AR038476A1 - Derivados de quinazolina - Google Patents
Derivados de quinazolinaInfo
- Publication number
- AR038476A1 AR038476A1 ARP030100315A ARP030100315A AR038476A1 AR 038476 A1 AR038476 A1 AR 038476A1 AR P030100315 A ARP030100315 A AR P030100315A AR P030100315 A ARP030100315 A AR P030100315A AR 038476 A1 AR038476 A1 AR 038476A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkyl
- alkoxy
- amino
- group
- hydroxy
- Prior art date
Links
- JWVCLYRUEFBMGU-UHFFFAOYSA-N quinazoline Chemical class N1=CN=CC2=CC=CC=C21 JWVCLYRUEFBMGU-UHFFFAOYSA-N 0.000 title 1
- 125000000217 alkyl group Chemical group 0.000 abstract 42
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 23
- 229910052739 hydrogen Inorganic materials 0.000 abstract 18
- 239000001257 hydrogen Substances 0.000 abstract 18
- 150000002431 hydrogen Chemical group 0.000 abstract 16
- 229910052757 nitrogen Inorganic materials 0.000 abstract 15
- 125000006273 (C1-C3) alkyl group Chemical group 0.000 abstract 13
- 125000001424 substituent group Chemical group 0.000 abstract 11
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 10
- 229910052736 halogen Inorganic materials 0.000 abstract 9
- 150000002367 halogens Chemical group 0.000 abstract 9
- 125000005842 heteroatom Chemical group 0.000 abstract 9
- 229910052760 oxygen Inorganic materials 0.000 abstract 9
- 229910052717 sulfur Inorganic materials 0.000 abstract 9
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 8
- 125000004043 oxo group Chemical group O=* 0.000 abstract 7
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 abstract 6
- 125000003342 alkenyl group Chemical group 0.000 abstract 6
- 125000003282 alkyl amino group Chemical group 0.000 abstract 6
- 125000004122 cyclic group Chemical group 0.000 abstract 6
- 125000000623 heterocyclic group Chemical group 0.000 abstract 6
- 125000000304 alkynyl group Chemical group 0.000 abstract 5
- 125000004103 aminoalkyl group Chemical group 0.000 abstract 5
- 150000001875 compounds Chemical class 0.000 abstract 5
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 5
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 abstract 4
- 125000003545 alkoxy group Chemical group 0.000 abstract 4
- -1 hydroxy C1-4 alkyl Chemical group 0.000 abstract 4
- 238000000034 method Methods 0.000 abstract 4
- 125000002853 C1-C4 hydroxyalkyl group Chemical group 0.000 abstract 3
- 125000004453 alkoxycarbonyl group Chemical group 0.000 abstract 3
- 125000004966 cyanoalkyl group Chemical group 0.000 abstract 3
- 125000006569 (C5-C6) heterocyclic group Chemical group 0.000 abstract 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 abstract 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 2
- 125000004471 alkyl aminosulfonyl group Chemical group 0.000 abstract 2
- 125000004397 aminosulfonyl group Chemical group NS(=O)(=O)* 0.000 abstract 2
- 125000006615 aromatic heterocyclic group Chemical group 0.000 abstract 2
- 125000003118 aryl group Chemical group 0.000 abstract 2
- 229910052799 carbon Inorganic materials 0.000 abstract 2
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 abstract 2
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 abstract 2
- 201000010099 disease Diseases 0.000 abstract 2
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 2
- AQYSYJUIMQTRMV-UHFFFAOYSA-N hypofluorous acid Chemical compound FO AQYSYJUIMQTRMV-UHFFFAOYSA-N 0.000 abstract 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 2
- UBQKCCHYAOITMY-UHFFFAOYSA-N pyridin-2-ol Chemical group OC1=CC=CC=N1 UBQKCCHYAOITMY-UHFFFAOYSA-N 0.000 abstract 2
- 150000003839 salts Chemical class 0.000 abstract 2
