ES2097496T3 - Derivados acilaminoindol como agonistas de 5-ht1. - Google Patents

Derivados acilaminoindol como agonistas de 5-ht1.

Info

Publication number
ES2097496T3
ES2097496T3 ES93907096T ES93907096T ES2097496T3 ES 2097496 T3 ES2097496 T3 ES 2097496T3 ES 93907096 T ES93907096 T ES 93907096T ES 93907096 T ES93907096 T ES 93907096T ES 2097496 T3 ES2097496 T3 ES 2097496T3
Authority
ES
Spain
Prior art keywords
aryl
alkyl
alkylaryl
hydrogen
pct
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
ES93907096T
Other languages
English (en)
Inventor
John E Macor
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.)
Pfizer Inc
Original Assignee
Pfizer Inc
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 Pfizer Inc filed Critical Pfizer Inc
Application granted granted Critical
Publication of ES2097496T3 publication Critical patent/ES2097496T3/es
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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
    • C07D403/06Heterocyclic 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 only aliphatic carbon atoms
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/04Centrally acting analgesics, e.g. opioids
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/06Antimigraine agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/20Hypnotics; Sedatives
    • 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/26Psychostimulants, e.g. nicotine, cocaine
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00Drugs for disorders of the metabolism
    • A61P3/04Anorexiants; Antiobesity agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • A61P9/12Antihypertensives
    • 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
    • C07D403/14Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing three or more hetero rings

Landscapes

  • Health & Medical Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Veterinary Medicine (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Public Health (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Engineering & Computer Science (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Biomedical Technology (AREA)
  • Neurosurgery (AREA)
  • Neurology (AREA)
  • Pain & Pain Management (AREA)
  • Psychiatry (AREA)
  • Anesthesiology (AREA)
  • Cardiology (AREA)
  • Child & Adolescent Psychology (AREA)
  • Diabetes (AREA)
  • Hematology (AREA)
  • Obesity (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Indole Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Supply Devices, Intensifiers, Converters, And Telemotors (AREA)
  • Materials For Photolithography (AREA)
  • Soft Magnetic Materials (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Polysaccharides And Polysaccharide Derivatives (AREA)
  • Pyrrole Compounds (AREA)

Abstract

COMPUESTOS DE FORMULA (I) DONDE N ES 0, 1 O 2; M ES 0 O 1; Y Y W SON CADA UNO UN RESIDUO AMINOACIDO; R1 ES HIDROGENO, ALQUILO C1-C6, ALQUENILO C3-C6, ALQUINILO C3-C6, ARILO, ALQUILARILO C1-C3, O ALQUILHETEROARILO C1-C3, Y -(CH2)PR3; R2 ES CF3, ALQUILO C1-C6, ARILO, ALQUILARILO C1-C3, Y -OR5; R3 ES CIANO, TRIFLUOROMETILO, O -OR4; R4 ES HIDROGENO, ALQUILO C1-C6, ALQUILARILO C1-C3, O ARILO; R5 ES ALQUILO C1-C6, ALQUILARILO C1-C3, O ARILO; R6 ES HIDROGENO, -OR7, O -NHCOR7; R7 ES HIDROGENO, ALQUILO C1 A C6, ARILO, O ALQUILO-ARILO C1 A C3; P ES 1,2, O 3; Y LOS GRUPOS ARILO ANTERIORES Y LAS FRACCIONES ARILO DE LOS GRUPOS ALQUILO-ARILO SON SELECCIONADOS INDEPENDIENTEMENTE DE FENILO Y FENILO SUSTITUIDO, EN DONDE DICHO FENILO SUSTITUIDO PUEDE SER SUSTITUIDO CON UNO A TRES GRUPOS SELECCIONADOS DE ALQUILO C1 A C4, HALOGENO, HIDROXI, CIANO, CARBOXIAMIDA, NITRO, Y ALCOXI C1 A C4 Y LAS SALES FARMACEUTICAMENTE ACEPTABLES DE ELLOS. ESTOS COMPUESTOS SE USAN EN TRATAMIENTO DE MIGRAÑA Y OTROS DESORDENES. ESTOSCOMPUESTOS SE USAN COMO PSICOTERAPEUTICOS Y SON POTENTES AGONISTAS (5-HT1) DE SEROTONINA Y SE PUEDEN USAR EN EL TRATAMIENTO DE DEPRESION, ANSIEDAD, DESORDENES ALIMENTARIOS, OBESIDAD, ABUSO DE DROGAS, CEFALEA EN RACIMO, MIGRAÑA, DOLOR, Y HEMICRANIA PAROXISMICA CRONICA Y CEFALEA ASOCIADA CON DESORDENES VASCULARES, Y OTROS DESORDENES SURGIDOS DE DEFICIENTE NEUROTRANSMISION SEROTONERGICA. LOS COMPUESTOS TAMBIEN PUEDEN SER USADOS COMO ANTIHIPERTENSIVOS Y VASODILATADORES QUE ACTUAN CENTRALMENTE.
ES93907096T 1992-04-10 1993-03-04 Derivados acilaminoindol como agonistas de 5-ht1. Expired - Lifetime ES2097496T3 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US86638292A 1992-04-10 1992-04-10

