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AR020875A1 - Compuesto acido (s)-2-etoxi-3-[4-(2-(4-metansulfoniloxi fenil)etoxi)fenil]-propanoico, proceso para su preparacion formulaicon farmaceutica, uso de dicho compuesto en la elaboracion de medicamentos, y formulacion farmaceutica - Google Patents

Compuesto acido (s)-2-etoxi-3-[4-(2-(4-metansulfoniloxi fenil)etoxi)fenil]-propanoico, proceso para su preparacion formulaicon farmaceutica, uso de dicho compuesto en la elaboracion de medicamentos, y formulacion farmaceutica

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Publication number
AR020875A1
AR020875A1 ARP990102635A ARP990102635A AR020875A1 AR 020875 A1 AR020875 A1 AR 020875A1 AR P990102635 A ARP990102635 A AR P990102635A AR P990102635 A ARP990102635 A AR P990102635A AR 020875 A1 AR020875 A1 AR 020875A1
Authority
AR
Argentina
Prior art keywords
treatment
preparation
disorders
compound
etoxi
Prior art date
Application number
ARP990102635A
Other languages
English (en)
Original Assignee
Astrazeneca Ab
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 Astrazeneca Ab filed Critical Astrazeneca Ab
Publication of AR020875A1 publication Critical patent/AR020875A1/es

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    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C303/00—Preparation of esters or amides of sulfuric acids; Preparation of sulfonic acids or of their esters, halides, anhydrides or amides
    • C07C303/26—Preparation of esters or amides of sulfuric acids; Preparation of sulfonic acids or of their esters, halides, anhydrides or amides of esters of sulfonic acids
    • C07C303/30—Preparation of esters or amides of sulfuric acids; Preparation of sulfonic acids or of their esters, halides, anhydrides or amides of esters of sulfonic acids by reactions not involving the formation of esterified sulfo groups
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00—Drugs for disorders of the metabolism
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00—Drugs for disorders of the metabolism
    • A61P3/04—Anorexiants; Antiobesity agents
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    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00—Drugs for disorders of the metabolism
    • A61P3/06—Antihyperlipidemics
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00—Drugs for disorders of the metabolism
    • A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00—Drugs for disorders of the metabolism
    • A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
    • A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P5/00—Drugs for disorders of the endocrine system
    • A61P5/48—Drugs for disorders of the endocrine system of the pancreatic hormones
    • A61P5/50—Drugs for disorders of the endocrine system of the pancreatic hormones for increasing or potentiating the activity of insulin
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    • C07C217/76—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having amino groups bound to carbon atoms of six-membered aromatic rings and etherified hydroxy groups bound to acyclic carbon atoms or to carbon atoms of rings other than six-membered aromatic rings of the same carbon skeleton
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    • C07C233/25—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by singly-bound oxygen atoms with the substituted hydrocarbon radical bound to the nitrogen atom of the carboxamide group by a carbon atom of a six-membered aromatic ring having the carbon atom of the carboxamide group bound to a hydrogen atom or to a carbon atom of an acyclic saturated carbon skeleton
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    • C07C233/24—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by singly-bound oxygen atoms with the substituted hydrocarbon radical bound to the nitrogen atom of the carboxamide group by a carbon atom of a six-membered aromatic ring
    • C07C233/29—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by singly-bound oxygen atoms with the substituted hydrocarbon radical bound to the nitrogen atom of the carboxamide group by a carbon atom of a six-membered aromatic ring having the carbon atom of the carboxamide group bound to an acyclic carbon atom of a carbon skeleton containing six-membered aromatic rings
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    • C07C235/42—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms having carbon atoms of carboxamide groups bound to carbon atoms of six-membered aromatic rings and singly-bound oxygen atoms bound to the same carbon skeleton
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    • C07C271/08—Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms
    • C07C271/26—Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms with the nitrogen atom of at least one of the carbamate groups bound to a carbon atom of a six-membered aromatic ring
    • C07C271/28—Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms with the nitrogen atom of at least one of the carbamate groups bound to a carbon atom of a six-membered aromatic ring to a carbon atom of a non-condensed six-membered aromatic ring
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    • C07C271/32—Esters of carbamic acids having oxygen atoms of carbamate groups bound to carbon atoms of rings other than six-membered aromatic rings
    • C07C271/38—Esters of carbamic acids having oxygen atoms of carbamate groups bound to carbon atoms of rings other than six-membered aromatic rings with the nitrogen atom of at least one of the carbamate groups bound to a carbon atom of a six-membered aromatic ring
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    • C07C271/44—Esters of carbamic acids having oxygen atoms of carbamate groups bound to carbon atoms of six-membered aromatic rings with the nitrogen atoms of the carbamate groups bound to hydrogen atoms or to acyclic carbon atoms to hydrogen atoms or to carbon atoms of unsubstituted hydrocarbon radicals
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    • C07C271/58—Esters of carbamic acids having oxygen atoms of carbamate groups bound to carbon atoms of six-membered aromatic rings with the nitrogen atom of at least one of the carbamate groups bound to a carbon atom of a six-membered aromatic ring
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    • C07C275/32—Derivatives of urea, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups having nitrogen atoms of urea groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton being further substituted by singly-bound oxygen atoms
    • C07C275/34—Derivatives of urea, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups having nitrogen atoms of urea groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton being further substituted by singly-bound oxygen atoms having nitrogen atoms of urea groups and singly-bound oxygen atoms bound to carbon atoms of the same non-condensed six-membered aromatic ring
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    • C07C311/01—Sulfonamides having sulfur atoms of sulfonamide groups bound to acyclic carbon atoms
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    • C07C2601/14—The ring being saturated

