AR048304A1 - Derivados de bencimidazolilo - Google Patents

Derivados de bencimidazolilo

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Publication number
AR048304A1
AR048304A1 ARP050100706A ARP050100706A AR048304A1 AR 048304 A1 AR048304 A1 AR 048304A1 AR P050100706 A ARP050100706 A AR P050100706A AR P050100706 A ARP050100706 A AR P050100706A AR 048304 A1 AR048304 A1 AR 048304A1
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AR
Argentina
Prior art keywords
cr5r6
group
independently
hal
kor13
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ARP050100706A
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English (en)
Inventor
Hans-Peter Buchstaller
Lars Thore Burgdorf
Frank Stieber
Christiane Amendt
Matthias Grell
Christian Sirrenberg
Frank Zenke
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Merck Patent Gmbh
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Publication of AR048304A1 publication Critical patent/AR048304A1/es

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    • C07C273/1818Preparation of urea or its derivatives, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups of substituted ureas with formation of the N-C(O)-N moiety from -N=C=O and XNR'R"
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Abstract

Derivados de bencimidazolilo y uso de los compuestos de formula (1) para preparar una composicion farmacéutica y a un método de tratamiento que comprende la administracion de dicha composicion farmacéutica a un paciente. Reivindicacion 1: derivados de bencimidazolilo e la formula (1) en donde Ar1 está seleccionado de hidrocarburos aromáticos que contienen 6 a 14 átomos de carbono y residuos heterocíclicos etilénicos insaturados o aromáticos que contienen 3 a 10 átomos de carbono y uno o dos heteroátomos, seleccionados de modo independiente de N, O y S, E es (CR5R6)n, en donde n es 1 o 2; D es (CR5R6)k, en donde k es 0 o 1; R5, R6 están seleccionados, en cada caso de modo independiente entre sí, de H y A; R8, R9, y R10 están seleccionados de modo independiente de un grupo integrado por H, A, cicloalquilo que comprende 3 a 7 átomos de C, Hal, CH2Hal, CH(Hal)2, C(Hal)3, NO2, (CH2)nCN, OHet, N(R11)Het, NR11COR13, NR11COOR13, CONR11R12, COOR13, (CR5R6)kHet, O(CR5R6)kHet, N(R11)(CR5R6)kHet, (CR5R6)kNR11R12, (CR5R6)kOR13, O(CR5R6)kNR11R12, NR11(CR5R6)kNR11R12, O(CR5R6)kR13, NR11(CR5R6)kR13, O(CR5R6)kOR13, NR11(CR5R6)kOR13, (CH2)nNR11R12, (CH2)nO(CH2)kNR11R12, (CH2)nNR11(CH2)kNR11R12, (CH2)nO(CH2)kOR11, (CH2)nNR11(CH2)kOR12, (CH2)nCOOR13, (CH2)nCOR13, (CH2)nCONR11R12, (CH2)nNR11COR13, (CH2)nNR11CONR11R12, (CH2)nNR11SO2A, (CH2)nSO2NR11R12, (CH2)nS(O)uR13, (CH2)nOC(O)R13, (CH2)nCOR13, (CH2)nSR11, CH=N-OA, CH2CH=N-OA, (CH2)nNHOA, (CH2)nCH=N-R11, (CH2)nOC(O) NR11R12, (CH2)nNR11COOR13, (CH2)nN(R11)CH2CH2OR13, (CH2)nN(R11)CH2CH2OCF3, (CH2)nN(R11)C(R13)HCOOR12, (CH2)nN(R11)C(R13)HCOR11, (CH2)nN(R11)CH2CH2N(R12)CH2COOR11, (CH2)n N(R11)CH2CH2 NR11R12, CH=CHCOOR13, CH=CHCH2 NR11R12, CH=CHCH2NR11R12, CH=CHCH2OR13, (CH2)nN(COOR13)COOR14, (CH2)nN(CONH2)COOR13, (CH2)nN(CONH2)CONH2, (CH2)nN(CH2COOR13)COOR14, (CH2)nN(CH2CONH2)COOR13, (CH2)nN(CH2CONH2)CONH2, (CH2)nCHR13COR14, (CH2)nCHR13COOR14, (CH2)nCHR13CH2OR14, (CH2)nOCN y (CH2)nNCO, en donde R11, R12 están seleccionados de modo independiente de un grupo integrado por H, A, (CH2)mAr3 y (CH2)mHet, o en NR11R12; R11 y R12 forman, junto con el átomo de N al que están unidos, un heterociclo de 5, 6 o 7 miembros que opcionalmente contiene 1 o 2 heteroátomos adicionales, seleccionados de N, O y S; R13 , R14 están seleccionados de modo independiente de un grupo integrado por H, Hal, A, (CH2)mAr4 y (CH2)mHet, A está seleccionado del grupo integrado por alquilo, alquenilo, cicloalquilo, alquilencicloalquilo, alcoxi, alcoxialquilo y heterociclilo saturado, con preferencia del grupo integrado por alquilo, alquenilo, cicloalquilo, alquilencicloalquilo, alcoxi y alcoxialquilo; Ar3, Ar4 son, de modo independiente entre sí, residuos hidrocarbonados aromáticos que comprenden 5 a 12 y con preferencia 5 a 10 átomos de C que están opcionalmente sustituidos con uno o varios sustituyentes, seleccionados de un grupo integrado por A, Hal, NO2, CN, OR15, NR15R16, COOR15, CONR15R16, NR15COR16, NR15CONR15R16, NR16SO2A, COR15, SO2NR15R16, S(O)uA y OOCR15, Het es un residuo heterocíclico saturado, insaturado o aromático que está opcionalmente sustituido con uno o varios sustituyentes, seleccionados de un grupo integrado por AQ, Hal, NO2, CN, OR15, NR15R16, COOR15, CONR15R16, NR15COR16, NR15CONR15R16, NR16SO2A, COR15, SO2NR15R16, SW(O)uA y OOCR15; R15, R16 están seleccionados de modo independiente de un grupo integrado por H, AQ y (CH2)mAr6, en donde Ar6 es un hidrocarburo aromático de 5 o 6 miembros que está opcionalmente sustituido con uno o varios sustituyentes seleccionados de un grupo integrado por metilo, etilo, propilo, 2-propilo, ter-butilo, Hal, CN, OH, NH2 y CF3, k, n y m son, de modo independiente entre sí, 0, 1, 2, 3, 4 o 5; Y esta seleccionado de O, S, NR21, C(R22)-NO2, C(R22)-CN y C(CN)2, en donde R21 está seleccionado de modo independiente de los significados dados para R13, R14 y R22 está seleccionado de modo independiente de los significados dados para R11, R12, p es, de modo independiente en cada caso, 0, 1, 2, 3, 4 o 5, q es 0, 1, 2, 3 o 4, con preferencia 0, 1 o 2, u es 0, 1, 2 o 3, con preferencia 0, 1 o 2, y Hal está seleccionado de modo independiente de un grupo integrado por F, Cl, Br e I; sus formas tautoméricas; y sus derivados, sales y solvatos farmacéuticamente aceptables.
ARP050100706A 2004-02-26 2005-02-25 Derivados de bencimidazolilo AR048304A1 (es)