Publications (1)

Publication Number Publication Date
ES2097496T3 true ES2097496T3 (es) 1997-04-01

Family

ID=25347493

Family Applications (1)

Application Number Title Priority Date Filing Date
ES93907096T Expired - Lifetime ES2097496T3 (es) 1992-04-10 1993-03-04 Derivados acilaminoindol como agonistas de 5-ht1.

Country Status (31)

Country Link
US (1) US5498626A (es)
EP (1) EP0635015B1 (es)
JP (1) JP2544704B2 (es)
KR (1) KR0179074B1 (es)
CN (1) CN1038506C (es)
AT (1) ATE148465T1 (es)
AU (1) AU670270B2 (es)
BR (1) BR9306221A (es)
CA (1) CA2132706C (es)
CZ (1) CZ282653B6 (es)
DE (1) DE69307875T2 (es)
DK (1) DK0635015T3 (es)
EG (1) EG20466A (es)
ES (1) ES2097496T3 (es)
FI (2) FI111256B (es)
GR (1) GR3022767T3 (es)
HR (1) HRP930753B1 (es)
HU (1) HUT64060A (es)
IL (1) IL105309A0 (es)
MX (1) MX9301996A (es)
MY (1) MY115278A (es)
NO (1) NO309860B1 (es)
NZ (1) NZ251047A (es)
PL (1) PL172232B1 (es)
RU (1) RU2110516C1 (es)
SK (1) SK278182B6 (es)
TW (1) TW394769B (es)
UA (1) UA34452C2 (es)
WO (1) WO1993021180A1 (es)
YU (1) YU48916B (es)
ZA (1) ZA932536B (es)

Families Citing this family (21)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5545644A (en) * 1990-10-15 1996-08-13 Pfizer Inc. Indole derivatives
US5607951A (en) * 1990-10-15 1997-03-04 Pfizer Inc Indole derivatives
US5559129A (en) * 1990-10-15 1996-09-24 Pfizer Inc Indole derivatives
US5578612A (en) * 1990-10-15 1996-11-26 Pfizer Inc. Indole derivatives
US5559246A (en) * 1990-10-15 1996-09-24 Pfizer Inc. Indole derivatives
AU670579B2 (en) 1992-04-07 1996-07-25 Pfizer Inc. Indole derivatives as 5-HT1 agonists
US6380233B1 (en) 1992-04-07 2002-04-30 Pfizer Inc Indole derivatives as 5-HT1 agonists
ES2070772B1 (es) * 1993-08-09 1996-02-16 Pfizer Derivados de acilaminoindol
DE69413240T2 (de) * 1993-08-31 1999-02-04 Pfizer 5-arylindolderivate
GB9402016D0 (en) * 1994-02-02 1994-03-30 Merck Sharp & Dohme Therapeutic agents
GB9402011D0 (en) * 1994-02-02 1994-03-30 Merck Sharp & Dohme Therapeutic agents
US5965582A (en) * 1994-08-03 1999-10-12 Asta Medica Aktiengesellschaft N-benzylindole and benzopyrazole derivatives with anti-asthmatic, anti-allergic, anti-inflammatory and immunemodulating effect
GB9417310D0 (en) 1994-08-27 1994-10-19 Pfizer Ltd Therapeutic agents
GB9420503D0 (en) * 1994-10-11 1994-11-23 Pfizer Ltd Therapeutic agents
GB9420529D0 (en) 1994-10-12 1994-11-30 Pfizer Ltd Indoles
WO1999053956A1 (fr) * 1998-04-16 1999-10-28 Yamanouchi Pharmaceutical Co., Ltd. Remedes contre l'obesite
US5994352A (en) * 1998-11-13 1999-11-30 Pfizer Inc. 5-arylindole derivatives
AU2004206909A1 (en) * 2003-01-22 2004-08-05 Gtx Inc. Treating androgen deficiency in female (ADIF)-associated conditions with sarms
MX2010006162A (es) * 2007-12-07 2010-06-25 Pfizer Sal tosilato de una trans-n-isobutil-3-fluoro-3-[3-fluoro-4-(pirro lidin-1-il-metil)fenil]ciclobutanocarboxamida.
CA2891122C (en) 2012-11-14 2021-07-20 The Johns Hopkins University Methods and compositions for treating schizophrenia
CN103408535B (zh) * 2013-08-13 2016-03-02 张家港威胜生物医药有限公司 一种依来曲普坦中间体-5-溴-3-(n-甲基吡咯啉-2-基甲基)-1h-吲哚合成工艺

