AR031230A1 - Agente terapeutico para la hepatitis c el cual comprende un compuesto de anillo fundido, dicho compuesto de anillo fundido, composicion farmaceutica, inhibidor y agente que lo comprenden, envase comercial que comprende dicha composicion, compuesto de benzimidazol y compuesto de tiazol - Google Patents

Agente terapeutico para la hepatitis c el cual comprende un compuesto de anillo fundido, dicho compuesto de anillo fundido, composicion farmaceutica, inhibidor y agente que lo comprenden, envase comercial que comprende dicha composicion, compuesto de benzimidazol y compuesto de tiazol

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Publication number
AR031230A1
AR031230A1 ARP000106947A ARP000106947A AR031230A1 AR 031230 A1 AR031230 A1 AR 031230A1 AR P000106947 A ARP000106947 A AR P000106947A AR P000106947 A ARP000106947 A AR P000106947A AR 031230 A1 AR031230 A1 AR 031230A1
Authority
AR
Argentina
Prior art keywords
optionally substituted
alkyl
group
substituent
atom
Prior art date
Application number
ARP000106947A
Other languages
English (en)
Inventor
Seizo Hashimoto
K Mizutani
Masanori Yoshida
Original Assignee
Japan Tobacco Inc
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Priority claimed from JP2000391904A external-priority patent/JP2001247550A/ja
Application filed by Japan Tobacco Inc filed Critical Japan Tobacco Inc
Publication of AR031230A1 publication Critical patent/AR031230A1/es

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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
    • C07D231/12—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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    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
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    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
    • A61K31/403—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil condensed with carbocyclic rings, e.g. carbazole
    • A61K31/404—Indoles, e.g. pindolol
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    • A61K31/33—Heterocyclic compounds
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    • 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
    • A61K31/4184—1,3-Diazoles condensed with carbocyclic rings, e.g. benzimidazoles
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
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    • A61K31/33—Heterocyclic compounds
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    • 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
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    • A61K31/425—Thiazoles
    • A61K31/427—Thiazoles not condensed and containing further heterocyclic rings
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    • A61K31/4353—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems
    • A61K31/437—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a five-membered ring having nitrogen as a ring hetero atom, e.g. indolizine, beta-carboline
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    • A61K31/4439—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. omeprazole
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    • A61K31/445—Non condensed piperidines, e.g. piperocaine
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    • A61K31/47—Quinolines; Isoquinolines
    • A61K31/4738—Quinolines; Isoquinolines ortho- or peri-condensed with heterocyclic ring systems
    • A61K31/4745—Quinolines; Isoquinolines ortho- or peri-condensed with heterocyclic ring systems condensed with ring systems having nitrogen as a ring hetero atom, e.g. phenantrolines
    • A—HUMAN NECESSITIES
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    • A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
