CA2165133A1 - Substituted 1h-imidazoles - Google Patents

Substituted 1h-imidazoles

Info

Publication number
CA2165133A1
CA2165133A1 CA002165133A CA2165133A CA2165133A1 CA 2165133 A1 CA2165133 A1 CA 2165133A1 CA 002165133 A CA002165133 A CA 002165133A CA 2165133 A CA2165133 A CA 2165133A CA 2165133 A1 CA2165133 A1 CA 2165133A1
Authority
CA
Canada
Prior art keywords
imidazole
tetrahydro
compound
naphthalenyl
imidazol
Prior art date
Legal status (The legal status 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 status listed.)
Abandoned
Application number
CA002165133A
Other languages
English (en)
French (fr)
Inventor
Jean-Pierre Geerts
Genevieve Motte
Edmond Differding
Jean-Pierre Henichart
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
UCB SA
Original Assignee
UCB SA
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 UCB SA filed Critical UCB SA
Publication of CA2165133A1 publication Critical patent/CA2165133A1/en
Abandoned legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
    • C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
    • C07D233/56—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, attached to ring carbon atoms
    • C07D233/58—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, attached to ring carbon atoms with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, attached to ring nitrogen atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
    • C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
    • C07D233/64—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with substituted hydrocarbon radicals attached to ring carbon atoms, e.g. histidine
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system
    • A61P9/10—Drugs 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
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system
    • A61P9/12—Antihypertensives

Landscapes

  • Organic Chemistry (AREA)
  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Public Health (AREA)
  • General Chemical & Material Sciences (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Medicinal Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Animal Behavior & Ethology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • General Health & Medical Sciences (AREA)
  • Cardiology (AREA)
  • Veterinary Medicine (AREA)
  • Urology & Nephrology (AREA)
  • Vascular Medicine (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
CA002165133A 1994-12-14 1995-12-13 Substituted 1h-imidazoles Abandoned CA2165133A1 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
GBGB9425211.1A GB9425211D0 (en) 1994-12-14 1994-12-14 Substituted 1H-imidazoles
GB9425211.1 1994-12-14

Publications (1)

Publication Number Publication Date
CA2165133A1 true CA2165133A1 (en) 1996-06-15

Family

ID=10765918

Family Applications (1)

Application Number Title Priority Date Filing Date
CA002165133A Abandoned CA2165133A1 (en) 1994-12-14 1995-12-13 Substituted 1h-imidazoles

Country Status (26)

Country Link
US (1) US5658938A (cg-RX-API-DMAC10.html)
EP (1) EP0717037A1 (cg-RX-API-DMAC10.html)
JP (1) JPH08208622A (cg-RX-API-DMAC10.html)
KR (1) KR960022474A (cg-RX-API-DMAC10.html)
CN (1) CN1054376C (cg-RX-API-DMAC10.html)
AR (1) AR002257A1 (cg-RX-API-DMAC10.html)
AU (1) AU693614B2 (cg-RX-API-DMAC10.html)
BG (1) BG63043B1 (cg-RX-API-DMAC10.html)
BR (1) BR9505815A (cg-RX-API-DMAC10.html)
CA (1) CA2165133A1 (cg-RX-API-DMAC10.html)
CZ (1) CZ327195A3 (cg-RX-API-DMAC10.html)
EE (1) EE9500064A (cg-RX-API-DMAC10.html)
FI (1) FI955927L (cg-RX-API-DMAC10.html)
GB (1) GB9425211D0 (cg-RX-API-DMAC10.html)
HU (1) HUT73980A (cg-RX-API-DMAC10.html)
IL (1) IL116325A (cg-RX-API-DMAC10.html)
IS (1) IS4311A (cg-RX-API-DMAC10.html)
MX (1) MX9505063A (cg-RX-API-DMAC10.html)
NO (1) NO305316B1 (cg-RX-API-DMAC10.html)
NZ (1) NZ280646A (cg-RX-API-DMAC10.html)
PL (1) PL311736A1 (cg-RX-API-DMAC10.html)
RO (1) RO113346B1 (cg-RX-API-DMAC10.html)
RU (1) RU2156239C2 (cg-RX-API-DMAC10.html)
SK (1) SK155095A3 (cg-RX-API-DMAC10.html)
TW (1) TW303362B (cg-RX-API-DMAC10.html)
ZA (1) ZA9510554B (cg-RX-API-DMAC10.html)

