ES2301859T3 - Nuevos derivados de piridazin-3(2h)-ona. - Google Patents

Nuevos derivados de piridazin-3(2h)-ona. Download PDF

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ES2301859T3
ES2301859T3 ES03782471T ES03782471T ES2301859T3 ES 2301859 T3 ES2301859 T3 ES 2301859T3 ES 03782471 T ES03782471 T ES 03782471T ES 03782471 T ES03782471 T ES 03782471T ES 2301859 T3 ES2301859 T3 ES 2301859T3
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amino
mono
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Vittorio Dal Piaz
Izquierdo Nuria Aguilar
Maria Antonia Buil Albero
Marta Carrascal Riera
Jordi Gracia Ferrer
Maria Paola Giovannoni
Claudia Vergelli
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Almirall SA
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    • A61P29/00Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
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    • A61P9/00Drugs for disorders of the cardiovascular system
    • A61P9/10Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
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    • C07DHETEROCYCLIC COMPOUNDS
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    • C07D237/02Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings not condensed with other rings
    • C07D237/06Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
    • C07D237/10Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings not condensed with other rings having three 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
    • C07D237/24Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen
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    • C07D401/12Heterocyclic 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 chain containing hetero atoms as chain links
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    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
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    • C07D417/02Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
    • C07D417/04Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond

Abstract

Un derivado de piridazin-3(2H)-ona de fórmula (I): (Ver fórmula) en la que R1 representa un grupo seleccionado de: * un grupo alquilo C1-C4 que está opcionalmente sustituido con uno o más; y * grupos de fórmula -(CH2)n-R6 en la que n es un número entero que varía de 1 a 3 y R6 representa un grupo cicloalquilo C3-C6, R2 es un átomo de hidrógeno, R3 representa un grupo arilo C5-C14 monocíclico o policíclico o un grupo heteroarilo de 5 a 14 miembros que contiene al menos un heteroátomo seleccionado de O, S y N, que está opcionalmente sustituido con uno o más, por ejemplo 1, 2, 3 ó 4 sustituyentes seleccionados de: * átomos de halógeno; * grupos alquilo C1-C20 y alquileno C1-C6, que están opcionalmente sustituidos con uno o más sustituyentes seleccionados de átomos de halógeno; y grupos fenilo, hidroxi, hidroxialquilo C1-C10, alcoxi C1-C10, ariloxi C5-C14, (alquil C1-C10)tio, oxo, amino, mono- o di-(alquil C1-C10)amino, acilamino, hidroxicarbonilo, (alcoxi C1-C10)carbonilo, carbamoilo, mono- o di-(alquil C1-C10)carbamoilo * grupos fenilo, hidroxi, hidroxialquilo C1-C10, alcoxi C1-C10, cicloalcoxi C3-C7, nitro, ariloxi C5-C14, (alquil C1-C10)tio, (alquil C1-C10)sulfinilo, (alquil C1-C10)sulfonilo, (alquil C1-C10)sulfamoilo, acilo, amino, mono- o di(alquil C1-C10)amino, acilamino, hidroxicarbonilo, (alcoxi C1-C10)carbonilo, carbamoilo, mono- o di(alquil C1-C10)carbamoilo, ureido, N''-(alquil C1-C10)ureido, N'',N''-di(alquil C1-C10)ureido, (alquil C1-C10)sulfamido, aminosulfonilo, mono- o di(alquil C1-C10)aminosulfonilo, ciano, difluorometoxi o trifluorometoxi; R5 representa un grupo -COOR7 o un grupo arilo C5-C14 monocíclico o