AR067869A1 - Derivados de piridina y pirimidina - Google Patents
Derivados de piridina y pirimidinaInfo
- Publication number
- AR067869A1 AR067869A1 ARP080103260A ARP080103260A AR067869A1 AR 067869 A1 AR067869 A1 AR 067869A1 AR P080103260 A ARP080103260 A AR P080103260A AR P080103260 A ARP080103260 A AR P080103260A AR 067869 A1 AR067869 A1 AR 067869A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkyl
- amino
- alkylamino
- alkoxy
- hydroxyl
- Prior art date
Links
- CZPWVGJYEJSRLH-UHFFFAOYSA-N Pyrimidine Chemical class C1=CN=CN=C1 CZPWVGJYEJSRLH-UHFFFAOYSA-N 0.000 title 1
- 229940083082 pyrimidine derivative acting on arteriolar smooth muscle Drugs 0.000 title 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 17
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 16
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 12
- 125000004916 (C1-C6) alkylcarbonyl group Chemical group 0.000 abstract 10
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 abstract 9
- 125000004890 (C1-C6) alkylamino group Chemical group 0.000 abstract 9
- 125000004739 (C1-C6) alkylsulfonyl group Chemical group 0.000 abstract 9
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 9
- 229910052736 halogen Inorganic materials 0.000 abstract 8
- 150000002367 halogens Chemical class 0.000 abstract 8
- 125000000623 heterocyclic group Chemical group 0.000 abstract 8
- 229910052739 hydrogen Inorganic materials 0.000 abstract 8
- 239000001257 hydrogen Substances 0.000 abstract 8
- 125000004750 (C1-C6) alkylaminosulfonyl group Chemical group 0.000 abstract 7
- 125000004457 alkyl amino carbonyl group Chemical group 0.000 abstract 6
- 125000004454 (C1-C6) alkoxycarbonyl group Chemical group 0.000 abstract 5
- 125000004738 (C1-C6) alkyl sulfinyl group Chemical group 0.000 abstract 5
- 125000004845 (C1-C6) alkylsulfonylamino group Chemical group 0.000 abstract 5
- 125000003302 alkenyloxy group Chemical group 0.000 abstract 5
- 125000003806 alkyl carbonyl amino group Chemical group 0.000 abstract 5
- 125000000217 alkyl group Chemical group 0.000 abstract 5
- 125000005133 alkynyloxy group Chemical group 0.000 abstract 5
- 125000004397 aminosulfonyl group Chemical group NS(=O)(=O)* 0.000 abstract 5
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 abstract 5
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 5
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 5
- 125000001424 substituent group Chemical group 0.000 abstract 5
- 125000004001 thioalkyl group Chemical group 0.000 abstract 5
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 abstract 4
- 125000004452 carbocyclyl group Chemical group 0.000 abstract 4
- 125000001072 heteroaryl group Chemical group 0.000 abstract 4
- 125000005915 C6-C14 aryl group Chemical group 0.000 abstract 3
- 125000003342 alkenyl group Chemical group 0.000 abstract 3
- 150000001875 compounds Chemical class 0.000 abstract 3
- 125000005843 halogen group Chemical group 0.000 abstract 3
- 125000001183 hydrocarbyl group Chemical group 0.000 abstract 3
- 150000002431 hydrogen Chemical class 0.000 abstract 3
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 3
- 125000006570 (C5-C6) heteroaryl group Chemical group 0.000 abstract 2
- 125000001313 C5-C10 heteroaryl group Chemical group 0.000 abstract 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 2
- 125000003545 alkoxy group Chemical group 0.000 abstract 2
- 125000002947 alkylene group Chemical group 0.000 abstract 2
- 125000000304 alkynyl group Chemical group 0.000 abstract 2
- 125000004122 cyclic group Chemical group 0.000 abstract 2
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 2
- 150000003839 salts Chemical class 0.000 abstract 2
- 125000006273 (C1-C3) alkyl group Chemical group 0.000 abstract 1
- 125000006583 (C1-C3) haloalkyl group Chemical group 0.000 abstract 1
- 125000006274 (C1-C3)alkoxy group Chemical group 0.000 abstract 1
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 abstract 1
- 125000006728 (C1-C6) alkynyl group Chemical group 0.000 abstract 1
- 125000004737 (C1-C6) haloalkoxy group Chemical group 0.000 abstract 1
- 125000006656 (C2-C4) alkenyl group Chemical group 0.000 abstract 1
- 125000006650 (C2-C4) alkynyl group Chemical group 0.000 abstract 1