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    • A—HUMAN NECESSITIES
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    • A61K31/498—Pyrazines or piperazines ortho- and peri-condensed with carbocyclic ring systems, e.g. quinoxaline, phenazine
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    • A61K31/503—Pyridazines; Hydrogenated pyridazines spiro-condensed
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    • A61K31/7052—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides
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    • A61K9/2013—Organic compounds, e.g. phospholipids, fats
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    • 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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Abstract

Un agente terapéutico para la hepatitis C, que comprende un compuesto de anillo fundido de la formula [1] o una sal farmacéuticamente aceptable del mismo como un ingrediente activo, donde: una línea punteada es un enlace simple o un enlace doble; G1 es C(-R1) o un átomo de nitrogeno; G2 es C(-R2) o un átomo de nitrogeno; G3 es C(-R3) o un átomo de nitrogeno; G4 es C(-R4) o un átomo de nitrogeno; G5, G6, G8 y G9 son, cada uno independientemente, un átomo de carbono o un átomo de nitrogeno; G7 es C(-R7), un átomo de oxígeno, un átomo de azufre, o un átomo de nitrogeno opcionalmente sustituido por R8; donde R1, R2, R3 y R4 son cada uno, independientemente, (1) un átomo de hidrogeno, (2) alcanoilo C1-6, (3) carboxilo, (4) ciano, (5) nitro, (6) alquilo C1-6 opcionalmente sustituido por 1 a 3 sustituyente(s) seleccionado(s) del siguiente grupo A, grupo A: un átomo de halogeno, un grupo hidroxilo, carboxilo, amino, alcoxi C1-6, alcoxicarbonilo C1-6 y alquilamino C1-6, (7) -COORa1 donde Ra1 es alquilo C1-6 opcionalmente sustituido (tal como se definio con anterioridad) o aril C6-14-alquilo C1-6 opcionalmente sustituido por 1 a 5 sustituyente(s) seleccionado(s) del siguiente grupo B, grupo B: un átomo de halogeno, ciano, nitro, alquilo C1-6, alquilo C1-6 halogenado, alcanoilo C1-6, -(CH2)r-COORb1, -(CH2)r-CONRb1Rb2, -(CH2)r-NRb1Rb2, -(CH2)r-NRb1-CORb2, -(CH2)r-NHSO2Rb1, -(CH2)rORb1, -(CH2)r-SRb1, -(CH2)r-SO2Rb1 y -(CH2)r-SO2NRb1Rb2, donde Rb1 y Rb2 son cada uno, independientemente, un átomo de hidrogeno o alquilo C1-6 y r es 0 o un numero entero de 1 a 6, (8) -CONRa2Ra3 donde Ra2 y Ra3 son cada uno, independientemente, un átomo de hidrogeno, alcoxi C1-6 o alquilo C1-6 opcionalmente sustituido (tal como se definio con anterioridad), (9) -C(=NRa4)NH2 donde Ra4 es un átomo de hidrogeno o un grupo hidroxilo, (10) -NHRa5 donde Ra5 es un átomo de hidrogeno, alcanoilo C1-6 o alquilsulfonilo C1-6, (11) -ORa6 donde Ra6 es un átomo de hidrogeno o alquilo C1-6 opcionalmente sustituido (tal como se definio con anterioridad), (12) -SO2Ra7 donde Ra7 es un grupo hidroxilo, amino, alquilo C1-6 o alquilamino C1-6, o (13) -P(=O)(ORa31)2 donde Ra31es un átomo de hidrogeno, alquilo C1-6 opcionalmente sustituido (tal como se definio con anterioridad) o aril C6-14-alquilo C1-6 opcionalmente sustituido por 1 a 5 sustituyente(s) seleccionado(s) del grupo anterior B; y R7 y R8 son cada uno un átomo de hidrogeno o alquilo C1-6 opcionalmente sustituido (tal como se definio con anterioridad); el anillo Cy es (1) cicloalquilo C3-8 opcionalmente sustituido por 1 a 5 sustituyente(s) seleccionado(s) del siguiente grupo C, grupo C: un grupo hidroxilo, un átomo de halogeno, alquilo C1-6 y alcoxi C1-6, (2) cicloalquenilo C3-8 opcionalmente sustituido por 1 a 5 sustituyente(s) seleccionado(s) del grupo anterior C, o (3) un resto de formulas [2], [3] o [4] donde u y v son cada uno, independientemente, un