AR051108A1 - Compuesto de 4- heteroaril- metil o 4-(heteroaril - metil substituido ) - imidazol2- tiona y su uso para preparar una coposicion farmaceutica - Google Patents
Compuesto de 4- heteroaril- metil o 4-(heteroaril - metil substituido ) - imidazol2- tiona y su uso para preparar una coposicion farmaceuticaInfo
- Publication number
- AR051108A1 AR051108A1 ARP050103995A ARP050103995A AR051108A1 AR 051108 A1 AR051108 A1 AR 051108A1 AR P050103995 A ARP050103995 A AR P050103995A AR P050103995 A ARP050103995 A AR P050103995A AR 051108 A1 AR051108 A1 AR 051108A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkyl
- independently selected
- substituted
- carbocyclic
- pain
- Prior art date
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- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
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- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/06—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
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Abstract
Un compuesto de 4-heteroaril-metil- o 4-(heteroaril-metil substituido)-imidazol-2-tiona de la formula (|1) donde m, n y q son enteros seleccionados de 0 , 1, 2, 3 y 4 con la condicion de que la suma de m, n y q sea 1, 2, 3 o 4; W, X e Y representan un CV o un heteroátomo independientemente seleccionados de N, O y S con la condicion de que al menos uno de los grupos mencionados W, X e Y representan un heteroátomo, las líneas punteadas representan una union o ausencia de una union con la condicion de que no haya más de 3 líneas punteadas presentes en el anillo y con la posterior condicion que ninguna línea punteada representando una union está conectada a un heteroátomo de O o de S; R1 es independientemente H, alquilo C1-4, F alquilo sustituido C1-4, (CH2)sCN, (CH2)s-OR2, (CH2)s-NR4R5, s es un entero seleccionado de 1, 2 y 3; R2 está independientemente H, alquilo C1-4, C(O)R8, arilo carbocíclico o arilo heterocíclico, que tiene 1 hasta 3 heteroátomos independientemente seleccionados de N, O y S; p es un entero seleccionado de 0, 1, 2, 3, 4, y 5; R3 es independientemente seleccionado de los grupos que consisten de alquilo C1-4, F alquilo substituido C1-4, alquenilo C2-4, alquinilo C2-4, F, Cl, Br, Y, N3, NO2, (CH2)t-OR2, (CH2)t-NR5R6, (CH2)t-CN, C(O)R4, C(O)OR4, (CH2)t-SO2R4, arilo carbocíclico o arilo heterocíclico que tiene 1 hasta 3 heteroátomos independientemente seleccionados de N, O y S; t es un entero seleccionado de 0, 1, 2 y 3; R4 y R5 son independientemente H o alquilo C1-4; R6 es independientemente H, alquilo C1-4, arilo carbocíclico o arilo heterocíclico que tiene 1 hasta 3 heteroátomos independientemente seleccionados de N, O y S. Opcionalmente R7 y R8 junto con los átomos a los que están unidos conjuntamente forman un anillo carbocíclico o heterocíclico, el anillo heterocíclico que tiene 5 o 6 átomos en el anillo y 1 hasta 3 heteroátomos independientemente seleccionados de N, O y S; dicho anillo carbocíclico o heterocíclico conjuntamente formado por R7 y R8 siendo opcionalmente substituidos con los grupos R9 desde 1 hasta 7; R9 está independientemente seleccionado de los gripos que consisten de alquilo C1-4, alquenilo C2-4, alquinilo C2-4, CH2OR2, CH2N(R2)2, CH2CN, C(O)R2, C(O)OR6, SO3R6, SO2N(R2)2, CH2SR2, F, Cl, Br, I, F