- 201000001320 Atherosclerosis Diseases 0.000 abstract 1
- -1 C1- alkylsulfonyl 6 Chemical group 0.000 abstract 1
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 abstract 1
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 abstract 1
- 206010009900 Colitis ulcerative Diseases 0.000 abstract 1
- 208000011231 Crohn disease Diseases 0.000 abstract 1
- 206010020751 Hypersensitivity Diseases 0.000 abstract 1
- 206010028980 Neoplasm Diseases 0.000 abstract 1
- 208000008589 Obesity Diseases 0.000 abstract 1
- 108091007960 PI3Ks Proteins 0.000 abstract 1
- 102000003993 Phosphatidylinositol 3-kinases Human genes 0.000 abstract 1
- 108090000430 Phosphatidylinositol 3-kinases Proteins 0.000 abstract 1
- 201000004681 Psoriasis Diseases 0.000 abstract 1
- 208000025747 Rheumatic disease Diseases 0.000 abstract 1
- 206010040070 Septic Shock Diseases 0.000 abstract 1
- 201000006704 Ulcerative Colitis Diseases 0.000 abstract 1
- 230000007815 allergy Effects 0.000 abstract 1
- 125000003118 aryl group Chemical group 0.000 abstract 1
- 201000011510 cancer Diseases 0.000 abstract 1
- 125000002837 carbocyclic group Chemical group 0.000 abstract 1
- 206010012601 diabetes mellitus Diseases 0.000 abstract 1
- 201000010099 disease Diseases 0.000 abstract 1
- 208000035475 disorder Diseases 0.000 abstract 1
- 239000003814 drug Substances 0.000 abstract 1
- 125000004438 haloalkoxy group Chemical group 0.000 abstract 1
- 230000005764 inhibitory process Effects 0.000 abstract 1
- 238000004519 manufacturing process Methods 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
- 125000004433 nitrogen atom Chemical group N* 0.000 abstract 1
- 235000020824 obesity Nutrition 0.000 abstract 1
- 201000008482 osteoarthritis Diseases 0.000 abstract 1
- 230000002062 proliferating effect Effects 0.000 abstract 1
- 208000023504 respiratory system disease Diseases 0.000 abstract 1
- 208000037803 restenosis Diseases 0.000 abstract 1
- 206010039073 rheumatoid arthritis Diseases 0.000 abstract 1
- 239000012453 solvate Substances 0.000 abstract 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more 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, directly attached to ring carbon atoms
- C07D239/32—One oxygen, sulfur or nitrogen atom
- C07D239/34—One oxygen atom
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
-
- 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
-
- 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
-
- 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]
-
- 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
- A61P3/04—Anorexiants; Antiobesity agents
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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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- 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
-
- 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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- 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
- A61P37/08—Antiallergic agents
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- A—HUMAN NECESSITIES
- 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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- 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
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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
- A61P9/10—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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more 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, directly attached to ring carbon atoms
- C07D239/32—One oxygen, sulfur or nitrogen atom
- C07D239/42—One nitrogen atom
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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
- C07D401/02—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
- C07D401/12—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 chain containing hetero atoms as chain links
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—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
- 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
- C07D405/12—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 linked by a chain containing hetero atoms as chain links
