CO4700285A1 - Derivados de 1-oxo-2-(fenilsulfonilamino)pentilpiperidina, su preparacion y su aplciacion en la terapeutica - Google Patents

Derivados de 1-oxo-2-(fenilsulfonilamino)pentilpiperidina, su preparacion y su aplciacion en la terapeutica

Info

Publication number
CO4700285A1
CO4700285A1 CO95061143A CO95061143A CO4700285A1 CO 4700285 A1 CO4700285 A1 CO 4700285A1 CO 95061143 A CO95061143 A CO 95061143A CO 95061143 A CO95061143 A CO 95061143A CO 4700285 A1 CO4700285 A1 CO 4700285A1
Authority
CO
Colombia
Prior art keywords
carbon atoms
straight
group
alkyl group
chain
Prior art date
Application number
CO95061143A
Other languages
English (en)
Inventor
Jean Michel Altenburger
Gilbert Lasalle
Original Assignee
Synthelabo
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 Synthelabo filed Critical Synthelabo
Publication of CO4700285A1 publication Critical patent/CO4700285A1/es

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic 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
    • C07D401/02Heterocyclic 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
    • C07D401/12Heterocyclic 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K5/00Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
    • C07K5/04Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
    • C07K5/06Dipeptides
    • C07K5/06139Dipeptides with the first amino acid being heterocyclic
    • 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K38/00Medicinal preparations containing peptides

Landscapes

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

Abstract

Compuestos que responden a la Fórmula (I):en la que R1 representa ya sea un átomo de hidrógeno, o bien un grupo alquilo con 1 a 4 atómos de carbono, R2 representa, ya sea un átomo de hidrógeno, o bien un grupo alquilo de 1 a 4 átomos de carbono de cadena recta o ramificada, R3 representa un grupo alquilo de 1 a 7 átomos de carbono, de cadena recta o ramificada, o bien un grupo -(CH2 )n OCH3 (en la cual n es 1, 2 o 3), o bien un grupo -CH2 O(C2 H4 O)m CH3 (en la cual m es 1, 2 o 3), R4 representa, ya sea un átomo de hidrógeno, o bien, un átomo de halógeno,R5 representa un grupo alquilo con 1 a 4 átomos de carbono, de cadena recta o ramificada yA representa, ya sea un grupo fenilo eventualmente substituido por uno o varios substituyentes seleccionados entre los átomos de halógeno, y los grupos alquilo con 1 a 4 átomos de carbono de cadena recta o ramificada, alcoxi con 1 a 4 átomos de carbono de cadena recta o ramificada y trifluorometilo, o bien, un heterociclo seleccionado entre los grupos piridinilo, tienilo, furilo, eventualmente substituidos como arriba, o bien un grupo cicloalquilo con 5 a 8 átomos de carbono, en forma de base libre, o de sales de adición a ácidos farmacéuticamente aceptables.
CO95061143A 1994-12-23 1995-12-22 Derivados de 1-oxo-2-(fenilsulfonilamino)pentilpiperidina, su preparacion y su aplciacion en la terapeutica CO4700285A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
FR9415549A FR2728570B1 (fr) 1994-12-23 1994-12-23 Derives de 1-oxo-2-(phenylsulfonylamino)pentylpiperidine, leur preparation et leur application en therapeutique

Publications (1)

Publication Number Publication Date
CO4700285A1 true CO4700285A1 (es) 1998-12-29

Family

ID=9470166

Family Applications (1)

Application Number Title Priority Date Filing Date
CO95061143A CO4700285A1 (es) 1994-12-23 1995-12-22 Derivados de 1-oxo-2-(fenilsulfonilamino)pentilpiperidina, su preparacion y su aplciacion en la terapeutica

Country Status (21)

Country Link
US (2) US5602149A (es)
EP (1) EP0718307A2 (es)
JP (1) JPH08239380A (es)
KR (1) KR960022504A (es)
CN (1) CN1131153A (es)
AR (1) AR002259A1 (es)
AU (1) AU4062995A (es)
BR (1) BR9506062A (es)
CA (1) CA2166032A1 (es)
CO (1) CO4700285A1 (es)
CZ (1) CZ346095A3 (es)
FI (1) FI956251A (es)
FR (1) FR2728570B1 (es)
HU (1) HUT75114A (es)
IL (1) IL116532A0 (es)
NO (1) NO955242L (es)
NZ (1) NZ280735A (es)
PL (1) PL312028A1 (es)
SK (1) SK163895A3 (es)
TW (1) TW321647B (es)
ZA (1) ZA9510930B (es)

