BR0015401A - [(indol-3-yl) -cycloalkyl] -3-substituted azetidines for the treatment of central nervous system disorders - Google Patents

[(indol-3-yl) -cycloalkyl] -3-substituted azetidines for the treatment of central nervous system disorders

Info

Publication number
BR0015401A
BR0015401A BR0015401-6A BR0015401A BR0015401A BR 0015401 A BR0015401 A BR 0015401A BR 0015401 A BR0015401 A BR 0015401A BR 0015401 A BR0015401 A BR 0015401A
Authority
BR
Brazil
Prior art keywords
carbon atoms
cycloalkyl
treatment
nervous system
central nervous
Prior art date
Application number
BR0015401-6A
Other languages
Portuguese (pt)
Inventor
Magda Asselin
John Watson Ellingboe
Richard Eric Mewshaw
Original Assignee
Wyeth Corp
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 Wyeth Corp filed Critical Wyeth Corp
Publication of BR0015401A publication Critical patent/BR0015401A/en

Links

Classifications

    • 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
    • C07D403/08Heterocyclic 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 alicyclic rings
    • 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

Landscapes

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

Abstract

Patente de Invenção: "[(INDOL-3-IL)-CICLOALQUIL]-3-AZETIDINAS SUBSTITUìDAS PARA O TRATAMENTO DE DISTúRBIOS DO SISTEMA NERVOSO CENTRAL". Esta invenção refere-se aos novos compostos, composições farmacêuticas e processos de uso dos compostos no tratamento de distúrbios do sistema nervoso central, tais como, ansiedade e depressão, os compostos possuindo a fórmula (I), em que: X é N-R, O, S(O)~ m~ é 0 a 2; n é 0 a 4; Ar é um grupo arila de 6 a 12 átomos de carbono, opcionalmente substituído com 1 a 3 grupos R~ 3~ ou um grupo hetoroarila de 4 a 10 átomos de carbono, opcionalmente substituído com 1 a 3 grupos R~ 3~; R e R~ 2~ são independentemente H, alquila de cadeia linear de 1 a 6 átomos de carbono, alquila ramificada de 3 a 6 átomos de carbono, cicloalquila de 3 a 6 átomos de carbono, alcoxicarbonila de 1 a 6 átomos de carbono, alquilcarbonila de 1 a 6 átomos de carbono, aminocarbonila ou alquilaminocarbonila de 1 a 4 átomos de carbono; R~ 1~ e R~ 3~ são independentemente H, alquila de cadeia linear de 1 a 4 átomos de carbono, alquila ramificada de 3 a 6 átomos de carbono, cicloalquila de 3 a 8 átomos de carbono, halo, grupo alcóxi de 1 a 4 átomos de carbono, haloalquila de 1 a 4 átomos de carbono, OH, nitro, amino, sulfonila, CN, carbóxi, alcoxicarbonila de 1 a 4 átomos de carbono, alquilcarbonila de 1 a 4 átomos de carbono, aminocarbonila ou alquilaminocarbonila de 1 a 4 átomos de carbono; e todas as formas cristalinas ou um sal farmaceuticamente aceitável das mesmas.Invention Patent: "[(INDOL-3-IL) -CYCLOLOQUIL] -3-SUBSTITUTED AZETIDINES FOR THE TREATMENT OF DISORDERS OF THE CENTRAL NERVOUS SYSTEM". This invention relates to the new compounds, pharmaceutical compositions and processes of use of the compounds in the treatment of disorders of the central nervous system, such as anxiety and depression, the compounds having the formula (I), in which: X is NR, O , S (O) ~ m ~ is 0 to 2; n is 0 to 4; Ar is an aryl group of 6 to 12 carbon atoms, optionally substituted with 1 to 3 R ~ 3 ~ groups or a hetoroaryl group of 4 to 10 carbon atoms, optionally substituted with 1 to 3 R ~ 3 ~ groups; R and R ~ 2 ~ are independently H, straight chain alkyl of 1 to 6 carbon atoms, branched alkyl of 3 to 6 carbon atoms, cycloalkyl of 3 to 6 carbon atoms, alkoxycarbonyl of 1 to 6 carbon atoms, alkylcarbonyl of 1 to 6 carbon atoms, aminocarbonyl or alkylaminocarbonyl of 1 to 4 carbon atoms; R ~ 1 ~ and R ~ 3 ~ are independently H, straight chain alkyl of 1 to 4 carbon atoms, branched alkyl of 3 to 6 carbon atoms, cycloalkyl of 3 to 8 carbon atoms, halo, alkoxy group of 1 to 4 carbon atoms, haloalkyl of 1 to 4 carbon atoms, OH, nitro, amino, sulfonyl, CN, carboxy, alkoxycarbonyl of 1 to 4 carbon atoms, alkylcarbonyl of 1 to 4 carbon atoms, aminocarbonyl or 1-alkylaminocarbonyl to 4 carbon atoms; and all crystalline forms or a pharmaceutically acceptable salt thereof.