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pharmacology & Pharmacy (AREA)
- Engineering & Computer Science (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Immunology (AREA)
- Diabetes (AREA)
- Obesity (AREA)
- Hematology (AREA)
- Cardiology (AREA)
- Pulmonology (AREA)
- Rheumatology (AREA)
- Heart & Thoracic Surgery (AREA)
- Pain & Pain Management (AREA)
- Urology & Nephrology (AREA)
- Transplantation (AREA)
- Vascular Medicine (AREA)
- Child & Adolescent Psychology (AREA)
- Emergency Medicine (AREA)
- Endocrinology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Physical Education & Sports Medicine (AREA)
- Dermatology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
Abstract
Composiciones y uso de los compuestos en el tratamiento de enfermedades mejoradas por la inhibicion de fosfatidilinositol 3-cinasa Reivindicacion 1: Un compuesto de la formula 1 o una sal, adecuadamente una sal farmacéuticamente aceptable, o un solvato del mismo, caracterizado porque: R1 es hidrogeno; R2 es hidrogeno o amino; A es CR3; B es CR3a o N; Ar' es la formula 2; o un arilo de C6-14 alternativo o un grupo heteroarilo de 5-10 miembros, donde cada arilo o heteroarilo es opcionalmente sustituido por uno o más sustituyentes seleccionados de la Lista X; E es CH o N; R3 y R3a son independientemente hidrogeno, alquilo de C1-6, haloalquilo de C1-6, carbociclilo de C4-8, un heterociclilo de 5-8 miembros o un grupo -Y-Z, donde los anillos son sustituidos opcionalmente por uno o más sustituyentes seleccionados de la Lista X; Y es un enlace directo, -O-(CH2)n- o -N(R4)-(CH2)o-; Z es fenilo o un heteroarilo de 5-6 miembros, donde los anillos son opcionalmente sustituidos por uno o más sustituyentes seleccionados de la Lista X; R4 es hidrogeno o alquilo de C1-6; R5 es hidroxilo, alquilo de C1-6, haloalquilo de C1-6, SO2NR7R8, NR9SO2R10, NR11C(O)R12, C(O)NR13R14 o NR15R16; R6 es hidrogeno, halo, hidroxilo, ciano, alquilo de C1-3, haloalquilo de C1-3, alcoxi de C1-3 o haloalcoxi de C1-3 o R5 y R6 juntos forman un heteroarilo de 5-6 miembros o un heterociclilo de 5-8 miembros, donde cada anillo es opcionalmente sustituido por uno o más sustituyentes seleccionados de la Lista X; R7, R9, R11, R13 y R15 son independientemente hidrogeno o alquilo de C1-6; R8, R10, R12, R14 y R16 son independientemente hidrogeno, alquilo de C1-C6 o -(CH2)p-R17, o R10 y R12 son independientemente de manera adicional alcoxi de C1-6, donde los grupos alquilo y alcoxi pueden ser sustituidos por uno a cinco de halo o por hidroxilo, alcoxi de C1-6, NR18R19 o CN; R17 es arilo de C6-14, heteroarilo de 5-10 miembros, carbociclilo de C4-8, un heterociclilo de 4-8 miembros, un arilo de C6-14 fusionado con un carbociclilo de C4-C8 o un heterociclilo de 4-8 miembros o un heteroarilo de 5-10 miembros fusionado con un carbociclilo de C4-8 o un heterociclilo de 4-8 miembros, donde los anillos son opcionalmente sustituidos por uno o más sustituyentes seleccionados de la Lista X; o R7 y R8, R13 y R14 o R15 y R16 pueden formar un heterociclilo de 4-8 miembros que contiene al menos un átomo de N en el anillo, donde el anillo es opcionalmente sustituido por halo, hidroxilo, alquilo de C1-6, haloalquilo de C1-6, alcoxi de C1-6 o haloalcoxi de C1-6 o ciano; R18 y R19 son independientemente hidrogeno o alquilo de C1-6; n es un numero entero de 0-2, o es un numero entero de 0-2 y p es un numero entero de 0-2; la Lista X está representada por hidroxilo, ciano, nitro, alquilo de C1-6, alquenilo de C2-6, alquinilo de C2-6, alcoxi de C1-6, alqueniloxi de C1-6, alquiniloxi de C2-6, -O-(alquileno de C1-4)-R20, -O-(alquileno de C2-4)-R21, halogeno, alquilcarbonilo de C1-6, carboxi, alcoxicarbonilo de C1-6, amino, alquilamino de C1-6, di-alquilamino de C1-6, alquilaminocarbonilo de C1-6, di-alquilaminocarbonilo de C1-6, alquilcarbonilamino de C1-6, alquilcarbonilo de C1-6- (alquilo de C1-6)amino, alquilsulfonilamino de C1-6, alquilsulfonilo de C1-6(alquilo de C1-6)amino, tioalquilo de C1-6, alquilsulfinilo de C1-6, alquilsulfonilo de C1-6, aminosulfonilo, alquilaminosulfonilo de C1-6, di-alquilaminosulfonilo de C1-6, fenilo o heteroarilo de 5-6 miembros