AR038002A1 - Antagonistas del receptor de neuroquinina-1, composiciones farmaceuticas y el uso de dichos antagonistas para la preparacion de un medicamento - Google Patents
Antagonistas del receptor de neuroquinina-1, composiciones farmaceuticas y el uso de dichos antagonistas para la preparacion de un medicamentoInfo
- Publication number
- AR038002A1 AR038002A1 ARP020104337A ARP020104337A AR038002A1 AR 038002 A1 AR038002 A1 AR 038002A1 AR P020104337 A ARP020104337 A AR P020104337A AR P020104337 A ARP020104337 A AR P020104337A AR 038002 A1 AR038002 A1 AR 038002A1
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- Prior art keywords
- group
- alkyl
- independently selected
- cycloalkyl
- atom
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Abstract
Antagonistas del receptor de la neuroqinina-1 que comprenden un compuesto que tiene la fórmula (1) o una sal farmacéuticamente aceptable del mismo, donde Ar1 y Ar2 están cada uno independientemente seleccionado del grupo que consiste en R17-heteroarilo- y como se muestra en estructura (2); X1 es -O-, -S-, -SO-, SO2, -NR18a, -N(COR12)- o -N(SO2R15)-; X2 es C, S, o SO; cuando X2 es C, entonces Y es O, S, o NR11, cuando X2 es S o SO, entonces Y es O, cuando X1 es -SO-, -SO2-, -N(COR12)- o -N(SO2R15)-, entonces; R1 y R2 están cada uno independientemente seleccionados del grupo que consiste en H, alquilo C1-6, hidroxi(alquilo C1-3), -cicloalquilo C3-8, -cicloalquilalquilo C4-8, -CH2F, -CHF2 y -CF3; o R1 y R2, uno con el otro conjuntamente, y el átomo de C al cual están ambos unidos, forman un anillo alquileno C3-6; cuando X1 es -O-, -S- o NR18a, entonces R1 y R2, están cada uno independientemente seleccionados del grupo que consiste en H, -alquilo C1-6, hidroxi(alquilo C1-3), -cicloalquiloC3-8, -cicloalquilalquilo C4-8, -CH2F, -CHF2 u -CF3, o R1 y R2, conjuntamente uno con el otro y con el átomo de C al cual están ambos unidos forman un anillo alquileno C3-6; o R1 y R2 conjuntamente uno con el otro y con el átomo de C al cual están ambos unidos forman un grupo C=O; R3 está seleccionado del grupo que consiste en H, -alquilo C1-6, hidroxi-(alquiloC1-3); -cicloalquilo C3-8, -CH2F, -CHF2 y -CF3; cada R6 está independientemente seleccionado del grupo que consiste en H, alquilo C1-6, -OR13 y -SR18; cada R7 está independientemente seleccionado del grupo que consiste en H, y alquilo C1-6, o R6 y R7, conjuntamente uno con el otro y con el átomo de C al cual están ambos unidos forman un grupo C=O; n2 es de 1 a 4; R4 y R5 están cada uno independientemente seleccionados del grupo que consiste en -(CR28R29)n1-G y -C(O)(CR28R29)n4-G, donde n1 es de 0 a 5; n4 es de 1 a 5 y G es H, -CF3, -CHF2, -CH2F, -OH, -O-(alquilo C1-6), -SO2R13, -O-(cicloalquilo C3-8), -NR13R14, -SO2NR13R14, -NR13SO2R15, -NR13COR12, -NR12(CONR13R14), -NR12COC(R12)2NR13R14, -CONR13R14, -COOR12, cicloalquilo C3-8(R19)r arilo-, (R19)r heteroarilo-, OC(O)R14, -OC(O)NR13R14, o como se muestra en las estructuras (3) o R4 y R5, conjuntamente uno con el otro y con el átomo de C al cual están