AR002984A1 - Derivados de 1,3-dihidro-2h-imidazol-2-ona, procedimiento para su preparacion, composicion que los comprende, procedimiento para preparar dicha composicion y el uso de dichos derivados para fabricar medicamentos. - Google Patents

Derivados de 1,3-dihidro-2h-imidazol-2-ona, procedimiento para su preparacion, composicion que los comprende, procedimiento para preparar dicha composicion y el uso de dichos derivados para fabricar medicamentos.

Info

Publication number
AR002984A1
AR002984A1 ARP960102075A AR10207596A AR002984A1 AR 002984 A1 AR002984 A1 AR 002984A1 AR P960102075 A ARP960102075 A AR P960102075A AR 10207596 A AR10207596 A AR 10207596A AR 002984 A1 AR002984 A1 AR 002984A1
Authority
AR
Argentina
Prior art keywords
substituted
alkyl
piperidinyl
derivatives
procedure
Prior art date
Application number
ARP960102075A
Other languages
English (en)
Original Assignee
Janssen Pharmaceutica Nv
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 Janssen Pharmaceutica Nv filed Critical Janssen Pharmaceutica Nv
Publication of AR002984A1 publication Critical patent/AR002984A1/es

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Classifications

    • 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
    • C07D405/04Heterocyclic 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 directly linked by a ring-member-to-ring-member bond
    • 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
    • A61K31/41Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/4151,2-Diazoles
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00Drugs for disorders of the respiratory system
    • 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
    • C07D233/00Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
    • C07D233/04Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
    • C07D233/28Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D233/30Oxygen or sulfur atoms
    • C07D233/32One oxygen atom
    • 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
    • C07D233/66Heterocyclic 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 hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D233/70One oxygen atom

Landscapes

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

Abstract

La presente invención se relaciona con derivados de 1,3-dihidro-2H-imidazol -2-ona de la fórmula (I), las formas de N-óxido, las sales de adición de ácidoo base farmacéuticamente aceptables y las formas estereoquímicamente isoméricas de las mismas,e n las cuales:R1 y R2 consisten independientemente en hidrógeno,alquilo C1-6, difluorometilo, trifluorometilo, cicloalquilo C2-6,un heterociclo saturado de 5-, 6- ó 7- elementos que contiene uno o dos heteroátomosseleccionados entre oxígeno, azufreo nitrógeno; indanilo, biciclo [2.2.1]-2- heptenilo; biciclo [2.2.1] heptanilo; alquilsulfonilo C1-6; arilsulfonilo; óalquilo C1-10 sustituido;R3 es H, halo o alquiloxi C1-16;donde X es O; alquilo; >C = NOR5; un anillo de metilenos; Alc esalcanodiil o C1-4;-A-B- es un radicalbivalente de la fórmula: -CR6=CR7-; ó -CHR6-CHR7-; L es H, alquilo C1-6; optativamente sustituido alquilcarbonilo C1-6;alquiloxicarbonilo C1-6,alqueniloC3-6; optativamente sustituido; piperidinilooptativamente sustit uido; alquilsulfonilo C1-6 o arilsulfonilo; arilo es fenilo optativamente sustituido.Het 1 es piridinilo, piridinilo sustituido con alquilo C1-4; furanilo, furanilo sustituido con alquilo C1-4;tienilo, tienilosustituido con alquilcarbonilam inoC1-4; hidroxipiridinilo, hidroxipiridinilo sustituido con alquilo C1-4 ó C1-4 alcoxi C1-4 alquilo, imidazolilo, imidazolilo sustituido con alquilo C1-4;tiazolilo,tiazolilo sustituido con alquilo C1-4;oxazolilo;oxazolilo sustituido con alquilo C 1-4; isoquinolinilo; isoquinolinilo sustituido con alquilo C1-4;quinolinonilo; quinolinonilo sustituido con alquilo C1-4; morfolinilo; piperidinilo; piperidinilo sustituido con alquilo C1-4,alquiloxicarbonilo C1-4ó aril C1-4alquilo;y Het2 e s morfolinilo;piperidinilo, piperidinilo sustituido con alquilo C1-4; o aril C1-4alquilo; piperazinilo; piperazinilo sustituido con
ARP960102075A 1995-04-06 1996-04-03 Derivados de 1,3-dihidro-2h-imidazol-2-ona, procedimiento para su preparacion, composicion que los comprende, procedimiento para preparar dicha composicion y el uso de dichos derivados para fabricar medicamentos. AR002984A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
EP95200870 1995-04-06

Publications (1)

Publication Number Publication Date
AR002984A1 true AR002984A1 (es) 1998-05-27

Family

ID=8220175

Family Applications (1)

Application Number Title Priority Date Filing Date
ARP960102075A AR002984A1 (es) 1995-04-06 1996-04-03 Derivados de 1,3-dihidro-2h-imidazol-2-ona, procedimiento para su preparacion, composicion que los comprende, procedimiento para preparar dicha composicion y el uso de dichos derivados para fabricar medicamentos.

