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PE20011325A1 - Heterociclilalquilaminas como antagonistas de los receptores muscarinicos - Google Patents

Heterociclilalquilaminas como antagonistas de los receptores muscarinicos

Info

Publication number
PE20011325A1
PE20011325A1 PE2001000457A PE2001000457A PE20011325A1 PE 20011325 A1 PE20011325 A1 PE 20011325A1 PE 2001000457 A PE2001000457 A PE 2001000457A PE 2001000457 A PE2001000457 A PE 2001000457A PE 20011325 A1 PE20011325 A1 PE 20011325A1
Authority
PE
Peru
Prior art keywords
alkyl
antagonists
heterocyclylalkylamines
metansulfonylphenyl
ona
Prior art date
Application number
PE2001000457A
Other languages
English (en)
Inventor
Charles Alois Dvorak
Lawrence Emerson Fisher
Keena Lynn Green
Russell Stephen Stabler
Hans Maag
Anthony Prince
David Bruce Repke
Ralph New Harris Iii
Original Assignee
Hoffmann La Roche
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 Hoffmann La Roche filed Critical Hoffmann La Roche
Publication of PE20011325A1 publication Critical patent/PE20011325A1/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
    • C07D207/18—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 one double bond between ring members or between a ring member and a non-ring member
    • C07D207/22—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 one double bond between ring members or between a ring member and a non-ring member 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
    • C07D207/24—Oxygen or sulfur atoms
    • C07D207/26—2-Pyrrolidones
    • C07D207/263—2-Pyrrolidones with only hydrogen atoms or radicals containing only hydrogen and carbon atoms directly attached to other ring carbon atoms
    • C07D207/27—2-Pyrrolidones with only hydrogen atoms or radicals containing only hydrogen and carbon atoms directly attached to other ring carbon atoms with substituted hydrocarbon radicals directly attached to the ring nitrogen atom
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    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/55—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
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    • A61K31/551—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole having two nitrogen atoms, e.g. dilazep
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    • A61K31/553—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole having at least one nitrogen and one oxygen as ring hetero atoms, e.g. loxapine, staurosporine
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Abstract

SE REFIERE A DERIVADOS DE HETEROCICLILALQUILAMINA DE FORMULA I DONDE R1, R2, R3 SON H, HALOGENO, ALQUILO C1-C6, OR', NR'R", ENTRE OTROS; R1 Y R2 JUNTO A LOS CARBONOS FORMAN UN ANILLO DE 5-7 MIEMBROS; R' Y R" SON H, ALQUILO C1-C6, ALQUIL C0-C3-ALCOXILO, ARILO, HETEROCICLILO, HETEROARILO, ENTRE OTROS; R4 ES ALQUILO C1-C6; R5 ES ALQUILO C1-C6, ALQUENILO C1-C6, CICLOALQUILO, ENTRE OTROS; UNO DE X, Y Z ES S, O, CH2, NR6 LOS OTROS SON CH2; R6 ES H, ALQUILO C1-C6, HALOGENOALQUILO, ENTRE OTROS; m ES 0-3; n ES 1-6. SON COMPUESTOS PREFERIDOS 1-(4-{[2-(4-METANSULFONILFENIL)-1-METILETIL]PROPILAMINO}-BUTIL)-PIPERAZIN-2-ONA 4-(4-{ALIL-[2-(4-METANSULFONILFENIL)-1-METILETIL]AMINO}-BUTIL)-[1,4]DIAZEPAN-5-ONA, ENTRE OTROS; TAMBIEN SE REFIERE A UN PROCEDIMIENTO PARA LA PREPARACION. LOS COMPUESTOS I SON ANTAGONISTAS DE LOS RECEPTORES MUSCARINICOS M2/M3 Y PUEDE SER UTIL PARA EL TRATAMIENTO DE ENFERMEDADES DEL TRACTO GASTROINTESTINAL, GENITOURINARIO, ESTADOS RESPIRATORIOS
PE2001000457A 2000-05-25 2001-05-21 Heterociclilalquilaminas como antagonistas de los receptores muscarinicos PE20011325A1 (es)

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