ES2159345T3 - Indazolcarboxamidas. - Google Patents

Indazolcarboxamidas.

Info

Publication number
ES2159345T3
ES2159345T3 ES96301682T ES96301682T ES2159345T3 ES 2159345 T3 ES2159345 T3 ES 2159345T3 ES 96301682 T ES96301682 T ES 96301682T ES 96301682 T ES96301682 T ES 96301682T ES 2159345 T3 ES2159345 T3 ES 2159345T3
Authority
ES
Spain
Prior art keywords
sub
rent
naftil
sup
phenyl
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
ES96301682T
Other languages
English (en)
Inventor
John Thomas Catlow
Marlene Lois Cohen
Michael John Martinelli
John Mehnert Schaus
Steven Phillip Swanson
Dennis Charles Thompson
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.)
Eli Lilly and Co
Original Assignee
Eli Lilly and Co
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 US08/485,956 external-priority patent/US5654320A/en
Application filed by Eli Lilly and Co filed Critical Eli Lilly and Co
Application granted granted Critical
Publication of ES2159345T3 publication Critical patent/ES2159345T3/es
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
    • C07D231/54—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings condensed with carbocyclic rings or ring systems
    • C07D231/56—Benzopyrazoles; Hydrogenated benzopyrazoles
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00—Drugs for disorders of the alimentary tract or the digestive 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
    • 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
    • A61P25/28—Drugs 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
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system
    • A61P9/06—Antiarrhythmics
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D401/00—Heterocyclic 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
    • C07D401/02—Heterocyclic 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
    • C07D401/12—Heterocyclic 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

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Veterinary Medicine (AREA)
  • Biomedical Technology (AREA)
  • Neurology (AREA)
  • Neurosurgery (AREA)
  • Psychiatry (AREA)
  • Cardiology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Hospice & Palliative Care (AREA)
  • Anesthesiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Macromolecular Compounds Obtained By Forming Nitrogen-Containing Linkages In General (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Paper (AREA)
  • Luminescent Compositions (AREA)

Abstract

LAS INDAZOLCARBOXAMIDAS SE USAN COMO ANTAGONISTAS Y AGONISTAS PARCIALES DEL RECEPTOR DE LA SEROTONINA 5-HT4 Y PROPORCIONAN METODOS TERAPEUTICOS PARA EL TRATAMIENTO DE LOS DESORDENES CAUSADOS POR O AFECTADOS POR UNA DISFUNCION DEL RECEPTOR 5-HT4. LAS INDAZOLCARBOXAMIDAS TIENEN POR FORMULA EN DONDE R ES HIDROGENO, C{SUB,1}-C{SUB,6} ALQUIL, C{SUB,3}-C{SUB,6} CICLOALQUIL; R{SUP,1} ES HIDROGENO, HALO, C{SUB,1}-C{SUB,4} ALQUIL, HIDROXI, C{SUB,1}-C{SUB,4} ALCOXI O ALQUILTIO, CIANO, TRIFLUOROMETIL, CARBOXAMIDO, MONO- O DI(C{SUB,1}-C{SUB,4} ALQUIL)CARBOXAMIDO; M, N Y O SON INDEPENDIENTEMENTE 0-5, DE MODO QUE LA SUMA DE M,N Y O SEA 2-5; R{SUP,2} ES HIDROGENO O C{SUB,1}-C{SUB,4} ALQUIL; R{SUP,3} Y R{SUP,4} SE COMBINAN JUNTO CON EL ATOMO DE NITROGENO AL CUAL ESTAN ADHERIDOS PARA FORMAR 1-PIRROLIDINIL, 1PIPERAZINIL, 1,2,3,4 TETRAHIDRO-2-ISOQUINOLINIL, 2,3-DIHIDRO-1INDOLINIL, 4-MORFOLINIL, 1-PIPERIDINIL O 1-HEXAMETILENIMINIL, SUSTITUIDO CON FENIL, NAFTIL, (FENIL O NAFTIL) (C{SUB,1}-C{SUB,3} ALQUIL), (FENIL O NAFTIL) (C{SUB,1}-C{SUB,3} ALCANOIL), AMINO, MONO- O DI(C{SUB,1}-C{SUB,4} ALQUIL)AMINO O UN GRUPO DE LA FORMULA -NH-Y-R{SUP,5}; CON TAL QUE UN GRUPO PIPERAZINIL O MORFOLINIL NO PUEDA SER SUSTITUIDO CON AMINO, MONOO DI(C{SUB,1}-C{SUB,4} ALQUIL)AMINO O -NH-Y-R{SUP,5}; EN DONDE UN GRUPO FENIL O NAFTIL ES SUSTITUIDO O NO SUSTITUIDO CON 1-3 HALO, C{SUB,1}-C{SUB,3} ALQUIL O GRUPOS C{SUB,1}-C{SUB,3} DE ALCOXI; Y ES CARBONIL, SULFONIL, AMINOCARBONIL U OXICARBONIL; R{SUP,5} ES C{SUB,1}-C{SUB,6} ALQUIL, C{SUB,3}-C{SUB,8} CICLOALQUIL, C{SUB,6}-C{SUB,11} BICICLO- O TRICICLOALQUIL, (FENIL O NAFTIL) (C{SUB,1}-C{SUB,3} ALQUIL), FENIL O NAFTIL; EN DONDE UN GRUPO CICLOALQUIL, BICICLO- O TRICICLOALQUIL, FENIL O NAFTIL ES SUSTITUIDO O NO SUSTITUIDO CON GRUPOS DE 1-3 HIDROXI, HALO, C{SUB,1}-C{SUB,3} ALQUIL O C{SUB,1}-C{SUB,3} ALCOXI; O SALES DE ELLAS FARMACEUTICAMENTE ACEPTABLES.
ES96301682T 1995-03-16 1996-03-12 Indazolcarboxamidas. Expired - Lifetime ES2159345T3 (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US40511995A 1995-03-16 1995-03-16
US08/485,956 US5654320A (en) 1995-03-16 1995-06-07 Indazolecarboxamides

