AR060800A1 - Derivados de aminometilpiridina su preparacion y su aplicacion en terapeutica - Google Patents
Derivados de aminometilpiridina su preparacion y su aplicacion en terapeuticaInfo
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- AR060800A1 AR060800A1 ARP070101551A ARP070101551A AR060800A1 AR 060800 A1 AR060800 A1 AR 060800A1 AR P070101551 A ARP070101551 A AR P070101551A AR P070101551 A ARP070101551 A AR P070101551A AR 060800 A1 AR060800 A1 AR 060800A1
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- Prior art keywords
- group
- alkyl
- substituted
- unsubstituted
- nalk
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Abstract
Reivindicacion 1: Compuesto que responde a la formula (1) en la que: - Z representa un grupo N(R3)XR4, N(R3)COOR5 o OCON(R3)R5; - X representa un grupo -CO-, -SO2-, -CON(R6)- o -CSN(R6)-; - R1 y R2 representan cada uno independientemente uno del otro un átomo de hidrogeno o un alquilo (C1-7) o R1 y R2 junto con el átomo de nitrogeno al que están unidos constituyen un radical heterocíclico saturado o insaturado, de 3 a 8 eslabones que puede contener uno o varios otros heteroátomos seleccionados entre un átomo de oxígeno, de azufre o de nitrogeno, estando dicho radical sin sustituir o sustituido con uno o varios grupos alquilo (C1-4); - R3 representa un átomo de hidrogeno o un grupo alquilo (C1-4); - R4 representa: un grupo alquilo (C3-10) sin sustituir o sustituido con un grupo CF3; un radical carbocíclico no aromático en (C3-12), sin sustituir o sustituido o varias veces por sustituyentes idénticos o diferentes seleccionados entre un grupo alquilo (C1-4), hidroxilo, alcoxi (C1-4), alquiltio (C1-4), ciano; un radical heterocíclico de 3 a 8 átomos oxigenado, sulfurado o nitrogenado saturado o insaturado sin sustituir o sustituido con uno o varios sustituyentes idénticos o diferentes seleccionados entre un átomo de halogeno, un grupo alquilo (C1-4), hidroxilo, trifluorometilo, alcoxi (C1-4), trifluorometoxi, trifluorometiltio, alquiltio (C1-4), ciano, nitro o por un grupo oxo; un indolilo sin sustituir o sustiluido con un átomo de halogeno o por un grupo alquilo (C1-4), trifluorometilo, hidroxilo, alcoxi (C1-4), trifluorometoxi, trifluorometiltio, alquiltio (C1-4), ciano, nitro; un tetrahidronaftalenilo; un naftalenilo; un benzotiofenilo o un benzofurilo; un fenilo sin sustituir o sustituido o varias veces por sustituyentes idénticos o diferentes seleccionados entre un átomo de halogeno, un grupo alquilo (C1-4), trifluorometilo, trifluorometoxi, hidroxilo, alcoxi (C1-4), alquiltio (C1-4), trifluorometiltio, ciano, nitro, alcanoilo (C1- 4), fenilo, un grupo S(O)nAlk, OS(O)nAlk o NR7R8; un benzodioxilo; un fenoximetileno, un 1-fenoxietileno, estando los grupos fenilo sin sustituir o sustituidos una o varias veces por sustituyentes idénticos o diferentes seleccionados entre un átomo de halogeno, un grupo alquilo (C1-4), trifluorometilo, trifluorometoxi, hidroxilo, alcoxi (C1-4), alquiltio (C1-4), trifluorometiltio, ciano, nitro, alcanoilo (C1-4), fenilo, un grupo S(O)nAlk, OS(O)nAlk o NR7R8; los grupos metileno o estando el etileno sin sustituir o sustituido una o varias veces por un grupo alquilo (C1-4) o por un cicloalquilo (C3-7); un grupo fenilciclopropilo, estando el grupo fenilo sin