AR075868A1 - 2-acetamido-5-aril-1,2,4-triazolonas sustituidas y su uso - Google Patents
2-acetamido-5-aril-1,2,4-triazolonas sustituidas y su usoInfo
- Publication number
- AR075868A1 AR075868A1 ARP100100847A ARP100100847A AR075868A1 AR 075868 A1 AR075868 A1 AR 075868A1 AR P100100847 A ARP100100847 A AR P100100847A AR P100100847 A ARP100100847 A AR P100100847A AR 075868 A1 AR075868 A1 AR 075868A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkyl
- represents hydrogen
- cycloalkyl
- substituted
- trifluoromethyl
- Prior art date
Links
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 40
- 229910052739 hydrogen Inorganic materials 0.000 abstract 24
- 239000001257 hydrogen Substances 0.000 abstract 24
- 125000000623 heterocyclic group Chemical group 0.000 abstract 22
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 22
- 125000006272 (C3-C7) cycloalkyl group Chemical group 0.000 abstract 19
- 125000001424 substituent group Chemical group 0.000 abstract 18
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 abstract 18
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 13
- 125000004043 oxo group Chemical group O=* 0.000 abstract 9
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 abstract 8
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical group FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 abstract 8
- 125000004433 nitrogen atom Chemical group N* 0.000 abstract 8
- 229910052731 fluorine Inorganic materials 0.000 abstract 7
- 239000011737 fluorine Substances 0.000 abstract 7
- 229910052757 nitrogen Inorganic materials 0.000 abstract 6
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 6
- 125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 abstract 5
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 4
- 125000001153 fluoro group Chemical group F* 0.000 abstract 4
- -1 C1-4alkoxycarbonyl Chemical group 0.000 abstract 3
- 125000004429 atom Chemical group 0.000 abstract 3
- 229910052736 halogen Inorganic materials 0.000 abstract 3
- 150000002367 halogens Chemical class 0.000 abstract 3
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 3
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 abstract 2
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 2
- RFEBDZANCVHDLP-UHFFFAOYSA-N 3-[(4-cyanophenyl)methylamino]-6-(trifluoromethyl)quinoxaline-2-carboxylic acid Chemical compound OC(=O)C1=NC2=CC=C(C(F)(F)F)C=C2N=C1NCC1=CC=C(C#N)C=C1 RFEBDZANCVHDLP-UHFFFAOYSA-N 0.000 abstract 2
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 abstract 2
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 abstract 2
- YZCKVEUIGOORGS-OUBTZVSYSA-N Deuterium Chemical compound [2H] YZCKVEUIGOORGS-OUBTZVSYSA-N 0.000 abstract 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 2
- LFMFPKKYRXFHHZ-UHFFFAOYSA-N R24 Chemical compound C1=C(Cl)C(C)=CC=C1NC1=NC(N)=C(C=CC=C2)C2=N1 LFMFPKKYRXFHHZ-UHFFFAOYSA-N 0.000 abstract 2
- NFGODEMQGQNUKK-UHFFFAOYSA-M [6-(diethylamino)-9-(2-octadecoxycarbonylphenyl)xanthen-3-ylidene]-diethylazanium;chloride Chemical group [Cl-].CCCCCCCCCCCCCCCCCCOC(=O)C1=CC=CC=C1C1=C2C=CC(=[N+](CC)CC)C=C2OC2=CC(N(CC)CC)=CC=C21 NFGODEMQGQNUKK-UHFFFAOYSA-M 0.000 abstract 2
- 125000000217 alkyl group Chemical group 0.000 abstract 2
- KCNKJCHARANTIP-SNAWJCMRSA-N allyl-{4-[3-(4-bromo-phenyl)-benzofuran-6-yloxy]-but-2-enyl}-methyl-amine Chemical group C=1OC2=CC(OC/C=C/CN(CC=C)C)=CC=C2C=1C1=CC=C(Br)C=C1 KCNKJCHARANTIP-SNAWJCMRSA-N 0.000 abstract 2
- 125000004196 benzothienyl group Chemical group S1C(=CC2=C1C=CC=C2)* 0.000 abstract 2
- SYGWYBOJXOGMRU-UHFFFAOYSA-N chembl233051 Chemical compound C1=CC=C2C3=CC(C(N(CCN(C)C)C4=O)=O)=C5C4=CC=CC5=C3SC2=C1 SYGWYBOJXOGMRU-UHFFFAOYSA-N 0.000 abstract 2
- 229910052805 deuterium Inorganic materials 0.000 abstract 2
- 230000006806 disease prevention Effects 0.000 abstract 2
- 125000002541 furyl group Chemical group 0.000 abstract 2
- ORTFAQDWJHRMNX-UHFFFAOYSA-N hydroxidooxidocarbon(.) Chemical group O[C]=O ORTFAQDWJHRMNX-UHFFFAOYSA-N 0.000 abstract 2
- 125000001624 naphthyl group Chemical group 0.000 abstract 2
- 150000003839 salts Chemical class 0.000 abstract 2
