CL2008003832A1 - Compuestos derivados del acido 2-(4-(2-(((2-cloro-fenil)sulfonil)metil)-4-(carbamoil)fenoxi)-2-fluorofenil) acetico, forma cristalina anhidra ll de un compuesto especifico; procesos de preparacion; compuestos intermediario, composicion farmaceutica; y uso en el tratamiento de enfermedades inflamatorias, tales como epoc, rinitis, asma y la dermatitis. - Google Patents

Compuestos derivados del acido 2-(4-(2-(((2-cloro-fenil)sulfonil)metil)-4-(carbamoil)fenoxi)-2-fluorofenil) acetico, forma cristalina anhidra ll de un compuesto especifico; procesos de preparacion; compuestos intermediario, composicion farmaceutica; y uso en el tratamiento de enfermedades inflamatorias, tales como epoc, rinitis, asma y la dermatitis.

Info

Publication number
CL2008003832A1
CL2008003832A1 CL2008003832A CL2008003832A CL2008003832A1 CL 2008003832 A1 CL2008003832 A1 CL 2008003832A1 CL 2008003832 A CL2008003832 A CL 2008003832A CL 2008003832 A CL2008003832 A CL 2008003832A CL 2008003832 A1 CL2008003832 A1 CL 2008003832A1
Authority
CL
Chile
Prior art keywords
copd
rhinitis
dermatitis
pharmaceutical composition
acetic acid
Prior art date
Application number
CL2008003832A
Other languages
English (en)
Inventor
Liu Jiwen
C Medina Julio
Grillo Mark
Li An-Rong
Su Yongli
Wang Yingcai
Jona Janan
Allgeier Alan
Milne Jacqueline
m Jerry
Original Assignee
Amgen Inc
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 Amgen Inc filed Critical Amgen Inc
Publication of CL2008003832A1 publication Critical patent/CL2008003832A1/es

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C311/00Amides of sulfonic acids, i.e. compounds having singly-bound oxygen atoms of sulfo groups replaced by nitrogen atoms, not being part of nitro or nitroso groups
    • C07C311/22Sulfonamides, the carbon skeleton of the acid part being further substituted by singly-bound oxygen atoms
    • C07C311/29Sulfonamides, the carbon skeleton of the acid part being further substituted by singly-bound oxygen atoms having the sulfur atom of at least one of the sulfonamide groups bound to a carbon atom of a six-membered aromatic ring
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00Drugs for disorders of the respiratory system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00Drugs for disorders of the respiratory system
    • A61P11/02Nasal agents, e.g. decongestants
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00Drugs for disorders of the respiratory system
    • A61P11/06Antiasthmatics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P17/00Drugs for dermatological disorders
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00Drugs for immunological or allergic disorders
    • A61P37/08Antiallergic agents
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C311/00Amides of sulfonic acids, i.e. compounds having singly-bound oxygen atoms of sulfo groups replaced by nitrogen atoms, not being part of nitro or nitroso groups
    • C07C311/15Sulfonamides having sulfur atoms of sulfonamide groups bound to carbon atoms of six-membered aromatic rings
    • C07C311/21Sulfonamides having sulfur atoms of sulfonamide groups bound to carbon atoms of six-membered aromatic rings having the nitrogen atom of at least one of the sulfonamide groups bound to a carbon atom of a six-membered aromatic ring
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2601/00Systems containing only non-condensed rings
    • C07C2601/02Systems containing only non-condensed rings with a three-membered ring
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2601/00Systems containing only non-condensed rings
    • C07C2601/04Systems containing only non-condensed rings with a four-membered ring

Landscapes

  • Health & Medical Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical & Material Sciences (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Veterinary Medicine (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Engineering & Computer Science (AREA)
  • Pulmonology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Immunology (AREA)
  • Otolaryngology (AREA)
  • Dermatology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)

Abstract

Compuestos derivados del ácido fluorofenil acético, procedimiento de preparación, compuestos intermediarios, composición farmacéutica, útiles para tratar el asma, la epoc, la rinitis, la dermatitis.
CL2008003832A 2007-12-19 2008-12-19 Compuestos derivados del acido 2-(4-(2-(((2-cloro-fenil)sulfonil)metil)-4-(carbamoil)fenoxi)-2-fluorofenil) acetico, forma cristalina anhidra ll de un compuesto especifico; procesos de preparacion; compuestos intermediario, composicion farmaceutica; y uso en el tratamiento de enfermedades inflamatorias, tales como epoc, rinitis, asma y la dermatitis. CL2008003832A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US843307P 2007-12-19 2007-12-19

Publications (1)

Publication Number Publication Date
CL2008003832A1 true CL2008003832A1 (es) 2010-03-26

Family

ID=40564868

Family Applications (1)

Application Number Title Priority Date Filing Date
CL2008003832A CL2008003832A1 (es) 2007-12-19 2008-12-19 Compuestos derivados del acido 2-(4-(2-(((2-cloro-fenil)sulfonil)metil)-4-(carbamoil)fenoxi)-2-fluorofenil) acetico, forma cristalina anhidra ll de un compuesto especifico; procesos de preparacion; compuestos intermediario, composicion farmaceutica; y uso en el tratamiento de enfermedades inflamatorias, tales como epoc, rinitis, asma y la dermatitis.

