EA200100783A1 - Соединения - агонисты дофаминовых рецепторов d1 - Google Patents

Соединения - агонисты дофаминовых рецепторов d1

Info

Publication number
EA200100783A1
EA200100783A1 EA200100783A EA200100783A EA200100783A1 EA 200100783 A1 EA200100783 A1 EA 200100783A1 EA 200100783 A EA200100783 A EA 200100783A EA 200100783 A EA200100783 A EA 200100783A EA 200100783 A1 EA200100783 A1 EA 200100783A1
Authority
EA
Eurasian Patent Office
Prior art keywords
hydrogen
halogen
together form
cyclohexane ring
compounds
Prior art date
Application number
EA200100783A
Other languages
English (en)
Other versions
EA004745B1 (ru
Inventor
Гари Тилбрук
Original Assignee
Синес Лимитед
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 Синес Лимитед filed Critical Синес Лимитед
Publication of EA200100783A1 publication Critical patent/EA200100783A1/ru
Publication of EA004745B1 publication Critical patent/EA004745B1/ru

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D223/00Heterocyclic compounds containing seven-membered rings having one nitrogen atom as the only ring hetero atom
    • C07D223/14Heterocyclic compounds containing seven-membered rings having one nitrogen atom as the only ring hetero atom condensed with carbocyclic rings or ring systems
    • C07D223/16Benzazepines; Hydrogenated benzazepines
    • 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
    • A61P25/28Drugs 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
    • 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D409/00Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
    • C07D409/02Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
    • C07D409/04Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings directly linked by a ring-member-to-ring-member bond

Landscapes

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

Abstract

Данное изобретение предлагает 2,3,4,5-тетрагидро-1H-3-бензазепины общей формулы (I), где Rпредставляет собой водород, галоген, C-C-алкил или CF; Rпредставляет собой водород, метил или низший алкенил с 3-5 атомами углерода; Rи Rвместе образуют фурановое, дигидрофурановое, тиофеновое, дигидротиофеновое, циклопентановое или циклогексановое кольцо и Rпредставляет собой водород или Rи Rвместе образуют фурановое, дигидрофурановое, тиофеновое, дигидротиофеновое, циклопентановое или циклогексановое кольцо и Rпредставляет собой водород; Rпредставляет собой водород, галоген, CF, CN, NO, или NH; Rпредставляет собой водород, галоген, CF, CN, NOили NH. Исключена определенная комбинация заместителей: R=H, R=H, и Rи R, вместе образуют циклогексановое кольцо, а именно 1-(5,6,7,8-тетрагидронафтален-2-ил)-2,3,4,5-тетрагидро-1H-бензол[d]азепин-7,8-диол. Соединения по изобретению предложены в качестве терапевтических агентов, которые селективно позитивно взаимодействуют с постсинаптическими дофаминовыми рецепторами D1 в полосатом теле, прямо или косвенно, (называемые дофаминовыми D1-агонистами) и являются чрезвычайно полезными в качестве антипаркинсонических агентов.Международная заявка была опубликована вместе с отчетом о международном поиске.
EA200100783A 1999-02-17 2000-02-17 Тетрагидробензазепиновые производные в качестве агонистов дофаминовых рецепторов d1 EA004745B1 (ru)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
GBGB9903671.7A GB9903671D0 (en) 1999-02-17 1999-02-17 Dopamine D-1 receptor agonist compounds
PCT/GB2000/000570 WO2000049000A1 (en) 1999-02-17 2000-02-17 Dopamine d1 receptor agonist compounds

Publications (2)

Publication Number Publication Date
EA200100783A1 true EA200100783A1 (ru) 2002-02-28
EA004745B1 EA004745B1 (ru) 2004-08-26

Family

ID=10847990

Family Applications (1)

Application Number Title Priority Date Filing Date
EA200100783A EA004745B1 (ru) 1999-02-17 2000-02-17 Тетрагидробензазепиновые производные в качестве агонистов дофаминовых рецепторов d1

Country Status (17)

