AR050969A1 - 5-heterociclil pirimidinas inhibidoras del vih; composiciones farmaceuticas que las contienen y uso de las mismas como medicamentos - Google Patents
5-heterociclil pirimidinas inhibidoras del vih; composiciones farmaceuticas que las contienen y uso de las mismas como medicamentosInfo
- Publication number
- AR050969A1 AR050969A1 ARP050104153A ARP050104153A AR050969A1 AR 050969 A1 AR050969 A1 AR 050969A1 AR P050104153 A ARP050104153 A AR P050104153A AR P050104153 A ARP050104153 A AR P050104153A AR 050969 A1 AR050969 A1 AR 050969A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkyl
- cyano
- halo
- independently
- nr9r10
- Prior art date
Links
- 239000008194 pharmaceutical composition Substances 0.000 title abstract 2
- 229940079593 drug Drugs 0.000 title 1
- 239000003814 drug Substances 0.000 title 1
- 239000003112 inhibitor Substances 0.000 title 1
- 150000003230 pyrimidines Chemical class 0.000 title 1
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 33
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 32
- 125000005843 halogen group Chemical group 0.000 abstract 26
- 125000001424 substituent group Chemical group 0.000 abstract 21
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 abstract 17
- 125000000217 alkyl group Chemical group 0.000 abstract 15
- 125000004453 alkoxycarbonyl group Chemical group 0.000 abstract 11
- 125000003545 alkoxy group Chemical group 0.000 abstract 9
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 8
- -1 hydroxy, mercapto Chemical class 0.000 abstract 8
- 229920006395 saturated elastomer Polymers 0.000 abstract 8
- 125000004916 (C1-C6) alkylcarbonyl group Chemical group 0.000 abstract 7
- 125000006684 polyhaloalkyl group Polymers 0.000 abstract 7
- 125000006272 (C3-C7) cycloalkyl group Chemical group 0.000 abstract 6
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 abstract 6
- 125000002485 formyl group Chemical group [H]C(*)=O 0.000 abstract 6
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 6
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 abstract 5
- 229910052739 hydrogen Inorganic materials 0.000 abstract 5
- 239000001257 hydrogen Substances 0.000 abstract 5
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 5
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 5
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 5
- 125000004103 aminoalkyl group Chemical group 0.000 abstract 4
- 125000003118 aryl 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
- 125000006700 (C1-C6) alkylthio group Chemical group 0.000 abstract 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 abstract 3
- 125000003710 aryl alkyl group Chemical group 0.000 abstract 3
- 125000006577 C1-C6 hydroxyalkyl group Chemical group 0.000 abstract 2
- 101100240519 Caenorhabditis elegans nhr-13 gene Chemical group 0.000 abstract 2
- 125000004448 alkyl carbonyl group Chemical group 0.000 abstract 2
- 125000002837 carbocyclic group Chemical group 0.000 abstract 2
- 229910052799 carbon Inorganic materials 0.000 abstract 2
- 125000004432 carbon atom Chemical group C* 0.000 abstract 2
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 abstract 2
- 150000001875 compounds Chemical class 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
- 229910052757 nitrogen Inorganic materials 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
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 abstract 1
- 208000031886 HIV Infections Diseases 0.000 abstract 1
