LU91571I2 - Une combinaison de olmesartan medoxomil, facultativement sous forme d'un sel pharmaceutiquement acceptable, et d'un bésylate d'amplodipine - Google Patents

Une combinaison de olmesartan medoxomil, facultativement sous forme d'un sel pharmaceutiquement acceptable, et d'un bésylate d'amplodipine

Info

Publication number
LU91571I2
LU91571I2 LU91571C LU91571C LU91571I2 LU 91571 I2 LU91571 I2 LU 91571I2 LU 91571 C LU91571 C LU 91571C LU 91571 C LU91571 C LU 91571C LU 91571 I2 LU91571 I2 LU 91571I2
Authority
LU
Luxembourg
Prior art keywords
alkyl
aryl
alkoxy
substd
halo
Prior art date
Application number
LU91571C
Other languages
English (en)
Original Assignee
Daiichi Sankyo Co Ltd
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=27549327&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=LU91571(I2) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Daiichi Sankyo Co Ltd filed Critical Daiichi Sankyo Co Ltd
Publication of LU91571I2 publication Critical patent/LU91571I2/fr

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
    • C07D403/10—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a carbon chain containing aromatic rings
    • 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
    • A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/415—1,2-Diazoles
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • 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
    • A61P9/12—Antihypertensives
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
    • C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
    • C07D233/66—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members 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
    • C07D233/90—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
    • C07D405/12—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/14—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero rings
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
    • C07F7/02—Silicon compounds
    • C07F7/08—Compounds having one or more C—Si linkages
    • C07F7/18—Compounds having one or more C—Si linkages as well as one or more C—O—Si linkages
    • C07F7/1804—Compounds having Si-O-C linkages
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P20/00—Technologies relating to chemical industry
    • Y02P20/50—Improvements relating to the production of bulk chemicals
    • Y02P20/55—Design of synthesis routes, e.g. reducing the use of auxiliary or protecting groups
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P20/00—Technologies relating to chemical industry
    • Y02P20/50—Improvements relating to the production of bulk chemicals
    • Y02P20/582—Recycling of unreacted starting or intermediate materials

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Epidemiology (AREA)
  • Cardiology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Breeding Of Plants And Reproduction By Means Of Culturing (AREA)
  • Dental Preparations (AREA)
  • Phenolic Resins Or Amino Resins (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
LU91571C 1991-02-21 2009-05-11 Une combinaison de olmesartan medoxomil, facultativement sous forme d'un sel pharmaceutiquement acceptable, et d'un bésylate d'amplodipine LU91571I2 (fr)

Applications Claiming Priority (6)

Application Number Priority Date Filing Date Title
JP2709891 1991-02-21
JP9658891 1991-04-26
JP13488991 1991-06-06
JP16713891 1991-07-08
JP17397291 1991-07-15
JP18484191 1991-07-24

Publications (1)

Publication Number Publication Date
LU91571I2 true LU91571I2 (fr) 2009-07-13

Family

ID=27549327

Family Applications (4)

Application Number Title Priority Date Filing Date
LU91056C LU91056I2 (fr) 1991-02-21 2004-01-26 Dérivés de 1-biphénylimidazole, leur préparation et leur utilisation thérapeutique.
LU91330C LU91330I2 (fr) 1991-02-21 2007-04-02 Une combinaison d'olmesartan medoxomil, optionnellement sous la forme d'un sel pharmaceutiquement acceptable et d'hydrochlorothiazide (olmetec plus)
LU91571C LU91571I2 (fr) 1991-02-21 2009-05-11 Une combinaison de olmesartan medoxomil, facultativement sous forme d'un sel pharmaceutiquement acceptable, et d'un bésylate d'amplodipine
LU91847C LU91847I2 (fr) 1991-02-21 2011-07-26 Combinaison de olmesartan medoxomil, optionnellement sous forme d'un sel pharmaceutiquement acceptable, et amlodipine besylate et hydrochlorothiazide

Family Applications Before (2)

Application Number Title Priority Date Filing Date
LU91056C LU91056I2 (fr) 1991-02-21 2004-01-26 Dérivés de 1-biphénylimidazole, leur préparation et leur utilisation thérapeutique.
LU91330C LU91330I2 (fr) 1991-02-21 2007-04-02 Une combinaison d'olmesartan medoxomil, optionnellement sous la forme d'un sel pharmaceutiquement acceptable et d'hydrochlorothiazide (olmetec plus)