ambos unidos forman un grupo C=O o C=NR12, o R4 y R5 conjuntamente uno con el otro y con el átomo de C al cual están ambos unidos forman un anillo de 4 a 7 miembros que contiene de 0 a 3 heteroátomos que están cada uno independientemente seleccionados del grupo que consiste en -O-, -S-, -S(O)-, -SO2-, y -NR18- estando el anillo opcionalmente sustituido con 1 o 2 sustituyentes que están independientemente seleccionados del grupo que consiste en: R30 o R31; o cuando R4 y R5 no forman un anillo, y n2 es 1 o 2, entonces R4 y R6 o R4 y R7 que están carbonos adyacentes, pueden formar un enlace; X3 es -NR20-, -N(CONR13R14)-, -N(CO2R13), -N(SO2R15)-, -N(COR12)-, -N(SO2NHR13), -O-, -S-,-S(O)-, -SO2-, -CH2-, -CF2-, o -CR12F-; R8, R9 y R10 están cada uno independientemente seleccionados del grupo que consiste en H, alquilo C1-6, cicloalquilo C3-8, -OR18, halógeno, -CN, -NO2, -CF3, -CHF2, -CH2F, -CH2CF3, -OCF3, -OCHF2, -OCH2F, -OCH2CF3, -COOR12, -CONR21R22, -NR21COR12, -NR21CO2R15, -NR21CONR21R22, -NR21SO2R15, -NR21R22, -SO2NR21R22, -S(O)n5R15, (R19),arilo- y (R19)r heteroarilo-; R11 es H, -alquilo C1-6, -cicloalquilo C3-8, -cicloalquilalquilo C4-8, -NO2, -CN, o -OR18, R12 es H, -alquilo C1-6, -cicloalquilo C3-6 o -cicloalquilalquilo C4-8; R13 y R14 están cada uno independientemente seleccionados del grupo que consiste en H, alquilo C1-6, cicloalquilo C3-8 o cicloalquilalquilo C4-8, o R13 y R14 conjuntamente uno con el otro forman una cadena alquileno C3 a C6, y con el N al cual están ambos unidos forman un anillo de 4 a 7 miembros que está opcionalmente sustituido con -OR12, donde uno de los átomos de C en la cadena alquileno C3-6 químicamente factible es, opcionalmente , reemplazada con un heteroátomo seleccionado del grupo que consiste en -O-, -S- y -NR18-, R15 es -alquilo C1-6, -cicloalquilo C3-8, cicloalquilalquilo C4-8 o -CF3; R17 es H, -alquilo C1-6, -cicloalquilo C3-8, -cicloalquilo C4-8, -COOR12, -CONR21R22, -NR21R22, -NR21COR12, -NR21CO2R12, -NR21CONR21R22, -NR21SO2R15 o -S(O)n5R15, cada R18 está independientemente seleccionado del grupo que consiste en H, alquilo C1-6, cicloalquilo C3-8, cicloalquilalquilo C4-8 y P(O)(OH)2; cada R18a está independientemente seleccionado del grupo que consiste en H, alquilo C1-6, -cicloalquilo C3-8 y cicloalquilalquilo C4-8, cada R19 está sustituido en el anillo arilo o heteroarilo al cual está unido y está independientemente seleccionado del grupo que consiste en H, -alquilo C1-6, -cicloalquilo C3-8, -cicloalquilalquilo C4-8, -alcoxi C1-6, -OH, -halógeno, -CN, -NO2, -CF3, -CHF2, -OCF3, -OCHF2, -OCH2F, -O-alquilo C1-6, -O-cicloalquiloC3-8, -COOR12, -CONR21R22, -NR21R22, -NR21COR12, -NR21CO2R12, -NR21CONR21R22, -NR21SO2R15 y -S(O)n 5R15; r es de 1 a 3; R20 es H, alquilo C1-6, cicloalquilo C3-8, cicloalquilalquilo C4-8 o -(CH2)n6-heterocicloalquilo; R21 y R22 están cada uno independientemente seleccionados del grupo que consiste en H, -alquilo C1-6, -cicloalquilo C3-8, -cicloalquilalquilo C4-8 y bencilo; o R21 y R22 conjuntamente uno con el otro forman una