AR052266A1 - Derivados de pirroles, su preparacion, y su uso como compuestos farmaceuticos - Google Patents

Derivados de pirroles, su preparacion, y su uso como compuestos farmaceuticos

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Publication number
AR052266A1
AR052266A1 ARP050105197A ARP050105197A AR052266A1 AR 052266 A1 AR052266 A1 AR 052266A1 AR P050105197 A ARP050105197 A AR P050105197A AR P050105197 A ARP050105197 A AR P050105197A AR 052266 A1 AR052266 A1 AR 052266A1
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AR
Argentina
Prior art keywords
alkyl
amino
group
atoms
membered heterocyclic
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ARP050105197A
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English (en)
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Novartis Ag
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Application filed by Novartis Ag filed Critical Novartis Ag
Publication of AR052266A1 publication Critical patent/AR052266A1/es

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    • 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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    • 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
    • A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
    • A61K31/4025—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil not condensed and containing further heterocyclic rings, e.g. cromakalim
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    • C07D207/30—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 two double bonds between ring members or between ring members and non-ring members
    • C07D207/34—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 two double bonds between ring members or between ring members and non-ring members 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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    • C07—ORGANIC CHEMISTRY
    • 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
    • C07D401/04—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 directly linked by a ring-member-to-ring-member bond
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    • C07D405/02—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
    • C07D405/04—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 directly linked by a ring-member-to-ring-member bond

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  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Veterinary Medicine (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Public Health (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Pulmonology (AREA)
  • Immunology (AREA)
  • Diabetes (AREA)
  • Dermatology (AREA)
  • Hematology (AREA)
  • Physical Education & Sports Medicine (AREA)
  • Ophthalmology & Optometry (AREA)
  • Rheumatology (AREA)
  • Urology & Nephrology (AREA)
  • Vascular Medicine (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Orthopedic Medicine & Surgery (AREA)
  • Obesity (AREA)
  • Cardiology (AREA)
  • Neurology (AREA)
  • Child & Adolescent Psychology (AREA)
  • Pain & Pain Management (AREA)
  • Communicable Diseases (AREA)
  • Biomedical Technology (AREA)
  • Tropical Medicine & Parasitology (AREA)
  • Neurosurgery (AREA)
  • Endocrinology (AREA)
  • Gastroenterology & Hepatology (AREA)
  • Oncology (AREA)
  • Otolaryngology (AREA)