policíclico o un grupo heteroarilo de 5 a 14 miembros que contiene al menos un heteroátomo seleccionado de O, S y N, que está opcionalmente sustituido con uno o más sustituyentes seleccionados de: * átomos de halógeno; * grupos alquilo C1-C20 y alquileno C2-C20, que están opcionalmente sustituidos con uno o más sustituyentes seleccionados de átomos de halógeno y grupos fenilo, hidroxi, hidroxialquilo C1-C10, alcoxi C1-C10, ariloxi C5-C14, (alquil C1-C10)tio, oxo, amino, mono- o di-(alquil C1-C10)amino, acilamino, hidroxicarbonilo, (alcoxi C1-C10)carbonilo, carbamoilo, mono- o di(alquil C1-C10)carbamoilo; y * grupos fenilo, hidroxi, (alquileno C1-C6)dioxi, alcoxi C1-C10, cicloalcoxi C3-C7, nitro, (alquil C1-C10)tio, (alquil C1-C10)sulfinilo, (alquil C1-C10)sulfonilo, (alquil C1-C10)sulfamoilo, amino, mono- o di(alquil C1-C10)amino, acilamino, nitro, acilo, hidroxicarbonilo, (alcoxi C1-C10)carbonilo, carbamoilo, mono- o di(alquil C1-C10)carbamoilo, ureido, N''-(alquil C1-C10)ureido, N'',N''-di(alquil C1-C10)ureido, (alquil C1-C10)sulfamido, aminosulfonilo, mono- o di(alquil C1-C10)aminosulfonilo, ciano, difluorometoxi o trifluorometoxi; en el que R7 representa un alquilo C1-C20 que está opcionalmente sustituido con uno o más sustituyentes seleccionados de átomos de halógeno y grupos hidroxi, alcoxi C1-C10, ariloxi C5-C14, (alquil C1-C10)tio, oxo, amino, mono- o di(alquil C1-C10)amino, acilamino, hidroxicarbonilo, (alcoxi C1-C10)carbonilo, carbamoilo, mono- o di-(alquil C1-C10)carbamoilo o un grupo de fórmula -(CH2)m-R11 en la que m es un número entero de 0 a 4 y R11 representa: * un grupo cicloalquilo C3-C7 o cicloalquenilo C3-C7; * un grupo arilo C5-C14, que está opcionalmente sustituido con uno o más sustituyentes seleccionados de átomos de halógeno y grupos alquilo C1-C20, hidroxi, alcoxi C1-C10, (alquileno C1-C6)dioxi, (alquil C1-C10)tio, amino, mono- o di(alquil C1-C10)amino, nitro, acilo, hidroxicarbonilo, (alcoxi C1-C10)carbonilo, carbamoilo, mono- o di-(alquil C1-C10)carbamoilo, ciano, trifluorometilo, difluorometoxi o trifluorometoxi; * o un anillo de 3 a 7 miembros que comprende de 1 a 4 heteroátomos seleccionados de nitrógeno, oxígeno y azufre, anillo que puede estar opcionalmente sustituido con uno o más sustituyentes seleccionados de átomos de halógeno y grupos alquilo C1-C20, hidroxi, alcoxi C1-C10, (alquileno C1-C6)dioxi, amino, mono- o di(alquil C1-C10)amino, nitro, ciano o trifluorometilo; y R4 representa * un grupo alquilo que tiene de 1 a 6 átomos de carbono y que está opcionalmente sustituido con uno o más sustituyentes seleccionados de átomos de halógeno y grupo hidroxi; * un grupo mono-(alquil C1-C4)amino o di-(alquil C1-C4)amino no sustituido; * un grupo alquilo C1-C4 que está no sustituido o sustituido con uno o más sustituyentes seleccionados de grupos hidroxi, alcoxi C1-C4, amino, mono(alquil C1-C4)amino y di(alquil C1-C4)amino; * un grupo fenil(alquilo C1-C4)- no sustituido; o * un grupo de fórmula -(CH2)p-R12 en la que p es 2 y R12 representa un radical seleccionado de fenilo, piridilo y tienilo opcionalmente sustituido con uno o más sustituyentes seleccionados de átomos de halógeno y grupos alquilo C1-C20, hidroxi, alcoxi C1-C10, (alquileno C1-C6)dioxi, amino, mono- o di(alquil C1-C10)amino, nitro, ciano y trifluorometilo, siendo cada resto acilo en R3, R5 y R11 un radical C2-C20 unido a un radical carbonilo; asi como los N-óxidos obtenibles de los radicales heteroarilo presentes en la estructura cuando dichos radicales comprenden átomos de nitrógeno y sus sales farmacéuticamente aceptables, con la condición de que cuando R5 no es un grupo heteroarilo opcionalmente sustituido ni un grupo COOR7, entonces R3 es un grupo heteroarilo opcionalmente sustituido.
