AR032676A1 - Quinazolinas como inhibidores de mmp-13 - Google Patents

Quinazolinas como inhibidores de mmp-13

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Publication number
AR032676A1
AR032676A1 ARP020100470A ARP020100470A AR032676A1 AR 032676 A1 AR032676 A1 AR 032676A1 AR P020100470 A ARP020100470 A AR P020100470A AR P020100470 A ARP020100470 A AR P020100470A AR 032676 A1 AR032676 A1 AR 032676A1
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AR
Argentina
Prior art keywords
alkyl
oxygen
nitrogen
sulfur
nr10r11
Prior art date
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ARP020100470A
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English (en)
Inventor
Bernard Gaudilliere
Henry Jacobelli
Daniel Fred Ortwine
William Chester Patt
Catherine Rose Kostlan
Charles Andrianjara
Barvian Nicole Chantel
Michael William Wilson
Ly Phan
Original Assignee
Warner Lambert Co
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Publication of AR032676A1 publication Critical patent/AR032676A1/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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    • 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
    • A61K31/495—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
    • A61K31/517—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with carbocyclic ring systems, e.g. quinazoline, perimidine
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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
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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
    • A61K31/525—Isoalloxazines, e.g. riboflavins, vitamin B2
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    • C07D—HETEROCYCLIC COMPOUNDS
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    • C07D239/70—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings condensed with carbocyclic rings or ring systems
    • C07D239/72—Quinazolines; Hydrogenated quinazolines
    • C07D239/95—Quinazolines; Hydrogenated quinazolines with hetero atoms directly attached in positions 2 and 4
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    • C07D239/72—Quinazolines; Hydrogenated quinazolines
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    • C07D471/04—Ortho-condensed systems

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  • Plural Heterocyclic Compounds (AREA)
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Abstract

Compuesto de quinazolinas substituidas de formula (1), donde R1 es hidrogeno, amino, C1-6alquilo , C3-6alquenilo, alquinilo C3-6, mono C1-6 alquilamino C1-6 alquilo, di C1-6 alquilamino C1-6 alquilo, arilo, aril C1-6 alquilo, heterociclo y cicloalquil C1-6 alquil de 3 a 6 miembros, insustituidos o sustituidos con uno o más grupos amino, C1-6 alquilo, ciano, halo C1-6 alquilo, C(=O)OR4, OR4 y SR4; R4 representa hidrogeno o C1-6 alquilo, en donde R4 es tal como se define en la memoria; W es oxígeno, azufre, o =N-R'; R' representa C1-6 alquilo, hidroxilo o ciano; X1, X2 y X3 representan, nitrogeno o -C-R6 y R6 es tal como se define en la memoria; Y representan oxígeno, azufre, -NH y -N C1-6 alquilo; Z es oxígeno, azufre o -NR7, y R7 es tal como se define en la memoria; n es de 1 a 8 inclusive; Z1 representa -CR8R9, y R8 y R9 son tal como se definen en la memoria; A representa un monociclo de 5 o 6 miembros, aromático o no aromático, con 0 a 4 heteroátomos nitrogeno, oxígeno y azufre, y un biciclo, de dos anillos de 5 o 6 miembros, aromáticos o no aromáticos, idénticos o diferentes, con 0 a 4 heteroátomos nitrogeno, oxígeno y azufre; m es 0 a 7 inclusive; R2 es C1-6 alquilo, halogeno, -CN, NO2, SCF3, -CF3, -OCF3, -NR10R11, -OR10, -SR10, SOR10, -SO2R10, (CH2)kSO2NR10R11, -X5(CH2)kC(=O)OR10, -(CH2)kC(=O)OR10, -X5(CH2)kC(=O)NR10R11, -(CH2)kC(=O)NR10R11, y -X4-R12, en los cuales X5, k, R10, R11, X4 y R12 son tal como se definen en la memoria; R3 representa hidrogeno, C1-6 alquilo, C3-6 alquenilo, C3-6 alquinilo, insustituidos o sustituidos con amino, ciano , halo C1-6 alquilo, cicloalquilo, -C(=O)NR10R11, -C(=O)OR10, OR10, y S10, donde R10 y R11, son como se definen en la memoria; y, cuando el anillo es heterocíclico, comprende de 1 a 4 heteroátomos nitrogeno, oxígeno y azufre, con la condicion de que cuando X1 representa un nitrogeno, X2 no puede representar un carbono sustituido por un grupo metilo o por NH-CH3, las formas racémicas, isomeros, N-oxido, y sales farmacéuticamente aceptables. Se incluyen compuestos intermediarios, los procesos de fabricacion y el uso de esos compuestos para preparar un producto medicinal para una terapia de inhibicion de la metaloproteasa de matriz de tipo 13 (MMP-13), como ser para tratar artritis, artritis reumatoide, osteoartritis, osteoporosis, afecciones periodontales, afeccion por inflamacion intestinal, psoriasis, esclerosis multiple, insuficiencia cardíaca, ateroesclerosis, asma, enfermedad de obstruccion pulmonar cronica (COPD), deterioro macular relacionado con la edad (ARMD) y cánceres.
ARP020100470A 2001-02-14 2002-02-13 Quinazolinas como inhibidores de mmp-13 AR032676A1 (es)