- 239000012453 solvate Substances 0.000 abstract 2
- 125000001544 thienyl group Chemical group 0.000 abstract 2
- 125000001313 C5-C10 heteroaryl group Chemical group 0.000 abstract 1
- 208000024172 Cardiovascular disease Diseases 0.000 abstract 1
- 125000004453 alkoxycarbonyl group Chemical group 0.000 abstract 1
- JYNZIOFUHBJABQ-UHFFFAOYSA-N allyl-{6-[3-(4-bromo-phenyl)-benzofuran-6-yloxy]-hexyl-}-methyl-amin Chemical compound C=1OC2=CC(OCCCCCCN(C)CC=C)=CC=C2C=1C1=CC=C(Br)C=C1 JYNZIOFUHBJABQ-UHFFFAOYSA-N 0.000 abstract 1
- 125000003277 amino group Chemical group 0.000 abstract 1
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 125000000000 cycloalkoxy group Chemical group 0.000 abstract 1
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 1
- 125000004786 difluoromethoxy group Chemical group [H]C(F)(F)O* 0.000 abstract 1
- 125000001028 difluoromethyl group Chemical group [H]C(F)(F)* 0.000 abstract 1
- 239000003814 drug Substances 0.000 abstract 1
- 125000005843 halogen group Chemical group 0.000 abstract 1
- 125000004029 hydroxymethyl group Chemical group [H]OC([H])([H])* 0.000 abstract 1
- 238000000034 method Methods 0.000 abstract 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 1
- 230000002265 prevention Effects 0.000 abstract 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
- C07D233/66—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D233/70—One oxygen atom
-
- A—HUMAN NECESSITIES
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- 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
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/4164—1,3-Diazoles
- A61K31/4166—1,3-Diazoles having oxo groups directly attached to the heterocyclic ring, e.g. phenytoin
-
- A—HUMAN NECESSITIES
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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
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/4196—1,2,4-Triazoles
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- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/42—Oxazoles
- A61K31/422—Oxazoles not condensed and containing further heterocyclic rings
-
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- A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
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- A61K9/0087—Galenical forms not covered by A61K9/02 - A61K9/7023
- A61K9/0095—Drinks; Beverages; Syrups; Compositions for reconstitution thereof, e.g. powders or tablets to be dispersed in a glass of water; Veterinary drenches
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- A61K9/2022—Organic macromolecular compounds
- A61K9/205—Polysaccharides, e.g. alginate, gums; Cyclodextrin
- A61K9/2054—Cellulose; Cellulose derivatives, e.g. hydroxypropyl methylcellulose
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/16—Drugs for disorders of the alimentary tract or the digestive system for liver or gallbladder disorders, e.g. hepatoprotective agents, cholagogues, litholytics
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- A61P7/00—Drugs for disorders of the blood or the extracellular fluid
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- C07C211/00—Compounds containing amino groups bound to a carbon skeleton
- C07C211/01—Compounds containing amino groups bound to a carbon skeleton having amino groups bound to acyclic carbon atoms
- C07C211/26—Compounds containing amino groups bound to a carbon skeleton having amino groups bound to acyclic carbon atoms of an unsaturated carbon skeleton containing at least one six-membered aromatic ring
- C07C211/29—Compounds containing amino groups bound to a carbon skeleton having amino groups bound to acyclic carbon atoms of an unsaturated carbon skeleton containing at least one six-membered aromatic ring the carbon skeleton being further substituted by halogen atoms or by nitro or nitroso groups
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- C07C215/00—Compounds containing amino and hydroxy groups bound to the same carbon skeleton
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- C07C215/22—Compounds containing amino and hydroxy groups bound to the same carbon skeleton having hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being unsaturated