cadena alquileno C3-6 químicamente factible, y con el N al cual están ambos unidos forman un anillo de 4 a 7 miembros químicamente factible, donde uno de los átomos de C en la cadena alquileno C3-6 químicamente factible está opcionalmente reemplazado con un heteroátomo seleccionado del grupo que consiste en -O-, -S-, o -NR18; R23 y R24 están cada uno independientemente seleccionados del grupo que consiste en H y alquilo C1-6 o R23 y R24, conjuntamente uno con el otro y con el átomo de C al cual están ambos unidos forman un grupo C=O o ciclopropilo; R25 y R26 están cada uno independientemente seleccionados del grupo que consiste en H y alquilo C1-6; o R25 y R26, conjuntamente uno con el otro con el átomo de C, al cual están ambos unidos forman un grupo C=O o ciclopropilo; R27 es H, -alquilo C1-6; R28 y R29 están uno independientemente seleccionados del grupo que consiste en H, -alquilo C1-2, -CH2F, -CHF2 y -CF3; R30 y R31 están cada uno independientemente seleccionados del grupo que consiste en H, -alquilo C1-2, -CH2F, -CHF2 y -CF3; o R30 y R31, conjuntamente uno con el otro y con el átomo de C al cual están ambos unidos forman un grupo C=O o ciclopropilo; n3 es de 1 a 5; n5 es de 0 a 2; y n6 es de 0 a 3; con la condición de que, cuando n5 es 0, y R25 y R26 son cada uno H, entonces X3 es -CH2-, -CF2- o CR12F- o un diaestereómero, enantiómero, estereoisómero, regioestereómero, rotómero, tautómero o prodroga del mismo, composiciones farmacéuticas y el uso de dichos antagonistas para la preparación de un medicamento para tratar emesis, náusea, depresión, ansiedad o tos; una enfermedad respiratoria, una enfermedad inflamatoria, un desorden de la piel, un desorden oftalmológico, fobia y desorden bipolar, dependencia del alcohol, y abuso de sustancias psicoactivas, epilepsia, nocicepción, psicosis, esquizofrenia, enfermedad de Alzheimer, demencia relacionada con Sida, enfermedad de Towne, desorden relacionado con estrés, desorden obsesivo/compulsivo, bulimia, anorexia nerviosa y excesos de comida, manía, síndrome pre-menstrual, desorden gastrointestinal ateroesclorosis, desorden fibrosante, obesidad, diabetes de Tipo II, dolores de cabeza, dolor neuropático, dolor post-operativo y síndromes de dolor crónico, desordenes vesicales y genitourinarios.
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EP (1) | EP1451153B1 (es) |
JP (2) | JP4459621B2 (es) |
CN (1) | CN100509782C (es) |
AR (1) | AR038002A1 (es) |
AT (1) | ATE374183T1 (es) |
CA (1) | CA2466465A1 (es) |
DE (1) | DE60222693T2 (es) |
ES (1) | ES2291538T3 (es) |
HK (1) | HK1063791A1 (es) |
MX (1) | MXPA04004477A (es) |
PE (1) | PE20030592A1 (es) |
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PE20030762A1 (es) | 2001-12-18 | 2003-09-05 | Schering Corp | Compuestos heterociclicos como antagonistas nk1 |
GB0308968D0 (en) * | 2003-04-17 | 2003-05-28 | Glaxo Group Ltd | Medicaments |
DE602005025755D1 (de) | 2004-06-04 | 2011-02-17 | Teva Pharma | Irbesartan enthaltende pharmazeutische zusammensetzung |
