AR059898A1 - Derivados de 3-ciano-piridona 1,4-disustituida y su uso como moduladores alostericos de los receptores mglur2 - Google Patents
Derivados de 3-ciano-piridona 1,4-disustituida y su uso como moduladores alostericos de los receptores mglur2Info
- Publication number
- AR059898A1 AR059898A1 ARP070101038A ARP070101038A AR059898A1 AR 059898 A1 AR059898 A1 AR 059898A1 AR P070101038 A ARP070101038 A AR P070101038A AR P070101038 A ARP070101038 A AR P070101038A AR 059898 A1 AR059898 A1 AR 059898A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkyl
- group
- het3
- radical
- pyridinyl
- Prior art date
Links
- 102100036837 Metabotropic glutamate receptor 2 Human genes 0.000 title abstract 3
- 230000003281 allosteric effect Effects 0.000 title abstract 2
- 101150016175 Grm2 gene Proteins 0.000 title 1
- -1 cyano, hydroxy, amino Chemical group 0.000 abstract 21
- 125000004432 carbon atom Chemical group C* 0.000 abstract 8
- 125000005843 halogen group Chemical group 0.000 abstract 8
- 125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 abstract 6
- 125000000217 alkyl group Chemical group 0.000 abstract 6
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 abstract 6
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 6
- 125000004043 oxo group Chemical group O=* 0.000 abstract 6
- 125000006684 polyhaloalkyl group Polymers 0.000 abstract 6
- 229920006395 saturated elastomer Polymers 0.000 abstract 6
- 229910003827 NRaRb Inorganic materials 0.000 abstract 5
- 125000003545 alkoxy group Chemical group 0.000 abstract 5
- 125000004076 pyridyl group Chemical group 0.000 abstract 5
- 125000006273 (C1-C3) alkyl group Chemical group 0.000 abstract 4
- 239000004215 Carbon black (E152) Substances 0.000 abstract 4
- 125000004448 alkyl carbonyl group Chemical group 0.000 abstract 4
- 150000001875 compounds Chemical class 0.000 abstract 4
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 4
- 229930195733 hydrocarbon Natural products 0.000 abstract 4
- 229910052739 hydrogen Inorganic materials 0.000 abstract 4
- 239000001257 hydrogen Substances 0.000 abstract 4
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 4
- 125000003118 aryl group Chemical group 0.000 abstract 3
- 201000010099 disease Diseases 0.000 abstract 3
- 125000001041 indolyl group Chemical group 0.000 abstract 3
- 125000003386 piperidinyl group Chemical group 0.000 abstract 3
- 125000000719 pyrrolidinyl group Chemical group 0.000 abstract 3
- 125000001424 substituent group Chemical group 0.000 abstract 3
- 125000004605 1,2,3,4-tetrahydroisoquinolinyl group Chemical group C1(NCCC2=CC=CC=C12)* 0.000 abstract 2
- 125000004183 alkoxy alkyl group Chemical group 0.000 abstract 2
- 125000004390 alkyl sulfonyl group Chemical group 0.000 abstract 2
- 125000003710 aryl alkyl group Chemical group 0.000 abstract 2
- 125000002102 aryl alkyloxo group Chemical group 0.000 abstract 2
- 125000004104 aryloxy group Chemical group 0.000 abstract 2
- 229910052799 carbon Inorganic materials 0.000 abstract 2
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical compound C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 abstract 2
- 125000002541 furyl group Chemical group 0.000 abstract 2
- 125000003387 indolinyl group Chemical group N1(CCC2=CC=CC=C12)* 0.000 abstract 2
- 125000000842 isoxazolyl group Chemical group 0.000 abstract 2
- 108010038421 metabotropic glutamate receptor 2 Proteins 0.000 abstract 2
- 125000002757 morpholinyl group Chemical group 0.000 abstract 2
- 125000004193 piperazinyl group Chemical group 0.000 abstract 2
- 230000002265 prevention Effects 0.000 abstract 2
- 125000003226 pyrazolyl group Chemical group 0.000 abstract 2
- 125000001412 tetrahydropyranyl group Chemical group 0.000 abstract 2
- 125000000335 thiazolyl group Chemical group 0.000 abstract 2
- 125000001544 thienyl group Chemical group 0.000 abstract 2
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 1