Abstract

Un proceso para prepararlos, y su uso como productos farmacéuticos. Reivindicacion 1: Un compuesto de la formula (1) en forma libre o de sal farmacéuticamente aceptable, en donde Q es [cR1R2]m; R1 y R2 son independientemente H, alquilo C1-8, o junto con el átomo de C con el que están unidos, forman un grupo cicloalifático divalente de 3 a 8 átomos de C; R3 y R4 se seleccionan independientemente a partir de H y alquilo C1-8; R5 se selecciona a partir de H, halogeno, alquilo C1-8, haloalquilo C1-8, un grupo carbocíclico de 3 a 15 átomos de C, nitro, ciano, SO2R5a, SOR5b, SR5c, alquilo C1-8-carbonilo, alcoxilo C1-8-carbonilo, alcoxilo C1-8, haloalcoxilo C1-8, carboxilo, carboxi-alquilo C1-8, amino, amino-(alquilo C1-8), alquilo C1-8-amino, di-(alquilo C1-8)-amino, SO2NR5dR5e, -C(O)NR5fR5g, un grupo carbocíclico aromático de 6 a 15 átomos de C, y un grupo heterocíclico de 4 a 10 miembros que tiene uno o más heteroátomos seleccionados a partir del grupo que consiste en O, N y S; R5a, R5b y R5c se seleccionan independientemente a partir de alquilo C1-8, hidroxialquilo C1-8, alquilo C1-8-amino-(alquilo C1-8), di-(alquilo C1-8)- amino-(alquilo C1-8), cianoalquilo C1-8, un grupo carbocíclico de 3 a 15 átomos de C, haloalquilo C1-8, y un grupo heterocíclico de 4 a 10 miembros que tiene uno o más heteroátomos seleccionados a partir del grupo que consiste en O, N, y S; R5d, R5e, R5f, y R5g son independientemente H, alquilo C1-8, hidroxialquilo C1-8, alquilo C1-8- amino-(alquilo C1-8), di-(alquilo C1-8)-amino-(alquilo C1-8), cianoalquilo C1-8, un grupo carbocíclico de 3 a 15 átomos de C, haloalquilo C1-8, y un grupo heterocíclico de 4 a 10 miembros que tiene uno o más heteroátomos seleccionados a partir del grupo que consiste en O, N, y S; o junto con el átomo de N con el que están unidos, forman un grupo heterocíclico de 4 a 10 átomos de C; R6 se selecciona a partir de H, halogeno, alquilo C1-8, haloalquilo C1-8, un grupo carbocíclico de 3 a 15 átomos de C, nitro, ciano, SO2R6a, alquilo C1-8-carbonilo, alcoxilo C1-8-carbonilo, alcoxilo C1-8, haloalcoxilo C1-8, -SR6b, carboxilo, carboxi-alquilo C1-8, amino, amino-(alquilo C1-8), alquilo C18-amino-(alquilo C1-8), di-(alquilo C1-8)-amino-(alquilo C1- 8), alquilo C1-8-amino, di-(alquilo C1-8)-amino, SO2NR6cR6d, -C(O)NR6eR6f, hidroxialquilo C1-8, NR6gSO2R6h, NR6i(CO)R6j, SOR6k, un grupo carbocíclico aromático de 6 a 15 átomos de C, y un grupo heterocíclico de 4 a 10 miembros que tiene uno o más heteroátomos seleccionados a partir del grupo que consiste en O, N y S; R6a, R6k, y R6b se seleccionan independientemente a partir de alquilo C1-8, hidroxialquilo C1-8, alquilo C1-8-amino-(alquilo C1-8), di-(alquilo C1-8)-amino-(alquilo C1-8), cianoalquilo C1-8, un grupo carbocíclico de 3 a 15 átomos de C, haloalquilo C1-8, y un grupo heterocíclico de 4 a 10 miembros que tiene uno o más heteroátomos seleccionados a partir del grupo que consiste en O, N y S; R6c, R6d,R6e, y R6f son independientemente H, alquilo C1-8, hidroxialquilo C1-8, alquilo C1-8-amino-(alquilo C1-8), di-(alquilo C1-8)-amino-(alquilo C1-8), cianoalquilo C1-8, un grupo carbocíclico de 3 a 15 átomos de C, haloalquilo C1-8, un grupo heterocíclico de 4 a 10 miembros que tiene uno o más heteroátomos seleccionados a partir del grupo que consiste en O, N, y S, o junto con el átomo de N con el que están unidos, forman un grupo heterocíclico de 4 a 10 átomos de C; R6g y R6i se seleccionan independientemente a partir de H, alquilo C1-8, hidroxialquilo C1-8, alquilo C1-8-amino-(alquilo C1-8), di-(alquilo C1-8)-amino-(alquilo C1-8), cianoalquilo C1-8, un grupo carbocíclico de 3 a 15 átomos de C, haloalquilo C1-8, y un grupo heterocíclico de 4 a 10 miembros que tiene uno o más heteroátomos seleccionados a partir del grupo que consiste en O, N, y S; R6h y R6j se seleccionan independientemente a partir de alquilo C1-8, un grupo carbocíclico de 3 a 15 átomos de C, un grupo heterocíclico de 4 a 10 miembros que tiene uno o más heteroátomos seleccionados a partir del grupo que consiste en O, N y S, hidroxialquilo C1-8, amino-(alquilo C1-8), alquilo C1-8-amino-(alquilo C1-8), di-(alquilo C1-8)-amino-(alquilo C1-8), y cianoalquilo C1-8;W se selecciona a partir de un grupo carbocíclico de 3 a 15 átomos de C, y un heterociclo de 4 a 10 miembros que tiene uno o más heteroátomos seleccionados a partir del grupo que consiste en O, N y S; m es un entero seleccionado a partir de 1 a 3; y n es un entero seleccionado a partir de 1 a 4.
ARP050105197A 2004-12-14 2005-12-12 Derivados de pirroles, su preparacion, y su uso como compuestos farmaceuticos AR052266A1 (es)

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GBGB0427381.9A GB0427381D0 (en) 2004-12-14 2004-12-14 Organic compounds

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AR052266A1 true AR052266A1 (es) 2007-03-07

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US (1) US20100087432A1 (es)
EP (1) EP1828172B1 (es)
JP (1) JP2008523130A (es)
KR (1) KR20070087605A (es)
CN (1) CN101072773B (es)
AR (1) AR052266A1 (es)
AT (1) ATE449772T1 (es)
AU (1) AU2005315881C1 (es)
BR (1) BRPI0518607A2 (es)
CA (1) CA2587934A1 (es)
DE (1) DE602005017935D1 (es)
ES (1) ES2335519T3 (es)
GB (1) GB0427381D0 (es)
GT (1) GT200500360A (es)
MX (1) MX2007007098A (es)
PE (1) PE20060736A1 (es)
PL (1) PL1828172T3 (es)
PT (1) PT1828172E (es)
RU (1) RU2007126761A (es)
TW (1) TW200635921A (es)
WO (1) WO2006063763A1 (es)

Families Citing this family (23)

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Publication number Priority date Publication date Assignee Title
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TW200848019A (en) * 2007-03-06 2008-12-16 Wyeth Corp Aryl sulfonamides useful for modulation of the progesterone receptor
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TW200635921A (en) 2006-10-16
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AU2005315881B2 (en) 2009-09-24
AU2005315881A1 (en) 2006-06-22
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