AR050970A1 - Pirimidinas 5-sustituidas con carbociclos o heterociclos inhibidoras del vih; composiciones farmaceuticas que las contienen y uso de las mismas como medicamentos. - Google Patents
Pirimidinas 5-sustituidas con carbociclos o heterociclos inhibidoras del vih; composiciones farmaceuticas que las contienen y uso de las mismas como medicamentos.Info
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- AR050970A1 AR050970A1 ARP050104154A ARP050104154A AR050970A1 AR 050970 A1 AR050970 A1 AR 050970A1 AR P050104154 A ARP050104154 A AR P050104154A AR P050104154 A ARP050104154 A AR P050104154A AR 050970 A1 AR050970 A1 AR 050970A1
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- Prior art keywords
- alkyl
- cyano
- independently
- halo
- nr9r10
- Prior art date
Links
- 239000008194 pharmaceutical composition Substances 0.000 title abstract 2
- 239000003814 drug Substances 0.000 title 1
- 230000002401 inhibitory effect Effects 0.000 title 1
- 150000003230 pyrimidines Chemical class 0.000 title 1
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 28
- 125000005843 halogen group Chemical group 0.000 abstract 24
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 23
- 125000001424 substituent group Chemical group 0.000 abstract 21
- 125000000217 alkyl group Chemical group 0.000 abstract 19
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 abstract 14
- -1 cyano, nitro, amino Chemical group 0.000 abstract 10
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 10
- 125000003545 alkoxy group Chemical group 0.000 abstract 9
- 125000004453 alkoxycarbonyl group Chemical group 0.000 abstract 9
- 229920006395 saturated elastomer Polymers 0.000 abstract 8
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 7
- 125000004916 (C1-C6) alkylcarbonyl group Chemical group 0.000 abstract 6
- 125000002485 formyl group Chemical group [H]C(*)=O 0.000 abstract 6
- 125000006684 polyhaloalkyl group Polymers 0.000 abstract 6
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 abstract 5
- 125000004103 aminoalkyl group Chemical group 0.000 abstract 5
- 125000003118 aryl group Chemical group 0.000 abstract 5
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 5
- 125000006272 (C3-C7) cycloalkyl group Chemical group 0.000 abstract 4
- 125000002619 bicyclic group Chemical group 0.000 abstract 4
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 4
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 abstract 3
- 150000001875 compounds Chemical class 0.000 abstract 3
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 3
- 125000006700 (C1-C6) alkylthio group Chemical group 0.000 abstract 2
- 125000006577 C1-C6 hydroxyalkyl group Chemical group 0.000 abstract 2
- 101100240519 Caenorhabditis elegans nhr-13 gene Chemical group 0.000 abstract 2
- 125000003342 alkenyl group Chemical group 0.000 abstract 2
- 125000004448 alkyl carbonyl group Chemical group 0.000 abstract 2
- 125000000304 alkynyl group Chemical group 0.000 abstract 2
- 125000003710 aryl alkyl group Chemical group 0.000 abstract 2
- 125000002837 carbocyclic group Chemical group 0.000 abstract 2
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 abstract 2
- 125000000623 heterocyclic group Chemical group 0.000 abstract 2
- 125000000717 hydrazino group Chemical group [H]N([*])N([H])[H] 0.000 abstract 2