sustituir o sustituido o varias veces por sustituyentes idénticos o diferentes seleccionados entre un átomo de halogeno, un grupo alquilo (C1-4), trifluorometilo, trifluorometoxi, hidroxilo, alcoxi (C1-4), alquiltio (C1-4), trifluorometiltio, ciano, nitro, alcanoilo (C1-4), fenilo, un grupo S(O)nAlk, OS(O)nAIk o NR7R8; un alquileno (C1-2) sustituido con uno o dos sustituyentes idénticos o diferentes seleccionados entre: (ii) un radical carbocíclico no aromático en C3-12, sin sustituir o sustituido una o varias veces por un grupo alquilo(C1-4); (ii) un fenilo sin sustituir o sustituido con uno o varios sustituyentes, idénticos o diferentes, seleccionados entre un átomo de halogeno, un grupo alquilo (C1-4), hidroxilo, trifluorometilo, alcoxi (C1-4), alquiltio (C1-4), trifluorometoxi, trifluorometiltio, alcanoilo (C1-4), ciano, nitro, fenilo, un grupo S(O)nAlk, OS(O)nAlk o NR7R8; un radical heterociclico de 3 a 8 átomos oxigenado, sulfurado o nitrogenado, saturado o insaturado, sin sustituir o sustituido con uno o varios sustituyentes idénticos o diferentes seleccionados entre un átomo de halogeno, un grupo alquilo (C1-4), hidroxilo, trifluorometilo, alcoxi (C1-4), trifluorometoxi, trifluorometiltio, alquiltio (C1-4), ciano, nitro; además cuando X representa un grupo -CON(R6)- o -CSN(R6)-, R4 puede representar un grupo alcanoilo (C1-6) o un grupo benzoilo o bencilcarbonilo, estando el grupo fenilo de dichos grupos sin sustituir o sustituido con sustituyentes idénticos o diferentes seleccionados entre un átomo de halogeno, un grupo alquilo (C1-4), trifluorometilo, trifluorometoxi, hidroxilo, alcoxi (C1-4), alquiltio (C1-4), trifluorometiltio, ciano, nitro, alcanoilo (C1-4), fenilo, un grupo S(O)nAlk, OS(O)nAlk o NR7R8; R5 representa un fenilo sin sustituir o sustituido una o varias veces por sustituyentes idénticos o diferentes seleccionados entre un átomo de halogeno, un grupo alquilo (C1-4), trifluorometilo, trifluorometoxi, ciano, nitro, alcoxi (C1-4), alquiltio (C1-4), trifluorometiltio, un grupo S(O)nAlk, OS(O)nAlk o NR7R8; R6 representa un átomo de hidrogeno o un grupo alquilo (C1-4); o R4 y R6 junto con el átomo de nitrogeno al que están unidos constituyen un radical heterociclico de 3 a 8 átomos, que contienen o no un segundo heteroátomo seleccionado entre un átomo de oxigeno, de azufre o de nitrogeno, sin sustituir o sustituido o varias veces por un grupo alquilo (C1-4); un grupo alcanoílo (C1-4); un grupo NR7R8 o CONR7R8; un grupo fenilo sin sustituir o sustituido o varias veces por un átomo de halogeno, un grupo alquilo (C1-4), alcoxi (C1-4) o trifluorometilo, alquiltio (C1-4), trifluorometoxi, trifluorornetiltio o un grupo OS(O)nAlk, S(O)nAlk o NR7R8; R7 y R8 representan cada uno independientemente del otro un átomo de hidrogeno, un grupo alquilo (C1-4) o R7 y R8 junto con el átomo de nitrogeno al que están unidos, constituyen un radical heterocíclico saturado de 4 a 8 átomo que puede contener otro heteroátomo seleccionado entre un átomo de nitrogeno, de oxígeno o de azufre; Ar1 y Ar2 representan cada uno independientemente del otro un fenilo sin sustituir o sustituido con un átomo de halogeno, un grupo alquilo (C1-6), alcoxi (C1-6), alquiltio (C1-6), trifluorometilo, trifluorometoxi, trifluorometiltio, ciano, nitro o un grupo S(Q)nAlk, OS(O)nAlk o NR7R8; n representa 0, 1 o 2; Alk representa un grupo alquilo(C1-7); en forma de base o de sal de adicion, así como en forma de hidrato o de solvato.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR0603382A FR2899899A1 (fr) | 2006-04-14 | 2006-04-14 | Derives d'aminomethyl pyridine, leur preparation et leur application en therapeutique |
