-02 2018-01-31 베링거 인겔하임 인터내셔날 게엠베하 동결건조된 다비가트란
HUP1000069A2 (en) 2010-02-02 2012-05-02 Egis Gyogyszergyar Nyilvanosan M Kod Ruszvunytarsasag New salts for the preparation of pharmaceutical composition
EA201201263A1 (ru) 2010-03-08 2013-04-30 Рациофарм Гмбх Фармацевтическая композиция, содержащая этексилат дабигатрана
WO2012004397A1 (en) 2010-07-09 2012-01-12 Esteve Química, S.A. Intermediates and process for preparing a thrombin specific inhibitor
MX2013000295A (es) 2010-07-09 2013-05-28 Esteve Quimica Sa Procedimiento de preparacion de un inhibidor especifico de la trombina.
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JP2014517843A (ja) 2011-05-24 2014-07-24 テバ ファーマシューティカル インダストリーズ リミティド 医薬組成物用の圧縮コア
WO2013110567A1 (en) * 2012-01-24 2013-08-01 Boehringer Ingelheim International Gmbh Novel orally administered dabigatran formulation
CN103304539A (zh) * 2012-03-07 2013-09-18 天津药物研究院 达比加群酯苹果酸盐及其制备方法和应用
WO2013144971A1 (en) 2012-03-27 2013-10-03 Cadila Healthcare Limited New solid forms of dabigatran etexilate bisulfate and mesylate and processes to prepare them
WO2013150545A2 (en) 2012-04-02 2013-10-10 Msn Laboratories Limited Process for the preparation of benzimidazole derivatives and salts thereof
WO2014049586A2 (en) 2012-09-28 2014-04-03 Ranbaxy Laboratories Limited Process for the preparation of dabigatran etexilate or pharmaceutically acceptable salt thereof
IN2015DN02616A (de) 2012-09-28 2015-09-18 Ranbaxy Lab Ltd
EP2722034B1 (de) 2012-10-19 2020-09-16 Sanovel Ilac Sanayi ve Ticaret A.S. Orale pharmazeutische zusammensetzungen enthaltend dabigatran
EP2722033A1 (de) 2012-10-19 2014-04-23 Sanovel Ilac Sanayi ve Ticaret A.S. Pharmazeutische Zusammensetzungen aus dabigatranfreier Base
CN103864756B (zh) * 2012-12-11 2018-06-15 四川海思科制药有限公司 丁二磺酸达比加群酯及其制备方法和用途
WO2014178017A1 (en) 2013-04-30 2014-11-06 Ranbaxy Laboratories Limited Dabigatran etexilate impurity, process of its preparation, and its use as a reference standard
WO2015124764A1 (en) 2014-02-24 2015-08-27 Erregierre S.P.A. Synthesis process of dabigatran etexilate mesylate, intermediates of the process and novel polymorph of dabigatran etexilate
CN104892574A (zh) 2014-03-04 2015-09-09 浙江海正药业股份有限公司 达比加群酯甲磺酸盐的晶型及其制备方法和用途
CN108947966A (zh) * 2014-04-04 2018-12-07 江苏天士力帝益药业有限公司 达比加群酯甲磺酸盐新晶型及其制备方法
WO2015155297A1 (en) 2014-04-11 2015-10-15 Sanovel Ilac Sanayi Ve Ticaret A.S. Pharmaceutical combinations of dabigatran and h2-receptor antagonists
WO2015155281A1 (en) 2014-04-11 2015-10-15 Sanovel Ilac Sanayi Ve Ticaret A.S. Pharmaceutical combinations of dabigatran and proton pump inhibitors
WO2017013106A1 (en) 2015-07-20 2017-01-26 Sanovel Ilac Sanayi Ve Ticaret A.S. Pharmaceutical formulations of dabigatran free base
TR201606697A2 (tr) 2016-05-20 2017-12-21 Sanovel Ilac Sanayi Ve Ticaret Anonim Sirketi Dabi̇gatranin yeni̇ oral farmasöti̇k formülasyonlari
TR201617984A2 (tr) 2016-12-07 2018-06-21 Sanovel Ilac Sanayi Ve Ticaret Anonim Sirketi Dabi̇gatranin farmasöti̇k kompozi̇syonlari
WO2018104387A1 (en) 2016-12-07 2018-06-14 Sanovel Ilac Sanayi Ve Ticaret A.S. Multilayered tablet compositions of dabigatran
TR201722186A2 (tr) 2017-12-27 2019-07-22 Sanovel Ilac Sanayi Ve Ticaret Anonim Sirketi Dabi̇gatranin farmasöti̇k kompozi̇syonlari
TR201722323A2 (tr) 2017-12-27 2019-07-22 Sanovel Ilac Sanayi Ve Ticaret Anonim Sirketi Dabi̇gatranin oral farmasöti̇k kompozi̇syonlari
TR201722630A2 (de) 2017-12-28 2019-07-22 Sanovel Ilac Sanayi Ve Ticaret Anonim Sirketi