- 125000000165 tricyclic carbocycle group Chemical group 0.000 abstract 2
- 125000000169 tricyclic heterocycle group Chemical group 0.000 abstract 2
- 125000006619 (C1-C6) dialkylamino group Chemical group 0.000 abstract 1
- 125000003830 C1- C4 alkylcarbonylamino group Chemical group 0.000 abstract 1
- 125000002853 C1-C4 hydroxyalkyl group Chemical group 0.000 abstract 1
- 208000031886 HIV Infections Diseases 0.000 abstract 1
- 208000037357 HIV infectious disease Diseases 0.000 abstract 1
- 125000004457 alkyl amino carbonyl group Chemical group 0.000 abstract 1
- 125000003282 alkyl amino group Chemical group 0.000 abstract 1
- 125000003277 amino group Chemical group 0.000 abstract 1
- 125000005018 aryl alkenyl group Chemical group 0.000 abstract 1
- 125000004104 aryloxy group Chemical group 0.000 abstract 1
- 125000004429 atom Chemical group 0.000 abstract 1
- 125000000499 benzofuranyl group Chemical group O1C(=CC2=C1C=CC=C2)* 0.000 abstract 1
- 125000004196 benzothienyl group Chemical group S1C(=CC2=C1C=CC=C2)* 0.000 abstract 1
- 125000004432 carbon atom Chemical group C* 0.000 abstract 1
- 125000004181 carboxyalkyl group Chemical group 0.000 abstract 1
- 125000004966 cyanoalkyl group Chemical group 0.000 abstract 1
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 1
- 125000002541 furyl group Chemical group 0.000 abstract 1
- 125000005842 heteroatom Chemical group 0.000 abstract 1
- 208000033519 human immunodeficiency virus infectious disease Diseases 0.000 abstract 1
- 125000002883 imidazolyl group Chemical group 0.000 abstract 1
- 125000000842 isoxazolyl group Chemical group 0.000 abstract 1
- 125000002757 morpholinyl group Chemical group 0.000 abstract 1
- 125000002971 oxazolyl group Chemical group 0.000 abstract 1
- 125000004193 piperazinyl group Chemical group 0.000 abstract 1
- 125000003386 piperidinyl group Chemical group 0.000 abstract 1
- 230000002265 prevention Effects 0.000 abstract 1
- 125000003226 pyrazolyl group Chemical group 0.000 abstract 1
- 125000004076 pyridyl group Chemical group 0.000 abstract 1
- 125000000719 pyrrolidinyl group Chemical group 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 125000001113 thiadiazolyl group Chemical group 0.000 abstract 1
- 125000000335 thiazolyl group Chemical group 0.000 abstract 1
- 125000001544 thienyl group Chemical group 0.000 abstract 1
Classifications
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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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
- A61P31/14—Antivirals for RNA viruses
- A61P31/18—Antivirals for RNA viruses for HIV
-
- 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
-
- 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
- C07D239/46—Two or more oxygen, sulphur or nitrogen atoms
- C07D239/48—Two nitrogen atoms
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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
- C07D239/46—Two or more oxygen, sulphur or nitrogen atoms
- C07D239/50—Three nitrogen atoms
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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
- 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
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
- C07D409/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms 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