Family Applications After (1)

Application Number Title Priority Date Filing Date
LU91847C LU91847I2 (fr) 1991-02-21 2011-07-26 Combinaison de olmesartan medoxomil, optionnellement sous forme d'un sel pharmaceutiquement acceptable, et amlodipine besylate et hydrochlorothiazide

Country Status (23)

Country Link
EP (2) EP0545912B1 (fr)
JP (1) JPH07121918B2 (fr)
KR (1) KR0128289B1 (fr)
CN (3) CN1045770C (fr)
AT (2) ATE200777T1 (fr)
CA (2) CA2061607C (fr)
CZ (1) CZ289194B6 (fr)
DE (6) DE10299043I2 (fr)
DK (2) DK0545912T3 (fr)
ES (2) ES2156866T3 (fr)
FI (2) FI112942B3 (fr)
GR (2) GR3035906T3 (fr)
HK (2) HK1011361A1 (fr)
HU (3) HU223338B1 (fr)
IE (1) IE920540A1 (fr)
IL (3) IL114996A (fr)
IS (1) IS1756B (fr)
LU (4) LU91056I2 (fr)
NL (3) NL300133I2 (fr)
NO (6) NO304516B3 (fr)
NZ (1) NZ241681A (fr)
PT (2) PT503785E (fr)
RU (1) RU2128173C1 (fr)

