MX2009005447A - Derivados de 2,5-dihidro-3h-pirazolo[4,3-c]piridazin-3-ona sustituidos, su preparacion y uso de los mismos como ligandos de los receptores cb1 de canabinoides. - Google Patents

Derivados de 2,5-dihidro-3h-pirazolo[4,3-c]piridazin-3-ona sustituidos, su preparacion y uso de los mismos como ligandos de los receptores cb1 de canabinoides.

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Publication number
MX2009005447A
MX2009005447A MX2009005447A MX2009005447A MX2009005447A MX 2009005447 A MX2009005447 A MX 2009005447A MX 2009005447 A MX2009005447 A MX 2009005447A MX 2009005447 A MX2009005447 A MX 2009005447A MX 2009005447 A MX2009005447 A MX 2009005447A
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Mexico
Prior art keywords
substituted
preparation
dfflydro
pyridazin
pyrazolo
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MX2009005447A
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English (en)
Inventor
Murielle Rinaldi-Carmona
Christian Congy
Didier Van Broeck
Victor Dos Santos
Arnaud Rouquette
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Sanofi Aventis
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Publication of MX2009005447A publication Critical patent/MX2009005447A/es

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    • C07D231/00Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
    • C07D231/02Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
    • C07D231/10Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • C07D231/14Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three 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
    • C07D231/18One oxygen or sulfur atom
    • C07D231/20One oxygen atom attached in position 3 or 5
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
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    • A61K31/495Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/50Pyridazines; Hydrogenated pyridazines
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    • C07D237/02Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings not condensed with other rings
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    • C07D249/02Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms not condensed with other rings
    • C07D249/081,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
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    • C07D487/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
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    • C07D495/02Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
    • C07D495/04Ortho-condensed systems

Abstract

La presente invención tiene por objeto compuestos que responden a la fórmula (I), en la cual: -R1 representa: un alquilo (C1-C12) no sustituido o sustituido; un radical carbocíclico no aromático en (C3-C12) no sustituido o sustituido; un fenilo no sustituido o sustituido; un bencilo no sustituido o sustituido; un fenetilo no sustituido o sustituido; un benzhidrilo; un benzhidrilmetilo; un radical heterocíclico aromático; - R2 representa un fenilo no sustituido o sustituido; - R3 representa un fenilo no sustituido o sustituido; - R4 representa un átomo de hidrógeno, un alquilo (C1-C4), un alcoxi (C1-C4), un hidroxi; -Alk representa un alquilo (C1-C4) no sustituido o sustituido. La invención también se refiere a un procedimiento para la preparación y aplicación de ellos en terapéutica, como ligandos de los receptores CB1 de los canabinoides localizados al nivel central y/o periférico.
MX2009005447A 2006-11-23 2007-11-19 Derivados de 2,5-dihidro-3h-pirazolo[4,3-c]piridazin-3-ona sustituidos, su preparacion y uso de los mismos como ligandos de los receptores cb1 de canabinoides. MX2009005447A (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
FR0610371A FR2909090B1 (fr) 2006-11-23 2006-11-23 Derives de 2,5-dihydro-3h-pyrazolo[4,3-c]pyridazin-3-one substitues,leur preparation et leur application en therapeutique.
PCT/FR2007/001889 WO2008068424A2 (fr) 2006-11-23 2007-11-19 Derives de 2, 5-dihydro-3h-pyrazolo [4, 3-c] pyridazin-3-one substitues, leur preparation et leur utilisation comme ligands des recepteurs cb1 des cannabinoides

Publications (1)

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MX2009005447A true MX2009005447A (es) 2009-08-07

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MX2009005447A MX2009005447A (es) 2006-11-23 2007-11-19 Derivados de 2,5-dihidro-3h-pirazolo[4,3-c]piridazin-3-ona sustituidos, su preparacion y uso de los mismos como ligandos de los receptores cb1 de canabinoides.

