AR077664A2 - Compuestos como ligandos de receptores de canabinoides - Google Patents
Compuestos como ligandos de receptores de canabinoidesInfo
- Publication number
- AR077664A2 AR077664A2 ARP100102555A ARP100102555A AR077664A2 AR 077664 A2 AR077664 A2 AR 077664A2 AR P100102555 A ARP100102555 A AR P100102555A AR P100102555 A ARP100102555 A AR P100102555A AR 077664 A2 AR077664 A2 AR 077664A2
- Authority
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- Argentina
- Prior art keywords
- cr1cr1d
- haloalkyl
- alkyl
- independently
- instance
- Prior art date
Links
- 150000001875 compounds Chemical class 0.000 title abstract 4
- 239000003446 ligand Substances 0.000 title 1
- 125000000217 alkyl group Chemical group 0.000 abstract 22
- 125000001188 haloalkyl group Chemical group 0.000 abstract 20
- 229910052739 hydrogen Inorganic materials 0.000 abstract 17
- 239000001257 hydrogen Substances 0.000 abstract 17
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 16
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 15
- 229910052736 halogen Chemical group 0.000 abstract 14
- 150000002367 halogens Chemical group 0.000 abstract 14
- 125000004765 (C1-C4) haloalkyl group Chemical group 0.000 abstract 11
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 9
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 9
- 125000000623 heterocyclic group Chemical group 0.000 abstract 8
- 125000004043 oxo group Chemical group O=* 0.000 abstract 8
- 125000001424 substituent group Chemical group 0.000 abstract 8
- 125000003545 alkoxy group Chemical group 0.000 abstract 5
- 125000004432 carbon atom Chemical group C* 0.000 abstract 5
- 125000000392 cycloalkenyl group Chemical group 0.000 abstract 5
- 125000004438 haloalkoxy group Chemical group 0.000 abstract 5
- 125000001072 heteroaryl group Chemical group 0.000 abstract 5
- 125000002950 monocyclic group Chemical group 0.000 abstract 5
- 125000002911 monocyclic heterocycle group Chemical group 0.000 abstract 5
- 229910052760 oxygen Inorganic materials 0.000 abstract 5
- 229910052717 sulfur Inorganic materials 0.000 abstract 5
- -1 = N-ORf Chemical group 0.000 abstract 4
- 125000003342 alkenyl group Chemical group 0.000 abstract 4
- 125000000304 alkynyl group Chemical group 0.000 abstract 4
- 125000003118 aryl group Chemical group 0.000 abstract 4
- 125000006656 (C2-C4) alkenyl group Chemical group 0.000 abstract 3
- 125000004183 alkoxy alkyl group Chemical group 0.000 abstract 3
- 229910052799 carbon Inorganic materials 0.000 abstract 3
- 125000004994 halo alkoxy alkyl group Chemical group 0.000 abstract 3
- 125000006650 (C2-C4) alkynyl group Chemical group 0.000 abstract 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 abstract 2
- 239000000203 mixture Substances 0.000 abstract 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 2
- 239000000651 prodrug Chemical class 0.000 abstract 2
- 229940002612 prodrug Drugs 0.000 abstract 2
- 150000003839 salts Chemical class 0.000 abstract 2
- 208000024172 Cardiovascular disease Diseases 0.000 abstract 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 1
