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PE20040563A1 - Compuesto de imidazol y metodo para su produccion - Google Patents

Compuesto de imidazol y metodo para su produccion

Info

Publication number
PE20040563A1
PE20040563A1 PE2003000593A PE2003000593A PE20040563A1 PE 20040563 A1 PE20040563 A1 PE 20040563A1 PE 2003000593 A PE2003000593 A PE 2003000593A PE 2003000593 A PE2003000593 A PE 2003000593A PE 20040563 A1 PE20040563 A1 PE 20040563A1
Authority
PE
Peru
Prior art keywords
methyl
ethyl
trifluoroetoxy
lil
sulfinyl
Prior art date
Application number
PE2003000593A
Other languages
English (en)
Inventor
Hiroshi Banno
Fumihiko Sato
Keiji Kamiyama
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
Publication of PE20040563A1 publication Critical patent/PE20040563A1/es

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D471/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
    • C07D471/04Ortho-condensed systems
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/04Drugs 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/04Antibacterial agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D233/00Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
    • C07D233/54Heterocyclic 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
    • C07D233/66Heterocyclic 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
    • C07D233/90Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic 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
    • C07D401/02Heterocyclic 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
    • C07D401/12Heterocyclic 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic 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
    • C07D401/14Heterocyclic 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 three or more hetero rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D405/00Heterocyclic 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
    • C07D405/02Heterocyclic 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
    • C07D405/04Heterocyclic 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 directly linked by a ring-member-to-ring-member bond
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D405/00Heterocyclic 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
    • C07D405/14Heterocyclic 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

Landscapes

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

Abstract

SE REFIERE A UN COMPUESTO DE FORMULA I DONDE, EL ANILLO A ES PIRIDINA; EL ANILLO B ES BENCENO, HETEROCICLO AROMATICO MONICICLICO; X1 Y X2 SON CADA UNO O, S; W ES HIDROCARBURO DE CADENA DIVALENTE; R ES HIDROCARBURO, GRUPO HETEROCICLO; R Y W PUEDEN ENLAZARSE; D1 Y D2 SON CADA UNO O, S, ENTRE OTROS; Y ES HIDROCARBURO, HETEROCICLO, ENTRE OTROS. SON COMPUESTOS PREFERIDOS: 2-[METIL[[(R)-2-[[[3-METIL-4-(2,2,2-TRIFLUOROETOXI)-2-PIRIDIL]METIL]SULFINIL]-1H-BENCIMIDAZO-1-LIL]CARBONIL]AMINO]ETIL ACETATO; ETIL-2-[METIL[[(R)-2-[[[3-METIL-4-(2,2,2-TRIFLUOROETOXI)-2-PIRIDIL]METIL]SULFINIL]-1H-BENCIMIDAZO-1-LIL]CARBONIL]AMINO]ETIL-CARBONATO Y 2-[METIL[[(R)-2-[[[3-METIL-4-(2,2,2-TRIFLUOROETOXI)-2-PIRIDIL]METIL]SULFINIL]-1H-BENCIMIDAZO-1-LIL]CARBONIL]AMINO]ETIL TETRAHIDROPIRA-4-NIL-CARBONATO, ENTRE OTROS. SE REFIERE TAMBIEN A UNA COMPOSICION FARMACEUTICA UTIL EN LA PROFILAXIS O TRATAMIENTO DE ULCERA PEPTICA, GASTRITIS, ESOFAGITIS PEPTICA, ENTRE OTROS
PE2003000593A 2002-06-14 2003-06-13 Compuesto de imidazol y metodo para su produccion PE20040563A1 (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP2002175086 2002-06-14
JP2003041085 2003-02-19

Publications (1)

Publication Number Publication Date
PE20040563A1 true PE20040563A1 (es) 2004-10-21

Family

ID=29738411

Family Applications (1)

Application Number Title Priority Date Filing Date
PE2003000593A PE20040563A1 (es) 2002-06-14 2003-06-13 Compuesto de imidazol y metodo para su produccion

Country Status (19)

Country Link
US (2) US7410981B2 (es)
EP (2) EP1513527B1 (es)
JP (1) JPWO2003106429A1 (es)
KR (1) KR20050009751A (es)
CN (1) CN1678315A (es)
AR (1) AR040221A1 (es)
AT (1) ATE437642T1 (es)
AU (2) AU2003242390A1 (es)
BR (1) BR0311801A (es)
CA (2) CA2489361A1 (es)
DE (1) DE60328603D1 (es)
IL (1) IL165562A0 (es)
MX (1) MXPA04012396A (es)
NO (1) NO20050141L (es)
OA (1) OA12867A (es)
PE (1) PE20040563A1 (es)
PL (1) PL373085A1 (es)
TW (1) TW200307544A (es)
WO (2) WO2003105845A1 (es)