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 abstract 2
- 125000004455 (C1-C3) alkylthio group Chemical group 0.000 abstract 1
- 125000006274 (C1-C3)alkoxy group Chemical group 0.000 abstract 1
- 125000002861 (C1-C4) alkanoyl group Chemical group 0.000 abstract 1
- 125000004765 (C1-C4) haloalkyl group Chemical group 0.000 abstract 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 abstract 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 abstract 1
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 abstract 1
- 241001465754 Metazoa Species 0.000 abstract 1
- 206010028980 Neoplasm Diseases 0.000 abstract 1
- 102000005789 Vascular Endothelial Growth Factors Human genes 0.000 abstract 1
- 108010019530 Vascular Endothelial Growth Factors Proteins 0.000 abstract 1
- 125000002431 aminoalkoxy group Chemical group 0.000 abstract 1
- 230000033115 angiogenesis Effects 0.000 abstract 1
- 230000001772 anti-angiogenic effect Effects 0.000 abstract 1
- 125000002619 bicyclic group Chemical group 0.000 abstract 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 abstract 1
- 229910052794 bromium Inorganic materials 0.000 abstract 1
- 201000011510 cancer Diseases 0.000 abstract 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 abstract 1
- 229910052801 chlorine Inorganic materials 0.000 abstract 1
- 239000000460 chlorine Substances 0.000 abstract 1
- 239000003814 drug Substances 0.000 abstract 1
- 229940079593 drug Drugs 0.000 abstract 1
- 230000000694 effects Effects 0.000 abstract 1
- 229910052731 fluorine Inorganic materials 0.000 abstract 1
- 239000011737 fluorine Substances 0.000 abstract 1
- 125000005113 hydroxyalkoxy group Chemical group 0.000 abstract 1
- 238000004519 manufacturing process Methods 0.000 abstract 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
- 125000002294 quinazolinyl group Chemical class N1=C(N=CC2=CC=CC=C12)* 0.000 abstract 1
- 206010039073 rheumatoid arthritis Diseases 0.000 abstract 1
- 229920006395 saturated elastomer Polymers 0.000 abstract 1
- 230000008728 vascular permeability Effects 0.000 abstract 1
Classifications
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- C—CHEMISTRY; METALLURGY
- 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
- C07D401/14—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 three or more hetero rings
-
- 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
- A61K31/495—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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K35/00—Medicinal preparations containing materials or reaction products thereof with undetermined constitution
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P13/00—Drugs for disorders of the urinary system
- A61P13/12—Drugs for disorders of the urinary system of the kidneys
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P15/00—Drugs for genital or sexual disorders; Contraceptives
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
- A61P17/02—Drugs for dermatological disorders for treating wounds, ulcers, burns, scars, keloids, or the like
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
- A61P17/06—Antipsoriatics
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
- A61P19/02—Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P27/00—Drugs for disorders of the senses
- A61P27/02—Ophthalmic agents
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
- A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
- A61P35/02—Antineoplastic agents specific for leukemia
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
- A61P37/06—Immunosuppressants, e.g. drugs for graft rejection