- JCXJVPUVTGWSNB-UHFFFAOYSA-N Nitrogen dioxide Chemical compound O=[N]=O JCXJVPUVTGWSNB-UHFFFAOYSA-N 0.000 abstract 1
- 125000004429 atom Chemical group 0.000 abstract 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 abstract 1
- 125000005605 benzo group Chemical group 0.000 abstract 1
- 208000015114 central nervous system disease Diseases 0.000 abstract 1
- 206010012601 diabetes mellitus Diseases 0.000 abstract 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 1
- 230000002526 effect on cardiovascular system Effects 0.000 abstract 1
- 125000002541 furyl group Chemical group 0.000 abstract 1
- 125000000842 isoxazolyl group Chemical group 0.000 abstract 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 1
- 229910052757 nitrogen Inorganic materials 0.000 abstract 1
- 125000001715 oxadiazolyl group Chemical group 0.000 abstract 1
- 125000002971 oxazolyl group Chemical group 0.000 abstract 1
- 239000001301 oxygen Substances 0.000 abstract 1
- 125000006413 ring segment Chemical group 0.000 abstract 1
- 239000012453 solvate Chemical class 0.000 abstract 1
- 125000001544 thienyl group Chemical group 0.000 abstract 1
Classifications
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- C—CHEMISTRY; METALLURGY
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- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—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
- 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
- C07D405/12—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 chain containing hetero atoms as chain links
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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
- A61K31/415—1,2-Diazoles
- A61K31/4155—1,2-Diazoles non condensed and containing further heterocyclic rings
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
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- A61P25/00—Drugs for disorders of the nervous system
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/04—Centrally acting analgesics, e.g. opioids
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- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
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- A—HUMAN NECESSITIES
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- 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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- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
- A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
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- 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
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- 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
- C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
- C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
- C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D231/14—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with 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
- C07D231/38—Nitrogen atoms
- C07D231/40—Acylated on said nitrogen atom