numero entero de 1 a 3; el anillo A es (1) arilo C6-14, (2) cicloalquilo C3-8, (3) cicloalquenilo C3-8 o (4) un grupo heterocíclico que tiene 1 a 4 heteroátomo(s) seleccionado(s) de un átomo de oxígeno, un átomo de nitrogeno y un átomo de azufre; R5 y R6 son cada uno, independientemente, (1) un átomo de hidrogeno, (2) un átomo de halogeno, (3) alquilo C1-6 opcionalmente sustituido (tal como se definio con anterioridad) o (4) -ORa8 donde Ra8 es un átomo de hidrogeno, alquilo C1-6 o aril C6-14-alquilo C1-6; y X es (1) un átomo de hidrogeno, (2) un átomo de halogeno, (3) ciano, (4) nitro, (5) amino, alcanoilamino C1-6, (6) alquilsulfonilo C1-6, (7) alquilo C1-6 opcionalmente sustituido (tal como se definio con anterioridad), (8) alquenilo C2-6 opcionalmente sustituido por 1 a 3 sustituyente(s) seleccionado(s) del grupo anterior A, (9) -COORa9 donde Ra9 es un átomo de hidrogeno o alquilo C1-6, (10) -CONH-(CH2)l-Ra10 donde Ra10 es alquilo C1-6 opcionalmente sustituido (tal como se definio con anterioridad), alcoxicarbonilo C1-6 o alcanoilamino C1-6 y l es 0 o un numero entero de 1 a 6, (11) -ORa11 donde Ra11 es un átomo de hidrogeno o alquilo C1-6 opcionalmente sustituido (tal como se definio con anterioridad), o (12) un compuesto de formula [5] donde el anillo B es (1') arilo C6-14, (2') cicloalquilo C3-8 o (3') un grupo heterocíclico (tal como se definio con anterioridad); cada Z es, independientemente, (1') un grupo seleccionado del siguiente grupo D, (2') arilo C6-14 opcionalmente sustituido por 1 a 5 sustituyente(s) seleccionado(s) del siguiente grupo D, (3') cicloalquilo C3-8 opcionalmente sustituido por 1 a 5 sustituyente(s) seleccionado(s) del siguiente grupo D, (4') aril C6-14-alquilo C1-6 opcionalmente sustituido por 1 a 5 sustituyente(s) seleccionado(s) del siguiente grupo D, o (5') un grupo heterocíclico opcionalmente sustituido por 1 a 5 sustituyente(s) seleccionado(s) del siguiente grupo D donde el grupo heterocíclico tiene 1 a 4 heteroátomo(s) seleccionado(s) de un átomo de oxígeno, un átomo de nitrogeno y un átomo de azufre; grupo D: (a) un átomo de hidrogeno, (b) un átomo de halogeno, (c) ciano, (d) nitro, (e) alquilo C1-6 opcionalmente sustituido (tal como se definio con anterioridad), (f) -(CH2)t-CORa18 (de ahora en adelante, cada t significa independientemente, 0 o un numero entero de 1 a 6), donde Ra18 es (1'') alquilo C1-6 opcionalmente sustituido (tal como se definio con anterioridad), (2'') arilo C6-14 opcionalmente sustituido por 1 a 5 sustituyente(s) seleccionado(s) del grupo anterior B o (3'') un grupo heterocíclico opcionalmente sustituido por 1 a 5 sustituyente(s) seleccionado(s) del grupo anterior B donde el grupo heterocíclico tiene 1 a 4 heteroátomo(s) seleccionado(s) de un átomo de oxígeno, un átomo de nitrogeno y un átomo de azufre, (g) -(CH2)t-COORa19 donde Ra19 es un átomo de hidrogeno, alquilo C1-6 opcionalmente sustituido (tal como se definio con anterioridad) o aril C6-14-alquilo C1-6 opcionalmente sustituido por 1 a 5 sustituyente(s) seleccionado(s) del grupo anterior B, (h) -(CH2)t-CONRa27Ra28 donde Ra27 y Ra28 son cada uno, independientemente, (1'') un átomo de hidrogeno, (2'') alquilo C1-6 opcionalmente sustituido (tal como se definio con anterioridad), (3'') arilo C6-14 opcionalmente sustituido por 1 a 5 sustituyente(s) seleccionado(s) del grupo anterior B, (4'') aril C6-14-alquilo C1-6 opcionalmente sustituido por 1 a 5 sustituyente(s) seleccionado(s) del grupo anterior B, (5'') un grupo heterocíclico opcionalmente sustituido por 1 a 5 sustituyente(s) seleccionado(s) del grupo anterior B, (6'') alquilo C1-6 heterocíclico opcionalmente sustituido por 1 a 5 sustituyente(s) seleccionado(s) del grupo anterior B, donde el alquilo C1-6 