WO2007088276A3 - Derives de sulfonamides, leur preparation et leur application en therapeutique - Google Patents

Derives de sulfonamides, leur preparation et leur application en therapeutique Download PDF

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Publication number
WO2007088276A3
WO2007088276A3 PCT/FR2007/000182 FR2007000182W WO2007088276A3 WO 2007088276 A3 WO2007088276 A3 WO 2007088276A3 FR 2007000182 W FR2007000182 W FR 2007000182W WO 2007088276 A3 WO2007088276 A3 WO 2007088276A3
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WIPO (PCT)
Prior art keywords
optionally substituted
preparation
several groups
sulfonamide derivatives
therapeutic application
Prior art date
Application number
PCT/FR2007/000182
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English (en)
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WO2007088276A2 (fr
Inventor
Gilles Courtemanche
Pierre Despeyroux
Evelyne Fontaine
Pierrick Rochard
Gal Claudine Serradeil-Le
Roedern Erich Von
Original Assignee
Sanofi Aventis
Gilles Courtemanche
Pierre Despeyroux
Evelyne Fontaine
Pierrick Rochard
Gal Claudine Serradeil-Le
Roedern Erich Von
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.)
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Publication date
Application filed by Sanofi Aventis, Gilles Courtemanche, Pierre Despeyroux, Evelyne Fontaine, Pierrick Rochard, Gal Claudine Serradeil-Le, Roedern Erich Von filed Critical Sanofi Aventis
Priority to EP07730899A priority Critical patent/EP1981842A2/fr
Priority to JP2008552847A priority patent/JP2009525312A/ja
Publication of WO2007088276A2 publication Critical patent/WO2007088276A2/fr
Publication of WO2007088276A3 publication Critical patent/WO2007088276A3/fr
Priority to US12/183,487 priority patent/US20090054439A1/en

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    • 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
    • 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
    • A61P1/00Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/12Antidiarrhoeals
    • 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
    • A61P1/14Prodigestives, e.g. acids, enzymes, appetite stimulants, antidyspeptics, tonics, antiflatulents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P13/00Drugs for disorders of the urinary system
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    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P15/00Drugs for genital or sexual disorders; Contraceptives
    • AHUMAN NECESSITIES
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    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P21/00Drugs for disorders of the muscular or neuromuscular system
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    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/04Centrally acting analgesics, e.g. opioids
    • AHUMAN NECESSITIES
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    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
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    • AHUMAN NECESSITIES
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    • A61P25/28Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • A61P29/02Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID] without antiinflammatory effect
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
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    • A61P3/00Drugs for disorders of the metabolism
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
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    • A61P3/06Antihyperlipidemics
    • AHUMAN NECESSITIES
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    • A61P3/08Drugs for disorders of the metabolism for glucose homeostasis
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    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D295/00Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
    • C07D295/04Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms
    • C07D295/12Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly or doubly bound nitrogen atoms
    • C07D295/125Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly or doubly bound nitrogen atoms with the ring nitrogen atoms and the substituent nitrogen atoms attached to the same carbon chain, which is not interrupted by carbocyclic rings
    • C07D295/13Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly or doubly bound nitrogen atoms with the ring nitrogen atoms and the substituent nitrogen atoms attached to the same carbon chain, which is not interrupted by carbocyclic rings to an acyclic saturated chain
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07BGENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
    • C07B2200/00Indexing scheme relating to specific properties of organic compounds
    • C07B2200/07Optical isomers