Families Citing this family (51)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB9425211D0 (en) * 1994-12-14 1995-02-15 Ucb Sa Substituted 1H-imidazoles
GB9520150D0 (en) 1995-10-03 1995-12-06 Orion Yhtymae Oy New imidazole derivatives
ZA981080B (en) * 1997-02-11 1998-08-12 Warner Lambert Co Bicyclic inhibitors of protein farnesyl transferase
US20030073850A1 (en) * 1998-08-07 2003-04-17 Altenbach Robert J. 4-Imidazole derivatives of benzyl and restricted benzyl sulfonamides, sulfamides, ureas, carbamates, and amides and their use
US6503935B1 (en) * 1998-08-07 2003-01-07 Abbott Laboratories Imidazoles and related compounds as α1A agonists
US6388090B2 (en) 2000-01-14 2002-05-14 Orion Corporation Imidazole derivatives
PT1280779E (pt) 2000-05-08 2005-11-30 Orion Corp Novos indanilimidazois policiclicos com actividade adrenergica alfa2
TW200930291A (en) * 2002-04-29 2009-07-16 Bayer Cropscience Ag Pesticidal heterocycles
US20040266776A1 (en) * 2003-06-25 2004-12-30 Gil Daniel W. Methods of preventing and reducing the severity of stress-associated conditions
FI20022007A0 (fi) * 2002-11-08 2002-11-08 Juvantia Pharma Ltd Oy Oromukosaalinen valmiste ja menetelmä sen valmistamiseksi
FI20022159A0 (fi) * 2002-12-05 2002-12-05 Orion Corp Uusia farmaseuttisia yhdisteitä
AU2007209382A1 (en) * 2006-01-27 2007-08-02 F. Hoffmann-La Roche Ag Use of 2-imidazoles for the treatment of CNS disorders
CN101528709B (zh) * 2006-10-19 2012-02-01 弗·哈夫曼-拉罗切有限公司 对痕量胺相关受体有亲和性的氨基甲基-2-咪唑类
CA2666762C (en) * 2006-10-19 2014-12-30 F. Hoffmann-La Roche Ag Aminomethyl-4-imidazoles
AU2007316257A1 (en) * 2006-11-02 2008-05-08 F. Hoffmann-La Roche Ag Substituted 2-imidazoles as modulators of the trace amine associated receptors
WO2008058867A2 (en) * 2006-11-16 2008-05-22 F. Hoffmann-La Roche Ag Substituted 4-imidazoles
CA2672617A1 (en) * 2006-12-13 2008-06-19 F. Hoffmann-La Roche Ag Novel 2-imidazoles as ligands for trace amine associated receptors (taar)
US20080146523A1 (en) 2006-12-18 2008-06-19 Guido Galley Imidazole derivatives
WO2008092785A1 (en) * 2007-02-02 2008-08-07 F. Hoffmann-La Roche Ag Novel 2-aminooxazolines as taar1 ligands for cns disorders
CA2678072A1 (en) * 2007-02-13 2008-08-21 Schering Corporation Functionally selective alpha2c adrenoreceptor agonists
CL2008000429A1 (es) * 2007-02-13 2008-08-18 Schering Corp Compuestos derivados de heterociclos condensados; composicion farmaceutica que comprende a dichos compuestos; y su uso para tratar afecciones asociadas con los receptores alfa2c adrenergicos, tales como congestion asociada a rinitis, polipos, resfrio
WO2008100456A2 (en) * 2007-02-13 2008-08-21 Schering Corporation Functionally selective alpha2c adrenoreceptor agonists
KR101222412B1 (ko) * 2007-02-15 2013-01-15 에프. 호프만-라 로슈 아게 Ｔａａｒ1 리간드로서의 2-아미노옥사졸린
WO2009003868A2 (en) 2007-07-02 2009-01-08 F. Hoffmann-La Roche Ag 2 -imidazolines having a good affinity to the trace amine associated receptors (taars)
JP2010531836A (ja) * 2007-07-03 2010-09-30 エフ．ホフマン−ラ ロシュ アーゲー ４−イミダゾリン及びそれらの抗うつ剤としての使用
