AR041594A1 - Derivados de 1,4 piperidina disustituida y su uso como inhibidores de 11-beta hidroxiesteroide dehidrogenasa tipo 1 - Google Patents

Derivados de 1,4 piperidina disustituida y su uso como inhibidores de 11-beta hidroxiesteroide dehidrogenasa tipo 1

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Publication number
AR041594A1
AR041594A1 ARP030103716A ARP030103716A AR041594A1 AR 041594 A1 AR041594 A1 AR 041594A1 AR P030103716 A ARP030103716 A AR P030103716A AR P030103716 A ARP030103716 A AR P030103716A AR 041594 A1 AR041594 A1 AR 041594A1
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AR
Argentina
Prior art keywords
alkyl
heterocyclyl
carbocyclyl
carbamoyl
amino
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ARP030103716A
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English (en)
Inventor
Peter Barton
Philip Jewsbury
Elizabeth Pease
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Astrazeneca Ab
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Priority claimed from GB0223573A external-priority patent/GB0223573D0/en
Priority claimed from GB0310446A external-priority patent/GB0310446D0/en
Application filed by Astrazeneca Ab filed Critical Astrazeneca Ab
Publication of AR041594A1 publication Critical patent/AR041594A1/es

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    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D401/00—Heterocyclic 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
    • C07D401/02—Heterocyclic 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
    • C07D401/06—Heterocyclic 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 carbon chain containing only aliphatic carbon atoms
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    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • 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
    • A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
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    • A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
    • A61K31/443—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with oxygen as a ring hetero atom
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    • A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
    • A61K31/444—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a six-membered ring with nitrogen as a ring heteroatom, e.g. amrinone
    • A—HUMAN NECESSITIES
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    • 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
    • A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/445—Non condensed piperidines, e.g. piperocaine
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    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P19/00—Drugs for skeletal disorders
    • A61P19/08—Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease
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    • A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
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    • C07D211/00—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
    • C07D211/04—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D211/06—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings 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
    • C07D211/08—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings 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 or substituted hydrocarbon radicals directly attached to ring carbon atoms
    • C07D211/18—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings 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 or substituted hydrocarbon radicals directly attached to ring carbon atoms with substituted hydrocarbon radicals attached to ring carbon atoms
    • C07D211/30—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings 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 or substituted hydrocarbon radicals directly attached to ring carbon atoms with substituted hydrocarbon radicals attached to ring carbon atoms with hydrocarbon radicals, substituted by doubly bound oxygen or sulfur atoms or by two oxygen or sulfur atoms singly bound to the same carbon atom
    • C07D211/32—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings 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 or substituted hydrocarbon radicals directly attached to ring carbon atoms with substituted hydrocarbon radicals attached to ring carbon atoms with hydrocarbon radicals, substituted by doubly bound oxygen or sulfur atoms or by two oxygen or sulfur atoms singly bound to the same carbon atom by oxygen atoms
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    • C07D405/06—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
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    • C07D417/06—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
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    • C07D513/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains two hetero rings
    • C07D513/04—Ortho-condensed systems

