AR068057A1 - Esteres de 1-fenil-2-(3,5-dicloro)-piridina, metodo de preparacion de los mismos, composiciones farmaceuticas que los contienen y usos de los mismos para el tratamiento de enfermedades del tracto respiratorio. - Google Patents

Esteres de 1-fenil-2-(3,5-dicloro)-piridina, metodo de preparacion de los mismos, composiciones farmaceuticas que los contienen y usos de los mismos para el tratamiento de enfermedades del tracto respiratorio.

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Publication number
AR068057A1
AR068057A1 ARP080103461A ARP080103461A AR068057A1 AR 068057 A1 AR068057 A1 AR 068057A1 AR P080103461 A ARP080103461 A AR P080103461A AR P080103461 A ARP080103461 A AR P080103461A AR 068057 A1 AR068057 A1 AR 068057A1
Authority
AR
Argentina
Prior art keywords
alkyl
branched
linear
phenyl
cycloalkyl
Prior art date
Application number
ARP080103461A
Other languages
English (en)
Inventor
Maurizio Delcanale
Gabriele Armari
Elisabetta Armani
Original Assignee
Chiesi Farma Spa
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 Chiesi Farma Spa filed Critical Chiesi Farma Spa
Publication of AR068057A1 publication Critical patent/AR068057A1/es

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    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
    • C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/24—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with substituted hydrocarbon radicals attached to ring carbon atoms
    • C07D213/28—Radicals substituted by singly-bound oxygen or sulphur atoms
    • C07D213/30—Oxygen atoms
    • A—HUMAN NECESSITIES
    • 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
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
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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
    • A61K31/4433—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a six-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
    • A61K31/4439—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. omeprazole
    • A—HUMAN NECESSITIES
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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
    • A61K31/444—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
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    • A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/445—Non condensed piperidines, e.g. piperocaine
    • A61K31/4523—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems
    • A61K31/4545—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems containing a six-membered ring with nitrogen as a ring hetero atom, e.g. pipamperone, anabasine
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    • A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/455—Nicotinic acids, e.g. niacin; Derivatives thereof, e.g. esters, amides
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    • A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/519—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
    • A61K31/52—Purines, e.g. adenine
    • A61K31/522—Purines, e.g. adenine having oxo groups directly attached to the heterocyclic ring, e.g. hypoxanthine, guanine, acyclovir
    • A—HUMAN NECESSITIES
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    • A61K31/535—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
    • A61K31/5375—1,4-Oxazines, e.g. morpholine
    • A61K31/5377—1,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
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    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
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    • A61K31/535—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
    • A61K31/5375—1,4-Oxazines, e.g. morpholine
    • A61K31/538—1,4-Oxazines, e.g. morpholine ortho- or peri-condensed with carbocyclic ring systems
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    • A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
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    • C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/24—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with substituted hydrocarbon radicals attached to ring carbon atoms
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    • C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
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    • C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom 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
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    • C07D473/08—Heterocyclic compounds containing purine ring systems with oxygen, sulphur, or nitrogen atoms directly attached in positions 2 and 6 two oxygen atoms with radicals containing only hydrogen and carbon atoms, attached in position 1 or 3 with methyl radicals in positions 1 and 3, e.g. theophylline