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US (1) US20020193377A1 (es)
EP (1) EP1368324A1 (es)
JP (1) JP2004523546A (es)
KR (1) KR20030074827A (es)
CN (1) CN1537105A (es)
AP (1) AP2003002841A0 (es)
AR (1) AR032676A1 (es)
BG (1) BG108091A (es)
BR (1) BR0207268A (es)
CA (1) CA2437122A1 (es)
CZ (1) CZ20032142A3 (es)
EA (1) EA200300792A1 (es)
EC (1) ECSP034730A (es)
EE (1) EE200300384A (es)
HU (1) HUP0303164A2 (es)
IL (1) IL157109A0 (es)
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MA (1) MA26994A1 (es)
MX (1) MXPA03007248A (es)
NO (1) NO20033593L (es)
OA (1) OA12550A (es)
PA (1) PA8539401A1 (es)
PE (1) PE20021005A1 (es)
PL (1) PL367396A1 (es)
SK (1) SK10012003A3 (es)
SV (1) SV2003000876A (es)
TN (1) TNSN03045A1 (es)
UY (1) UY27173A1 (es)
WO (1) WO2002064572A1 (es)
ZA (1) ZA200306008B (es)

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US6924276B2 (en) 2001-09-10 2005-08-02 Warner-Lambert Company Diacid-substituted heteroaryl derivatives as matrix metalloproteinase inhibitors
MXPA04002537A (es) 2001-10-12 2004-05-31 Warner Lambert Co Alquinos como inhibidores de metaloproteinasa de matriz.
US6962922B2 (en) 2001-10-12 2005-11-08 Warner-Lambert Company Llc Alkynylated quinazoline compounds
US6894057B2 (en) 2002-03-08 2005-05-17 Warner-Lambert Company Oxo-azabicyclic compounds
US6747147B2 (en) 2002-03-08 2004-06-08 Warner-Lambert Company Oxo-azabicyclic compounds
AU2002249275A1 (en) * 2002-03-08 2003-09-22 Warner-Lambert Company Llc Oxo azabicyclic compounds
US20040006077A1 (en) * 2002-06-25 2004-01-08 Bernard Gaudilliere Thiazine and oxazine derivatives as MMP-13 inhibitors
EP1531904A1 (en) * 2002-07-17 2005-05-25 Warner-Lambert Company LLC Combination of an allosteric inhibitor of matrix metalloproteinase-13 with a selective inhibitor of cyclooxygenase-2 that is not celecoxib or valdecoxib
MXPA05000754A (es) * 2002-07-17 2005-04-19 Warner Lambert Co Combinacion de un inhibidor carboxilico alosterico de la metaloproteinasa de matriz-13 con celecoxib o valdecoxib.
BR0312727A (pt) * 2002-07-17 2005-04-19 Warner Lambert Co Combinação de um inibidor alostérico da metaloproteinase-13 de matriz com celecoxib ou valdecoxib
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