AR071541A1 - Inhibidores de la polimerasa virica - Google Patents

Inhibidores de la polimerasa virica

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Publication number
AR071541A1
AR071541A1 ARP080103381A ARP080103381A AR071541A1 AR 071541 A1 AR071541 A1 AR 071541A1 AR P080103381 A ARP080103381 A AR P080103381A AR P080103381 A ARP080103381 A AR P080103381A AR 071541 A1 AR071541 A1 AR 071541A1
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alkyl
cycloalkyl
independently selected
het
optionally substituted
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Timothy A Stammers
Pierre L Beaulieu
Martin Poirier
Jean Rancourt
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Boehringer Ingelheim Int
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Publication of AR071541A1 publication Critical patent/AR071541A1/es

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    • C07D333/04Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom
    • C07D333/26Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur 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
    • C07D333/38Carbon 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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    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/12Antivirals
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    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/12Antivirals
    • A61P31/14Antivirals for RNA viruses
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    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
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    • A61P31/12Antivirals
    • A61P31/14Antivirals for RNA viruses
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    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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    • C07D213/04Heterocyclic 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
    • C07D213/60Heterocyclic 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
    • C07D213/78Carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen, e.g. ester or nitrile radicals
    • C07D213/81Amides; Imides
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    • C07D231/00Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
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    • C07D231/10Heterocyclic 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
    • C07D231/14Heterocyclic 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
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    • C07D277/20Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • C07D277/32Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole 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
    • C07D277/56Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen
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    • C07D401/00Heterocyclic 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
    • C07D401/02Heterocyclic 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
    • C07D401/12Heterocyclic 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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    • C07D409/00Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
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    • C07D417/00Heterocyclic 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
    • C07D417/02Heterocyclic 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
    • C07D417/12Heterocyclic 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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    • C07D471/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
    • C07D471/04Ortho-condensed systems

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  • Pulmonology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
  • Thiazole And Isothizaole Compounds (AREA)
  • Pyridine Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Heterocyclic Compounds Containing Sulfur Atoms (AREA)

