AR047384A1 - Derivados de tipo ariloxialquilcarbamatos, su preparacion y su aplicacion en terapeutica - Google Patents

Derivados de tipo ariloxialquilcarbamatos, su preparacion y su aplicacion en terapeutica

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Publication number
AR047384A1
AR047384A1 ARP050100111A ARP050100111A AR047384A1 AR 047384 A1 AR047384 A1 AR 047384A1 AR P050100111 A ARP050100111 A AR P050100111A AR P050100111 A ARP050100111 A AR P050100111A AR 047384 A1 AR047384 A1 AR 047384A1
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Argentina
Prior art keywords
group
atom
cycloalkyl
alkyl
alkylene
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ARP050100111A
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English (en)
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Ahmed Abouabdellah
Garcia Antonio Almario
Jacques Froissant
Christian Hoornaert
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Sanofi Aventis
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Publication of AR047384A1 publication Critical patent/AR047384A1/es

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    • C07D207/02Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D207/04Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
    • C07D207/08Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon radicals, substituted by hetero atoms, attached to ring carbon atoms
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    • C07C271/00Derivatives of carbamic acids, i.e. compounds containing any of the groups, the nitrogen atom not being part of nitro or nitroso groups
    • C07C271/06Esters of carbamic acids
    • C07C271/08Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms
    • C07C271/10Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms with the nitrogen atoms of the carbamate groups bound to hydrogen atoms or to acyclic carbon atoms
    • C07C271/16Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms with the nitrogen atoms of the carbamate groups bound to hydrogen atoms or to acyclic carbon atoms to carbon atoms of hydrocarbon radicals substituted by singly-bound oxygen atoms
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    • C07D211/08Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms
    • C07D211/18Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms with substituted hydrocarbon radicals attached to ring carbon atoms
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    • C07D211/22Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms with substituted hydrocarbon radicals attached to ring carbon atoms with hydrocarbon radicals, substituted by singly bound oxygen or sulphur atoms by oxygen atoms
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    • C07D211/06Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
    • C07D211/36Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no 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
    • C07D211/40Oxygen atoms
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    • C07D213/04Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/60Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom 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
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Abstract

Compuesto que responde a la formula (1): en la cual: m representa 0, 1, 2 o 3; n representa 0, 1, 2, o 3, X representa un átomo de O o de S o un grupo SO o SO2; %R1 y R2 representan, independientemente entre sí, un átomo de H o un grupo alquilo C1- 3, o R1 y R2 forman juntos un grupos -(CH2)p-, donde p representa un numero entero que va de 1 a 5 de forma tal que, n + p, sea un numero entero que vaya de 2 a 5 R3 representa un átomo de H o de F o un grupo hidroxi o metilo; R4 representa un grupo de formula general CHR5CONHR6 en la cual: R5 representa un átomo de H o un grupo alquilo C1-6 y R6 representa un átomo de H o un grupo alquilo C1-6, cicloalquilo C3-7, cicloalquilo C3-7-alquileno C1-6; Y representa: un grupo Y1 elegido, especialmente, entre un fenilo, piridinilo, piridazinilo, pirimidinilo, pirazinilo, triazinilo, tiazolilo, naftilo, quinolinilo, isoquinolinilo, ftalazinilo, quinazolinilo, quinoxalinilo, naftiridinilo, cinolinilo, benzofuranilo, dihidrobenzofuranilo, benzotienilo, dihidrobenzotienilo, indolilo, isoindolilo, indolinilo, benzimidazolilo, benzoxazolilo, benzisoxazolilo, benzotiazolilo, benzisotiazolilo, benzotriazolilo, benzoxadiazolilo, benzotiadiazolilo; el grupo Y1 está sustituido, eventualmente, por uno o varios sustituyentes Y2, idénticos o diferentes entre sí, o por un grupo Y3; Y2 representa un átomo de halogeno, un grupo ciano, nitro, alquilo C1-8, alcoxi C1-8, tioalquilo C1-8, fluoroalquilo C1-8, fluoroalcoxi C1-8, fluorotioalquilo C1-8, cicloalquilo C3-7, cicloalquiloxi C3-7, cicloalquilo C3-7-alquileno C1-8, cicloalquilo C3-7-alquiloxi C1-8, hidroxi, NR7R8, NHCOR7, NHSO2R7, COR7, CO2R7, CONR7R8, SO2R7, SO2NR7R8, -O-(alquileno C1-3)-O-, feniloxi, feniltio, fenilalquileno C1-8, fenilalquiloxi C1-8 o fenilalquiltio C1-8; Y3 representa un grupo elegido, especialmente, entre un fenilo, piridinilo, pirimidinilo, pirazinilo o piridazinilo; el o los grupos Y3 pueden ser sustituidos por uno o varios grupos Y2 idénticos o diferentes entre sí, R7 y R8 representan, independientemente entre sí, un átomo de H o un grupo alquilo C1-6, o forman con el átomo de N que los lleva un ciclo azetidina, pirrolidina, piperidina, morfolina, tiomorfolina, azepina, piperazina, eventualmente sustituido por un grupo alquilo C1-3 o bencilo; en estado de base, de sal de adicion con un ácido, de hidrato o de solvato.
ARP050100111A 2004-01-16 2005-01-13 Derivados de tipo ariloxialquilcarbamatos, su preparacion y su aplicacion en terapeutica AR047384A1 (es)

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FR0400389A FR2865205B1 (fr) 2004-01-16 2004-01-16 Derives de type aryloxyalkylcarbamates, leur preparation et leur application en therapeutique

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AR047384A1 true AR047384A1 (es) 2006-01-18

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EP (1) EP1708994B1 (es)
JP (1) JP4705590B2 (es)
KR (1) KR101171462B1 (es)
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AR (1) AR047384A1 (es)
AT (1) ATE369336T1 (es)
AU (1) AU2005212868B2 (es)
BR (1) BRPI0506918A (es)
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FR2866888B1 (fr) * 2004-02-26 2006-05-05 Sanofi Synthelabo Derives de alkylpiperazine- et alkylhomopiperazine- carboxylates, leur preparation et leur application en therapeutique
FR2866884B1 (fr) * 2004-02-26 2007-08-31 Sanofi Synthelabo Derives d'aryl-et d'heteroaryl-piperidinecarboxylates, leur preparation et leur application en therapeutique
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KR101063585B1 (ko) 2005-02-17 2011-09-07 아스텔라스세이야쿠 가부시키가이샤 피리딜 비방향족 질소 함유 헤테로환-1-카르복실산에스테르 유도체
US8197472B2 (en) 2005-03-25 2012-06-12 Maquet Cardiovascular, Llc Tissue welding and cutting apparatus and method
US7918848B2 (en) 2005-03-25 2011-04-05 Maquet Cardiovascular, Llc Tissue welding and cutting apparatus and method
PE20070099A1 (es) 2005-06-30 2007-02-06 Janssen Pharmaceutica Nv N-heteroarilpiperazinil ureas como moduladores de la amida hidrolasa del acido graso
EP2065369A4 (en) * 2006-08-23 2011-12-28 Astellas Pharma Inc UREA CONNECTION OR SALT THEREOF
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MA28343A1 (fr) 2006-12-01
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NZ548530A (en) 2010-02-26
FR2865205A1 (fr) 2005-07-22
TWI402067B (zh) 2013-07-21
RU2006129640A (ru) 2008-02-27
DK1708994T3 (da) 2007-11-26
WO2005077898A1 (fr) 2005-08-25
PT1708994E (pt) 2007-10-02
KR101171462B1 (ko) 2012-08-07
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