ES2196806T3 - Derivados de fenilurea y de feniltiourea. - Google Patents

Derivados de fenilurea y de feniltiourea.

Info

Publication number
ES2196806T3
ES2196806T3 ES99923540T ES99923540T ES2196806T3 ES 2196806 T3 ES2196806 T3 ES 2196806T3 ES 99923540 T ES99923540 T ES 99923540T ES 99923540 T ES99923540 T ES 99923540T ES 2196806 T3 ES2196806 T3 ES 2196806T3
Authority
ES
Spain
Prior art keywords
alkyl
alkoxy
sulfur
phenyl
nitrogen
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.)
Expired - Lifetime
Application number
ES99923540T
Other languages
English (en)
Inventor
Amanda Johns
Roderick Alan Porter
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.)
SmithKline Beecham Ltd
Original Assignee
SmithKline Beecham Ltd
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
Priority claimed from GBGB9809988.0A external-priority patent/GB9809988D0/en
Priority claimed from GBGB9809972.4A external-priority patent/GB9809972D0/en
Priority claimed from GBGB9903268.2A external-priority patent/GB9903268D0/en
Application filed by SmithKline Beecham Ltd filed Critical SmithKline Beecham Ltd
Application granted granted Critical
Publication of ES2196806T3 publication Critical patent/ES2196806T3/es
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
    • C07D471/04—Ortho-condensed systems
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P15/00—Drugs for genital or sexual disorders; Contraceptives
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/04—Centrally acting analgesics, e.g. opioids
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/18—Antipsychotics, i.e. neuroleptics; Drugs for mania or schizophrenia
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/20—Hypnotics; Sedatives
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/22—Anxiolytics
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/24—Antidepressants
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00—Drugs for disorders of the metabolism
    • A61P3/04—Anorexiants; Antiobesity agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00

Landscapes

  • Health & Medical Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical & Material Sciences (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Veterinary Medicine (AREA)
  • General Health & Medical Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Medicinal Chemistry (AREA)
  • Public Health (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Neurosurgery (AREA)
  • Neurology (AREA)
  • Biomedical Technology (AREA)
  • Psychiatry (AREA)
  • Pain & Pain Management (AREA)
  • Obesity (AREA)
  • Hematology (AREA)
  • Diabetes (AREA)
  • Child & Adolescent Psychology (AREA)
  • Anesthesiology (AREA)
  • Endocrinology (AREA)
  • Reproductive Health (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)

Abstract

1. Un compuesto de fórmula (I): en la cual: uno de X e Y es N, y el otro es CH; Z representa oxígeno o azufre; R1 representa alquilo(C1-6), alquenilo(C2-6) o alcoxi(C1-6); halógeno, R7CO- ó NR8R9CO-; R2, R3, R4, R5 y R6 representan independientemente alquilo(C1-6), alquenilo(C2-6), alcoxi(C1-6) o tioalquilo(C1-6); hidrógeno, halógeno, nitro, ciano, fenoxi, naftiloxi, fenilalcoxi(C1-6), naftilalcoxi(C1-6), fenilalquilo(C1-6), naftilalquilo(C1-6), R7CO-, R7SO2NH-, R7CON(R10)-, NR8R9-, NR8R9CO-, -COOR8, un anillo monocíclico o bicíclico de 5 a 10 miembros, que puede estar insaturado o saturado, que contiene 1 a 3 heteroátomos seleccionados entre oxígeno, nitrógeno o azufre, o un alquilo(C1-6) sustituido con un anillo monocíclico o bicíclico de 5 a 10 miembros, que puede estar insaturado o saturado, que contiene 1 a 3 heteroátomos seleccionados entre oxígeno, nitrógeno o azufre; o un par adyacente de R2, R3, R4, R5 y R6 junto con los átomos de carbono a los cuales están unidos, forman un anillocarbocíclico o heterocíclico aromático o no aromático de 5 a 7 miembros, en el que el anillo heterocíclico contiene 1, 2 ó o 3 heteroátomos seleccionados entre oxígeno, nitrógeno y azufre, y en el que el anillo carbocíclico o heterocíclico puede estar insustituido o sustituido en el carbono o nitrógeno con uno o más sustituyentes seleccionados entre =O, alquilo(C1-4), fenilalquilo(C1-4), naftilalquilo(C1-4), fenilo, naftilo, alcoxi(C1-4), alcoxi(C1-4)alquil(C1-4)hidroxi, hidroxialquilo(C1-4), RaCO2-, RaCO2alquilo(C1-4), ciano, cianoalquilo(C1-4), RaRbN y RaRbNalquilo(C1-4); en el cual, Ra y Rb son independientemente seleccionados entre hidrógeno y alquilo(C1-4); R7 es alquilo(C1-6), fenilo o naftilo; R8 y R9 representan independientemente hidrógeno, alquilo (C1-6), fenilo, naftilo, fenilalquilo(C1-6) o naftilalquilo(C1-6); R10 es hidrógeno o alquilo(C1-6); y n es 0, 1, 2 ó 3; en donde alquilo puede ser una cadena lineal, ramificada o cíclica; o una sal farmacéuticamente aceptable del mismo.
ES99923540T 1998-05-08 1999-05-04 Derivados de fenilurea y de feniltiourea. Expired - Lifetime ES2196806T3 (es)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
GBGB9809988.0A GB9809988D0 (en) 1998-05-08 1998-05-08 Compounds
GBGB9809972.4A GB9809972D0 (en) 1998-05-08 1998-05-08 Compounds
GBGB9903268.2A GB9903268D0 (en) 1999-02-12 1999-02-12 Compounds