Country Link
EP (1) EP1157009A1 (ru)
JP (1) JP2002537288A (ru)
KR (1) KR20010108228A (ru)
CN (1) CN1142916C (ru)
AU (1) AU767332B2 (ru)
BR (1) BR0008329A (ru)
CA (1) CA2363695A1 (ru)
CZ (1) CZ20012973A3 (ru)
EA (1) EA004745B1 (ru)
GB (1) GB9903671D0 (ru)
HU (1) HUP0200057A3 (ru)
IL (1) IL144810A0 (ru)
MX (1) MXPA01008294A (ru)
NO (1) NO20013978L (ru)
PL (1) PL349838A1 (ru)
WO (1) WO2000049000A1 (ru)
ZA (1) ZA200106478B (ru)

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB0130576D0 (en) * 2001-12-20 2002-02-06 Cenes Ltd Dopamine D1 receptor agonist pro-drug compounds & derivatives
GEP20125566B (en) * 2005-07-15 2012-07-10 Amr Technology Inc Aryl-and heteroaryl-substituded tetrahydro-benzazepines and use thereof to block reuptake of norepinephrine, dopamine and serotonin
CN101296943A (zh) * 2005-08-03 2008-10-29 米亚·利维特 通过多巴胺d1r激动剂杀伤人类淋巴瘤和白血病癌细胞和tcr活化的人类正常细胞
CN101684096A (zh) * 2008-09-23 2010-03-31 中国科学院上海药物研究所 一类新型苯并氮杂卓类化合物及其制备方法和用途
CN102276531A (zh) * 2011-05-30 2011-12-14 扬子江药业集团广州海瑞药业有限公司 一种甲磺酸非诺多泮的制备方法
CN105324376B (zh) 2013-06-27 2017-06-23 辉瑞大药厂 杂芳族化合物及其作为多巴胺d1配体的用途

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB1561305A (en) * 1975-07-02 1980-02-20 Smithkline Corp Benzazepine derivatives and pharmeceutical compositions containing them
US4111957A (en) * 1977-02-02 1978-09-05 Smithkline Corporation Substituted 1-thienyl and furyl-2,3,4,5-tetrahydro-1H-3-benzazepine compounds
US4265889A (en) * 1978-05-05 1981-05-05 Smithkline Corporation 6-Lower alkyl-7,8-dihydroxy-1-phenyl-2,3,4,5-tetrahydro-1H-3-benzazepines
US4707483A (en) * 1985-12-20 1987-11-17 Smithkline Beckman Corporation 1-phenyl-3-benzazepines and their use for treating gastrointestinal motility disorders
US4861771A (en) * 1989-01-27 1989-08-29 Smithkline Beckman Corporation Carbamates of 6-chloro-7,8-dihydroxy-1-(4'-hydroxyphenyl)-2,3,4,5-tetrahydro-1H-3-benzazepine as prodrugs

Also Published As

Publication number Publication date
MXPA01008294A (es) 2002-07-02
KR20010108228A (ko) 2001-12-07
NO20013978D0 (no) 2001-08-15
PL349838A1 (en) 2002-09-23
AU2563200A (en) 2000-09-04
CN1341102A (zh) 2002-03-20
EA004745B1 (ru) 2004-08-26
BR0008329A (pt) 2002-01-29
GB9903671D0 (en) 1999-04-14
JP2002537288A (ja) 2002-11-05
CZ20012973A3 (cs) 2002-01-16
HUP0200057A2 (en) 2002-08-28
HUP0200057A3 (en) 2004-03-29
IL144810A0 (en) 2002-06-30
WO2000049000A1 (en) 2000-08-24
CN1142916C (zh) 2004-03-24
CA2363695A1 (en) 2000-08-24
AU767332B2 (en) 2003-11-06
ZA200106478B (en) 2002-02-07
EP1157009A1 (en) 2001-11-28
NO20013978L (no) 2001-08-15

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MM4A Lapse of a eurasian patent due to non-payment of renewal fees within the time limit in the following designated state(s)

Designated state(s): AM AZ BY KZ KG MD TJ TM RU