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- C07D—HETEROCYCLIC COMPOUNDS
- C07D285/00—Heterocyclic compounds containing rings having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by groups C07D275/00 - C07D283/00
- C07D285/01—Five-membered rings
- C07D285/02—Thiadiazoles; Hydrogenated thiadiazoles
- C07D285/04—Thiadiazoles; Hydrogenated thiadiazoles not condensed with other rings
- C07D285/12—1,3,4-Thiadiazoles; Hydrogenated 1,3,4-thiadiazoles
- C07D285/125—1,3,4-Thiadiazoles; Hydrogenated 1,3,4-thiadiazoles with oxygen, sulfur or nitrogen atoms, directly attached to ring carbon atoms, the nitrogen atoms not forming part of a nitro radical
- C07D285/135—Nitrogen atoms
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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
- C07D403/12—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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- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
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- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
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- C07—ORGANIC CHEMISTRY
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- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
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- Chemical & Material Sciences (AREA)
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- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Diabetes (AREA)
- Immunology (AREA)
- Hematology (AREA)
- Obesity (AREA)
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- Neurosurgery (AREA)
- Pain & Pain Management (AREA)
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- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Pyridine Compounds (AREA)
- Thiazole And Isothizaole Compounds (AREA)
- Nitrogen- Or Sulfur-Containing Heterocyclic Ring Compounds With Rings Of Six Or More Members (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Se divulgan asimismo composiciones que comprenden dichos compuestos y métodos para el tratamiento de condiciones y trastornos usando dichos compuestos y composiciones para diabetes, trastornos cardiovasculares y del sistema nervioso central. Reivindicacion 1: Un compuesto caracterizado porque tiene la formula (1), o una sal, solvato, prodroga, o sal de prodroga farmacéuticamente aceptable o combinacion de los mismos donde X4 es O, S, S(O), S(O)2, o N(Rbx); donde Rbx es hidrogeno, alquilo, haloalquilo, alcoxialquilo, -C(O)O(alquilo), cicloalquilo monocíclico, -(CR1cR1d)q3-(cicloalquilo monocíclico), o haloalcoxialquilo; y A1 es -G1a-G1b, -(CR1aR1b)q1-G1c, -(CR1aR1b)q1-A2, -(CR1gR1h)q2-A4, -N(Rb)C(O)Ra, -N(Rb)C(O)ORd, -N(Rb)C(O)N(Rb)(Rc), -N(Rb)(Rc), o -N=C(Rp)Rq); o X4 y A1 juntos son N=N(Rcx); A2 es -C(O)Ra, -S(O)2Rd, -SRd, -C(O)ORa, -C(O)N(Rb)(Rc), -C(S)N(Rb)(Rc), -S(O)2N(Rb)(Rc), -C(=NORf)Ra, -CN, -N(Rc)C(O)Ra, -N(Rc)C(O)ORd, -N(Rc)S(O)2Rd, -N(Rc)C(O)N(Rb)(Rc), -N(Rc)S(O)2N(Rb)(Rc), -ORm, o -N(Rb)(Rn); A3 es