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
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- Chemical Kinetics & Catalysis (AREA)
- Public Health (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmacology & Pharmacy (AREA)
- Virology (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Bioinformatics & Cheminformatics (AREA)
- AIDS & HIV (AREA)
- Tropical Medicine & Parasitology (AREA)
- Molecular Biology (AREA)
- Engineering & Computer Science (AREA)
- Communicable Diseases (AREA)
- Oncology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
Abstract
Composiciones farmacéuticas que comprenden estos compuestos como componente activo y el uso de estos compuestos para la prevencion o el tratamiento de la infeccion con VIH. Reivindicacion 1: Un compuesto de formula (1), un n-oxido, una sal de adicion aceptable desde el punto de vista farmacéutico, una amina cuaternaria o una forma estereoquímicamente isomérica de este, en el cual -a1=a2-a3=a4- representa un radical bivalente de formula -CH=CH-CH=CH- (a-1); -N=CH-CH=CH- (a-2); -N=CH-N=CH- (a-3); -N=CH-CH=N- (a-4); -N=N-CH=CH- (a-5); -b1=b2-b3=b4- representa un radical bivalente de formula -CH=CH-CH=CH- (b-1); -N=CH-CH=CH- (b-2); -N=CH-N=CH- (b-3); -N=CH-CH=N- (b-4); -N=N-CH=CH- (b-5); n es 0, 1, 2, 3 en el caso que -a1=a2-a3=a4- es (a-1), entonces n también puede ser 4; m es 0, 1, 2, 3 en el caso que -b1=b2-b3=b4- es (b-1), entonces m también puede ser 4; cada R1 en forma independiente es H, arilo, formilo, alquilcarbonilo C1-6, alquilo C1-6, alquiloxicarbonilo C1-6, alquilo C1-6 sustituido con formilo, alquilcarbonilo C1-6, alquiloxicarbonilo C1-6, o con alquilcarboniloxi C1-6, cada R2 en forma independiente es hidroxi, halo, alquilo C1-6 sustituido en forma opcional con 1, 2 o 3 sustituyentes seleccionados, cada uno en forma independiente, de halo, ciano o -C(=O)R6, cicloalquilo C3-7, alquenilo C2-6 sustituido en forma opcional con 1, 2 o 3 sustituyentes seleccionados, cada uno en forma independiente, de halo, ciano o -C(=O)R6, alquinilo C2-6 sustituido en forma opcional con 1, 2 o 3 sustituyentes seleccionados, cada uno en forma independiente, de halo, ciano o -C(=O)R6, alquiloxicarbonilo C1-6, carboxilo, ciano, nitro, amino, mono- o di(alquil C1-6)amino, polihalometilo, polihalometiltio, -S(=O)rR6, - NH-S(=O)rR6, -C(=O)R6, -NHC(=O)H, -C(=O)NHNH2, NHC(=O)R6, C(=NH)R6; R2a es ciano, aminocarbonilo, amino, alquilo C1-6, halo, alquiloxi C1-6 donde alquilo C1-6 puede estar sustituido en forma opcional con ciano, NHR13, NR13R14, -C(=O)-NHR13, -C(=O)- NR13R14, -C(=O)-R15, -CH=N-NH-C(=O)-R16, alquilo C1-6 sustituido con 1, 2 o 3 sustituyentes seleccionados, cada uno en forma independiente, de halo, ciano, NR9R10, -C(=O)-NR9R10, -C(=O)-alquilo C1-6 o R7; alquilo C1-6 sustituido con hidroxi y un segundo sustituyente seleccionado de halo, ciano, NR9R10, -C(=O)-NR9R10, -C(=O)-alquilo C1-6 o R7, alquiloxi C1-6alquilo C1-6 sustituido en forma opcional con 1, 2 o 3 sustituyentes seleccionados, cada uno en forma independiente, de halo, ciano, NR9R10, -C(=O)-NR9R10, -C(=O)-alquilo C1-6 o R7, alquenilo C2-6 sustituido con 1, 2 o 3 sustituyentes seleccionados, cada uno en forma independiente, de halo, ciano, NR9R10, -C(=O)-NR9R10, -C(=O)-alquilo C1-6 o R7, alquinilo C2-6 sustituido con 1, 2 o 3 sustituyentes seleccionados, cada