AR075255A1 - Derivados diazolicos y/o triazolicos agonistas de receptores tgr5 acoplado a proteina g, composiciones farmaceuticas que los contienen y uso de los mismos en el tratamiento de la obesidad, diabetes y otros trastornos metabolicos. - Google Patents
Derivados diazolicos y/o triazolicos agonistas de receptores tgr5 acoplado a proteina g, composiciones farmaceuticas que los contienen y uso de los mismos en el tratamiento de la obesidad, diabetes y otros trastornos metabolicos.Info
- Publication number
- AR075255A1 AR075255A1 ARP100100417A ARP100100417A AR075255A1 AR 075255 A1 AR075255 A1 AR 075255A1 AR P100100417 A ARP100100417 A AR P100100417A AR P100100417 A ARP100100417 A AR P100100417A AR 075255 A1 AR075255 A1 AR 075255A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkyl
- optionally substituted
- heterocycloalkyl
- groups
- halo
- Prior art date
Links
- 102100025353 G-protein coupled bile acid receptor 1 Human genes 0.000 title 1
- 101000857733 Homo sapiens G-protein coupled bile acid receptor 1 Proteins 0.000 title 1
- 208000008589 Obesity Diseases 0.000 title 1
- 206010012601 diabetes mellitus Diseases 0.000 title 1
- 208000030159 metabolic disease Diseases 0.000 title 1
- 235000020824 obesity Nutrition 0.000 title 1
- 239000008194 pharmaceutical composition Substances 0.000 title 1
- 102000004169 proteins and genes Human genes 0.000 title 1
- 108090000623 proteins and genes Proteins 0.000 title 1
- 125000000217 alkyl group Chemical group 0.000 abstract 22
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 abstract 20
- 125000001475 halogen functional group Chemical group 0.000 abstract 18
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 17
- 229910052739 hydrogen Inorganic materials 0.000 abstract 15
- 239000001257 hydrogen Substances 0.000 abstract 15
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 13
- 229910052799 carbon Inorganic materials 0.000 abstract 13
- 229910052757 nitrogen Inorganic materials 0.000 abstract 13
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 abstract 12
- -1 heterocycloalkyl carbon Chemical group 0.000 abstract 10
- 125000001072 heteroaryl group Chemical group 0.000 abstract 9
- 238000006467 substitution reaction Methods 0.000 abstract 8
- 125000000592 heterocycloalkyl group Chemical group 0.000 abstract 7
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 5
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 4
- 125000001424 substituent group Chemical group 0.000 abstract 4
- 125000006273 (C1-C3) alkyl group Chemical group 0.000 abstract 3
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 3
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 abstract 3
- 125000003118 aryl group Chemical group 0.000 abstract 2
- 125000004122 cyclic group Chemical group 0.000 abstract 2
- 125000004366 heterocycloalkenyl group Chemical group 0.000 abstract 2
- 150000002431 hydrogen Chemical class 0.000 abstract 2
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 abstract 2
- 125000004765 (C1-C4) haloalkyl group Chemical group 0.000 abstract 1
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 1
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 abstract 1
- KTZQTRPPVKQPFO-UHFFFAOYSA-N 1,2-benzoxazole Chemical compound C1=CC=C2C=NOC2=C1 KTZQTRPPVKQPFO-UHFFFAOYSA-N 0.000 abstract 1
- 125000002853 C1-C4 hydroxyalkyl group Chemical group 0.000 abstract 1
- 125000003545 alkoxy group Chemical group 0.000 abstract 1
- 125000005037 alkyl phenyl group Chemical group 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 1
- 229910052736 halogen Inorganic materials 0.000 abstract 1