C(O)Rh, -S(O)2Re, -C(O)N(Rh)2, -C(S)N(Rh)2, -S(O)2N(Rh)2, -C(=NORh)Rh, -N(Rh)C(O)Rh, -N(Rh)C(O)ORe, -N(Rh)S(O)2Re, -N(Rh)C(O)N(Rh)2, -N(Rh)S(O)2N(Rh1)2, -CN, -ORh, o -N(Rh)2; A4 es cicloalquilo, alcoxi, haloalcoxi, o N(R1m)2 donde cada instancia de R1m es en forma independiente hidrogeno o alquilo; cada instancia de Ra y Rc, es en forma independiente hidrogeno, alquilo, haloalquilo, -(CR1aR1b)q3-A3, G1d, o -(CR1aR1b)q3-G1d; Rb, en cada instancia, es en forma independiente hidrogeno, alquilo, haloalquilo, alcoxialquilo, cicloalquilo monocíclico, -(CR1cR1d)q3-(cicloalquilo monocíclico), o haloalcoxialquilo; Rd, en cada instancia, es en forma independiente alquilo, haloalquilo, -(CR1aR1b)q3-A3, G1d, o -(CR1aR1b)q3-G1d; Rcx es alquilo, haloalquilo, -(CR1aR1b)q3-A3, G1d, o -(CR1aR1b)q3-G1d; Rm es hidrogeno, -(CR1aR1b)q3-A3, G1d, o -(CR1aR1b)q3-G1d; Rn es haloalquilo, -(CR1aR1b)q3-A3, G1d, o -(CR1aR1b)q3-G1d; Rp es hidrogeno, alquilo, haloalquilo, -(CR1aR1b)q3-A3, -C(O)ORd, -C(O)Rd, G1d, o -(CR1aR1b)q3-G1d; Rq es hidrogeno, alquilo, haloalquilo, -N(Rb)(Rc), -(CR1aR1b)q3-A3, G1d, o -(CR1aR1b)q3-G1d; o Rp y Rq, junto con el átomo de carbono al cual están unidos, forman un anillo monocíclico de 5, 6, 7 u 8 miembros, opcionalmente sustituido con 1, 2, 3, 4, o 5 sustituyentes seleccionados en forma independiente entre el grupo que consiste en oxo, alquilo, haloalquilo, y halogeno; A5 representa la formula (a), (b), (c), (d), o (e), G1a y G1b son en forma independiente cicloalquilo, cicloalquenilo, heterociclo, arilo, o heteroarilo; G1c es cicloalquenilo, heterociclo, arilo, o heteroarilo; el anillo representado por G1a está opcionalmente sustituido con 1, 2, 3, 4, o 5 sustituyentes seleccionados en forma independiente entre el grupo que consiste en alquilo, alquenilo, alquinilo, halogeno, haloalquilo, =N-CN, =N-ORf, -CN, oxo, -ORf, -OC(O)Rf, -OC(O)N(Rf)2, -S(O)2Re, -S(O)2N(Rf)2, -C(O)Rf, -C(O)ORf, -C(O)N(Rf)2, -N(Rf)2, -N(Rf)C(O)Rf, -N(Rf)S(O)2Re, -N(Rf)C(O)O(Re), -N(Rf)C(O)N(Rf)2, -(CR1cR1d)q3-ORf, -(CR1cR1d)q3-OC(O)Rf, -(CR1cR1d)q3-OC(O)N(Rf)2, -(CR1cR1d)q3-S(O)2Re, -(CR1cR1d)q3-S(O)2N(Rf)2, -(CR1cR1d)q3-C(O)Rf, -(CR1cR1d)q3-C(O)ORf, -(CR1cR1d)q3-C(O)N(Rf)2, -(CR1cR1d)q3-N(Rf)2, -(CR1cR1d)q3-N(Rf)C(O)Rf, -(CR1cR1d)q3-N(Rf)S(O)2Re, -(CR1cR1d)q3-N(Rf)C(O)O(Re), -(CR1cR1d)q3-N(Rf)C(O)N(Rf)2, y -(CR1cR1d)q3-CN; los anillos representados por G1b, G1c, y el cicloalquilo de A4 están opcionalmente sustituidos en cada caso con 1, 2, 3, 4, o 5 sustituyentes seleccionados en forma independiente entre el grupo que consiste G1d, alquilo, alquenilo, alquinilo, halogeno, haloalquilo, =N-CN, =N-ORf, -CN, oxo, -ORf, -OC(O)Rf -OC(O)N(Rf)2, -S(O)2Re, -S(O)2N(Rf)2, -C(O)Rf, -C(O)ORf, -C(O)N(Rf)2, -N(Rf)2, -N(Rf)C(O)Rf, -N(Rf)S(O)2Re, -N(Rf)C(O)O(Re), -N(Rf)C(O)N(Rf)2, -(CR1cR1d)q3-G1d, -(CR1cR1d)q3-ORf, -(CR1cR1d)q3-OC(O)Rf, -(CR1cR1d)q3-OC(O)N(Rf)2, -(CR1cR1d)q3-S(O)2Re, -(CR1cR1d)q3-S(O)2N(Rf)2, -(CR1cR1d)q3-C(O)Rf, -(CR1cR1d)q3-C(O)ORf, -(CR1cR1d)q3-C(O)N(Rf)2, -(CR1cR1d)q3-N(Rf)2, -(CR1cR1d)q3-N(Rf)C(O)Rf, -(CR1cR1d)q3-N(Rf)S(O)2Re, -(CR1cR1d)q3-N(Rf)C(O)O(Re), -(CR1cR1d)q3-N(Rf)C(O)N(Rf)2 y -(CR1cR1d)q3-CN; G1d, en