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AR051802A1 - Heterociclos antagonistas de mchr1 - Google Patents

Heterociclos antagonistas de mchr1

Info

Publication number
AR051802A1
AR051802A1 ARP050105335A ARP050105335A AR051802A1 AR 051802 A1 AR051802 A1 AR 051802A1 AR P050105335 A ARP050105335 A AR P050105335A AR P050105335 A ARP050105335 A AR P050105335A AR 051802 A1 AR051802 A1 AR 051802A1
Authority
AR
Argentina
Prior art keywords
optionally substituted
alkyl group
fluorine
group
benzofurane
Prior art date
Application number
ARP050105335A
Other languages
English (en)
Original Assignee
Astrazeneca Ab
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
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=36602060&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=AR051802(A1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Priority claimed from SE0403119A external-priority patent/SE0403119D0/sv
Application filed by Astrazeneca Ab filed Critical Astrazeneca Ab
Publication of AR051802A1 publication Critical patent/AR051802A1/es

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    • 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/04Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
    • AHUMAN NECESSITIES
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    • A61P15/00Drugs for genital or sexual disorders; Contraceptives
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    • A61P25/08Antiepileptics; Anticonvulsants
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    • A61P25/00Drugs for disorders of the nervous system
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    • 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
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    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
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    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/18Antipsychotics, i.e. neuroleptics; Drugs for mania or schizophrenia
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    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/22Anxiolytics
    • AHUMAN NECESSITIES
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    • 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
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    • A61P25/30Drugs for disorders of the nervous system for treating abuse or dependence
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
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    • A61P25/00Drugs for disorders of the nervous system
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    • A61P25/32Alcohol-abuse
    • AHUMAN NECESSITIES
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    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/30Drugs for disorders of the nervous system for treating abuse or dependence
    • A61P25/34Tobacco-abuse
    • AHUMAN NECESSITIES
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    • A61P25/30Drugs for disorders of the nervous system for treating abuse or dependence
    • A61P25/36Opioid-abuse
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    • 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
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    • A61P29/00Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • A61P29/02Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID] without antiinflammatory effect
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    • 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
    • C07D401/12Heterocyclic 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 chain containing hetero atoms as chain links
    • 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
    • C07D401/14Heterocyclic 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 three or more hetero 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
    • C07D405/14Heterocyclic 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 three or more hetero rings
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    • C07DHETEROCYCLIC COMPOUNDS
    • C07D413/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
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    • C07DHETEROCYCLIC COMPOUNDS
    • C07D417/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
    • C07D417/14Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing three or more hetero rings

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  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Medicinal Chemistry (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Neurosurgery (AREA)
  • Biomedical Technology (AREA)
  • Neurology (AREA)
  • Addiction (AREA)
  • Psychiatry (AREA)
  • Pain & Pain Management (AREA)
  • Diabetes (AREA)
  • Endocrinology (AREA)
  • Hematology (AREA)
  • Obesity (AREA)
  • Psychology (AREA)
  • Rheumatology (AREA)
  • Immunology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Emergency Medicine (AREA)
  • Hospice & Palliative Care (AREA)
  • Child & Adolescent Psychology (AREA)
  • Cardiology (AREA)
  • Reproductive Health (AREA)
  • Pulmonology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)