Abstract

Son utiles como inhibidores de la polimerasa NS5B del virus de la hepatitis C. Reivindicacion 1: Un compuesto caracterizado porque tiene la formula (1): en donde: X se selecciona de O y S; R2 es Het o arilo, opcionalmente sustituido con 1 a 5 sustituyentes R20, en donde R20, en cada caso, se selecciona independientemente de: a) halogeno, ciano o nitro; b) R7, -C(=O)-R7, -C(=O)-O-R7, -O-R7, -S-R7, -SO-R7, -SO2-R7, -alquilen C1-6-R7, -alquilen C1-6-C(=O)-R7, -alquilen C1-6-C(=O)-O-R7, -alquilen C1-6-O-R7, alquilen C1-6-S-R7, alquilen C1-6-SO-R7 o alquilen C1-6-SO2-R7; en donde R7 en cada caso se selecciona independientemente de H, alquilo C1-6, alquenilo C2-6, alquinilo C2-6, halogenoalquilo C1-6, cicloalquilo C3-7, arilo y Het; en donde el alquilo C1-6, alquenilo C2-6, alquinilo C2-6, cicloalquilo C3-7, y alquileno C1-6 están opcionalmente sustituidos con 1 o 2 sustituyentes, cada uno independientemente seleccionado de -OH, -alquilo C1-6, halogeno, -halogenoalquilo C1-6, cicloalquilo C3-7, -O-alquilo C1-6, ciano, COOH, -NH2, -NH-alquilo C1-4, -Nhcicloalquilo C3-7, -N(alquil C1-4)cicIoalquilo 3-7 y -N(alquilo C1-4)2; y en donde cada uno del arilo y Het está opcionalmente sustituido con 1 a 3 sustituyentes, cada uno independientemente seleccionado de i) halogeno, ciano, oxo, tioxo, imino, -OH, -O-alquilo C1-6, -O-halogenoalquilo C1-6, cicloalquilo C3-7, halogenoalquilo C1-6, -C(=O)-alquilo C1-6, -SO2-alquilo C1-6, -C(=O)-NH2, -C(=O)-NH-alquilo C1-4, -C(=O)-N(alquilo C1-4)2, -C(=O)-NH-cicloalquilo C3-7, -C(=O)-N(alquil C1-4)-cicloalquilo C3-7, -NH2, -Nhalquilo C1-4, -N(alquilo C1-4)2, -NH-cicloalquilo C3-7, -N(alquil C1-4)-cicloalquilo C3-7 o -NH-C(=O)-alquilo C1-4; ii) alquilo C1-6 opcionalmente sustituido con -OH, -O-halogenoalquilo C1-6 o -O-alquilo C1-6; y iii) arilo o Het, en donde cada uno del arilo y Het está opcionalmente sustituido con halo o alquilo C1-6; y c) -N(R8)R9, -C(=O)-N(R8)R9, -O-C(=O)-N(R8)R9, -SO2-N(R8)R9, -alquilen C1-6-N(R8)R9, -alquilen C1-6-C(=O)-N(R8)R9, -alquilen C1-6-O-C(=O)-N(R8)R9 o -alquilen C1-6-SO2-N(R8)R9; en donde el alquileno C1-6 está opcionalmente sustituido con 1 o 2 sustituyentes, cada uno independientemente seleccionado de -OH, -alquilo C1-6, halogeno, -halogenoalquilo C1-6, cicloalquilo C3-7, -O-alquilo C1-6, ciano, COOH, -NH2, -NH-alquilo C1-4, -NH-cicloaIquilo C3-7, -N(alquil C1-4)cicloalquiIo C3-7 y -N(alquilo C1-4)2; R8 en cada caso se selecciona independientemente de H, alquilo C1-6 y cicloalquilo C3-7; y R9 en cada caso se selecciona independientemente de R7, -O-alquilo C1-6, -alquilen C1-6-R7, -SO2-R7, -C(=O)-R7, -C(=O)OR7 y -C(=O)N(R8)R7; en donde R7 y R8 son como se han definido antes; o R8 y R9, junto con el N al que están unidos, están unidos para formar un heterociclo de 4 a 7 miembros que además opcionalmente contiene 1 a 3 heteroátomos, cada uno independientemente seleccionado de N, O y S, en donde cada heteroátomo de S, independientemente y cuando sea posible, puede existir en un estado oxidado de modo que está además unido a uno o dos átomos de oxígeno para formar los grupos SO o SO2, en donde el heterociclo está opcionalmente sustituido con 1 a 3 sustituyentes cada uno independientemente seleccionado de alquilo C1-6, halogenoalquilo C1-6, halogeno, oxo, -OH, SH, -O-alquilo C1-6, S-alquilo C1-6, cicloalquilo C3-7, -NH2, -NH-alquilo C1-6, -N(alquilo C1-6)2, -NH-cicloalquilo C3-7, -N(alquil C1-4)cicloalquilo C3-7, -C(=O)-alquilo C1-6 y -NHC(=O)-alquilo C1-6; R3 se selecciona de H, halogeno, CN, alquilo C1-4, -OH, -O-alquilo C1-4, -S-alquilo C1-4, -NH, -NH-alquilo C1-4, -NH-cicloalquilo C3-7, -N(alquil C1-4)cicloalquilo