cada instancia, es en forma independiente un heterociclo monocíclico, un heteroarilo monocíclico, un fenilo, un cicloalquilo monocíclico, o un cicloalquenilo monocíclico; donde G1d está opcionalmente sustituido con 1, 2, 3, o 4 sustituyentes seleccionados en forma independiente entre el grupo que consiste en -N(Rh)2, -CN, oxo, alquilo, haloalquilo, alcoxi, haloalcoxi, halogeno, y OH; Re, en cada instancia, es en forma independiente alquilo C1-4, haloalquilo C1-4, cicloalquilo monocíclico, heterociclo monocíclico, o -(CR1cR1d)q3-(cicloalquilo monocíclico); Rf, en cada instancia, es en forma independiente hidrogeno, alquilo C1-4, haloalquilo C1-4, -(CR1cR1d)q3-ORh, heterociclo monocíclico, cicloalquilo monocíclico, o -(CR1cR1d)q3-(cicloalquilo monocíclico); Rh, en cada instancia, es en forma independiente hidrogeno, alquilo C1-4, haloalquilo C1-4, cicloalquilo monocíclico, o -(CR1cR1d)q3-(cicloalquilo monocíclico); R21, R22, R23, R24, y R25 es en forma independiente alquilo, alquenilo, alquinilo, haloalquilo, -(CR2aR2b)q4-OH, -(CR2aR2b)q4-O-aIquilo, -(CR2aR2b)q4-O-haloalquilo, -(CR2aR2b)q4-O-G2a, -(CR2aR2b)q4-O-(CR2cR2d)q3-G2a, -(CR2aR2b)q5-C(O)-Ra, -(CR2aR2b)q5-C(=N-ORf)Ra, -(CR2aR2b)q5-SO2-Rd, -(CR2aR2b)q5-G2b, -(CR2aR2b)q5-C(O)N(Rb)(Rc), o -(CR2aR2b)q5-CN; cada instancia de G2a es en forma independiente cicloalquilo, heterociclo, arilo, o heteroarilo; G2b es un anillo monocíclico seleccionado entre el grupo que consiste en cicloalquilo, cicloalquenilo, tienilo, fenilo, furanilo, oxazolilo, isoxazolilo, oxadiazolilo, y heterociclo; donde el heterociclo contiene 0 o 1 doble enlace, 1 o 2 oxígenos, y 0 o 1 nitrogeno como átomos del anillo; dos átomos no adyacentes de dicho anillo heterociclo pueden estar opcionalmente unidos por medio de un puente alquenileno de 2, 3, o 4 átomos de carbono, u opcionalmente unidos por un puente alquileno de 1, 2, 3, o 4 átomos de carbono; cada anillo G2b está opcionalmente fusionado con un anillo monocíclico seleccionado entre el grupo que consiste en benzo, cicloalquilo, cicloalquenilo, heterociclo y heteroarilo; cada instancia de G2a y G2b en forma independiente no está sustituida o está sustituida con 1, 2, 3, 4, 5, o 6 sustituyentes seleccionados en forma independiente entre el grupo que consiste en oxo, alquilo, halogeno, -OH, alcoxi, haloalcoxi, y haloalquilo; X1 es O o S; X2 es O, S, o N(R10) donde R10 es alquilo, alcoxialquilo, haloalcoxialquilo, o haloalquilo; X3 es O o S; R3, R4, R5, R6, R7, R8, R9, R11, y R12 es en forma independiente G3, hidrogeno, alquilo, alquenilo, alquinilo, -NO2, -CN, halogeno, -ORh, N(Rh)2, - C(O)Rh, -C(O)O(Rh), haloalquilo, -(CR3aR3b)q6-ORh, -(CR3aR3b)q6-N(Rh)2, -(CR3aR3b)q6-C(O)Rh, o -(CR3aR3b)q6-C(O)O(Rh); R13 y R14 es en forma independiente G3, hidrogeno, alquilo, haloalquilo, o -(CR3aR3b)q6-ORh; o R13 y R14 tomados junto con el átomo de carbono al cual están unidos forman un anillo heterociclo monocíclico o un anillo cicloalquilo monocíclico, donde cada uno de los cuales en forma independiente no está sustituido o está sustituido con 1, 2, 3, o 4 sustituyentes