Families Citing this family (17)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
PT1740571E (pt) 2004-04-28 2009-09-02 Hetero Drugs Ltd Processo para preparar compostos de piridinilmetil-1hbenzimidazol na forma enantiomericamente enriquecida ou como enantiómeros únicos
CA2784881C (en) 2005-02-25 2016-02-09 Takeda Pharmaceutical Company Limited Method for producing granules
KR101148399B1 (ko) * 2005-06-22 2012-05-23 일양약품주식회사 항궤양제 및 점막보호제를 함유하는 경구용 위장질환치료용 약제 조성물
US20100317689A1 (en) * 2006-09-19 2010-12-16 Garst Michael E Prodrugs of proton pump inhibitors including the 1h-imidazo[4,5-b] pyridine moiety
MX2009004475A (es) 2006-10-27 2009-08-12 Univ Missouri Composiciones que comprenden agentes acido labiles que inhiben la bomba de protones, por lo menos otro agente farmaceuticamente activo y metodos de uso de las misma.
CA2716367C (en) 2008-02-20 2015-05-26 The Curators Of The University Of Missouri Composition comprising a combination of omeprazole and lansoprazole, and a buffering agent, and methods of using same
ES2601226T3 (es) 2009-10-28 2017-02-14 Newlink Genetics Corporation Derivados de imidazol como inhibidores de IDO
US8916563B2 (en) 2010-07-16 2014-12-23 The Trustees Of Columbia University In The City Of New York Aldose reductase inhibitors and uses thereof
WO2016172436A1 (en) * 2015-04-23 2016-10-27 Temple University-Of The Commonwealth System Of Higher Education Polycationic amphiphiles and polymers thereof as antimicrobial agents and methods using same
DK3352754T3 (da) 2016-06-21 2020-12-07 Univ Columbia Aldosereduktaseinhibitorer og fremgangsmåder til anvendelse deraf
US11111216B2 (en) 2016-10-26 2021-09-07 Temple University-Of The Commonwealth System Of Higher Education Polycationic amphiphiles as antimicrobial agents and methods using same
CN119633117A (zh) 2017-07-28 2025-03-18 应用治疗公司 用于治疗半乳糖血症的组合物和方法
JP7623292B2 (ja) 2019-04-01 2025-01-28 アプライド セラピューティクス, インコーポレイテッド アルドースレダクターゼの阻害剤
CA3136100A1 (en) 2019-05-07 2020-11-12 Stephan L. ZUCHNER Treatment and detection of inherited neuropathies and associated disorders
HUE070031T2 (hu) * 2020-06-17 2025-05-28 Ildong Pharmaceutical Co Ltd Új savszekréciós inhibitor és alkalmazása
IT202200001022A1 (it) * 2022-01-21 2023-07-21 Exo Lab Italia Composti farmaceutici ibridi ottenuti mediante coniugazione di un inibitore delle pompe protoniche e un inibitore delle anidrasi carboniche
CN120590773B (zh) * 2025-08-06 2025-12-26 广州仕天材料科技有限公司 一种增强型聚碳酸酯和制备方法及在汽车照明系统中的应用

Family Cites Families (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
SE416649B (sv) 1974-05-16 1981-01-26 Haessle Ab Forfarande for framstellning av foreningar som paverkar magsyrasekretionen
SE8300736D0 (sv) 1983-02-11 1983-02-11 Haessle Ab Novel pharmacologically active compounds
KR890000387B1 (ko) 1984-09-24 1989-03-16 디 엎존 캄파니 2-(피리딜알켄술 피닐)벤즈 이미드아졸류의 n-치환 유도체의 제조방법
IL76839A (en) 1984-10-31 1988-08-31 Byk Gulden Lomberg Chem Fab Picoline derivatives,processes for the preparation thereof and pharmaceutical compositions containing the same
SE8505112D0 (sv) 1985-10-29 1985-10-29 Haessle Ab Novel pharmacological compounds
US4965269A (en) 1989-12-20 1990-10-23 Ab Hassle Therapeutically active chloro substituted benzimidazoles
US5614549A (en) * 1992-08-21 1997-03-25 Enzon, Inc. High molecular weight polymer-based prodrugs
US6093734A (en) 1998-08-10 2000-07-25 Partnership Of Michael E. Garst, George Sachs, And Jai Moo Shin Prodrugs of proton pump inhibitors
BR0009653A (pt) * 1999-04-09 2002-01-08 Basf Ag Composto, medicamento, e, uso de compostos
US6765019B1 (en) * 1999-05-06 2004-07-20 University Of Kentucky Research Foundation Permeable, water soluble, non-irritating prodrugs of chemotherapeutic agents with oxaalkanoic acids
EP1334104A2 (en) * 2000-07-07 2003-08-13 Neotherapeutics, Inc. Methods for treatment of drug-induced peripheral neuropathy and related conditions
AU2001294228A1 (en) 2000-10-12 2002-04-22 Takeda Chemical Industries Ltd. Benzimidazole compounds, process for producing the same and use thereof
MXPA03011094A (es) * 2001-05-31 2004-12-06 Medarex Inc Citotoxinas, profarmacos, ligadores, y estabilizadores utiles para ello.
US20040248941A1 (en) 2001-09-25 2004-12-09 Keiji Kamiyama Benzimidazone compound, process for producing the same, and use thereof

Also Published As

Publication number Publication date
EP1513527A1 (en) 2005-03-16
EP1514870A4 (en) 2006-08-23
EP1514870A1 (en) 2005-03-16
DE60328603D1 (de) 2009-09-10
PL373085A1 (en) 2005-08-08
CA2489361A1 (en) 2003-12-24
NO20050141D0 (no) 2005-01-11
CA2489470A1 (en) 2003-12-24
AU2003242388A1 (en) 2003-12-31
WO2003105845A1 (en) 2003-12-24
KR20050009751A (ko) 2005-01-25
ATE437642T1 (de) 2009-08-15
BR0311801A (pt) 2005-04-12
AU2003242390A1 (en) 2003-12-31
US7410981B2 (en) 2008-08-12
EP1513527B1 (en) 2009-07-29
IL165562A0 (en) 2006-01-15
AR040221A1 (es) 2005-03-16
US20050222210A1 (en) 2005-10-06
WO2003106429A1 (ja) 2003-12-24
US20060293371A1 (en) 2006-12-28
NO20050141L (no) 2005-01-27
OA12867A (en) 2006-09-15
JPWO2003106429A1 (ja) 2005-10-13
MXPA04012396A (es) 2005-06-17
CN1678315A (zh) 2005-10-05
TW200307544A (en) 2003-12-16

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