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- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
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- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P7/00—Drugs for disorders of the blood or the extracellular fluid
- A61P7/02—Antithrombotic agents; Anticoagulants; Platelet aggregation inhibitors
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- A61P9/00—Drugs for disorders of the cardiovascular system
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- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
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- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/14—Vasoprotectives; Antihaemorrhoidals; Drugs for varicose therapy; Capillary stabilisers
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic 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
- C07D403/12—Heterocyclic 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 linked by a chain containing hetero atoms as chain links
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D491/00—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
- C07D491/02—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
- C07D491/04—Ortho-condensed systems
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Diabetes (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Immunology (AREA)
- Hematology (AREA)
- Rheumatology (AREA)
- Dermatology (AREA)
- Epidemiology (AREA)
- Endocrinology (AREA)
- Vascular Medicine (AREA)
- Urology & Nephrology (AREA)
- Obesity (AREA)
- Pain & Pain Management (AREA)
- Transplantation (AREA)
- Ophthalmology & Optometry (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Physical Education & Sports Medicine (AREA)
- Reproductive Health (AREA)
- Emergency Medicine (AREA)
- Oncology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
Abstract
Derivados de quinazolina, su uso en la fabricación de un medicamento que se usa para producir un efecto antiangiogénico y/o reducir la permeabilidad vascular en animales de sangre caliente; procesos para la preparación de dichos compuestos; intermediarios utilizados en dichos procesos; procesos para preparar dichos intermediarios; composiciones farmacéuticas que contienen un compuesto de la fórmula (1) o una sal aceptable para uso farmacéutico del mismos y métodos para tratar estados de enfermedad que involucran angiogénesis mediante la administración de un compuesto de la fórmula (1) o una sal aceptable para uso farmacéutico del mismo. Los compuestos de la fórmula (1) inhiben los efectos de VEGF, una propiedad valiosa en el tratamiento de una cantidad de estados de enfermedad entre los que se incluyen el cáncer y la artritis reumatoide. Reivindicación 1: Un compuesto caracterizado porque responde a la formula (1) donde: el anillo C es una porción bicíclica o tricíclica de 8, 9, 10, 12 ó 13 miembros; dicha porción puede ser saturada o insaturada, que puede ser aromática o no aromática, y que opcionalmente puede contener 1-3 heteroátomos seleccionados independientemente entre O, N y S; Z es -O-, -NH- ó -S-; n es 0, 1, 2, 3, 4 ó 5; m es 0, 1, 2 ó 3; R2 representa hidrógeno, hidroxi, halógeno, ciano, nitro, trifluorometilo, alquilo C1-3, alcoxi C1-3, alquilsulfanilo C1-3, -NR3R4 (donde R3 y R4, que pueden ser iguales o diferentes, cada uno representa hidrógeno o alquilo C1-3), ó R5X1- (donde X1 representa un enlace directo, -O-, -CH2-, -OC(O)-, -C(O)-, -S-, -SO-, -SO2-, -NR6C(O)-, -C(O)NR7-, -SO2NR8-, -NR9SO2- ó -NR10- (donde R6, R7, R8, R9 y R10 cada uno independientemente representa hidrógeno, alquilo