alquilo sustituido C1-4, CN, N3, NO2, N(R2)2, OR2, SR2 o R8 es O o S unido doble a un C de dicho anillo carbocíclico o heterocíclico, con la condicion de que el anillo de formula (2) no representa un imidazol, un imidazol substituido, una furanona o 2-furanona substituido. Son agonistas de receptores adrenérgicos alfa2 y algunos no tienen o tienen mínima actividad cardiovascular y/o sedante. Son utiles para el tratamiento del dolor y otras condiciones con efectos secundarios mínimos. Su uso para preparar una composicion farmacéutica util para tratar dolor cronico, dolor visceral, dolor neuropático, dolor en la cornea, glaucoma, presion intraocular elevada, neuropatías isquémicas, , enfermedades neurodegenerativas, diarrea, congestion nasal, espasticidad muscular, diuresis, síndrome de abstinencia, neuropatía optica, isquemia espinal, derrame cerebral, déficit de la memoria y del conocimiento, desordenes de déficit de atencion, psicosis, desordenes maníacos, ansiedad, depresion, hipertension, falla cardíaca congestiva, isquemia cardíaca, artritis, espondilitis, artritis gotosa, osteoartritis, artritis juvenil, enfermedades autoinmunes, lupus eritematoso, inflamaciones gastrointestinales cronicas, enfermedad de Crohn, gastritis, síndrome del intestino irritable (IBS), dispepsia funcional o colitis ulcerosa.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US61294504P | 2004-09-24 | 2004-09-24 |
Publications (1)
Publication Number | Publication Date |
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AR051108A1 true AR051108A1 (es) | 2006-12-20 |
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ID=35636634
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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ARP050103995A AR051108A1 (es) | 2004-09-24 | 2005-09-26 | Compuesto de 4- heteroaril- metil o 4-(heteroaril - metil substituido ) - imidazol2- tiona y su uso para preparar una coposicion farmaceutica |
Country Status (9)
Country | Link |
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US (2) | US7399868B2 (es) |
EP (1) | EP1791832A1 (es) |
JP (1) | JP2008514603A (es) |
AR (1) | AR051108A1 (es) |
AU (1) | AU2005290008A1 (es) |
BR (1) | BRPI0516025A (es) |
CA (1) | CA2581828A1 (es) |
TW (1) | TW200624430A (es) |
WO (1) | WO2006036507A1 (es) |
Families Citing this family (17)
Publication number | Priority date | Publication date | Assignee | Title |
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JP2008514603A (ja) * | 2004-09-24 | 2008-05-08 | アラーガン、インコーポレイテッド | α2アドレナリン作動剤としての4−(ヘテロアリール−メチルおよび置換ヘテロアリール−メチル)−イミダゾール−2−チオン |
US8003624B2 (en) * | 2005-08-25 | 2011-08-23 | Schering Corporation | Functionally selective ALPHA2C adrenoreceptor agonists |
CN101374830A (zh) * | 2005-08-25 | 2009-02-25 | 先灵公司 | α2C肾上腺素受体激动剂 |
ATE517883T1 (de) * | 2005-08-25 | 2011-08-15 | Schering Corp | Imidazolderivate als funktionelle selektive agonisten des alpha2c-adrenorezeptors |
JP2010510184A (ja) * | 2006-11-16 | 2010-04-02 | エフ.ホフマン−ラ ロシュ アーゲー | 置換4−イミダゾール類 |
WO2008088937A1 (en) * | 2007-01-12 | 2008-07-24 | Allergan, Inc. | Quinolynylmethylimidizoles as therapeutic agents |
US7868020B2 (en) | 2007-01-12 | 2011-01-11 | Allergan, Inc. | Quinolynylmethylimidizoles as therapeutic agents |