Publications (1)

Publication Number Publication Date
ES2196806T3 true ES2196806T3 (es) 2003-12-16

Family

ID=27269308

Family Applications (1)

Application Number Title Priority Date Filing Date
ES99923540T Expired - Lifetime ES2196806T3 (es) 1998-05-08 1999-05-04 Derivados de fenilurea y de feniltiourea.

Country Status (8)

Country Link
US (1) US6372757B1 (es)
EP (1) EP1075478B1 (es)
JP (1) JP4633925B2 (es)
AU (1) AU4037799A (es)
CA (1) CA2331735A1 (es)
DE (1) DE69906960T2 (es)
ES (1) ES2196806T3 (es)
WO (1) WO1999058533A1 (es)

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US6093820A (en) 1997-10-02 2000-07-25 Taro Pharmaceutical Industries Ltd. Method and reagents for N-alkylating ureides
WO2000047576A1 (en) * 1999-02-12 2000-08-17 Smithkline Beecham Plc Cinnamide derivatives as orexin-1 receptors antagonists
EP1144409B1 (en) * 1999-02-12 2004-11-17 SmithKline Beecham plc Phenyl urea and phenyl thiourea derivatives
EP1150664B1 (en) * 1999-02-12 2003-05-28 SmithKline Beecham plc Novel use of orexin receptor antagonists
JP4009460B2 (ja) 2000-03-14 2007-11-14 アクテリオン ファマシューティカルズ リミテッド １，２，３，４−テトラヒドロイソキノリン誘導体
CA2408343A1 (en) * 2000-05-11 2002-11-07 Banyu Pharmaceutical Co., Ltd. N-acyltetrahydroisoquinoline derivatives
PT1289955E (pt) * 2000-06-16 2005-08-31 Smithkline Beecham Plc Piperidinas para utilizacao como antagonistas dos receptores da orexina
US6756379B2 (en) * 2001-07-26 2004-06-29 Taro Pharmaceutical Industries Ltd. Non-sedating barbiturate compounds as neuroprotective agents
US7683071B2 (en) * 2000-07-26 2010-03-23 Taro Pharmaceuticals Industries Ltd. Composition and method for improved bioavailability and enhanced brain delivery of 5,5-diphenyl barbituric acid
US6939873B2 (en) * 2000-07-26 2005-09-06 Taro Pharmaceuticals Industries Limited Non-sedating barbituric acid derivatives
JP4309135B2 (ja) 2001-05-05 2009-08-05 スミスクライン ビーチャム ピー エル シー Ｎ−アロイルサイクリックアミン
GB0115862D0 (en) 2001-06-28 2001-08-22 Smithkline Beecham Plc Compounds
GB0130335D0 (en) * 2001-12-19 2002-02-06 Smithkline Beecham Plc Compounds
RU2005103398A (ru) 2002-07-09 2006-06-27 Актелион Фармасьютикалз Лтд. (Ch) Производные 7,8,9,10-тетрагидро-6h-азепино-, 6,7,8,9-тетрагидропиридо-и 2,3-дигидро-2h-пирроло-[2,1-b]-хиназолинона
AU2003294671A1 (en) 2002-10-11 2004-05-04 Actelion Pharmaceuticals Ltd. Sulfonylamino-acetic derivatives and their use as orexin receptor antagonists
TWI334780B (en) 2002-12-11 2010-12-21 Taro Pharmaceuticals Ireland Ltd Method of treating movement disorders using barbituric acid derivatives
CA2520839A1 (en) 2003-04-28 2004-11-11 Actelion Pharmaceuticals Ltd Quinoxalinone-3- one derivatives as orexin receptor antagonists
US20050032794A1 (en) * 2003-08-05 2005-02-10 Padia Janak K. Diamine derivatives of quinone and uses thereof