donde cada uno de los grupos hidrocarburo mencionados anteriormente pueden ser opcionalmente sustituidos por uno o más de halogeno, hidroxilo, alcoxi de C1-6, amino, alquilamino de C1-6, di-alquilamino de C1-6 o ciano, y donde el grupo fenilo o heteroarilo puede ser opcionalmente sustituido por uno o más grupos seleccionados de grupos hidroxilo, ciano, nitro, alquilo de C1-6, haloalquilo de C1-6, alquenilo de C1-6, alquinilo de C1-6, alcoxi de C1-6, alqueniloxi de C1-6, alquiniloxi de C1-6, halogeno, alquilcarbonilo de C1-6, carboxi, alcoxicarbonilo de C1-6, amino, alquilamino de C1-6, di-alquilamino de C1-6, alquilaminocarbonilo de C1-6, di-alquilaminocarbonilo de C1-6, alquilcarbonilamino de C1-6, alquilcarbonilo de C1-6(alquilo de C1-6)amino, alquilsulfonilamino de C1-6, alquilsulfonilo de C1-6(alquilo de C1-6)amino, tioalquilo de C1-6, alquilsulfinilo de C1-6, alquilsulfonilo de C1-6, aminosulfonilo, alquilaminosulfonilo de C1-6 o di-alquilaminosulfonilo de C1-6; R20 representa alquenilo de C2-4, alquinilo de C2-4, halogeno, ciano, nitro, alquilcarbonilo de C1-6, carboxi, alcoxicarbonilo de C1-6, tioalquilo de C1-6, alquilsulfinilo de C1-6, alquilsulfonilo de C1-6, aminosulfonilo, alquilaminosulfonilo de C1-6, di-alquilaminosulfonilo de C1-6, fenilo, un grupo heteroarilo enlazado con C de 5-6 miembros, un grupo carbocíclico de C4-6 o un grupo heterociclilo enlazado con C de 5-6 miembros, donde los grupos fenilo o cíclicos pueden ser opcionalmente sustituidos por uno o más grupos hidroxilo, ciano, nitro, alquilo de C1-6, alquenilo de C1-6, alquinilo de C1-6, alcoxi de C1-6, alqueniloxi de C1-6, alquiniloxi de C1-6, halogeno, alquilcarbonilo de C1-6, carboxi, alcoxicarbonilo de C1-6, amino, alquilamino de C1-6, di-alquilamino de C1-6, alquilaminocarbonilo de C1-6, di-alquilaminocarbonilo de C1-6, alquilcarbonilamino de C1-6, alquilcarbonilo de C1-6(alquilo de C1-6)amino, alquilsulfonilamino de C1-6, alquilsulfonilo de C1-6(alquilo de C1-6)amino, tioalquilo de C1-6, alquilsulfinilo de C1-6, alquilsulfonilo de C1-6, aminosulfonilo, alquilaminosulfonilo de C1-6 o di-alquilaminosulfonilo de C1-6, donde cada uno de los grupos hidrocarburo mencionados anteriormente pueden ser opcionalmente sustituidos por uno o más de halogeno, hidroxilo, alcoxi de C1-6, amino, alquilamino de C1-6, di-alquilamino de C1-6 o ciano; y R21 representa hidroxilo, alcoxi de C1-4, alqueniloxi de C2-4, alquiniloxi de C2-4, amino, alquilamino de C1-6, di-alquilamino de C1-6, alquilaminocarbonilo de C1-6, di-alquilaminocarbonilo de C1-6, alquilcarbonilamino de C1-6, alquilcarbonilo de C1-6(alquilo de C1-6)amino, alquilsulfonilamino de C1-6, alquilsulfonilo de C1-6(alquilo de C1-6)amino, un grupo heteroarilo enlazado con N de 5-6 miembros o un heterociclilo enlazado con N de 5-6 miembros donde el grupo cíclico puede ser opcionalmente sustituido por uno o más grupos hidroxilo, nitro, alquilo de C1-6, alquenilo de C1-6, alquinilo de C1-6, alcoxi de C1-6, alqueniloxi de C1-6, alquiniloxi de C1-6, halogeno, alquilcarbonilo de C1-6, carboxi, alcoxicarbonilo de C1-6, amino, alquilamino de C1-6, di-alquilamino de C1-6, alquilaminocarbonilo de C1-6, di-alquilaminocarbonilo de C1-6, alquilcarbonilamino de C1-6, alquilcarbonilo de C1-6(alquilo de C1-6)amino, alquilsulfonilamino de C1-6, alquilsulfonilo de C1-6(alquilo de C1-6)amino, tioalquilo de C1-6, alquilsulfinilo de C1-6, alquilsulfonilo de C1-6, aminosulfonilo, alquilaminosulfonilo de C1-6, o di-alquilaminosulfonilo de C1-6, donde cada uno de los grupos hidrocarburo mencionados anteriormente puede ser opcionalmente sustituido por uno o más de halogeno, hidroxilo, alcoxi de C1-6, amino, alquilamino de C1-6, di-alquilamino de C1-6 o ciano. Reivindicacion 14: Uso de un compuesto de conformidad con cualquiera de las reivindicaciones 1 a 10 en la fabricacion de un medicamento para el tratamiento de enfermedades respiratorias, alergias, artritis reumatoide, osteoartritis, trastornos reumáticos, psoriasis, colitis ulcerativa, enfermedad de Crohn, choque séptico, trastornos proliferativos tales como cáncer, aterosclerosis, rechazo de aloinjerto después de un trasplante, diabetes, stroke (apoplejía), obesidad o restenosis.