US8013169B2 (en) | 2007-01-12 | 2011-09-06 | Allergan, Inc | Naphthylmethylimidizoles as therapeutic agents |
AU2008251324B2 (en) * | 2007-05-14 | 2014-05-01 | Allergan, Inc. | ((Phenyl)imidazolyl)methylheteroaryl compounds |
WO2009052072A1 (en) * | 2007-10-18 | 2009-04-23 | Allergan, Inc. | Treating motor disorders with 4-(1-(2,3-dimethylphenyl)ethyl)-1h-imidazole-2(3h)-thione |
US8455548B2 (en) * | 2007-10-18 | 2013-06-04 | Allergan, Inc. | Method of treating sensorimotor disorders with alpha-2 adrenergic receptor agonists |
US7902247B2 (en) * | 2008-01-09 | 2011-03-08 | Allergan, Inc. | Substituted-aryl-2-phenylethyl-1H-imidazole compounds as subtype selective modulators of alpha 2B and/or alpha 2C adrenergic receptors |
WO2009105504A2 (en) * | 2008-02-21 | 2009-08-27 | Schering Corporation | Functionally selective alpha2c adrenoreceptor agonists |
BRPI0912604A2 (pt) * | 2008-05-13 | 2019-09-10 | Allergan Inc | quinolinilmetilimidazóis como agentes terapêuticos |
CA2728480A1 (en) * | 2008-07-24 | 2010-01-28 | F. Hoffmann-La Roche Ag | 4,5-dihydro-oxazol-2-yl derivatives |
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JP2012517433A (ja) * | 2009-02-06 | 2012-08-02 | アラーガン インコーポレイテッド | アルファ2bおよび/またはアルファ2cアドレナリンレセプターのサブタイプ選択的モジュレーターとしてのピリジン化合物 |
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JP2002097312A (ja) | 2000-09-26 | 2002-04-02 | Bridgestone Corp | タイヤ |
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US6534542B2 (en) | 2001-02-27 | 2003-03-18 | Allergen Sales, Inc. | (2-hydroxy)ethyl-thioureas useful as modulators of α2B adrenergic receptors |
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US7091232B2 (en) * | 2002-05-21 | 2006-08-15 | Allergan, Inc. | 4-(substituted cycloalkylmethyl) imidazole-2-thiones, 4-(substituted cycloalkenylmethyl) imidazole-2-thiones, 4-(substituted cycloalkylmethyl) imidazol-2-ones and 4-(substituted cycloalkenylmethyl) imidazol-2-ones and related compounds |
JP2008514603A (ja) * | 2004-09-24 | 2008-05-08 | アラーガン、インコーポレイテッド | α2アドレナリン作動剤としての4−(ヘテロアリール−メチルおよび置換ヘテロアリール−メチル)−イミダゾール−2−チオン |
-
2005
- 2005-09-07 JP JP2007533518A patent/JP2008514603A/ja active Pending
- 2005-09-07 AU AU2005290008A patent/AU2005290008A1/en not_active Abandoned
- 2005-09-07 BR BRPI0516025-1A patent/BRPI0516025A/pt not_active IP Right Cessation
- 2005-09-07 CA CA002581828A patent/CA2581828A1/en not_active Abandoned
- 2005-09-07 WO PCT/US2005/032128 patent/WO2006036507A1/en active Application Filing
- 2005-09-07 EP EP05796248A patent/EP1791832A1/en not_active Withdrawn
- 2005-09-20 US US11/232,323 patent/US7399868B2/en not_active Expired - Fee Related
- 2005-09-23 TW TW094133123A patent/TW200624430A/zh unknown
- 2005-09-26 AR ARP050103995A patent/AR051108A1/es not_active Application Discontinuation
-
2008
- 2008-05-20 US US12/123,578 patent/US20080221152A1/en not_active Abandoned
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TW200624430A (en) | 2006-07-16 |
JP2008514603A (ja) | 2008-05-08 |
AU2005290008A1 (en) | 2006-04-06 |
BRPI0516025A (pt) | 2008-08-19 |
US20080221152A1 (en) | 2008-09-11 |
WO2006036507A1 (en) | 2006-04-06 |
US7399868B2 (en) | 2008-07-15 |
US20060069143A1 (en) | 2006-03-30 |
EP1791832A1 (en) | 2007-06-06 |
CA2581828A1 (en) | 2006-04-06 |
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