- 208000037357 HIV infectious disease Diseases 0.000 abstract 1
- 150000001204 N-oxides Chemical class 0.000 abstract 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 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
- 125000005196 alkyl carbonyloxy group Chemical group 0.000 abstract 1
- 125000003277 amino group Chemical group 0.000 abstract 1
- 125000004104 aryloxy group Chemical group 0.000 abstract 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 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
- 125000004181 carboxyalkyl group Chemical group 0.000 abstract 1
- 125000004966 cyanoalkyl group Chemical group 0.000 abstract 1
- 125000004122 cyclic 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
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 abstract 1
- 125000001715 oxadiazolyl group Chemical group 0.000 abstract 1
- 125000002971 oxazolyl group Chemical group 0.000 abstract 1
- 229910052760 oxygen Inorganic materials 0.000 abstract 1
- 239000001301 oxygen Substances 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
- 125000002943 quinolinyl group Chemical group N1=C(C=CC2=CC=CC=C12)* 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 229910052717 sulfur Inorganic materials 0.000 abstract 1
- 239000011593 sulfur Substances 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
-
- 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
- C07D405/04—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 directly linked by a ring-member-to-ring-member bond
-
- 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
-
- 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
-
- 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
-
- 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
- C07D401/04—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 directly linked by a ring-member-to-ring-member bond
-
- 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
- C07D403/04—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 directly linked by a ring-member-to-ring-member bond
-
- 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
- C07D409/04—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 directly linked by a ring-member-to-ring-member bond
-
- 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
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- 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
- C07D417/04—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 directly linked by a ring-member-to-ring-member bond
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Medicinal Chemistry (AREA)
- Veterinary Medicine (AREA)
- Virology (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Oncology (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Communicable Diseases (AREA)
- AIDS & HIV (AREA)
- Tropical Medicine & Parasitology (AREA)
- Molecular Biology (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
Abstract
Uso de estos compuestos para la prevencion o el tratamiento de la infeccion con VIH, composicion farmacéuticas que los contienen. 