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Abstract

Se describe el uso de un compuesto en la fabricación de un medicamento para usar en la inhibición de 11 HSD1, también reivindica proceso y composiciones farmacéuticas y compuestos. Reivindicación 1: El uso de un compuesto caracterizado porque responde a la fórmula (1) donde: El anillo A se selecciona entre carbociclilo o heterociclilo; donde si dicho heterociclilo contiene una porción -NH- este N puede estar sustituido opcionalmente con un grupo seleccionado entre R9. R1 es un sustituyente sobre C y se selecciona entre halo, nitro, ciano, hidroxi, amino, carboxi, carbamoilo, mercapto, sulfamoilo, C1-4 alquilo, C2-4 alquenilo, C2-4 alquinilo, C1-4 alcoxi, C1-4 alcanoilo, C1-4alcanoiloxi, N-(C1-4 alquil)amino, N,N-(C1-4 alquil)2amino, C1-4 alcanoilamino, N-(C1-4 alquil)carbamoilo, N,N-(C1-4alquil)2carbamoilo, C1-4 alquilS(O)a donde a es entre 0 y 2, C1-4 alcoxicarbonilo, N-(C1-4 alquil)sulfamoilo, N,N-(C1-4 alquil)2sulfamoilo, C1-4 alquilsulfonilamino, carbociclilo, heterociclilo, carbociclil C0-4 alquilen-Z- y heterociclil C0-4 alquilen-Z-; donde R1 puede estar sustituido opcionalmente sobre C con uno o más grupos seleccionados entre R3; y donde si dicho heterociclilo contiene una porción -NH- este N puede estar sustituido opcionalmente con un grupo seleccionado entre R4; n es 0-5; donde los valores de R1 pueden ser iguales o diferentes; X es un enlace simple, -C(O)-, -S(O)2, -C(O)NR11, -C(S)NR11, -C(O)O-, -C(=NR11)- o -CH2-; donde R11 se selecciona entre H, C1-4 alquilo, carbociclilo y heterociclilo; Y es H, C1-6 alquilo, C2-6 alquenilo, C2-6 alquinilo, carbociclilo o heterociclilo; donde Y puede estar sustituido opcionalmente sobre C con uno o más R2; donde si dicho heterociclilo contiene una porción -NH- este N puede estar sustituido opcionalmente con un grupo seleccionado entre R5; R2 es un sustituyente sobre C y se selecciona entre halo, nitro, ciano, hidroxi, amino, carboxi, carbamoilo, mercapto, sulfamoilo, trifluorometilo, trifluorometoxi, C1-4 alquilo, C2-4 alquenilo, C2-4 alquinilo, C1-4 alcoxi, C1-4 alcanoilo, C1-4 alcanoiloxi, N-(C1-4 alquil)amino, N,N-(C1-4 alquil)2amino, C1-4 alcanoilamino, N,(C1-4 alquil)carbamoilo, N,N-(C1-4 alquil)2carbamoilo, C1-4 alquilS(O)a donde a es entre 0 y 2, C1-4 alcoxicarbonilo, C1-4 alcoxicarbonilamino, C1-4 alcoxicarbonil-N-(C1-4 alquil)amino, N-(C1-4 alquil)sulfamoilo, N,N-(C1-4 alquil)2sulfamoilo, C1-4 alquilsulfonilamino, aminotiocarboniltio, N-(C1-4 alquil)aminotiocarboniltio, N,N-(C1-4 alquil)2 aminotiocarboniltio, carbociclilo, heterociclilo, carbociclil C0-4 alquilen-Z- y heterociclil C0-4 alquilen-Z-; donde R2 puede estar sustituido opcionalmente sobre C con uno o más grupos seleccionados entre R6, y donde si dicho heterociclilo contiene una porción -NH- este N puede estar sustituido opcionalmente con un grupo seleccionado entre R7; R3 y R6 se seleccionan en forma independiente entre halo, nitro, ciano, hidroxi, amino, carboxi, carbamoilo, mercapto, sulfamoilo, trifluorometilo, trifluorometoxi, C1-4 alquilo, C2-4 alquenilo, C2-4 alquinilo, C1-4 alcoxi, C1-4 alcanoilo, C1-4 alcanoiloxi, N-(C1-4 alquil)amino, N,N-(C1-4 alquil)2amino, C1-4 alcanoilamino, N-(C1-4 alquil)carbamoilo, N,N-(C1-4 alquil)2carbamoilo, C1-4 alquilS(O)a donde a es entre 0 y 2, C1-4 alcoxicarbonilo, C1-4 alcoxicarbonilamino, C1-4 alcoxicarbonil-N-(C1-4 alquil)amino, N-(C1-4 alquil)sulfamoilo, N,N-(C1-4 alquil)2sulfamoilo, C1-4 alquilsulfonilamino, carbociclilo, heterociclilo, carbociclil C0-4 alquilen-Z- y heterociclil C0-4 alquilen-Z- donde R3 y R6 pueden estar sustituidos opcionalmente en forma independiente sobre C con uno o más R8; y donde si dicho heterociclilo contiene una porción -NH- este N puede estar sustituido opcionalmente con un grupo seleccionado entre R13; R4, R5, R7, R9 y R13 se seleccionan en forma independiente entre C1-4 alquilo, C1-4 alcanoilo, C1-4 alquilsulfonilo, C1-4 alcoxicarbonilo, carbamoilo, N-(C1-4 alquil)carbamoilo, N,N-(C1-4 alquil)2carbamoilo, bencilo, benciloxicarbonilo, benzoilo y fenilsulfonilo; R8 se selecciona entre halo, nitro, ciano, hidroxi, trifluorometoxi, trifluorometilo, amino, carboxi, carbamoilo, mercapto, sulfamoilo, metilo, etilo, metoxi, etoxi, acetilo, acetoxi, metilamino, etilamino, dimetilamino, dietilamino, N-metil-N-etilamino, acetilamino, N-metilcarbamoilo, N-etilcarbamoilo, N,N-dimetilcarbamoilo, N,N-dietilcarbamoilo, N-metil-N-etilcarbamoilo, metilito, etiltio, metilsulfinilo, etilsulfinilo, mesilo, etilsulfonilo, metoxicarbonilo, etoxicarbonilo, N-metilsulfamoilo, N-etilsulfamoilo, N,N-dimetilsulfamoilo, N,N-dietilsulfamoilo o N-metil-N-etilsulfamoilo; Z es -S(O)a-, -O-, -NR10-, -C(O)-, -C(O)NR11-, -NR10C(O)-, -OC(O)NR10- o -SO2NR10-; donde a es entre 0 y 2; donde R10 se selecciona entre H y C1-4 alquilo; R12 es hidroxi, metilo, etilo o propilo; m es 0 o 1; q es 0 o 1; o una sal aceptable para uso farmacéutico del mismo, en la fabricación de un medicamento para usar en la inhibición de 11betaHSD1.
ARP030103716A 2002-10-11 2003-10-10 Derivados de 1,4 piperidina disustituida y su uso como inhibidores de 11-beta hidroxiesteroide dehidrogenasa tipo 1 AR041594A1 (es)

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GB0223573A GB0223573D0 (en) 2002-10-11 2002-10-11 Chemical compounds
GB0310446A GB0310446D0 (en) 2003-05-07 2003-05-07 Chemical compounds

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US (1) US20050256159A1 (es)
EP (1) EP1556349A1 (es)
JP (1) JP2006506451A (es)
KR (1) KR20050051691A (es)
AR (1) AR041594A1 (es)
AU (1) AU2003269242A1 (es)
BR (1) BR0315166A (es)
CA (1) CA2501611A1 (es)
MX (1) MXPA05003632A (es)
NO (1) NO20051600L (es)
TW (1) TW200413318A (es)
UY (1) UY28014A1 (es)
WO (1) WO2004033427A1 (es)

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MXPA01007099A (es) * 1999-01-13 2002-03-27 Univ New York State Res Found Metodo novedoso para disenar inhibidores de la proteina cinasa.
US7005445B2 (en) * 2001-10-22 2006-02-28 The Research Foundation Of State University Of New York Protein kinase and phosphatase inhibitors and methods for designing them
GB0325745D0 (en) * 2003-11-05 2003-12-10 Astrazeneca Ab Chemical compounds
GB0326029D0 (en) * 2003-11-07 2003-12-10 Astrazeneca Ab Chemical compounds
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