AR075071A1 - COMPUESTOS DERIVADOS DE SULFONAMIDAS , USO DE LOS MISMOS PARA LA PREPARACIoN DE MEDICAMENTOS , COMPOSICIONES FARMACÉUTICAS Y PROCESO DE PREPARACIoN DE LOS MISMOS - Google Patents
COMPUESTOS DERIVADOS DE SULFONAMIDAS , USO DE LOS MISMOS PARA LA PREPARACIoN DE MEDICAMENTOS , COMPOSICIONES FARMACÉUTICAS Y PROCESO DE PREPARACIoN DE LOS MISMOSInfo
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- AR075071A1 AR075071A1 ARP090102946A ARP090102946A AR075071A1 AR 075071 A1 AR075071 A1 AR 075071A1 AR P090102946 A ARP090102946 A AR P090102946A AR P090102946 A ARP090102946 A AR P090102946A AR 075071 A1 AR075071 A1 AR 075071A1
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- Prior art keywords
- carbon atoms
- optionally substituted
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- alkyl
- atoms
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- 150000001875 compounds Chemical class 0.000 title abstract 7
- 238000000034 method Methods 0.000 title abstract 3
- 239000003814 drug Substances 0.000 title abstract 2
- 239000008194 pharmaceutical composition Substances 0.000 title abstract 2
- 125000004432 carbon atom Chemical group C* 0.000 abstract 45
- 125000000217 alkyl group Chemical group 0.000 abstract 22
- 125000000623 heterocyclic group Chemical group 0.000 abstract 11
- 125000002837 carbocyclic group Chemical group 0.000 abstract 9
- 125000005843 halogen group Chemical group 0.000 abstract 8
- 229910052736 halogen Inorganic materials 0.000 abstract 6
- 150000002367 halogens Chemical class 0.000 abstract 6
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 6
- 125000003545 alkoxy group Chemical group 0.000 abstract 5
- 125000002947 alkylene group Chemical group 0.000 abstract 5
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 5
- 125000000392 cycloalkenyl group Chemical group 0.000 abstract 4
- 125000001033 ether group Chemical group 0.000 abstract 4
- 125000001424 substituent group Chemical group 0.000 abstract 4
- 108091008648 NR7C Proteins 0.000 abstract 3
- 125000004122 cyclic group Chemical group 0.000 abstract 3
- 125000004430 oxygen atom Chemical group O* 0.000 abstract 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 abstract 2
- 101001043818 Mus musculus Interleukin-31 receptor subunit alpha Proteins 0.000 abstract 2
- 125000003341 7 membered heterocyclic group Chemical group 0.000 abstract 1
- 206010027654 Allergic conditions Diseases 0.000 abstract 1
- 101100212791 Saccharomyces cerevisiae (strain ATCC 204508 / S288c) YBL068W-A gene Proteins 0.000 abstract 1
- 101000585507 Solanum tuberosum Cytochrome b-c1 complex subunit 7 Proteins 0.000 abstract 1
- 208000026935 allergic disease Diseases 0.000 abstract 1
- 125000004429 atom Chemical group 0.000 abstract 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 abstract 1
- 229910052799 carbon Inorganic materials 0.000 abstract 1
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 1
- 239000003937 drug carrier Substances 0.000 abstract 1
- 150000004677 hydrates Chemical class 0.000 abstract 1
- 229910052739 hydrogen Inorganic materials 0.000 abstract 1
- 239000001257 hydrogen Substances 0.000 abstract 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 1
- 230000002757 inflammatory effect Effects 0.000 abstract 1
- 238000004519 manufacturing process Methods 0.000 abstract 1
- 229910052757 nitrogen Inorganic materials 0.000 abstract 1
- 239000000546 pharmaceutical excipient Substances 0.000 abstract 1
- 150000003839 salts Chemical class 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
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/24—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with substituted hydrocarbon radicals attached to ring carbon atoms
- C07D213/44—Radicals substituted by doubly-bound oxygen, sulfur, or nitrogen atoms, or by two such atoms singly-bound to the same carbon atom
- C07D213/52—Sulfur atoms
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- 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