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 del mismo, en el cual: -a1 = a2 - a3 = a4- representa un radical bivalente de formulas (2) a (6); -b1 = b2 - b3 = b4- representa un radical bivalente de formulas (2) a (6); n es 0,1, 2, 3 y en el caso que -a1 = a2 - a3 = a4 es una formula (2), entonces n también puede ser 4; m es 0, 1, 2, 3 y en el caso que -b1 = b2 - b3 = b4- es una formula (2), entonces m también puede ser 4; cada R1 es en forma independiente es hidrogeno; arilo; formilo; alquilcarbonilo C1-6; alquilo C1-6; alquiloxiC1-6carbonilo; alquilo C1-6 sustituido con formilo, alquilC1-6carbonilo, alquiloxiC1-6carbonilo, o con alquilC1-6carboniloxi; cada R2 es en forma independiente es hidroxi; halo; alquilo C1-6 sustituido en forma opcional con uno, dos o tres 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 uno, dos o tres sustituyentes seleccionados, cada uno en forma independiente, de halo, ciano o -C(=O)R6; alquinilo C2-6 sustituido en forma opcional con uno, dos o tres sustituyentes seleccionados, cada uno en forma independiente, de halo, ciano o -C(=O)R6; alquiloxiC1-6carbonilo; carboxilo; ciano; nitro; amino; mono- o di(alquilC1-6)amino; polihalometilo; polihalometiltio; -S(=O)pR6, -NH-S(=O)pR6, -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 uno, dos o tres sustituyentes seleccionados, cada uno en forma independiente, de halo, ciano, NR9R10; -C(=O)-NR9R10, -C(=O)-alquiloC1-6 o R7; alquilo C1-6 sustituido con hidroxi y un segundo sustituyente seleccionado de halo, ciano, NR9R10, -C(=O)-NR9R10, -C(=O)-alquiloC1-6 o R7; alquiloxiC1- 6alquiloC1-6 sustituido en forma opcional con uno, dos o tres sustituyentes seleccionados, cada uno en forma independiente, de halo, ciano, NR9R10, -C(=O)-NR9R10, -C(=O)-alquiloC1-6 o R7; alquenilo C2-6 sustituido con uno, dos o tres sustituyentes seleccionados, cada uno en forma independiente, de halo, ciano, NR9R10, -C(=O)-NR9R10, -C(=O)-alquiloC1-6 o R7; alquinilo C2-6 sustituido con uno, dos o tres sustituyentes seleccionados, cada uno en forma independiente, de halo, ciano, NR9R10, - C(=O)-NR9R10, -C(=O)-alquiloC1-6 o R7; -C(=N-O-R8)-alquiloC1-4; R7 o -X3-R7; X1 es -NR1-, -O-, -C(=O)-, -CH2-, -CHOH-, -S-, -S(=O)p-; 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 uno, dos o tres sustituyentes seleccionados, cada uno en forma independiente, de halo, ciano, NR9R10; -C(=O)-NR9R10, - C(=O)-alquiloC1-6 o R7; alquilo C1-6 sustituido con hidroxi y un segundo sustituyente seleccionado de halo, ciano, NR9R10, -C(=O)-NR9R10, -C(=O)-alquiloC1-6 o R7; alquiloxiC1-6alquiloC1-6 sustituido en forma opcional con uno, dos o tres sustituyentes seleccionados, cada uno en forma independiente, de halo, ciano, NR9R10, -C(=O)-NR9R10, -C(=O)-alquiloC1-6 o R7; alquenilo C2-6 sustituido con uno, dos o tres sustituyentes seleccionados, cada uno en forma independiente, de halo, ciano, NR9R10, -C(=O)-NR9R10, -C(=O)-alquiloC1-6 o R7; alquinilo C2-6 sustituido con uno, dos o tres sustituyentes seleccionados, cada uno en forma independiente, de halo, ciano, NR9R10, -C(=O)-NR9R10, -C(=O)-alquiloC1-6 o R7; -C(=N-O-R8)-alquiloC1-4; R7 o -X3-R7; X3 es -NR1-, -O-, -C(=O)-, -S-, -S(=O)p-; R4 es halo; R4 es halo; hidroxi; alquilo C1-6 sustituido en forma opcional con uno, dos o tres sustituyentes seleccionados, cada uno en forma independiente, de halo, ciano, o -C(=O)R6; alquenilo C2-6 sustituido en forma opcional con uno, dos o tres sustituyentes seleccionados, cada uno en forma independiente, de halo, ciano o -C(=O)R6; alquinilo C2-6 sustituido en forma opcional con uno, dos o tres 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; alquiloxiC1-6carbonilo; alquilC1-6carbonilo; formilo; amino; mono- o di(alquil C1-4)amino o R7; R5 es un sistema anular completamente insaturado de 5 o 6 miembros en el cual uno, dos, tres o cuatro miembros del anillo son heteroátomos seleccionados, cada uno en forma independiente, del grupo formado por