uno en forma independiente, de halo, ciano, NR9R10, -C(=O)-NR9R10, -C(=O)-alquilo C1-6 o R7, -C(=N-O-R8)-alquilo C1-4, R7 o -X3-R7; X1 es -NR1-, -O-, -C(=O)-, -CH2-, -CHOH-, -S-, -S(=O)r-; R3 es ciano, aminocarbonilo, amino, alquilo C1-6, halo, alquiloxi C1-6 donde alquilo C1-6 puede estar sustituido en forma opcional con ciano, NHR13, NR13R14, -C(=O)-NHR13, -C(=O)-NR13R14, -C(=O)-R15, -CH=N-NH-C(=O)-R16, alquilo C1-6 sustituido con 1, 2 o 3 sustituyentes seleccionados, cada uno en forma independiente, de halo, ciano, NR9R10, -C(=O)-NR9R10, -C(=O)-alquilo C1-6 o R7; alquilo C1-6 sustituido con hidroxi y un segundo sustituyente seleccionado de halo, ciano, NR9R10, -C(=O)-NR9R10, -C(=O)- alquilo C1-6 o R7, alquiloxi C1-6alquilo C1-6 sustituido en forma opcional con 1, 2 o 3 sustituyentes seleccionados, cada uno en forma independiente, de halo, ciano, NR9R10, -C(=O)-NR9R10, -C(=O)-alquilo C1-6 o R7, alquenilo C2-6 sustituido con 1, 2 o 3 sustituyentes seleccionados, cada uno en forma independiente, de halo, ciano, NR9R10, -C(=O)-NR9R10, -C(=O)-alquilo C1-6 o R7, alquinilo C2-6 sustituido con 1, 2 o 3 sustituyentes seleccionados, cada uno en forma independiente, de halo, ciano, NR9R10, -C(=O)-NR9R10, -C(=O)-alquilo C1-6 o R7, -C(=N-O-R8)-alquilo C1-4, R7 o -X3-R7; X3 es -NR1-, -O-, -C(=O)-, -S-, -S(=O)r-; R4 es halo, hidroxi, alquilo C1-6 sustituido en forma opcional con 1, 2 o 3 sustituyentes seleccionados, cada uno en forma independiente, de halo, ciano o -C(=O)R6, alquenilo C2-6 sustituido en forma opcional con 1, 2 o 3 sustituyentes seleccionados, cada uno en forma independiente, de halo, ciano o -C(=O)R6, alquinilo C2-6 sustituido en forma opcional con 1, 2 o 3 sustituyentes seleccionados, cada uno en forma independiente, de halo, ciano o -C(=O)R6, cicloalquilo C3-7, alquiloxi C1-6, ciano, nitro, polihaloalquilo C1-6, polihaloalquiloxi C1-6, aminocarbonilo, mono- o di(alquil C1-4)aminocarbonilo, alquiloxicarbonilo C1-6, alquilcarbonilo C1-6, formilo, amino, mono- o di(alquil C1-4)amino o R7, R5 es un radical e formula -Y-Alk-L, -Alk'-Y-L o -Alk'-Y-Alk-L; cada Alk o Alk' en forma independiente es un grupo alquilo C1-6 o alquenilo C2-6 bivalente; L es arilo o Het; Y es O, S, -S(=O)r-, NR1, -CH=N-O; Het es un sistema completamente insaturado de 5 o 6 miembros en el cual 1, 2, 3 o 4 miembros del anillo son heteroátomos seleccionados, cada uno en forma independiente, del grupo formado por N, O y S, y en el cual el resto de los miembros del anillo son átomos de C; y, donde sea posible, cualquier miembro n el anillo puede estar sustituido en forma opcional con alquilo C1-6, sistema anular que puede estar condensado en forma opcional con un anillo bencénico, y en el cualquier átomo de c del anillo, incluyendo cualquier C de un anillo bencénico condensado en forma opcional, puede, cada uno en forma independiente, de manera opcional estar sustituido con un sustituyente seleccionado de halo, hidroxi, mercapto, ciano, alquilo C1-6, hidroxialquilo C1-4, carboxialquilo C1-4, alquiloxi C1-4alquilo C1-4,alquiloxicarbonil C1-4alquilo C1-4, cianoalquilo C1-4, mono- y di(alquil C1-4)aminoalquilo C1-4, Het1alquilo C1-4, arilalquilo C1-4, polihaloalquilo C1-4, cicloalquilo C3-7, alquenilo C2-6, aril-alquenilo C2-4, alquiloxi C1-4, -OCONH2, polihaloalquiloxi C1-4, ariloxi, amino, mono- y