AR070569A2 - Compuestos de arilvinilazacicloalcano, composiciones farmaceuticas que los comprenden, un proceso para prepararlos y su uso en la fabricacion de medicamentos para el tratamiento de trastornos neurodegenerativos. - Google Patents
Compuestos de arilvinilazacicloalcano, composiciones farmaceuticas que los comprenden, un proceso para prepararlos y su uso en la fabricacion de medicamentos para el tratamiento de trastornos neurodegenerativos.Info
- Publication number
- AR070569A2 AR070569A2 ARP090100388A ARP090100388A AR070569A2 AR 070569 A2 AR070569 A2 AR 070569A2 AR P090100388 A ARP090100388 A AR P090100388A AR P090100388 A ARP090100388 A AR P090100388A AR 070569 A2 AR070569 A2 AR 070569A2
- Authority
- AR
- Argentina
- Prior art keywords
- alkyl
- heteroaryl
- aryl
- nr8r9
- heterocyclyl
- Prior art date
Links
- 150000001875 compounds Chemical class 0.000 title abstract 6
- 239000003814 drug Substances 0.000 title abstract 2
- 238000004519 manufacturing process Methods 0.000 title abstract 2
- 208000015122 neurodegenerative disease Diseases 0.000 title abstract 2
- 239000008194 pharmaceutical composition Substances 0.000 title abstract 2
- 238000000034 method Methods 0.000 title 1
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 26
- 125000003118 aryl group Chemical group 0.000 abstract 12
- 229910052739 hydrogen Inorganic materials 0.000 abstract 12
- 239000001257 hydrogen Substances 0.000 abstract 12
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 8
- 125000001072 heteroaryl group Chemical group 0.000 abstract 8
- 125000000623 heterocyclic group Chemical group 0.000 abstract 8
- 150000002431 hydrogen Chemical group 0.000 abstract 8
- 229910052736 halogen Inorganic materials 0.000 abstract 5
- 150000002367 halogens Chemical group 0.000 abstract 5
- -1 vinyl cycloalkane compound Chemical class 0.000 abstract 5
- 229910052794 bromium Inorganic materials 0.000 abstract 4
- 229910052801 chlorine Inorganic materials 0.000 abstract 4
- 229910052731 fluorine Inorganic materials 0.000 abstract 4
- 229910052740 iodine Inorganic materials 0.000 abstract 4
- 125000005592 polycycloalkyl group Polymers 0.000 abstract 4
- 125000001424 substituent group Chemical group 0.000 abstract 4
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 3
- 208000035475 disorder Diseases 0.000 abstract 3
- 150000003839 salts Chemical class 0.000 abstract 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 2
- 101100477978 Hypocrea jecorina (strain QM6a) sor6 gene Proteins 0.000 abstract 2
- 102000019315 Nicotinic acetylcholine receptors Human genes 0.000 abstract 2
- 108050006807 Nicotinic acetylcholine receptors Proteins 0.000 abstract 2
- 125000004429 atom Chemical group 0.000 abstract 2
- 210000005095 gastrointestinal system Anatomy 0.000 abstract 2
- 125000004415 heterocyclylalkyl group Chemical group 0.000 abstract 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 2
- 239000000203 mixture Substances 0.000 abstract 2
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 2
- RIOQSEWOXXDEQQ-UHFFFAOYSA-N triphenylphosphine Chemical compound C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 RIOQSEWOXXDEQQ-UHFFFAOYSA-N 0.000 abstract 2
- 229920002554 vinyl polymer Polymers 0.000 abstract 2
- RHXWCCJQAYTDFH-UHFFFAOYSA-N 3-[2-(1-methylpyrrolidin-3-yl)ethenyl]-5-propan-2-yloxypyridine Chemical compound CC(C)OC1=CN=CC(C=CC2CN(C)CC2)=C1 RHXWCCJQAYTDFH-UHFFFAOYSA-N 0.000 abstract 1
- QZNRBEKGFAQMIJ-UHFFFAOYSA-N 3-propan-2-yloxy-5-(2-pyrrolidin-3-ylethenyl)pyridine Chemical compound CC(C)OC1=CN=CC(C=CC2CNCC2)=C1 QZNRBEKGFAQMIJ-UHFFFAOYSA-N 0.000 abstract 1
- 208000024827 Alzheimer disease Diseases 0.000 abstract 1
- AIZGOZXVRHEYPQ-UHFFFAOYSA-N CCOc1cncc(C=CC2CCN(C)C2)c1 Chemical compound CCOc1cncc(C=CC2CCN(C)C2)c1 AIZGOZXVRHEYPQ-UHFFFAOYSA-N 0.000 abstract 1
- OOYOEYPWZJQDAF-UHFFFAOYSA-N CN1CCC(C1)C=Cc1cccnc1 Chemical compound CN1CCC(C1)C=Cc1cccnc1 OOYOEYPWZJQDAF-UHFFFAOYSA-N 0.000 abstract 1
- IFUGTMPFBCYPSJ-UHFFFAOYSA-N CN1CCC(C1)C=Cc1cncc(Oc2ccccc2)c1 Chemical compound CN1CCC(C1)C=Cc1cncc(Oc2ccccc2)c1 IFUGTMPFBCYPSJ-UHFFFAOYSA-N 0.000 abstract 1
- 208000019430 Motor disease Diseases 0.000 abstract 1