Publications (1)
Publication Number | Publication Date |
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AR060800A1 true AR060800A1 (es) | 2008-07-16 |
Family
ID=37434008
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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ARP070101551A AR060800A1 (es) | 2006-04-14 | 2007-04-12 | Derivados de aminometilpiridina su preparacion y su aplicacion en terapeutica |
Country Status (18)
Country | Link |
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US (1) | US20090203699A1 (es) |
EP (1) | EP2010492A2 (es) |
JP (1) | JP2009533400A (es) |
KR (1) | KR20080108540A (es) |
CN (1) | CN101421240A (es) |
AR (1) | AR060800A1 (es) |
AU (1) | AU2007239344A1 (es) |
BR (1) | BRPI0710741A2 (es) |
CA (1) | CA2645961A1 (es) |
DO (1) | DOP2007000067A (es) |
FR (1) | FR2899899A1 (es) |
IL (1) | IL194573A0 (es) |
MX (1) | MX2008013208A (es) |
PE (1) | PE20071224A1 (es) |
RU (1) | RU2008144952A (es) |
TW (1) | TW200813037A (es) |
UY (1) | UY30285A1 (es) |
WO (1) | WO2007119001A2 (es) |
Families Citing this family (10)
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EP2025674A1 (de) | 2007-08-15 | 2009-02-18 | sanofi-aventis | Substituierte Tetrahydronaphthaline, Verfahren zu ihrer Herstellung und ihre Verwendung als Arzneimittel |
AU2011281132B2 (en) * | 2010-07-20 | 2014-01-30 | Council Of Scientific & Industrial Research | Pyridin- 2 - YL sulfanyl acid esters and process for the preparation thereof |
GB201103419D0 (es) | 2011-02-28 | 2011-04-13 | Univ Aberdeen | |
WO2012120054A1 (de) | 2011-03-08 | 2012-09-13 | Sanofi | Di- und trisubstituierte oxathiazinderivate, verfahren zu deren herstellung, ihre verwendung als medikament sowie sie enthaltendes arzneimittel und deren verwendung |
EP2766349B1 (de) | 2011-03-08 | 2016-06-01 | Sanofi | Mit carbozyklen oder heterozyklen substituierte oxathiazinderivate, verfahren zu deren herstellung, diese verbindungen enthaltende arzneimittel und deren verwendung |
EP2683700B1 (de) | 2011-03-08 | 2015-02-18 | Sanofi | Tetrasubstituierte oxathiazinderivate, verfahren zu deren herstellung, ihre verwendung als medikament sowie sie enthaltendes arzneimittel und deren verwendung |
WO2012120053A1 (de) | 2011-03-08 | 2012-09-13 | Sanofi | Verzweigte oxathiazinderivate, verfahren zu deren herstellung, ihre verwendung als medikament sowie sie enthaltendes arzneimittel und deren verwendung |
WO2012120055A1 (de) | 2011-03-08 | 2012-09-13 | Sanofi | Di- und trisubstituierte oxathiazinderivate, verfahren zu deren herstellung, ihre verwendung als medikament sowie sie enthaltendes arzneimittel und deren verwendung |
US8809372B2 (en) | 2011-09-30 | 2014-08-19 | Asana Biosciences, Llc | Pyridine derivatives |
US9199975B2 (en) | 2011-09-30 | 2015-12-01 | Asana Biosciences, Llc | Biaryl imidazole derivatives for regulating CYP17 |
Family Cites Families (8)