- A61K31/16—Amides, e.g. hydroxamic acids
- A61K31/18—Sulfonamides
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- 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
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
- A61P17/02—Drugs for dermatological disorders for treating wounds, ulcers, burns, scars, keloids, or the like
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
- A61P19/02—Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
- A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/08—Antiallergic agents
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- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C311/00—Amides of sulfonic acids, i.e. compounds having singly-bound oxygen atoms of sulfo groups replaced by nitrogen atoms, not being part of nitro or nitroso groups
- C07C311/48—Amides of sulfonic acids, i.e. compounds having singly-bound oxygen atoms of sulfo groups replaced by nitrogen atoms, not being part of nitro or nitroso groups having nitrogen atoms of sulfonamide groups further bound to another hetero atom
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- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/24—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with substituted hydrocarbon radicals attached to ring carbon atoms
- C07D213/36—Radicals substituted by singly-bound nitrogen atoms
- C07D213/38—Radicals substituted by singly-bound nitrogen atoms having only hydrogen or hydrocarbon radicals attached to the substituent nitrogen atom
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- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
- C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
- C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D231/12—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
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- C07D241/00—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings
- C07D241/02—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings
- C07D241/10—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
- C07D241/12—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
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- C07—ORGANIC CHEMISTRY
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- C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
- C07D307/02—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings
- C07D307/04—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having no double bonds between ring members or between ring members and non-ring members
- C07D307/10—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having no double bonds between ring members or between ring members and non-ring members with substituted hydrocarbon radicals attached to ring carbon atoms
- C07D307/14—Radicals substituted by nitrogen atoms not forming part of a nitro radical
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- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
- C07D307/02—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings
- C07D307/34—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D307/38—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with substituted hydrocarbon radicals attached to ring carbon atoms
- C07D307/40—Radicals substituted by oxygen atoms
- C07D307/42—Singly bound oxygen atoms
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- C07D—HETEROCYCLIC COMPOUNDS
- C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
- C07D307/02—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings
- C07D307/34—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D307/38—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with substituted hydrocarbon radicals attached to ring carbon atoms
- C07D307/52—Radicals substituted by nitrogen atoms not forming part of a nitro radical
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- C07D333/00—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom
