ES2098357T3 - Derivado de indol. - Google Patents

Derivado de indol.

Info

Publication number
ES2098357T3
ES2098357T3 ES91911488T ES91911488T ES2098357T3 ES 2098357 T3 ES2098357 T3 ES 2098357T3 ES 91911488 T ES91911488 T ES 91911488T ES 91911488 T ES91911488 T ES 91911488T ES 2098357 T3 ES2098357 T3 ES 2098357T3
Authority
ES
Spain
Prior art keywords
alkyl
group
carbonyl
carbon atoms
hydrogen atom
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
ES91911488T
Other languages
English (en)
Inventor
Hiroshi Nagase
Akira Mizusuna
Yoshihiro Onoda
Koji Kawai
Shu Matsumoto
Takashi Endo
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.)
Toray Industries Inc
Original Assignee
Toray Industries 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 Toray Industries Inc filed Critical Toray Industries Inc
Application granted granted Critical
Publication of ES2098357T3 publication Critical patent/ES2098357T3/es
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
    • C07D471/04—Ortho-condensed systems
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00—Drugs for immunological or allergic disorders
    • A61P37/02—Immunomodulators
    • A61P37/06—Immunosuppressants, e.g. drugs for graft rejection
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D217/00—Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems
    • C07D217/02—Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems with only hydrogen atoms or radicals containing only carbon and hydrogen atoms, directly attached to carbon atoms of the nitrogen-containing ring; Alkylene-bis-isoquinolines
    • C07D217/06—Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems with only hydrogen atoms or radicals containing only carbon and hydrogen atoms, directly attached to carbon atoms of the nitrogen-containing ring; Alkylene-bis-isoquinolines with the ring nitrogen atom acylated by carboxylic or carbonic acids, or with sulfur or nitrogen analogues thereof, e.g. carbamates
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D217/00—Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems
    • C07D217/22—Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to carbon atoms of the nitrogen-containing ring
    • C07D217/24—Oxygen atoms

Landscapes

  • Organic Chemistry (AREA)
  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Immunology (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Animal Behavior & Ethology (AREA)
  • Transplantation (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Plural Heterocyclic Compounds (AREA)

Abstract

Un procedimiento para preparar un derivado de indol representado por la **fórmula** en la cual R1 es un grupo alquilo C1-5, cicloalquil C4-7-alquilo, cicloalquenil C5-7-alquilo, aralquilo C7-14, trans-alquenilo C4-5, alilo, furanil-2-il-alquilo C1-5, tienil-2-il-alquilo C1-5, viniloxicarbonilo, tricloro-etoxicarbonilo, benciloxicarbonilo, alcanólo que tiene hasta 5 átomos de carbono, aralquil C7-14-carbonilo, 2-furólo, tiofeno-2-carbonilo, cicloalquil C4-7-carbonilo, alquenil C3-8-carbonilo, o anisólo,R2 es un átomo de hidrógeno o un grupo alquilo C1-3, bencilo o alcanólo que tiene hasta 5 átomos de carbono, R3 es un átomo de hidrógeno, fluor,cloro o bromo o ungruponitro o alquilo C1-5, R4 es un átomo de hidrógeno o un grupo alquilo C1-5, bencilo o fenilo, y R5 es un átomo de hidrógeno o un grupo hidroxi o alcanoiloxi que tiene hasta 5 átomos de carbono, y en el cual la fórmula general (1) abarca una forma (+), una forma (-) y una forma (+-) o una de sus sales farmacológicamente aceptables.
ES91911488T 1990-06-05 1991-06-05 Derivado de indol. Expired - Lifetime ES2098357T3 (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP14817990 1990-06-05
JP33545890 1990-11-29

Publications (1)

Publication Number Publication Date
ES2098357T3 true ES2098357T3 (es) 1997-05-01

Family

ID=26478480

Family Applications (1)

Application Number Title Priority Date Filing Date
ES91911488T Expired - Lifetime ES2098357T3 (es) 1990-06-05 1991-06-05 Derivado de indol.

Country Status (9)

Country Link
US (2) US5244904A (es)
EP (2) EP0735026A1 (es)
JP (1) JP3180344B2 (es)
KR (1) KR950002885B1 (es)
CA (2) CA2064853C (es)
DE (1) DE69125099T2 (es)
ES (1) ES2098357T3 (es)
FI (1) FI920480A0 (es)
WO (1) WO1991018901A1 (es)