ES03782471T 2002-12-26 2003-12-22 Nuevos derivados de piridazin-3(2h)-ona. Expired - Lifetime ES2301859T3 (es)

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ES200203003 2002-12-26

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Families Citing this family (71)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7214687B2 (en) 1999-07-14 2007-05-08 Almirall Ag Quinuclidine derivatives and medicinal compositions containing the same
ES2165768B1 (es) 1999-07-14 2003-04-01 Almirall Prodesfarma Sa Nuevos derivados de quinuclidina y composiciones farmaceuticas que los contienen.
ES2211344B1 (es) * 2002-12-26 2005-10-01 Almirall Prodesfarma, S.A. Nuevos derivados de piridazin-3(2h)-ona.
ES2232306B1 (es) * 2003-11-10 2006-08-01 Almirall Prodesfarma, S.A. Nuevos derivados de piridazin-3(2h)-ona.
DE602005022499D1 (de) 2004-05-31 2010-09-02 Almirall Sa Kombinationen mit Antimuskarin-Wirkstoffen und PDE4-Hemmern
ES2257152B1 (es) 2004-05-31 2007-07-01 Laboratorios Almirall S.A. Combinaciones que comprenden agentes antimuscarinicos y agonistas beta-adrenergicos.
ES2251866B1 (es) 2004-06-18 2007-06-16 Laboratorios Almirall S.A. Nuevos derivados de piridazin-3(2h)-ona.
ES2251867B1 (es) * 2004-06-21 2007-06-16 Laboratorios Almirall S.A. Nuevos derivados de piridazin-3(2h)-ona.
CA2584261A1 (en) * 2004-10-13 2006-04-20 Kyowa Hakko Kogyo Co., Ltd. Pharmaceutical composition
EP1810692A1 (en) * 2004-10-13 2007-07-25 Kyowa Hakko Kogyo Co., Ltd. Remedies/preventives for chronic skin disease
ES2265276B1 (es) 2005-05-20 2008-02-01 Laboratorios Almirall S.A. Derivados de 4-(2-amino-1-hidroxietil)fenol como agonistas del receptor beta2 adrenergico.
ES2354627T3 (es) 2005-10-05 2011-03-16 F. Hoffmann-La Roche Ag Derivados de naftiridina.
JO2769B1 (en) 2005-10-26 2014-03-15 جانسين فارماسوتيكا ان. في Rapid decomposition of physiologically antagonistic agents of the 2-dopamine receptor
KR20080094921A (ko) * 2006-01-16 2008-10-27 우베 고산 가부시키가이샤 피롤로피리다지논 화합물
ES2298049B1 (es) 2006-07-21 2009-10-20 Laboratorios Almirall S.A. Procedimiento para fabricar bromuro de 3(r)-(2-hidroxi-2,2-ditien-2-ilacetoxi)-1-(3-fenoxipropil)-1-azoniabiciclo (2.2.2) octano.
JO2849B1 (en) 2007-02-13 2015-03-15 جانسين فارماسوتيكا ان. في Dopamine 2 receptor antagonists are rapidly hydrolyzed
ES2320955B1 (es) 2007-03-02 2010-03-16 Laboratorios Almirall S.A. Nuevos derivados de 3-((1,2,4)triazolo(4,3-a)piridin-7-il)benzamida.
