AR038172A1 - Compuesto de ciclohexano y ciclohexeno, su uso para preparar una composicion farmaceutica, dicha composicion farmaceutica, procedimiento para preparar el compuesto y compuestos intermediarios en dicho procedimiento - Google Patents
Compuesto de ciclohexano y ciclohexeno, su uso para preparar una composicion farmaceutica, dicha composicion farmaceutica, procedimiento para preparar el compuesto y compuestos intermediarios en dicho procedimientoInfo
- Publication number
- AR038172A1 AR038172A1 ARP020101914A ARP020101914A AR038172A1 AR 038172 A1 AR038172 A1 AR 038172A1 AR P020101914 A ARP020101914 A AR P020101914A AR P020101914 A ARP020101914 A AR P020101914A AR 038172 A1 AR038172 A1 AR 038172A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkyl
- alkenyl
- optionally substituted
- sulfonyl
- hydroxy
- Prior art date
Links
- 150000001875 compounds Chemical class 0.000 title abstract 4
- 239000008194 pharmaceutical composition Substances 0.000 title 2
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 abstract 30
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 23
- 125000006656 (C2-C4) alkenyl group Chemical group 0.000 abstract 20
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 17
- -1 amino, piperidyl Chemical group 0.000 abstract 17
- 125000003277 amino group Chemical group 0.000 abstract 13
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 13
- 125000000217 alkyl group Chemical group 0.000 abstract 10
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 abstract 10
- 125000004916 (C1-C6) alkylcarbonyl group Chemical group 0.000 abstract 9
- 125000004454 (C1-C6) alkoxycarbonyl group Chemical group 0.000 abstract 8
- 125000004739 (C1-C6) alkylsulfonyl group Chemical group 0.000 abstract 8
- 125000004453 alkoxycarbonyl group Chemical group 0.000 abstract 7
- 125000003118 aryl group Chemical group 0.000 abstract 7
- 125000006574 non-aromatic ring group Chemical group 0.000 abstract 7
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 7
- 125000003342 alkenyl group Chemical group 0.000 abstract 6
- 125000004448 alkyl carbonyl group Chemical group 0.000 abstract 6
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 abstract 5
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 abstract 5
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 abstract 5
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 abstract 4
- 101000585507 Solanum tuberosum Cytochrome b-c1 complex subunit 7 Proteins 0.000 abstract 4
- 125000004423 acyloxy group Chemical group 0.000 abstract 4
- 125000004429 atom Chemical group 0.000 abstract 4
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 abstract 4
- 229910052760 oxygen Inorganic materials 0.000 abstract 4
- 229910052717 sulfur Inorganic materials 0.000 abstract 4
- 125000004769 (C1-C4) alkylsulfonyl group Chemical group 0.000 abstract 3
- 125000006577 C1-C6 hydroxyalkyl group Chemical group 0.000 abstract 3
- 101150020251 NR13 gene Proteins 0.000 abstract 3
- 125000002252 acyl group Chemical group 0.000 abstract 3
- 125000005225 alkynyloxycarbonyl group Chemical group 0.000 abstract 3
- 125000005097 aminocarbonylalkyl group Chemical group 0.000 abstract 3
- 125000004397 aminosulfonyl group Chemical group NS(=O)(=O)* 0.000 abstract 3
- 229910052736 halogen Inorganic materials 0.000 abstract 3
- 150000002367 halogens Chemical group 0.000 abstract 3
- 125000001424 substituent group Chemical group 0.000 abstract 3
- 125000001889 triflyl group Chemical group FC(F)(F)S(*)(=O)=O 0.000 abstract 3
- 125000001414 1,2,4-triazol-5-yl group Chemical group [H]N1N=C([H])N=C1[*] 0.000 abstract 2
- 125000005035 acylthio group Chemical group 0.000 abstract 2
- 125000003545 alkoxy group Chemical group 0.000 abstract 2
- 125000000304 alkynyl group Chemical group 0.000 abstract 2
- 125000003739 carbamimidoyl group Chemical group C(N)(=N)* 0.000 abstract 2
- 229910052799 carbon Inorganic materials 0.000 abstract 2
- HGCIXCUEYOPUTN-UHFFFAOYSA-N cyclohexene Chemical compound C1CCC=CC1 HGCIXCUEYOPUTN-UHFFFAOYSA-N 0.000 abstract 2
- 125000002485 formyl group Chemical group [H]C(*)=O 0.000 abstract 2
- 125000002795 guanidino group Chemical group C(N)(=N)N* 0.000 abstract 2
- 125000005843 halogen group Chemical group 0.000 abstract 2
- 125000000623 heterocyclic group Chemical group 0.000 abstract 2
- 125000005647 linker group Chemical group 0.000 abstract 2
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 2
- 229910052757 nitrogen Inorganic materials 0.000 abstract 2
- 125000005740 oxycarbonyl group Chemical group [*:1]OC([*:2])=O 0.000 abstract 2
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 abstract 1
- 125000002853 C1-C4 hydroxyalkyl group Chemical group 0.000 abstract 1
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 abstract 1
- 241000790917 Dioxys <bee> Species 0.000 abstract 1
- 239000008896 Opium Substances 0.000 abstract 1