- C07D333/02—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings
- C07D333/04—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom
- C07D333/26—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D333/30—Hetero atoms other than halogen
- C07D333/36—Nitrogen atoms
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- 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
- C07D413/12—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 linked by a chain containing hetero atoms as chain links
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Abstract
Reivindicacion 1: Un compuesto de la formula 1: o solvatos, hidratos o sales farmacéuticamente aceptables del mismo, en donde: R1 es H, un grupo carbocíclico de 3 a 10 miembros opcionalmente sustituido por uno o más grupos Z, un grupo heterocíclico de 3 a 10 miembros opcionalmente sustituido por uno o más grupos Z, (alquilo de 1 a 4 átomos de carbono)-grupo carbocíclico de 3 a 10 miembros opcionalmente sustituido por uno o más grupos Z, (alquilo de 1 a 4 átomos de carbono)-grupo heterocíclico de 3 a 10 miembros opcionalmente sustituido por uno o más grupos Z, alquilo de 1 a 6 átomos de carbono opcionalmente sustituido por uno o más átomos de halogeno, grupos CN u OH, alcoxilo de 1 a 6 átomos de carbono opcionalmente sustituido por uno o más átomos de halogeno o grupos OH, o un grupo éter que contiene de 2 a 10 átomos de carbono y de 1 a 3 átomos de oxígeno, en donde el grupo éter está opcionalmente sustituido por uno o más sustituyentes, cada uno independientemente seleccionado a partir de OH, halogeno, un grupo carbocíclico de 3 a 10 miembros opcionalmente sustituido por uno o más grupos Z, y un grupo heterocíclico de 3 a 10 miembros opcionalmente sustituido por uno o más grupos Z; R2 es un grupo carbocíclico de 3 a 10 miembros opcionalmente sustituido por uno o más grupos Z, un grupo heterocíclico de 3 a 10 miembros opcionalmente sustituido por uno o más grupos Z, (alquilo de 1 a 4 átomos de carbono)-grupo carbocíclico de 3 a 10 miembros opcionalmente sustituido por uno o más grupos Z, (alquilo de 1 a 4 átomos de carbono)-grupo heterocíclico de 3 a 10 miembros opcionalmente sustituido por uno o más grupos Z, alquilo de 1 a 6 átomos de carbono opcionalmente sustituido por uno o más átomos de halogeno, grupos CN u OH, alcoxilo de 1 a 6 átomos de carbono opcionalmente sustituido por uno o más átomos de halogeno o grupos OH, o un grupo éter que contiene de 2 a 10 átomos de carbono y de 1 a 3 átomos de oxígeno, en donde el grupo éter está opcionalmente sustituido por uno o más sustituyentes, cada uno independientemente seleccionado a partir de OH, halogeno, un grupo carbocíclico de 3 a 10 miembros opcionalmente sustituido por uno o más grupos Z, y un grupo heterocíclico de 3 a 10 miembros opcionalmente sustituido por uno o más grupos Z; o R1 y R2 junto con el átomo de carbono con el que están unidos, forman un grupo carbocíclico de 3 a 10 miembros opcionalmente sustituido por uno o más grupos Z, o un grupo heterocíclico de 3 a 10 miembros opcionalmente sustituido por uno o más grupos Z; R3 es hidrogeno, halogeno o ciano; R4 es H, alquilo de 1 a 8 átomos de carbono, cicloalquilo de 3 a 8 átomos de carbono, cicloalquenilo de 5 a 8 átomos de carbono o (alquilo de 1 a 4 átomos de carbono)-R6, en donde los grupos alquilo están cada uno opcionalmente sustituidos por uno o más átomos de halogeno; R5 es alquilo de 1 a 8 átomos de carbono, cicloalquilo de 3 a 8 átomos de carbono, cicloalquenilo de 5 a 8 átomos de carbono, (alquilo de 1 a 4 átomos de carbono) cicloalquilo de 3 a 8 átomos de carbono o (alquilo de 1 a 4 átomos de carbono)-cicloalquenilo de 5 a 8 átomos de carbono, en donde los grupos alquilo están cada uno opcionalmente sustituidos por uno o más átomos de halogeno: o R4 y R5, junto con los átomos de nitrogeno y oxígeno con los que están unidos, forman un grupo heterocíclico de 5 a 10 miembros opcionalmente