Families Citing this family (103)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5616599A (en) * 1991-02-21 1997-04-01 Sankyo Company, Limited Angiotensin II antagosist 1-biphenylmethylimidazole compounds and their therapeutic use
PT573218E (pt) * 1992-06-02 2001-06-29 Sankyo Co 4-carbonilimidazoles como antagonistas de angiotensina ii e sua utilizacao terapeutica
RU2109736C1 (ru) * 1992-12-17 1998-04-27 Санкио Компани Лимитед Производные бифенила и способ их получения
US5395844A (en) * 1993-06-10 1995-03-07 The Du Pont Merck Pharmaceutical Company Imidazole 5-position substituted angiotensin II antagonists
RU2123847C1 (ru) * 1994-03-16 1998-12-27 Санкио Компани Лимитед Лекарственное средство и способ лечения повышенного глазного давления и/или глаукомы
TW442301B (en) 1995-06-07 2001-06-23 Sanofi Synthelabo Pharmaceutical compositions containing irbesartan
AUPN786896A0 (en) 1996-02-02 1996-02-29 Telstra Corporation Limited A network fault system
RU2183128C2 (ru) 1996-07-15 2002-06-10 Санкио Компани Лимитед Фармацевтическая композиция
WO1998034922A1 (fr) * 1997-02-05 1998-08-13 Sankyo Company, Limited Agent destine a la prophylaxie ou la therapie des complications diabetiques
WO2000078727A1 (fr) * 1999-06-22 2000-12-28 Takeda Chemical Industries, Ltd. Methode de preparation de derives d'imidazole
SE9903028D0 (sv) 1999-08-27 1999-08-27 Astra Ab New use
PE20010781A1 (es) 1999-10-22 2001-08-08 Takeda Chemical Industries Ltd Compuestos 1-(1h-imidazol-4-il)-1-(naftil-2-sustituido)etanol, su produccion y utilizacion
JP4521844B2 (ja) * 2000-04-18 2010-08-11 日本曹達株式会社 ４，５−ジシアノイミダゾールの製造方法
AU2001284413A1 (en) * 2000-08-30 2002-03-13 Sankyo Company Limited Medicinal compositions for preventing or treating heart failure
US8168616B1 (en) 2000-11-17 2012-05-01 Novartis Ag Combination comprising a renin inhibitor and an angiotensin receptor inhibitor for hypertension
NZ525913A (en) * 2000-11-21 2004-05-28 Sankyo Co A pharmaceutical composition
NZ531346A (en) * 2001-08-28 2005-10-28 Sankyo Co Medicinal compositions containing angiotensin II receptor antagonist
KR101194453B1 (ko) 2003-01-31 2012-10-24 다이이찌 산쿄 가부시키가이샤 동맥 경화 및 고혈압증의 예방 및 치료를 위한 의약
CN1197866C (zh) * 2003-03-21 2005-04-20 上海医药工业研究院 4，6－二氢呋喃并[3,4－d]咪唑－6－酮衍生物及其盐和制备方法
EP1614428A4 (fr) * 2003-04-15 2010-01-06 Sankyo Co Medicament destine a la prevention ou au traitement des maladies oculaires angiogeniques
US7732162B2 (en) 2003-05-05 2010-06-08 Probiodrug Ag Inhibitors of glutaminyl cyclase for treating neurodegenerative diseases
GB0316546D0 (en) 2003-07-15 2003-08-20 Novartis Ag Process for the manufacture of organic compounds
EP2428516A1 (fr) 2003-11-19 2012-03-14 Metabasis Therapeutics, Inc. Nouvelles substances thyromimetiques contenant du phosphore
GB0327839D0 (en) 2003-12-01 2003-12-31 Novartis Ag Organic compounds
JP2005206603A (ja) * 2004-01-21 2005-08-04 Teva Pharmaceutical Industries Ltd カンデサルタンシレキセチルの調製
GB0402262D0 (en) 2004-02-02 2004-03-10 Novartis Ag Process for the manufacture of organic compounds
US7692023B2 (en) 2004-02-11 2010-04-06 Teva Pharmaceutical Industries Ltd. Candesartan cilexetil polymorphs
US7157584B2 (en) 2004-02-25 2007-01-02 Takeda Pharmaceutical Company Limited Benzimidazole derivative and use thereof
US20080161321A1 (en) 2004-03-17 2008-07-03 David Louis Feldman Use of Renin Inhibitors in Therapy
US7528258B2 (en) * 2004-09-02 2009-05-05 Teva Pharmaceutical Industries Ltd Preparation of olmesartan medoxomil
EP1799199B1 (fr) 2004-10-08 2012-03-28 Novartis AG Utilisation d'inhibiteurs de renine pour la prevention ou le traitement du dysfonctionnement diastolique ou de la cardiopathie diastolique
WO2006046593A1 (fr) 2004-10-27 2006-05-04 Daiichi Sankyo Company, Limited Composé du benzène ayant deux ou plus de deux substituants