Country Status (20)

Country Link
US (1) US8183293B2 (es)
EP (1) EP2231595B1 (es)
JP (1) JP5437267B2 (es)
KR (1) KR20100102668A (es)
CN (1) CN101903338A (es)
AR (1) AR071279A1 (es)
AU (1) AU2008343924B2 (es)
BR (1) BRPI0821197A2 (es)
CA (1) CA2707789A1 (es)
CL (1) CL2008003832A1 (es)
CO (1) CO6321234A2 (es)
CR (1) CR11572A (es)
EA (1) EA201001029A1 (es)
ES (1) ES2471919T3 (es)
IL (1) IL206069A0 (es)
MA (1) MA32013B1 (es)
PE (1) PE20091526A1 (es)
TN (1) TN2010000223A1 (es)
TW (1) TW200940051A (es)
WO (1) WO2009085177A1 (es)

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP2457900A1 (en) 2010-11-25 2012-05-30 Almirall, S.A. New pyrazole derivatives having CRTh2 antagonistic behaviour
EP2790696A1 (en) 2011-12-16 2014-10-22 Atopix Therapeutics Limited Combination of crth2 antagonist and a proton pump inhibitor for the treatment of eosinophilic esophagitis
US9974759B2 (en) * 2013-05-31 2018-05-22 Indiana University Research And Technology Corporation Beta 2 adrenoceptor antagonists for treating orthostatic hypotension
US20180021302A1 (en) * 2015-02-13 2018-01-25 Institut National De La Sante Et De La Recherche Medicale (Inserm) Ptgdr-1 and/or ptgdr-2 antagonists for preventing and/or treating systemic lupus erythematosus
HUE057460T2 (hu) 2016-03-22 2022-05-28 Merck Sharp & Dohme Nikotinos acetilkolin receptorok alloszterikus modulátorai
ES2733477T3 (es) * 2017-07-04 2019-11-29 Fis Fabbrica Italiana Sintetici Spa Procedimiento eficaz para la preparación de sitagliptina a través de una preparación muy eficaz del intermedio ácido 2,4,5-trifluorofenilacético

