AR073990A1 - Derivados de fenilamida y piridilamida - Google Patents

Derivados de fenilamida y piridilamida

Info

Publication number
AR073990A1
AR073990A1 ARP090104130A ARP090104130A AR073990A1 AR 073990 A1 AR073990 A1 AR 073990A1 AR P090104130 A ARP090104130 A AR P090104130A AR P090104130 A ARP090104130 A AR P090104130A AR 073990 A1 AR073990 A1 AR 073990A1
Authority
AR
Argentina
Prior art keywords
alkyl
alkoxy
halogen
group
alkoxycarbonyl
Prior art date
Application number
ARP090104130A
Other languages
English (en)
Original Assignee
Hoffmann La Roche
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
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=41426925&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=AR073990(A1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Hoffmann La Roche filed Critical Hoffmann La Roche
Publication of AR073990A1 publication Critical patent/AR073990A1/es

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    • C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
    • C07D209/04—Indoles; Hydrogenated indoles
    • C07D209/08—Indoles; Hydrogenated indoles with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, directly attached to carbon atoms of the hetero ring
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    • 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
    • A61K31/435—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
    • A61K31/47—Quinolines; Isoquinolines
    • A61K31/4709—Non-condensed quinolines and containing further heterocyclic rings
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    • C07C235/42—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms having carbon atoms of carboxamide groups bound to carbon atoms of six-membered aromatic rings and singly-bound oxygen atoms bound to the same carbon skeleton
    • C07C235/44—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms having carbon atoms of carboxamide groups bound to carbon atoms of six-membered aromatic rings and singly-bound oxygen atoms bound to the same carbon skeleton with carbon atoms of carboxamide groups and singly-bound oxygen atoms bound to carbon atoms of the same non-condensed six-membered aromatic ring
    • C07C235/58—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms having carbon atoms of carboxamide groups bound to carbon atoms of six-membered aromatic rings and singly-bound oxygen atoms bound to the same carbon skeleton with carbon atoms of carboxamide groups and singly-bound oxygen atoms bound to carbon atoms of the same non-condensed six-membered aromatic ring with carbon atoms of carboxamide groups and singly-bound oxygen atoms, bound in ortho-position to carbon atoms of the same non-condensed six-membered aromatic ring
    • C07C235/64—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms having carbon atoms of carboxamide groups bound to carbon atoms of six-membered aromatic rings and singly-bound oxygen atoms bound to the same carbon skeleton with carbon atoms of carboxamide groups and singly-bound oxygen atoms bound to carbon atoms of the same non-condensed six-membered aromatic ring with carbon atoms of carboxamide groups and singly-bound oxygen atoms, bound in ortho-position to carbon atoms of the same non-condensed six-membered aromatic ring having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a six-membered aromatic ring
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    • C07D213/02—Heterocyclic 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
    • C07D213/04—Heterocyclic 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
    • C07D213/60—Heterocyclic 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
    • C07D213/78—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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    • C07D213/02—Heterocyclic 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
    • C07D213/04—Heterocyclic 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
    • C07D213/60—Heterocyclic 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
    • C07D213/78—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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    • C07D215/04—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, directly attached to the ring carbon atoms
    • C07D215/08—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, directly attached to the ring carbon atoms with acylated ring nitrogen atom
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    • C07D215/16—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms 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
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    • C07D241/36—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings condensed with carbocyclic rings or ring systems
    • C07D241/38—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings condensed with carbocyclic rings or ring systems with only hydrogen or carbon atoms directly attached to the ring nitrogen atoms
    • C07D241/40—Benzopyrazines
    • C07D241/42—Benzopyrazines with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to carbon atoms of the hetero ring
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    • C07D265/34—1,4-Oxazines; Hydrogenated 1,4-oxazines condensed with carbocyclic rings
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    • 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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Abstract