sustituido por uno o más grupos Z; R6 se selecciona a partir de un grupo carbocíclico de 3 a 10 miembros opcionalmente sustituido por uno o más grupos Z, un grupo heterocíclico de 3 a 10 miembros opcionalmente sustituido por uno o más grupos Z, NR7R9, NR7(SO2)R9, (SO2)NR7R8, (SO2)R9, NR7C(O)R9, C(O)NR7R9, NR7C(O)NR8R9, NR7C(O)OR9, C(O)OR7, OC(O)R9, OC(O)NR7, C(O)R9, SR7, CN y NO2; R7 y R8 se seleccionan cada uno independientemente a partir de H, alquilo de 1 a 6 átomos de carbono, cicloalquilo de 3 a 10 átomos de carbono, cicloalquenilo de 5 a 10 átomos de carbono y -(alquileno de 1 a 3 átomos de carbono)-cicloalquilo de 3 a 10 átomos de carbono; R9 se selecciona a partir de H, alquilo de 1 a 6 átomos de carbono, -(alquileno de 1 a 3 átomos de carbono)-cicloalquilo de 3 a 10 átomos de carbono, un grupo carbocíclico de 3 a 10 miembros, y un grupo heterocíclico de 3 a 10 miembros, en donde cada uno de los grupos alquilo y sistemas de anillos está opcionalmente sustituido por OH, halogeno, alquilo de 1 a 3 átomos de carbono, y alcoxilo de 1 a 3 átomos de carbono; X es CR14 o N; Z se selecciona independientemente a partir de OH; un grupo carbocíclico de 3 a 10 miembros: un grupo heterocíclico de 3 a 10 miembros; bencilo; alquilo de 1 a 6 átomos de carbono opcionalmente sustituido por uno o más átomos de halogeno, grupos CN u OH; alcoxilo de 1 a 6 átomos de carbono opcionalmente sustituido por uno o más átomos de halogeno, grupos CN u OH; -Oarilo; -Obencilo; -O(CH2)aC(O)E; NR10(SO2)R12 (SO2)NR10R11; (SO2)R12; NR10C(O)R12; C(O)NR10R12; NR10C(O)NR11R12; NR10C(O)OR12; NR10R12; C(O)OR10; OC(O)R12; OC(O)NR10; C(O)R12; SR12; CN; NO2 y halogeno; o en donde hay dos o más sustituyentes Z, dos sustituyentes Z junto con los átomos con los que están unidos opcionalmente forman un sustituyente carbocíclico de 5 a 7 miembros o heterocíclico de 4 a 7 miembros fusionado con el sistema de anillos; a es 0, 1, 2, 3 o 4, en donde el grupo alquileno está opcionalmente sustituido por OH o NH, cuando a es 1, 2, 3 o 4; E es NR10R12 u OR12; cada R10 y R11 se selecciona independientemente a partir de H, alquilo de 1 a 6 átomos de carbono, cicloalquilo de 3 a 10 átomos de carbono, cicloalquenilo de 5 a 10 átomos de carbono y -(alquileno de 1 a 3 átomos de carbono)-cicloalquilo de 3 a 10 átomos de carbono; cada R12 se selecciona a partir de H, alquilo de 1 a 6 átomos de carbono, -(alquileno de 1 a 3 átomos de carbono)-cicloalquilo de 3 a 10 átomos de carbono, un grupo carbocíclico de 3 a 10 miembros, y un grupo heterocíclico de 3 a 10 miembros, en donde cada uno de los sistemas de anillos está opcionalmente sustituido por OH, halogeno, alquilo de 1 a 3 átomos de carbono, y alcoxilo de 1 a 3 átomos de carbono; y R14 es H o alquilo de 1 a 6 átomos de carbono. Reivindicacion 10: El uso de un compuesto de acuerdo con cualquiera de las reivindicaciones 1 a 8, en la fabricacion de un medicamento para el tratamiento de condiciones o enfermedades inflamatorias o alérgicas. Reivindicacion 12: Una composicion farmacéutica, la cual comprende un compuesto de acuerdo con cualquiera de las reivindicaciones 1 a 8, junto con un vehiculo o excipiente farmacéuticamente aceptable. Reivindicacion 14: Un proceso para la preparacion de un compuesto de acuerdo con cualquiera de las reivindicaciones 1 a 8, cuyo proceso comprende hacer reaccionar un compuesto de la formula 2: en donde R3, R4 y R5 son como se definen en la reivindicacion 1, con un compuesto de la formula 3: en donde X, R1 y R2 son como se definen en la reivindicacion 1; aislar el producto.
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| JP (1) | JP5303645B2 (es) |
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| AR (1) | AR075071A1 (es) |
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| BR (1) | BRPI0916995B8 (es) |
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Families Citing this family (33)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| UA103198C2 (en) | 2008-08-04 | 2013-09-25 | Новартис Аг | Squaramide derivatives as cxcr2 antagonists |