Families Citing this family (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2728570B1 (fr) * 1994-12-23 1997-04-11 Synthelabo Derives de 1-oxo-2-(phenylsulfonylamino)pentylpiperidine, leur preparation et leur application en therapeutique
FR2749584B1 (fr) * 1996-06-11 1998-07-10 Synthelabo Derives de 1-oxo-2-(1h-imidazol-4-yl)pentylpiperidine, leur preparation et leur application en therapeutique
FR2756285B1 (fr) * 1996-11-22 1998-12-18 Synthelabo Derives de n-(imidazolylbutyle)benzenesulfonamide, leur preparation et leur application en therapeutique
FR2758326B1 (fr) * 1997-01-16 1999-02-12 Synthelabo Derives de pyridone, leur prepaparation et leur utilisation comme intermediaires de synthese
FR2765220B1 (fr) * 1997-06-25 1999-07-30 Synthelabo Derives de 1-oxo-2-(phenylsulfonyl)aminopentyle, leur preparation et leur application en therapeutique
FR2771094B1 (fr) * 1997-11-19 2000-02-04 Synthelabo Derives de piperidine-2-carboxylate, leur preparation et leur application en therapeutique
FR2806722B1 (fr) * 2000-03-23 2002-05-17 Sanofi Synthelabo Derives de n-(heterocyclylbutyl) benzene-ou pyridine sulfonamide, leur preparation et leur application en therapeutique

Family Cites Families (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA1338645C (en) * 1987-01-06 1996-10-15 George R. Pettit Isolation, structural elucidation and synthesis of novel antineoplastic substances denominated "combretastatins"
US5312828A (en) * 1989-06-14 1994-05-17 Finkelstein Joseph A Substituted imidazoles having angiotensin II receptor blocking activity
US5136043A (en) * 1989-06-17 1992-08-04 Hoechst Aktiengesellschaft Process for the preparation of aromatic sulfonyl chlorides
US5492895A (en) * 1992-02-14 1996-02-20 Corvas International, Inc. Inhibitors of thrombosis
FR2689130B1 (fr) * 1992-03-30 1994-05-27 Synthelabo Derives de 1-[2 (arylsulfonylamino)ethyl-1-oxo] piperidine, leur preparation et leur application en therapeutique.
US5401851A (en) * 1992-06-03 1995-03-28 Eli Lilly And Company Angiotensin II antagonists
US5612360A (en) * 1992-06-03 1997-03-18 Eli Lilly And Company Angiotensin II antagonists
DE4240708A1 (de) * 1992-12-03 1994-06-09 Bayer Ag Verfahren zur Herstellung von Natriumsalzen nitrogruppenhaltiger aromatischer Sulfinsäuren
FR2710066B1 (fr) 1993-09-14 1995-10-20 Synthelabo Dérivés de 1-[2-amino-5-[1-(triphénylméthyl-1H-imidazol-4-yl]-1-oxopentyl]piperidine, leur préparation et leur utilisation comme intermédiaires de synthèse.
ATE260924T1 (de) * 1993-12-29 2004-03-15 Syngenta Participations Ag Vinylcarboxamid-derivate als insectizide und akarizide
DE4423061C1 (de) * 1994-07-01 1996-01-18 Hoechst Ag Verfahren zur Herstellung von Biphenylen mit Palladacyclen als Katalysatoren
FR2728570B1 (fr) * 1994-12-23 1997-04-11 Synthelabo Derives de 1-oxo-2-(phenylsulfonylamino)pentylpiperidine, leur preparation et leur application en therapeutique

Also Published As

Publication number Publication date
CN1131153A (zh) 1996-09-18
TW321647B (es) 1997-12-01
FR2728570B1 (fr) 1997-04-11
AR002259A1 (es) 1998-03-11
EP0718307A3 (es) 1996-08-07
ZA9510930B (en) 1996-06-24
BR9506062A (pt) 1997-12-23
CA2166032A1 (fr) 1996-06-24
JPH08239380A (ja) 1996-09-17
PL312028A1 (en) 1996-06-24
NZ280735A (en) 1997-06-24
IL116532A0 (en) 1996-03-31
NO955242D0 (no) 1995-12-22
NO955242L (no) 1996-06-24
FI956251A0 (fi) 1995-12-22
US5753667A (en) 1998-05-19
KR960022504A (ko) 1996-07-18
AU4062995A (en) 1996-07-04
FI956251A (fi) 1996-06-24
HUT75114A (en) 1997-04-28
US5602149A (en) 1997-02-11
FR2728570A1 (fr) 1996-06-28
SK163895A3 (en) 1996-09-04
HU9503782D0 (en) 1996-05-28
EP0718307A2 (fr) 1996-06-26
CZ346095A3 (en) 1996-07-17

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