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  • Health & Medical Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical & Material Sciences (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • General Chemical & Material Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Veterinary Medicine (AREA)
  • Medicinal Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Neurology (AREA)
  • Neurosurgery (AREA)
  • Biomedical Technology (AREA)
  • Diabetes (AREA)
  • Hematology (AREA)
  • Obesity (AREA)
  • Endocrinology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Pain & Pain Management (AREA)
  • Psychiatry (AREA)
  • Cardiology (AREA)
  • Urology & Nephrology (AREA)
  • Hospice & Palliative Care (AREA)
  • Nutrition Science (AREA)
  • Emergency Medicine (AREA)
  • Vascular Medicine (AREA)
  • Psychology (AREA)
  • Rheumatology (AREA)
  • Anesthesiology (AREA)
  • Child & Adolescent Psychology (AREA)
  • Orthopedic Medicine & Surgery (AREA)
  • Physical Education & Sports Medicine (AREA)
  • Reproductive Health (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)

Abstract

La présente invention a pour objet des dérivés de sulfonamides répondant à la formule générale (I) : Ar1 représente un aryle éventuellement substitué par un ou plusieurs groupes, un groupe hétérocyclyle, éventuellement substitué ; T représente un -(CH2)n- ou un groupe Ar2 représente un aryle éventuellement substitué par un ou plusieurs groupes, un groupe hétérocyclyle éventuellement substitué ; Ar3 représente un aryle, éventuellement substitué par un ou plusieurs groupes, ou bien un hétérocyclyle éventuellement substitué ; R représentent un hydrogène ou un (C1-C4) alkyle; R' représente un (C1-C4) alkyle éventuellement substitué; un acide carboxylique, un (C1-C4) carboxylate, une carboxamide éventuellement substitué; à l'état de base, de sel d'addition à un acide, d'hydrate ou de solvat, sous forme d'énantiomères, de diastéréoisomères, de rotamères, d'atropoisomères ou de leurs mélanges. Elle concerne également le procédé de préparation ainsi que l'utilisation en thérapeutique des composés de formule (I).
PCT/FR2007/000182 2006-02-02 2007-02-01 Derives de sulfonamides, leur preparation et leur application en therapeutique WO2007088276A2 (fr)

Priority Applications (3)

Application Number Priority Date Filing Date Title
EP07730899A EP1981842A2 (fr) 2006-02-02 2007-02-01 Derives de sulfonamides, leur preparation et leur application en therapeutique
JP2008552847A JP2009525312A (ja) 2006-02-02 2007-02-01 スルホンアミド誘導体、これの調製および治療への応用
US12/183,487 US20090054439A1 (en) 2006-02-02 2008-07-31 Sulfonamide derivatives, preparation and therapeutic application thereof

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
FR0600955 2006-02-02
FR0600955A FR2896799B1 (fr) 2006-02-02 2006-02-02 Derives de sulfonamides, leur preparation et leur application en therapeutique

Related Child Applications (1)

Application Number Title Priority Date Filing Date
US12/183,487 Continuation US20090054439A1 (en) 2006-02-02 2008-07-31 Sulfonamide derivatives, preparation and therapeutic application thereof

Publications (2)

Publication Number Publication Date
WO2007088276A2 WO2007088276A2 (fr) 2007-08-09
WO2007088276A3 true WO2007088276A3 (fr) 2007-10-25

Family

ID=37499618

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PCT/FR2007/000182 WO2007088276A2 (fr) 2006-02-02 2007-02-01 Derives de sulfonamides, leur preparation et leur application en therapeutique

Country Status (5)

Country Link
US (1) US20090054439A1 (fr)
EP (1) EP1981842A2 (fr)
JP (1) JP2009525312A (fr)
FR (1) FR2896799B1 (fr)
WO (1) WO2007088276A2 (fr)

