AR035716A1 - Compuestos agonistas del receptor beta3-adrenergico, uso de los mismos en la fabricacion de medicamentos y composiciones farmaceuticas conteniendo los mismos - Google Patents
Compuestos agonistas del receptor beta3-adrenergico, uso de los mismos en la fabricacion de medicamentos y composiciones farmaceuticas conteniendo los mismosInfo
- Publication number
- AR035716A1 AR035716A1 ARP010104923A ARP010104923A AR035716A1 AR 035716 A1 AR035716 A1 AR 035716A1 AR P010104923 A ARP010104923 A AR P010104923A AR P010104923 A ARP010104923 A AR P010104923A AR 035716 A1 AR035716 A1 AR 035716A1
- Authority
- AR
- Argentina
- Prior art keywords
- compounds
- nr9so2r10
- prodrugs
- stereoisomers
- halogen
- Prior art date
Links
- 150000001875 compounds Chemical class 0.000 title abstract 12
- 239000003814 drug Substances 0.000 title abstract 2
- 239000000556 agonist Substances 0.000 title 1
- 238000004519 manufacturing process Methods 0.000 title 1
- 239000000203 mixture Substances 0.000 title 1
- 229910052736 halogen Inorganic materials 0.000 abstract 8
- 150000002367 halogens Chemical group 0.000 abstract 8
- 229910052739 hydrogen Inorganic materials 0.000 abstract 8
- 239000001257 hydrogen Substances 0.000 abstract 8
- 239000000651 prodrug Substances 0.000 abstract 8
- 229940002612 prodrug Drugs 0.000 abstract 8
- 125000000623 heterocyclic group Chemical group 0.000 abstract 7
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 7
- 125000003118 aryl group Chemical group 0.000 abstract 6
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 abstract 4
- 150000002431 hydrogen Chemical group 0.000 abstract 4
- 229910052760 oxygen Inorganic materials 0.000 abstract 4
- 239000001301 oxygen Substances 0.000 abstract 4
- 150000003839 salts Chemical class 0.000 abstract 4
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 3
- 125000003545 alkoxy group Chemical group 0.000 abstract 3
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 3
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 abstract 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical group N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 abstract 2
- 125000005055 alkyl alkoxy group Chemical group 0.000 abstract 2
- 239000000883 anti-obesity agent Substances 0.000 abstract 2
- 229940125710 antiobesity agent Drugs 0.000 abstract 2
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 2
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 2
- 125000002883 imidazolyl group Chemical group 0.000 abstract 2
- 239000008194 pharmaceutical composition Substances 0.000 abstract 2
- 125000004076 pyridyl group Chemical group 0.000 abstract 2
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 1
- 241000124008 Mammalia Species 0.000 abstract 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 abstract 1
- 125000000217 alkyl group Chemical group 0.000 abstract 1
- 102000016959 beta-3 Adrenergic Receptors Human genes 0.000 abstract 1
- 108010014502 beta-3 Adrenergic Receptors Proteins 0.000 abstract 1
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 1
- 201000010099 disease Diseases 0.000 abstract 1
- 125000005842 heteroatom Chemical group 0.000 abstract 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 1
- 239000000543 intermediate Substances 0.000 abstract 1
- 125000001786 isothiazolyl group Chemical group 0.000 abstract 1
- 125000000842 isoxazolyl group Chemical group 0.000 abstract 1
- 230000001404 mediated effect Effects 0.000 abstract 1
- 229910052757 nitrogen Chemical group 0.000 abstract 1
- 125000001715 oxadiazolyl group Chemical group 0.000 abstract 1
- 125000002971 oxazolyl group Chemical group 0.000 abstract 1
- 125000003226 pyrazolyl group Chemical group 0.000 abstract 1