ES2320954B1 (es) * 2007-03-02 2010-03-16 Laboratorio Almirall S.A. Nuevo procedimiento de preparacion de 3-metil-4-fenilisoxazolo (3,4-d)iridazin-7(6h)-ona.
PT2148873E (pt) 2007-04-23 2012-11-20 Janssen Pharmaceutica Nv Derivados da 4-alcoxipiridazina antagonistas de dissociação rápida do recetor da dopamina 2
MX2009011416A (es) 2007-04-23 2009-11-05 Janssen Pharmaceutica Nv Tia(di)azoles como antagonistas del receptor de dopamina 2 de disociacion rapida.
EP2096105A1 (en) 2008-02-28 2009-09-02 Laboratorios Almirall, S.A. Derivatives of 4-(2-amino-1-hydroxyethyl)phenol as agonists of the b2 adrenergic receptor
EP2100599A1 (en) 2008-03-13 2009-09-16 Laboratorios Almirall, S.A. Inhalation composition containing aclidinium for treatment of asthma and chronic obstructive pulmonary disease
EP2100598A1 (en) 2008-03-13 2009-09-16 Laboratorios Almirall, S.A. Inhalation composition containing aclidinium for treatment of asthma and chronic obstructive pulmonary disease
EP2108641A1 (en) 2008-04-11 2009-10-14 Laboratorios Almirall, S.A. New substituted spiro[cycloalkyl-1,3'-indo]-2'(1'H)-one derivatives and their use as p38 mitogen-activated kinase inhibitors
EP2113503A1 (en) 2008-04-28 2009-11-04 Laboratorios Almirall, S.A. New substituted indolin-2-one derivatives and their use as p39 mitogen-activated kinase inhibitors
CN102171189B (zh) 2008-07-31 2013-11-20 詹森药业有限公司 作为快速解离多巴胺2受体拮抗剂的哌嗪-1-基-三氟甲基取代的吡啶
WO2010065153A1 (en) * 2008-12-06 2010-06-10 Intra-Cellular Therapies, Inc. Organic compounds
EP2196465A1 (en) 2008-12-15 2010-06-16 Almirall, S.A. (3-oxo)pyridazin-4-ylurea derivatives as PDE4 inhibitors
UY32297A (es) 2008-12-22 2010-05-31 Almirall Sa Sal mesilato de 5-(2-{[6-(2,2-difluoro-2-fenilitoxi) hexil]amino}-1-hidroxietil)-8-hidroxiquinolin-2( 1h)-ona como agonista del receptor b(beta)2 acrenérgico
EP2221297A1 (en) 2009-02-18 2010-08-25 Almirall, S.A. 5-(2-{[6-(2,2-difluoro-2-phenylethoxy)hexyl]amino}-1-hydroxyethyl)-8-hydroxyquinolin-2(1h)-one and its use in the treatment of pulmonary diseases
EP2221055A1 (en) 2009-02-18 2010-08-25 Almirall, S.A. 5-(2-{[6-(2,2-difluoro-2-phenylethoxy)hexyl]amino}-1-hydroxyethyl)-8-hydroxyquinolin-2(1H)-one for the treatment of lung function
EP2228368A1 (en) 2009-03-12 2010-09-15 Almirall, S.A. Process for manufacturing 5-(2-{[6-(2,2-difluoro-2-phenylethoxy) hexyl]amino}-1-hydroxyethyl)-8-hydroxyquinolin-2(1H)-one
EP2322176A1 (en) 2009-11-11 2011-05-18 Almirall, S.A. New 7-phenyl-[1,2,4]triazolo[4,3-a]pyridin-3(2H)-one derivatives
WO2011075415A1 (en) * 2009-12-14 2011-06-23 Inspire Pharmaceuticals, Inc. Bridged bicyclic rho kinase inhibitor compounds, composition and use
EP2338888A1 (en) 2009-12-24 2011-06-29 Almirall, S.A. Imidazopyridine derivatives as JAK inhibitors
EP2528915B1 (en) * 2010-01-29 2015-10-28 Boehringer Ingelheim International GmbH Substituted naphthyridines and their use as syk kinase inhibitors