Abstract

Los compuestos de formula (1), procesos para preparar tales compuestos, su utilizacion en el tratamiento de la obesidad, trastornos siquiátricos, trastornos cognitivos, trastornos de la memoria, esquizofrenia, epilepsia y afecciones relacionadas, y trastornos neurologicos tales como demencia, esclerosis multiple, mal de Parkinson, corea de Huntington y mal de Alzheimer y trastornos relacionados con el dolor y a composiciones farmacéuticas que los contienen. Reivindicacion 1: Un compuesto de formula (1), A representa N, un grupo alquilo C1-4, un grupo alquenilo C2-4, cicloalquilo C3-8, adamantilo, azetidinilo, pirrolidinilo, piperidinilo, piperazinilo, morfolinilo, 1,3-oxazidinilo, tetrahidro-piridinilo, o espiro[inden-1,4'- piperidinilo]; donde dicho grupo alquilo C1-4 o grupo alquenilo C2-4 está opcionalmente sustituido con uno o más fluor; X representa un enlace o NR3; donde A y X ambos no presentan nitrogeno; donde cuando A es azetidinilo, 1,3-oxazidinilo, pirrolidinilo, piperidinilo, piperazinilo, morfolinilo, tetrahidropiridinilo, o espiro[1,4'-piperidinilo]; el átomo de nitrogeno en A está directamente unido a C(O); R1 y R2 representan independientemente H, alquilo C1-6, un grupo alquenilo C2-6, cicloalquilo C3-10, CONRaRb en el cual Ra y Rb representan independientemente H, un grupo alquilo C1-4 o Ra y Rb, junto con el nitrogeno al cual están unidos, forman un anillo heterocíclico de 4 a 8 miembros; fenilo o naftilo; o un grupo heterocíclico seleccionado entre pirrolilo, imidazolilo, furilo, tienilo, tiazolilo, isotiazolilo, tiadiazolilo, pirazolilo, oxazolilo, isoxazolilo, piridilo, pirazinilo, pirimidinilo, piridazinilo, quinolinilo, isoquinolilo, quinazolilo, indolilo, benzofuranilo, benzo[b]tienilo, benzimidazolilo, benzotiazolilo, 1,4-benzodioxinilo, 1,3-benzodioxolilo, piperidinilo, morfolinilo, 1,4-oxazepanilo, o 4,4-dioxotiomorfolinilo; donde R1 o R2 está opcionalmente sustituido con uno o más de los siguientes: ciano; halo; hidroxi; oxo; un grupo alquilo C1-4 opcionalmente sustituido con uno o más fluor; un grupo alcoxi C1-4 opcionalmente sustituido con uno o más fluor; un grupo NCORaRb o CONRaRb en el cual Ra y Rb representan independientemente un grupo alquilo C1-3; un grupo SO2alquiloC1-4, opcionalmente sustituido con uno o más fluor, un grupo arilo o heteroarilo seleccionado entre tiadiazolilo, pirazolilo, fenilo, fenoxi, 2-piridilo o 3-piridilo donde dicho grupo arilo o heteroarilo puede estar opcionalmente adicionalmente sustituido con uno o más de los siguientes; ciano; halo; hidroxi; un grupo alquilo C1-4 opcionalmente sustituido con uno o más fluor; un grupo alcoxi C1-4 opcionalmente sustituido con uno o más fluor; un grupo NCORaRb o CONRaRb en el que Ra y Rb representan independientemente un grupo alquilo C1-3; un grupo SO2alquiloC1-4, opcionalmente sustituido con uno o más fluor; R1 y/o R2 está unido opcionalmente a A por medio de oxígeno o por medio de un grupo alquilo C1-4, donde uno de los átomos de carbono en dicho grupo alquilo C1-4 opcionalmente se reemplaza con un átomo de oxígeno; Y representa NR3, C(R5R6) o un enlace; donde al menos uno de A, X o Y es N, NR3 o un anillo heterocíclico que contiene nitrogeno; R3, R5 y R6 representan independientemente H o un grupo alquilo C1-4, D representa (CH2)n, donde n es 0 o 1 y E representa (CH2)m, donde m es 0 o 1; R4 representa H o, cuando m y n ambos son 1, R4 representa H o F; Z representa 2,5-tienilo, 2,5-furilo, o pirrolilo, opcionalmente sustituido con uno o más de los siguientes: ciano, halo, un grupo alquilo C1-4 opcionalmente sustituido con uno o más fluor, un grupo alcoxi C1-4 opcionalmente sustituido con uno o más fluor; W representa fenilo, 2-piridilo o 3-piridilo cada uno de los cuales está opcionalmente sustituido con uno o más de los siguientes: ciano, halo, un grupo alquilo C1-4 opcionalmente sustituido con uno o más fluor, un grupo alcoxi C1-4 opcionalmente sustituido con uno o más fluor; un grupo trifluormetilsulfonilo o un grupo 2,2'-difluor-oxolanilo (fusionado con dos átomos de carbono aromáticos adyacentes en W); así como también sus tautomeros, isomeros opticos y sus racematos así como también sus sales farmacéuticamente aceptables; con la condicion de que cuando Y representa NR3 entonces A-X no representa OCH2, CH2CH2 o CH=CH, donde cada átomo de carbono puede estar opcionalmente sustituido con 1 o 2 grupos metilo y/o 1 o 2 fluor.
ARP050105335A 2004-12-21 2005-12-19 Heterociclos antagonistas de mchr1 AR051802A1 (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
SE0403119A SE0403119D0 (sv) 2004-12-21 2004-12-21 Therapeutic agents
SE0501686 2005-07-15

Publications (1)