JP2007525504A (ja) * 2004-12-30 2007-09-06 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 ２．５よりも高いｐＨでオルメサルタンメドキソミルを調製するための方法
WO2006073519A1 (fr) * 2005-01-03 2006-07-13 Teva Pharmaceutical Industries Ltd. Olmesartan medoxomil a teneur reduite en impuretes
DE602006010364D1 (de) * 2005-04-22 2009-12-24 Daiichi Sankyo Co Ltd Pharmazeutikum zur prävention oder behandlung von metabolischer knochenkrankheit
US7943779B2 (en) * 2005-07-29 2011-05-17 Krka Process for the preparation of olmesartan medoxomil
EP1816131A1 (fr) * 2006-02-06 2007-08-08 KRKA, tovarna zdravil, d.d., Novo mesto Procédé pour la préparation du olmesartan medoxomil
CZ299265B6 (cs) * 2005-10-20 2008-05-28 Zentiva, A. S. Zpusob výroby 1-(cyklohexyloxykarbonyloxy)ethyl-2-ethoxy-1-[[2'-(1H-tetrazol-5-yl)bifenyl-4-yl]methyl]benzimidazol-7-karboxylátu (candesartan cilexetilu)
CZ299902B6 (cs) * 2005-10-27 2008-12-29 Zentiva, A. S Zpusob odstranování trifenylmethanové chránicí skupiny u prekurzoru antihypertenzních léciv
EP1801111B1 (fr) * 2005-12-20 2014-07-16 LEK Pharmaceuticals d.d. Formes polymorphes du Olmesartan Medoxomil
JP5047156B2 (ja) * 2006-02-27 2012-10-10 武田薬品工業株式会社 医薬パッケージ
ATE526963T1 (de) 2006-05-04 2011-10-15 Lek Pharmaceuticals Pharmazeutische zusammensetzung mit olmesartan- medoxomil
WO2007148344A2 (fr) * 2006-06-19 2007-12-27 Matrix Laboratories Limited Procédé de préparation d'olmésartan médoxomil
US8242151B2 (en) 2007-02-07 2012-08-14 Kyowa Hakko Kirin Co., Ltd. Tricyclic compounds
CA2679446C (fr) 2007-03-01 2016-05-17 Probiodrug Ag Nouvelle utilisation d'inhibiteurs de la glutaminyl cyclase
EP2141160A4 (fr) * 2007-03-23 2011-06-29 Daiichi Sankyo Co Ltd Cristal moulu d'olmésartan médoxomil
US9656991B2 (en) 2007-04-18 2017-05-23 Probiodrug Ag Inhibitors of glutaminyl cyclase
TWI448284B (zh) * 2007-04-24 2014-08-11 Theravance Inc 雙效抗高血壓劑
CN101311168B (zh) * 2007-05-21 2010-12-08 上海医药工业研究院 4-(1-羟基-1-甲基乙基)-2-丙基咪唑-5-羧酸酯的制备方法
CN101311169B (zh) * 2007-05-21 2011-03-16 上海医药工业研究院 4-(1-羟基-1-甲基乙基)-2-丙基咪唑-5-羧酸乙酯的制备方法
EP2170930B3 (fr) 2007-06-04 2013-10-02 Synergy Pharmaceuticals Inc. Agonistes de guanylase cyclase utiles pour le traitement de troubles gastro-intestinaux, d'inflammation, de cancer et d'autres troubles
US8969514B2 (en) 2007-06-04 2015-03-03 Synergy Pharmaceuticals, Inc. Agonists of guanylate cyclase useful for the treatment of hypercholesterolemia, atherosclerosis, coronary heart disease, gallstone, obesity and other cardiovascular diseases
GB0710680D0 (en) * 2007-06-05 2007-07-11 Generics Uk Ltd Novel crystalline form of olmesartan medoxmil
WO2009001661A1 (fr) * 2007-06-22 2008-12-31 Daiichi Sankyo Company, Limited Agent médicamenteux pour la prévention ou le traitement de la maladie d'alzheimer
JP2011522828A (ja) 2008-06-04 2011-08-04 シナジー ファーマシューティカルズ インコーポレイテッド 胃腸障害、炎症、癌、およびその他の障害の治療のために有用なグアニル酸シクラーゼのアゴニスト
ES2540062T3 (es) 2008-06-09 2015-07-08 Daiichi Sankyo Company, Limited Procedimiento de producción de un compuesto de 1-bifenilmetilimidazol
AU2009270833B2 (en) 2008-07-16 2015-02-19 Bausch Health Ireland Limited Agonists of guanylate cyclase useful for the treatment of gastrointestinal, inflammation, cancer and other disorders
JP5559689B2 (ja) 2008-08-06 2014-07-23 協和発酵キリン株式会社 ３環系化合物
WO2010054515A1 (fr) 2008-11-17 2010-05-20 上海医药工业研究院 Procédé de préparation de 4-(1-hydroxy-1-méthyléthyl)-2-propyl-imidazole-5-carboxylates
JP2009102340A (ja) * 2008-12-04 2009-05-14 Daiichi Sankyo Co Ltd イミダゾール誘導体の製造法（２）
WO2010093601A1 (fr) 2009-02-10 2010-08-19 Metabasis Therapeutics, Inc. Nouveaux thyromimetiques contenant de l'acide sulfonique et methodes d'utilisation associees
WO2010126014A1 (fr) 2009-04-28 2010-11-04 第一三共株式会社 Nouveaux cristaux solvates
TWI539948B (zh) 2009-04-28 2016-07-01 第一三共股份有限公司 奧美沙坦酯之製造方法
