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AR052655A1 - Derivados de n-[(4,5-difenil-3-alquil-2-tienil)metil]amina(amida,sulfonamida,carbamato,urea) - Google Patents

Derivados de n-[(4,5-difenil-3-alquil-2-tienil)metil]amina(amida,sulfonamida,carbamato,urea)

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Publication number
AR052655A1
AR052655A1 ARP050105403A ARP050105403A AR052655A1 AR 052655 A1 AR052655 A1 AR 052655A1 AR P050105403 A ARP050105403 A AR P050105403A AR P050105403 A ARP050105403 A AR P050105403A AR 052655 A1 AR052655 A1 AR 052655A1
Authority
AR
Argentina
Prior art keywords
alkyl
unsubstituted
trifluoromethyl
halogen atom
substituents independently
Prior art date
Application number
ARP050105403A
Other languages
English (en)
Inventor
Francis Barth
Christian Congy
Jean Philippe Ducoux
Murielle Rinaldi-Carmona
Original Assignee
Sanofi Aventis
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 Sanofi Aventis filed Critical Sanofi Aventis
Publication of AR052655A1 publication Critical patent/AR052655A1/es

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    • C07D333/00Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom
    • C07D333/02Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings
    • C07D333/04Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom
    • C07D333/06Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to the ring carbon atoms
    • C07D333/14Radicals substituted by singly bound hetero atoms other than halogen
    • C07D333/20Radicals substituted by singly bound hetero atoms other than halogen by nitrogen atoms
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Abstract

Método de preparacion, composiciones farmacéuticas que los contienen y usos en terapéutica. Reivindicacion 1: Un compuesto que responde a la formula (1) en la que: X representa un grupo -C(O)-, -SO-, -SO2, -C(O)-N(R6)-, - C(O)-O-; R1 representa alquilo C1-7, un radical carbocíclico no aromático en C3-12 no sustituido o sustituido una o varias veces con un alquilo C1-4; cicloalquil C3-7-metilo no sustituido o sustituido una o varias veces sobre el carbociclo con un alquilo C1-4; un fenilo no sustituido o mono-, di- o trisustituido con sustituyentes seleccionados independientemente entre un átomo de halogeno, alquilo C1-4, alcoxi C1-4, alquil C1-4-amino, di-alquil C1-4-amino, ciano, un radical trifluorometilo, trifluorometoxi, un grupo S(O)nAlk, un alquil C1-4- carbonilo, o entre un radical fenilo, fenoxi, pirrolilo, imidazolilo, piridilo o pirazolilo, estando dichos radicales no sustituidos o sustituidos una o varias veces con un alquilo C1-4, bencilo no sustituido o mono- o disustituido sobre el fenilo con sustituyentes seleccionados independientemente entre un átomo de halogeno, alquilo C1-4, alcoxi C1-4m trifluorometilo o sustituido en alfa con uno o dos grupos semejantes o diferentes seleccionados entre alquilo C1-4 cicloalquilo C3-7; fenetilo no sustituido o mono- o disustituido sobre el fenilo con sustituyentes seleccionados independientemente entre un átomo de halogeno, alquilo C1-4, alcoxi C1-4, trifluorometilo, bencidrilo, bencidrilmetilo, un radical heterocíclico aromático seleccionado entre un pirrolilo, imidazolilo, furilo, tienilo, pirazolilo, indolilo no sustituido o sustituido una o varias veces con sustituyentes seleccionados independientemente entre un átomo de halogeno, alquilo C1-4 o trifluorometilo, R2 representa H o alquilo C1-3; R3 representa alquilo C1-5 o cicloalquilo C3-7; R4 representa fenilo no sustituido o mono-, di- o trisustituido con sustituyentes seleccionados independientemente entre un átomo de halogeno, alquilo C1-4, alcoxi C1-4, trifluorometilo o un grupo S(O)nAlk; R5 representa fenilo no sustituido o mono-, di- o trisustituido con sustituyentes seleccionados independientemente entre un átomo de halogeno, alquilo C1-4, alcoxi C1-4 trifluorometilo o un grupo S(O)nAlk; R6 representa un átomo de H o alquilo C1-3; n representa 0, 1 o 2; Alk representa alquilo C1-4, así como sus hidratos o sus solvatos.
ARP050105403A 2004-12-23 2005-12-21 Derivados de n-[(4,5-difenil-3-alquil-2-tienil)metil]amina(amida,sulfonamida,carbamato,urea) AR052655A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
FR0413898A FR2880023B1 (fr) 2004-12-23 2004-12-23 Derives de n-[(4,5-diphenyl-3-alkyl-2-thienyl) methyl] amine leur preparation et leur application en therapeutique

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AR052655A1 true AR052655A1 (es) 2007-03-28

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US (1) US7674821B2 (es)
EP (1) EP1833812A1 (es)
JP (1) JP2008525388A (es)
KR (1) KR20070094614A (es)
CN (1) CN101107239A (es)
AR (1) AR052655A1 (es)
AU (1) AU2005321171A1 (es)
BR (1) BRPI0519291A2 (es)
CA (1) CA2590681A1 (es)
FR (1) FR2880023B1 (es)
IL (1) IL183996A0 (es)
MX (1) MX2007007725A (es)
PE (1) PE20060770A1 (es)
RU (1) RU2007127864A (es)
TW (1) TW200633996A (es)
UY (1) UY29302A1 (es)
WO (1) WO2006070106A1 (es)

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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
US8841334B2 (en) 2006-05-31 2014-09-23 Abbvie Inc. Compounds as cannabinoid receptor ligands and uses thereof
EP2024349B1 (en) 2006-05-31 2017-08-02 AbbVie Inc. Compounds as cannabinoid receptor ligands and uses thereof
WO2008028094A1 (en) * 2006-08-31 2008-03-06 Abbott Laboratories Compounds as cb2 cannabinoid receptor ligands
WO2008028093A1 (en) * 2006-08-31 2008-03-06 Abbott Laboratories Compounds as cb2 cannabinoid receptor ligands
US7875640B2 (en) 2007-03-28 2011-01-25 Abbott Laboratories Compounds as cannabinoid receptor ligands
US7872033B2 (en) 2007-04-17 2011-01-18 Abbott Laboratories Compounds as cannabinoid receptor ligands
WO2008144360A1 (en) 2007-05-18 2008-11-27 Abbott Laboratories Novel compounds as cannabinoid receptor ligands
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US7674821B2 (en) 2010-03-09
RU2007127864A (ru) 2009-01-27
EP1833812A1 (fr) 2007-09-19
AU2005321171A1 (en) 2006-07-06
WO2006070106A1 (fr) 2006-07-06
CN101107239A (zh) 2008-01-16
IL183996A0 (en) 2007-10-31
MX2007007725A (es) 2007-08-22
PE20060770A1 (es) 2006-10-03
JP2008525388A (ja) 2008-07-17
CA2590681A1 (fr) 2006-07-06
FR2880023A1 (fr) 2006-06-30
BRPI0519291A2 (pt) 2009-01-06
UY29302A1 (es) 2006-07-31
KR20070094614A (ko) 2007-09-20
US20070270470A1 (en) 2007-11-22
TW200633996A (en) 2006-10-01

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