EP2360158A1 (en) 2010-02-18 2011-08-24 Almirall, S.A. Pyrazole derivatives as jak inhibitors
UY33213A (es) 2010-02-18 2011-09-30 Almirall Sa Derivados de pirazol como inhibidores de jak
EP2386555A1 (en) 2010-05-13 2011-11-16 Almirall, S.A. New cyclohexylamine derivatives having beta2 adrenergic agonist and m3 muscarinic antagonist activities
EP2394998A1 (en) * 2010-05-31 2011-12-14 Almirall, S.A. 3-(5-Amino-6-oxo-1,6-dihydropyridazin-3-yl)-biphenyl derivatives as PDE4 inhibitors
EP2397482A1 (en) 2010-06-15 2011-12-21 Almirall, S.A. Heteroaryl imidazolone derivatives as jak inhibitors
JP5790348B2 (ja) 2010-09-08 2015-10-07 住友化学株式会社 ピリダジノン化合物の製造法およびその製造中間体
EP2441755A1 (en) 2010-09-30 2012-04-18 Almirall, S.A. Pyridine- and isoquinoline-derivatives as Syk and JAK kinase inhibitors
EP2457900A1 (en) 2010-11-25 2012-05-30 Almirall, S.A. New pyrazole derivatives having CRTh2 antagonistic behaviour
EP2463289A1 (en) 2010-11-26 2012-06-13 Almirall, S.A. Imidazo[1,2-b]pyridazine derivatives as JAK inhibitors
EP2489663A1 (en) 2011-02-16 2012-08-22 Almirall, S.A. Compounds as syk kinase inhibitors
EP2510928A1 (en) 2011-04-15 2012-10-17 Almirall, S.A. Aclidinium for use in improving the quality of sleep in respiratory patients
EP2518070A1 (en) 2011-04-29 2012-10-31 Almirall, S.A. Pyrrolotriazinone derivatives as PI3K inhibitors
EP2518071A1 (en) 2011-04-29 2012-10-31 Almirall, S.A. Imidazopyridine derivatives as PI3K inhibitors
EP2526945A1 (en) 2011-05-25 2012-11-28 Almirall, S.A. New CRTH2 Antagonists
EP2527344A1 (en) 2011-05-25 2012-11-28 Almirall, S.A. Pyridin-2(1H)-one derivatives useful as medicaments for the treatment of myeloproliferative disorders, transplant rejection, immune-mediated and inflammatory diseases
EP2548876A1 (en) 2011-07-18 2013-01-23 Almirall, S.A. New CRTh2 antagonists
EP2548863A1 (en) 2011-07-18 2013-01-23 Almirall, S.A. New CRTh2 antagonists.
EP2554544A1 (en) 2011-08-01 2013-02-06 Almirall, S.A. Pyridin-2(1h)-one derivatives as jak inhibitors
EP2578570A1 (en) 2011-10-07 2013-04-10 Almirall, S.A. Novel process for preparing 5-(2-{[6-(2,2-difluoro-2-phenylethoxy)hexyl]amino}-1(r)-hydroxyethyl)-8-hydroxyquinolin-2(1h)-one via novel intermediates of synthesis.
EP2592078A1 (en) 2011-11-11 2013-05-15 Almirall, S.A. New cyclohexylamine derivatives having beta2 adrenergic agonist and M3 muscarinic antagonist activities
EP2592077A1 (en) 2011-11-11 2013-05-15 Almirall, S.A. New cyclohexylamine derivatives having beta2 adrenergic agonist and M3 muscarinic antagonist activities
EP2641900A1 (en) 2012-03-20 2013-09-25 Almirall, S.A. Novel polymorphic Crystal forms of 5-(2-{[6-(2,2-difluoro-2-phenylethoxy) hexyl]amino}-1-(R)-hydroxyethyl)-8-hydroxyquinolin-2(1h)-one, heminapadisylate as agonist of the ß2 adrenergic receptor.