nitrogeno, oxígeno y azufre, y en el cual el resto de los miembros del anillo son átomos de carbono; y, cuando sea posible, cualquier nitrogeno miembro del 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 donde cualquier átomo de carbono del anillo, incluyendo cualquier carbono 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, alquiloxiC1-4alquiloC1-4, cianoalquilo C1-4, di(alquil C1-4)aminoalquiloC1-4, Het-alquiloC1-4, arilalquilo C1-4, polihaloalquilo C1-4, cicloalquilo C3-7, alquenilo C2-6, arilalquenilo C2-4, alquiloxi C1-4, -OCONH2, polihaloalquiloxi C1-4, ariloxi, amino, mono- y di-alquilaminoC1-4, alquilC1-4carbonilamino, formilo, alquilC1-4carbonilo, alquiloxiC1-4carbonilo, aminocarbonilo, mono- y di-alquilaminoC1-4carbonilo, arilo, Het; donde Het es piridilo, tienilo, furanilo, oxazolilo, isoxazolilo, imidazolilo, pirazolilo, tiazolilo, tiadiazolilo, oxadiazolilo, quinolinilo, benzotienilo, benzofuranilo; de los cuales cada uno puede estar sustituido en forma opcional con uno o dos radicales alquilo C1-4; Q es hidrogeno, 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 uno, dos, tres, cuatro o cinco 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)aminoalquiloC1-6, formilo, alquilC1-6carbonilo, cicloalquilo C3-7, alquiloxi C1-6, alquiloxiC1-6carbonilo, alquiltio C1-6, ciano, nitro, polihaloalquilo C1-6, polihaloalquiloxi C1-6, aminocarbonilo, -CH(=N-O- R8), R7a, -X3-R7a o R7a-alquiloC1-4; R7a es un carbocíclico 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 uno, dos, tres, cuatro o cinco 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)aminoalquiloC1-6, formilo, alquilC1-6carbonilo, cicloalquilo C3-7, alquiloxi C1-6, alquiloxiC1-6carbonilo, alquiltio C1-6, ciano, nitro, polihaloalquilo C1-6, polihaloalquiloxi C1-6, aminocarbonilo, -CH(=N-O-R8); R8 es hidrogeno, alquilo C1-4, arilo o arilalquilo C1-4; R9 y R10 son, cada uno en forma independiente hidrogeno; alquilo C1-6; alquilC1-6carbonilo; alquiloxiC1-6carbonilo; amino; mono- o di(alquil C1-6)aminocarbonilo; - CH(=N-O-R11), R7, donde cada uno de los grupos alquilo C1-6 antes mencionados puede estar sustituido 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, alquiloxiC1-6carbonilo, ciano, amino, imino, mono- o di(alquil C1-4)amino, polihalometilo, polihalometiloxi, polihalometiltio, -S(=O)pR6, -NH-S(=O)pR6, -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 formulas: -CH2-CH2-CH2-CH2-; -CH2-CH2-CH2-CH2-CH2-; -CH2-CH2-O-CH2-CH2-; -CH2-CH2-S-CH2-CH2-; -CH2-CH2-NR12-CH2-CH2-; -CH2-CH=CH-CH2-; =CH-CH=CH-CH=CH-; 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; alquilC1-4carbonilo; alquiloxiC1-4carbonilo; aminocarbonilo; mono- o di(alquil C1-4)aminocarbonilo; R12 es hidrogeno 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 p es 1 o 2; cada arilo es fenilo o fenilo sustituido con uno, dos, tres, cuatro o cinco 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)aminoalquiloC1-6, alquilC1-6carbonilo, cicloalquilo C3-7, alquiloxi C1-6, alquiloxiC1-6carbonilo, alquiltio C1-6, ciano, nitro, polihaloalquilo C1-6, polihaloalquiloxi C1-6, aminocarbonilo, Het o -X3-
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| US (1) | US8575342B2 (es) |
| EP (1) | EP1797069B1 (es) |
| JP (1) | JP5008567B2 (es) |
| KR (1) | KR20070057899A (es) |
| CN (1) | CN101031558B (es) |
| AR (1) | AR050969A1 (es) |
| AT (1) | ATE520680T1 (es) |
| AU (1) | AU2005288864B2 (es) |
| BR (1) | BRPI0516746A (es) |
| CA (1) | CA2577467C (es) |
