PE20010349A1 - Derivados de triazol e imidazol - Google Patents

Derivados de triazol e imidazol

Info

Publication number
PE20010349A1
PE20010349A1 PE2000000707A PE0007072000A PE20010349A1 PE 20010349 A1 PE20010349 A1 PE 20010349A1 PE 2000000707 A PE2000000707 A PE 2000000707A PE 0007072000 A PE0007072000 A PE 0007072000A PE 20010349 A1 PE20010349 A1 PE 20010349A1
Authority
PE
Peru
Prior art keywords
alkyl
phenyl
triazole
benzyl
compounds
Prior art date
Application number
PE2000000707A
Other languages
English (en)
Inventor
Bernd Buettelmann
Alexander Alanine
Emmanuel Pinard
Neidhart Marie-Paule Heitz
Georg Jaeschke
Rene Wyler
Original Assignee
Hoffmann La Roche
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 Hoffmann La Roche filed Critical Hoffmann La Roche
Publication of PE20010349A1 publication Critical patent/PE20010349A1/es

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D233/00Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
    • C07D233/54Heterocyclic 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
    • C07D233/64Heterocyclic 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P21/00Drugs for disorders of the muscular or neuromuscular system
    • A61P21/04Drugs for disorders of the muscular or neuromuscular system for myasthenia gravis
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/14Drugs for disorders of the nervous system for treating abnormal movements, e.g. chorea, dyskinesia
    • A61P25/16Anti-Parkinson drugs
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/18Antipsychotics, i.e. neuroleptics; Drugs for mania or schizophrenia
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/22Anxiolytics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/24Antidepressants
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/28Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
    • 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
    • C07D249/00Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
    • C07D249/02Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms not condensed with other rings
    • C07D249/081,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
    • 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D403/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
    • C07D403/10Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a carbon chain containing aromatic rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D405/00Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/02Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
    • C07D405/10Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a carbon chain containing aromatic rings

Abstract

SE REFIERE A COMPUESTOS DERIVADOS DE TRIAZOL E IMIDAZOL DE FORMULA I DONDE R1-R4 ES H, CF3, OCF3, OCHF2, ALQUILO, ALCOXILO, HALOGENO, HIDROXILO, FENILO, BENCILO, AMINO, NITRO, PIRROL-1-ILO, ALQUIL-SULFONILO, ENTRE OTROS; R2 Y R3 SON -O-(CH2)2-O-, -O-CH2-O-, -O-(CH2)2-, ENTRE OTROS; X ES -N=, -N(R8)-, -CH=; Y ES -N=, =N-, N(R8), -CH=, UNO DE X O Y ES N; R5 ES -CH2-NR6R7; R6 Y R7 SON H, ALQUILO, C(O)-ALQUILO, HIDROXI-ALQUILO, ALQUENILO, COCH2OH; R6 Y R7 JUNTO A N SON -(CH2)2-O-(CH2)2, -CH2-CH[OC(O)CH3]-(CH2)2, ENTRE OTROS; R8 ES H, ALQUILO, ALQUENILO, ALQUINILO, (CH2)m-O-ALQUILO, (CH2)m-OH, ENTRE OTROS; m ES 0-4. SON COMPUESTOS PREFERIDOS {3-[5-(4-DIFLUOROMETOXI-FENIL)-1H-[1,2,4]TRIAZOL-3-IL]-BENCIL}-DIMETIL-AMINO (MEZCLA DE TAUTOMEROS), {3-[5-(4-FLUOROMETOXI-FENIL)-1H-[1,2,4]TRIAZOL-3-IL]-BENCIL}-DIMETIL-AMINA (MEZCLA DE TAUTOMEROS), 5-(4-DIFLUOROMETOXI-FENIL)-3-(3-PIRROLIDIN-3-ILMETIL-FENIL)-1H-[1,2,4]TRIAZOL (MEZCLA DE TAUTOMEROS), ENTRE OTROS. SE REFIERE TAMBIEN A UN PROCEDIMIENTO PARA LA PREPARACION. LOS COMPUESTOS I SON BLOQUEADORES SELECTIVOS DEL RECEPTOR NMDA POR LO QUE PUEDEN SER UTILES EN EL TRATAMIENTO DE ENFERMEDADES DE ALZHEIMER, PARKINSON, HUNTINGTON
PE2000000707A 1999-07-21 2000-07-17 Derivados de triazol e imidazol PE20010349A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
EP99114313 1999-07-21