Abstract

Se refiere a inhibidores de la enzima fosfodiesterasa 4 (PDE4). Más en particular, se refiere a compuestos que son derivados de alcoholes de 1-fenil-2-piridinilalquilo, a métodos de preparacion de tales compuestos, a composiciones que los contienen y a su uso terapéutico. Reivindicacion 1: Un compuesto de la formula general (1) caracterizado porque Z está seleccionado del grupo que consiste en (CH2)m, en donde m = 0, 1 o 2; (CH2)nO, en donde n = 1, 2 o 3; O(CH2)p, en donde p = 0, 1, 2 o 3; CH2SO2; CHNR6; CH2NR6; NR6, en donde R6 es H o alquilo C1-4 lineal o ramificado; OCOR4R5; y CR4R5, en donde R4 está seleccionado, de modo independiente, de H o alquilo C1-4 lineal o ramificado, con preferencia metilo, opcionalmente sustituido con un cicloalquilo C1-4 y R5 está seleccionado, de modo independiente, del grupo que consiste en alquilo C1-4 lineal o ramificado, con preferencia metilo; fenilo; bencilo; NH2; y -HNCOOR', en donde R' es alquilo C1-4 lineal o ramificado, con preferencia t-butilo; R1 y R2 son diferentes o iguales y están seleccionados, de modo independiente, del grupo que consiste en H; alquilo C1-6 lineal o ramificado opcionalmente sustituido con uno o varios sustituyentes seleccionados de cicloalquilo C3-7 o cicloalquenilo C5-7; cicloalquilo C3-7; cicloalquenilo C5-7; alquenilo C2-6 lineal o ramificado; y alquinilo C2-6 lineal o ramificado; R3 es uno o varios sustituyentes seleccionados, de modo independiente, del grupo que consiste en H, CN, NO2, CF3 y átomos de halogeno; A es un sistema de anillos, es decir, un anillo mono- o bicíclico que puede estar saturado, parcialmente insaturado o insaturado, tales como arilo, cicloalquilo C3-8 o heteroarilo, en donde dicho sistema de anillos A tiene 5 a 10 átomos del anillo, en donde al menos un átomo del anillo es un heteroátomo (por ejemplo, N, S o O), en donde el sustituyente opcional Rx en el sistema de anillos A puede ser uno o varios, puede ser igual o diferente, y está seleccionado, de modo independiente, del grupo que consiste en: alquilo C1-6 lineal o ramificado opcionalmente sustituido con uno o varios cicloalquilo C3-7; alquenilo C2-6 lineal o ramificado opcionalmente sustituido con uno o varios cicloalquilo C3-7; alquinilo C2-6 lineal o ramificado opcionalmente sustituido con uno o varios cicloalquilo C3-7; cicloalquenilo C5-7; fenilo; heterocicloalquilo C3-7; OR7, en donde R7 está seleccionado del grupo que consiste en H; alquilo C1-10 opcionalmente sustituido con uno o varios cicloalquilo C3-7; cicloalquilo C3-7; alquil C1-4-heterocicloalquilo C3-7; CO alquilo C1-6; COO alquilo C1-6; fenilo; bencilo; alquil C1-10-NR8R9, en donde R8 y R9 están seleccionados, de modo independiente, del grupo que consiste en H, alquilo C1-6 lineal o ramificado y forman, con el átomo de nitrogeno al que están unidos, un anillo saturado, parcialmente saturado o insaturado, con preferencia NR8R9 está unido a alquilo C1-10 que forma, por ejemplo anillos piperidina, oxazina, imidazol saturados, parcialmente saturados o insaturados, en donde estos anillos están opcionalmente sustituidos con alquilo C1-4; y átomos de halogeno; CN; NO2; NR10R11, en donde R10 y R11 son diferentes o iguales y están seleccionados, de modo independiente, del grupo que consiste en H; alquilo C1-6 lineal o ramificado opcionalmente sustituido con fenilo o cicloalquilo C3-7; - COC6H5; CO-alquilo C1-4; COO-alquilo C1-4; CONH-alquil C1-6-R12, en donde R12 está seleccionado del grupo que consiste en H; alquilo C1-4; OR4R5; y CONH-alquil C1-4-N-alquilo C1-4; o forman, con el átomo de nitrogeno al que están unidos, un anillo saturado o parcialmente saturado, con preferencia un anillo piperidilo; alquil C1-4-NR10R11; COR12, en donde R12 es fenilo o alquilo C1-6 lineal o ramificado; oxo; HNSO2R13, en donde R13 es alquilo C1-4 o un fenilo opcionalmente sustituido con átomos de halogeno o con un grupo alquilo C1-4; SO2R14, en donde R14 es alquilo C1-4, OH o NR10R11, en donde R10 y R11 son como se definieron con anterioridad; SOR15, en donde R15 es fenilo o alquilo C1-4; SR16, en donde R16 es H, fenilo o alquilo C1-4; COOR17, en donde R17 es H, alquilo C1-4, fenilo o bencilo; y (CH2)qOR18, en donde q = 1, 2, 3 o 4 y R18 es H o cicloalquilo C1-4; y sus sales y N-oxidos farmacéuticamente aceptables en el anillo piridina.
ARP080103461A 2007-08-08 2008-08-07 Esteres de 1-fenil-2-(3,5-dicloro)-piridina, metodo de preparacion de los mismos, composiciones farmaceuticas que los contienen y usos de los mismos para el tratamiento de enfermedades del tracto respiratorio. AR068057A1 (es)

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