Publication Number Publication Date
AR051802A1 true AR051802A1 (es) 2007-02-07

Family

ID=36602060

Family Applications (1)

Application Number Title Priority Date Filing Date
ARP050105335A AR051802A1 (es) 2004-12-21 2005-12-19 Heterociclos antagonistas de mchr1

Country Status (6)

Country Link
US (1) US20080306055A1 (es)
EP (1) EP1831194A4 (es)
JP (1) JP2008524325A (es)
AR (1) AR051802A1 (es)
TW (1) TW200635589A (es)
WO (1) WO2006068594A1 (es)

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WO2005063704A1 (ja) * 2003-12-25 2005-07-14 Ono Pharmaceutical Co., Ltd. アゼチジン環化合物およびその医薬
WO2010080864A1 (en) * 2009-01-12 2010-07-15 Array Biopharma Inc. Piperidine-containing compounds and use thereof
SA110310332B1 (ar) * 2009-05-01 2013-12-10 Astrazeneca Ab مركبات ميثانون (3 استبدال -ازيتيدين -1-يل )(5- فينيل -1، 3، 4- أوكساديازول -2-يل )
WO2012004588A2 (en) 2010-07-06 2012-01-12 Astrazeneca Ab Therapeutic agents 976
WO2012113103A1 (en) 2011-02-25 2012-08-30 Helsinn Healthcare S.A. Asymmetric ureas and medical uses thereof
WO2012177893A2 (en) 2011-06-24 2012-12-27 Amgen Inc. Trpm8 antagonists and their use in treatments
AU2012272898A1 (en) 2011-06-24 2013-04-11 Amgen Inc. TRPM8 antagonists and their use in treatments
UY34194A (es) 2011-07-15 2013-02-28 Astrazeneca Ab ?(3-(4-(espiroheterocíclico)metil)fenoxi)azetidin-1-il)(5-(fenil)-1,3,4-oxadiazol-2-il)metanona en el tratamiento de la obesidad?
WO2013078413A1 (en) * 2011-11-22 2013-05-30 The United States Of America, As Represented By The Secretary, Department Of Health And Human Services Modulators of lipid storage
US8952009B2 (en) 2012-08-06 2015-02-10 Amgen Inc. Chroman derivatives as TRPM8 inhibitors
JP6223563B2 (ja) 2013-10-14 2017-11-01 エーザイ・アール・アンド・ディー・マネジメント株式会社 選択的に置換されたキノリン化合物
RU2671496C2 (ru) 2013-10-14 2018-11-01 Эйсай Ар Энд Ди Менеджмент Ко., Лтд. Производные 5-пиперидин-8-цианохинолина
TW201627299A (zh) * 2014-10-29 2016-08-01 美國禮來大藥廠 用於抑制微粒體前列腺素e合成酶1之新穎羧酸化合物
BR112017015291B1 (pt) 2015-01-16 2022-10-11 Nederlandse Organisatie Voor Toegepast- Natuurwetenschappelijk Onderzoek Tno Método para preparar um estabilizador de nitrocelulose derivado de ureia aromática
BR112018014788B1 (pt) 2016-03-22 2022-03-22 Helsinn Healthcare Sa Composto e uso de um composto

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SE9902987D0 (sv) * 1999-08-24 1999-08-24 Astra Pharma Prod Novel compounds
US6727264B1 (en) * 2001-07-05 2004-04-27 Synaptic Pharmaceutical Corporation Substituted anilinic piperidines as MCH selective antagonists
EP1432693A2 (en) * 2001-10-01 2004-06-30 Taisho Pharmaceutical Co. Ltd. Mch receptor antagonists
JP2005506338A (ja) * 2001-10-09 2005-03-03 ニューロクライン バイオサイエンシーズ, インコーポレイテッド メラノコルチンレセプターのリガンドならびに関連の配合物および方法
JP2005532368A (ja) * 2002-06-12 2005-10-27 アボット・ラボラトリーズ メラニン濃縮ホルモン受容体の拮抗薬
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EP1464335A3 (en) * 2003-03-31 2007-05-09 Taisho Pharmaceutical Co. Ltd. Quinoline, tetrahydroquinoline and pyrimidine derivatives as mch antagonist

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WO2006068594A1 (en) 2006-06-29
EP1831194A1 (en) 2007-09-12
TW200635589A (en) 2006-10-16
US20080306055A1 (en) 2008-12-11
JP2008524325A (ja) 2008-07-10
EP1831194A4 (en) 2009-12-02

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