C1-3 ó alcoxi C1-3-alquilo C2-3), y R5 se selecciona entre uno de los siguientes veintidós grupos: 1) hidrógeno, oxiranil-alquilo C1-4 ó alquilo C1-5 que puede ser insustituido o que puede estar sustituido con uno o más grupos seleccionados entre hidroxi, flúor, cloro, bromo y amino; 2) alquil C1-5-X2C(O)R11 (donde X2 representa -O- ó -NR12- (en donde R12 representa hidrógeno, alquilo C1-3 ó alcoxi C1-3-alquilo C2-3) y R11 representa alquilo C1-3, -NR13R14 ó -OR15 (donde R13, R14 y R15 que pueden ser iguales o diferentes cada uno representa hidrógeno, alquilo C1-5 ó alcoxi C1-3-alquilo C2-3)); 3) alquilo C1-5-X3R16 (donde X3 representa -O-, -S-, -SO-, -SO2-, -OC(O)-, -NR17C(O)-, -C(O)NR18-, -SO2NR19-, -NR20SO2- ó -NR21- (donde R17, R18, R19, R20 y R21 cada uno independientemente representa hidrógeno, alquilo C1-3 ó alcoxi C1-3-alquilo C2-3) y R16 representa hidrógeno, alquilo C1-3, ciclopentilo, ciclohexilo ó un grupo heterocíclico saturado de 5-6 miembros con 1-2 heteroátomos, seleccionados independientemente entre O, S y N, donde dicho grupo alquilo C1-3 puede tener 1 ó 2 sustituyentes seleccionados entre oxo, hidroxi, halógeno y alcoxi C1-4 y donde el grupo cíclico puede tener 1 ó 2 sustituyentes seleccionados entre oxo, hidroxi, halógeno, ciano, cianoalquilo C1-4, alquilo C1-4, hidroxialquilo C1-4, alcoxi C1-4, alcoxi C1-4-alquilo C1-4, alquilsulfonil C1-4-alquilo C1-4, alcoxicarbonilo C1-4, aminoalquilo C1-4, alquilamino C1-4, di(alquil C1-4)amino, alquilamino C1-4-alquilo C1-4, di(alquil C1-4)amino-alquilo C1-4, alquilamino C1-4-alcoxi C1-4, di(alquil C1-4)amino alcoxi C1-4 y un grupo -(-O-)f(alquil C1-4)g-anillo D (donde f es 0 ó 1, g es 0 ó 1 y el anillo D es un grupo heterocíclico saturado de 5-6 miembros con 1-2 heteroátomos, seleccionados independientemente entre O, S y N, donde el grupo cíclico puede tener uno o más sustituyentes seleccionado entre alquilo C1-4)); 4) alquil C1-5-X4-alquil C1-5-X5-R22 (donde X4 y X5 que pueden ser iguales o diferentes son cada uno -O-, -S-, -SO-, -SO2-, -NR23C(O)-, -C(O)NR24-, -SO2NR25-, -NR26SO2- ó - NR27- (donde R23, R24, R25, R26 y R27 cada uno independientemente representa hidrógeno, alquilo C1-3 ó alcoxi C1-3-alquilo C2-3) y R22 representa hidrógeno, alquilo C1-3 ó alcoxi C1-3-alquilo C2-3); 5) R28 (donde R28 es un grupo heterocíclico saturado de 5-6 miembros (unidos a través de carbono o nitrógeno) con 1-2 heteroátomos, seleccionados independientemente entre O, S y N, donde dicho grupo heterocíclico puede tener 1 ó 2 sustituyentes seleccionados entre oxo, hidroxi, halógeno, ciano, cianoalquilo C1-4, alquilo C1-4, hidroxialquilo C1-4, alcoxi C1-4, alcoxi C1-4-alquilo C1-4, alquilsulfonil C1-4-alquilo C1-4, alcoxi C1-4-carbonilo, aminoalquilo C1-4, alquil C1-4-amino, di(alquil C1-4)amino, alquilamino C1-4-alquilo C1-4, di(alquil C1-4)amino-alquilo C1-4, alquilamino C1-4-alcoxi C1-4, di(alquil C1-4)amino-alcoxi C1-4, y un grupo -(-O-)f(alquil C1-4)g-anillo D (donde f es 0 ó 1, g es 0 ó 1 y el anillo D es un grupo heterocíclico saturado de 5-6 miembros con 1-2 heteroátomos, seleccionados independientemente entre O, S y N, donde el grupo cíclico puede tener uno o más sustituyentes seleccionados entre alquilo C1-4)); 6) alquil C1-5-R28 (donde R28 tiene los valores definidos en la presente); 7) alquenil C2-5-R28 (donde R28 tiene los valores definidos en la presente); 8) alquinil C2-5-R28 (donde R28 tiene los valores definidos en la presente); 9) R29 (donde R29 representa un grupo piridona, un grupo fenilo ó un grupo heterocíclico aromático de 5-6 miembros (unidos a través de carbono o nitrógeno) con 