- 150000002367 halogens Chemical class 0.000 abstract 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 1
- HFZNPKDYLSOGBE-SCEMAYBHSA-N nrc-12 Chemical compound C([C@@H](C(=O)N[C@@H](CC(C)C)C(C)=O)NC(=O)[C@H](CC=1NC=NC=1)NC(=O)[C@H](CC(O)=O)NC(=O)[C@@H](NC(=O)[C@H](C)NC(=O)[C@H](CC(C)C)NC(=O)CNC(=O)CNC(=O)[C@@H](NC(=O)[C@@H](NC(=O)[C@H](CCCCN)NC(=O)CNC(=O)[C@@H](NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCCCN)NC(=O)[C@H](C)NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](CC=1C=CC=CC=1)NC(=O)[C@H](CC=1C2=CC=CC=C2NC=1)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CC=1C2=CC=CC=C2NC=1)NC(=O)CN)C(C)C)[C@@H](C)O)C(C)C)C(C)C)C1=CC=C(O)C=C1 HFZNPKDYLSOGBE-SCEMAYBHSA-N 0.000 abstract 1
- 229920000642 polymer Polymers 0.000 abstract 1
- 125000002943 quinolinyl group Chemical group N1=C(C=CC2=CC=CC=C12)* 0.000 abstract 1
- 125000001567 quinoxalinyl group Chemical group N1=C(C=NC2=CC=CC=C12)* 0.000 abstract 1
- 150000003839 salts Chemical class 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
- C07D233/84—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
- A61K31/33—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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- 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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- 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
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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
- A61P3/04—Anorexiants; Antiobesity agents
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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
- A61P3/06—Antihyperlipidemics
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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
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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
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P5/00—Drugs for disorders of the endocrine system
- A61P5/48—Drugs for disorders of the endocrine system of the pancreatic hormones
- A61P5/50—Drugs for disorders of the endocrine system of the pancreatic hormones for increasing or potentiating the activity of insulin
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
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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
- C07D233/64—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 substituted hydrocarbon radicals attached to ring carbon atoms, e.g. histidine
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- 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
- C07D233/90—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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- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- 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
- C07D249/12—Oxygen or sulfur atoms
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- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
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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
- C07D401/12—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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- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/06—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
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- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
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- C07D403/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing three or more hetero rings
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- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Abstract