Family Cites Families (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
ZA795239B (en) * 1978-10-12 1980-11-26 Glaxo Group Ltd Heterocyclic compounds
GB2083463B (en) * 1980-08-12 1984-05-10 Glaxo Group Ltd Heterocyclic compounds
ZA815541B (en) * 1980-08-12 1983-03-30 Glaxo Group Ltd Heterocyclic compounds
GB8600397D0 (en) * 1986-01-08 1986-02-12 Glaxo Group Ltd Chemical compounds
GB8719167D0 (en) * 1987-08-13 1987-09-23 Glaxo Group Ltd Chemical compounds
GB8724912D0 (en) * 1987-10-23 1987-11-25 Wellcome Found Indole derivatives
GB8819024D0 (en) * 1988-08-10 1988-09-14 Glaxo Group Ltd Chemical compounds
IL96891A0 (en) * 1990-01-17 1992-03-29 Merck Sharp & Dohme Indole-substituted five-membered heteroaromatic compounds,their preparation and pharmaceutical compositions containing them
CA2042295A1 (fr) * 1990-05-15 1991-11-16 Jacques Chauveau Derives de mediateurs endogenes, leurs sels, procede de preparation, applications, et compositions les renfermant
HU219974B (hu) * 1990-06-07 2001-10-28 Astrazeneca Ab, Heterociklusos csoporttal helyettesített indolszármazék, előállítása és a vegyületet hatóanyagként tartalmazó gyógyszerkészítmények
HUT64326A (en) * 1990-10-15 1993-12-28 Pfizer Process for production indole derivatives and pharmaceutical preparations containing these compounds
US5208248A (en) * 1991-01-11 1993-05-04 Merck Sharpe & Dohme, Ltd. Indazole-substituted five-membered heteroaromatic compounds
SK278998B6 (sk) * 1991-02-01 1998-05-06 Merck Sharp & Dohme Limited Deriváty imidazolu, triazolu a tetrazolu, spôsob i
DE69230803T2 (de) * 1991-11-25 2000-12-07 Pfizer 5-(hetero- oder carbocyclylamino)-indol derivate, deren herstellung und deren verwendung als 5-ht1 agonisten

Also Published As

Publication number Publication date
AU3782193A (en) 1993-11-18
NZ251047A (en) 1996-09-25
SK120794A3 (en) 1995-05-10
NO309860B1 (no) 2001-04-09
PL172232B1 (pl) 1997-08-29
UA34452C2 (uk) 2001-03-15
TW394769B (en) 2000-06-21
BR9306221A (pt) 1998-06-30
DE69307875T2 (de) 1997-05-22
JPH07501831A (ja) 1995-02-23
CN1038506C (zh) 1998-05-27
FI111256B (fi) 2003-06-30
HRP930753A2 (en) 1994-10-31
YU48916B (sh) 2002-11-15
RU2110516C1 (ru) 1998-05-10
EP0635015A1 (en) 1995-01-25
ATE148465T1 (de) 1997-02-15
ZA932536B (en) 1994-10-08
CZ282653B6 (cs) 1997-08-13
SK278182B6 (en) 1996-03-06
FI931613A0 (fi) 1993-04-08
HUT64060A (en) 1993-11-29
CA2132706A1 (en) 1993-10-28
GR3022767T3 (en) 1997-06-30
EP0635015B1 (en) 1997-01-29
YU25593A (sh) 1996-10-09
MX9301996A (es) 1994-03-31
CA2132706C (en) 1998-08-04
US5498626A (en) 1996-03-12
CZ247794A3 (en) 1995-07-12
JP2544704B2 (ja) 1996-10-16
KR950700903A (ko) 1995-02-20
CN1080288A (zh) 1994-01-05
HRP930753B1 (en) 2000-10-31
FI20010214A (fi) 2001-02-05
NO943803L (no) 1994-10-07
AU670270B2 (en) 1996-07-11
RU94045902A (ru) 1996-08-27
MY115278A (en) 2003-05-31
EG20466A (en) 1999-05-31
WO1993021180A1 (en) 1993-10-28
IL105309A0 (en) 1993-08-18
FI931613A (fi) 1993-10-11
DK0635015T3 (da) 1997-03-17
KR0179074B1 (ko) 1999-03-20
HU9301048D0 (en) 1993-06-28
NO943803D0 (no) 1994-10-07
DE69307875D1 (de) 1997-03-13

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