di-alquilamino C1-4, pirrolidinilo, piperidinilo, morfolinilo, piperazinilo, 4- alquilpiperazinilo C1-6, alquilcarbonilamino C1-4, formilo, alquilcarbonilo C1-4, alquiloxi C1-4carbonilo, aminocarbonilo, mono- y di-alquilamino C1-4carbonilo, arilo, Het1; Het1 es piridilo, tienilo, furanilo, oxazolilo, isoxazolilo, imidazolilo, pirazolilo, tiazolilo, tiadiazolilo, oxadiazolil quinolinilo, benzotienilo, benzofuranilo; de los cuales cada uno puede estar sustituido en forma opcional con 1 o 2 radicales alquilo C1-4; Q es H, alquilo C1-6, halo, polihaloalquilo C1-6, o -NR9R10; R6 es alquilo C1-4, amino, mono- o di(alquil C1-4)amino o polihaloalquilo C1-4; R7 es un carbociclo monocíclico, bicíclico o tricíclico saturado, parcialmente saturado o aromático o un heterociclo monocíclico, bicíclico o tricíclico saturado, parcialmente saturado o aromático, donde cada uno de dichos sistemas anulares carbocíclicos o heterocíclicos puede estar sustituido en forma opcional con 1, 2, 3, 4 o 5 sustituyentes seleccionados, cada uno en forma independiente, de halo, hidroxi, mercapto, alquilo C1-6, hidroxialquilo C1-6, aminoalquilo C1-6, mono o di(alquil C1-6)aminoalquilo C1-6, formilo, alquil C1-6carbonilo, cicloalquilo C3-7, alquiloxi C1-6. alquiloxi C1-6carbonilo, alquiltio C1-6, ciano, nitro, polihaloalquilo C1-6, polihaloalquiloxi C1-6, aminocarbonilo, -CH(=N-O-R8), R7a, -X3-R7a o R7a-alquilo C1-4-; R7a es un carbociclo monocíclico, bicíclico o tricíclico saturado, parcialmente saturado o aromático o un heterociclo monocíclico, bicíclico o tricíclico saturado, parcialmente saturado o aromático, donde cada uno de dichos sistemas anulares carbocíclicos o heterocíclicos puede estar sustituido en forma opcional con 1, 2, 3, 4 o 5 sustituyentes seleccionados, cada uno en forma independiente, de halo, hidroxi, mercapto, alquilo C1-6, hidroxialquilo C1-6, aminoalquilo C1-6, mono o di(alquil C1-6)aminoalquilo C1-6, formilo, alquil C1-6carbonilo, cicloalquilo C3-7, alquiloxi C1-6, alquiloxi C1-6carbonilo, alquiltio C1-6, ciano, nitro, polihaloalquilo C1-6, polihaloalquiloxi C1-6, aminocarbonilo, -CH(=N-O-R8); R8 es H, alquilo C1-4, arilo o arilalquilo C1-4; R9 y R10 son, cada uno en forma independiente H, alquilo C1-6, alquil C1-6carbonilo, alquiloxi C1-6carbonilo, amino, mono- o di(alquil C1-6)aminocarbonilo, -CH(=NR11) o R7, donde cada uno de los grupos alquilo C1-6 antes mencionados pueden estar sustituidos en forma opcional y cada uno en forma individual con uno o dos sustituyentes seleccionados, cada uno en forma independiente, de hidroxi, alquiloxi C1-6, hidroxialquiloxi C1-6, carboxilo, alquiloxi C1-6carbonilo, ciano, amino, imino, mono- o di(alquil C1-4)amino, polihalometilo, polihalometiloxi, polihalometiltio, -S(=O)rR6, -NH-S(=O)rR6, C(=O)R6, -NHC(=O)H, -C(=O)NHNH2, -NHC(=O)R6, -C(=NH)R6, R7; o R9 y R10 pueden tomarse juntos para formar un radical bivalente o trivalente de formula: -CH2-CH2-CH2-CH2- (d-1); -CH2-CH2-CH2-CH2-CH2- (d-2); -CH2-CH2-O-CH2-CH2- (d-3); -CH2-CH2-S-CH2-CH2- (d-4); -CH2-CH2- NR12-CH2-CH2- (d-5); -CH2CH=CH-CH2- (d-6); =CH-CH=CH-CH=CH- (d-7); R11 es ciano, alquilo C1-4 sustituido en forma opcional con alquiloxi C1-4, ciano, amino, mono- o di(alquil C1-4)amino o aminocarbonilo, alquil C1-4carbonilo, alquiloxi C1- 4carbonilo, aminocarbonilo, mono- o di(alquil