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US5481005A (en) * | 1990-07-31 | 1996-01-02 | Sanofi | N-sulfonylindoline derivatives, their preparation and the pharmaceutical compositions in which they are present |
US5686470A (en) * | 1995-02-10 | 1997-11-11 | Weier; Richard M. | 2, 3-substituted pyridines for the treatment of inflammation |
CA2479744A1 (en) * | 2002-03-28 | 2003-10-09 | Paul E. Finke | Substituted 2,3-diphenyl pyridines |
FR2838439B1 (fr) * | 2002-04-11 | 2005-05-20 | Sanofi Synthelabo | Derives de terphenyle, leur preparation, les compositions pharmaceutqiues en contenant |
FR2838438A1 (fr) * | 2002-04-11 | 2003-10-17 | Sanofi Synthelabo | Derives de diphenylpyridine,leur preparation, les compositions pharmaceutiques en contenant |
FR2856684B1 (fr) * | 2003-06-26 | 2008-04-11 | Sanofi Synthelabo | Derives de diphenylpyridine, leur preparation et leur application en therapeutique |
FR2864958B1 (fr) * | 2004-01-12 | 2006-02-24 | Sanofi Synthelabo | Derive de n-[(1,5-diphenyl-1h-pyrazol-3-yl)methyl] sulfonamide, leur preparation et leur application en therapeutique. |
FR2876691B1 (fr) * | 2004-10-18 | 2006-12-29 | Sanofi Aventis Sa | Derives de pyridine, leur preparation, leur application en therapeutique |
-
2006
- 2006-04-14 FR FR0603382A patent/FR2899899A1/fr not_active Withdrawn
-
2007
- 2007-04-10 DO DO2007000067A patent/DOP2007000067A/es unknown
- 2007-04-11 TW TW096112757A patent/TW200813037A/zh unknown
- 2007-04-12 KR KR1020087024954A patent/KR20080108540A/ko not_active Application Discontinuation
- 2007-04-12 MX MX2008013208A patent/MX2008013208A/es not_active Application Discontinuation
- 2007-04-12 PE PE2007000452A patent/PE20071224A1/es not_active Application Discontinuation
- 2007-04-12 CN CNA2007800131701A patent/CN101421240A/zh active Pending
- 2007-04-12 BR BRPI0710741-2A patent/BRPI0710741A2/pt not_active IP Right Cessation
- 2007-04-12 WO PCT/FR2007/000620 patent/WO2007119001A2/fr active Application Filing
- 2007-04-12 JP JP2009504782A patent/JP2009533400A/ja not_active Withdrawn
- 2007-04-12 EP EP07731288A patent/EP2010492A2/fr not_active Withdrawn
- 2007-04-12 RU RU2008144952/04A patent/RU2008144952A/ru not_active Application Discontinuation
- 2007-04-12 AU AU2007239344A patent/AU2007239344A1/en not_active Abandoned
- 2007-04-12 AR ARP070101551A patent/AR060800A1/es unknown
- 2007-04-12 CA CA002645961A patent/CA2645961A1/fr not_active Abandoned
- 2007-04-13 UY UY30285A patent/UY30285A1/es unknown
-
2008
- 2008-10-06 IL IL194573A patent/IL194573A0/en unknown
- 2008-10-10 US US12/249,140 patent/US20090203699A1/en not_active Abandoned
Also Published As
Publication number | Publication date |
---|---|
WO2007119001A2 (fr) | 2007-10-25 |
AU2007239344A1 (en) | 2007-10-25 |
IL194573A0 (en) | 2009-09-22 |
WO2007119001A3 (fr) | 2007-12-13 |
RU2008144952A (ru) | 2010-05-20 |
US20090203699A1 (en) | 2009-08-13 |
TW200813037A (en) | 2008-03-16 |
JP2009533400A (ja) | 2009-09-17 |
KR20080108540A (ko) | 2008-12-15 |
FR2899899A1 (fr) | 2007-10-19 |
DOP2007000067A (es) | 2007-10-31 |
CA2645961A1 (fr) | 2007-10-25 |
UY30285A1 (es) | 2007-11-30 |
MX2008013208A (es) | 2008-10-27 |
CN101421240A (zh) | 2009-04-29 |
PE20071224A1 (es) | 2008-01-23 |
EP2010492A2 (fr) | 2009-01-07 |
BRPI0710741A2 (pt) | 2011-06-07 |
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