| US8648070B2 (en) | 2010-12-17 | 2014-02-11 | Boehringer Ingelheim International Gmbh | Bicyclic ring system substituted sulfonamide functionalised phenols as medicaments |
| US8648118B2 (en) | 2010-12-17 | 2014-02-11 | Boehringer Ingelheim International Gmbh | Bicyclic ring system substituted amide functionalised phenols as medicaments |
| AU2016201916A1 (en) * | 2011-09-02 | 2016-04-21 | Novartis Ag | Choline salt of an anti-inflammatory substituted cyclobutenedione compound |
| PL2760821T3 (pl) * | 2011-09-02 | 2018-04-30 | Novartis Ag | Sól cholinowa przeciwzapalnego związku podstawionego cyklobutenodionem |
| FR2981934B1 (fr) * | 2011-10-28 | 2013-12-20 | Galderma Res & Dev | Nouveaux composes di-substitues de la diamino-3,4-cyclobutene-3-dione-1,2 utiles dans le traitement de pathologies mediees par des chimiokines. |
| FR2981935B1 (fr) * | 2011-10-28 | 2015-08-07 | Galderma Res & Dev | Nouveaux composes di-substitues de la diamino-3,4-cyclobutene-3-dione-1,2 utiles dans le traitement de pathologies mediees par des chimiokines. |
| EP2764866A1 (en) | 2013-02-07 | 2014-08-13 | IP Gesellschaft für Management mbH | Inhibitors of nedd8-activating enzyme |
| HK1223978A1 (zh) | 2013-06-18 | 2017-08-11 | New York University | 参与金黄色葡萄球菌杀白细胞素的细胞毒性的细胞因素:新型治疗靶点 |
| FR3030515B1 (fr) | 2014-12-23 | 2017-01-20 | Galderma Res & Dev | Nouveaux composes antagonistes des recepteurs cxcr1 et cxcr2 aux chimiokines, et leur utilisation dans le traitement de pathologies mediees par des chimiokines |
| TWI734715B (zh) | 2015-11-19 | 2021-08-01 | 美商卡默森屈有限公司 | 趨化因子受體調節劑 |
| TWI724056B (zh) | 2015-11-19 | 2021-04-11 | 美商卡默森屈有限公司 | Cxcr2抑制劑 |
| US10660909B2 (en) | 2016-11-17 | 2020-05-26 | Syntrix Biosystems Inc. | Method for treating cancer using chemokine antagonists |
| CA3072671A1 (en) * | 2017-08-14 | 2019-02-21 | Allergan, Inc. | 3,4-disubstituted 3-cyclobutene-1,2-diones and use thereof |
| WO2019099838A1 (en) | 2017-11-16 | 2019-05-23 | Novartis Ag | Combination therapies |
| US11207294B2 (en) | 2018-01-08 | 2021-12-28 | Chemocentryx, Inc. | Methods of treating generalized pustular psoriasis with an antagonist of CCR6 or CXCR2 |
| WO2019165315A1 (en) | 2018-02-23 | 2019-08-29 | Syntrix Biosystems Inc. | Method for treating cancer using chemokine antagonists alone or in combination |
| AR116109A1 (es) | 2018-07-10 | 2021-03-31 | Novartis Ag | Derivados de 3-(5-amino-1-oxoisoindolin-2-il)piperidina-2,6-diona y usos de los mismos |
| WO2020058869A1 (en) | 2018-09-21 | 2020-03-26 | Pfizer Inc. | N-substituted-dioxocyclobutenylamino-3-hydroxy-picolinamides useful as ccr6 inhibitors |
| CN113271945A (zh) | 2018-12-20 | 2021-08-17 | 诺华股份有限公司 | 包含3-(1-氧代异吲哚啉-2-基)哌啶-2,6-二酮衍生物的给药方案和药物组合 |
| MX2021009764A (es) | 2019-02-15 | 2021-09-08 | Novartis Ag | Derivados de 3-(1-oxoisoindolin-2-il)piperidina-2,6-diona sustituidos y usos de los mismos. |
| MX2021009763A (es) | 2019-02-15 | 2021-09-08 | Novartis Ag | Derivados de 3-(1-oxo-5-(piperidin-4-il)isoindolin-2-il)piperidina -2,6-diona y usos de los mismos. |
| CN112759549B (zh) * | 2019-11-05 | 2023-07-28 | 中国医学科学院药物研究所 | 3-取代氨基-4-((取代吡啶基)氨基)环丁-3-烯-1,2-二酮类化合物 |
| CN112851635B (zh) * | 2019-11-28 | 2022-09-16 | 中国医学科学院药物研究所 | 环状砜类化合物及其制备方法、用途和药物组合物 |
| JP2023507190A (ja) | 2019-12-20 | 2023-02-21 | ノバルティス アーゲー | 増殖性疾患を治療するための抗TGFβ抗体及びチェックポイント阻害薬の使用 |
| EP4168007A1 (en) | 2020-06-23 | 2023-04-26 | Novartis AG | Dosing regimen comprising 3-(1-oxoisoindolin-2-yl)piperidine-2,6-dione derivatives |
| EP4188549A1 (en) | 2020-08-03 | 2023-06-07 | Novartis AG | Heteroaryl substituted 3-(1-oxoisoindolin-2-yl)piperidine-2,6-dione derivatives and uses thereof |
| IL302553A (en) * | 2020-11-05 | 2023-07-01 | Icahn School Med Mount Sinai | Cxcr1/cxcr2 inhibitors for use in treating myelofibrosis |
| TW202304979A (zh) | 2021-04-07 | 2023-02-01 | 瑞士商諾華公司 | 抗TGFβ抗體及其他治療劑用於治療增殖性疾病之用途 |