CA2694362A1 (en) * 2007-07-27 2009-02-05 F. Hoffmann-La Roche Ag 2-azetidinemethaneamines and 2-pyrrolidinemethaneamines as taar-ligands
BRPI0815038A2 (pt) * 2007-08-02 2015-03-17 Hoffmann La Roche Uso de derivados de benzamida para o tratamento de transtornos do cns
KR101167773B1 (ko) * 2007-08-03 2012-07-24 에프. 호프만-라 로슈 아게 Ｔａａｒ１ 리간드로서의 피리딘카복스아마이드 및 벤즈아마이드 유도체
CL2008003553A1 (es) * 2007-12-05 2009-11-27 Grindeks Jsc Proceso para preparar atipamezol o clorhidrato de 5-(2-etil-2,3-dihidro-1h-inden-2-il)-1h-imidazol: y loa compuestos intermediarios considerados en el proceso
EP2257546B1 (en) 2008-02-21 2012-08-15 Merck Sharp & Dohme Corp. Functionally selective alpha2c adrenoreceptor agonists
CN102083805A (zh) * 2008-07-24 2011-06-01 弗·哈夫曼-拉罗切有限公司 4,5-二氢-唑-2-基衍生物
US8242153B2 (en) * 2008-07-24 2012-08-14 Hoffmann-La Roche Inc. 4,5-dihydro-oxazol-2YL derivatives
WO2010017120A1 (en) * 2008-08-04 2010-02-11 Schering Corporation Cyclopropylchromene derivatives as modulators of the alpha-2c receptor
TW201026691A (en) 2008-10-07 2010-07-16 Schering Corp Biaryl spiroaminooxazoline analogues as alpha2C adrenergic receptor modulators
US20100311798A1 (en) * 2009-06-05 2010-12-09 Decoret Guillaume 2-aminooxazolines as taar1 ligands
US8354441B2 (en) * 2009-11-11 2013-01-15 Hoffmann-La Roche Inc. Oxazoline derivatives
US9452980B2 (en) 2009-12-22 2016-09-27 Hoffmann-La Roche Inc. Substituted benzamides
US8673950B2 (en) 2010-11-02 2014-03-18 Hoffmann-Laroche Inc. Dihydrooxazol-2-amine derivatives
US8802673B2 (en) 2011-03-24 2014-08-12 Hoffmann-La Roche Inc Heterocyclic amine derivatives
US9073911B2 (en) 2011-06-09 2015-07-07 Hoffmann-La Roche Inc. Pyrazole derivatives
US9029370B2 (en) 2011-06-10 2015-05-12 Hoffmann-La Roche Inc. Substituted benzamide derivatives
JP5872069B2 (ja) 2012-01-12 2016-03-01 エフ．ホフマン−ラ ロシュ アーゲーＦ． Ｈｏｆｆｍａｎｎ−Ｌａ Ｒｏｃｈｅ Ａｋｔｉｅｎｇｅｓｅｌｌｓｃｈａｆｔ 微量アミン関連受容体（ｔａａｒ）としての複素環誘導体
BR112015004511B1 (pt) 2012-09-14 2022-08-02 F. Hoffmann-La Roche Ag Derivados de pirazol carboxamida como moduladores de taar para uso no tratamento de diversas desordens, tais como depressão, diabetes e doença de parkinson
MX361761B (es) 2012-09-17 2018-12-17 Hoffmann La Roche Derivados de triazol carboxamida.
WO2015165085A1 (en) 2014-04-30 2015-11-05 F.Hoffmann-La Roche Ag Morpholin-pyridine derivatives
WO2016030310A1 (en) 2014-08-27 2016-03-03 F. Hoffmann-La Roche Ag Substituted azetidine derivatives as taar ligands
MX2016016190A (es) 2014-08-27 2017-03-08 Hoffmann La Roche Derivados de pirazino[2,1-a]isoquinolina sustituida para el tratamiento de trastornos del sistema nervioso central.
EA036086B1 (ru) * 2016-03-17 2020-09-24 Фмк Корпорейшн Способ превращения s-энантиомера в его рацемическую форму
RS60825B1 (sr) 2016-03-17 2020-10-30 Hoffmann La Roche Aktivnost derivata 5-etiol-4-metil-pirazol-3-karboksamida kao agonista taar-a
CN116496261B (zh) * 2023-03-09 2025-06-27 中国人民解放军军事科学院军事医学研究院 4-(1h)-咪唑类衍生物及其医药用途
CN118684628B (zh) * 2024-05-20 2025-06-17 中国人民解放军军事科学院军事医学研究院 取代二氢茚基咪唑类化合物及其制备方法和用途