- 125000006272 (C3-C7) cycloalkyl group Chemical group 0.000 abstract 1
- 125000004607 1,2,3,4-tetrahydroquinolinyl group Chemical group N1(CCCC2=CC=CC=C12)* 0.000 abstract 1
- 125000005955 1H-indazolyl group Chemical group 0.000 abstract 1
- QSVDFJNXDKTKTJ-UHFFFAOYSA-N 4,5,6,7-tetrahydro-1h-indene Chemical compound C1CCCC2=C1CC=C2 QSVDFJNXDKTKTJ-UHFFFAOYSA-N 0.000 abstract 1
- 208000019901 Anxiety disease Diseases 0.000 abstract 1
- WHUUTDBJXJRKMK-VKHMYHEASA-N L-glutamic acid Chemical compound OC(=O)[C@@H](N)CCC(O)=O WHUUTDBJXJRKMK-VKHMYHEASA-N 0.000 abstract 1
- 208000019695 Migraine disease Diseases 0.000 abstract 1
- 125000000815 N-oxide group Chemical group 0.000 abstract 1
- 208000012902 Nervous system disease Diseases 0.000 abstract 1
- 208000025966 Neurological disease Diseases 0.000 abstract 1
- 239000002253 acid Substances 0.000 abstract 1
- 125000003342 alkenyl group Chemical group 0.000 abstract 1
- 125000004453 alkoxycarbonyl group Chemical group 0.000 abstract 1
- 125000005196 alkyl carbonyloxy group Chemical group 0.000 abstract 1
- 125000004414 alkyl thio group Chemical group 0.000 abstract 1
- 230000036506 anxiety Effects 0.000 abstract 1
- 125000005018 aryl alkenyl group Chemical group 0.000 abstract 1
- 125000005129 aryl carbonyl group Chemical group 0.000 abstract 1
- 125000005160 aryl oxy alkyl group Chemical group 0.000 abstract 1
- 125000004391 aryl sulfonyl group Chemical group 0.000 abstract 1
- 125000005164 aryl thioalkyl group Chemical group 0.000 abstract 1
- 125000002393 azetidinyl group Chemical group 0.000 abstract 1
- 125000005605 benzo group Chemical group 0.000 abstract 1
- 125000000499 benzofuranyl group Chemical group O1C(=CC2=C1C=CC=C2)* 0.000 abstract 1
- 125000001164 benzothiazolyl group Chemical group S1C(=NC2=C1C=CC=C2)* 0.000 abstract 1
- 125000004196 benzothienyl group Chemical group S1C(=CC2=C1C=CC=C2)* 0.000 abstract 1
- 125000004541 benzoxazolyl group Chemical group O1C(=NC2=C1C=CC=C2)* 0.000 abstract 1
- 235000010290 biphenyl Nutrition 0.000 abstract 1
- 239000004305 biphenyl Substances 0.000 abstract 1
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 abstract 1
- 210000003169 central nervous system Anatomy 0.000 abstract 1
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 1
- 208000035475 disorder Diseases 0.000 abstract 1
- 230000004064 dysfunction Effects 0.000 abstract 1
- 206010015037 epilepsy Diseases 0.000 abstract 1
- 125000002485 formyl group Chemical group [H]C(*)=O 0.000 abstract 1
- 125000004613 furo[2,3-c]pyridinyl group Chemical group O1C(=CC=2C1=CN=CC2)* 0.000 abstract 1
- 229930195712 glutamate Natural products 0.000 abstract 1
- 125000004356 hydroxy functional group Chemical group O* 0.000 abstract 1
- 125000002883 imidazolyl group Chemical group 0.000 abstract 1
- 125000003392 indanyl group Chemical group C1(CCC2=CC=CC=C12)* 0.000 abstract 1
- 125000005956 isoquinolyl group Chemical group 0.000 abstract 1
- 125000001786 isothiazolyl group Chemical group 0.000 abstract 1
- 102000006239 metabotropic receptors Human genes 0.000 abstract 1
- 108020004083 metabotropic receptors Proteins 0.000 abstract 1
- 238000000034 method Methods 0.000 abstract 1
- 206010027599 migraine Diseases 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
- 125000001624 naphthyl group Chemical group 0.000 abstract 1
- 230000000926 neurological effect Effects 0.000 abstract 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 1
- 125000001715 oxadiazolyl group Chemical group 0.000 abstract 1
- 125000002971 oxazolyl group Chemical group 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
- 125000005542 phthalazyl group Chemical group 0.000 abstract 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 1
- 208000020016 psychiatric disease Diseases 0.000 abstract 1
- 125000003373 pyrazinyl group Chemical group 0.000 abstract 1
- 150000005299 pyridinones Chemical class 0.000 abstract 1