seleccionados entre el grupo que consiste en alquilo, OH, alcoxi, haloalcoxi, haloalquilo, y oxo; R15 y R16 es en forma independiente G3, hidrogeno, alquilo, haloalquilo, o -(CR3aR3b)q6-ORh; o R5 y R16 tomados junto con el átomo de carbono al cual están unidos forman un anillo cicloalquilo monocíclico o un anillo heterociclo monocíclico; donde cada uno de los cuales en forma independiente no está sustituido o está sustituido con 1, 2, 3, o 4 sustituyentes seleccionados entre el grupo que consiste en alquilo, OH, alcoxi, haloalcoxi, haloalquilo, y oxo; G3, en cada instancia, es en forma independiente cicloalquilo, cicloalquenilo, arilo, heterociclo, o heteroarilo, donde cada G3 en forma independiente no está sustituida o está sustituida con 1, 2, 3 o 4 sustituyentes seleccionados entre el grupo que consiste en alquilo C1-4, alquenilo C2-4, alquinilo C2-4, halogeno, haloalquilo C1-4, =N-CN, =N-ORh, -CN, oxo, -ORh, -OC(O)Rh, -OC(O)N(Rh)2, -S(O)2Re, -S(O)2N(Rh)2, -C(O)Rh, -C(O)Orh, -C(O)N(Rh)2, -N(Rh)2, -N(Rh)C(O)Rh, -N(Rh)S(O)2Re, -N(Rh)C(O)O(Re), y -N(Rh)C(O)N(Rh)2; R1a en cada instancia, es en forma independiente hidrogeno, halogeno, alquilo C1-4 o haloalquilo C1-4; R1b en cada instancia, es en forma independiente hidrogeno, halogeno, alquilo C1-4, alquenilo C2-4, haloalquilo C1-4, -ORh, -N(Rh)2, -N(Rh)C(O)Rh, -N(Rh)C(O)ORe, o -N(Rh)S(O)2Re; R1g en cada instancia, es en forma independiente hidrogeno, halogeno, alquilo C1-4, haloalquilo C1-4, -ORh, -N(Rh)2, -N(Rh)C(O)Rh, -N(Rh)C(O)ORe, o -N(Rh)S(O)2Re; con la condicion de que al menos una instancia de R1g es halogeno, haloalquilo C1-4, -ORh, -N(Rh)2, -N(Rh)C(O)Rh, -N(Rh)C(O)ORe, o -N(Rh)S(O)2Re; R1h, en cada instancia, es en forma independiente hidrogeno, halogeno, alquilo C1-4, o haloalquilo C1-4; R1c, R1d, R2a, R2b, R2c, R2d, R3a y R3b, en cada instancia, es en forma independiente hidrogeno, halogeno, alquilo C1-4, o haloalquilo C1-4; Rx en cada instancia, es en forma independiente G1d, alquilo C1-4, alquenilo C2-4, alquinilo C2-4, halogeno, haloalquilo C1-4, NO2, -CN, -ORf, -OC(O)Rf, -OC(O)N(Rf)2, S(O)2Re, -S(O)2N(Rf)2, -C(O)Rf, -C(O)ORf, -C(O)N(Rf)2, -N(Rf)2, -N(Rf)C(O)Rf, -N(Rf)S(O)2Re, -N(Rf)C(O)O(Re), -N(Rf)C(O)N(Rf)2, -(CR1cR1d)q3-ORf, -(CR1cR1d)q3-OC(O)Rf, -(CR1cR1d)q3-OC(O)N(Rf)2, -(CR1cR1d)q3-S(O)2Re, -(CR1cR1d)q3-S(O)2N(Rf)2, -(CR1cR1d)q3-C(O)Rf, -(CR1cR1d)q3-C(O)ORf, -(CR1cR1d)q3-C(O)N(Rf)2, -(CR1cR1d)q3-N(Rf)2, -(CR1cR1d)q3-N(Rf)C(O)Rf, -(CR1cR1d)q3-N(Rf)S(O)2Re, -(CR1cR1d)q3-N(Rf)C(O)O(Re), -(CR1cR1d)q3-N(Rf)C(O)N(Rf)2, o -(CR1cR1d)q3-CN; q1, en cada instancia, es en forma independiente 1, 2, 3, o 4; q2 y q4, en cada instancia, son en forma independiente 2, 3, 4, o 5; q3, en cada instancia, es 1, 2 o 3; q5 y q6, en cada instanc
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-
2009
- 2009-09-16 TW TW098131294A patent/TW201016692A/zh unknown
- 2009-09-16 KR KR1020117008389A patent/KR20110061619A/ko not_active Withdrawn
- 2009-09-16 EP EP15151451.0A patent/EP2896615A1/en not_active Withdrawn
- 2009-09-16 ES ES11192134.2T patent/ES2556752T3/es active Active