C1-4)aminocarbonilo,; R12 es H o alquilo C1-4; R13 y R14 son, cada uno en forma independiente alquilo C1-6 sustituido en forma opcional con ciano o aminocarbonilo, alquenilo C2-6 sustituido en forma opcional con ciano o aminocarbonilo, alquinilo C2-6 sustituido en forma opcional con ciano o aminocarbonilo; R15 es alquilo C1-6 sustituido con ciano o aminocarbonilo; R16 es alquilo C1-6 sustituido en forma opcional con ciano o aminocarbonilo, o R7; cada r es 1 o 2; cada arilo es fenilo o fenilo sustituido con 1, 2, 3, 4 o 5 sustituyentes seleccionados, cada uno en forma independiente
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| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP04104814 | 2004-09-30 |
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| Publication Number | Publication Date |
|---|---|
| AR050970A1 true AR050970A1 (es) | 2006-12-06 |
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| Application Number | Title | Priority Date | Filing Date |
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| ARP050104154A AR050970A1 (es) | 2004-09-30 | 2005-09-30 | Pirimidinas 5-sustituidas con carbociclos o heterociclos inhibidoras del vih; composiciones farmaceuticas que las contienen y uso de las mismas como medicamentos. |
Country Status (17)
| Country | Link |
|---|---|
| US (1) | US7531548B2 (es) |
| EP (1) | EP1797048B1 (es) |
| JP (1) | JP5162245B2 (es) |
| KR (1) | KR20070057798A (es) |
| CN (1) | CN101031550B (es) |
| AR (1) | AR050970A1 (es) |
| AT (1) | ATE520672T1 (es) |
| AU (1) | AU2005288865B2 (es) |
| BR (1) | BRPI0515935B8 (es) |
| CA (1) | CA2573976C (es) |
| ES (1) | ES2371924T3 (es) |
| IL (1) | IL180760A (es) |
| MX (1) | MX2007003798A (es) |
| RU (1) | RU2403244C2 (es) |
| TW (1) | TW200626560A (es) |
| WO (1) | WO2006035068A2 (es) |
| ZA (1) | ZA200702655B (es) |
Families Citing this family (33)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| RS53109B (sr) | 2003-07-30 | 2014-06-30 | Rigel Pharmaceuticals Inc. | Jedinjenja 2,4 pirimidindiamina za upotrebu u tretmanu ili prevenciji autoimunih bolesti |
| EP1797047B1 (en) * | 2004-09-30 | 2012-01-25 | Tibotec Pharmaceuticals | Hiv inhibiting 5-substituted pyrimidines |
| US8575342B2 (en) * | 2004-09-30 | 2013-11-05 | Tibotech Pharmaceuticals Ltd. | HIV inhibiting 5-heterocyclyl pyrimidines |
| CN105348203B (zh) | 2005-06-08 | 2018-09-18 | 里格尔药品股份有限公司 | 抑制jak途径的组合物和方法 |
| US20070203161A1 (en) | 2006-02-24 | 2007-08-30 | Rigel Pharmaceuticals, Inc. | Compositions and methods for inhibition of the jak pathway |
| AU2007233737B2 (en) * | 2006-03-30 | 2012-11-29 | Janssen Sciences Ireland Uc | HIV inhibiting 5-amido substituted pyrimidines |
| JP5070278B2 (ja) * | 2006-03-30 | 2012-11-07 | テイボテク・フアーマシユーチカルズ | Hivを阻害する5−(ヒドロキシメチレンおよびアミノメチレン)置換されたピリミジン |
| ES2550152T3 (es) | 2006-12-13 | 2015-11-04 | F. Hoffmann-La Roche Ag | Derivados de 2-(piperidin-4-il)-4-fenoxi-o fenilamino-pirimidina como inhibidores no nucleósidos de transcriptasa inversa |
| EP2114902B1 (en) * | 2006-12-29 | 2014-09-17 | Janssen R&D Ireland | Hiv inhibiting 5,6-substituted pyrimidines |
| ES2470570T3 (es) * | 2006-12-29 | 2014-06-24 | Janssen R&D Ireland | Pirimidinas sustituidas en posición 6 inhibidoras del HIV |
| US7834024B2 (en) | 2007-03-26 | 2010-11-16 | Rigel Pharmaceuticals, Inc. | Compositions and methods for inhibition of the JAK pathway |