C3-7 y N(alquilo C1-4)2; R5 es H, alquilo C1-6, cicloalquilo C3-7, cicloalquil C3-7-alquilo C1-6- o Het; el alquilo C1-6 y el Het están cada uno opcionalmente sustituido con 1 a 4 sustituyentes, cada uno independientemente seleccionado de alquilo C1-6, halogenoalquilo C1-6, cicloalquilo C3-7, Het, -OH, -COOH, -C(=O)-alquilo C1-6, -C(=O)-O-alquilo C1-6, -SO2-alquilo C1-6) y -C(=O)-N(R51)R52; en donde R51 es H, alquilo C1-6 o cicloalquilo C3-7; y R52 es H, alquilo C1-6, cicloalquilo C3-7, arilo, Het, aril-alquilo C1-3- o Het-alquilo C1-3-; en donde cada uno de los alquilo C1-6, cicloalquilo C3-7, arilo, Het, aril-alquilo C1-3- y Het-alquilo C1-3- está opcionalmente sustituido con 1 a 3 sustituyentes, cada uno independientemente seleccionado de alquilo C1-6, halogenoalquilo C1-6, halogeno, oxo, -OH, -O-aIquiIo C1-6, -NH2, -NH-alquilo C1-6), -N(alquilo C1-6)2, -NH-cicloalquilo C3-7, -N(alquil C1-4)cicloalquilo C3-7, -C(=O)alquilo C1-6 y -NHC(=O)-alquilo C1-6; en donde el alquilo C1-6 está opcionalmente sustituido con OH; o R51 y R52, junto con el N al que están unidos, están unidos para formar un heterociclo de 4 a 7 miembros que además opcionalmente contiene 1 a 3 heteroátomos, cada uno independientemente seleccionado de N, O y S, en donde cada heteroátomo de S, independientemente y cuando sea posible, puede existir en un estado oxidado de modo que está además unido a uno o dos átomos de oxígeno para formar los grupos SO o SO2; en donde el heterociclo está opcionalmente sustituido con 1 a 3 sustituyentes cada uno independientemente seleccionado de alquilo C1-6, halogenoalquilo C1-6, halogeno, oxo, -OH, -O-alquilo C1-6, -NH2, -NH-alquilo C1-6, -N(alquilo C1-6)2, -Nhcicloalquilo C3-7), -N(alquil C1-4)cicloalquilo C3-7, -C(=O)-alquilo C1-6 y -NHC(=O)-alquilo C1-6; en donde el alquilo C1-6 está opcionalmente sustituido con OH; R6 es Het; que está opcionalmente sustituido con 1 a 5 sustituyentes, cada uno independientemente seleccionado de halogeno, alquilo C1-6, halogenoalquilo C1-6, cicloalquilo C3-7, -OH, -SH, -O-alquilo C1-4, -S-alquilo C1-4 y -N(R8)R9; en donde R8 y R9 son como se ha definido antes; y Het es un heterociclo de 4 a 7 miembros saturado, insaturado o aromático que tiene 1 a 4 heteroátomos, cada uno independientemente seleccionado de O, N y S, o un heteropoliciclo de 7 a 14 miembros saturado, insaturado o aromático que tiene, donde sea posible, 1 a 5 heteroátomos, cada uno independientemente seleccionado de O, N y S; en donde cada heteroátomo de N, independientemente y cuando sea posible, puede existir en un estado oxidado de modo que además está unido a un átomo de oxígeno para formar un grupo N-oxido y en donde cada heteroátomo de S, independientemente y cuando sea posible, existe en un estado oxidado de modo que está además unido a uno o dos átomos de oxigeno para formar los grupos SO o SO2 o una de sus sales o ésteres; con la salvedad que cuando X es O, R2 es fenilo, R3 es H y R5 es H, entonces R6 no es como en formula 2.
ARP080103381A 2007-08-03 2008-08-01 Inhibidores de la polimerasa virica AR071541A1 (es)

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CA2693495A1 (en) * 2007-08-03 2009-02-12 Boehringer Ingelheim International Gmbh Viral polymerase inhibitors
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US8410091B1 (en) 2009-09-11 2013-04-02 Boehringer Ingelheim International Gmbh Process for preparation of substituted 2-amino-5-(5-(heterocyclemethyl)pyridin-2-yloxy)benzoic acid
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CN103601671B (zh) * 2013-10-22 2016-08-17 上海泰坦科技股份有限公司 碘代三氟甲基吡啶的制备方法

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