- 2009-09-16 MX MX2011002811A patent/MX2011002811A/es not_active Application Discontinuation
- 2009-09-16 EP EP11192134.2A patent/EP2428507B1/en active Active
- 2009-09-16 US US12/560,893 patent/US8859596B2/en not_active Expired - Fee Related
- 2009-09-16 BR BRPI0919135A patent/BRPI0919135A2/pt not_active IP Right Cessation
- 2009-09-16 CN CN2009801455637A patent/CN102216277A/zh active Pending
- 2009-09-16 EP EP09792591A patent/EP2334646A2/en not_active Withdrawn
- 2009-09-16 RU RU2011115087/04A patent/RU2011115087A/ru not_active Application Discontinuation
- 2009-09-16 PA PA20098842501A patent/PA8842501A1/es unknown
- 2009-09-16 CA CA2737199A patent/CA2737199A1/en not_active Abandoned
- 2009-09-16 US US12/560,897 patent/US8188135B2/en not_active Expired - Fee Related
- 2009-09-16 WO PCT/US2009/057088 patent/WO2010033543A2/en not_active Ceased
- 2009-09-16 PE PE2011000626A patent/PE20110804A1/es not_active Application Discontinuation
- 2009-09-16 JP JP2011527056A patent/JP2012502917A/ja active Pending
- 2009-09-16 AU AU2009293319A patent/AU2009293319A1/en not_active Abandoned
- 2009-09-16 UY UY0001032125A patent/UY32125A/es not_active Application Discontinuation
- 2009-09-16 AR ARP090103558A patent/AR073599A1/es not_active Application Discontinuation
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2010
- 2010-07-14 AR ARP100102555A patent/AR077664A2/es not_active Application Discontinuation
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2011
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- 2011-03-01 ZA ZA2011/01590A patent/ZA201101590B/en unknown
- 2011-03-15 DO DO2011000081A patent/DOP2011000081A/es unknown
- 2011-03-15 CL CL2011000544A patent/CL2011000544A1/es unknown
- 2011-03-23 CO CO11035303A patent/CO6361998A2/es not_active Application Discontinuation
- 2011-04-12 EC EC2011010974A patent/ECSP11010974A/es unknown
Also Published As
| Publication number | Publication date |
|---|---|
| PE20110804A1 (es) | 2011-11-30 |
| RU2011115087A (ru) | 2012-10-27 |
| WO2010033543A2 (en) | 2010-03-25 |
| US8188135B2 (en) | 2012-05-29 |
| US20100069349A1 (en) | 2010-03-18 |
| EP2428507A3 (en) | 2012-06-13 |
| ZA201101590B (en) | 2012-08-29 |
| EP2896615A1 (en) | 2015-07-22 |
| JP2012502917A (ja) | 2012-02-02 |
| US20100069348A1 (en) | 2010-03-18 |
| BRPI0919135A2 (pt) | 2015-12-08 |
| CA2737199A1 (en) | 2010-03-25 |
| DOP2011000081A (es) | 2011-07-15 |
| EP2428507B1 (en) | 2015-10-21 |
| CN102216277A (zh) | 2011-10-12 |
| ECSP11010974A (es) | 2011-05-31 |
| EP2428507A2 (en) | 2012-03-14 |
| CL2011000544A1 (es) | 2011-06-17 |
| EP2334646A2 (en) | 2011-06-22 |
| UY32125A (es) | 2010-04-30 |
| KR20110061619A (ko) | 2011-06-09 |
| PA8842501A1 (es) | 2010-04-21 |
| MX2011002811A (es) | 2011-04-12 |
| US8859596B2 (en) | 2014-10-14 |
| TW201016692A (en) | 2010-05-01 |
| WO2010033543A3 (en) | 2010-11-18 |
| IL211406A0 (en) | 2011-05-31 |
| CO6361998A2 (es) | 2012-01-20 |
| AU2009293319A1 (en) | 2010-03-25 |
| ES2556752T3 (es) | 2016-01-20 |
| AR073599A1 (es) | 2010-11-17 |
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