UY26020A1 - Inhibidores de la recaptacion de monoaminas para el tratamiento de trastornos del snc. - Google Patents

Inhibidores de la recaptacion de monoaminas para el tratamiento de trastornos del snc.

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Publication number
UY26020A1
UY26020A1 UY26020A UY26020A UY26020A1 UY 26020 A1 UY26020 A1 UY 26020A1 UY 26020 A UY26020 A UY 26020A UY 26020 A UY26020 A UY 26020A UY 26020 A1 UY26020 A1 UY 26020A1
Authority
UY
Uruguay
Prior art keywords
treatment
phenyl ring
alkyl
disorders
serotonin
Prior art date
Application number
UY26020A
Other languages
English (en)
Inventor
Mark Leonard Elliot
Harry Ralph Howard Jr
Cristopher Joseph Schmidt
Thomas Francis Seeger
Original Assignee
Pfizer Prod 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 Pfizer Prod Inc filed Critical Pfizer Prod Inc
Publication of UY26020A1 publication Critical patent/UY26020A1/es

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    • C07D207/02—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D207/04—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom 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
    • C07D207/08—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom 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 radicals, substituted by hetero atoms, attached to ring carbon atoms
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    • C07C217/54—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having etherified hydroxy groups bound to carbon atoms of at least one six-membered aromatic ring and amino groups bound to acyclic carbon atoms or to carbon atoms of rings other than six-membered aromatic rings of the same carbon skeleton
    • C07C217/56—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having etherified hydroxy groups bound to carbon atoms of at least one six-membered aromatic ring and amino groups bound to acyclic carbon atoms or to carbon atoms of rings other than six-membered aromatic rings of the same carbon skeleton with amino groups linked to the six-membered aromatic ring, or to the condensed ring system containing that ring, by carbon chains not further substituted by singly-bound oxygen atoms
    • C07C217/58—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having etherified hydroxy groups bound to carbon atoms of at least one six-membered aromatic ring and amino groups bound to acyclic carbon atoms or to carbon atoms of rings other than six-membered aromatic rings of the same carbon skeleton with amino groups linked to the six-membered aromatic ring, or to the condensed ring system containing that ring, by carbon chains not further substituted by singly-bound oxygen atoms with amino groups and the six-membered aromatic ring, or the condensed ring system containing that ring, bound to the same carbon atom of the carbon chain
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    • C07C217/78—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having amino groups and etherified hydroxy groups bound to carbon atoms of six-membered aromatic rings of the same carbon skeleton
    • C07C217/80—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having amino groups and etherified hydroxy groups bound to carbon atoms of six-membered aromatic rings of the same carbon skeleton having amino groups and etherified hydroxy groups bound to carbon atoms of non-condensed six-membered aromatic rings
    • C07C217/82—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having amino groups and etherified hydroxy groups bound to carbon atoms of six-membered aromatic rings of the same carbon skeleton having amino groups and etherified hydroxy groups bound to carbon atoms of non-condensed six-membered aromatic rings of the same non-condensed six-membered aromatic ring
    • C07C217/90—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having amino groups and etherified hydroxy groups bound to carbon atoms of six-membered aromatic rings of the same carbon skeleton having amino groups and etherified hydroxy groups bound to carbon atoms of non-condensed six-membered aromatic rings of the same non-condensed six-membered aromatic ring the oxygen atom of at least one of the etherified hydroxy groups being further bound to a carbon atom of a six-membered aromatic ring, e.g. amino-diphenylethers
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    • C07C233/16—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
    • C07C233/17—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 an acyclic carbon atom
    • C07C233/18—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 an acyclic carbon atom 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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    • C07C235/32—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms having carbon atoms of carboxamide groups bound to acyclic carbon atoms and singly-bound oxygen atoms bound to the same carbon skeleton the carbon skeleton containing six-membered aromatic rings
    • C07C235/34—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms having carbon atoms of carboxamide groups bound to acyclic carbon atoms and singly-bound oxygen atoms bound to the same carbon skeleton the carbon skeleton containing six-membered aromatic rings having the nitrogen atoms of the carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms
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    • C07C255/37—Carboxylic acid nitriles having cyano groups bound to acyclic carbon atoms having cyano groups bound to acyclic carbon atoms of a carbon skeleton containing at least one six-membered aromatic ring the carbon skeleton being further substituted by etherified hydroxy groups
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    • C07C311/22—Sulfonamides, the carbon skeleton of the acid part being further substituted by singly-bound oxygen atoms
    • C07C311/29—Sulfonamides, the carbon skeleton of the acid part being further substituted by singly-bound oxygen atoms having the sulfur atom of at least one of the sulfonamide groups bound to a carbon atom of a six-membered aromatic ring
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Abstract

COMPUESTOS QUE SON UTILES Y PRESENTAN ACTIVIDAD COMO INHIBIDORES DE LA RECAPTACION DE LA SEROTONINA, NOREPINEFRINA Y DOPAMINA, A SUS SALES FARMACEUTICAMENTE ACEPTABLES, Y A SU USO EN EL TRATAMIENTO DE TRASTORNOS DEL SISTEMA NERVIOSO CENTRAL Y OTROS TRASTORNOS Un compuesto de fórmula (I) en la que: el anillo de fenilo A y el anillo de fenilo B pueden reemplazarse cada uno, independiente por un grupo naftilo y el anillo de fenilo A se reemplaza por un grupo naftilo; m y n son 1,2 o 3; R1 y R2 son H, alquilo C1-4, alquenilo C2-4 y alquinilo C2-4; R3 y R4 son H y alquilo C1-4 sustituído con uno o tres átomos de fluor; X se selecciona entre H, halo (Cloro, fluoro, bromo o yodo); Y es H, alquilo C1-6 y halo, o una sal farmacéutica del mismo. Este compuesto es útil en el tratamiento de hipertensión , depresión, Parkinson, fobias, obesidad, eyaculación precoz, trastornos de alimentación, adiccion al alcohol, a la cocaína, a la heroína, trastorno de pánico, trastornos de la memoria, síndrome premenstrual. También al inhibir la recaptación de serotonina, dopamina o norepinefrina, es antidepresiv. Tambíen para tratar hipertensión, depresión por cáncer, anorexia nerviosa, Alzheimer, síndrome de Tourette, etc. Ejemplo: 2-fluoro-6-(P-toliloxi)bencilamina
UY26020A 1999-02-23 2000-02-21 Inhibidores de la recaptacion de monoaminas para el tratamiento de trastornos del snc. UY26020A1 (es)

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US12131399P 1999-02-23 1999-02-23

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UY26020A1 true UY26020A1 (es) 2000-09-29

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UY26020A UY26020A1 (es) 1999-02-23 2000-02-21 Inhibidores de la recaptacion de monoaminas para el tratamiento de trastornos del snc.

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US (2) US6677378B2 (es)
EP (1) EP1154984A1 (es)
JP (1) JP3916871B2 (es)
KR (1) KR100446893B1 (es)
CN (1) CN1157365C (es)
AP (1) AP2001002252A0 (es)
AR (1) AR035479A1 (es)
AU (1) AU763884B2 (es)
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CO (3) CO5690130A1 (es)
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