EA200001009A1 - Производные пиридина, ингибирующие фосфодиэстеразу iv - Google Patents

Производные пиридина, ингибирующие фосфодиэстеразу iv

Info

Publication number
EA200001009A1
EA200001009A1 EA200001009A EA200001009A EA200001009A1 EA 200001009 A1 EA200001009 A1 EA 200001009A1 EA 200001009 A EA200001009 A EA 200001009A EA 200001009 A EA200001009 A EA 200001009A EA 200001009 A1 EA200001009 A1 EA 200001009A1
Authority
EA
Eurasian Patent Office
Prior art keywords
hydrogen
substituted
alkyl
calkyl
calkenyl
Prior art date
Application number
EA200001009A
Other languages
English (en)
Other versions
EA004207B1 (ru
Inventor
Эдди Жан Эдгар Фрейн
Гастон Станислас Марселла Дильс
Мария Энкарнасьон Матесанс-Бальестерос
Адольфо Диас-Мартинес
Original Assignee
Янссен Фармацевтика Н.В.
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 Янссен Фармацевтика Н.В. filed Critical Янссен Фармацевтика Н.В.
Publication of EA200001009A1 publication Critical patent/EA200001009A1/ru
Publication of EA004207B1 publication Critical patent/EA004207B1/ru

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • 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
    • C07D401/06Heterocyclic 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/4427Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
    • A61K31/4439Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. omeprazole
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00Drugs for disorders of the respiratory system
    • A61P11/06Antiasthmatics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P17/00Drugs for dermatological disorders
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00Drugs for immunological or allergic disorders
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00Drugs for immunological or allergic disorders
    • A61P37/08Antiallergic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D407/00Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00
    • C07D407/14Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00 containing three or more hetero rings

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Pulmonology (AREA)
  • Immunology (AREA)
  • Pain & Pain Management (AREA)
  • Rheumatology (AREA)
  • Dermatology (AREA)
  • Epidemiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Pyridine Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)

Abstract

Настоящее изобретение касается производных пиридина, имеющих формулу (I), их N-оксидных форм, фармацевтически приемлемых аддитивных солей и стереохимически изомерных форм, где L обозначает водород; Cалкил; Cалкилкарбонил; Cалкилоксикарбонил; замещенный Cалкил; Cалкенил; замещенный Cалкенил; пиперидил; замещенный пиперидил; Cалкилсульфонил или арилсульфонил; -A-B- обозначает -CR=CR- или-CHR-CHR-; D обозначает O или NR; Rобозначает водород или Cалкил; Rобозначает водород; галоген; Cалкил; трифторметил; Cциклоалкил; карбоксил; Cалкил оксикарбонил; Cциклоалкиламинокарбонил; арил; Het; или замещенный Cалкил; или Rобозначает -O-Rили -NH-R; Rобозначает водород; галоген; гидрокси; Cалкил или Cалкилокси; или Rи Rили Rи R, взятые вместе, могут образовывать двухвалентный радикал; Q обозначает дизамещенный пиридин; Rи R, каждый независимо, обозначает водород; Cалкил; дифторметил; трифторметил; Cциклоалкил; насыщенный 5-, 6- или 7-членный гетероцикл, содержащий один или два гетероатома, выбранных из кислорода, серы или азота; инданил; 6, 7-дигидро-5H-циклопентапиридил; бицикло [2.2.1] -2-гептенил; бицик-ло[2.2.1]гептанил; Cалкилсульфонил; арилсульфонил; или замещенный Cалкил; имеющих ингибирующую активность в отношении PDE IV и цитокина. Изобретение также относится к способам получения соединений формулы (I), их фармацевтическим композициям и их применению в качестве медикамента.Международная заявка была опубликована вместе с отчетом о международном поиске.
EA200001009A 1998-04-01 1999-03-24 Производные пиридина, ингибирующие фосфодиэстеразу iv EA004207B1 (ru)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
EP98201020 1998-04-01
PCT/EP1999/002045 WO1999050262A1 (en) 1998-04-01 1999-03-24 Pde iv inhibiting pyridine derivatives

Publications (2)

Publication Number Publication Date
EA200001009A1 true EA200001009A1 (ru) 2001-02-26
EA004207B1 EA004207B1 (ru) 2004-02-26

Family

ID=8233543

Family Applications (1)

Application Number Title Priority Date Filing Date
EA200001009A EA004207B1 (ru) 1998-04-01 1999-03-24 Производные пиридина, ингибирующие фосфодиэстеразу iv

Country Status (34)