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| KR (1) | KR20100025006A (es) |
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| US8268834B2 (en) * | 2008-03-19 | 2012-09-18 | Novartis Ag | Pyrazine derivatives that inhibit phosphatidylinositol 3-kinase enzyme |
| GB0815947D0 (en) * | 2008-09-02 | 2008-10-08 | Univ Dundee | Compounds |
| EP2408773A2 (en) | 2009-03-20 | 2012-01-25 | Amgen, Inc | Inhibitors of pi3 kinase |
| UY32582A (es) | 2009-04-28 | 2010-11-30 | Amgen Inc | Inhibidores de fosfoinositida 3 cinasa y/u objetivo mamífero |
| JP4967004B2 (ja) * | 2009-09-14 | 2012-07-04 | 東京エレクトロン株式会社 | レジスト塗布現像装置およびレジスト塗布現像方法 |
| WO2015108881A1 (en) | 2014-01-14 | 2015-07-23 | Millennium Pharmaceuticals, Inc. | Heteroaryls and uses thereof |
| AP2016009368A0 (en) | 2014-01-14 | 2016-08-31 | Millennium Pharm Inc | Heteroaryls and uses thereof |
| JP6433509B2 (ja) | 2014-04-24 | 2018-12-05 | ノバルティス アーゲー | ホスファチジルイノシトール3−キナーゼ阻害薬としてのアミノピラジン誘導体 |
| BR112016024484A2 (pt) * | 2014-04-24 | 2017-08-15 | Novartis Ag | derivados de aminopiridina como inibidores de fosfatidilinositol 3-quinase |
| PL3134395T3 (pl) * | 2014-04-24 | 2018-07-31 | Novartis Ag | Pochodne pirazyny jako inhibitory 3-kinazy fosfatydyloinozytolu |
| RU2020124116A (ru) | 2017-12-22 | 2022-01-25 | Хиберселл, Инк. | Производные арил-бипиридинамина в качестве ингибиторов фосфатидилинозитолфосфаткиназы |
| CR20200464A (es) | 2018-03-08 | 2021-04-14 | Incyte Corp | Compuestos diólicos de aminopirazina como inhibidores de pi3k-y |
| US11046658B2 (en) | 2018-07-02 | 2021-06-29 | Incyte Corporation | Aminopyrazine derivatives as PI3K-γ inhibitors |
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| YU63802A (sh) * | 2000-02-25 | 2005-06-10 | F. Hoffmann-La Roche Ag. | Modulatori adenozinskih receptora |
| MY130778A (en) * | 2001-02-09 | 2007-07-31 | Vertex Pharma | Heterocyclic inhibitiors of erk2 and uses thereof |
| EP1412327A2 (en) * | 2001-05-30 | 2004-04-28 | LG Biomedical Institute | Inhibitors of protein kinase for the treatment of disease |
| AUPR688101A0 (en) * | 2001-08-08 | 2001-08-30 | Luminis Pty Limited | Protein domains and their ligands |
| WO2003030909A1 (en) * | 2001-09-25 | 2003-04-17 | Bayer Pharmaceuticals Corporation | 2- and 4-aminopyrimidines n-substtituded by a bicyclic ring for use as kinase inhibitors in the treatment of cancer |
| TWI330183B (es) * | 2001-10-22 | 2010-09-11 | Eisai R&D Man Co Ltd | |
| AU2002950853A0 (en) * | 2002-08-19 | 2002-09-12 | Fujisawa Pharmaceutical Co., Ltd. | Aminopyrimidine compound and pharmaceutical use thereof |
| US7405221B2 (en) * | 2002-09-27 | 2008-07-29 | Merck & Co., Inc. | Substituted pyrimidines |