Publications (1)

Publication Number Publication Date
PE20010349A1 true PE20010349A1 (es) 2001-03-26

Family

ID=8238635

Family Applications (1)

Application Number Title Priority Date Filing Date
PE2000000707A PE20010349A1 (es) 1999-07-21 2000-07-17 Derivados de triazol e imidazol

Country Status (29)

Country Link
US (1) US6265426B1 (es)
EP (1) EP1070708B1 (es)
JP (1) JP3628946B2 (es)
KR (1) KR100383776B1 (es)
CN (1) CN1148357C (es)
AR (1) AR024790A1 (es)
AT (1) ATE257827T1 (es)
AU (1) AU773463B2 (es)
BR (1) BR0003075A (es)
CA (1) CA2314009C (es)
CO (1) CO5190713A1 (es)
DE (1) DE60007697T2 (es)
DK (1) DK1070708T3 (es)
ES (1) ES2211420T3 (es)
HR (1) HRP20000482A2 (es)
HU (1) HUP0002792A3 (es)
ID (1) ID26599A (es)
IL (1) IL137328A0 (es)
MA (1) MA26747A1 (es)
MX (1) MXPA00007069A (es)
NO (1) NO20003723L (es)
NZ (1) NZ505766A (es)
PE (1) PE20010349A1 (es)
PL (1) PL341616A1 (es)
PT (1) PT1070708E (es)
SG (1) SG98422A1 (es)
TR (1) TR200002097A3 (es)
UY (1) UY26253A1 (es)
ZA (1) ZA200003680B (es)

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US5962490A (en) * 1987-09-25 1999-10-05 Texas Biotechnology Corporation Thienyl-, furyl- and pyrrolyl-sulfonamides and derivatives thereof that modulate the activity of endothelin
US6610723B2 (en) 2001-01-29 2003-08-26 Hoffmann-La Roche Inc. Imidazole derivatives
US7375136B2 (en) 2001-03-08 2008-05-20 Emory University pH-dependent NMDA receptor antagonists
US6951875B2 (en) * 2001-10-29 2005-10-04 Hoffmann-La Roche Inc. Conjugated aromatic compounds with a pyridine substituent
US7005432B2 (en) * 2002-05-16 2006-02-28 Hoffman-La Roche Inc. Substituted imidazol-pyridazine derivatives
CA2488117A1 (en) 2002-06-17 2003-12-24 Merck & Co., Inc. 1-((5-aryl-1,2,4-oxadiazol-3-yl)benzyl)azetidine-3-carboxylates and 1-((5-aryl-1,2,4-oxadiazol-3-yl)benzyl)pyrrolidine-3-carboxylates as edg receptor agonists
US20060004088A1 (en) * 2002-10-22 2006-01-05 Oct Inc. Furan derivatives for preventing and curing osteoporosis and pharmaceutical compositions containing the same
US7084145B2 (en) * 2002-10-25 2006-08-01 Pfizer Inc. Triazole compounds useful in therapy
CN1747936A (zh) * 2003-02-12 2006-03-15 特兰斯泰克制药公司 作为治疗试剂的取代吡咯衍生物
GB0303503D0 (en) * 2003-02-14 2003-03-19 Novartis Ag Organic compounds
GB0315111D0 (en) 2003-06-27 2003-07-30 Cancer Rec Tech Ltd Substituted 5-membered ring compounds and their use
DE602004027301D1 (de) * 2003-12-22 2010-07-01 Merck Sharp & Dohme Alpha-hydroxyamide als bradykininantagonisten oder inverse agonisten
NZ548208A (en) * 2004-02-12 2010-09-30 Transtech Pharma Inc Substituted azole derivatives, compositions, and methods of use
CN101374835B (zh) * 2006-01-30 2012-04-25 转化技术制药公司 作为PTPase抑制剂的取代的咪唑衍生物、组合物和使用方法
JO3019B1 (ar) * 2006-04-19 2016-09-05 Janssen Pharmaceutica Nv ثلاثي مستبدل 4،2،1-ثلاثي زولات
EP2118077B1 (en) 2007-02-08 2014-12-24 Synta Pharmaceuticals Corp. Triazole compounds that modulate hsp90 activity
EP2529623A3 (en) * 2007-04-03 2013-03-13 E. I. du Pont de Nemours and Company Substituted benzene fungicides
US20110158907A1 (en) * 2007-04-19 2011-06-30 The Trustees Of The Univeristy Of Pennsylvania Diphenyl-heteroaryl derivatives and their use for binding and imaging amyloid plaques
US8420680B2 (en) * 2007-06-29 2013-04-16 Emory University NMDA receptor antagonists for neuroprotection
JO2784B1 (en) 2007-10-18 2014-03-15 شركة جانسين فارماسوتيكا ان. في 5,3,1 - Triazole substitute derivative
RU2474579C2 (ru) 2007-10-18 2013-02-10 Янссен Фармацевтика Нв Тризамещенные 1,2,4-триазолы
AU2009226988B2 (en) 2008-03-19 2013-05-23 Janssen Pharmaceutica Nv Trisubstituted 1, 2, 4 -triazoles as nicotinic acetylcholine receptor modulators
WO2009118187A1 (en) * 2008-03-27 2009-10-01 Evotec Neurosciences Gmbh Methods for treating disorders using nmda nr2b-subtype selective antagonist
JP5486591B2 (ja) 2008-05-09 2014-05-07 ジヤンセン・フアーマシユーチカ・ナームローゼ・フエンノートシヤツプ アセチルコリン受容体モジュレーターとしての三置換ピラゾール
RU2532394C1 (ru) * 2013-10-29 2014-11-10 Общество с ограниченной ответственностью "Научно-производственное объединение "Фарматрон" (НПО "Фарматрон") ПРИМЕНЕНИЕ БРОМИДА 1-β-ФЕНИЛЭТИЛ)-4-АМИНО-1,2,4-ТРИАЗОЛИЯ (ГИПЕРТРИЛ) КАК АКТИВНОЙ ОСНОВЫ ЛЕКАРСТВЕННЫХ СРЕДСТВ ДЛЯ КОРРЕКЦИИ НАРУШЕНИЙ ФУНКЦИОНИРОВАНИЯ НИТРОКСИДЕРГИЧЕСКОЙ СИСТЕМЫ ОРГАНОВ-МИШЕНЕЙ ПРИ ГОМОЦИСТЕИНЕМИИ И ОСТРЫХ НАРУШЕНИЯХ МОЗГОВОГО КРОВООБРАЩЕНИЯ
BR112017003918B1 (pt) 2014-08-29 2022-05-03 Fmc Corporation Composto, composições e mistura herbicida e método para o controle do crescimento da vegetação
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US11912670B1 (en) 2023-10-25 2024-02-27 King Faisal University Ethyl 4-(5-(3-fluorophenyl)-4-phenyl-4H-1,2,4-triazol-3-ylthio)butanoate as an antimicrobial compound

