PE20061038A1 - Derivados del 1,5-difenil-1h-pirazol-3-il) oxadiazol como agentes antagonistas cb1 y su preparacion - Google Patents

Derivados del 1,5-difenil-1h-pirazol-3-il) oxadiazol como agentes antagonistas cb1 y su preparacion

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Publication number
PE20061038A1
PE20061038A1 PE2006000202A PE2006000202A PE20061038A1 PE 20061038 A1 PE20061038 A1 PE 20061038A1 PE 2006000202 A PE2006000202 A PE 2006000202A PE 2006000202 A PE2006000202 A PE 2006000202A PE 20061038 A1 PE20061038 A1 PE 20061038A1
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PE
Peru
Prior art keywords
chlorophenyl
oxadiazole
alkyl
alcoxy
halogen
Prior art date
Application number
PE2006000202A
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English (en)
Inventor
Francis Barth
Christian Congy
Broeck Didier Van
Patrick Geule
Original Assignee
Sanofi Aventis
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Publication date
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First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=35079215&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=PE20061038(A1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Sanofi Aventis filed Critical Sanofi Aventis
Publication of PE20061038A1 publication Critical patent/PE20061038A1/es

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    • C07ORGANIC CHEMISTRY
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    • C07D413/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/02Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
    • C07D413/04Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings directly linked by a ring-member-to-ring-member bond
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    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/41Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/4245Oxadiazoles
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Abstract

REFERIDA A UN COMPUESTO DERIVADO DE PIRAZOL DE FORMULA (I), DONDE RI ES UN HETEROCICLO, DONDE R1a ES ALQUILO C1-C7 OPCIONALMENTE SUSTITUIDO CON UNO O VARIOS ATOMOS DE HALOGENO, ALCOXI C1-C4, TRIFLUOROMETOXI, FENOXI, ENTRE OTROS, FENILO OPCIONALMENTE SUSTITUIDO CON HALOGENO, ALQUILO C1-C4, ALCOXI C1-C4, ENTRE OTROS; R1b ES ALQUILO C1-C7 OPCIONALMENTE SUSTITUIDO CON UNO O VARIOS ATOMOS DE HALOGENO, ALCOXI C1-C4, TRIFLUOROMETOXI, FENOXI, ENTRE OTROS; R2 ES ALQUILO C1-C5 O CIANO; R3 Y R4 SON FENILO OPCIONALMENTE SUSTITUIDO CON HALOGENO, ALQUILO C1-C4, ALCOXI C1-C4, RADICAL TRIFLUOROMETILO, ENTRE OTROS. SON COMPUESTOS PREFERIDOS: 2-TER-BUTIL-5-[1-(2-CLOROFENIL)-5-(4-CLOROFENIL)-4-METIL-1H-PIRAZOL-3-IL]-1,3,4-OXADIAZOL, 2-[1-(2-CLOROFENIL)-5-(4-CLOROFENIL)-4-METIL-1H-PIRAZOL-3-IL]-5-ISOPROPIL-1,3,4-OXADIAZOL, 2-TER-BUTIL-5-[5-(4-CLOROFENIL)-1-(2,4-DICLOROFENIL)-4-METIL-1H-PIRAZOL-3-IL]-1,3,4-OXADIAZOL, ENTRE OTROS. TAMBIEN SE REFIERE A UN PROCEDIMIENTO DE PREPARACION Y A UNA COMPOSICION FARMACEUTICA. DICHOS COMPUESTOS SON ANTAGONISTAS DE LOS RECEPTORES CANABINOIDES CB1 Y SON UTILES EN EL TRATAMIENTO DE TRASTORNOS PSIQUIATRICOS COMO LA ANSIEDAD, DEPRESION, INSOMNIO, PSICOSIS, ESQUIZOFRENIA, ENTRE OTRAS
PE2006000202A 2005-02-21 2006-02-17 Derivados del 1,5-difenil-1h-pirazol-3-il) oxadiazol como agentes antagonistas cb1 y su preparacion PE20061038A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
FR0501860A FR2882365B1 (fr) 2005-02-21 2005-02-21 Derives de 2-(1,5-diphenyl-1h-pyrazol-3-yl)-1,3,4-oxadiazole leur preparation et leur application en therapeutique

Publications (1)

Publication Number Publication Date
PE20061038A1 true PE20061038A1 (es) 2006-11-24

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PE2006000202A PE20061038A1 (es) 2005-02-21 2006-02-17 Derivados del 1,5-difenil-1h-pirazol-3-il) oxadiazol como agentes antagonistas cb1 y su preparacion

Country Status (25)

Country Link
US (1) US7632852B2 (es)
EP (1) EP1853595A1 (es)
JP (1) JP4812778B2 (es)
KR (1) KR20070107053A (es)
CN (1) CN101119990A (es)
AR (1) AR055560A1 (es)
AU (1) AU2006215443A1 (es)
BR (1) BRPI0606845A2 (es)
CA (1) CA2597359A1 (es)
DO (1) DOP2006000045A (es)
EA (1) EA200701779A1 (es)
FR (1) FR2882365B1 (es)
GT (1) GT200600082A (es)
IL (1) IL185163A0 (es)
MA (1) MA29261B1 (es)
MX (1) MX2007009994A (es)
NO (1) NO20074763L (es)
NZ (1) NZ560790A (es)
PA (1) PA8663901A1 (es)
PE (1) PE20061038A1 (es)
SV (1) SV2007002422A (es)
TW (1) TW200640916A (es)
UY (1) UY29388A1 (es)
WO (1) WO2006087480A1 (es)
ZA (1) ZA200706953B (es)

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US20080207704A1 (en) * 2007-02-27 2008-08-28 The Green Cross Corporation Heteroaryl-imidazole derivatives as cannabinoid cb1 receptor antagonists
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WO2009078498A1 (en) * 2007-12-17 2009-06-25 Green Cross Corporation Biarylpyrazole 4-carboxamides as cannabinoid cb1 receptor ligands
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KR101318689B1 (ko) 2008-09-25 2013-10-16 주식회사 녹십자 칸나비노이드 cb1 수용체 길항제로서 황 함유 피라졸-헤테로사이클 유도체
WO2010068601A1 (en) 2008-12-08 2010-06-17 Sanofi-Aventis A crystalline heteroaromatic fluoroglycoside hydrate, processes for making, methods of use and pharmaceutical compositions thereof
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SV2007002422A (es) 2007-01-17
BRPI0606845A2 (pt) 2009-07-21
PA8663901A1 (es) 2006-12-07
JP2008530188A (ja) 2008-08-07
ZA200706953B (en) 2009-03-25
IL185163A0 (en) 2007-12-03
US20080039510A1 (en) 2008-02-14
NO20074763L (no) 2007-11-16
KR20070107053A (ko) 2007-11-06
DOP2006000045A (es) 2006-11-15
FR2882365B1 (fr) 2007-09-07
AU2006215443A1 (en) 2006-08-24
US7632852B2 (en) 2009-12-15
WO2006087480A1 (fr) 2006-08-24
UY29388A1 (es) 2006-10-02
NZ560790A (en) 2009-08-28
EA200701779A1 (ru) 2008-02-28
AR055560A1 (es) 2007-08-22
GT200600082A (es) 2006-10-19
EP1853595A1 (fr) 2007-11-14
FR2882365A1 (fr) 2006-08-25
CA2597359A1 (fr) 2006-08-24
MX2007009994A (es) 2007-10-10
CN101119990A (zh) 2008-02-06
MA29261B1 (fr) 2008-02-01
TW200640916A (en) 2006-12-01
JP4812778B2 (ja) 2011-11-09

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