Publications (1)

Publication Number Publication Date
ES2159345T3 true ES2159345T3 (es) 2001-10-01

Family

ID=27018928

Family Applications (1)

Application Number Title Priority Date Filing Date
ES96301682T Expired - Lifetime ES2159345T3 (es) 1995-03-16 1996-03-12 Indazolcarboxamidas.

Country Status (23)

Country Link
US (2) US5798367A (es)
EP (1) EP0732333B1 (es)
JP (1) JPH11502230A (es)
CN (1) CN1112923C (es)
AT (1) ATE203748T1 (es)
AU (1) AU700842B2 (es)
BR (1) BR9608223A (es)
CA (1) CA2215359A1 (es)
DE (1) DE69614164T2 (es)
DK (1) DK0732333T3 (es)
EA (1) EA000699B1 (es)
ES (1) ES2159345T3 (es)
GR (1) GR3037029T3 (es)
HU (1) HU223973B1 (es)
IL (1) IL117438A (es)
NO (1) NO312833B1 (es)
NZ (1) NZ315971A (es)
PL (1) PL183867B1 (es)
PT (1) PT732333E (es)
RO (1) RO119617B1 (es)
SK (1) SK283924B6 (es)
TR (1) TR199700956T1 (es)
WO (1) WO1996033713A1 (es)

Families Citing this family (17)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
IT1291569B1 (it) * 1997-04-15 1999-01-11 Angelini Ricerche Spa Indazolammidi come agenti serotoninergici
US5914405A (en) * 1997-10-07 1999-06-22 Eli Lilly And Company Process for preparing 3-substituted indazoles
US6069152A (en) * 1997-10-07 2000-05-30 Eli Lilly And Company 5-HT4 agonists and antagonists
ID28510A (id) * 1998-08-21 2001-05-31 Novartis Ag Formulasi oral yang baru untuk agonis atau antagonis 5-ht4
JP3366323B2 (ja) 1998-09-10 2003-01-14 エフ.ホフマン−ラ ロシュ アーゲー 5−ht4受容体アンタゴニストとしてのジヒドロベンゾジオキシンカルボキサミド及びケトン誘導体
AU2001270304A1 (en) 2000-07-07 2002-01-21 The Administrators Of The Tulane Educational Fund Methods for protection of stratified squamous epithelium against injury by noxious substances and novel agents for use therefor
MXPA03001210A (es) * 2000-08-07 2004-08-12 Smithkline Beecham Corp Uso de antagonista del receptor 5-ht4 en la fabricacion de un medicamento para la profilaxis o tratamiento de fibrilacion atrial.
EP1321142A1 (en) * 2001-12-21 2003-06-25 Novartis AG Solid pharmaceutical composition for oral administration of Tegaserod
ATE401072T1 (de) * 2002-02-12 2008-08-15 Organon Nv 1-arylsulfonyl-3-substituierte indol und indolinederivate verwendbar zur behandlung von erkrankungen des zentralnervensystem
ITMI20030287A1 (it) * 2003-02-18 2004-08-19 Acraf Indazolammidi dotate di attivita' analgesica metodo, per
ITMI20031468A1 (it) * 2003-07-18 2005-01-19 Acraf Farmaco ativo nel dolore neuropatico
ITMI20031467A1 (it) * 2003-07-18 2005-01-19 Acraf Farmaco attivo nel dolore neuropatico
SE0401969D0 (sv) * 2004-08-02 2004-08-02 Astrazeneca Ab Piperidine derivatives
WO2007010390A1 (en) * 2005-07-22 2007-01-25 Pfizer Japan Inc. Indazolecarboxamide derivatives as 5ht4 receptor agonists
WO2009106980A2 (en) * 2008-02-29 2009-09-03 Pfizer Inc. Indazole derivatives
GB201511382D0 (en) 2015-06-29 2015-08-12 Imp Innovations Ltd Novel compounds and their use in therapy
CN119997982A (zh) 2022-09-09 2025-05-13 迈里克斯制药有限公司 包含nmt抑制剂的抗体药物偶联物及其用途