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Also Published As

Publication number Publication date
UY26253A1 (es) 2000-10-31
NO20003723L (no) 2001-01-22
TR200002097A2 (tr) 2001-02-21
ES2211420T3 (es) 2004-07-16
AU773463B2 (en) 2004-05-27
JP2001064263A (ja) 2001-03-13
CN1148357C (zh) 2004-05-05
ZA200003680B (en) 2001-01-22
CA2314009A1 (en) 2001-01-21
AU4865100A (en) 2001-01-25
EP1070708B1 (en) 2004-01-14
TR200002097A3 (tr) 2001-02-21
NZ505766A (en) 2002-03-28
KR100383776B1 (ko) 2003-05-12
PT1070708E (pt) 2004-05-31
NO20003723D0 (no) 2000-07-20
ID26599A (id) 2001-01-25
DK1070708T3 (da) 2004-05-10
KR20010049825A (ko) 2001-06-15
AR024790A1 (es) 2002-10-23
BR0003075A (pt) 2001-03-13
CN1281852A (zh) 2001-01-31
ATE257827T1 (de) 2004-01-15
SG98422A1 (en) 2003-09-19
HUP0002792A2 (hu) 2001-09-28
MA26747A1 (fr) 2004-12-20
US6265426B1 (en) 2001-07-24
IL137328A0 (en) 2001-07-24
DE60007697T2 (de) 2004-12-09
DE60007697D1 (de) 2004-02-19
EP1070708A1 (en) 2001-01-24
MXPA00007069A (es) 2002-04-24
HU0002792D0 (en) 2000-09-28
PL341616A1 (en) 2001-01-29
JP3628946B2 (ja) 2005-03-16
CA2314009C (en) 2008-09-30
CO5190713A1 (es) 2002-08-29
HUP0002792A3 (en) 2002-10-28
HRP20000482A2 (en) 2001-06-30

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