Country Status (15)

Country Link
US (1) US5869515A (es)
EP (1) EP0832071B1 (es)
JP (1) JP4115519B2 (es)
KR (1) KR100400159B1 (es)
CN (1) CN1103760C (es)
AR (1) AR002984A1 (es)
AT (1) ATE305455T1 (es)
CA (1) CA2216542C (es)
DE (1) DE69635224T2 (es)
ES (1) ES2250988T3 (es)
IL (1) IL117806A (es)
MY (1) MY117936A (es)
TW (1) TW375612B (es)
WO (1) WO1996031487A1 (es)
ZA (1) ZA962753B (es)

Families Citing this family (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5922751A (en) * 1994-06-24 1999-07-13 Euro-Celtique, S.A. Aryl pyrazole compound for inhibiting phosphodiesterase IV and methods of using same
IL129298A0 (en) * 1996-10-02 2000-02-17 Janssen Pharmaceutica Nv PDE iv inhibiting 2-cyanoiminoimidazole derivatives
WO1999050262A1 (en) * 1998-04-01 1999-10-07 Janssen Pharmaceutica N.V. Pde iv inhibiting pyridine derivatives
DE60043318D1 (de) 1999-08-21 2010-01-14 Nycomed Gmbh Synergistische kombination von pumafentrine und salmeterol
US20030175314A1 (en) * 2001-11-19 2003-09-18 Didriksen Erik Johannes Pharmaceutical composition for dermal application
FR2860514A1 (fr) 2003-10-03 2005-04-08 Sanofi Synthelabo Derives d'arylalkylcarbamates, leur preparation et leur application en therapeutique
BRPI0510453A (pt) 2004-04-30 2007-10-30 Warner Lambert Co composto substituìdos com morfolina para o tratamento de distúrbios do sistema nervoso central
WO2006078698A1 (en) * 2005-01-19 2006-07-27 Cengent Therapeutics, Inc. 2-imidazolone and 2-imidazolidinone heterocyclic inhibitors of tyrosine phosphatases
WO2007085357A1 (en) * 2006-01-30 2007-08-02 Euro-Celtique S.A. Cyclourea compounds as calcium channel blockers

Family Cites Families (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4636516A (en) * 1981-02-19 1987-01-13 Yamanouchi Pharmaceutical Co., Ltd. 3,5-di-tert-butyl-4-hydroxyphenyl-substituted heterocyclic compounds
CA1309096C (en) * 1985-08-13 1992-10-20 Sumitomo Chemical Co., Ltd. Butenoic acid derivatives, and their production and use
US4845233A (en) * 1987-09-11 1989-07-04 Iprx, Inc. Imidazolin-2-ones
US5401851A (en) * 1992-06-03 1995-03-28 Eli Lilly And Company Angiotensin II antagonists
JP3775684B2 (ja) * 1992-07-28 2006-05-17 ローン−プーラン・ロレ・リミテツド 脂肪族−またはヘテロ原子−含有連結基によりアリールまたはヘテロアリールに連結されたフェニル含有化合物
EP0711282B1 (en) * 1993-07-28 2002-06-05 Aventis Pharma Limited Compounds as pde iv and tnf inhibitors
GB9401460D0 (en) * 1994-01-26 1994-03-23 Rhone Poulenc Rorer Ltd Compositions of matter
GB9412672D0 (en) * 1994-06-23 1994-08-10 Celltech Ltd Chemical compounds
EP0766676B1 (en) * 1994-06-24 2002-05-22 Euroceltique S.A. Compounds for inhibiting phosphodiesterase iv

Also Published As

Publication number Publication date
CN1181073A (zh) 1998-05-06
JPH11504003A (ja) 1999-04-06
IL117806A (en) 2000-02-17
AU697390B2 (en) 1998-10-01
ZA962753B (en) 1997-10-06
TW375612B (en) 1999-12-01
JP4115519B2 (ja) 2008-07-09
CN1103760C (zh) 2003-03-26
CA2216542A1 (en) 1996-10-10
ES2250988T3 (es) 2006-04-16
ATE305455T1 (de) 2005-10-15
AU5497996A (en) 1996-10-23
DE69635224T2 (de) 2006-06-22
US5869515A (en) 1999-02-09
KR100400159B1 (ko) 2003-12-31
EP0832071A1 (en) 1998-04-01
WO1996031487A1 (en) 1996-10-10
EP0832071B1 (en) 2005-09-28
MY117936A (en) 2004-08-30
KR19980703448A (ko) 1998-11-05
DE69635224D1 (de) 2006-02-09
IL117806A0 (en) 1996-08-04
CA2216542C (en) 2009-01-13

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