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EP04004332 2004-02-26
EP04004967 2004-03-03

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AR048304A1 true AR048304A1 (es) 2006-04-19

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US (1) US20070191444A1 (es)
EP (1) EP1718637A2 (es)
JP (1) JP2007523929A (es)
AR (1) AR048304A1 (es)
AU (1) AU2005217042A1 (es)
CA (1) CA2557398A1 (es)
WO (1) WO2005082862A2 (es)

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SG10202110259QA (en) 2017-10-05 2021-10-28 Fulcrum Therapeutics Inc Use of p38 inhibitors to reduce expression of dux4
US10342786B2 (en) 2017-10-05 2019-07-09 Fulcrum Therapeutics, Inc. P38 kinase inhibitors reduce DUX4 and downstream gene expression for the treatment of FSHD

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JPS575785B2 (es) * 1973-12-18 1982-02-01
JP2004517080A (ja) * 2000-11-29 2004-06-10 グラクソ グループ リミテッド Tie−2および/またはvegfr−2の阻害剤として有用なベンゾイミダゾール誘導体
TWI236474B (en) * 2001-04-03 2005-07-21 Telik Inc Antagonists of MCP-1 function and methods of use thereof
CN1705645A (zh) * 2002-10-24 2005-12-07 默克专利有限公司 作为raf-激酶抑制剂的亚甲基脲衍生物
JP5229853B2 (ja) * 2003-02-28 2013-07-03 ニッポネックス インコーポレイテッド 癌その他の疾患の治療に有用な新規な二環尿素誘導体
WO2005054183A2 (en) * 2003-12-01 2005-06-16 The Scripps Research Institute Quinolinone based protein kinase inhibitors

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WO2005082862A2 (en) 2005-09-09
JP2007523929A (ja) 2007-08-23
CA2557398A1 (en) 2005-09-09
US20070191444A1 (en) 2007-08-16

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