ATE342263T1 - Salze von benzimidazol-derivaten und deren verwendung - Google Patents

Salze von benzimidazol-derivaten und deren verwendung

Info

Publication number
ATE342263T1
ATE342263T1 AT01954427T AT01954427T ATE342263T1 AT E342263 T1 ATE342263 T1 AT E342263T1 AT 01954427 T AT01954427 T AT 01954427T AT 01954427 T AT01954427 T AT 01954427T AT E342263 T1 ATE342263 T1 AT E342263T1
Authority
AT
Austria
Prior art keywords
salt
salts
benzimidazole derivatives
benzimidazole
äää3
Prior art date
Application number
AT01954427T
Other languages
English (en)
Inventor
Keiji Kamiyama
Hideo Hashimoto
Original Assignee
Takeda Pharmaceutical
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
Application filed by Takeda Pharmaceutical filed Critical Takeda Pharmaceutical
Application granted granted Critical
Publication of ATE342263T1 publication Critical patent/ATE342263T1/de

Links

Classifications

    • 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
    • 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
    • A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
    • A61K31/4439—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. omeprazole
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/04—Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/20—Hypnotics; Sedatives
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/04—Antibacterial agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Epidemiology (AREA)
  • Anesthesiology (AREA)
  • Biomedical Technology (AREA)
  • Neurology (AREA)
  • Neurosurgery (AREA)
  • Communicable Diseases (AREA)
  • Oncology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
AT01954427T 2000-08-04 2001-08-03 Salze von benzimidazol-derivaten und deren verwendung ATE342263T1 (de)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2000236651 2000-08-04

Publications (1)

Publication Number Publication Date
ATE342263T1 true ATE342263T1 (de) 2006-11-15

Family

ID=18728661

Family Applications (1)

Application Number Title Priority Date Filing Date
AT01954427T ATE342263T1 (de) 2000-08-04 2001-08-03 Salze von benzimidazol-derivaten und deren verwendung

Country Status (8)

Country Link
US (3) US7271182B2 (de)
EP (1) EP1306375B1 (de)
JP (1) JP5412023B2 (de)
AT (1) ATE342263T1 (de)
AU (1) AU2001276721A1 (de)
CA (2) CA2417311C (de)
DE (1) DE60123800T2 (de)
WO (1) WO2002012225A1 (de)