- C07C215/28—Compounds containing amino and hydroxy groups bound to the same carbon skeleton having hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being unsaturated and containing six-membered aromatic rings
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- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C233/00—Carboxylic acid amides
- C07C233/01—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms
- C07C233/34—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by amino groups
- C07C233/35—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by amino groups with the substituted hydrocarbon radical bound to the nitrogen atom of the carboxamide group by an acyclic carbon atom
- C07C233/36—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by amino groups with the substituted hydrocarbon radical bound to the nitrogen atom of the carboxamide group by an acyclic carbon atom having the carbon atom of the carboxamide group bound to a hydrogen atom or to a carbon atom of an acyclic saturated carbon skeleton
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- C07C271/06—Esters of carbamic acids
- C07C271/08—Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms
- C07C271/10—Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms with the nitrogen atoms of the carbamate groups bound to hydrogen atoms or to acyclic carbon atoms
- C07C271/12—Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms with the nitrogen atoms of the carbamate groups bound to hydrogen atoms or to acyclic carbon atoms to hydrogen atoms or to carbon atoms of unsubstituted hydrocarbon radicals
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- C07C271/14—Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms with the nitrogen atoms of the carbamate groups bound to hydrogen atoms or to acyclic carbon atoms to carbon atoms of hydrocarbon radicals substituted by halogen atoms or by nitro or nitroso groups
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- C07C271/20—Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms with the nitrogen atoms of the carbamate groups bound to hydrogen atoms or to acyclic carbon atoms to carbon atoms of hydrocarbon radicals substituted by nitrogen atoms not being part of nitro or nitroso groups
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- C07C311/01—Sulfonamides having sulfur atoms of sulfonamide groups bound to acyclic carbon atoms
- C07C311/02—Sulfonamides having sulfur atoms of sulfonamide groups bound to acyclic carbon atoms of an acyclic saturated carbon skeleton
- C07C311/03—Sulfonamides having sulfur atoms of sulfonamide groups bound to acyclic carbon atoms of an acyclic saturated carbon skeleton having the nitrogen atoms of the sulfonamide groups bound to hydrogen atoms or to acyclic carbon atoms
- C07C311/05—Sulfonamides having sulfur atoms of sulfonamide groups bound to acyclic carbon atoms of an acyclic saturated carbon skeleton having the nitrogen atoms of the sulfonamide groups bound to hydrogen atoms or to acyclic carbon atoms to acyclic carbon atoms of hydrocarbon radicals substituted by nitrogen atoms, not being part of nitro or nitroso groups
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- C07C317/28—Sulfones; Sulfoxides having sulfone or sulfoxide groups and nitrogen atoms, not being part of nitro or nitroso groups, bound to the same carbon skeleton with sulfone or sulfoxide groups bound to acyclic carbon atoms of the carbon skeleton
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- C07D233/04—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
- C07D233/28—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member 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
- C07D233/30—Oxygen or sulfur atoms
- C07D233/32—One oxygen atom
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- C07D249/00—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
- C07D249/02—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms not condensed with other rings