heterocíclico es alquilo C1-6 sustituido por un grupo heterocíclico opcionalmente sustituido por 1 a 5 sustituyente(s) seleccionado(s) del grupo anterior B, tal como se definio con anterioridad, (7'') cicloalquilo C3-8 opcionalmente sustituido por 1 a 5 sustituyente(s) seleccionado(s) del grupo anterior B, o (8'') cicloalquil C3-8 alquilo C1-6 opcionalmente sustituido por 1 a 5 sustituyente(s) seleccionado(s) del grupo anterior B, (i) -(CH2)t-C(=NRa33)NH2 donde Ra33 es un átomo de hidrogeno o alquilo C1-6, (j) -(CH2)t-ORa20 donde Ra20 es (1'') un átomo de hidrogeno, (2'') alquilo C1-6 opcionalmente sustituido (tal como se definio con anterioridad), (3'') alquenilo C2-6 opcionalmente sustituido (tal como se definio con anterioridad), (4'') alquinilo C2-6 opcionalmente sustituido por 1 a 3 sustituyente(s) seleccionado(s) del grupo anterior A, (5'') arilo C6-14 opcionalmente sustituido por 1 a 5 sustituyente(s) seleccionado(s) del grupo anterior B, (6'') aril C6-14-alquilo C1-6 opcionalmente sustituido por 1 a 5 sustituyente(s) seleccionado(s) del grupo anterior B, (7'') un grupo heterocíclico opcionalmente sustituido por 1 a 5 sustituyente(s) seleccionado(s) del grupo anterior B, (8'') alquilo C1-6 heterocíclico opcionalmente sustituido por 1 a 5 sustituyente(s) seleccionado(s) del grupo anterior B, (9'') cicloalquilo C3-8 opcionalmente sustituido por 1 a 5 sustituyente(s) seleccionado(s) del grupo anterior B, o (10'') cicloalquil C3-8-alquilo C1-6 opcionalmente sustituido por 1 a 5 sustituyente(s) seleccionado(s) del grupo anterior B, (k) -(CH2)t-O-(CH2)p-CORa21 donde Ra21 es alquilamino C1-6 o un grupo heterocíclico opcionalmente sustituido por 1 a 5 sustituyente(s) seleccionado(s) del grupo anterior B, y p es 0 o un numero entero de 1 a 6, (l) -(CH2)t-NRa22Ra23 donde Ra22 y Ra23 son cada uno, independientemente, (1'') un átomo de hidrogeno, (2'') alquilo C1-6 opcionalmente sustituido (tal como se definio con anterioridad), (3'') arilo C6-14 opcionalmente sustituido por 1 a 5 sustituyente(s) seleccionado(s) del grupo anterior B, (4'') aril C6-14-alquilo C1-6 opcionalmente sustituido por 1 a 5 sustituyente(s) seleccionado(s) del grupo anterior B o (5'') alquilo C1-6 heterocíclico opcionalmente sustituido por 1 a 5 sustituyente(s) seleccionado(s) del grupo anterior B, (m) -(CH2)t-NRa29CO-Ra24 donde Ra29 es un átomo de hidrogeno, alquilo C1-6 o alcanoilo C1-6 y Ra24 es alquilo C1-6 opcionalmente sustituido (tal como se definio con anterioridad), arilo C6-14 opcionalmente sustituido por 1 a 5 sustituyente(s) seleccionado(s) del grupo anterior B o un grupo heterocíclico opcionalmente sustituido por 1 a 5 sustituyente(s) seleccionado(s) del grupo anterior B, (n) -(CH2)t-NHSO2-Ra25 donde Ra25 es un átomo de hidrogeno, alquilo C1-6 opcionalmente sustituido (tal como se definio con anterioridad), arilo C6-14 opcionalmente sustituido por 1 a 5 sustituyente(s) seleccionado(s) del grupo anterior B o un grupo heterocíclico opcionalmente sustituido por 1 a 5 sustituyente(s) seleccionado(s) del grupo anterior B, (o) -(CH2)t-S(O)q-Ra25 donde Ra25 es tal como se definio con anterioridad y q es 0, 1 o 2, y (p) -(CH2)t-SO2-NHRa26 donde Ra26 es un átomo de hidrogeno, alquilo C1-6 opcionalmente sustituido (tal como se definio con anterioridad), arilo C6-14 opcionalmente sustituido por 1 a 5 sustituyente(s) sel
ARP000106947A 1999-12-27 2000-12-27 Agente terapeutico para la hepatitis c el cual comprende un compuesto de anillo fundido, dicho compuesto de anillo fundido, composicion farmaceutica, inhibidor y agente que lo comprenden, envase comercial que comprende dicha composicion, compuesto de benzimidazol y compuesto de tiazol AR031230A1 (es)

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