BR0015401-6A 1999-11-08 2000-10-31 [(indol-3-yl) -cycloalkyl] -3-substituted azetidines for the treatment of central nervous system disorders BR0015401A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US43611999A 1999-11-08 1999-11-08
PCT/US2000/029954 WO2001034598A1 (en) 1999-11-08 2000-10-31 [(indol-3-yl)-cycloalkyl]-3-substituted azetidines for the treatment of central nervous system disorders

Publications (1)

Publication Number Publication Date
BR0015401A true BR0015401A (en) 2002-07-02

Family

ID=23731187

Family Applications (1)

Application Number Title Priority Date Filing Date
BR0015401-6A BR0015401A (en) 1999-11-08 2000-10-31 [(indol-3-yl) -cycloalkyl] -3-substituted azetidines for the treatment of central nervous system disorders

Country Status (8)

Country Link
EP (1) EP1228065A1 (en)
JP (1) JP2003513970A (en)
CN (1) CN1414962A (en)
AU (1) AU1446601A (en)
BR (1) BR0015401A (en)
CA (1) CA2390531A1 (en)
MX (1) MXPA02004555A (en)
WO (1) WO2001034598A1 (en)

Families Citing this family (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1638939A2 (en) * 2003-06-24 2006-03-29 Neurosearch A/S Aza-ring derivatives and their use as monoamine neurotransmitter re-uptake inhibitors
TW200616967A (en) 2004-06-24 2006-06-01 Smithkline Beecham Corp Novel indazole carboxamides and their use
TW200626142A (en) 2004-09-21 2006-08-01 Glaxo Group Ltd Chemical compounds
US8063071B2 (en) 2007-10-31 2011-11-22 GlaxoSmithKline, LLC Chemical compounds
AR065804A1 (en) 2007-03-23 2009-07-01 Smithkline Beecham Corp COMPOSITE OF INDOL CARBOXAMIDE, PHARMACEUTICAL COMPOSITION THAT UNDERSTANDS IT AND USE OF THIS COMPOUND TO PREPARE A MEDICINAL PRODUCT
UY32312A (en) 2008-12-10 2010-06-30 Janssen Pharmaceutica Nv 4-AZETIDINIL-1-HETEROARIL-CICLOHEXANOL ANTAGONISTS OF CCR2
WO2010102968A1 (en) 2009-03-10 2010-09-16 Glaxo Group Limited Indole derivatives as ikk2 inhibitors
CN102459226B (en) 2009-04-17 2014-09-17 詹森药业有限公司 4-azetidinyl-1-heteroatom linked-cyclohexane antagonists of ccr2
EP2419419B1 (en) 2009-04-17 2014-12-03 Janssen Pharmaceutica NV 4-azetidinyl-1-phenyl-cyclohexane antagonists of ccr2
TW201211027A (en) 2010-06-09 2012-03-16 Janssen Pharmaceutica Nv Cyclohexyl-azetidinyl antagonists of CCR2
WO2011159854A1 (en) 2010-06-17 2011-12-22 Janssen Pharmaceutica Nv Cyclohexyl-azetidinyl antagonists of ccr2
JP6994767B2 (en) * 2016-06-21 2022-01-14 エックス4 ファーマシューティカルズ, インコーポレイテッド CXCR4 inhibitor and its use
CN116554168A (en) 2016-06-21 2023-08-08 X4 制药有限公司 CXCR4 inhibitors and uses thereof

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB9401436D0 (en) * 1994-01-26 1994-03-23 Wellcome Found Therapeutic heterocyclic compounds
ATE223379T1 (en) * 1998-04-08 2002-09-15 Wyeth Corp N-ARYLOXYETHYLAMINE DERIVATIVES FOR THE TREATMENT OF DEPRESSION
CN1166636C (en) * 1999-01-07 2004-09-15 惠氏 Arylpiperazinyl-cyclohexyl indole derivatives for the treatment of depression

Also Published As

Publication number Publication date
WO2001034598A1 (en) 2001-05-17
MXPA02004555A (en) 2004-09-10
CA2390531A1 (en) 2001-05-17
AU1446601A (en) 2001-06-06
CN1414962A (en) 2003-04-30
JP2003513970A (en) 2003-04-15
EP1228065A1 (en) 2002-08-07

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Legal Events

Date Code Title Description
B11A Dismissal acc. art.33 of ipl - examination not requested within 36 months of filing
B11Y Definitive dismissal acc. article 33 of ipl - extension of time limit for request of examination expired