- C07D249/08—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
- C07D249/10—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles 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
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- C07D263/02—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings
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- C07D263/18—Oxygen atoms
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- 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
La presente se refiere a procedimientos para su preparacion, a su uso solas o en combinaciones para el tratamiento y/o la prevencion de enfermedades, así como a su uso para la preparacion de medicamentos para el tratamiento y/o la prevencion de enfermedades, en particular para el tratamiento y/o la prevencion de enfermedades cardiovasculares. Reivindicacion 1: Compuesto de la formula (1) en la que A representa -C(R6AR6B)-* o -C(R6AR6B)-C(R7AR7B)-*, donde * representa el sitio de union a R3, R6A representa hidrogeno, alquilo C1-4 o trifluorometilo; R6B representa hidrogeno o alquilo C1-4; R7A representa hidrogeno, alquilo C1-4 o trifluorometilo; R7B representa hidrogeno o alquilo C1-4; Q representa CH o N; R1 representa alquilo C1-6, alquenilo C2-6, alquinilo C2-6 o cicloalquilo C3-7, pudiendo estar sustituidos el alquilo C1-6, el alquenilo C2-6 y el alquinilo C2-6 con 1 a .3 sustituyentes seleccionados independientemente unos de otros del grupo deuterio, halogeno, ciano, oxo, hidroxilo, trifluorometilo, cicloalquilo C3-7, alcoxi C1-6, trifluorometoxi y fenilo, pudiendo estar sustituido el cicloalquilo C3-7 con 1 o 2 sustituyentes seleccionados independientemente uno de otro del grupo alquilo C1-4, oxo, hidroxilo, alcoxi C1-4 y amino, y pudiendo estar sustituido el alcoxi C1-6 con 1 o 2 sustituyentes seleccionados independientemente uno de otro del grupo amino, hidroxilo, alcoxi C1-4, hidroxicarbonilo y alcoxicarbonilo C1-4 y pudiendo estar sustituido el fenilo con 1 a 3 sustituyentes seleccionados independientemente unos de otros del grupo halogeno, ciano, nitro, alquilo C1-4, trifluorometilo, hidroxilo, hidroximetilo, alcoxi C1-4, trifluorometoxi, alcoxi C1-4-metilo, hidroxicarbonilo, alcoxi C1-4-carbonilo, aminocarbonilo, monoalquil C1-4-aminocarbonilo y dialquil C1-4-aminocarbonilo, y pudiendo estar sustituido el cicloalquilo C3-7 con 1 o 2 sustituyentes seleccionados independientemente uno de otro del grupo fluor, alquilo C1-4, alcoxi C1-4, hidroxilo, amino y oxo, R2 representa benzotienilo, fenilo, tienilo o furilo, pudiendo estar sustituidos el benzotienilo, el fenilo, el tienilo y el furilo con 1 a 3 sustituyentes seleccionados independientemente unos de otros del grupo halogeno, ciano, nitro, alquilo C1-4, trifluorometilo, hidroxi, alcoxi C1-4 y trifluorometoxi, R3 representa trifluorometilo, hidroxilo, trifluorometoxi, alcoxi C1-4, cicloalcoxi C3-7, nitro, amino, NR8-C(=O)-R9, -NR10-SO2-R11, -SO2-NR12R13, -O-C(=O)-NR14R15, -NR16-C(=O)NR17R18, -NR19-C(=O)-OR20; -S(=O)R21, -O-SO2-NR24R25, -NR26-SO2-NR27R28 o -NR30R31 donde R8 representa hidrogeno o alquilo C1-4, R9 representa hidrogeno, alquilo C1-4 o cicloalquilo C3-7 o R8 y R9 conjuntamente con los átomos a los que están unidos, forman un heterociclo de 5 a 7 miembros pudiendo estar sustituido el heterociclo de 5 a 7 miembros con 1 o 2 sustituyentes seleccionados independientemente uno de otro del grupo fluor, alquilo C1-4 y trifluorometilo, R10 representa hidrogeno o alquilo C1-4, R11 representa alquilo C1-4 o cicloalquilo C3-7; o R10 y R11 conjuntamente con los átomos a los que están unidos, forman un heterociclo de 5 a 7 miembros, pudiendo estar sustituido el heterociclo de 5 a 7 miembros con 1 o 2 sustituyentes seleccionados independientemente uno de otro del grupo fluor, alquilo C1-4 y trifluorometilo, R12 representa hidrogeno, alquilo C1-4 o cicloalquilo C3-7; R13 representa hidrogeno, alquilo C1-4 o cicloalquilo C3-7; o R12 y R13 conjuntamente con el átomo de nitrogeno al que están unidos, forman un heterociclo de 4 a 7 miembros, pudiendo estar sustituido el heterociclo de 4 a 7 miembros con 1 o 2 sustituyentes