HUP0304101A3 (en) * 2003-12-22 2008-10-28 Sanofi Aventis Pyrazole derivatives, process for producing them, their use, pharmaceutical compositions containing them and their intermediates
HRP20150371T1 (hr) 2004-03-01 2015-05-08 Actelion Pharmaceuticals Ltd. Supstituirani derivati 1,2,3,4-tetrahidroizokinolina
EP2305352A1 (en) 2004-04-02 2011-04-06 Merck Sharp & Dohme Corp. 5-alpha-reductase inhibitors for use in the treatment of men with metabolic and anthropometric disorders
CA2572797A1 (en) * 2004-07-02 2006-01-12 Daniella Gutman A process for preparing 1-methoxymethyl-5,5-diphenylbarbituric acid
US20060178307A1 (en) * 2005-01-26 2006-08-10 The Regents Of The University Of California Modulation of NMDA receptor currents via orexin receptor and/or CRF receptor
US7501395B2 (en) 2005-04-25 2009-03-10 Eisai R & D Management Co., Ltd. Method of screening for antianxiety drugs
US7547782B2 (en) 2005-09-30 2009-06-16 Bristol-Myers Squibb Company Met kinase inhibitors
US8618102B2 (en) 2006-07-14 2013-12-31 Merck Sharp & Dohme Corp. Bridged diazepan orexin receptor antagonists
US20080132529A1 (en) * 2006-11-14 2008-06-05 Avraham Yacobi Method of improving bioavailability for non-sedating barbiturates
PE20081229A1 (es) 2006-12-01 2008-08-28 Merck & Co Inc Antagonistas de receptor de orexina de diazepam sustituido
CL2008001003A1 (es) 2007-04-11 2008-10-17 Actelion Pharmaceuticals Ltd Compuestos derivados de oxazolidinona; composicion farmaceutica que comprende a dichos compuestos; y su uso para preparar un medicamento para tratar una infeccion bacteriana.
AU2008255005B2 (en) 2007-05-18 2013-05-02 Merck Sharp & Dohme Corp. OXO bridged diazepan orexin receptor antagonists
US8030495B2 (en) 2007-05-23 2011-10-04 Coleman Paul J Cyclopropyl pyrrolidine orexin receptor antagonists
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JPH05213884A (ja) * 1991-06-14 1993-08-24 Upjohn Co:The 新規な４−アミノキノリン類およびこれを有効成分とする高血圧・鬱血性心不全の予防・治療剤
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AR016817A1 (es) * 1997-08-14 2001-08-01 Smithkline Beecham Plc Derivados de fenilurea o feniltiourea, procedimiento para su preparacion, coleccion de compuestos, compuestos intermediarios, composicion farmaceutica,metodo de tratamiento y uso de dichos compuestos para la manufactura de un medicamento

Also Published As

Publication number Publication date
EP1075478A1 (en) 2001-02-14
AU4037799A (en) 1999-11-29
US6372757B1 (en) 2002-04-16
JP4633925B2 (ja) 2011-02-16
CA2331735A1 (en) 1999-11-18
JP2003522101A (ja) 2003-07-22
DE69906960T2 (de) 2004-01-29
WO1999058533A1 (en) 1999-11-18
DE69906960D1 (en) 2003-05-22
EP1075478B1 (en) 2003-04-16

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