EA200400545A1 - Новые замещенные 4-фенил-4-[1h-имидазол-2-ил] пиперидиновые производные и их применение в качестве селективных непептидных агонистов дельта-опиоидов - Google Patents

Новые замещенные 4-фенил-4-[1h-имидазол-2-ил] пиперидиновые производные и их применение в качестве селективных непептидных агонистов дельта-опиоидов

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Publication number
EA200400545A1
EA200400545A1 EA200400545A EA200400545A EA200400545A1 EA 200400545 A1 EA200400545 A1 EA 200400545A1 EA 200400545 A EA200400545 A EA 200400545A EA 200400545 A EA200400545 A EA 200400545A EA 200400545 A1 EA200400545 A1 EA 200400545A1
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EA
Eurasian Patent Office
Prior art keywords
imidazol
phenyl
agonists
selective
nepeptida
Prior art date
Application number
EA200400545A
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English (en)
Other versions
EA006507B1 (ru
Inventor
Франс Эдуард Янссенс
Йозеф Элизабет Ленартс
Франсиско Хавьер Фернандес-Гадеа
Антонио Гомес-Санчес
Тео Франс Мерт
Original Assignee
Янссен Фармацевтика Н.В.
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Application filed by Янссен Фармацевтика Н.В. filed Critical Янссен Фармацевтика Н.В.
Publication of EA200400545A1 publication Critical patent/EA200400545A1/ru
Publication of EA006507B1 publication Critical patent/EA006507B1/ru

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    • C07ORGANIC CHEMISTRY
    • 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
    • C07D401/04Heterocyclic 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 directly linked by a ring-member-to-ring-member bond
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00Drugs for disorders of the alimentary tract or the digestive system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00Drugs for disorders of the alimentary tract or the digestive system
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    • AHUMAN NECESSITIES
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    • A61P1/00Drugs for disorders of the alimentary tract or the digestive system
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    • A61P13/00Drugs for disorders of the urinary system
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    • A61P25/00Drugs for disorders of the nervous system
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    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
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Abstract

Настоящее изобретение относится к новым 4-фенил-4-[1H-имидазол-2-ил]пиперидиновым производным формулы (I)их фармацевтически приемлемым солям присоединения кислот или оснований, их стереохимически изомерным формам, их таутомерным формам и их N-оксидам. В частности, заявлены соединения формулы (I), где A=B представляет собой C=O или SO, X представляет собой ковалентную связь, Rпредставляет собой алкилокси, алкилоксиалкил, Ar или NRR, где Rи R, каждый независимо, представляют собой водород или Ar; или A=B и Rвместе образуют радикал бензоксазолил; p равен нулю, Rпредставляет собой бензил, необязательно замещенный гидрокси, алкилом или алкилоксикарбонилом, и каждый из Rи Rпредставляет собой водород. Изобретение также относится к способам получения соединений по изобретению и их применению в медицине, в частности, в качестве селективных непептидных агонистов d-опиоидов, для применения при лечении различных болей.Международная заявка была опубликована вместе с отчетом о международном поиске.
EA200400545A 2001-10-15 2002-10-10 Новые замещенные 4-фенил-4-[1h-имидазол-2-ил] пиперидиновые производные и их применение в качестве селективных непептидных агонистов дельта-опиоидов EA006507B1 (ru)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
EP01203926 2001-10-15
PCT/EP2002/011372 WO2003033486A1 (en) 2001-10-15 2002-10-10 Novel substituted 4-phenyl-4-[1h-imidazol-2-yl]-piperidine derivatives and their use as selective non-peptide delta opioid agonists

Publications (2)

Publication Number Publication Date
EA200400545A1 true EA200400545A1 (ru) 2004-08-26
EA006507B1 EA006507B1 (ru) 2005-12-29

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ID=8181080

Family Applications (1)

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EA200400545A EA006507B1 (ru) 2001-10-15 2002-10-10 Новые замещенные 4-фенил-4-[1h-имидазол-2-ил] пиперидиновые производные и их применение в качестве селективных непептидных агонистов дельта-опиоидов

Country Status (26)