Reivindicacion 1: Un compuesto de formula (1) o una de sus sales farmacéuticamente aceptables, en donde: X es =N- o =C(R4)-; R1 es RC; o X puede ser =C(RC)- solo cuando R1 es fenilo opcionalmente sustituido con uno, dos o tres grupos RC10; RC está seleccionado de fenilo, -cicloalquilo C5-6, -CH2-fenilo, heteroarilo y -alquilo C1-4 opcionalmente sustituido con -ORC13, -N(RC13)2 o -S(RC13), en donde el grupo cíclico de RC puede estar opcionalmente sustituido con 1, 2, 3, 4 o 5 grupos RC10, en donde los 1, 2, 3, 4 o 5 grupos RC10 están seleccionados, de modo independiente, de RC10A y RC10B, siempre que RC no pueda estar sustituido con más de 2 grupos RC10B y siempre que la sustitucion de RC con RC10 solo pueda realizarse reemplazando un hidrogeno que está unido covalentemente con un carbono o un nitrogeno de RC; en donde cada RC10A está seleccionado, de modo independiente, de halo, ciano y -alquilo C1-4 opcionalmente sustituido con 1-3 grupos seleccionados de -OH y halo; cada RC10B está seleccionado, de modo independiente, de -C(O)NH2, heterocicloalquilo (de 5-6 miembros), -O-alquil C1-4-RC11, -C(O)ORC12, -OC(O)ORC12 y -O-alquilo C1-4 opcionalmente sustituido con -OH o -C(O)OH; RC11 es ciano, nitro, N(RC12)2, -ORC12, -SRC12, -C(O)RC12, -C(O)ORC12, -C(O)N(RC12)2, -S(O)N(RC12)2, -S(O)2N(RC12)2, -S(O)2RC12, -OC(O)RC12, -OC(O)ORC12, -OC(O)N(RC12)2, -N(RC12)C(O)RC12, -N(RC12)C(O)ORC12, -N(RC12)C(O)N(RC12)2 o -N(RC12)C(=NRC12)N(RC12)2; cada RC12 está seleccionado, de modo independiente, de hidrogeno, alquilo C1-4 y haloalquilo C1-4; cada RC13 está seleccionado, de modo independiente, de hidrogeno -alquilo C1-4 y -haloalquilo C1-4; R2 es -LD-RD1; LD es -[C(R)2]p-Y-[C(R)2]q-; p es 0 o 1; q es 0 o 1; cada R está seleccionado, de modo independiente, de H, -alquilo C1-3, halo, -OH y -CH2OH; Y es un enlace, -S-, -S(O)2-, -CH(OH)-, -O-, -C(H)=C(H)-, -C(O)-alquilo C1-4-, -alquil C1-4-S-alquilo C1-4-, -alquil C1-4-N(RY)-alquilo C1-4-, -C(H)(halo)-, -alquil C1-4-S(O)2-, -S(O)2-N(RY)-, -alquil C1-4-O- o -C(O)-N(RY)- en donde RY es H, -alquilo C1-4, hidroxialquilo C1-4, o -CsC-alquilo C1-3-; RD1 está seleccionado de -arilo C6-10, -N(H)-fenilo, cicloalquilo, heterocicloalquilo y heteroarilo, en donde RD1 puede estar opcionalmente sustituido con 1, 2, 3, 4 o 5 grupos RD10, siempre que la sustitucion de RD1 con RD10 solo pueda realizarse reemplazando un hidrogeno que está unido covalentemente con un carbono o un nitrogeno de RD1, en donde los 1-5 grupos RD10 están seleccionados, de modo independiente, de grupos A y grupos B, siempre que RD1 no pueda estar sustituido con más de 2 grupos B; cada grupo A, cuando aparece, está seleccionado, de modo independiente de halo, -CF3, -CN, -NO2, -OH, -O-alquilo C1-4 opcionalmente sustituido en el grupo alquilo con 1-3 sustituyentes seleccionados, de modo independiente, de -OH y halo y -alquilo C1-4 opcionalmente sustituido con 1-3 sustituyentes seleccionados, de modo independiente, de -OH y halo; cada grupo B, cuando aparece, está seleccionado, de modo independiente de -(alquil C1-4)N(RD11)2, -C(O)-NH2, -C(O)-N(H)-OH, -C(O)-N(H)-RD11C, -c(o)-alquilo C1-4 opcionalmente sustituido con RD11B, -C(O)OH, -S(O)2-alquil C1-4-N(RD11)2, -S(O)2-N(RD11)RD11C, -S(O)2-N(H)C(O)-N(RD11)RD11B, -C(=NH)-NH2, -C(O)O-alquilo C1-4 opcionalmente sustituido con RD11B, -O-alquilo C1-4 opcionalmente sustituido en el grupo alquilo con 1 o 2 RD11B, -C(O)-heterocicloalquilo, en donde el -C(O)-heterocicloalquilo puede estar opcionalmente sustituido con RD11B, siempre que la sustitucion de -C(O)-heterocicloalquilo con RD11B solo pueda realizarse reemplazando un hidrogeno que está unido covalentemente con un carbono o