AR002950A1 - Derivados de la piperazina, sus sales aceptables desde el punto de vista fisiologico, un procedimiento para su preparacion y medicamentos que contienenestos compuestos. - Google Patents

Derivados de la piperazina, sus sales aceptables desde el punto de vista fisiologico, un procedimiento para su preparacion y medicamentos que contienenestos compuestos.

Info

Publication number
AR002950A1
AR002950A1 ARP950100727A AR10072795A AR002950A1 AR 002950 A1 AR002950 A1 AR 002950A1 AR P950100727 A ARP950100727 A AR P950100727A AR 10072795 A AR10072795 A AR 10072795A AR 002950 A1 AR002950 A1 AR 002950A1
Authority
AR
Argentina
Prior art keywords
group
derivatives
acceptable salts
piperazine
compounds
Prior art date
Application number
ARP950100727A
Other languages
English (en)
Inventor
Frank Dr Himmelbach
Guenter Dr Linz
Helmut Dr Pieper
Volkhard Dr Prof Austel
Brian Dr Guth
Johannes Dr Weisenberger
Original Assignee
Thomae Gmbh Dr K
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 DE19944446301 external-priority patent/DE4446301A1/de
Application filed by Thomae Gmbh Dr K filed Critical Thomae Gmbh Dr K
Publication of AR002950A1 publication Critical patent/AR002950A1/es

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D211/00Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
    • C07D211/04Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D211/06Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
    • C07D211/36Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members 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 ring carbon atoms
    • C07D211/56Nitrogen atoms
    • C07D211/58Nitrogen atoms attached in position 4
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P7/00Drugs for disorders of the blood or the extracellular fluid
    • A61P7/02Antithrombotic agents; Anticoagulants; Platelet aggregation inhibitors
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D211/00Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
    • C07D211/04Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D211/06Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
    • C07D211/08Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms
    • C07D211/18Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms with substituted hydrocarbon radicals attached to ring carbon atoms
    • C07D211/34Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms with substituted hydrocarbon radicals attached to ring carbon atoms with hydrocarbon radicals, substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Diabetes (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Hematology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Hydrogenated Pyridines (AREA)

Abstract

La presente invención se refiere a los derivados de la piperazina de fórmula general (I), en la que Ra representa un grupo de 3-pirrolidinilo, 3-piperidinilo, 4-piperidinilo, 3-hexametileniminilo o 4-hexametileniminilo, Rb y Rc que pueden ser iguales o diferentes, representan átomos de H, grupos dealquilo C1-5, arilo o aril-alquilo C1-5, ó Rb y Rc junto con el puente de etileno situado entre ellos, representan un grupo de o-fenileno;Y1 representaun grupo -A1-, -CO-, -CO-CO-, -A1-CO-, -C0-A1-, -S02-A2-, -A2-SO2-, -CO-A1-CO-, -CO-NR1-CO-,-CO-NR1-A2-, -CO-NR1-A2-C0-,-CO-A2-NR1-CO-, -CO-A2-O ó -CO-A2-NR1-;Y2 representa un grupo de fenileno, ciclohexileno o piridinileno, un grupo 3- piperidinileno, 4-piperidinileno o 1,4-piperazinileno; Y3 representa un grupo-CO-, -A2-CO-, -CH2-CH(NHR2)-CO-, NR2-A3-CO-, -CH2-NR2-A3-CO-, -O-A3-CO-, -CO-A3-CO- ó -CO-NR1-A3-CO-; y E representa un grupo hidroxi, un grupo alcoxicon 1 a 6 átomos de carbono, un grupo de fenilalcoxi, un grupode cicloalcoxi con 3 a 9 átomos de C, un grupo de cicloalcoxi con 5 a 8 átomos de C, un grupode cicloalqueniloxi, un grupo de alqueniloxi, fenilalqueniloxi, alquiniloxi, un grupo de cicloalquilalcoxi, un grupo de bicicloalcoxi, un grupo de 1,3-dihidro-3-oxo-1-isobenzofuraniloxi o un grupo R5-CO-O-(R3CR4)-O,ó E representa un grupo alfa-amino de un aminoácido natural, y sus ésteres, sus tautómeros,sus estereoisómeros, incluidas sus mezclas, y sus sales, en particular, sus sales aceptables desde el punto de vista fisiológico, La invención también serefiere a un procedimiento para preparar estos derivados y a los medicamentos que los contienen. Los nuevos compuestos presentan valiosas propiedadesfarmacológicas, en particular, efectos inhibidores de la agregación.
ARP950100727A 1994-12-23 1995-12-22 Derivados de la piperazina, sus sales aceptables desde el punto de vista fisiologico, un procedimiento para su preparacion y medicamentos que contienenestos compuestos. AR002950A1 (es)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
DE19944446301 DE4446301A1 (de) 1994-12-23 1994-12-23 Piperazinderivate, diese Verbindungen enthaltende Arzneimittel, deren Verwendung und Verfahren zu ihrer Herstellung
DE19526678A DE19526678A1 (de) 1994-12-23 1995-07-21 Piperazinderivate, diese Verbindungen enthaltende Arzneimittel, deren Verwendung und Verfahren zu ihrer Herstellung
DE1995133639 DE19533639A1 (de) 1994-12-23 1995-09-12 Piperazinderivate, diese Verbindungen enthaltende Arzneimittel, deren Verwendung und Verfahren zu ihrer Herstellung