EP2647627A1 (en) 2012-04-02 2013-10-09 Almirall, S.A. Salts of 5-[(1r)-2-({2-[4-(2,2-difluoro-2-phenylethoxy)phenyl] ethyl}amino)-1-hydroxyethyl]-8-hydroxyquinolin-2(1h)-one.
EP2666465A1 (en) 2012-05-25 2013-11-27 Almirall, S.A. Novel dosage and formulation
EP2668941A1 (en) 2012-05-31 2013-12-04 Almirall, S.A. Novel dosage form and formulation of abediterol
WO2014060431A1 (en) 2012-10-16 2014-04-24 Almirall, S.A. Pyrrolotriazinone derivatives as pi3k inhibitors
EP2738172A1 (en) 2012-11-28 2014-06-04 Almirall, S.A. New bicyclic compounds as crac channel modulators
CN104869996A (zh) 2012-12-17 2015-08-26 阿尔米雷尔有限公司 阿地铵的新用途
EA201500651A1 (ru) 2012-12-18 2015-11-30 Альмираль, С.А. НОВЫЕ ПРОИЗВОДНЫЕ ЦИКЛОГЕКСИЛ- И ХИНУКЛИДИНИЛКАРБАМАТА, ОБЛАДАЮЩИЕ АГОНИСТИЧЕСКОЙ АКТИВНОСТЬЮ ПО ОТНОШЕНИЮ К β2 АДРЕНЕРГИЧЕСКОМУ РЕЦЕПТОРУ И АНТАГОНИСТИЧЕСКОЙ АКТИВНОСТЬЮ ПО ОТНОШЕНИЮ К МУСКАРИНОВОМУ РЕЦЕПТОРУ М3
AR094797A1 (es) 2013-02-15 2015-08-26 Almirall Sa Derivados de pirrolotriazina como inhibidores de pi3k
WO2014139150A1 (en) * 2013-03-15 2014-09-18 Merck Sharp & Dohme Corp. Substituted pyridizinone derivatives as pde10 inhibitors
EP2848615A1 (en) 2013-07-03 2015-03-18 Almirall, S.A. New pyrazole derivatives as CRAC channel modulators
LT3640241T (lt) 2013-10-18 2022-12-27 Celgene Quanticel Research, Inc. Bromodomeno inhibitoriai
JP2021527125A (ja) * 2018-06-07 2021-10-11 ディサーム・セラピューティクス・インコーポレイテッドDisarm Therapeutics, Inc. Sarm1阻害剤
KR102481635B1 (ko) * 2020-09-28 2022-12-26 서울대학교산학협력단 메타-치환된 니코틴 유도체의 신규 합성방법

Family Cites Families (24)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB1351569A (en) 1972-05-15 1974-05-01 Morishita Pharma 2-alkyl-4-alkoxy-5-morpholino-3-2h-pyridazinones and their method of preparation
DE2225218C2 (de) 1972-05-24 1983-01-13 Morishita Pharmaceutical Co., Ltd., Osaka 2-Alkyl-4-äthoxy-5-morpholino-3(2H)-pyridazinone und Verfahren zu deren Herstellung
HUT66969A (en) * 1991-10-09 1995-01-30 Syntex Inc Benzo- and pyrido-pyridazinone- and pyridazin-thion derivatives, pharmaceutical compositions containing the same and process for the production of thereof
US5679696A (en) * 1992-07-28 1997-10-21 Rhone-Poulenc Rorer Limited Compounds containing phenyl linked to aryl or heteroaryl by an aliphatic-or heteroatom-containing linking group
DE19533975A1 (de) * 1995-09-14 1997-03-20 Merck Patent Gmbh Arylalkyl-diazinone
DE19540475A1 (de) * 1995-10-20 1997-04-24 Schering Ag Chirale Methylphenyloxazolidinone
KR20000065219A (ko) * 1996-05-20 2000-11-06 마르크 젠너 티엔에프 저해제 및 피디이-4 저해제로서의 퀴놀린 카르복사미드
ES2137113B1 (es) 1997-07-29 2000-09-16 Almirall Prodesfarma Sa Nuevos derivados de triazolo-piridazinas heterociclicos.