Composicion farmacéutica y proceso de preparacion, así como sus sales farmacéuticamente aceptables. Estos compuestos son agonistas del GPBAR1 y pueden utilizarse como medicamentos para el tratamiento de enfermedades, por ejemplo la diabetes de tipo II. Reivindicacion 1: Compuestos de la formula (1) en la que A1 es CR12 o N; A2 es CR13 o N; R1 y R2 se eligen con independencia entre sí entre el grupo formado por hidrogeno alquilo C1-7, halogeno, ciano y alcoxi C1-7; R12 y R13 se eligen con independencia entre sí entre el grupo formado por hidrogeno, alquilo C1-7, halogeno, ciano, alcoxi C1-7, amino y alquilsulfanilo C1-7; R3 se elige entre el grupo formado por hidrogeno, alquilo C1-7, halogeno, alcoxi C1-7, ciano, cicloalquilo C3-7, N-heterociclilo, heteroarilo de cinco eslabones y fenilo; R4 se elige entre el grupo formado por metilo, etilo, isopropilo, difluormetilo, trifluormetilo, ciclopropilo y oxetanilo; o R3 y R4 juntos son -X-(CR14R15)n- y forman parte de un anillo; en el que X se elige entre el grupo formado por -CR16R17-, O, S, C=O y NR18; R14 y R15 se eligen con independencia entre sí entre hidrogeno y alquilo C1-7; R16 y R17 se eligen con independencia entre sí entre el grupo formado por hidrogeno, alquilo C1-7, alcoxi C1-7-carbonilo, heterociclilo sin sustituir y heterociclilo sustituido por uno o dos grupos elegidos entre alquilo C1-7 y halogeno, o R16 y R17 junto con el átomo de C al que están unidos forman un anillo ciclopropilo u oxetanilo o juntos forman un grupo =CH2 o =CF2; R18 se elige entre el grupo formado por hidrogeno, alquilo C1-7, halogeno-alquilo C1-7, cicloalquilo C3-7, cicloalquil C3-7-alquilo C1-7, heterociclilo, heterociclil-alquilo C1-7, heteroarilo, heteroaril-alquilo C1-7, carboxil-alquilo C1-7, alcoxi C1-7-carbonil-alquilo C1-7, alquil C1-7-carboniloxi-alquilo C1-7, fenilo, dicho fenilo está sin sustituir o sustituido por carboxil-alquilo C1-7, o alcoxi C1-7-carbonilo, fenilcarbonilo, cuyo fenilo está sin sustituir o sustituido por carboxil-alquilo C1-7 o alcoxi C1-7-carbonilo y fenilsulfonilo, cuyo fenilo está sin sustituir o sustituido por carboxil-alquilo C1-7, o alcoxi C1-7-carbonilo; o R18 y un R14 juntos son -(CH2)3- y forman parte de un anillo, o R18 junto con un par de R14 y R15 son -CH=CH-CH=, y forman parte de un anillo; y n es el numero 1, 2 o 3; B1 es N o CR19 y B2 es N o CR20, con la condicion de que como máximo uno de B1 y B2 sea N; y R19 y R20 se eligen con independencia entre sí entre el grupo formado por hidrogeno, alquilo C1-7, halogeno, halogeno-alquilo C1-7, alcoxi C1-7, halogeno-alcoxi C1-7, y ciano; R5 y R6 se eligen con independencia entre sí entre el grupo formado por hidrogeno, halogeno, alquilo C1-7, alcoxi C1-7, halogeno-alquilo C1-7, halogeno-alcoxi C1-7 y ciano, y por lo menos uno o, en el caso de que R4 sea metilo o etilo, por lo menos dos de R7, R8, R9, R10 y R11 se eligen entre el grupo formado por alquilo C1-7, halogeno, halogeno-alquilo C1-7, alcoxi C1-7, halogeno-alcoxi C1-7, ciano, carboxilo, alcoxi C1-7-carbonilo, hidroxi-alquilo C1-7, hidroxi-alquenilo C3-7, hidroxi-alquinilo C3-7, carboxil-alquilo C1-7, carboxil-alquenilo C2-7, carboxil-alquinilo C2-7, alcoxi C1-7-carbonil-alquilo C1-7, alcoxi C1-7-carbonil-alquenilo C2-7, alcoxi C1-7-carbonil-alquinilo C2-7, carboxil-alquil C1-7-aminocarbonilo, alcoxi C1-7-carbonil-alquil C1-7-aminocarbonilo, carboxil-alquil C1-7-aminocarbonil-alquilo C1-7, alcoxi C1-7-carbonil-alquil C1-7-aminocarbonil-alquilo C1-7, carboxil-alquil C1-7-alquilamino C1-7-carbonil-alquilo C1-7, alcoxi C1-7-carbonil-alquil C1-7-alquilamino C1-7-carbonil-alquilo C1-7, fenilo, dicho fenilo está sin sustituir o sustituido de una a tres veces por grupos elegidos entre halogeno, alcoxi C1-7, carboxilo o alcoxi C1-7-carbonilo, fenilcarbonilo, cuyo fenilo está sin sustituir o sustituido de una a tres veces por grupos elegidos entre halogeno, alcoxi C1-7, carboxilo o alcoxi C1-7-carbonilo, fenil-alquilo C1-7, cuyo fenilo está sin sustituir o sustituido de una a tres veces por grupos elegidos entre halogeno, alcoxi C1-7, carboxilo y alcoxi C1-7-carbonilo, fenil-alquinilo C2-7, cuyo fenilo está sin sustituir o sustituido de una a tres veces por grupos elegidos entre halogeno, alcoxi C1-7, carboxilo y alcoxi C1-7-carbonilo, y pirrolidinil-carbonil-alquilo C1-7, cuyo pirrolidinilo está sustituido por carboxilo, y los demás de R7, R8, R9, R10 y R11 son hidrogeno; o sus sales farmacéuticamente aceptables.
ARP090104130A 2008-10-29 2009-10-27 Derivados de fenilamida y piridilamida AR073990A1 (es)

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