| US11351168B1 (en) | 2008-06-27 | 2022-06-07 | Celgene Car Llc | 2,4-disubstituted pyrimidines useful as kinase inhibitors |
| US8338439B2 (en) | 2008-06-27 | 2012-12-25 | Celgene Avilomics Research, Inc. | 2,4-disubstituted pyrimidines useful as kinase inhibitors |
| BRPI0914682B8 (pt) | 2008-06-27 | 2021-05-25 | Avila Therapeutics Inc | compostos de heteroarila e composições compreendendo os referidos compostos |
| TW201024281A (en) | 2008-11-24 | 2010-07-01 | Boehringer Ingelheim Int | New compounds |
| AR074210A1 (es) | 2008-11-24 | 2010-12-29 | Boehringer Ingelheim Int | Derivados de pirimidina como inhibidores de ptk2-quinasa |
| US9908884B2 (en) | 2009-05-05 | 2018-03-06 | Dana-Farber Cancer Institute, Inc. | EGFR inhibitors and methods of treating disorders |
| NZ607845A (en) | 2010-08-10 | 2015-03-27 | Celgene Avilomics Res Inc | Besylate salt of a btk inhibitor |
| CN103269704B (zh) | 2010-11-01 | 2018-07-06 | 西建卡尔有限责任公司 | 杂环化合物和其用途 |
| US9238629B2 (en) | 2010-11-01 | 2016-01-19 | Celgene Avilomics Research, Inc. | Heteroaryl compounds and uses thereof |
| EP2637502B1 (en) | 2010-11-10 | 2018-01-10 | Celgene CAR LLC | Mutant-selective egfr inhibitors and uses thereof |
| TW201325593A (zh) | 2011-10-28 | 2013-07-01 | Celgene Avilomics Res Inc | 治療布魯頓(bruton’s)酪胺酸激酶疾病或病症之方法 |
| CN108658873B (zh) | 2012-03-15 | 2021-09-14 | 西建卡尔有限责任公司 | 表皮生长因子受体激酶抑制剂的固体形式 |
| JP6317320B2 (ja) | 2012-03-15 | 2018-04-25 | セルジーン シーエーアール エルエルシー | 上皮成長因子受容体キナーゼ阻害剤の塩 |
| EP2935226A4 (en) | 2012-12-21 | 2016-11-02 | Celgene Avilomics Res Inc | HETEROARYL COMPOUNDS AND USES THEREOF |
| CA2900012A1 (en) | 2013-02-08 | 2014-08-14 | Celgene Avilomics Research, Inc. | Erk inhibitors and uses thereof |
| US9492471B2 (en) | 2013-08-27 | 2016-11-15 | Celgene Avilomics Research, Inc. | Methods of treating a disease or disorder associated with Bruton'S Tyrosine Kinase |
| US9415049B2 (en) | 2013-12-20 | 2016-08-16 | Celgene Avilomics Research, Inc. | Heteroaryl compounds and uses thereof |
| DK3179858T3 (da) | 2014-08-13 | 2019-07-22 | Celgene Car Llc | Forme og sammensætninger af en ERK-inhibitor |
| NZ786735A (en) | 2020-02-19 | 2025-08-29 | Pharmasyntez Joint Stock Company | Pyrimidine-based bicycles as antiviral agents for the treatment and prevention of hiv infection |
| US11351149B2 (en) | 2020-09-03 | 2022-06-07 | Pfizer Inc. | Nitrile-containing antiviral compounds |
| KR20230155351A (ko) * | 2022-05-03 | 2023-11-10 | 한국화학연구원 | 5-클로로-2,4-다이아미노피리미딘을 포함하는 키나아제 억제 화합물, 이의 제조방법 및 이를 유효성분으로 함유하는 암의 예방 또는 치료용 약학적 조성물 |
| WO2024103400A1 (zh) * | 2022-11-18 | 2024-05-23 | 水木未来(北京)科技有限公司 | 作为gpr75激活剂的多环化合物、包含其的药物组合物及其用途 |
Family Cites Families (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB9012592D0 (en) | 1990-06-06 | 1990-07-25 | Smithkline Beecham Intercredit | Compounds |
| TW440563B (en) * | 1996-05-23 | 2001-06-16 | Hoffmann La Roche | Aryl pyrimidine derivatives and a pharmaceutical composition thereof |
| NO311614B1 (no) | 1996-10-01 | 2001-12-17 | Janssen Pharmaceutica Nv | Substituerte diamino-1,3,5-triazinderivater |
| EP0945447A1 (en) | 1998-03-27 | 1999-09-29 | Janssen Pharmaceutica N.V. | Trisubstituted 1,3,5-triazine derivatives for treatment of HIV infections |
| ES2361146T3 (es) * | 1998-03-27 | 2011-06-14 | Janssen Pharmaceutica Nv | Derivados de la piramidina inhibitatoria de vih. |