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US20050220870A1 (en) * 2003-02-20 2005-10-06 Bonnie Hepburn Novel formulation, omeprazole antacid complex-immediate release for rapid and sustained suppression of gastric acid
WO2004085424A1 (ja) * 2003-03-24 2004-10-07 Eisai Co., Ltd. スルホキシド誘導体またはその塩のアモルファスの製造方法
US20070060556A1 (en) * 2003-05-05 2007-03-15 Yatendra Kumar Barium salt of benzimidazole derivative
MXPA05013316A (es) 2003-06-10 2006-03-17 Teva Pharma Proceso para preparar bencimidazoles 2[-(piridinil)metil]sulfinil-sustituidos y derivados clorados novedosos de pantoprazol.
US8993599B2 (en) 2003-07-18 2015-03-31 Santarus, Inc. Pharmaceutical formulations useful for inhibiting acid secretion and methods for making and using them
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GB0403165D0 (en) * 2004-02-12 2004-03-17 Ct Novel uses for proton pump inhibitors
WO2005082888A1 (en) * 2004-03-01 2005-09-09 Milen Merkez Ilac Endustrisi A.S. Process for the preparation of magnesium salt of omeprazole
US20050239845A1 (en) * 2004-04-16 2005-10-27 Santarus, Inc. Combination of proton pump inhibitor, buffering agent, and prokinetic agent
US8815916B2 (en) 2004-05-25 2014-08-26 Santarus, Inc. Pharmaceutical formulations useful for inhibiting acid secretion and methods for making and using them
US8906940B2 (en) 2004-05-25 2014-12-09 Santarus, Inc. Pharmaceutical formulations useful for inhibiting acid secretion and methods for making and using them
EP1768668A2 (de) 2004-06-16 2007-04-04 Tap Pharmaceutical Products, Inc. Multi-ppi-dosierform
FR2871800B1 (fr) * 2004-06-17 2006-08-25 Sidem Pharma Sa Sa Sel de sodium monohydrate du s-tenatoprazole et application en therapeutique
CA2570795C (en) * 2004-06-24 2013-05-28 Astrazeneca Ab Process for the preparation of crystal modifications for use in the preparation of esomeprazole sodium salt
US7244765B2 (en) * 2004-06-25 2007-07-17 Cytokine Pharmasciences, Inc Guanylhydrazone salts, compositions, processes of making and methods of using
ES2246149B1 (es) * 2004-07-02 2007-06-01 Esteve Quimica, S.A. Formas solidas de la sal magnesica de s-omeprazol y procedimientos para su preparacion.
CN104958270A (zh) 2004-08-25 2015-10-07 伊森舍丽斯有限公司 钾atp通道开放剂的药物制剂及其应用
WO2006132217A1 (ja) * 2005-06-07 2006-12-14 Takeda Pharmaceutical Company Limited ベンズイミダゾール化合物の塩の結晶
WO2006131338A2 (en) * 2005-06-08 2006-12-14 Lek Pharmaceuticals D.D. Crystalline solvate of omeprazole sodium
WO2007041790A1 (en) * 2005-10-14 2007-04-19 Jon Pty Limited Salts of proton pump inhibitors and process for preparing same
PL1968601T3 (pl) * 2006-01-05 2012-03-30 Essentialis Inc Sole związków otwierających kanały potasowe ATP i ich zastosowanie
EP1960388A1 (de) * 2006-11-06 2008-08-27 Teva Pharmaceutical Industries Ltd. Verfahren zur herstellung von substantiell reinem pantoprazol-magnesium
CN102014638A (zh) * 2007-10-12 2011-04-13 武田制药北美公司 与食物摄入无关的治疗胃肠病症的方法
EP2222663A1 (de) * 2007-12-18 2010-09-01 Watson Pharma Private Limited Verfahren zur herstellung von stabilem amorphem r-lansoprazol
CN101250182B (zh) * 2008-03-26 2010-09-01 江苏奥赛康药业有限公司 兰索拉唑钠
BRPI0912478A2 (pt) 2008-05-14 2016-02-10 Watson Pharma Private Ltd sal de r-(+)-lansoprazol alquilamina, processo para preparar um sal de r-(+)-lansoprazol alquilamina estável e forma de dosagem farmacêutica
US20110009637A1 (en) * 2009-02-10 2011-01-13 Dario Braga Crystals of Dexlansoprazole
WO2011004387A2 (en) 2009-06-18 2011-01-13 Matrix Laboratories Ltd Process for the preparation of dexlansoprazole polymorphic forms
AU2010283928A1 (en) * 2009-08-19 2012-04-12 Apotex Pharmachem Inc. Forms of dexlansoprazole and processes for the preparation thereof
CA2795110C (en) 2010-03-31 2015-06-09 Ranbaxy Laboratories Limited Process for the preparation of dexlansoprazole
US9085556B2 (en) 2010-03-31 2015-07-21 Ranbaxy Laboraotories Limited Salts of dexlansoprazole and their preparation
CN102399212B (zh) * 2010-08-23 2014-07-16 江苏豪森医药集团有限公司 一种右兰索拉唑晶型及其制备方法
WO2012095859A1 (en) * 2011-01-12 2012-07-19 Hetero Research Foundation Polymorphs of dexlansoprazole salts
WO2012104805A1 (en) 2011-02-01 2012-08-09 Ranbaxy Laboratories Limited Process for the preparation of dexlansoprazole
EP2723728A1 (de) 2011-06-21 2014-04-30 Ranbaxy Laboratories Limited Verfahren zur herstellung von dexlansoprazol
WO2013140120A1 (en) 2012-03-22 2013-09-26 Cipla Limited Glycerol solvate forms of (r) - 2 - [ [ [3 -methyl -4 (2,2, 2 - trifluoroethoxy) pyridin- 2 - yl] methyl] sulphinyl] - 1h - ben zimidazole
WO2013179194A1 (en) 2012-05-31 2013-12-05 Ranbaxy Laboratories Limited Process for the preparation of crystalline dexlansoprazole
CN102942557A (zh) * 2012-11-26 2013-02-27 北京阜康仁生物制药科技有限公司 右兰索拉唑的新药用盐
US9011934B2 (en) 2013-06-14 2015-04-21 SatisPharma, LLC Multi-purpose anti-itch treatment
CN103788068B (zh) * 2014-02-26 2016-04-06 南京海融医药科技有限公司 高熔点的手性苯并咪唑类化合物钠盐、制备方法及其用途
CN105017216A (zh) * 2014-04-16 2015-11-04 天津药物研究院 右兰索拉唑晶型iii及其制备方法和用途
US9452178B1 (en) 2014-10-22 2016-09-27 SatisPharma, LLC Acne formulations, treatments, and pressure sensitive patches for delivery of acne formulations

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JPS6150978A (ja) 1984-08-16 1986-03-13 Takeda Chem Ind Ltd ピリジン誘導体およびその製造法
JPS62277322A (ja) * 1986-02-13 1987-12-02 Takeda Chem Ind Ltd 安定化された腸溶性抗潰瘍固形組成物
DE4035455A1 (de) 1990-11-08 1992-05-14 Byk Gulden Lomberg Chem Fab Enantiomerentrennung
SE9301830D0 (sv) 1993-05-28 1993-05-28 Ab Astra New compounds
SE9302396D0 (sv) 1993-07-09 1993-07-09 Ab Astra A novel compound form
SE504459C2 (sv) * 1994-07-15 1997-02-17 Astra Ab Förfarande för framställning av substituerade sulfoxider
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SE508669C2 (sv) * 1996-04-26 1998-10-26 Astra Ab Nytt förfarande
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Also Published As

Publication number Publication date
EP1306375A4 (de) 2004-03-31
WO2002012225A1 (en) 2002-02-14
CA2775616A1 (en) 2002-02-14
CA2417311C (en) 2012-07-10
US8809542B2 (en) 2014-08-19
US20130281704A1 (en) 2013-10-24
JP5412023B2 (ja) 2014-02-12
AU2001276721A1 (en) 2002-02-18
EP1306375A1 (de) 2003-05-02
US20070254924A1 (en) 2007-11-01
EP1306375B1 (de) 2006-10-11
CA2417311A1 (en) 2003-01-27
US20030181487A1 (en) 2003-09-25
JP2002114779A (ja) 2002-04-16
CA2775616C (en) 2013-09-17
US7271182B2 (en) 2007-09-18
DE60123800T2 (de) 2007-10-11
DE60123800D1 (de) 2006-11-23

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Legal Events

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RER Ceased as to paragraph 5 lit. 3 law introducing patent treaties