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WO1998037075A1 (de) * 1997-02-18 1998-08-27 Boehringer Ingelheim Pharma Kg Disubstituierte bicyclische heterocyclen, ihre herstellung und ihre verwendung als arzneimittel
WO2004014894A1 (de) * 2002-08-02 2004-02-19 Boehringer Ingelheim Pharma Gmbh & Co. Kg Neue prodrugs von 1-methyl-2(4-amidinophenylaminomethyl)-benzimidazol-5-yl-carbonsäure-(n-2-pyridil-n-2-hydroxycarbonylethyl)-amid, ihre herstellung und ihre verwendung als arzneimittel
WO2005018615A1 (de) * 2003-08-16 2005-03-03 Boehringer Ingelheim International Gmbh Tablette enthaltend 3-[(2-{[4-(hexyloxycarbonylamino-imino-methyl)-phenylamino]-methyl}-1-methyl-1h-benzimidazol-5-carbonyl)-pyridin-2-yl-amino]-propionsäure-ethylester oder dessen salze
WO2005028468A1 (de) * 2003-08-29 2005-03-31 Boehringer Ingelheim International Gmbh 3-[(2-{[4-(hexyloxycarbonylamino-imino-methyl)-phenylamino]-methyl}-1-methyl-1h-benzimidazol-5-carbonyl)-pyridin-2-yl-amino]-propionsäure-ethylester -methansulfonat und dessen verwendung als arzneimittel
WO2006000353A1 (de) * 2004-06-25 2006-01-05 Boehringer Ingelheim International Gmbh Verfahren zur herstellung von 4-(benzimidazolylmethylamino)- benzamidinen

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US6414008B1 (en) * 1997-04-29 2002-07-02 Boehringer Ingelheim Pharma Kg Disubstituted bicyclic heterocycles, the preparation thereof, and their use as pharmaceutical compositions
US20030181488A1 (en) * 2002-03-07 2003-09-25 Boehringer Ingelheim Pharma Gmbh & Co. Kg Administration form for the oral application of 3-[(2-{[4-(hexyloxycarbonylamino-imino-methyl)-phenylamino]-methyl}-1-methyl-1H-benzimidazol-5-carbonyl)-pyridin-2-yl-amino]-propionic acid ethyl ester and the salts thereof

Patent Citations (5)

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Publication number Priority date Publication date Assignee Title
WO1998037075A1 (de) * 1997-02-18 1998-08-27 Boehringer Ingelheim Pharma Kg Disubstituierte bicyclische heterocyclen, ihre herstellung und ihre verwendung als arzneimittel
WO2004014894A1 (de) * 2002-08-02 2004-02-19 Boehringer Ingelheim Pharma Gmbh & Co. Kg Neue prodrugs von 1-methyl-2(4-amidinophenylaminomethyl)-benzimidazol-5-yl-carbonsäure-(n-2-pyridil-n-2-hydroxycarbonylethyl)-amid, ihre herstellung und ihre verwendung als arzneimittel
WO2005018615A1 (de) * 2003-08-16 2005-03-03 Boehringer Ingelheim International Gmbh Tablette enthaltend 3-[(2-{[4-(hexyloxycarbonylamino-imino-methyl)-phenylamino]-methyl}-1-methyl-1h-benzimidazol-5-carbonyl)-pyridin-2-yl-amino]-propionsäure-ethylester oder dessen salze
WO2005028468A1 (de) * 2003-08-29 2005-03-31 Boehringer Ingelheim International Gmbh 3-[(2-{[4-(hexyloxycarbonylamino-imino-methyl)-phenylamino]-methyl}-1-methyl-1h-benzimidazol-5-carbonyl)-pyridin-2-yl-amino]-propionsäure-ethylester -methansulfonat und dessen verwendung als arzneimittel
WO2006000353A1 (de) * 2004-06-25 2006-01-05 Boehringer Ingelheim International Gmbh Verfahren zur herstellung von 4-(benzimidazolylmethylamino)- benzamidinen

Also Published As

Publication number Publication date
TW200716610A (en) 2007-05-01
AR054261A1 (es) 2007-06-13
JP2008539199A (ja) 2008-11-13
DE102005020002A1 (de) 2006-11-02
PE20061321A1 (es) 2007-01-15
US20060247278A1 (en) 2006-11-02
EP1877395A2 (de) 2008-01-16
WO2006114415A2 (de) 2006-11-02
UY29493A1 (es) 2006-11-30
CA2606090A1 (en) 2006-11-02
US20090042948A1 (en) 2009-02-12

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