| ES (1) | ES2371923T3 (es) |
| IL (1) | IL180959A (es) |
| MX (1) | MX2007003797A (es) |
| RU (1) | RU2405778C2 (es) |
| TW (1) | TW200626574A (es) |
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| MX2007003797A (es) | 2004-09-30 | 2007-04-23 | Tibotec Pharm Ltd | 5-heterociclil pirimidinas inhibidoras del virus de inmunodeficiencia humana. |
| BRPI0607811B8 (pt) * | 2005-02-18 | 2021-05-25 | Janssen R & D Ireland | derivados de óxido de pirimidina de 2-(4-cianofenilamino) inibidores de hiv, composição farmacêutica compreendendo os mesmos, processo para preparar a referida composição e uso |
| BRPI0709690B8 (pt) | 2006-03-30 | 2021-05-25 | Janssen R & D Ireland | 5-amido pirimidinas substituídas e composição farmacêutica que as compreende |
| RU2469032C2 (ru) | 2006-12-13 | 2012-12-10 | Ф.Хоффманн-Ля Рош Аг | Производные 2-(пиперидин-4-ил)-4-фенокси- или фениламинопиримидина в качестве ненуклеозидных ингибиторов обратной транскриптазы |
| KR20090094073A (ko) | 2006-12-29 | 2009-09-03 | 티보텍 파마슈티칼즈 리미티드 | Hiv를 억제하는 6-치환된 피리미딘 |
| CN101573342A (zh) | 2006-12-29 | 2009-11-04 | 泰博特克药品有限公司 | 抑制hiv的5,6-取代的嘧啶类化合物 |
| TW201016676A (en) * | 2008-10-03 | 2010-05-01 | Astrazeneca Ab | Heterocyclic derivatives and methods of use thereof |
| EP2571361A4 (en) | 2010-05-19 | 2013-11-13 | Univ North Carolina | PYRAZOLOPYRIMIDINE COMPOUNDS FOR CANCER TREATMENT |
| US8729079B2 (en) | 2011-08-23 | 2014-05-20 | Endo Pharmaceuticals Inc. | Pyrimido-pyridazinone compounds and methods of use thereof |
| KR102063098B1 (ko) | 2011-10-03 | 2020-01-08 | 더 유니버시티 오브 노쓰 캐롤라이나 엣 채플 힐 | 암 치료를 위한 피롤로피리미딘 화합물 |
| CN104302627A (zh) * | 2012-05-22 | 2015-01-21 | 北卡罗来纳大学教堂山分校 | 用于治疗癌症的嘧啶化合物 |
| WO2014062774A1 (en) | 2012-10-17 | 2014-04-24 | The University Of North Carolina At Chapel Hill | Pyrazolopyrimidine compounds for the treatment of cancer |
| EP2925752A4 (en) | 2012-11-27 | 2016-06-01 | Univ North Carolina | PYRIMIDINE COMPOUNDS FOR CANCER TREATMENT |
| RU2547844C1 (ru) * | 2013-10-29 | 2015-04-10 | Федеральное государственное бюджетное учреждение науки Институт органического синтеза им. И.Я. Постовского Уральского отделения Российской академии наук | Способ получения 5-(гет)арил-4-(2-тиенил)-2-(тио)морфолилпиримидина |
| WO2015157123A1 (en) | 2014-04-11 | 2015-10-15 | The University Of North Carolina At Chapel Hill | Mertk-specific pyrrolopyrimidine compounds |
| RS58124B1 (sr) * | 2014-04-28 | 2019-02-28 | Medicines For Malaria Venture Mmv | Triaminopirimidin jedinjenja korisna za prevenciju ili tretman malarije |
| TWI803187B (zh) * | 2014-08-08 | 2023-05-21 | 日商中外製藥股份有限公司 | 包含4環性化合物的非晶質體之固體分散體及製劑 |
| US10709708B2 (en) | 2016-03-17 | 2020-07-14 | The University Of North Carolina At Chapel Hill | Method of treating cancer with a combination of MER tyrosine kinase inhibitor and an epidermal growth factor receptor (EGFR) inhibitor |
| WO2018201131A1 (en) | 2017-04-28 | 2018-11-01 | Asana Biosciences, Llc | Formulations, methods, kits, and dosage forms for treating atopic dermatitis and for improved stability of an active pharmaceutical ingredient |
| WO2019222538A1 (en) * | 2018-05-16 | 2019-11-21 | The University Of North Carolina At Chapel Hill | Aminopyrimidines and aminopyridines as mertk inhibitors and their application in cancer treatment |
| AU2021224460A1 (en) | 2020-02-19 | 2022-12-15 | Pharmasyntez, Joint Stock Company | Pyrimidine-based bicycles as antiviral agents for the treatment and prevention of HIV infection |