Families Citing this family (24)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR100241662B1 (ko) * 1991-07-05 2000-03-02 지오르지오 스치니나 히드로이소퀴놀린 유도체
FR2697850B1 (fr) * 1992-11-10 1994-12-02 Univ Pasteur Nouveaux polypeptides ayant une activité de récepteur opioïde, acides nucléiques codant pour ces polypeptides et utilisations.
US5464841A (en) * 1993-11-08 1995-11-07 Univ Minnesota Use of delta opioid receptor antagonists to treat immunoregulatory disorders
US5578725A (en) * 1995-01-30 1996-11-26 Regents Of The University Of Minnesota Delta opioid receptor antagonists
AU6470996A (en) * 1995-07-20 1997-02-18 Toray Industries, Inc. 4a-aryldecahydroisoquinoline compounds and medicinal uses thereof
US5994327A (en) * 1995-11-17 1999-11-30 Astra Ab Process for the preparation of morphinans
US7232829B2 (en) * 2001-04-06 2007-06-19 Regents Of The University Of Minnesota Therapeutic compounds and methods
JP2005530685A (ja) * 2002-01-25 2005-10-13 リージェンツ オブ ザ ユニバーシティ オブ ミネソタ 選択的鎮痛剤
EP1768662A2 (en) 2004-06-24 2007-04-04 Novartis Vaccines and Diagnostics, Inc. Small molecule immunopotentiators and assays for their detection
WO2006045096A2 (en) * 2004-10-20 2006-04-27 Resverlogix Corp. Flavanoids and isoflavanoids for the prevention and treatment of cardiovascular diseases
AU2006275514B2 (en) 2005-07-29 2012-04-05 Resverlogix Corp. Pharmaceutical compositions for the prevention and treatment of complex diseases and their delivery by insertable medical devices
US8053440B2 (en) 2007-02-01 2011-11-08 Resverlogix Corporation Compounds for the prevention and treatment of cardiovascular diseases
CA2711103C (en) 2008-06-26 2016-08-09 Resverlogix Corp. Methods of preparing quinazolinone derivatives
EP2382194B1 (en) 2009-01-08 2014-03-12 Resverlogix Corp. Compounds for the prevention and treatment of cardiovascular disease
JP5795304B2 (ja) 2009-03-18 2015-10-14 レスバーロジックス コーポレイション 新規抗炎症剤
KR101892987B1 (ko) 2009-04-22 2018-08-30 리스버로직스 코퍼레이션 신규한 소염제
DK2773354T3 (da) 2011-11-01 2019-08-05 Resverlogix Corp Oralformuleringer med øjeblikkelig frigivelse for substituerede quinazolinoner
WO2014080290A2 (en) 2012-11-21 2014-05-30 Rvx Therapeutics Inc. Cyclic amines as bromodomain inhibitors
WO2014080291A2 (en) 2012-11-21 2014-05-30 Rvx Therapeutics Inc. Biaryl derivatives as bromodomain inhibitors
AU2013365926B9 (en) 2012-12-21 2019-01-17 Zenith Epigenetics Ltd. Novel heterocyclic compounds as bromodomain inhibitors
KR102662814B1 (ko) 2015-03-13 2024-05-03 리스버로직스 코퍼레이션 보체 관련 질환을 치료하기 위한 조성물 및 치료 방법
EP3749667A1 (en) 2018-02-05 2020-12-16 Alkermes, Inc. Compounds for the treatment of pain
US20230146716A1 (en) 2021-10-14 2023-05-11 Biosense Webster (Israel) Ltd. Digital twin of atria for atrial fibrillation patients
US20240020926A1 (en) 2022-07-14 2024-01-18 Biosense Webster (Israel) Ltd. Correcting a segmentation curve in an anatomical model

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE2336559A1 (de) * 1972-07-20 1974-01-31 Du Pont 4a-aryl-trans-decahydrochinoline und verfahren zu ihrer herstellung
US4419517A (en) * 1973-06-01 1983-12-06 E. I. Du Pont De Nemours & Co. 4a-Aryl-trans-decahydroisoquinolines
US3933827A (en) * 1974-10-29 1976-01-20 Hoffmann-La Roche Inc. 9-Acyloxy-5,11-dimethyl-6H-pyrido[4,3-B]carbazoles
US4310667A (en) * 1976-04-22 1982-01-12 Agence Nationale De Valorisation De La Recherche (Anvar) 2-N Quaternary ammonium salt derivatives of 9-hydroxy ellipticine
US4189583A (en) * 1978-04-26 1980-02-19 The United States Of America As Represented By The Department Of Health, Education And Welfare Synthesis of 4A-aryl-decahydroisoquinolines
FR2436786A1 (fr) * 1978-09-21 1980-04-18 Anvar Nouveaux derives des pyrido (4,3-b) carbazoles (ellipticines), substitues en position 1 par une chaine polyaminee, leur obtention et leur application a titre de medicaments

Also Published As

Publication number Publication date
DE69125099T2 (de) 1997-06-19
CA2224047A1 (en) 1991-12-06
US5244904A (en) 1993-09-14
CA2064853C (en) 1999-08-24
EP0485636B1 (en) 1997-03-12
US5539119A (en) 1996-07-23
EP0735026A1 (en) 1996-10-02
EP0485636A1 (en) 1992-05-20
CA2064853A1 (en) 1991-12-06
JP3180344B2 (ja) 2001-06-25
KR950002885B1 (ko) 1995-03-28
KR920702360A (ko) 1992-09-03
FI920480A0 (fi) 1992-02-04
EP0485636A4 (en) 1992-11-19
DE69125099D1 (de) 1997-04-17
WO1991018901A1 (fr) 1991-12-12

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