seleccionados independientemente uno de otro del grupo fluor, oxo, hidroxilo, alquilo C1-4 y trifluorometilo, R14 representa hidrogeno, alquilo C1-4 o cicloalquilo C3-7, R15 representa hidrogeno, alquilo C1-4 o cicloalquilo C3-7, o R14 y R15 conjuntamente con el átomo de nitrogeno al que están unidos, forman un heterociclo de 4 a 7 miembros pudiendo estar sustituido el heterociclo de 4 a 7 miembros con 1 o 2 sustituyentes seleccionados independientemente uno de otro del grupo fluor, oxo, hidroxilo, alquilo C1-4 y trifluorometilo, R16 representa hidrogeno o alquilo C1-4, R17 representa hidrogeno, alquilo C1-4 o cicloalquilo C3-7, R18 representa hidrogeno, alquilo C1-4 o cicloalquilo C3-7, o R16 y R17 conjuntamente con los átomos de nitrogeno a los que están unidos, forman un heterociclo de 5 a 7 miembros, pudiendo estar sustituido el heterociclo de 5 a 7 miembros con 1 o 2 sustituyentes seleccionados independientemente uno de otro del grupo fluor, trifluorometilo y alquilo C1-4, o R17 y R18 conjuntamente con el átomo de nitrogeno al que están unidos, forman un heterociclo de 4 a 7 miembros,. pudiendo estar sustituido el heterociclo de 4 a 7 miembros con 1 o 2 sustituyentes seleccionados independientemente uno de otro del grupo fluor, oxo, hidroxilo, alquilo C1-4 y trifluorometilo, R19 representa hidrogeno o alquilo C1-4, R20 representa alquilo C1-4 o cicloalquilo C3-7, R19 y R20 conjuntamente con los átomos a los que están unidos, forman un heterociclo de 5 a 7 miembros pudiendo estar sustituido el heterociclo de 5 a 7 miembros con 1 o 2 sustituyentes seleccionados independientemente uno de otro del grupo fluor, alquilo C1-4 y trifluorometilo, n representa el numero 0, 1 o 2, R21 representa hidrogeno, alquilo C1-4 o cicloalquilo C3-7, R24 representa hidrogeno, alquilo C1-4 o cicloalquilo C3-7, R25 representa hidrogeno, alquilo C1-4 o cicloalquilo C3-7, o R24 y R25 conjuntamente con el átomo de nitrogeno al que están unidos, forman un heterociclo de 4 a 7 miembros, pudiendo estar sustituido el heterociclo de 4 a 7 miembros con 1 o 2 sustituyentes seleccionados independientemente uno de otro del grupo fluor, oxo, hidroxilo, alquilo C1-4 y trifluorometilo, R26 representa hidrogeno o alquilo C1-4; R27 representa hidrogeno, alquilo C1-4 o cicloalquilo C3-7, R28 representa hidrogeno, alquilo C1-4 o cicloalquilo C3-7, o R26 y R27 conjuntamente con los átomos de nitrogeno a los que están unidos, forman un heterociclo de 5 a 7 miembros, pudiendo estar sustituido el heterociclo de 5 a 7 miembros con 1 o 2 sustituyentes seleccionados independientemente uno de otro del grupo fluor, trifluorometilo y alquilo C1-4, o R27 y R28 conjuntamente con el átomo de nitrogeno al que están unidos, forman un heterociclo de 4 a 7 miembros, pudiendo estar sustituido el heterociclo de 4 a 7 miembros con 1 o 2 sustituyentes seleccionados independientemente uno de otro del grupo fluor, oxo, hidroxilo y alquilo C1-4, R30 representa hidrogeno, alquilo C1-4 o cicloalquilo C3-7, R31 representa alquilo C1-4 o cicloalquilo C3-7, o R30 y R31 conjuntamente con el átomo de nitrogeno al que están unidos, forman un heterociclo de 4 a 7 miembros, pudiendo estar sustituido el heterociclo de 4 a 7 miembros con 1 o 2 sustituyentes seleccionados independientemente uno de otro del grupo fluor, oxo, hidroxilo, alquilo C1-4 y trifluorometilo, R4 representa fenilo, naftilo o un heteroarilo de 5 a 10 miembros, pudiendo estar sustituidos el fenilo, el naftilo y el heteroarilo de 5 a 10 miembros con 1 a 3 sustituyentes seleccionados independientemente unos de otros del grupo halogeno, ciano, nitro, alquilo C1-4, difluorometilo, trifluorometilo, hidroxilo, alcoxi C1-4, difluorometoxi y trifluorometoxi, R5 representa hidrogeno, deuterio, trifluorometilo o alquilo C1-4, R29 representa hidrogeno o alquilo C1-4, y sus sales, solvatos y solvatos de las sales.
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| DE102010001064A DE102010001064A1 (de) | 2009-03-18 | 2010-01-20 | Substituierte 2-Acetamido-5-Aryl-1,2,4-triazolone und deren Verwendung |
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