AU2012216435B8 (en) * | 2004-07-01 | 2015-02-19 | Opko Health, Inc. | Piperidine derivatives as NK1 antagonists |
WO2006007540A2 (en) * | 2004-07-01 | 2006-01-19 | Schering Corporation | Piperidine derivatives as nk1 antagonists |
BRPI0619154A2 (pt) * | 2005-12-01 | 2011-09-20 | Hoffmann La Roche | inibidores do transportador da serotonina (sert) |
KR20080108319A (ko) | 2006-04-05 | 2008-12-12 | 쉐링 코포레이션 | 약제학적 제형: 8-[{1-(3,5-비스-(트리플루오로메틸)페닐)-에톡시}-메틸]-8-페닐-1,7-디아자-스피로[4,5]데칸-2-온의 염 및이를 사용한 치료 방법 |
AR066191A1 (es) * | 2007-03-22 | 2009-08-05 | Schering Corp | Proceso e intermediarios para la sintesis de compuestos 8- [ ( 1- (3,5- bis- ( trifluorometil) fenil) - etoxi ) - metil]- 8 fenil - 1,7- diaza - espiro (4, 5) decan -2 ona |
WO2010028232A1 (en) | 2008-09-05 | 2010-03-11 | Schering Corporation | Process and intermediates for the synthesis of 8-[{1-(3,5-bis-(trifluoromethyl)phenyl)-ethoxy}-methyl]-8-phenyl-1,7-diaza-spiro[4.5]decan-2-one compounds |
MX336071B (es) | 2009-08-14 | 2016-01-06 | Opko Health Inc | Formulaciones intravenosas de antagonistas de neurocinina 1. |
JP5934787B2 (ja) | 2011-05-10 | 2016-06-15 | ギリアード サイエンシーズ, インコーポレイテッド | イオンチャネルモジュレーターとしての縮合複素環式化合物 |
NO3175985T3 (es) | 2011-07-01 | 2018-04-28 | ||
TW201837023A (zh) | 2011-07-01 | 2018-10-16 | 美商基利科學股份有限公司 | 作為離子通道調節劑之稠合雜環化合物 |
JP6723930B2 (ja) * | 2014-02-07 | 2020-07-15 | エムティーエー タモガトット クタトクソポルトク イロダジャ | シグマ−1−受容体アゴニスト化合物の新規使用 |
CN105367510B (zh) * | 2015-11-02 | 2017-07-21 | 叶海伟 | 一种(2R,4S)‑3‑Cbz‑2,4‑二苯基‑1,3‑恶唑烷‑5‑酮的制备方法 |
CN106967000B (zh) * | 2017-04-19 | 2021-02-02 | 成都百特万合医药科技有限公司 | 用于防治肿瘤化疗的医药中间体的制备方法 |
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ATE188472T1 (de) | 1992-10-28 | 2000-01-15 | Merck Sharp & Dohme | 4-arylmethyloxymethyl piperidine als tachykinin antagonisten |
AU682838B2 (en) | 1992-12-14 | 1997-10-23 | Merck Sharp & Dohme Limited | 4-aminomethyl/thiomethyl/sulfonylmethyl-4-phenylpiperidines as tachykinin receptor antagonists |
EP0739336B1 (en) | 1994-01-13 | 1998-08-26 | MERCK SHARP & DOHME LTD. | Gem-disubstituted azacyclic tachykinin antagonists |
US6162805A (en) | 1997-04-24 | 2000-12-19 | Merck Sharp & Dohme Limited | Use of an NK-1 receptor antagonist and an SSRI for treating obesity |
WO2001044200A2 (en) * | 1999-12-17 | 2001-06-21 | Schering Corporation | Selective neurokinin antagonists |
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JP2010090163A (ja) | 2010-04-22 |
HK1063791A1 (en) | 2005-01-14 |
CA2466465A1 (en) | 2003-05-22 |
WO2003042173A8 (en) | 2003-10-02 |
JP2005509031A (ja) | 2005-04-07 |
EP1451153A1 (en) | 2004-09-01 |
CN1585748A (zh) | 2005-02-23 |
ATE374183T1 (de) | 2007-10-15 |
US20030144270A1 (en) | 2003-07-31 |
DE60222693T2 (de) | 2008-07-17 |
CN100509782C (zh) | 2009-07-08 |
ES2291538T3 (es) | 2008-03-01 |
JP4459621B2 (ja) | 2010-04-28 |
TW200300347A (en) | 2003-06-01 |
US7122677B2 (en) | 2006-10-17 |
EP1451153B1 (en) | 2007-09-26 |
WO2003042173A1 (en) | 2003-05-22 |
PE20030592A1 (es) | 2003-07-07 |
DE60222693D1 (de) | 2007-11-08 |
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