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  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)

Abstract

Derivados del ácido 3-aril-2-hidroxipropionico que tiene la formula general (1) y las sales, solvatos y formas cristalinas farmacéuticamente aceptables delmismo. Proceso para su preparacion, formulacion farmacéutica que lo contiene, uso de dichocomp uesto en la elaboracion de un medicamento para la profilaxis y/otratamiento de trastornos clínicos asociados con la resistencia a la insulina, y formulacion farmacéutica para usar en la profilaxis y/o tratamiento detrastornos clínicos asociadoscon l a resistencia a la insulina. Los compuestos de la formula (1) son adecuados para la profilaxis y/o tratamiento de trastornosclínicos asociados con la sensibilidad a la insulina reducida (resistencia a la insulina) y trastornos metabolicosrelacionado s. Estos trastornos clínicosincluyen, aunque no se limitan a, obesidad abdominal, hipertension arterial, hiperinsulinemia, hiperglucemia, diabetes mellitus no insulinodependiente (NIDDM)y la dislipidemia (trastornos de la lipoproteínaplasmática) que aparece como signo característico de la resistencia a la insulina. Esta dislipidemia, tambiénconocida como perfil de lipoproteína aterogénica del fenotipo B, se caracteriza por un nivel de ácidos grasos no esterificados moderadamenteelevado, nivele levado de triglicéridos lipoproteínas de muy baja densidad (VLDL), bajo nivel de colesterol de lipoproteínas de alta densidad (HDL) y presencia de pequenas ydensas lipoproteínas de baja densidad (LDL). Se espera que el tratamientocon los presentes c ompuestos reduzca la morbilidad y mortalidad asociadas con laaterosclerosis. Estos trastornos típicos de la enfermedad cardiovascular incluyen macroangiopatías causantes del infarto de miocardio, enfermedadcerebrovascular einsuficiencia arterial per iférica de las extremidades inferiores. Debido a su efecto sensibilizante a la insulina, también se espera que elcompuesto de la formula (1) reduzca el proceso de afecciones clínicas asociadas con la hiperglucemia cronicaen la diabetes, como las mic roangiopatíascausantes de enfermedad renal y dano a la retina. Además, los compuestos pueden ser de utilidad en el tratamiento de diversos trastornos ajenos al sistema
ARP990102635A 1998-06-04 1999-06-03 Compuesto acido (s)-2-etoxi-3-[4-(2-(4-metansulfoniloxi fenil)etoxi)fenil]-propanoico, proceso para su preparacion formulaicon farmaceutica, uso de dicho compuesto en la elaboracion de medicamentos, y formulacion farmaceutica AR020875A1 (es)

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ARP000102487A AR024061A2 (es) 1998-06-04 2000-05-22 Intermediario acido 2-etoxi-3(-(2[4-metansulfoniloxifenil*etoxi*fenil*propanoico

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