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6048972A (ja) * 1983-08-25 1985-03-16 Dai Ichi Seiyaku Co Ltd テトラヒドロナフタレン誘導体
GB2167408B (en) * 1984-11-23 1988-05-25 Farmos Oy Substituted imidazole derivatives and their preparation and use
GB8626287D0 (en) * 1986-11-04 1986-12-03 Ucb Sa Substituted 1h-imidazoles
GB2206880B (en) * 1987-07-16 1991-04-24 Farmos Oy Optical isomers of an imidazole derivative
US5151526A (en) * 1990-10-11 1992-09-29 The United States Of America As Represented By The Secretary Of The Army 4-[1-(1-naphthalenyl)ethyl]-1H-imidazole, method of making and use as an anesthetic
JPH04210680A (ja) * 1990-12-01 1992-07-31 Nissan Chem Ind Ltd イミダゾール誘導体および植物生長調節剤
GB9425211D0 (en) * 1994-12-14 1995-02-15 Ucb Sa Substituted 1H-imidazoles

Also Published As

Publication number Publication date
MX9505063A (es) 1997-01-31
SK155095A3 (en) 1997-02-05
AU693614B2 (en) 1998-07-02
BR9505815A (pt) 1998-01-06
PL311736A1 (en) 1996-06-24
CN1133837A (zh) 1996-10-23
NZ280646A (en) 1996-08-27
EP0717037A1 (fr) 1996-06-19
AR002257A1 (es) 1998-03-11
NO955034L (no) 1996-06-17
IS4311A (is) 1996-06-15
JPH08208622A (ja) 1996-08-13
FI955927A7 (fi) 1996-06-15
GB9425211D0 (en) 1995-02-15
IL116325A0 (en) 1996-03-31
AU4036895A (en) 1996-06-20
FI955927L (fi) 1996-06-15
HUT73980A (en) 1996-10-28
US5658938A (en) 1997-08-19
IL116325A (en) 1999-10-28
FI955927A0 (fi) 1995-12-11
CZ327195A3 (en) 1996-07-17
TW303362B (cg-RX-API-DMAC10.html) 1997-04-21
CN1054376C (zh) 2000-07-12
RU2156239C2 (ru) 2000-09-20
ZA9510554B (en) 1996-06-13
HU9503549D0 (en) 1996-02-28
BG100208A (bg) 1996-07-31
RO113346B1 (ro) 1998-06-30
KR960022474A (ko) 1996-07-18
NO305316B1 (no) 1999-05-10
BG63043B1 (bg) 2001-02-28
NO955034D0 (no) 1995-12-12
EE9500064A (et) 1996-06-17

Similar Documents

Publication Publication Date Title
US5658938A (en) Substituted 1H-imidazoles
EP0721455B1 (fr) Tetrahydropyridine-(ou 4-hydroxypiperidine) alkylazoles ayant une activite pour les recepteurs sigma et/ou 5ht1a
US5001134A (en) Piperidines, processes of preparation and medications containing them
Alabaster et al. 2 (1H)-Quinolinones with cardiac stimulant activity. 2. Synthesis and biological activities of 6-(N-linked, five-membered heteroaryl) derivatives
JP2840288B2 (ja) 置換１―（１ｈ―イミダゾール―４―イル）アルキル―ベンズアミド
US4851526A (en) 1-(4-Substituted phenyl)-1H-imidazoles compounds
JPS61176571A (ja) イミダゾール誘導体およびその製造方法
FI63226C (fi) Foerfarande foer framstaellning av nya terapeutiskt anvaendbara 1-difenylmetyl-3-metyl-3-bensylpiperazinderivat
KR100254690B1 (ko) 트라조돈의 알킬 유도체
EP0198235B1 (en) Imidazole derivatives having antimycotic and antibacterial activities, a process for the preparation thereof and pharmaceutical compositions containing them
WO1999031089A1 (fr) Derives de 1-(1h-imidazol-2-yl)pyrrolidines et 1-(1h-imidazol-2-ylpiperidines), leur preparation et leur application en therapeutique
US4288448A (en) N-Substituted imidazole derivatives, and their use
HU195645B (en) Process for preparing novel 3(2h)-pyridazinone derivatives and pharmaceutical compositions comprising the same
US4874761A (en) 4-arylcarbonyl-1-[(4-morpholinyl)-lower-alkyl]-1H-indoles
US5726178A (en) Alkyl derivatives of trazodone with CNS activity
US4840950A (en) 4-arylcarbonyl-1-[(4-morpholinyl)-lower-alkyl]-1H-indoles
IE850985L (en) Salts of fosfomycin with imidazole
FI85853C (fi) Foerfarande foer framstaellning av 4- metoxi-2'-/2-(1-metyl-2-piperidyl) etyl/bentsanilidhydroklorid och 1-(2-nitrofenyl)-2-/2-(1-metyl) pyridiniummetylsulfat/etanol.
PL162554B1 (pl) S posób wytwarzania nowych pochodnych imidazolu PL PL PL PL PL
CA2051803A1 (en) Aromatase inhibiting 4(5)-imidazoles
WO2000006552A1 (fr) Derives de 4-phenyl- et de 4,5-diphenylimidazoles, leur preparation et leur application en therapeutique
GB2209748A (en) Imidazolinyl derivatives of dihydronapthalene and tetrahydronapthalene
HU202861B (en) Process for producing new 1- and 4-substituted 2:2'-bi-1h-imidazol derivatives and pharmaceutical compositions containing them as active components
KR20010072407A (ko) Ｎ-치환 아자비시클로헵탄 유도체, 그의 제조 및 용도
JPS63190875A (ja) 新規な置換ペピリジン又はアゼピン、その製造方法及び治療におけるその使用

Legal Events

Date Code Title Description
FZDE Discontinued