MX2012002993A (es) 2009-09-11 2012-04-19 Probiodrug Ag Derivados heterociclicos como inhibidores de ciclasa glutaminilo.
CN102050816A (zh) * 2009-10-28 2011-05-11 北京万全阳光医学技术有限公司 一种合成奥美沙坦酯的方法
HUP0900788A2 (en) 2009-12-16 2011-11-28 Sanofi Aventis Process for producing 4-bromomethyl-biphenyl derivatives
WO2011083112A2 (fr) 2010-01-05 2011-07-14 Ratiopharm Gmbh Forme posologique orale solide contenant de l'olmésartan médoxomil
WO2011107530A2 (fr) 2010-03-03 2011-09-09 Probiodrug Ag Nouveaux inhibiteurs
JP5688745B2 (ja) 2010-03-10 2015-03-25 プロビオドルグ エージー グルタミニルシクラーゼ（ｑｃ、ｅｃ２．３．２．５）の複素環阻害剤
EP2560953B1 (fr) 2010-04-21 2016-01-06 Probiodrug AG Inhibiteurs de glutaminyl cyclase
JP5137996B2 (ja) * 2010-04-28 2013-02-06 日本曹達株式会社 ４，５−ジシアノイミダゾールの製造方法
IT1400311B1 (it) 2010-05-10 2013-05-24 Menarini Int Operations Lu Sa Associazione di inibitori della xantina ossidasi e antagonisti del recettore dell'angiotensina ii e loro uso.
EP2425859A1 (fr) 2010-08-08 2012-03-07 Abdi Ibrahim Ilac Sanayi ve Ticaret Anonim Sirketi Formulations de l'olmesartane
US9616097B2 (en) 2010-09-15 2017-04-11 Synergy Pharmaceuticals, Inc. Formulations of guanylate cyclase C agonists and methods of use
CN102060778B (zh) * 2010-12-24 2012-05-23 江苏江神药物化学有限公司 一种4-(1-羟基-1-甲基乙基)-2-丙基咪唑-5-羧酸乙酯的合成方法
CN102206208A (zh) * 2010-12-24 2011-10-05 上海现代制药股份有限公司 含低水平杂质的奥美沙坦酯的制备方法
ES2570167T3 (es) 2011-03-16 2016-05-17 Probiodrug Ag Derivados de benzimidazol como inhibidores de glutaminil ciclasa
TW201311678A (zh) 2011-08-03 2013-03-16 Kyowa Hakko Kirin Co Ltd 二苯并氧呯衍生物
BR112014014527A2 (pt) 2011-12-15 2017-06-13 Takeda Pharmaceuticals Usa Inc combinações de azilsartan e clorotalidona para tratar hipertensão em pacientes negros
CN103304550B (zh) * 2012-03-16 2016-01-27 湖南欧亚生物有限公司 一种奥美沙坦酯的制备方法
US9624181B2 (en) 2012-08-31 2017-04-18 Api Corporation Method for producing biaryl compound
JP5881837B2 (ja) 2012-09-26 2016-03-09 株式会社エーピーアイ コーポレーション テトラゾール化合物の脱保護方法
JP6218084B2 (ja) 2012-10-04 2017-10-25 国立研究開発法人国立循環器病研究センター 悪性腫瘍転移抑制用医薬
CN103012382B (zh) * 2012-12-05 2016-10-05 迪沙药业集团有限公司 一种奥美沙坦酯的制备方法
CN103044407A (zh) * 2012-12-20 2013-04-17 安徽悦康凯悦制药有限公司 奥美沙坦酯的制备方法
CN103965167A (zh) * 2013-01-29 2014-08-06 通化济达医药有限公司 咪唑羧酸衍生物
JP2014152127A (ja) * 2013-02-06 2014-08-25 Tokuyama Corp オルメサルタンメドキソミルの製造方法
CA2905435A1 (fr) 2013-03-15 2014-09-25 Synergy Pharmaceuticals Inc. Compositions utiles pour le traitement de troubles gastro-intestinaux
WO2014151206A1 (fr) 2013-03-15 2014-09-25 Synergy Pharmaceuticals Inc. Agonistes de la guanylate cyclase et leurs utilisations
EP3004138B1 (fr) 2013-06-05 2024-03-13 Bausch Health Ireland Limited Agonistes ultra-purs de guanylate cyclase c, leur procédé de production et d'utilisation
EP3025711B1 (fr) 2013-07-23 2020-11-18 Daiichi Sankyo Company, Limited Médicament destiné à la prévention ou au traitement de l'hypertension artérielle
CN103880825B (zh) * 2014-03-14 2019-03-05 浙江华海药业股份有限公司 一种高纯的三苯甲基奥美沙坦酯的制备工艺
CN104356069B (zh) * 2014-11-18 2016-09-14 黄冈鲁班药业有限公司 奥美沙坦酯中间体4-(1-羟基-1-甲基乙基)-2-丙基咪唑-5-羧酸乙酯的制备方法及应用
CN104447564B (zh) * 2014-11-24 2016-08-31 广州天赐高新材料股份有限公司 高纯度4,5-二氰基-2-三氟甲基咪唑及其盐的制备方法
CN104402873A (zh) * 2014-12-02 2015-03-11 千辉药业（安徽）有限责任公司 一种奥美沙坦酯中间体的制备方法
CN105481842A (zh) * 2015-12-15 2016-04-13 江苏中邦制药有限公司 一种奥美沙坦酯的制备方法
EP3434284A4 (fr) 2016-03-24 2019-11-13 Daiichi Sankyo Company, Limited Médicament pour le traitement d'une maladie rénale
CN106749195A (zh) * 2016-12-30 2017-05-31 青岛黄海制药有限责任公司 一种奥美沙坦酯中间体杂质合成、鉴定的方法
CN107474042A (zh) * 2017-09-07 2017-12-15 浙江华海致诚药业有限公司 一种三苯甲基奥美沙坦酯的晶型h
ES2812698T3 (es) 2017-09-29 2021-03-18 Probiodrug Ag Inhibidores de glutaminil ciclasa
CN109081812B (zh) * 2018-08-30 2022-08-16 黄冈鲁班药业股份有限公司 4-(1-羟基-1-甲基乙基)-2-丙基咪唑-5-羧酸乙酯一水合物
KR102131359B1 (ko) 2018-09-07 2020-07-07 오토텔릭바이오 주식회사 안정성이 향상된 의약 조성물
CN112778209B (zh) * 2019-11-04 2024-05-14 宜昌东阳光长江药业股份有限公司 一种二酸的制备方法