Country Link
US (2) US7282508B2 (ru)
EP (1) EP1438304B1 (ru)
JP (1) JP4417108B2 (ru)
KR (1) KR100898562B1 (ru)
CN (1) CN100354273C (ru)
AR (1) AR037506A1 (ru)
AT (1) ATE347549T1 (ru)
AU (1) AU2002346994B2 (ru)
BR (1) BR0213327A (ru)
CA (1) CA2462953C (ru)
CY (1) CY1106356T1 (ru)
DE (1) DE60216627T2 (ru)
EA (1) EA006507B1 (ru)
ES (1) ES2278065T3 (ru)
HR (1) HRP20040324A2 (ru)
HU (1) HUP0600447A3 (ru)
IL (2) IL161348A0 (ru)
MX (1) MXPA04003479A (ru)
MY (1) MY137356A (ru)
NO (1) NO327602B1 (ru)
NZ (1) NZ531679A (ru)
PL (1) PL367967A1 (ru)
PT (1) PT1438304E (ru)
UA (1) UA76224C2 (ru)
WO (1) WO2003033486A1 (ru)
ZA (1) ZA200402818B (ru)

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TW200403058A (en) * 2002-04-19 2004-03-01 Bristol Myers Squibb Co Heterocyclo inhibitors of potassium channel function
CA2484936A1 (en) * 2002-05-08 2004-05-21 Neurogen Corporation Substituted imidazolylmethyl pyridine and pyrazine derivatives and their use as gabaa receptor ligands
DE60330794D1 (de) * 2002-07-03 2010-02-11 Glaxo Group Ltd Substituierte 4-phenylpiperidinamide als tachykininantagonisten und serotoninwiederaufnahmehemmer
CL2004000754A1 (es) * 2003-04-11 2005-02-25 Janssen Pharmaceutica Nv Uso de compuestos derivados de 4-fenil-4-(1h-imidazol-2-il)piperidina, como agonistas delta-opioides no peptidicos, para preparar un medicamento util en prevenir o tratar trastornos del sistema nervioso central.
NZ546834A (en) 2003-10-01 2010-03-26 Adolor Corp Spirocyclic heterocyclic derivatives and methods of their use
SI2653465T1 (sl) 2004-03-15 2016-10-28 Janssen Pharmaceutica N.V. Modulatorji opiodnih receptorjev
AU2013205089B2 (en) * 2004-03-15 2013-12-19 Janssen Pharmaceutica, N.V. Novel compounds as opioid receptor modulators
US7598261B2 (en) 2005-03-31 2009-10-06 Adolor Corporation Spirocyclic heterocyclic derivatives and methods of their use
US7576207B2 (en) 2006-04-06 2009-08-18 Adolor Corporation Spirocyclic heterocyclic derivatives and methods of their use
JP2010503669A (ja) 2006-09-12 2010-02-04 アドラー コーポレーション 認知機能の強化のためのn含有スピロ化合物の使用
IT1396951B1 (it) * 2009-12-18 2012-12-20 Neuroscienze Pharmaness S C A R L Composti farmaceutici
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TWI652264B (zh) * 2013-09-26 2019-03-01 東麗股份有限公司 Cyclic amine derivatives and their medical uses
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Also Published As

Publication number Publication date
ATE347549T1 (de) 2006-12-15
EA006507B1 (ru) 2005-12-29
HUP0600447A3 (en) 2008-03-28
ES2278065T3 (es) 2007-08-01
JP4417108B2 (ja) 2010-02-17
KR100898562B1 (ko) 2009-05-20
EP1438304B1 (en) 2006-12-06
NZ531679A (en) 2005-02-25
HUP0600447A2 (en) 2006-09-28
IL161348A0 (en) 2004-09-27
US20080096925A1 (en) 2008-04-24
PT1438304E (pt) 2007-03-30
UA76224C2 (en) 2006-07-17
NO20041666L (no) 2004-04-22
DE60216627D1 (de) 2007-01-18
EP1438304A1 (en) 2004-07-21
AU2002346994B2 (en) 2007-09-06
US20040260096A1 (en) 2004-12-23
KR20050035121A (ko) 2005-04-15
MY137356A (en) 2009-01-30
IL161348A (en) 2010-11-30
CN100354273C (zh) 2007-12-12
ZA200402818B (en) 2005-06-29
WO2003033486A1 (en) 2003-04-24
JP2005505625A (ja) 2005-02-24
CA2462953C (en) 2011-01-04
NO327602B1 (no) 2009-08-31
HRP20040324A2 (en) 2005-04-30
PL367967A1 (en) 2005-03-07
MXPA04003479A (es) 2004-07-30
AR037506A1 (es) 2004-11-17
US7282508B2 (en) 2007-10-16
CN1568321A (zh) 2005-01-19
CY1106356T1 (el) 2011-10-12
CA2462953A1 (en) 2003-04-24
BR0213327A (pt) 2004-10-13
DE60216627T2 (de) 2007-09-20

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