- 101100030361 Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) pph-3 gene Proteins 0.000 abstract 1
- 208000018737 Parkinson disease Diseases 0.000 abstract 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 abstract 1
- 230000001154 acute effect Effects 0.000 abstract 1
- 229940035676 analgesics Drugs 0.000 abstract 1
- 239000000730 antalgic agent Substances 0.000 abstract 1
- 230000003542 behavioural effect Effects 0.000 abstract 1
- 210000003169 central nervous system Anatomy 0.000 abstract 1
- 208000015114 central nervous system disease Diseases 0.000 abstract 1
- 230000001684 chronic effect Effects 0.000 abstract 1
- 208000010877 cognitive disease Diseases 0.000 abstract 1
- 206010013663 drug dependence Diseases 0.000 abstract 1
- 230000004064 dysfunction Effects 0.000 abstract 1
- 125000002485 formyl group Chemical class [H]C(*)=O 0.000 abstract 1
- 208000027866 inflammatory disease Diseases 0.000 abstract 1
- 239000003446 ligand Substances 0.000 abstract 1
- 229910052698 phosphorus Inorganic materials 0.000 abstract 1
- 239000011574 phosphorus Substances 0.000 abstract 1
- 125000006239 protecting group Chemical group 0.000 abstract 1
- 230000000306 recurrent effect Effects 0.000 abstract 1
- 208000011117 substance-related disease Diseases 0.000 abstract 1
Classifications
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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
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/506—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
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- 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
- C07D401/06—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 carbon chain containing only aliphatic carbon atoms
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Abstract
Se revelan compuestos vinilazacicloalcano los cuales son ligandos de diversos nAChRs. Los compuestos y sus sales farmacéuticamente aceptables pueden utilizarse para preparar composiciones farmacéuticas y/o medicamentos para prevenir o tratar trastornos asociados con la disfuncion de nAChRs, especialmente dentro del sistema nervioso central o el sistema gastrointestinal. Ejemplos de tipos de trastornos que pueden tratarse incluyen trastornos neurodegenerativos, que incluyen trastornos del sistema nervioso central tales como enfermedad de Alzheimer, trastornos cognitivos, trastornos motores tales como enfermedad de Parkinson, adiccion las drogas, trastornos de conducta y trastornos inflamatorios dentro del sistema gastrointestinal. Los compuestos también pueden servir como analgésicos en el tratamiento del dolor agudo, cronico o recurrente. Reivindicacion 1: Un compuesto vinilazacicloalcano caracterizado por la formula (1) en donde la línea ondulante representa la geometría variable (E o Z) alrededor del enlace doble; X es CR2; R1 es hidrogeno, alquilo C1-6, halogeno, -OR4, -OR4R5, o -SR4; R2 es hidrogeno, alquilo C1-6, arilo, aril-alquilo C1-6, heteroarilo, heteroaril-alquilo C1-6, heterociclilo, heterociclil-alquilo C1-6, cicloalquilo, policicloalquilo, -OR6, -NR6R7, -SR6, -SOR6 o -SO2R6; en donde los grupos alquilo C1-6, cicloalquilo, heterociclilo, heteroarilo o arilo se pueden sustituir con uno o más sustituyentes seleccionados del grupo formado por F, Cl, Br, I, -R8, -OR8, -NR8R9, -CF3, -OCF3, -CN, -NO2, -SR8, -S(O)R8, -SO2R8, -O-SO2R8, -C(=O)NR6R9, -NR8C(=O)R9, -C(=O)OR8, -OC(=O) R8, -NHSO2R8, -SO2NR8R9, -C(S)NR8R9, y -NHC(S)R8; R3 es hidrogeno o metilo; R4 y R5 son, independientemente, hidrogeno o alquilo C1-6; R6 y R7 son, independientemente, hidrogeno, alquilo C1-6, arilo, aril-alquilo C1-6, heteroarilo, heteroaril-alquilo C1-6, heterociclilo, heterociclilalquilo, cicloalquilo o policicloalquilo, en donde los grupos alquilo C1-6, cicloalquilo, heterociclilo, heteroarilo y arilo se pueden sustituir con uno o más sustituyentes seleccionados del grupo formado por F, Cl, Br, I, -R8, -NR8R9, -CF3, -CN, -NO2, -C2R8, -N3, -SO2CH3, -OR8, -SR8, -C(=O)NR8R9, -NR8C(=O)R8, -C(=O)R8, -C(=O)OR8, -(CH2)qOR8, -OC(=O) R8, -OC(=O)NR8R9, y -NR8C(=O)OR8; R8 y R9 son, independientemente, hidrogeno, alquilo C1-6, o una especie que