Family Cites Families (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5671074A (en) * 1979-11-12 1981-06-13 Takeda Chem Ind Ltd 1,2-disubstituted-4-halogenoimidazole-5-acetic acid derivative
JPS5671073A (en) * 1979-11-12 1981-06-13 Takeda Chem Ind Ltd Imidazole derivative
IE802177L (en) 1980-10-21 1981-05-12 Takeda Chemical Industries Ltd Imidazol-5-ylacetic acid derivatives
US4812462A (en) 1986-04-01 1989-03-14 Warner-Lambert Company 4,5,6,7-tetrahydro-1H-imidazo[4,5-c]pyridine-6-carboxylic acid analogs having antihypertensive activity
CA1334092C (fr) 1986-07-11 1995-01-24 David John Carini Imidazoles bloquant les recepteurs de l'angiotensine ii
CA1338238C (fr) 1988-01-07 1996-04-09 David John Carini Imidazoles bloquant les recepteurs de l'angiotensine ii et combinaisons de ces imidazoles avec des diuretiques et des anti-inflammatoires non steroidiens
US5015651A (en) * 1988-01-07 1991-05-14 E. I. Du Pont De Nemours And Company Treatment of hypertension with 1,2,4-angiotensin II antagonists
US4916129A (en) 1989-01-19 1990-04-10 E. I. Du Pont De Nemours And Company Combination β-blocking/angiotensin II blocking antihypertensives
CA2016710A1 (fr) 1989-05-15 1990-11-15 Prasun K. Chakravarty Benzimidazoles substitues comme antagonistes de l'antiotensine ii
GB8911854D0 (en) 1989-05-23 1989-07-12 Ici Plc Heterocyclic compounds
IE64514B1 (en) 1989-05-23 1995-08-09 Zeneca Ltd Azaindenes
US5064825A (en) * 1989-06-01 1991-11-12 Merck & Co., Inc. Angiotensin ii antagonists
WO1991012002A1 (fr) * 1990-02-13 1991-08-22 Merck & Co., Inc. Agents antagonistes de l'angiotensine ii a base d'imidazoles dans lesquels est incorpore un element de benzyle substitue
US5140037A (en) * 1990-03-20 1992-08-18 E. I. Du Pont De Nemours And Company Treatment of central nervous system disorders with imidazole angiotensin-ii receptor antagonists