Country Status (20)

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US (1) US7915258B2 (es)
EP (1) EP2094706B1 (es)
JP (1) JP2010510297A (es)
KR (1) KR20090092774A (es)
CN (1) CN101541802A (es)
AR (1) AR063898A1 (es)
AT (1) ATE494290T1 (es)
AU (1) AU2007330652A1 (es)
BR (1) BRPI0719291A2 (es)
CA (1) CA2668196A1 (es)
CL (1) CL2007003346A1 (es)
DE (1) DE602007011815D1 (es)
FR (1) FR2909090B1 (es)
IL (1) IL198523A0 (es)
MX (1) MX2009005447A (es)
PE (1) PE20081496A1 (es)
RU (1) RU2009123841A (es)
TW (1) TW200836739A (es)
UY (1) UY30742A1 (es)
WO (1) WO2008068424A2 (es)

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US8933236B2 (en) 2012-05-22 2015-01-13 Xenon Pharmaceuticals Inc. N-substituted benzamides and methods of use thereof
US20090074717A1 (en) * 2007-07-13 2009-03-19 Martin Robert Leivers Anti-viral compounds, compositions, and methods of use
US8293744B2 (en) 2009-04-20 2012-10-23 Merck Sharp & Dohme Corp. Heterocyclic fused cinnoline M1 receptor positive allosteric modulators
JP5800813B2 (ja) 2010-08-04 2015-10-28 武田薬品工業株式会社 複素環化合物
EP3030549B8 (en) * 2013-09-12 2019-04-10 Janssen BioPharma, Inc. Pyridazinone compounds and uses thereof
CA2923075C (en) 2013-09-12 2022-07-26 Alios Biopharma, Inc. Aza-pyridone compounds and uses thereof
JP6422164B2 (ja) 2013-12-26 2018-11-14 塩野義製薬株式会社 含窒素6員環誘導体およびそれらを含有する医薬組成物
AU2016229147C1 (en) 2015-03-11 2021-03-25 Janssen Biopharma, Inc. Aza-pyridone compounds and uses thereof
DK3287443T3 (da) 2015-04-24 2022-02-07 Shionogi & Co 6-leddet heterocyklisk derivat og farmaceutisk sammensætning, som omfatter dette
WO2018074390A1 (ja) 2016-10-17 2018-04-26 塩野義製薬株式会社 二環性含窒素複素環誘導体およびそれらを含有する医薬組成物
TW202321229A (zh) 2021-08-18 2023-06-01 美商富曼西公司 殺真菌的取代的雜環化合物

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US4345934A (en) 1977-03-10 1982-08-24 Rohm And Haas Company Method of producing hybrid cereal grain seeds by application of 1-aryl-1,4-dihydro-4-oxo(thio)-pyridazines
FR2692575B1 (fr) 1992-06-23 1995-06-30 Sanofi Elf Nouveaux derives du pyrazole, procede pour leur preparation et compositions pharmaceutiques les contenant.
FR2713225B1 (fr) 1993-12-02 1996-03-01 Sanofi Sa N-pipéridino-3-pyrazolecarboxamide substitué.
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US5808082A (en) * 1996-05-08 1998-09-15 Merck & Co., Inc. Method of preparing phosphodiesterase IV inhibitors
FR2789079B3 (fr) 1999-02-01 2001-03-02 Sanofi Synthelabo Derive d'acide pyrazolecarboxylique, sa preparation, les compositions pharmaceutiques en contenant
WO2004072029A2 (en) * 2003-02-06 2004-08-26 Vertex Pharmaceuticals Incorporated Pyrazolopyridazines useful as inhibitors of protein kinases
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US8299257B2 (en) * 2007-09-20 2012-10-30 Glaxo Group Limited Compounds which have activity at M1receptor and their uses in medicine

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DE602007011815D1 (de) 2011-02-17
JP2010510297A (ja) 2010-04-02
TW200836739A (en) 2008-09-16
CA2668196A1 (fr) 2008-06-12
FR2909090A1 (fr) 2008-05-30
ATE494290T1 (de) 2011-01-15
FR2909090B1 (fr) 2009-01-09
WO2008068424A2 (fr) 2008-06-12
KR20090092774A (ko) 2009-09-01
PE20081496A1 (es) 2009-01-04
RU2009123841A (ru) 2010-12-27
CN101541802A (zh) 2009-09-23
WO2008068424A3 (fr) 2008-07-24
IL198523A0 (en) 2010-02-17
CL2007003346A1 (es) 2008-07-04
US20090281107A1 (en) 2009-11-12
EP2094706B1 (fr) 2011-01-05
US7915258B2 (en) 2011-03-29
UY30742A1 (es) 2008-07-03
AU2007330652A1 (en) 2008-06-12
EP2094706A2 (fr) 2009-09-02
AR063898A1 (es) 2009-02-25
WO2008068424A8 (fr) 2009-07-02
BRPI0719291A2 (pt) 2014-02-25

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