| CZ299380B6 (cs) | 1998-03-27 | 2008-07-09 | Janssen Pharmaceutica N. V. | Pyrimidinová sloucenina, použití této slouceniny pro prípravu léciva, farmaceutický prostredek tutoslouceninu obsahující, zpusob prípravy tohoto prostredku a uvedené slouceniny a kombinace a produktuvedenou slouceninu obsahující |
| HU227453B1 (en) * | 1998-11-10 | 2011-06-28 | Janssen Pharmaceutica Nv | Hiv replication inhibiting pyrimidines, and pharmaceutical compositions containing them |
| GB9828511D0 (en) * | 1998-12-24 | 1999-02-17 | Zeneca Ltd | Chemical compounds |
| JP5230050B2 (ja) * | 2000-05-08 | 2013-07-10 | ジヤンセン・フアーマシユーチカ・ナームローゼ・フエンノートシヤツプ | Hiv複製阻害剤 |
| MXPA03005609A (es) * | 2000-12-21 | 2003-10-06 | Vertex Pharma | Compuestos de pirazol utiles como inhibidores de la proteina cinasa. |
| JO3429B1 (ar) * | 2001-08-13 | 2019-10-20 | Janssen Pharmaceutica Nv | مشتقات برميدينات مثبطة فيروس الايدز |
| RS20050363A (sr) * | 2002-11-28 | 2007-11-15 | Schering Aktiengesellschaft, | Chk-,Pdk- I Akt-INHIBITORNI PIRIMIDINI, NJIHOVA PROIZVODNJA I UPOTREBA KAO FARMACEUTSKIH SREDSTAVA |
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- 2005-09-29 CN CN200580033118.3A patent/CN101031550B/zh not_active Expired - Fee Related
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- 2005-09-29 AT AT05803358T patent/ATE520672T1/de not_active IP Right Cessation
- 2005-09-29 MX MX2007003798A patent/MX2007003798A/es active IP Right Grant
- 2005-09-29 AU AU2005288865A patent/AU2005288865B2/en not_active Ceased
- 2005-09-29 KR KR1020077003634A patent/KR20070057798A/ko not_active Ceased
- 2005-09-29 RU RU2007116161/04A patent/RU2403244C2/ru active
- 2005-09-29 TW TW094134106A patent/TW200626560A/zh unknown
- 2005-09-29 WO PCT/EP2005/054931 patent/WO2006035068A2/en not_active Ceased
- 2005-09-29 US US11/576,068 patent/US7531548B2/en not_active Expired - Lifetime
- 2005-09-29 BR BRPI0515935A patent/BRPI0515935B8/pt not_active IP Right Cessation
- 2005-09-29 ES ES05803358T patent/ES2371924T3/es active Active
- 2005-09-29 EP EP05803358A patent/EP1797048B1/en not_active Expired - Lifetime
- 2005-09-30 AR ARP050104154A patent/AR050970A1/es not_active Application Discontinuation
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Also Published As
| Publication number | Publication date |
|---|---|
| MX2007003798A (es) | 2007-04-23 |
| JP5162245B2 (ja) | 2013-03-13 |
| CN101031550B (zh) | 2015-05-27 |
| RU2007116161A (ru) | 2008-11-10 |
| BRPI0515935B1 (pt) | 2019-11-19 |
| WO2006035068A2 (en) | 2006-04-06 |
| AU2005288865A1 (en) | 2006-04-06 |
| WO2006035068A3 (en) | 2006-08-31 |
| CN101031550A (zh) | 2007-09-05 |
| ES2371924T3 (es) | 2012-01-11 |
| JP2008514680A (ja) | 2008-05-08 |
| BRPI0515935A (pt) | 2008-08-12 |
| EP1797048B1 (en) | 2011-08-17 |
| US7531548B2 (en) | 2009-05-12 |
| KR20070057798A (ko) | 2007-06-07 |
| US20070208022A1 (en) | 2007-09-06 |
| ZA200702655B (en) | 2008-09-25 |
| CA2573976A1 (en) | 2006-04-06 |
| EP1797048A2 (en) | 2007-06-20 |
| TW200626560A (en) | 2006-08-01 |
| BRPI0515935B8 (pt) | 2021-05-25 |
| IL180760A (en) | 2013-02-28 |
| IL180760A0 (en) | 2007-06-03 |
| RU2403244C2 (ru) | 2010-11-10 |
| CA2573976C (en) | 2014-04-29 |
| AU2005288865B2 (en) | 2012-07-19 |
| ATE520672T1 (de) | 2011-09-15 |
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