Publications (1)

Publication Number Publication Date
AR002950A1 true AR002950A1 (es) 1998-05-27

Family

ID=27207101

Family Applications (1)

Application Number Title Priority Date Filing Date
ARP950100727A AR002950A1 (es) 1994-12-23 1995-12-22 Derivados de la piperazina, sus sales aceptables desde el punto de vista fisiologico, un procedimiento para su preparacion y medicamentos que contienenestos compuestos.

Country Status (20)

Country Link
US (1) US5922717A (es)
EP (1) EP0799202A1 (es)
JP (1) JPH10511374A (es)
CN (1) CN1183770A (es)
AR (1) AR002950A1 (es)
AU (1) AU4432496A (es)
BG (1) BG101582A (es)
BR (1) BR9510360A (es)
CA (1) CA2207618A1 (es)
CZ (1) CZ189197A3 (es)
EE (1) EE9700141A (es)
FI (1) FI972646A (es)
HR (1) HRP950609A2 (es)
IL (1) IL116517A0 (es)
MX (1) MX9704745A (es)
NO (1) NO972881L (es)
PL (1) PL321003A1 (es)
SK (1) SK79797A3 (es)
TR (1) TR199501634A2 (es)
WO (1) WO1996020173A1 (es)

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UY25225A1 (es) 1997-10-29 2000-12-29 Smithkline Beecham Plc Derivados de pleuromutilina utiles como agentes antimicrobianos
EP1070712A4 (en) * 1998-04-09 2005-01-05 Meiji Seika Kaisha NITROGEN-CONTAINING HETEROCYCLES WITH ANTI-BLOOD INFLAMMATION AND THEIR MEDICAL USE
CZ20011872A3 (cs) * 1999-09-29 2002-03-13 Ortho-Mcneil Pharmaceutical, Inc. Isonipekotamidy pro léčbu onemocnění zprostředkovaných integriny
EP1533310A1 (en) * 1999-09-29 2005-05-25 Ortho-McNeil Pharmaceutical, Inc. Isonipecotamides for the treatment of integrin-mediated disorders
USRE39921E1 (en) 1999-10-07 2007-11-13 Smithkline Beecham Corporation Chemical compounds
GB9923748D0 (en) 1999-10-07 1999-12-08 Glaxo Group Ltd Chemical compounds
GB0025354D0 (en) 2000-10-17 2000-11-29 Glaxo Group Ltd Chemical compounds
JP2004529918A (ja) * 2001-04-09 2004-09-30 オーソ−マクニール・フアーマシユーチカル・インコーポレーテツド インテグリンに由来する疾患の治療のためのキナゾリンおよびキナゾリン類似化合物
ATE530184T1 (de) 2001-08-24 2011-11-15 Univ Yale Piperazinon-verbindungen als tumor- und krebsbekämpfende wirkstoffe
FR2829766A1 (fr) * 2001-09-14 2003-03-21 Lipha Derives d'oxamates comportant un heterocycle azote diversement substitue
EP1472222A1 (en) 2002-02-08 2004-11-03 Glaxo Group Limited Piperidylcarboxamide derivatives and their use in the treatment of tachykinim-mediated diseases