contiene un grupo aromático; en donde la especie que contiene un grupo aromático se puede sustituir con uno o más de alquilo C1-6, halogeno o amino; o R6 y R7 juntos o R8 y R9 juntos con los átomos a los cuales están unidos forman un anillo de 3 a 10 miembros; m es 1, 2, 3 o 4; y n es 1, 2 o 3; o un isomero, mezcla, enantiomero, diastereomero, tautomero o una sal farmacéuticamente aceptable de ellos; siempre que, sin embargo, el compuesto no sea: 3-(2-(1-metilpirrolidin-3-il)vinil)piridina; 3-isopropoxi-5-(2-(1-metilpirrolidin-3-il)vinil)piridina; 3-isopropoxi-5-(2-(pirrolidin-3-il)vinil)piridina; 5-(2-(1-metilpirrolidin-3-il)vinil)-3-fenoxipiridina; o 3-etoxi-5-(2-(1-metilpirrolidin-3-il)vinil)piridina. Reivindicacion 30: Un proceso para preparar compuestos arilvinilazacicloalcano de acuerdo con las reivindicaciones 1 a 12, de la formula (1) en donde: la línea ondulante representa la geometría variable (E o Z) alrededor del enlace doble; X es CR2; R1 es hidrogeno, alquilo C1-6, halogeno, -OR4, -OR4R5, o -SR4; R2 es hidrogeno, alquilo C1-6, arilo, aril-alquilo C1-6, heteroarilo, heteroaril-alquilo C1-6, heterociclilo, heterociclil-alquilo C1-6, cicloalquilo, policicloalquilo, -OR6, -NR6R7, -SR6, -SOR6 o -SO2R6; en donde los grupos alquilo C1-6, cicloalquilo, heterociclilo, heteroarilo o arilo se pueden sustituir con uno o más sustituyentes seleccionados del grupo formado por F, Cl, Br, I, -R8, -OR8, -NR8R9, -CF3, -OCF3, -CN, -NO2, -SR8, -S(O)R8, -SO2R8, -O-SO2R8, -C(=O)NR6R9, -NR8C(=O)R9, -C(=O)OR8, -OC(=O) R8, -NHSO2R8, -SO2NR8R9, -C(S)NR8R9, y -NHC(S)R8; R3 es hidrogeno o metilo; R4 y R5 son, independientemente, hidrogeno o alquilo C1-6; R6 y R7 son, independientemente, hidrogeno, alquilo C1-6, arilo, aril-alquilo C1-6, heteroarilo, heteroaril-alquilo C1-6, heterociclilo, heterociclilalquilo, cicloalquilo o policicloalquilo, en donde los grupos alquilo C1-6, cicloalquilo, heterociclilo, heteroarilo y arilo se pueden sustituir con uno o más sustituyentes seleccionados del grupo formado por F, Cl, Br, I, -R8, -NR8R9, -CF3, -CN, -NO2, -C2R8, -N3, -SO2CH3, -OR8, -SR8, -C(=O)NR8R9, -NR8C(=O)R8, -C(=O)R8, -C(=O)OR8, -(CH2)qOR8, -OC(=O) R8, -OC(=O)NR8R9, y -NR8C(=O)OR8; R8 y R9 son, independientemente, hidrogeno, alquilo C1-6, o una especie que contiene un grupo aromático; en donde la especie que contiene un grupo aromático se puede sustituir con uno o más de alquilo C1-6, halogeno o amino; o R6 y R7 juntos o R8 y R9 juntos con los átomos a los cuales están unidos forman un anillo de 3 a 10 miembros; m es 1, 2, 3 o 4; y n es 1, 2 o 3; o un isomero, mezcla, enantiomero, diastereomero, tautomero o una sal farmacéuticamente aceptable de ellos, caracterizado porque comprende: a) hacer reaccionar un aldehído de la formula (2) en donde m es 1, 2, o 3 y n es 1, 2 o 3, con una fosforano ilida de la formula PPh3=CH2 para dar un vinilazacicloalcano de la formula (3); b) hacer reaccionar el vinilazacicloalcano con un haluro de heteroarilo de la formula (4) en donde X y R1 son lo definido anteriormente e Y es halogeno; y c) remover todos los grupos protectores remanentes.
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| US10/379,868 US7098331B2 (en) | 2003-03-05 | 2003-03-05 | Arylvinylazacycloalkane compounds and methods of preparation and use thereof |
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| ARP090100389A AR070570A2 (es) | 2003-03-05 | 2009-02-05 | Compuesto de arilvinilazacicloalcano, una composicion farmaceutica que lo comprende y su uso en el tratamiento de enfermedades mediadas por alfa4beta2 nachr. |
| ARP090100388A AR070569A2 (es) | 2003-03-05 | 2009-02-05 | Compuestos de arilvinilazacicloalcano, composiciones farmaceuticas que los comprenden, un proceso para prepararlos y su uso en la fabricacion de medicamentos para el tratamiento de trastornos neurodegenerativos. |
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| ARP090100389A AR070570A2 (es) | 2003-03-05 | 2009-02-05 | Compuesto de arilvinilazacicloalcano, una composicion farmaceutica que lo comprende y su uso en el tratamiento de enfermedades mediadas por alfa4beta2 nachr. |
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