Country Link
US (1) US6656959B1 (ru)
EP (1) EP1068194B1 (ru)
JP (1) JP4778612B2 (ru)
KR (1) KR100596664B1 (ru)
CN (1) CN1172930C (ru)
AR (1) AR014972A1 (ru)
AT (1) ATE253569T1 (ru)
AU (1) AU760771B2 (ru)
BG (1) BG64705B1 (ru)
BR (1) BR9909326A (ru)
CA (1) CA2326045C (ru)
CZ (1) CZ298747B6 (ru)
DE (1) DE69912590T2 (ru)
DK (1) DK1068194T3 (ru)
EA (1) EA004207B1 (ru)
EE (1) EE04718B1 (ru)
ES (1) ES2211061T3 (ru)
HK (1) HK1033579A1 (ru)
HR (1) HRP20000619B1 (ru)
HU (1) HU229412B1 (ru)
ID (1) ID27207A (ru)
IL (2) IL138745A0 (ru)
MY (1) MY124696A (ru)
NO (1) NO319531B1 (ru)
NZ (1) NZ507022A (ru)
PL (1) PL196026B1 (ru)
PT (1) PT1068194E (ru)
SI (1) SI1068194T1 (ru)
SK (1) SK284468B6 (ru)
TR (1) TR200002801T2 (ru)
TW (1) TWI242558B (ru)
UA (1) UA66842C2 (ru)
WO (1) WO1999050262A1 (ru)
ZA (1) ZA200006190B (ru)

Families Citing this family (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6639077B2 (en) 2000-03-23 2003-10-28 Merck Frosst Canada & Co. Tri-aryl-substituted-ethane PDE4 inhibitors
MY123585A (en) 2000-03-23 2006-05-31 Merck Canada Inc Tri-aryl-substituted-ethane pde4 inhibitors.
DE10130397A1 (de) * 2001-06-23 2003-01-09 Bayer Cropscience Gmbh Herbizide substituierte Pyridine, Verfahren zu ihrer Herstellung und ihre Verwendung als Herbzide und Pflanzenwachstumsregulatoren
DE10318610A1 (de) * 2003-04-24 2004-11-11 Elbion Ag 7-Azaindole und deren Verwendung als Therapeutika
CA2564994A1 (en) 2004-04-30 2005-11-10 Warner-Lambert Company Llc Substituted morpholine compounds for the treatment of central nervous system disorders
US7863446B2 (en) 2006-01-19 2011-01-04 Orchid Research Laboratories Limited Heterocycles
JP2009525269A (ja) 2006-01-30 2009-07-09 ユーロ−セルティーク エス.エイ. カルシウムチャネルブロッカーとしての環状尿素化合物
ES2357340T3 (es) 2006-10-18 2011-04-25 Pfizer Products Inc. Compuestos de biaril éter urea.
RU2572616C2 (ru) 2008-02-01 2016-01-20 Оркид Рисерч Лабораториз Лимитед Новые гетероциклы
JOP20190060A1 (ar) 2016-09-26 2019-03-26 Chugai Pharmaceutical Co Ltd مشتق بيرازولو بيريدين له تأثير مساعد لمستقبل glp-1

Family Cites Families (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3876657A (en) * 1971-06-03 1975-04-08 Ashland Oil Inc Preparation of 1-substituted-2-imidazolidinones
US4600430A (en) 1985-02-22 1986-07-15 Eli Lilly And Company Pyridinylimidazolidinone compounds
ZA945609B (en) 1993-07-28 1995-05-12 Rhone Poulenc Rorer Ltd [Di(ether or thioether)heteroaryl or fluoro substituted aryl] compounds
GB9401460D0 (en) * 1994-01-26 1994-03-23 Rhone Poulenc Rorer Ltd Compositions of matter
WO1996004186A1 (en) * 1994-08-03 1996-02-15 Gics & Vermee, L.P. Ovenable food package
TW332201B (en) * 1995-04-06 1998-05-21 Janssen Pharmaceutica Nv 1,3-Dihydro-1-(phenylalkyl)-2H-imidazol-2-one derivatives
TW375612B (en) 1995-04-06 1999-12-01 Janssen Pharmaceutica Nv 1,3-dihydro-2H-imidazol-2-one derivatives for the treatment of disease states related to an abnormal enzymatic or catalytic activity of phosphodiesterase type IV, preparation thereof and pharmaceutical composition containing the same
TW424087B (en) * 1995-04-06 2001-03-01 Janssen Pharmaceutica Nv 1,3-dihydro-1-(phenylalkenyl)-2H-imidazol-2-one derivatives
WO1997003967A1 (en) * 1995-07-22 1997-02-06 Rhone-Poulenc Rorer Limited Substituted aromatic compounds and their pharmaceutical use
WO1997024122A1 (en) * 1995-12-29 1997-07-10 Smithkline Beecham Corporation Vitronectin receptor antagonists
SI0934280T1 (en) 1996-10-02 2003-12-31 Janssen Pharmaceutica N.V. Pde iv inhibiting 2-cyanoiminoimidazole derivatives