un nitrogeno de -C(O)-heterocicloalquilo, -C(O)-N(H)-alquilo C1-6 opcionalmente sustituido en el grupo alquilo con 1 o 2 RD11B, heterocicloalquilo opcionalmente sustituido con oxo o RD11, siempre que la sustitucion del heterocicloalquilo con RD11 solo pueda realizarse reemplazando un hidrogeno que está unido covalentemente con un carbono o un nitrogeno del heterocicloalquilo, heterocicloalquenilo opcionalmente sustituido con oxo o RD11, siempre que la sustitucion del heterocicloalquenilo con RD11 solo pueda realizarse reemplazando un hidrogeno que está unido covalentemente con un carbono o un nitrogeno del heterocicloalquenilo, heteroarilo opcionalmente sustituido con RD11, siempre que la sustitucion del heteroarilo con RD11 solo pueda realizarse reemplazando un hidrogeno que está unido covalentemente con un carbono o un nitrogeno del heteroarilo, -s(O)2-heterocicloalquilo (de 4-6 miembros) opcionalmente sustituido con RD11C, siempre que la sustitucion del -s(o)2-heterocicloalquilo (de 4-6 miembros) con RD11C solo pueda realizarse reemplazando un hidrogeno que está unido covalentemente con un carbono o un nitrogeno del -S(O)2-heterocicloalquilo (de 4-6 miembros), -S(O)2-N(H)C(O)-alquilo C1-4 opcionalmente sustituido con RD11B, -S(O)2-N(H)C(O)O-alquilo C1-4 opcionalmente sustituido con RD11B, -S(O)2-alquilo C1-4 opcionalmente sustituido con RD11B, -N(H)-C(O)-alquilo C1-4 opcionalmente sustituido en el grupo alquilo con 1 o 2 RD11B, -N(H)-C(O)N(H)-alquilo C1-3 opcionalmente sustituido en el grupo alquilo con RD11B, -alquilo C1-6 opcionalmente sustituido con 1 o 2 RD11B y -CsC-alquilo C1-3 opcionalmente sustituido con RD11B; cada RD11 está seleccionado de modo independiente, de H, -cicloalquilo C3-6, -OH, -haloalquilo C1-4, -alquilo C1-4 opcionalmente sustituido con halo, -OH, -C(O)OH, -S(O)2OH, C(O)OH, -NH2 o N(H)C(=NH)NH2 y -alquil C1-3-fenilo opcionalmente sustituido en el grupo fenilo con 1-3 sustituyentes seleccionados de metoxi, hidroxilo y halo; RD11B está seleccionado de H, -OH, -CF3, un polímero PEG, -N(RD11)2, -C(O)OH, -O-alquilo C1-4, -S(O)2OH, -C(=NH)-NH2, -N(H)C(=NH)NH2, -C(H)=NC(=NH)NH2, -C(H)=NN(H)C(=NH)NH2, -N(H)C(=NH)-N(H)C(=NH)NH2, -C(O)-alquilo C1-3, -O-alquil C1-4-C(O)OH, heteroarilo (de 5-6 miembros), -alquilo C1-4 opcionalmente sustituido con 1-3 grupos seleccionados de modo independiente de halo, -OH, -S(O)2OH, -C(O)OH, -NH2 y N(H)C(=NH)NH2, -alquil C0-3-heterocicloalquilo (de 5-8 miembros), opcionalmente sustituido con 1, 2 o 3 RD11, siempre que la sustitucion de -alquil C0-3-heterocicloalquilo (de 5-8 miembros) con RD11 solo pueda realizarse reemplazando un hidrogeno que está unido covalentemente con un carbono o un nitrogeno de -alquil C0-3-heterocicloalquilo (de 5-8 miembros), -alquil C0-3-cicloalquilo C3-6 opcionalmente sustituido con RD11 y arilo opcionalmente sustituido con 1-5 halo; o RD11 y RD11B, cuando ambos existen y están cada uno unidos al nitrogeno, se pueden unir con el nitrogeno al que están unidos para formar un heterocicloalquilo (de 5-6 miembros) opcionalmente sustituido con un grupo seleccionado de -cicloalquilo C3-6, -haloalquilo C1-4, -OH, -S(O)2OH, -C(O)OH, -NH2, -N(H)C(=NH)NH2, -alquilo C1-4 opcionalmente sustituido con halo, -OH o -C(O)OH y -alquil C1-3-fenilo opcionalmente sustituido en el grupo fenilo con 1-3 sustituyentes seleccionados de metoxi, hidroxilo y halo, siempre que la sustitucion del heterocicloalquilo (de 5-6 miembros) solo pueda realizarse reemplazando un hidrogeno que está unido covalentemente con un carbono o un nitrogeno del heterocicloalquilo (de 5-6 miembros); RD11C está seleccionado de H, -OH, -CF3, -O-alquilo C1-4, -alquil