- 229910052717 sulfur Inorganic materials 0.000 abstract 1
- 239000011593 sulfur Chemical group 0.000 abstract 1
- 125000001113 thiadiazolyl group Chemical group 0.000 abstract 1
- 125000000335 thiazolyl group Chemical group 0.000 abstract 1
- 125000004306 triazinyl group Chemical group 0.000 abstract 1
- 125000001425 triazolyl group Chemical group 0.000 abstract 1
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 abstract 1
Classifications
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- 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
- C07D231/12—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 only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
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- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
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- C07D233/56—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 only hydrogen atoms or radicals containing only hydrogen and carbon atoms, attached to ring carbon atoms
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- C07D249/00—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
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- C07D249/08—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
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- C07D263/32—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
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- C07D285/01—Five-membered rings
- C07D285/02—Thiadiazoles; Hydrogenated thiadiazoles
- C07D285/04—Thiadiazoles; Hydrogenated thiadiazoles not condensed with other rings
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- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
Se proporcionan además productos intermedios útiles para la preparación de los compuestos de Fórmula (1); combinaciones de los compuestos de Fórmula (1), los estereoisómeros y profármacos de los mismos, y las sales farmacéuticamente aceptables de los compuestos, estereoisómeros y profármacos, con agentes antiobesidad; composiciones farmacéuticas que comprenden los compuestos de Fórmula (1), los estereoisómeros y profármacos de los mismos, y las sales farmacéuticamente aceptables de los compuestos, estereoisómeros y profármacos, o composiciones farmacéuticas que comprenden los compuestos de la Fórmula (1), los estereoisómeros y profármacos de los mismos, y las sales farmacéuticamente aceptables de los compuestos, estereoisómeros y profármacos, y agentes antiobesidad; y uso de los compuestos para preparar medicamentos para tratar enfermedades, estados o trastornos mediados por el receptor beta3-adrenérgico en un mamífero. Reivindicación 1: Un compuesto caracterizado porque es de la fórmula (1), los estereoisómeros y profármacos del mismo, y las sales farmacéuticamente aceptables de dichos compuestos, estereoisómeros y profármacos, fórmula en la cual Ar es piridilo o fenilo; R es hidrógeno, hidroxilo, halógeno, -CF3, -alquilo (C1-6), -alcoxilo (C1-6), -cicloalquilo (C3-8), -NR9R10, -NR9SO2R10, -NR9COR10, ó -SO2R9; R1 es hidrógeno, -alquilo (C1-6), halógeno, -alcoxilo (C1-6), o hidroxilo; R2, R3 y R4 son independientemente hidrógeno, o -alquilo (C1-6); R5 es un heterociclo aromático con anillo de 5 ó 6 miembros, que tiene de 1 a 4 heteroátomos seleccionados del grupo que consiste en oxígeno, azufre y nitrógeno; R6 y R7 son independientemente hidrógeno, halógeno, ciano, -acilo (C1-6), -CO2R9, -NR9R10, hidroxilo, -alcoxilo (C1-6), -CONR9R10, -NR9SO2R10, -SO2NR9R10, ó -SO2R9; -alquilo (C1-6) opcionalmente sustituido con -cicloalquilo (C3-8), halógeno, arilo, alcoxilo (C1-6), -haloalquilo (C1-6), alquilalcoxilo, hidroxilo, -NR9R10, -NR9SO2R10, -SO2NR9R10, -SO2R9, o