Also Published As

Publication number Publication date
HRP20000619A2 (en) 2001-10-31
EE200000569A (et) 2002-04-15
EE04718B1 (et) 2006-10-16
SI1068194T1 (en) 2004-04-30
HK1033579A1 (en) 2001-09-07
EA004207B1 (ru) 2004-02-26
KR20010040681A (ko) 2001-05-15
HUP0101239A3 (en) 2002-09-30
NO319531B1 (no) 2005-08-29
NZ507022A (en) 2002-06-28
CZ20003338A3 (cs) 2001-02-14
HU229412B1 (en) 2013-12-30
CA2326045C (en) 2008-12-09
JP4778612B2 (ja) 2011-09-21
AU3147499A (en) 1999-10-18
PL343194A1 (en) 2001-07-30
PL196026B1 (pl) 2007-11-30
EP1068194B1 (en) 2003-11-05
US6656959B1 (en) 2003-12-02
TWI242558B (en) 2005-11-01
KR100596664B1 (ko) 2006-07-06
JP2002509927A (ja) 2002-04-02
DE69912590D1 (de) 2003-12-11
CN1172930C (zh) 2004-10-27
HRP20000619B1 (en) 2004-06-30
ES2211061T3 (es) 2004-07-01
NO20004906L (no) 2000-11-28
NO20004906D0 (no) 2000-09-29
ATE253569T1 (de) 2003-11-15
TR200002801T2 (tr) 2000-12-21
SK13872000A3 (sk) 2001-11-06
CZ298747B6 (cs) 2008-01-16
WO1999050262A1 (en) 1999-10-07
DE69912590T2 (de) 2004-09-16
HUP0101239A2 (hu) 2002-05-29
BR9909326A (pt) 2000-12-12
MY124696A (en) 2006-06-30
IL138745A0 (en) 2001-10-31
BG64705B1 (bg) 2005-12-30
EP1068194A1 (en) 2001-01-17
IL138745A (en) 2007-06-17
CN1295571A (zh) 2001-05-16
UA66842C2 (ru) 2004-06-15
PT1068194E (pt) 2004-03-31
ZA200006190B (en) 2001-10-31
DK1068194T3 (da) 2004-03-15
AU760771B2 (en) 2003-05-22
CA2326045A1 (en) 1999-10-07
AR014972A1 (es) 2001-04-11
ID27207A (id) 2001-03-08
BG104718A (en) 2001-04-30
SK284468B6 (sk) 2005-04-01

Similar Documents

Publication Publication Date Title
NO986055D0 (no) Nye heterocykliske forbindelser, deres fremstilling, farmas÷ytiske preparat
NO883587D0 (no) Fremgangsmaate for fremstilling av terapeutisk aktive indolderivater.
TR200100300T2 (tr) Sitokinlerin üretiminde engelleyici olarak kullanışlı amid türevleri
DE69633607D1 (de) Piperidinderivate mit tachykinin-antagonistischer wirkung
RU2004122481A (ru) Производные альфа-(n-сульфонамидо)ацетамида как ингибиторы бета-амилоида
MY116980A (en) Pde iv inhibiting 2-cyanoiminoimidazole derivatives
AR039566A1 (es) Inhibidores de la histona deacetilasa, composicion farmaceutica que los contiene y sus procesos de preparacion
DK0620216T3 (da) Benzamidderivater og deres anvendelse som vasopressinantagonister
NO20062905L (no) Nye hydroksaminsyreestere og farmasoytisk anvendelse derav
DE60103133D1 (de) Imidazol-2-carbonsäureamid derivate als raf kinase inhibitoren
NO884202D0 (no) Fremgangsmaate for fremstilling av terapeutisk aktive benzimidazolin-2-okso-1-karboksylsyrederivater.
MY101208A (en) Phenyl-piperazine anti-arrhythmia agents.
MY119254A (en) 1, 3-dihydro-1-(phenylalkyl)-2h-imidazol-2-one derivatives
HUT62264A (en) Process for producing amidino compounds and pharmaceutical compositions comprising same as active ingredient
DE69431069D1 (de) Cyclische amidderivate als neurokinin a antagonisten
EA200001009A1 (ru) Производные пиридина, ингибирующие фосфодиэстеразу iv
AR003412A1 (es) Derivados de 1,3-dihidro-1-(fenilalquenil)-2h-imidazol-2-ona, procedimiento para su preparacion, composicion que los comprenden, procedimiento para obtenerdicha composicion y uso de dichos compuestos para preparar medicamentos.
MY117936A (en) 1,3-dihydro-2h-imidazol-2-one derivatives
NO932382L (no) Heterocykliske forbindelser
AR013889A1 (es) Nuevos derivados del acido 4-(1-piperazinil)-benzoico, procedimiento para obtenerlos y composiciones farmaceuticas que lo contienen.
FI894125A (fi) Analogiamenetelmä terapeuttisesti käyttökelpoisen 3-piperidinyyli-indatsolin valmistamiseksi

Legal Events

Date Code Title Description
MM4A Lapse of a eurasian patent due to non-payment of renewal fees within the time limit in the following designated state(s)

Designated state(s): AM AZ BY KZ KG MD TJ TM

MK4A Patent expired

Designated state(s): RU