| CA3216717A1 (en) | 2021-04-30 | 2022-11-03 | Mind Medicine, Inc. | Lsd salt crystal forms |
| AR125874A1 (es) | 2021-05-18 | 2023-08-23 | Novartis Ag | Terapias de combinación |
| US12527786B2 (en) | 2021-08-19 | 2026-01-20 | Mind Medicine, Inc. | Immediate release formulations of d-lysergic acid diethylamide for therapeutic applications |
| WO2025149577A1 (en) * | 2024-01-11 | 2025-07-17 | Julius-Maximilians-Universitaet Wuerzburg | 18f-cxcr2 pet tracer |
Family Cites Families (27)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5354763A (en) * | 1993-11-17 | 1994-10-11 | American Home Products Corporation | Substituted N-heteroaryl and N-aryl-1,2-diaminocyclobutene-3,4-diones |
| US6166050A (en) | 1998-12-14 | 2000-12-26 | American Home Products Corporation | 3,4-diamino-3-cyclobutene-1,2-dione derivatives which inhibit leukocyte adhesion mediated by VLA-4 |
| JP2002534498A (ja) * | 1999-01-13 | 2002-10-15 | ワーナー−ランバート・カンパニー | Mek阻害剤としてのベンゼンスルホンアミド誘導体およびその使用 |
| DE60216229T2 (de) * | 2001-01-16 | 2007-10-04 | Smithkline Beecham Corp. | Il-8-rezeptorantagonisten |
| US20040110954A1 (en) | 2001-03-30 | 2004-06-10 | Palovich Michael R. | Methods of synthesizing phenol-contining compounds |
| PL208928B1 (pl) | 2001-04-16 | 2011-06-30 | Pharmacopeia | 3, 4-di-podstawione cyklobuten-1, 2-diony jako ligandy receptora CXC chemokiny |
| US20040106794A1 (en) | 2001-04-16 | 2004-06-03 | Schering Corporation | 3,4-Di-substituted cyclobutene-1,2-diones as CXC-chemokine receptor ligands |
| US7132445B2 (en) | 2001-04-16 | 2006-11-07 | Schering Corporation | 3,4-Di-substituted cyclobutene-1,2-diones as CXC-chemokine receptor ligands |
| MXPA04009127A (es) | 2002-03-18 | 2005-01-25 | Schering Corp | Tratamiento de enfermedades mediadas por quimiocinas. |
| JP2007519751A (ja) | 2004-01-30 | 2007-07-19 | シェーリング コーポレイション | Cxc−ケモカインレセプターリガンドの結晶多形 |
| DE102005001053A1 (de) | 2005-01-07 | 2006-07-20 | Merck Patent Gmbh | Quadratsäurederivate |
| JP2008530284A (ja) | 2005-02-10 | 2008-08-07 | ワッカー ケミー アクチエンゲゼルシャフト | 保護されたイソシアネート基を有する粒子を含有する塗料 |
| WO2006088920A1 (en) | 2005-02-16 | 2006-08-24 | Schering Corporation | Amine-linked pyridyl and phenyl substituted piperazine-piperidines with cxcr3 antagonist activity |
| DE102005035742A1 (de) | 2005-07-29 | 2007-02-01 | Merck Patent Gmbh | Quadratsäurederivate II |
| AU2007269572A1 (en) | 2006-07-07 | 2008-01-10 | Pharmacopeia, Inc. | 3,4-di-substituted cyclobutene-1,2-diones as CXC-chemokine receptor ligands |
| EP2139852A1 (en) * | 2006-12-19 | 2010-01-06 | Pharmos Corporation | Sulfonamide derivatives with therapeutic indications |
| US8450348B2 (en) | 2007-02-21 | 2013-05-28 | Forma Tm, Llc | Derivatives of squaric acid with anti-proliferative activity |
| BRPI0812222A2 (pt) * | 2007-06-06 | 2014-12-16 | Novartis Ag | Compostos ciclobutenodiona substituídos anti-inflamatórios. |
| CN101932553A (zh) | 2007-07-03 | 2010-12-29 | 先灵公司 | 合成1,2-取代的3,4-二氧代-1-环丁烯化合物的方法和中间体 |
| CN101778836A (zh) | 2007-07-05 | 2010-07-14 | 先灵公司 | 在1,2-取代的3,4-二氧-1-环丁烯化合物中控制的晶体大小的方法 |
| WO2009012375A2 (en) | 2007-07-19 | 2009-01-22 | Wyeth | Squarate kinase inhibitors |
| US20110009482A1 (en) | 2007-12-04 | 2011-01-13 | Schering Corporation | Methods of treating copd |
| PT2444120T (pt) | 2007-12-10 | 2018-01-03 | Novartis Ag | Análogos da amilorida espirocíclicos como bloqueadores de enac |
| UA103198C2 (en) | 2008-08-04 | 2013-09-25 | Новартис Аг | Squaramide derivatives as cxcr2 antagonists |
| WO2010063802A1 (en) | 2008-12-05 | 2010-06-10 | Novartis Ag | 3, 4-di-substituted cyclobutene- 1, 2 -diones as cxcr2 receptor antagonists |
| WO2010091543A1 (en) | 2009-02-10 | 2010-08-19 | Merck Sharp & Dohme Corp. | Novel hydrazino-cyclobut-3-ene-1, 2-dione derivatives as cxcr2 antagonists |
| PL2760821T3 (pl) | 2011-09-02 | 2018-04-30 | Novartis Ag | Sól cholinowa przeciwzapalnego związku podstawionego cyklobutenodionem |
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