Family Cites Families (41)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB8704158D0 (en) 1987-02-23 1987-04-01 Wellcome Found Substituted hydantoin compounds
US5849780A (en) 1992-01-30 1998-12-15 Sanofi 1-benzenesulfonyl-1-1,3-dihydroindol-2-one derivatives, their preparation and pharmaceutical compositions in which they are present
JP3894949B2 (ja) 1993-06-30 2007-03-22 ザ、ウェルカム、ファンデーション、リミテッド 抗アテローム性動脈硬化症ジアリール化合物
US5545669A (en) * 1994-06-02 1996-08-13 Adams; Jerry L. Anti-inflammatory compounds
BR9510533A (pt) 1994-12-20 1998-07-14 Hoffmann La Roche Derivados de aril-e hetarilsulfonamida sua preparação e seu uso como antagonistas de endotelina
US6008234A (en) * 1996-09-12 1999-12-28 Berlex Laboratories, Inc. Benzamidine derivatives substituted by cyclic amino acid and cyclic hydroxy acid derivatives and their use as anti-coagulants
CN1234798A (zh) 1996-09-12 1999-11-10 舍林股份公司 环状氨基酸和环状羟基羧酸衍生物取代的苄脒衍生物和它们用作抗凝剂的用途
TW523506B (en) 1996-12-18 2003-03-11 Ono Pharmaceutical Co Sulfonamide or carbamide derivatives and drugs containing the same as active ingredients
JPH11202458A (ja) 1998-01-16 1999-07-30 Fuji Photo Film Co Ltd ハロゲン化銀写真感光材料
US5929250A (en) 1997-01-23 1999-07-27 Smithkline Beecham Corporation IL-8 receptor antagonists
JP2002512997A (ja) 1998-04-29 2002-05-08 バーテックス ファーマシューティカルズ インコーポレイテッド Impdh酵素のインヒビター
AR023659A1 (es) 1998-09-18 2002-09-04 Vertex Pharma Un compuesto inhibidor de p38, una composicion farmaceutica que lo comprende y el uso de dicha composicion en el tratamiento y prevencion de estados patologicos
US6248739B1 (en) 1999-01-08 2001-06-19 Pharmacia & Upjohn Company Quinolinecarboxamides as antiviral agents
IL144765A0 (en) 1999-03-01 2002-06-30 Pfizer Prod Inc Oxamic acids and derivatives as thyroid receptor ligands
JP3828364B2 (ja) 1999-03-10 2006-10-04 塩野義製薬株式会社 [2.2.1]および[3.1.1]ビシクロ骨格を有するpgd2/txa2両受容体拮抗性医薬組成物
EP1211513B1 (en) 1999-08-23 2006-01-04 BML, Inc. Method of identifying modulators of prostaglandin d2 receptors
US6531291B1 (en) * 1999-11-10 2003-03-11 The Trustees Of Columbia University In The City Of New York Antimicrobial activity of gemfibrozil and related compounds and derivatives and metabolites thereof
EP1255750A1 (en) 2000-02-01 2002-11-13 Millenium Pharmaceuticals, Inc. INDOLE AND BENZIMIDAZOLE INHIBITORS OF FACTOR Xa
US20010047027A1 (en) 2000-04-12 2001-11-29 Marc Labelle Prostaglandin D2 receptor antagonists
JPWO2001094309A1 (ja) 2000-06-02 2004-02-05 塩野義製薬株式会社 Pgd2/txa2両受容体拮抗性医薬組成物
US6878522B2 (en) * 2000-07-07 2005-04-12 Baiyong Li Methods for the identification of compounds useful for the treatment of disease states mediated by prostaglandin D2
AU2002229611A1 (en) 2000-12-08 2002-06-18 Institut National De La Sante Et De La Recherche Medicale (Inserm) Use of active compounds capable of modulating the intracellular pathway triggered by the dp receptor in langerhans cells
JP2004517851A (ja) 2000-12-27 2004-06-17 バイエル アクチェンゲゼルシャフト 甲状腺受容体のリガンドとしてのインドール誘導体
EP1395590B1 (en) 2001-05-23 2006-09-27 Merck Frosst Canada & Co. Dihydropyrrolo¬1,2-a|indole and tetrahydropyrido¬1,2-a|indole derivatives as prostaglandin d2 receptor antagonists
IL160253A0 (en) 2001-08-09 2004-07-25 Ono Pharmaceutical Co Carboxylic acid derivative compounds and drugs comprising these compounds as the active ingredient
SE0200356D0 (sv) 2002-02-05 2002-02-05 Astrazeneca Ab Novel use
SE0200411D0 (sv) 2002-02-05 2002-02-05 Astrazeneca Ab Novel use
MXPA04009095A (es) 2002-03-19 2004-12-06 Ono Pharmaceutical Co Compuesto de acido carboxilico y agente farmaceutico que comprende el compuesto como ingrediente activo.
EP2423190A1 (en) 2002-05-16 2012-02-29 Shionogi&Co., Ltd. Compounds Exhibiting PGD 2 Receptor Antagonism
JPWO2003097042A1 (ja) 2002-05-16 2005-09-15 塩野義製薬株式会社 Pgd2受容体拮抗剤
GB2388540A (en) 2002-05-17 2003-11-19 Bayer Ag New use of Ramatroban
SE0201635D0 (sv) 2002-05-30 2002-05-30 Astrazeneca Ab Novel compounds
TW200307542A (en) 2002-05-30 2003-12-16 Astrazeneca Ab Novel compounds
GB0224557D0 (en) 2002-10-22 2002-11-27 Glaxo Group Ltd Novel compounds
AU2003297398B2 (en) * 2002-12-20 2009-09-24 Amgen Inc. Asthma and allergic inflammation modulators
DE602004011985T2 (de) 2003-11-25 2009-03-05 Eli Lilly And Co., Indianapolis Modulatoren des peroxisomproliferatoraktivierten rezeptors
US8148572B2 (en) * 2005-10-06 2012-04-03 Astrazeneca Ab Compounds
BRPI0720254A2 (pt) * 2006-12-15 2014-01-07 Glaxo Group Ltd Derivados de benzamida como agonistas do receptor ep4
US7960567B2 (en) * 2007-05-02 2011-06-14 Amgen Inc. Compounds and methods useful for treating asthma and allergic inflammation
CN102596199A (zh) 2009-07-31 2012-07-18 潘米拉制药公司 Dp2受体拮抗剂的眼用医药组合物
WO2011014588A2 (en) 2009-07-31 2011-02-03 Amira Pharmaceuticals, Inc. Dermal formulations of dp2 receptor antagonists

Also Published As

Publication number Publication date
ES2471919T3 (es) 2014-06-27
EP2231595B1 (en) 2014-04-23
AU2008343924A2 (en) 2011-02-17
EA201001029A1 (ru) 2011-06-30
EP2231595A1 (en) 2010-09-29
CA2707789A1 (en) 2009-07-09
CR11572A (es) 2010-08-13
AU2008343924A1 (en) 2009-07-09
US8183293B2 (en) 2012-05-22
KR20100102668A (ko) 2010-09-24
JP2011507847A (ja) 2011-03-10
PE20091526A1 (es) 2009-11-01
TN2010000223A1 (en) 2011-11-11
MA32013B1 (fr) 2011-01-03
AR071279A1 (es) 2010-06-09
TW200940051A (en) 2009-10-01
AU2008343924B2 (en) 2013-01-17
CO6321234A2 (es) 2011-09-20
CN101903338A (zh) 2010-12-01
US20090275659A1 (en) 2009-11-05
JP5437267B2 (ja) 2014-03-12
IL206069A0 (en) 2010-11-30
WO2009085177A1 (en) 2009-07-09
BRPI0821197A2 (pt) 2015-06-16

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