| CN111875548A (zh) * | 2020-07-16 | 2020-11-03 | 山东大学 | 一种5位芳环取代的二芳基嘧啶类衍生物及其制备方法与应用 |
| US11351149B2 (en) | 2020-09-03 | 2022-06-07 | Pfizer Inc. | Nitrile-containing antiviral compounds |
| WO2022059996A1 (ko) * | 2020-09-15 | 2022-03-24 | 서울대학교 기술지주 주식회사 | 혈액 순환 미세체외소체 매개 암 치료용 조성물 |
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| US3459731A (en) | 1966-12-16 | 1969-08-05 | Corn Products Co | Cyclodextrin polyethers and their production |
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| EP0945447A1 (en) | 1998-03-27 | 1999-09-29 | Janssen Pharmaceutica N.V. | Trisubstituted 1,3,5-triazine derivatives for treatment of HIV infections |
| ATE232521T1 (de) | 1998-03-27 | 2003-02-15 | Janssen Pharmaceutica Nv | Hiv hemmende pyrimidin derivate |
| AU762523C (en) * | 1998-11-10 | 2004-02-12 | Janssen Pharmaceutica N.V. | HIV replication inhibiting pyrimidines |
| GB9828511D0 (en) | 1998-12-24 | 1999-02-17 | Zeneca Ltd | Chemical compounds |
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| GB0016877D0 (en) * | 2000-07-11 | 2000-08-30 | Astrazeneca Ab | Chemical compounds |
| ATE354573T1 (de) * | 2000-12-21 | 2007-03-15 | Vertex Pharma | ßPYRAZOLVERBINDUNGEN, DIE SICH ALS PROTEINKINASEINHIBITOREN EIGNENß |
| JO3429B1 (ar) | 2001-08-13 | 2019-10-20 | Janssen Pharmaceutica Nv | مشتقات برميدينات مثبطة فيروس الايدز |
| TWI329105B (en) * | 2002-02-01 | 2010-08-21 | Rigel Pharmaceuticals Inc | 2,4-pyrimidinediamine compounds and their uses |
| WO2004046143A1 (en) | 2002-11-15 | 2004-06-03 | Tibotec Pharmaceuticals Ltd. | Substituted indolepyridinium as anti-infective compounds |
| US7504396B2 (en) | 2003-06-24 | 2009-03-17 | Amgen Inc. | Substituted heterocyclic compounds and methods of use |
| EP1797047B1 (en) | 2004-09-30 | 2012-01-25 | Tibotec Pharmaceuticals | Hiv inhibiting 5-substituted pyrimidines |
| CA2573976C (en) | 2004-09-30 | 2014-04-29 | Tibotec Pharmaceuticals Ltd. | Hiv inhibiting 5-carbo- or heterocyclic substituted pyrimidines |
| MX2007003797A (es) | 2004-09-30 | 2007-04-23 | Tibotec Pharm Ltd | 5-heterociclil pirimidinas inhibidoras del virus de inmunodeficiencia humana. |
| BRPI0709690B8 (pt) | 2006-03-30 | 2021-05-25 | Janssen R & D Ireland | 5-amido pirimidinas substituídas e composição farmacêutica que as compreende |
| CN101573342A (zh) | 2006-12-29 | 2009-11-04 | 泰博特克药品有限公司 | 抑制hiv的5,6-取代的嘧啶类化合物 |
| KR20090094073A (ko) | 2006-12-29 | 2009-09-03 | 티보텍 파마슈티칼즈 리미티드 | Hiv를 억제하는 6-치환된 피리미딘 |
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Also Published As
| Publication number | Publication date |
|---|---|
| EP1797069B1 (en) | 2011-08-17 |
| KR20070057899A (ko) | 2007-06-07 |
| CN101031558A (zh) | 2007-09-05 |
| CA2577467C (en) | 2013-05-28 |
| RU2007116152A (ru) | 2008-11-10 |
| ZA200702653B (en) | 2008-08-27 |
| AU2005288864A1 (en) | 2006-04-06 |
| WO2006035067A2 (en) | 2006-04-06 |
| BRPI0516746A (pt) | 2008-09-23 |
| US20090181993A1 (en) | 2009-07-16 |
| WO2006035067A3 (en) | 2006-08-24 |
| IL180959A (en) | 2012-08-30 |
| TW200626574A (en) | 2006-08-01 |
| ES2371923T3 (es) | 2012-01-11 |
| MX2007003797A (es) | 2007-04-23 |
| RU2405778C2 (ru) | 2010-12-10 |
| CN101031558B (zh) | 2011-10-05 |
| ATE520680T1 (de) | 2011-09-15 |
| IL180959A0 (en) | 2007-07-04 |
| EP1797069A2 (en) | 2007-06-20 |
| CA2577467A1 (en) | 2006-04-06 |
| US8575342B2 (en) | 2013-11-05 |
| JP5008567B2 (ja) | 2012-08-22 |
| JP2008514679A (ja) | 2008-05-08 |
| AU2005288864B2 (en) | 2012-08-23 |
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