- 125000000714 pyrimidinyl group Chemical group 0.000 abstract 1
- 125000000168 pyrrolyl group Chemical group 0.000 abstract 1
- 150000003242 quaternary ammonium salts Chemical class 0.000 abstract 1
- 125000002294 quinazolinyl group Chemical group N1=C(N=CC2=CC=CC=C12)* 0.000 abstract 1
- 125000005493 quinolyl group Chemical group 0.000 abstract 1
- 125000001567 quinoxalinyl group Chemical group N1=C(C=NC2=CC=CC=C12)* 0.000 abstract 1
- 102000005962 receptors Human genes 0.000 abstract 1
- 108020003175 receptors Proteins 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 229930195734 saturated hydrocarbon Natural products 0.000 abstract 1
- 201000000980 schizophrenia Diseases 0.000 abstract 1
- 125000003831 tetrazolyl group Chemical group 0.000 abstract 1
- 125000001113 thiadiazolyl group Chemical group 0.000 abstract 1
- BUGOPWGPQGYYGR-UHFFFAOYSA-N thiane 1,1-dioxide Chemical compound O=S1(=O)CCCCC1 BUGOPWGPQGYYGR-UHFFFAOYSA-N 0.000 abstract 1
- 125000001425 triazolyl group Chemical group 0.000 abstract 1
Classifications
-
- 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
- C07D213/60—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 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
- C07D213/78—Carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen, e.g. ester or nitrile radicals
- C07D213/84—Nitriles
- C07D213/85—Nitriles in position 3
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- 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
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/4412—Non condensed pyridines; Hydrogenated derivatives thereof having oxo groups directly attached to the heterocyclic ring
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- 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
- C07D213/60—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 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
- C07D213/62—Oxygen or sulfur atoms
- C07D213/63—One oxygen atom
- C07D213/64—One oxygen atom attached in position 2 or 6
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- C—CHEMISTRY; METALLURGY
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- 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
- C07D213/60—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 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
- C07D213/78—Carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen, e.g. ester or nitrile radicals
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- 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
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- C07D401/10—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 aromatic 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
- C07D401/12—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
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- 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
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- 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
- C07D405/06—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 carbon chain containing only aliphatic carbon atoms
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Abstract
Derivados de piridinona donde todos los radicales se definen en la memoria descriptiva y en las reivindicaciones. Los compuestos son moduladores alostéricos positivos de los receptores metabotropicos-sub-tipo 2 (ômGIuR2ö) que son utiles para el tratamiento o la prevencion de trastornos neurologicos y psiquiátricos asociados con disfuncion de glutamato y enfermedades en las cuales el subtipo mGluR2 de los receptores metabotropicos está involucrado. En particular, dichas enfermedades son trastornos del sistema nervioso central del grupo de la ansiedad, esquizofrenia, migrana, depresion y epilepsia, se refiere, además, a composiciones farmacéuticas y procesos para preparar dichos compuestos y composiciones, como también al uso de