CO5170501A1 - AZOLES SUSTITUIDOS UTILES PARA EL TRATAMIENTO DE ENFERMEDADES MEDIADAS POR TNFa eIL-1 Y ENFERMEDADES DEL METABOLISMO OSEO - Google Patents

AZOLES SUSTITUIDOS UTILES PARA EL TRATAMIENTO DE ENFERMEDADES MEDIADAS POR TNFa eIL-1 Y ENFERMEDADES DEL METABOLISMO OSEO

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Publication number
CO5170501A1
CO5170501A1 CO00026470A CO00026470A CO5170501A1 CO 5170501 A1 CO5170501 A1 CO 5170501A1 CO 00026470 A CO00026470 A CO 00026470A CO 00026470 A CO00026470 A CO 00026470A CO 5170501 A1 CO5170501 A1 CO 5170501A1
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Colombia
Prior art keywords
carbon atoms
alkyl
halogen
optionally substituted
atoms
Prior art date
Application number
CO00026470A
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English (en)
Inventor
Revesz Laszlo
Achim Schlapbach
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Novartis Ag
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Publication date
Priority claimed from GBGB9908532.6A external-priority patent/GB9908532D0/en
Priority claimed from GBGB9908531.8A external-priority patent/GB9908531D0/en
Application filed by Novartis Ag filed Critical Novartis Ag
Publication of CO5170501A1 publication Critical patent/CO5170501A1/es

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    • C07D401/14Heterocyclic 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 three or more hetero rings
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    • C07D403/04Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
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Abstract

La presente invención se relaciona con un compuesto de la fórmula I :<EMI FILE="00026470_1" ID="1" IMF=JPEG >en donde: a es N o C;b es CH cuando a es N, u O cuando a es C;--- denota un enlace sencillo o doble, dependiendo de si el anillo de azol es un anillo de imidazol o de oxazol;Z es N o CH;W es -NR6-Y-, -O-, ó -S-,en donde R6 es H, alquilo de 1 a 4 átomos de carbono, cicloalquilo de 3 a 8 átomos de carbono, cicloalquilo de 3 a 8 átomos de carbono-alquilo de 1 a 3 átomos de carbono, arilo de 6 a 18 átomos de carbono, heteroarilo de 3 a 18 átomos de carbono, aralquilo de 7 a 19 átomos de carbono, o heteroaralquilo de 4 a 19 átomos de carbono, e - Y - es alquileno de 1 a 4 átomos de carbono, o un enlace directo;R2 es fenilo, opcionalmente sustituido por uno o más sustituyentes, cada uno de los cuales se selecciona independientemente a partir de halógeno, CF3, ciano, amido, o tioamido, carboxilato o tiocarboxilato, alcoxilo de 1 a 4 átomos de carbono, alquilo de 1 a 4 átomos de carbono, o NH2 que está opcionalmente sustituido por mono- o di-N-alquilo de 1 a 4 átomos de carbono;R3 es H, halógeno, alquilo de 1 a 10 átomos de carbono, cicloalquilo de 3 a 10 átomos de carbono, heterocicloalquilo de 3 a 18 átomos de carbono, arilo de 6 a 18 átomos de carbono, heteroarilo de 3 a 18 átomos de carbono, o metilenaminoguanidinilo (es decir, -CH=N-NH-C(NH).NH2), cada uno de los cuales está opcionalmente sustituido por hasta cuatro sustituyentes seleccionados por separado a partir de alquilo de 1 a 4 átomos de carbono, halógeno, alquilo de 1 a 4 átomos de carbono sustituido por halógeno, hidroxilo, alcoxilo de 1 a 4 átomos de carbono, tioalquilo de 1 a 4 átomos de carbono, o amino opcionalmente sustituido por mono- o di-N-alquilo de 1 a 4 átomos de carbono, o por N-heterociclilo que contiene de 5 a 7 átomos del anillo, y que contiene opcionalmente un heteroátomo adicional;R5 es arilo de 6 a 18 átomos de carbono, heteroarilo de 3 a 18 átomos de carbono, o cicloalquilo de 3 a 12 átomos de carbono, cada uno de los cuales está opcionalmente sustituido por hasta cuatro sustituyentes seleccionados por separado a partir de alquilo de 1 a 4 átomos de carbono, halógeno, alquilo de 1 a 4 átomos de carbono sustituido por halógeno, hidroxilo, alcoxilo de 1 a 4 átomos de carbono, tioalquilo de 1 a 4 átomos de carbono, o amino opcionalmente sustituido por mono- o di-N-alquilo de 1 a 4 átomos de carbono, o por N-heterociclilo que contiene de 5 a 7 átomos del anillo, y que opcionalmente contiene un heteroátomo adicional, o un ésteres del mismo y sales de adición de ácido del mismo. Igualmente, se refiere a una composición farmacéutica que contiene dicho compuesto y el proceso para la preparación del mismo.
CO00026470A 1999-04-14 2000-04-11 AZOLES SUSTITUIDOS UTILES PARA EL TRATAMIENTO DE ENFERMEDADES MEDIADAS POR TNFa eIL-1 Y ENFERMEDADES DEL METABOLISMO OSEO CO5170501A1 (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
GBGB9908532.6A GB9908532D0 (en) 1999-04-14 1999-04-14 Organic compounds
GBGB9908531.8A GB9908531D0 (en) 1999-04-14 1999-04-14 Organic compounds

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CO5170501A1 true CO5170501A1 (es) 2002-06-27

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CO00026470A CO5170501A1 (es) 1999-04-14 2000-04-11 AZOLES SUSTITUIDOS UTILES PARA EL TRATAMIENTO DE ENFERMEDADES MEDIADAS POR TNFa eIL-1 Y ENFERMEDADES DEL METABOLISMO OSEO

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Country Link
US (1) US6579874B2 (es)
EP (1) EP1224180B1 (es)
JP (1) JP2003503311A (es)
KR (1) KR20010108504A (es)
CN (1) CN1378544A (es)
AR (1) AR023465A1 (es)
AT (1) ATE244236T1 (es)
AU (1) AU4295300A (es)
BR (1) BR0010598A (es)
CA (1) CA2370417A1 (es)
CO (1) CO5170501A1 (es)
CZ (1) CZ20013696A3 (es)
DE (1) DE60003709T2 (es)
DK (1) DK1224180T3 (es)
ES (1) ES2202114T3 (es)
HU (1) HUP0302747A2 (es)
IL (1) IL145836A0 (es)
MX (1) MXPA01010434A (es)
NO (1) NO20014987L (es)
PE (1) PE20010031A1 (es)
PL (1) PL364789A1 (es)
PT (1) PT1224180E (es)
SK (1) SK14562001A3 (es)
TR (1) TR200102967T2 (es)
WO (1) WO2000063204A2 (es)

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AU4295300A (en) 2000-11-02
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KR20010108504A (ko) 2001-12-07
AR023465A1 (es) 2002-09-04
JP2003503311A (ja) 2003-01-28
US20020049220A1 (en) 2002-04-25
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PE20010031A1 (es) 2001-02-23
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EP1224180A2 (en) 2002-07-24
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ATE244236T1 (de) 2003-07-15
WO2000063204A2 (en) 2000-10-26
CN1378544A (zh) 2002-11-06
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CA2370417A1 (en) 2000-10-26
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