GB0203020D0 (en) 2002-02-08 2002-03-27 Glaxo Group Ltd Chemical compounds
GB0203022D0 (en) 2002-02-08 2002-03-27 Glaxo Group Ltd Chemical compounds
KR20070004769A (ko) * 2004-02-27 2007-01-09 암젠 인코포레이션 대사 장애의 치료에 사용되는 화합물, 약제학적 조성물 및그 사용방법
WO2007016496A2 (en) * 2005-08-02 2007-02-08 Neurogen Corporation Dipiperazinyl ketones and related analogues
EP1942893A4 (en) * 2005-10-28 2011-10-12 Merck Sharp & Dohme PIPERIDINE Glycine-TRANSPORTER INHIBITORS
PL2041088T3 (pl) 2006-06-28 2014-07-31 Amgen Inc Inhibitory transportera-1 glicyny
US9090604B2 (en) 2006-07-27 2015-07-28 E I Du Pont De Nemours And Company Fungicidal azocyclic amides
WO2008013622A2 (en) * 2006-07-27 2008-01-31 E. I. Du Pont De Nemours And Company Fungicidal azocyclic amides
KR101227072B1 (ko) * 2007-01-16 2013-01-29 시오노기세이야쿠가부시키가이샤 Orl-1 리간드로서의 헤테로시클릭-치환 피페리딘
MX2010002449A (es) 2007-08-31 2010-09-07 Purdue Pharma Lp Compuestos de piperidina tipo quinoxalina sustituida y uso de los mismsos.
WO2010081851A1 (en) 2009-01-14 2010-07-22 Genoscience Pharma Piperidin-4-ylpiperazine compounds for the treatment of hcv infection
JP2014527511A (ja) 2011-06-24 2014-10-16 アムジエン・インコーポレーテツド Trpm8拮抗剤及び治療におけるそれらの使用
WO2012177896A1 (en) 2011-06-24 2012-12-27 Amgen Inc. Trpm8 antagonists and their use in treatments
CN104334541A (zh) 2012-02-16 2015-02-04 纽约大学 使用低聚氧代哌嗪非肽螺旋模拟物对低氧诱导基因表达的控制
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AU2014207311A1 (en) 2013-01-19 2015-08-20 New York University Oligooxopiperazines for p53 reactivation
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Also Published As

Publication number Publication date
FI972646A0 (fi) 1997-06-19
JPH10511374A (ja) 1998-11-04
NO972881D0 (no) 1997-06-20
EP0799202A1 (de) 1997-10-08
US5922717A (en) 1999-07-13
SK79797A3 (en) 1997-11-05
CN1183770A (zh) 1998-06-03
BR9510360A (pt) 1997-12-23
TR199501634A2 (tr) 1996-07-21
HRP950609A2 (en) 1997-10-31
CZ189197A3 (cs) 1998-01-14
AU4432496A (en) 1996-07-19
EE9700141A (et) 1997-12-15
CA2207618A1 (en) 1996-07-04
MX9704745A (es) 1997-10-31
NO972881L (no) 1997-06-20
FI972646A (fi) 1997-08-19
WO1996020173A1 (de) 1996-07-04
IL116517A0 (en) 1996-03-31
PL321003A1 (en) 1997-11-24
BG101582A (en) 1998-01-30

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