dichos compuestos para la prevencion y el tratamiento de dichas enfermedades en las cuales mGluR2 está involucrado. Reivindicacion 1: Compuesto de acuerdo con la Formula general (1), una de sus sales de adicion con ácido o base aceptables desde el punto de vista farmacéutico, una de sus formas estereoquímicamente isoméricas, una de sus formas de N-oxido o una de sus sales de amonio cuaternario, donde V1 se selecciona del grupo de un enlace covalente y un radical hidrocarbonado bivalente recto o ramificado, saturado o insaturado que tiene desde 1 hasta 6 átomos de carbono; M1 se selecciona del grupo de hidrogeno; cicloalquilo C3-7; arilo; alquilcarbonilo; alquiloxi; ariloxi; arilalquiloxi; arilcarbonilo; hexahidrotiopiranilo; y Het1; L se selecciona del grupo de un enlace covalente; -O-; -OCH2-; -OCH2CH2-; -OCH2CH2O-; -OCH2CH2OCH2-; -S-; -NR7-; -NR7CH2-; -NR7cicloC3-7 -NR7CH2CH2-; -OCH2CH2N(R7)CH2-; -CH2-; -CH2CH2-; -CH2CH2CH2 -C:::C-; -C=O-; y -C(R8)=C(R9)-; donde cada uno de R7, en forma independiente entre sí, se selecciona del grupo de hidrogeno y alquilo C1-3 y donde R8 y R9, en forma independiente entre si, se seleccionan del grupo de hidrogeno, halo y alquilo C1-3; R2 y R3 son cada uno en forma independiente entre sí hidrogeno, halo o alquilo; A es Het2 o fenilo, donde cada radical está sustituido en forma opcional con n radicales R4, en los cuales n es un numero entero igual a cero, 1, 2 o 3; R4 se selecciona del grupo de halo; ciano; hidroxi: oxo; formilo, etanoílo; carboxilo; nitro; tio; alquilo; alquiloxi; alquiloxialquilo; alquiloxicarbonilo; alquiloxicarbonilalquilo; alquilcarbonilo; alquilcarboniloxi; alquilcarbonilalquiloxi; polihaloalquilo C1-3, polihaloalquiloxi C1-3, polihaloalquiltio C1-3, alquiltio; alquilsulfonilo; Het3, Het3-alquilo; Het3-oxi; Het3-oxialquilo; Het3-alquiloxi; Het3-oxialquiloxi; Het3-carbonilo; Het3-carbonilalquilo; Het3-tio; Het3-tioalquilo; Het3-sulfonilo; arilo; arilalquilo; ariloxi; ariloxialquilo; arilalquiloxi; arilalquenilo; arilcarbonilalquilo; ariltioalquilo; arilsulfonilo; -NRaRb; alquil-NRaRb; O-alquil-NRaRb, -C(=O)-NraRb, -C(=O)-alquil-NRaRb; y O-alquiI-C(=O)NRaRb; donde Ra y Rb se seleccionan del grupo de hidrogeno, alquilo, alquilcarbonilo, arilalquilo, alquiloxialquilo, Het3, Het3alquilo, alquilsulfonilo, alquil-NRcRd y C(=O)alquil-NRcRd, donde Rc y Rd se seleccionan del grupo de hidrogeno, alquilo y alquilcarbonilo; o dos radicales R4 pueden combinarse para formar un radical bivalente -X1-C1-6-X2- donde C1-6 es un radical hidrocarbonado saturado o insaturado, recto o ramificado que tiene 1 hasta 6 átomos de carbono y X1 y X2 son cada uno de manera independiente C, O o NH; donde el radical bivalente está sustituido en forma opcional con uno o más radicales seleccionados del grupo de halo, polihaloalquilo C1-3, ciano, hidroxi, amino, oxo, carboxilo, nitro, tio, formilo y etanoílo; Het1 se selecciona del grupo de tetrahidropiranilo; y piridinilo; donde cada radical está sustituido en forma opcional con 1, 2 o 3 sustituyentes, cada uno independientemente entre si, seleccionados del grupo de halo, alquilo C1-3, polihaloalquilo C1-3, polihaloalquiloxi C1-3, ciano, hidroxi, amino, oxo, carboxilo, nitro, tio, formilo, etanoílo y alquiloxi C1-3; Het2 se selecciona del grupo de piperazinilo; piperidinilo; tienilo; furanilo; 1H-indazolilo; 1H-bencimidazolilo; 1,2,3,4-tetrahidro-isoquinolinilo; 2,5-diaza-biciclo[2.2.1]heptilo; pirrolidinilo; azetidinilo; 2,7-diaza-espiro[3.5]nonilo; piridinilo; pirazolilo; indolinilo; 1 H-indolilo; 1 H-indazolilo; benzomorfolinilo; tiazolilo; 1,2,3,4-tetrahidroquinolinilo; 3,9-diazaespiro[5.5]undecilo; 1,2,3,4,4a,5,6,10b-octahidro- benzo[f]quinolinilo; 1,2,3,4,4a,10a-hexahidro-benzo[5,6][1,4]dioxino[2,3-c]-piridinilo; 2,3,4,9tetrahidro-1H-indeno[2,1-c]piridinilo; 2,3,4,9-tetrahidro-1H-beta-carboIinilo; 1,2,3,4-tetrahidro-benzo[4.5]furo-[2,3-c]piridinilo; 