PE20040163A1 - Derivados de ciclopenteno - Google Patents

Derivados de ciclopenteno

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Publication number
PE20040163A1
PE20040163A1 PE2003000288A PE2003000288A PE20040163A1 PE 20040163 A1 PE20040163 A1 PE 20040163A1 PE 2003000288 A PE2003000288 A PE 2003000288A PE 2003000288 A PE2003000288 A PE 2003000288A PE 20040163 A1 PE20040163 A1 PE 20040163A1
Authority
PE
Peru
Prior art keywords
hydroxy
hydrogen
cyclopenten
ona
alkyl
Prior art date
Application number
PE2003000288A
Other languages
English (en)
Inventor
Barbara Albrecht
Matthias Breuning
Lars Barfacker
Gunter Schmidt
Walter Hubsch
Elisabeth Perzborn
Christiane Faeste
Original Assignee
Bayer Ag
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 Bayer Ag filed Critical Bayer Ag
Publication of PE20040163A1 publication Critical patent/PE20040163A1/es

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    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D309/00Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings
    • C07D309/02Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings having no double bonds between ring members or between ring members and non-ring members
    • C07D309/04Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings having no double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
    • C07D309/06Radicals substituted by oxygen atoms
    • 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
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
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    • C07C205/00Compounds containing nitro groups bound to a carbon skeleton
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    • C07C205/08Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by halogen atoms having nitro groups bound to acyclic carbon atoms
    • C07C205/09Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by halogen atoms having nitro groups bound to acyclic carbon atoms of an unsaturated carbon skeleton
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    • C07C251/44Oximes with oxygen atoms of oxyimino groups bound to hydrogen atoms or to carbon atoms of unsubstituted hydrocarbon radicals with the carbon atom of at least one of the oxyimino groups being part of a ring other than a six-membered aromatic ring
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    • C07C255/00Carboxylic acid nitriles
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    • C07C35/00Compounds having at least one hydroxy or O-metal group bound to a carbon atom of a ring other than a six-membered aromatic ring
    • C07C35/21Compounds having at least one hydroxy or O-metal group bound to a carbon atom of a ring other than a six-membered aromatic ring polycyclic, at least one hydroxy group bound to a non-condensed ring
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    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
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    • C07C45/70Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by isomerisation; by change of size of the carbon skeleton by increase in the number of carbon atoms by reaction with functional groups containing oxygen only in singly bound form
    • C07C45/71Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by isomerisation; by change of size of the carbon skeleton by increase in the number of carbon atoms by reaction with functional groups containing oxygen only in singly bound form being hydroxy groups
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    • C07C45/72Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by isomerisation; by change of size of the carbon skeleton by increase in the number of carbon atoms by reaction of compounds containing >C = O groups with the same or other compounds containing >C = O groups
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    • C07C49/00Ketones; Ketenes; Dimeric ketenes; Ketonic chelates
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Abstract

SE REFIERE A DERIVADOS DE CICLOPENTENO DE FORMULA I DONDE R1 ES ARILO C6-C10 O HETEROARILO DE 5 O 6 MIEMBROS, ENTRE OTROS; A ES UN ENLACE, ALCANO(C1-C4)DIILO, ALQUENO C2-C4, ENTRE OTROS; R2 Y R5 SON PIRIDILO, TIENILO, BENZOFURANILO, TETRAHIDROPIRANILO, ENTRE OTROS; R3 Y R4 SON HIDROGENO, ALQUILO C1-C6, CICLOALQUILO C6-C8, ENTRE OTROS; R6 ES HIDROGENO, ALQUILO C1-C6, -C(O)-C(O)-R14; R14 ES HIDROGENO O ALQUILO C1-C6; R7 ES HIDROGENO; R8 ES HIDROXI. SON COMPUESTOS PREFERIDOS:2-(4-FLUOROFENIL)-4 HIDROXI-5-METIL-3,4-DIFENIL-2-CICLOPENTEN-1-ONA,4-HIDROXI-2,3,4-TRIFENIL-5-PROPIL-2-CICLOPENTEN-1-ONA,3,4-BIS-(2-FLUOROFENIL)-4-HIDROXI-5-METIL-2-FENIL-2-CICLOPENTEN-1-ONA. SE REFIERE TAMBIEN A UNA COMPOSICION FARMACEUTICA. LOS COMPUESTOS MENCIONADOS ACTUAN SOBRE LA UNION DE ADP AL RECEPTOR P2Y-1 E INHIBEN LA AGREGACION DE TROMBOCITOSIS Y SON UTILES PARA EL TRATAMIENTO DE ENFERMEDADES TROMBOEMBOLICAS
PE2003000288A 2002-03-25 2003-03-24 Derivados de ciclopenteno PE20040163A1 (es)

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DE10213228A DE10213228A1 (de) 2002-03-25 2002-03-25 Cyclopenten-Derivate

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AR (1) AR039041A1 (es)
AU (1) AU2003209728A1 (es)
DE (1) DE10213228A1 (es)
GT (1) GT200300066A (es)
HN (1) HN2003000104A (es)
PE (1) PE20040163A1 (es)
TW (1) TW200400936A (es)
UY (1) UY27733A1 (es)
WO (1) WO2003080553A1 (es)

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US7550499B2 (en) 2004-05-12 2009-06-23 Bristol-Myers Squibb Company Urea antagonists of P2Y1 receptor useful in the treatment of thrombotic conditions
ATE499370T1 (de) 2005-01-19 2011-03-15 Bristol Myers Squibb Co 2-phenoxy-n-(1,3,4-thiadizol-2-yl)pyridin-3- aminderivate und verwandte verbindungen als p2y1- rezeptor-hemmer zur behandlung thromboembolischer erkrankungen
US7728008B2 (en) 2005-06-27 2010-06-01 Bristol-Myers Squibb Company N-linked heterocyclic antagonists of P2Y1 receptor useful in the treatment of thrombotic conditions
US7714002B2 (en) 2005-06-27 2010-05-11 Bristol-Myers Squibb Company Carbocycle and heterocycle antagonists of P2Y1 receptor useful in the treatment of thrombotic conditions
ES2352796T3 (es) 2005-06-27 2011-02-23 Bristol-Myers Squibb Company Antagonistas cíclicos unidos a c del receptor p2y1 útiles en el tratamiento de afecciones trombóticas.
DE602006020871D1 (de) 2005-06-27 2011-05-05 Bristol Myers Squibb Co Lineare harnstoffmimetika-antagonisten des p2y1-rezeptors zur behandlung von thromboseleiden
TWI499414B (zh) 2006-09-29 2015-09-11 Lexicon Pharmaceuticals Inc 鈉與葡萄糖第2型共同運輸體(co-transporter 2)的抑制物與其應用方法
US7960569B2 (en) 2006-10-17 2011-06-14 Bristol-Myers Squibb Company Indole antagonists of P2Y1 receptor useful in the treatment of thrombotic conditions
WO2008109591A1 (en) 2007-03-08 2008-09-12 Lexicon Pharmaceuticals, Inc. Phlorizin analogs as inhibitors of sodium glucose co-transporter 2
US11884640B2 (en) * 2021-06-02 2024-01-30 Chirogate International Inc. Processes and intermediates for the preparations of benzoprostacyclin analogues and benzoprostacyclin analogues prepared therefrom

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