1-3 heteroátomos seleccionados entre O, N y S, donde dicho grupo piridona, fenilo ó grupo heterocíclico aromático puede contener hasta 5 sustituyentes seleccionados entre oxo, hidroxi, halógeno, amino, alquilo C1-4, alcoxi C1-4, hidroxialquilo C1-4, aminoalquilo C1-4, alquilamino C1-4, hidroxialcoxi C1-4, carboxi, trifluorometilo, ciano, -C(O)NR30R31, -NR32C(O)R33 (donde R30, R31, R32 y R33, que pueden ser iguales o diferentes, cada uno representa hidrógeno, alquilo C1-4 ó alcoxi C1-3 alquilo C2-3) y un grupo -(-O-)f(alquil C1-4)g-anillo D (donde f es 0 ó 1, g es 0 ó 1 y el anillo D es un grupo heterocíclico saturado de 5-6 miembros con 1-2 heteroátomos, seleccionados independientemente entre O, N y S, donde el grupo cíclico puede tener uno o más sustituyentes seleccionados entre alquilo C1-4)); 10) alquil C1-5-R29 (donde R29 tiene los valores definidos en la presente); 11) alquenil C2-5-R29 (donde R29 tiene los valores definidos en la presente); 12) alquinil C2-5-R29 (donde R29 tiene los valores definidos en la presente); 13) alquil C1-5-X6R29 (donde X6 representa -O-, -S-, -SO-, -SO2-, -NR34C(O)-, -C(O)NR35-, -SO2NR36-, -NR37SO2- ó -NR38- (donde R34, R35, R36, R37 y R38 cada uno independientemente representa hidrógeno, alquilo C1-3 ó alcoxi C1-3-alquilo C2-3) y R29 tiene los valores definidos en la presente); 14) alquenil C2-5-X7R29 (donde X7 representa -O-, -S-, -SO-, -SO2-, -NR39C(O)-, -C(O)NR40-, -SO2NR41-, -NR42SO2- ó -NR43- (donde R39, R40, R41, R42 y R43 cada uno independientemente representa hidrógeno, alquilo C1-3 ó alcoxi C1-3-alquilo C2-3) y R29 tiene los valores definidos en la presente); 15) alquinil C2-5-X8R29 (donde X8 representa -O-, -S-, -SO-, -SO2-, -NR44C(O)-, -C(O)NR45-, -SO2NR46-, -NR47SO2- ó -NR48- (donde R44, R45, R46, R47 y R48 cada uno independientemente representa hidrógeno, alquilo C1-3 ó alcoxi C1-3-alquilo C2-3) y R29 tiene los valores definidos en la presente); 16) alquil C1-4-X9-alquil C1-4-R29 (donde X9 representa -O-, -S-, -SO-, -SO2-, -NR49C(O)-, -C(O)NR50-, -SO2NR51-, -NR52SO2- ó -NR53- (donde R49, R50, R51, R52 y R53 cada uno independientemente representa hidrógeno, alquilo C1-3 ó alcoxi C1-3-alquilo C2-3) y R29 tiene los valores definidos en la presente); 17) alquil C1-4-X9-alquil C1-4-R28 (donde X9 y R28 tienen los valores que se han definido); 18) alquenilo C2-5 que puede ser insustituido o que puede ser sustituido con uno o más grupos seleccionados entre hidroxi, flúor, amino, alquilamino C1-4, N,N-di(alquil C1-4)amino, aminosulfonilo, N-alquil C1-4-aminosulfonilo y N,N-di(alquil C1-4)aminosulfonilo; 19) alquinilo C2-5 que puede ser insustituido o que puede ser sustituido con uno o más grupos seleccionados entre hidroxi, flúor, amino, alquilamino C1-4, N,N-di(alquil C1-4)amino, aminosulfonilo, N-alquil C1-4-aminosulfonilo y N,N-di(alquil C1-4)aminosulfonilo; 20) alquenil C2-5-X9-alquil C1-4-R28 (donde X9 y R28 tienen los valores que se han definido); 21) alquinilo C2-5-X9-alquil C1-4-R28 (donde X9 y R28 tienen los valores que se han definido); y 22) alquil C1-4-R54-(alquil C1-4)q(X9)rR55 (donde X9 tiene los valores definidos en la presente, q es 0 ó 1, r es 0 ó 1, y R54 y R55 son cada uno seleccionados independientemente entre hidrógeno, alquilo C1-3, ciclopentilo, ciclohexilo y un grupo heterocíclico saturado de 5-6 miembros con 1-2 heteroátomos, seleccionados independientemente entre O, S y N, donde dicho grupo alquilo C1-3 puede tener 1 ó 2 sustituyentes seleccionado entre oxo, hidroxi, halógeno y alcoxi C1-4 y donde el grupo cíclico puede tener 1 ó 2 sustituyentes seleccionados entre