ECSP066695A - Derivados de n-(1,5-difenil-1h-pirazol-3-il) sulfonamida con afinidad por los receptores cb1 - Google Patents

Derivados de n-(1,5-difenil-1h-pirazol-3-il) sulfonamida con afinidad por los receptores cb1

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Publication number
ECSP066695A
ECSP066695A EC2006006695A ECSP066695A ECSP066695A EC SP066695 A ECSP066695 A EC SP066695A EC 2006006695 A EC2006006695 A EC 2006006695A EC SP066695 A ECSP066695 A EC SP066695A EC SP066695 A ECSP066695 A EC SP066695A
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EC
Ecuador
Prior art keywords
alkyl
unsubstituted
halogen atom
group
alkoxy
Prior art date
Application number
EC2006006695A
Other languages
English (en)
Inventor
Francis Barth
Christian Congy
Serge Martinez
Murielle Rinaldi-Carmona
Original Assignee
Sanofi Aventis
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Filing date
Publication date
Application filed by Sanofi Aventis filed Critical Sanofi Aventis
Publication of ECSP066695A publication Critical patent/ECSP066695A/es

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    • 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
    • C07D231/12Heterocyclic 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 only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
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Abstract

Compuesto que responde a la fórmula (I):en la que - R1 representa" alquilo(C1-C6);" cicloalquilo(C3-C7) no sustituido o sustituido una o varias veces con un grupo alquilo (C1-C3);" cicloalquilmetilo(C3-C7) no sustituido o sustituido una o varias veces en el carbociclo con alquilo(C1-C3);" fenilo no sustituido o mono, di o trisustituido con un sustituyente elegido de manera independiente entre un átomo de halógeno, alquilo(C1-C4), alcoxi(C1-C3), ciano, radical trifluorometilo, radical trifluorometoxi, grupo S(O)nAlk, grupo alquilcarbonilo(C1-C3) o fenilo;" bencilo no sustituido o mono o disustituido con un sustituyente elegido de manera independiente entre un átomo de halógeno, alquilo(C1-C3), alcoxi(C1-C3) o radical trifluorometilo;" tienilo no sustituido o sustituido con un átomo de halógeno o con un isoxazolilo;- R2 representa un átomo de hidrógeno o alquilo(C1-C3);- R3 representa un átomo de hidrógeno o alquilo(C1-C5);- R4, R5, R6, R7, R8 y R9 representan cada uno de manera independiente un átomo de hidrógeno, átomo de halógeno, alquilo(C1-C7), alcoxi(C1-C5), radical trifluorometilo o grupo S(O)nAlk;- n representa 0, 1 ó 2;- Alk representa alquilo(C1-C4).en forma de base o de sal de adición de ácido, así como en forma de hidrato o solvato.
EC2006006695A 2004-01-12 2006-07-11 Derivados de n-(1,5-difenil-1h-pirazol-3-il) sulfonamida con afinidad por los receptores cb1 ECSP066695A (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
FR0400257A FR2864958B1 (fr) 2004-01-12 2004-01-12 Derive de n-[(1,5-diphenyl-1h-pyrazol-3-yl)methyl] sulfonamide, leur preparation et leur application en therapeutique.

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ECSP066695A true ECSP066695A (es) 2006-10-31

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EC2006006695A ECSP066695A (es) 2004-01-12 2006-07-11 Derivados de n-(1,5-difenil-1h-pirazol-3-il) sulfonamida con afinidad por los receptores cb1

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US (1) US7294645B2 (es)
EP (1) EP1720837B1 (es)
JP (1) JP4723514B2 (es)
KR (1) KR20060105050A (es)
CN (1) CN1910157A (es)
AR (1) AR047096A1 (es)
AT (1) ATE465995T1 (es)
AU (1) AU2005209441B2 (es)
CA (1) CA2551141C (es)
CR (1) CR8468A (es)
CY (1) CY1110651T1 (es)
DE (1) DE602005020907D1 (es)
DK (1) DK1720837T3 (es)
EC (1) ECSP066695A (es)
ES (1) ES2344850T3 (es)
FR (1) FR2864958B1 (es)
HR (1) HRP20100283T8 (es)
IL (1) IL176710A0 (es)
MA (1) MA28422B1 (es)
NO (1) NO20063621L (es)
NZ (1) NZ548442A (es)
PL (1) PL1720837T3 (es)
PT (1) PT1720837E (es)
RS (1) RS51365B (es)
RU (1) RU2366657C2 (es)
SI (1) SI1720837T1 (es)
TN (1) TNSN06203A1 (es)
TW (1) TWI323255B (es)
UA (1) UA85079C2 (es)
WO (1) WO2005073197A1 (es)
ZA (1) ZA200605657B (es)

Families Citing this family (26)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7030141B2 (en) * 2001-11-29 2006-04-18 Christopher Franklin Bigge Inhibitors of factor Xa and other serine proteases involved in the coagulation cascade
FR2880023B1 (fr) 2004-12-23 2007-02-23 Sanofi Aventis Sa Derives de n-[(4,5-diphenyl-3-alkyl-2-thienyl) methyl] amine leur preparation et leur application en therapeutique
FR2880890B1 (fr) * 2005-01-19 2007-03-30 Sanofi Aventis Sa Derives de n-[(4,5-diphenyl-2-thienyl)methyl]sulfonamide, leur preparation et leur application en therapeutique
FR2881744B1 (fr) 2005-02-09 2007-04-27 Sanofi Aventis Sa Derives de n-[(4,5-diphenyl-2-thienyl)methyl]amine, leur preparation et leur application en therapeutique
FR2894579B1 (fr) * 2005-12-12 2008-01-18 Sanofi Aventis Sa Derives diaryltriazolmethylamine, leur preparation et leur application en therapeutique.
FR2894578B1 (fr) 2005-12-12 2008-02-01 Sanofi Aventis Sa Derives heterocycliques, leur preparation et leur application en therapeutique.
EP1829867A1 (en) 2006-03-03 2007-09-05 Laboratorios Del Dr. Esteve, S.A. Imidazole compounds having pharmaceutical activity towards the sigma receptor
FR2899899A1 (fr) * 2006-04-14 2007-10-19 Sanofi Aventis Sa Derives d'aminomethyl pyridine, leur preparation et leur application en therapeutique
ATE469129T1 (de) * 2006-07-11 2010-06-15 Sanofi Aventis N-ä(1,5-diphenyl-1h-pyrazol-3- yl)methylüsulfonamid-derivate antagonisten der cb1 rezeptoren der cannabinoide
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EP1720837A1 (fr) 2006-11-15
TNSN06203A1 (en) 2007-11-15
US20070021486A1 (en) 2007-01-25
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TWI323255B (en) 2010-04-11
US7294645B2 (en) 2007-11-13
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ATE465995T1 (de) 2010-05-15
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FR2864958A1 (fr) 2005-07-15
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