Families Citing this family (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP2025674A1 (fr) 2007-08-15 2009-02-18 sanofi-aventis Tetrahydronaphthaline substituée, son procédé de fabrication et son utilisation en tant que médicament
EP2491038B1 (fr) 2009-10-23 2016-04-06 Janssen Pharmaceutica N.V. Octahydropyrrolo[3,4-c]pyrroles disubstitués en tant que modulateurs de récepteur d'orexine
US8828994B2 (en) 2011-03-08 2014-09-09 Sanofi Di- and tri-substituted oxathiazine derivatives, method for the production thereof, use thereof as medicine and drug containing said derivatives and use thereof
WO2012120053A1 (fr) 2011-03-08 2012-09-13 Sanofi Dérivés oxathiazine ramifiés, procédé pour leur préparation, utilisation en tant que médicament, agents pharmaceutiques contenant ces dérivés et leur utilisation
WO2012120056A1 (fr) 2011-03-08 2012-09-13 Sanofi Dérivés oxathiazine tétra-substitués, procédé pour leur préparation, utilisation en tant que médicament, agent pharmaceutique contenant ces dérivés et utilisation
WO2012120055A1 (fr) 2011-03-08 2012-09-13 Sanofi Dérivés oxathiazine di- et tri-substitués, procédé pour leur préparation, utilisation en tant que médicament, agent pharmaceutique contenant ces dérivés et utilisation
US8901114B2 (en) 2011-03-08 2014-12-02 Sanofi Oxathiazine derivatives substituted with carbocycles or heterocycles, method for producing same, drugs containing said compounds, and use thereof
CA2863413A1 (fr) 2012-02-07 2013-08-15 Eolas Therapeutics, Inc. Piperidines/prolines substituees en tant qu'antagonistes du recepteur de l'orexine
US9440982B2 (en) 2012-02-07 2016-09-13 Eolas Therapeutics, Inc. Substituted prolines/piperidines as orexin receptor antagonists
AR101558A1 (es) 2014-08-13 2016-12-28 Eolas Therapeutics Inc Difluoropirrolidinas como moduladores del receptor de orexina
TWI710557B (zh) 2016-02-12 2020-11-21 美商伊歐拉斯治療學公司 作為食慾素受體調節劑之經鹵素取代之六氫吡啶
CA2960253A1 (fr) 2016-03-10 2017-09-10 Janssen Pharmaceutica Nv Methodes de traitement de la depression au moyen d'antagonistes du recepteur orexine-2

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0358571A1 (fr) * 1988-09-08 1990-03-14 Pierre Fabre Medicament Thioformamidines, leur préparation et leur application en tant que médicaments
US20060014783A1 (en) * 2002-10-11 2006-01-19 Hamed Aissaoui Sulfonylamino-acetic acid derivatives

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2000047284A2 (fr) 1999-02-12 2000-08-17 Smithkline Beecham P.L.C. Nouvelle utilisation des antagonistes des recepteurs de l'orexine
EP1150977B1 (fr) * 1999-02-12 2004-08-25 SmithKline Beecham plc Derives de phenyluree et de phenylthiouree utilises comme antagonistes des recepteurs de l'orexine
AP2001002307A0 (en) * 2000-10-20 2001-12-31 Pfizer Prod Inc B3 adrenergic receptor agonists and uses thereof.
HUP0304101A3 (en) * 2003-12-22 2008-10-28 Sanofi Aventis Pyrazole derivatives, process for producing them, their use, pharmaceutical compositions containing them and their intermediates
HUP0400405A3 (en) * 2004-02-10 2009-03-30 Sanofi Synthelabo Pyrimidine derivatives, process for producing them, their use, pharmaceutical compositions containing them and their intermediates
FR2874011B1 (fr) * 2004-08-03 2007-06-15 Sanofi Synthelabo Derives de sulfonamides, leur preparation et leur application en therapeutique

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0358571A1 (fr) * 1988-09-08 1990-03-14 Pierre Fabre Medicament Thioformamidines, leur préparation et leur application en tant que médicaments
US20060014783A1 (en) * 2002-10-11 2006-01-19 Hamed Aissaoui Sulfonylamino-acetic acid derivatives

Also Published As

Publication number Publication date
FR2896799A1 (fr) 2007-08-03
JP2009525312A (ja) 2009-07-09
WO2007088276A2 (fr) 2007-08-09
EP1981842A2 (fr) 2008-10-22
US20090054439A1 (en) 2009-02-26
FR2896799B1 (fr) 2008-03-28

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