ATE296630T1 - Substituierte 8-arylchinoline als pde4-hemmer - Google Patents

Substituierte 8-arylchinoline als pde4-hemmer

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Publication number
ATE296630T1
ATE296630T1 AT02742600T AT02742600T ATE296630T1 AT E296630 T1 ATE296630 T1 AT E296630T1 AT 02742600 T AT02742600 T AT 02742600T AT 02742600 T AT02742600 T AT 02742600T AT E296630 T1 ATE296630 T1 AT E296630T1
Authority
AT
Austria
Prior art keywords
sup
pde4 inhibitors
arylcinolines
substituted
arthritis
Prior art date
Application number
AT02742600T
Other languages
English (en)
Inventor
Daniel Dube
Yves Girard
Dwight Macdonald
Anthony Mastracchio
Michel Gallant
Patrick Lacombe
Denis Deschenes
Original Assignee
Merck Frosst Canada Inc
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Merck Frosst Canada Inc filed Critical Merck Frosst Canada Inc
Application granted granted Critical
Publication of ATE296630T1 publication Critical patent/ATE296630T1/de

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    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic 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
    • C07D401/02Heterocyclic 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
    • C07D401/08Heterocyclic 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 alicyclic rings
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    • A61P1/00Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/04Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
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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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D215/00Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
    • C07D215/02Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom
    • C07D215/12Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom with substituted hydrocarbon radicals attached to ring carbon atoms
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    • C07D215/12Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom with substituted hydrocarbon radicals attached to ring carbon atoms
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    • C07F9/00Compounds containing elements of Groups 5 or 15 of the Periodic Table
    • C07F9/02Phosphorus compounds
    • C07F9/547Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
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    • C07F9/02Phosphorus compounds
    • C07F9/547Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
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    • C07F9/657181Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having phosphorus atoms, with or without nitrogen, oxygen, sulfur, selenium or tellurium atoms, as ring hetero atoms having phosphorus and oxygen atoms as the only ring hetero atoms the ring phosphorus atom being bound to at least one carbon atom the ring phosphorus atom and, at least, one ring oxygen atom being part of a (thio)phosphonic acid derivative

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AT02742600T 2001-06-27 2002-06-26 Substituierte 8-arylchinoline als pde4-hemmer ATE296630T1 (de)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US30122001P 2001-06-27 2001-06-27
US30347201P 2001-07-06 2001-07-06
PCT/CA2002/000953 WO2003002118A1 (en) 2001-06-27 2002-06-26 Substituted 8-arylquinoline pde4 inhibitors

Publications (1)

Publication Number Publication Date
ATE296630T1 true ATE296630T1 (de) 2005-06-15

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Application Number Title Priority Date Filing Date
AT02742600T ATE296630T1 (de) 2001-06-27 2002-06-26 Substituierte 8-arylchinoline als pde4-hemmer

Country Status (9)

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US (1) US6919353B2 (de)
EP (1) EP1404330B1 (de)
JP (1) JP2005501822A (de)
AT (1) ATE296630T1 (de)
AU (1) AU2002344885C1 (de)
CA (1) CA2450686A1 (de)
DE (1) DE60204463T2 (de)
ES (1) ES2242036T3 (de)
WO (1) WO2003002118A1 (de)

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EP1487797B1 (de) * 2002-03-18 2009-05-27 Merck Frosst Canada Ltd. Pde4-inhibitoren mit heterobrückensubstituiertem 8-arylchinolin
WO2004026794A2 (en) * 2002-09-17 2004-04-01 Merck & Co., Inc. Removal of aldehyde impurity by reactive polystyrene resin
CA2523336A1 (en) * 2003-04-30 2004-11-11 Merck Frosst Canada Ltd. 8-(3-biaryl)phenylquinoline phosphodiesterase-4-inhibitors
WO2005091752A2 (en) * 2004-03-25 2005-10-06 Synta Pharmaceuticals Corp. Acrylonitrile derivatives for inflammation and immune-related uses
CN100425591C (zh) * 2005-09-26 2008-10-15 山东大学 含有磺酰基二苯基乙烯桥化合物及其制法和药物应用
JP2009514969A (ja) 2005-11-09 2009-04-09 コンビナトアールエックス インコーポレーティッド 医学的状態を治療するための方法、組成物、およびキット
ES2443342T3 (es) * 2006-07-05 2014-02-19 Takeda Gmbh Combinación de inhibidor de la HMG-CoA reductasa rosuvastatina con un inhibidor de la fosfodiesterasa 4, tal como roflumilast, roflumilast-N-óxido para el tratamiento de enfermedades pulmonares inflamatorias
CN101910159B (zh) * 2007-12-26 2013-06-19 卫材R&D管理有限公司 杂环取代吡啶衍生物的制备方法
CA2796826A1 (en) 2010-05-10 2011-11-17 Gilead Sciences, Inc. Bifunctional quinoline derivatives
UY33373A (es) 2010-05-10 2011-12-30 Gilead Sciences Inc ?Compuestos de pirazolopiridina bifuncionales, su uso en terapia y composiciones que los comprenden?.
ITMI20110362A1 (it) * 2011-03-09 2012-09-10 F I S Fabbrica Italiana Sint P A Procedimento per la preparazione di 1-(6-metilpiridin-3-il)-2-[4-(metilsolfonil)fenil]etanone, un intermedio dell'etoricoxib.
ITMI20120394A1 (it) * 2012-03-14 2013-09-15 Zach System Spa Processo di sintesi di un chetosolfone derivato
ITVI20130014A1 (it) * 2013-01-22 2014-07-23 Italiana Sint Spa Procedimento molto efficiente per preparare un intermedio di etoricoxib
BR112015019276A2 (pt) 2013-02-19 2017-07-18 Pfizer compostos de azabenzimidazol como inibidores de isoenzimas de pde4 para o tratamento de distúrbios do snc e outros distúrbios
WO2016012896A1 (en) 2014-07-24 2016-01-28 Pfizer Inc. Pyrazolopyrimidine compounds
MD20170011A2 (ro) 2014-08-06 2017-08-31 Pfizer Inc. Compuşi imidazopiridazinici
CA3053734A1 (en) * 2017-02-26 2018-08-30 Oat Agrio Co., Ltd. Thiazole compounds and herbicide
CN119504834B (zh) * 2024-11-21 2025-10-17 南开大学 一种以含硅基团为疏水标签的pd-l1蛋白降解剂及其制备方法、药物组合物和应用

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* Cited by examiner, † Cited by third party
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US5455252A (en) * 1993-03-31 1995-10-03 Syntex (U.S.A.) Inc. Optionally substituted 6,8-quinolines
MY134008A (en) * 1999-12-22 2007-11-30 Merck Frosst Canada Inc Subtituted 8-arylquinoline phospohodiestrase-4 inhibitors

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DE60204463T2 (de) 2006-05-18
US6919353B2 (en) 2005-07-19
JP2005501822A (ja) 2005-01-20
US20040162314A1 (en) 2004-08-19
EP1404330A1 (de) 2004-04-07
AU2002344885C1 (en) 2006-11-09
AU2002344885B2 (en) 2006-06-29
WO2003002118A1 (en) 2003-01-09
CA2450686A1 (en) 2003-01-09
ES2242036T3 (es) 2005-11-01
EP1404330B1 (de) 2005-06-01

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