heterociclo; -cicloalquilo (C3-8) opcionalmente sustituido con -alquilo (C1-6), -cicloalquilo (C3-8), halógeno, arilo, alcoxilo (C1-6), -haloalquilo (C1-6), alquilalcoxilo, hidroxilo, -NR9R10, -NR9SO2R10, -SO2NR9R10, -SO2R9, o heterociclo; arilo opcionalmente sustituido con -alquilo (C1-6), -cicloalquilo (C3-7), halógeno, arilo, -alcoxilo (C1-6), -haloalquilo (C1-6), alquilalcoxilo, hidroxilo, -NR9R10, -NR9SO2R10, -SO2NR9R10, -SO2R9, o heterociclo; o heterociclo opcionalmente sustituido con -alquilo (C1-6), -cicloalquilo (C3-8), halógeno, arilo, -alcoxilo (C1-6), -haloalquilo (C1-6), alquilacoxilo, hidroxilo, -NR9R10, -NR9SO2R10, -SO2NR9R10, -SO2R9, o heterociclo; R8 es hidrógeno, -alquilo (C1-4) o halógeno; y R9 y R10 son independientemente hidrógeno, -alquilo (C1-6), alquilalcoxilo, -cicloalquilo (C3-8), -haloalquilo (C1-6), -alcoxilo (C1-6), arilo, o heterociclo; X es un enlace directo u oxígeno; e Y es un enlace directo, -alquilo (C1-6), -OCH2-, -CH2O- u oxígeno; con tal que: (i) cuando Ar sea fenilo, R sea -NR9SO2R10, -SO2NR9R10, o -SO2R9, y (ii) cuando Ar sea fenilo, -NR9SO2R10, y tanto R6 como R7 sean hidrógeno, R5 no sea entonces imidazolilo. Reivindicación 2: Un compuesto de acuerdo con la reivindicación 1, caracterizado porque Ar es piridilo; R, R1, R2, R3, R4 y R8 son hidrógeno; X es oxígeno; Y es un enlace directo; y R5 es un heterociclo con anillo de cinco o seis miembros, seleccionado del grupo que consiste en imidazolilo, isotiazolilo, isoxazolilo, oxadiazolilo, oxazolilo, pirazolilo, tiadiazolilo, tiazolilo, triazinilo y triazolilo.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US24227400P | 2000-10-20 | 2000-10-20 |
Publications (1)
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|---|---|
| AR035716A1 true AR035716A1 (es) | 2004-07-07 |
Family
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Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP010104923A AR035716A1 (es) | 2000-10-20 | 2001-10-19 | Compuestos agonistas del receptor beta3-adrenergico, uso de los mismos en la fabricacion de medicamentos y composiciones farmaceuticas conteniendo los mismos |
Country Status (34)
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| JP (1) | JP2004511555A (es) |
| KR (1) | KR20030044013A (es) |
| CN (1) | CN1469876A (es) |
| AP (1) | AP2001002307A0 (es) |
| AR (1) | AR035716A1 (es) |
| AU (1) | AU2001292161A1 (es) |
| BG (1) | BG107652A (es) |
| BR (1) | BR0114836A (es) |
| CA (1) | CA2423792A1 (es) |
| CR (1) | CR6935A (es) |
| CZ (1) | CZ20031012A3 (es) |
| DO (1) | DOP2001000270A (es) |
| EA (1) | EA200300305A1 (es) |
| EC (1) | ECSP034562A (es) |
| EE (1) | EE200300191A (es) |
| GT (1) | GT200100210A (es) |
| HR (1) | HRP20030297A2 (es) |
| HU (1) | HUP0301382A2 (es) |
| IL (1) | IL154911A0 (es) |
| IS (1) | IS6748A (es) |
| MA (1) | MA26954A1 (es) |
| MX (1) | MXPA03003455A (es) |
| NO (1) | NO20031573L (es) |
| PA (1) | PA8530401A1 (es) |
| PE (1) | PE20020541A1 (es) |
| PL (1) | PL362076A1 (es) |
| SK (1) | SK4612003A3 (es) |
| SV (1) | SV2003000697A (es) |
| TN (1) | TNSN01148A1 (es) |
| UY (1) | UY26974A1 (es) |
| WO (1) | WO2002032897A1 (es) |
| ZA (1) | ZA200302191B (es) |
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| GB9812709D0 (en) * | 1998-06-13 | 1998-08-12 | Glaxo Group Ltd | Chemical compounds |
| GB2356197A (en) | 1999-10-12 | 2001-05-16 | Merck & Co Inc | Amide derivatives as beta 3 agonists |
| US6465501B2 (en) | 2000-07-17 | 2002-10-15 | Wyeth | Azolidines as β3 adrenergic receptor agonists |
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- 2001-10-04 CN CNA018176267A patent/CN1469876A/zh active Pending
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