| EP2316831B1 (en) | 2002-11-21 | 2013-03-06 | Novartis AG | 2-(morpholin-4-yl)pyrimidines as phosphotidylinositol (PI) 3-kinase inhibitors and their use in the treatment of cancer |
| CN1735607B (zh) * | 2002-11-21 | 2010-06-09 | 诺华疫苗和诊断公司 | 2,4,6-三取代的嘧啶作为磷脂酰肌醇(pi)3-激酶抑制剂及其在治疗癌症中的应用 |
| US7230098B2 (en) * | 2003-02-26 | 2007-06-12 | Sugen, Inc. | Aminoheteroaryl compounds as protein kinase inhibitors |
| SE0301010D0 (sv) * | 2003-04-07 | 2003-04-07 | Astrazeneca Ab | Novel compounds |
| WO2005005380A2 (en) * | 2003-06-30 | 2005-01-20 | Merck & Co., Inc. | 17-acetamido-4-azasteroid derivatives as androgen receptor modulators |
| ES2229928B1 (es) * | 2003-10-02 | 2006-07-01 | Almirall Prodesfarma, S.A. | Nuevos derivados de pirimidin-2-amina. |
| EP1781654A1 (en) * | 2004-07-27 | 2007-05-09 | SGX Pharmaceuticals, Inc. | Pyrrolo-pyridine kinase modulators |
| SE0402735D0 (sv) * | 2004-11-09 | 2004-11-09 | Astrazeneca Ab | Novel compounds |
| PE20061067A1 (es) * | 2005-03-10 | 2006-11-30 | Bayer Pharmaceuticals Corp | Derivados de pirimidina |
| DE602007004092D1 (de) * | 2006-03-22 | 2010-02-11 | Vertex Pharma | C-met-proteinkinasehemmer zur behandlung proliferativer erkrankungen |
| GB0608820D0 (en) * | 2006-05-04 | 2006-06-14 | Piramed Ltd | Pharmaceutical compounds |
| GB0610242D0 (en) * | 2006-05-23 | 2006-07-05 | Novartis Ag | Organic compounds |
| PT2049502E (pt) * | 2006-07-28 | 2012-04-02 | Novartis Ag | Quinazolinas 2,4-substituídas como inibidores da lípido cinase |
| SG174086A1 (en) * | 2006-08-30 | 2011-09-29 | Cellzome Ltd | Triazole derivatives as kinase inhibitors |
| AR067354A1 (es) * | 2007-06-29 | 2009-10-07 | Sunesis Pharmaceuticals Inc | Compuestos utiles como inhibidores de la raf quinasa |
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| Publication number | Publication date |
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| TN2010000038A1 (en) | 2011-09-26 |
| EP2173722B1 (en) | 2012-08-29 |
| MA31594B1 (fr) | 2010-08-02 |
| CR11208A (es) | 2010-02-12 |
| EA201000104A1 (ru) | 2010-08-30 |
| EP2173722A2 (en) | 2010-04-14 |
| AU2008278966A1 (en) | 2009-01-29 |
| CA2694275A1 (en) | 2009-01-29 |
| AU2008278966B2 (en) | 2012-02-23 |
| SV2010003464A (es) | 2010-05-21 |
| JP2010534634A (ja) | 2010-11-11 |
| ES2394126T3 (es) | 2013-01-22 |
| PE20090880A1 (es) | 2009-08-06 |
| BRPI0813629A2 (pt) | 2018-07-10 |
| MX2010001020A (es) | 2010-03-01 |
| ECSP109900A (es) | 2010-02-26 |
| CN101765591B (zh) | 2013-11-27 |
| CO6290670A2 (es) | 2011-06-20 |
| WO2009013348A3 (en) | 2009-07-23 |
| WO2009013348A2 (en) | 2009-01-29 |
| JP5485884B2 (ja) | 2014-05-07 |
| TW200909426A (en) | 2009-03-01 |
| KR20100025006A (ko) | 2010-03-08 |
| CN101765591A (zh) | 2010-06-30 |
| CL2008002185A1 (es) | 2009-02-20 |
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