Family Cites Families (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3145215A (en) * 1961-12-19 1964-08-18 Sterling Drug Inc Indazole derivatives
JP2795460B2 (ja) * 1988-06-20 1998-09-10 協和醗酵工業株式会社 ピラゾロアクリドン誘導体
NZ230068A (en) * 1988-07-29 1991-07-26 Dainippon Pharmaceutical Co Indazole-3-carboxylic acid esters and amides of diaza compounds having 6,7, or 8 ring members: preparatory processes and pharmaceutical compositions
EP0410509A1 (en) * 1989-07-25 1991-01-30 Duphar International Research B.V New substituted 1H-indazole-3-carboxamides
HU211081B (en) * 1990-12-18 1995-10-30 Sandoz Ag Process for producing indole derivatives as serotonin antagonists and pharmaceutical compositions containing the same
NZ243993A (en) * 1991-08-20 1994-10-26 Smithkline Beecham Plc Pharmaceutical compositions having 5-ht4 receptor antagonist activity and selected compounds having such activity
WO1993005040A1 (en) * 1991-09-12 1993-03-18 Smithkline Beecham Plc Azabicyclic compounds as 5-ht4 receptor antagonists
US5763459A (en) * 1992-05-23 1998-06-09 Smithkline Beecham P.L.C. Medicaments for the treatment of anxiety
JPH07508276A (ja) * 1992-06-27 1995-09-14 スミスクライン・ビーチャム・パブリック・リミテッド・カンパニー 5−ht↓4受容体アンタゴニスト含有医薬品
MX9305947A (es) * 1992-09-29 1994-06-30 Smithkline Beecham Plc Compuestos antagonistas del receptor 5-ht4, procedimiento para su preparacion y composiciones farmaceuticas que las contienen.
TW251287B (es) * 1993-04-30 1995-07-11 Nissei Co Ltd
GB9310582D0 (en) * 1993-05-22 1993-07-07 Smithkline Beecham Plc Pharmaceuticals

Also Published As

Publication number Publication date
EP0732333A1 (en) 1996-09-18
EA199700242A1 (ru) 1998-04-30
EA000699B1 (ru) 2000-02-28
NO312833B1 (no) 2002-07-08
JPH11502230A (ja) 1999-02-23
TR199700956T1 (xx) 1998-02-21
HUP9801386A2 (hu) 1999-06-28
AU6894896A (en) 1996-11-18
DE69614164T2 (de) 2002-04-25
IL117438A (en) 2001-12-23
RO119617B1 (ro) 2005-01-28
AU700842B2 (en) 1999-01-14
US5817676A (en) 1998-10-06
NO974221L (no) 1997-10-27
IL117438A0 (en) 1996-07-23
PT732333E (pt) 2001-11-30
SK283924B6 (sk) 2004-05-04
WO1996033713A1 (en) 1996-10-31
DE69614164D1 (de) 2001-09-06
SK124297A3 (en) 1998-02-04
DK0732333T3 (da) 2001-10-08
NO974221D0 (no) 1997-09-12
US5798367A (en) 1998-08-25
HU223973B1 (hu) 2005-03-29
EP0732333B1 (en) 2001-08-01
MX9706967A (es) 1997-11-29
NZ315971A (en) 1999-01-28
ATE203748T1 (de) 2001-08-15
HUP9801386A3 (en) 2000-03-28
PL322362A1 (en) 1998-01-19
GR3037029T3 (en) 2002-01-31
CN1112923C (zh) 2003-07-02
PL183867B1 (pl) 2002-07-31
BR9608223A (pt) 1998-12-29
CA2215359A1 (en) 1996-10-31
CN1183041A (zh) 1998-05-27

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