C1-4-N(H)C(=NH)-NH2, -alquil C0-3-heteroarilo (de 5-6 miembros), -alquilo C1-4 opcionalmente sustituido con 1-3 grupos seleccionados, de modo independiente, de halo, -OH, -S(O)2OH, -C(O)OH, -NH2 y - N(H)C(=NH)NH, -alquil C0-3-heterocicloalquilo (de 5-6 miembros) opcionalmente sustituido con un heteroarilo (de 5-6 miembros) siempre que la sustitucion del -alquil C0-3-heterocicloalquilo (de 5-6 miembros) con heteroarilo (de 5-6 miembros) solo pueda realizarse reemplazando un hidrogeno que está unido covalentemente con un carbono o un nitrogeno del -alquil C0-3-heterocicloalquilo (de 5-6 miembros), -alquil C0-3-heterocicloalquilo (de 5-6 miembros) sustituido con 1, 2 o 3 grupos seleccionados de OH y -alquilo C1-3, siempre que la sustitucion del -alquil C1-3-heterocicloalquilo (de 5-6 miembros) solo pueda realizarse reemplazando un hidrogeno que está unido covalentemente con un carbono o un nitrogeno del -alquil C0-3-heterocicloalquilo (de 5-6 miembros) y -alquil C0-3-arilo opcionalmente sustituido en el grupo arilo con 1-3 halo; R4 es H, -alquilo C1-3 o halo; r5 es -[C(R8)2]-fenilo, -[C(R8)2]-naftalenilo o -[C(R8)2]-heteroarilo (de 5-10 miembros), en donde el heteroarilo está seleccionado de (benzo[d] [1,3]dioxolilo, benzo[d]isoxazol, quinoxalinilo, quinolinilo y 2,3,4a,8a-tetrahidrobenzo[b][1,4]dioxinilo, en donde el grupo cíclico de r5 está opcionalmente sustituido con 1, 2, 3, 4 o 5 grupos RA10, siempre que la sustitucion de r5 con RA10 solo pueda realizarse reemplazando un hidrogeno que está unido covalentemente con un carbono o un nitrogeno de r5, en donde los 1-5 grupos RA10 están seleccionados, de modo independiente, de grupos RA10A y grupos RA10B, siempre que r5 no pueda estar sustituido con más de 2 grupos RA10B; cada RA10A, cuando aparece, está seleccionado, de modo independiente, de halo, alcoxilo, hidroxilo, -CN, -OCF3, -alquilo C1-4 y -Nh2; cada RA10B, cuando aparece, está seleccionado de -O-alquil C1-4-RA11, -S(O)2-NH2, -S(O)2CH3, -N(H)-S(O)2CH3, -S(O)2N(H)-CH3, -C(O)OH, -alquil C1-4-OH, -C(O)NH2 y -alquilo C1-4 sustituido con 1-3 grupos seleccionados de -OH y halo; RA11 está seleccionado de -C(O)OH, heterocicloalquilo (de 5-6 miembros), halogeno, ciano, nitro, -alquilo C1-4, -N(RA12)2, -ORA12, -SRA12, -N(ORA12)RA12, -C(O)RA12, -C(O)ORA12, -c(o)N(RA12)2, -N(RA12)S(O)RA12, -N(RA12)S(O)2RA12, -S(O)N(RA12)2, -S(O)2N(RA12)2, -S(O)2RA12, -OC(O)RA12, -OC(O)ORA12, -OC(O)N(RA12), -N(RA12)C(O)RA12, -N(RA12)S(O)2RA12, -N(RA12)C(O)ORA12, -N(RA12)C(O)N(RA12)2, -N(RA12)C(=NRA12)N(RA12)2 y heteroarilo, en donde cada RA12 es, de modo independiente, hidrogeno, -alquilo C1-4 o -haloalquilo C1-4; y cada R8 es, de modo independiente,
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| AR (1) | AR075255A1 (es) |
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2010
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- 2010-02-12 WO PCT/US2010/023981 patent/WO2010093845A1/en not_active Ceased
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- 2010-02-12 TW TW099104908A patent/TW201040168A/zh unknown
- 2010-02-12 KR KR1020117021128A patent/KR20110119790A/ko not_active Withdrawn
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| Publication number | Publication date |
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| KR20110119790A (ko) | 2011-11-02 |
| EP2396304A1 (en) | 2011-12-21 |
| US20120040985A1 (en) | 2012-02-16 |
| WO2010093845A1 (en) | 2010-08-19 |
| CN102395567A (zh) | 2012-03-28 |
| US8785488B2 (en) | 2014-07-22 |
| JP2012517479A (ja) | 2012-08-02 |
| JP2014240421A (ja) | 2014-12-25 |
| TW201040168A (en) | 2010-11-16 |
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