US6162830A (en) * 1997-11-25 2000-12-19 Warner-Lambert Company Benzenesulfonamide inhibitors of PDE-IV and their therapeutic use
CZ300570B6 (cs) * 1998-10-27 2009-06-17 Abbott Laboratories Inhibitory biosyntézy prostaglandin endoperoxid H synthasy
AU764005B2 (en) * 1999-02-25 2003-08-07 Merck Frosst Canada & Co. PDE IV inhibiting compounds, compositions and methods of treatment
US6313156B1 (en) 1999-12-23 2001-11-06 Icos Corporation Thiazole compounds as cyclic-AMP-specific phosphodiesterase inhibitors
US6699890B2 (en) * 2000-12-22 2004-03-02 Memory Pharmaceuticals Corp. Phosphodiesterase 4 inhibitors
RU2340600C2 (ru) * 2001-10-16 2008-12-10 Мемори Фармасьютиклз Корпорейшн Производные 4-(4-алкокси-3-гидроксифенил)-2-пирролидона в качестве ингибиторов pde-4 для лечения неврологических синдромов
MY130622A (en) * 2001-11-05 2007-07-31 Novartis Ag Naphthyridine derivatives, their preparation and their use as phosphodiesterase isoenzyme 4 (pde4) inhibitors
US6972936B2 (en) * 2002-03-29 2005-12-06 Robert Allan Morris Pre-emptive circuit breaker with arc fault and fault lockout short circuit protection
ES2195785B1 (es) * 2002-05-16 2005-03-16 Almirall Prodesfarma, S.A. Nuevos derivados de piridazin-3(2h)-ona.
BR0315705A (pt) * 2002-11-19 2005-09-06 Memory Pharm Corp Inibidores de fosfodiesterase-4
ES2211344B1 (es) * 2002-12-26 2005-10-01 Almirall Prodesfarma, S.A. Nuevos derivados de piridazin-3(2h)-ona.
BRPI0409888A (pt) * 2003-04-18 2006-05-23 Memory Pharm Corp derivados de pirazol como inibidores de fosfodiesterase 4, composto, composição farmacêutica, método para efetuar a inibição da enzima pde4, incrementar a cognição e/ou tratar a psicose em um paciente, método para o tratamento de um paciente que tem uma doença que envolve nìveis de camp diminuìdos, método para o tratamento de um paciente que sofre de uma doença alérgica ou inflamatória e método para o tratamento de um paciente que sofre de neurodegeneração resultante de uma doença ou de um ferimento
ES2232306B1 (es) 2003-11-10 2006-08-01 Almirall Prodesfarma, S.A. Nuevos derivados de piridazin-3(2h)-ona.
ES2251866B1 (es) * 2004-06-18 2007-06-16 Laboratorios Almirall S.A. Nuevos derivados de piridazin-3(2h)-ona.
ES2251867B1 (es) * 2004-06-21 2007-06-16 Laboratorios Almirall S.A. Nuevos derivados de piridazin-3(2h)-ona.
ES2320954B1 (es) * 2007-03-02 2010-03-16 Laboratorio Almirall S.A. Nuevo procedimiento de preparacion de 3-metil-4-fenilisoxazolo (3,4-d)iridazin-7(6h)-ona.

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