oxo, hidroxi, halógeno, ciano, cianoalquilo C1-4, alquilo C1-4, hidroxialquilo C1-4, alcoxi C1-4, alcoxi C1-4-alquilo C1-4, alquilsulfonil C1-4-alquilo C1-4, alcoxi C1-4-carbonilo, aminoalquilo C1-4, alquilamino C1-4, di(alquil C1-4)amino, alquilamino C1-4-alquilo C1-4, di(alquil C1-4)aminoalquilo C1-4, alquilamino C1-4-alcoxi C1-4, di(alquil C1-4)aminoalcoxi C1-4 y un grupo -(-O-)f(alquil C1-4)g-anillo D (donde f es 0 ó 1, g es 0 ó 1 y el anillo D es un grupo heterocíclico saturado de 5-6 miembros con 1-2 heteroátomos, seleccionados independientemente entre O, S y N, donde el grupo cíclico puede tener uno o más sustituyentes seleccionados entre alquilo C1-4), con la condición de que R54 no puede ser hidrógeno); y además donde cualquier grupo alquilo C1-5, alquenilo C2-5 ó alquinilo C2-5 en R5X1- que está unido a X1 puede tener uno o más sustituyentes seleccionados entre hidroxi, halógeno y amino); R1 representa hidrógeno, oxo, halógeno, hidroxi, alcoxi C1-4, alquilo C1-4, alcoxi C1-4-metilo, alcanoílo C1-4, haloalquilo C1-4, ciano, amino, alquenilo C
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2003
- 2003-01-28 MX MXPA04007459A patent/MXPA04007459A/es not_active Application Discontinuation
- 2003-01-28 EP EP10185282A patent/EP2292615A1/en not_active Withdrawn
- 2003-01-28 AT AT03700951T patent/ATE549329T1/de active
- 2003-01-28 BR BR0307151-0A patent/BR0307151A/pt not_active IP Right Cessation
- 2003-01-28 CA CA2473572A patent/CA2473572C/en not_active Expired - Fee Related
- 2003-01-28 DK DK03700951.1T patent/DK1474420T3/da active
- 2003-01-28 CN CNA038031248A patent/CN1625555A/zh active Pending
- 2003-01-28 AU AU2003202094A patent/AU2003202094B2/en not_active Ceased
- 2003-01-28 PT PT03700951T patent/PT1474420E/pt unknown
- 2003-01-28 KR KR1020047011872A patent/KR101093345B1/ko not_active Expired - Fee Related
- 2003-01-28 RU RU2008100766/04A patent/RU2362774C1/ru not_active IP Right Cessation
- 2003-01-28 SI SI200332134T patent/SI1474420T1/sl unknown
- 2003-01-28 PL PL03371486A patent/PL371486A1/xx unknown
- 2003-01-28 CN CNA2009101521170A patent/CN101607958A/zh active Pending
- 2003-01-28 JP JP2003564036A patent/JP4608215B2/ja not_active Expired - Fee Related
- 2003-01-28 RU RU2004126612/04A patent/RU2365588C2/ru not_active IP Right Cessation
- 2003-01-28 HU HU0402588A patent/HUP0402588A3/hu unknown
- 2003-01-28 NZ NZ534171A patent/NZ534171A/en not_active IP Right Cessation
- 2003-01-28 RU RU2008100767/04A patent/RU2362775C1/ru not_active IP Right Cessation
- 2003-01-28 EP EP03700951A patent/EP1474420B1/en not_active Expired - Lifetime
- 2003-01-28 ES ES03700951T patent/ES2381781T3/es not_active Expired - Lifetime
- 2003-01-28 WO PCT/GB2003/000343 patent/WO2003064413A1/en not_active Ceased
- 2003-01-28 UA UA20040807063A patent/UA81619C2/ru unknown
- 2003-01-28 US US10/502,538 patent/US7268230B2/en not_active Expired - Fee Related
- 2003-01-30 MY MYPI20030343A patent/MY144042A/en unknown
- 2003-01-30 TW TW092102248A patent/TWI337866B/zh not_active IP Right Cessation
- 2003-01-31 AR ARP030100315A patent/AR038476A1/es not_active Application Discontinuation
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2004
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- 2004-07-22 NO NO20043162A patent/NO328731B1/no not_active IP Right Cessation
- 2004-07-22 IS IS7362A patent/IS7362A/is unknown
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2007
- 2007-02-12 US US11/705,035 patent/US8293902B2/en not_active Expired - Fee Related
- 2007-08-02 US US11/882,604 patent/US20090156821A1/en not_active Abandoned
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