Also Published As

Publication number Publication date
IL101034A (en) 1996-10-16
CN1065063A (zh) 1992-10-07
ES2156866T3 (es) 2001-08-01
DK0545912T3 (da) 2001-06-18
CN1101384C (zh) 2003-02-12
CN1189490A (zh) 1998-08-05
EP0503785B1 (fr) 2001-04-25
DE69231801D1 (de) 2001-05-31
CA2229000C (fr) 2002-04-09
HU223667B1 (hu) 2004-11-29
DK0503785T3 (da) 2001-06-18
CA2229000A1 (fr) 1992-08-22
IL114996A (en) 1997-07-13
HU9601179D0 (en) 1996-07-29
ES2157895T7 (es) 2012-06-14
FI112942B3 (fi) 2012-03-13
NO920688D0 (no) 1992-02-21
NO304516B3 (no) 2012-06-11
KR920016429A (ko) 1992-09-24
RU95101430A (ru) 1997-02-20
IE970752A1 (en) 2000-02-23
NO2003009I2 (en) 2007-12-11
CN1045770C (zh) 1999-10-20
NZ241681A (en) 1993-07-27
CN1121859C (zh) 2003-09-24
AU1112592A (en) 1992-08-27
NO2006012I1 (no) 2006-10-30
AU647887B2 (en) 1994-03-31
FI920749A0 (fi) 1992-02-20
HU223338B1 (hu) 2004-06-28
NO304517B1 (no) 1999-01-04
IL114996A0 (en) 1995-12-08
ES2157895T3 (es) 2001-09-01
NO954507D0 (no) 1995-11-09
CN1188645A (zh) 1998-07-29
GR3035906T3 (en) 2001-08-31
JPH07121918B2 (ja) 1995-12-25
HU9200578D0 (en) 1992-05-28
NL300133I1 (nl) 2003-10-01
PT503785E (pt) 2001-08-30
CA2061607A1 (fr) 1992-08-22
IE920540A1 (en) 1992-08-26
EP0545912A2 (fr) 1993-06-09
DE122011000011I1 (de) 2011-06-16
GR3035909T3 (en) 2001-08-31
DE69231798T3 (de) 2012-07-12
DE10299043I1 (de) 2003-03-27
NO2011013I1 (no) 2011-08-22
CZ51692A3 (en) 1993-03-17
IS3819A (is) 1992-08-22
NO920688L (no) 1992-08-24
ATE200778T1 (de) 2001-05-15
NO304516B1 (no) 1999-01-04
LU91056I2 (fr) 2004-10-19
DE69231801T2 (de) 2001-12-06
IS1756B (is) 2000-12-28
FI955248A0 (fi) 1995-11-02
NO2009019I1 (no) 2009-09-21
FI955248A (fi) 1995-11-02
FI112942B (fi) 2004-02-13
DE10299043I2 (de) 2003-08-07
DE69231798D1 (de) 2001-05-31
CZ289194B6 (cs) 2001-11-14
HU211934A9 (en) 1996-01-29
JPH0578328A (ja) 1993-03-30
HUT60475A (en) 1992-09-28
NO954507L (no) 1992-08-24
DE122009000024I1 (de) 2009-09-17
CA2061607C (fr) 1999-01-19
EP0545912B1 (fr) 2001-04-25
IL101034A0 (en) 1992-11-15
FI112941B (fi) 2004-02-13
LU91330I2 (fr) 2007-06-04
EP0503785A1 (fr) 1992-09-16
RU2128173C1 (ru) 1999-03-27
EP0545912A3 (fr) 1993-06-16
DE69231798T2 (de) 2001-12-06
DE122005000051I1 (de) 2006-01-26
NL300375I1 (nl) 2009-04-01
PT545912E (pt) 2001-08-30
FI920749A (fi) 1992-08-22
NL300133I2 (nl) 2004-03-01
HK1011969A1 (en) 1999-07-23
KR0128289B1 (ko) 1998-04-02
HK1011361A1 (en) 1999-07-09
LU91847I2 (fr) 2011-09-26
ATE200777T1 (de) 2001-05-15
EP0503785B3 (fr) 2012-02-29
NL300227I1 (nl) 2006-06-01

Similar Documents

Publication Publication Date Title
LU91571I2 (fr) Une combinaison de olmesartan medoxomil, facultativement sous forme d'un sel pharmaceutiquement acceptable, et d'un bésylate d'amplodipine