1,2,3,4- tetrahidrobenzo[4.5]tieno[2,3-c]piridinilo; [1,4]diazepilo; isoxazolilo; indanilo; e indolilo; Het3 se selecciona del grupo de piridinilo; pirimidinilo; piridazililo; pirazinilo; piperidinilo; pirrolilo; pirrolidinilo; piperazinilo; triazolilo; tetrazolilo; indolilo; tienilo; furanilo; tetrahidropiranilo; tetrahidro-tiopiran-1,1-dioxido; tiazolilo; tiadiazolilo; isotiazolilo; oxazolilo; morfolinilo; oxadiazolilo; isoxazolilo; imidazolilo; pirazolilo; benzoimidazolilo; benzoxazolilo; benzotienilo; benzotiazolilo; benzofuranilo; benzomorfolinilo; 1,2,3,4-tetrahidro-isoquinolinilo; tionaftilo; indolilo; indolinilo; quinolilo; isoquinolilo; quinoxalilo; ftalazilo; benzo[1,3]dioxilo; y quinazolilo; donde cada radical está sustituido en forma opcional con 1, 2 o 3 sustituyentes, cada uno independientemente entre sí, seleccionados del grupo de halo, alquilo C1-6, polihaloalquilo C1-3, ciano, hidroxi, amino, oxo, carboxilo, nitro, tio, formilo, etanoílo, fenilo, pirrolidinilo, piperidinilo, piridinilo, morfolinilo, mono- y di(alquil)amino, y alquiloxi C1-3; arilo es naftilo, fenilo, o bifenilo; donde cada radical está sustituido en forma opcional con 1, 2 o 3 sustituyentes, cada uno independientemente entre sí seleccionados del grupo de halo, alquilo C1-3, polihaloalquilo C1-3, polihaloalquiloxi C1-3, ciano, hidroxi, amino, oxo, carboxilo, nitro, tio, formilo, etanoílo, etiloxicarbonilo, y alquiloxi C1-3; alquilo es un radical hidrocarbonado saturado, recto o ramificado que tiene desde 1 hasta 6 átomos de carbono; o es un radical hidrocarbonado saturado, cíclico que tiene desde 3 hasta 7 átomos de carbono; o es un radical hidrocarbonado saturado desde 4 hasta 12 átomos de carbono, que comprende por lo menos un radical hidrocarbonado saturado, recto o ramificado que tiene desde 1 hasta 6 átomos de carbono y por lo menos un radical hidrocarbonado saturado, cíclico que tiene desde 3 hasta 7 átomos de carbono; donde cada átomo de carbono puede estar sustituido en forma opcional con uno o más radicales seleccionados del grupo de halo, polihaloalquilo C1-3, ciano, hidroxi, amino, oxo, carboxilo, nitro, tio, formilo, etanoílo, carbamoílo; fenilo; y un radical bivalente -OCH2CH2O-; y alquenilo es alquilo, que contiene, en forma adicional, uno o más dobles enlaces.
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- 2007-03-15 JP JP2008558820A patent/JP5393161B2/ja not_active Expired - Fee Related
- 2007-03-15 KR KR1020087022610A patent/KR101289156B1/ko not_active Expired - Fee Related
- 2007-03-15 CN CN201210472507.8A patent/CN103012259B/zh not_active Expired - Fee Related
- 2007-03-15 PL PL07726932T patent/PL1994004T3/pl unknown
- 2007-03-15 EP EP11181481.0A patent/EP2426125B1/en not_active Not-in-force
- 2007-03-15 AU AU2007224431A patent/AU2007224431B8/en not_active Ceased
- 2007-03-15 KR KR1020127018962A patent/KR20130006429A/ko not_active Withdrawn
- 2007-03-15 WO PCT/EP2007/052442 patent/WO2007104783A2/en not_active Ceased
- 2007-03-15 DK DK07726932.2T patent/DK1994004T3/da active
- 2007-03-15 CA CA2640534A patent/CA2640534C/en not_active Expired - Fee Related
- 2007-03-15 PT PT07726932T patent/PT1994004E/pt unknown
- 2007-03-15 MX MX2008011412A patent/MX2008011412A/es active IP Right Grant
- 2007-03-15 EP EP07726932.2A patent/EP1994004B9/en active Active
- 2007-03-15 ES ES11181481.0T patent/ES2558346T3/es active Active
- 2007-03-15 EA EA200801934A patent/EA017914B8/ru not_active IP Right Cessation
- 2007-03-15 NZ NZ570096A patent/NZ570096A/en not_active IP Right Cessation
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2008
- 2008-07-17 IL IL192868A patent/IL192868A0/en unknown
- 2008-08-13 NO NO20083500A patent/NO20083500L/no not_active Application Discontinuation
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2014
- 2014-07-02 US US14/322,177 patent/US9266834B2/en not_active Expired - Fee Related
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