- 125000004442 acylamino group Chemical group 0.000 abstract 1
- 125000005196 alkyl carbonyloxy group Chemical group 0.000 abstract 1
- 125000002947 alkylene group Chemical group 0.000 abstract 1
- 125000005087 alkynylcarbonyl group Chemical group 0.000 abstract 1
- 125000003710 aryl alkyl group Chemical group 0.000 abstract 1
- 125000005129 aryl carbonyl group Chemical group 0.000 abstract 1
- 125000004391 aryl sulfonyl group Chemical group 0.000 abstract 1
- 125000005361 aryl sulfoxide group Chemical group 0.000 abstract 1
- 125000005110 aryl thio group Chemical group 0.000 abstract 1
- 125000004104 aryloxy group Chemical group 0.000 abstract 1
- 125000000852 azido group Chemical group *N=[N+]=[N-] 0.000 abstract 1
- 125000002619 bicyclic group Chemical group 0.000 abstract 1
- 125000002837 carbocyclic group Chemical group 0.000 abstract 1
- 125000004432 carbon atom Chemical group C* 0.000 abstract 1
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 1
- 125000004966 cyanoalkyl group Chemical group 0.000 abstract 1
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 1
- 150000002148 esters Chemical class 0.000 abstract 1
- 125000004438 haloalkoxy group Chemical group 0.000 abstract 1
- 125000001188 haloalkyl group Chemical group 0.000 abstract 1
- 125000005223 heteroarylcarbonyl group Chemical group 0.000 abstract 1
- 125000005842 heteroatom Chemical group 0.000 abstract 1
- 125000005844 heterocyclyloxy group Chemical group 0.000 abstract 1
- 229910052739 hydrogen Inorganic materials 0.000 abstract 1
- 125000002768 hydroxyalkyl group Chemical group 0.000 abstract 1
- 229960001027 opium Drugs 0.000 abstract 1
- 125000004043 oxo group Chemical group O=* 0.000 abstract 1
- 125000005936 piperidyl group Chemical group 0.000 abstract 1
- RAHZWNYVWXNFOC-UHFFFAOYSA-N sulfur dioxide Inorganic materials O=S=O RAHZWNYVWXNFOC-UHFFFAOYSA-N 0.000 abstract 1
- 125000003718 tetrahydrofuranyl group Chemical group 0.000 abstract 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 abstract 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—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
- C07D401/02—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
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/04—Antibacterial agents
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic 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
- C07D471/02—Heterocyclic 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
- C07D471/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D491/00—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
- C07D491/02—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
- C07D491/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D513/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00
- C07D513/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains two hetero rings
- C07D513/04—Ortho-condensed systems
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmacology & Pharmacy (AREA)
- Communicable Diseases (AREA)
- Animal Behavior & Ethology (AREA)
- Oncology (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Plural Heterocyclic Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Compuesto de ciclohexano y ciclohexeno de la fórmula (1) o un derivado del mismo farmacéuticamente aceptable, en donde: uno de Z1, Z2, Z3, Z4 y Z5 es N, uno es CR1a y el resto son CH, o uno de Z1. Z2, Z3, Z4 y Z5 es CR1a y el resto son CH, Rv y Rw son H o Rv y Rw juntos son un enlace; R1 y R1a se seleccionan independientemente del grupo formado por H, hidroxi, alcoxi C1-6 opcionalmente sustituido con alcoxi C1-6, amino, piperidilo, guanidino o amidino cualquiera de los cuales está opcionalmente N-sustituido con uno o dos grupos alquilo C1-6, acilo o alquil(C1-6)sulfonilo, CONH2, hidroxi, alquil(C1-6)tio, heterocicliltio, heterocicliloxi, ariltio, ariloxi, aciltio, aciloxi o alquil(C1-6)sulfoniloxi; alquilo(C1-6) sustituido con alcoxi C1-6; halógeno; alquilo C1-6, alquil(C1-6)tio; trifluorometilo, nitro, azido, acilo, aciloxi, aciltio, alquil(C1-6)sulfonilo, alquil(C1-6)sulfóxido; arilsulfonilo; arilsulfóxido o un grupo amino; piperidilo, guanidino o amidino opcionalmente N-sustituido con uno o dos grupos alquilo (C1-6), acilo o alquil(C1-6)sulfonilo, o cuando Z1 es CR1a, R1 y R1a juntos pueden representar alquilen(C1-2)dioxi, o cuando Z5 es CR1a, R1a puede ser en vez de ciano, hidroximetil o carboxi, con la condición de que, cuando Z1, Z2, Z3, Z4 y Z5 son CR1a o CH, entonces R1 no sea H; R2 es H, o alquilo C1-4 o alquenilo C2-4 opcionalmente sustituido con 1 a 3 grupos seleccionados entre : amino opcionalmente sustituido con 1 o 2 alquilo C1-4 grupos; carboxi; alcoxi(C1-4)carbonilo; alquil(C1-4)carbonilo; alquenil(C2-4)oxicarbonilo; alquenil(C2-4)carbonilo; aminocarbonilo en donde el grupo amino está opcionalmente sustituido con hidroxi, alquilo C1-4, hidroxialquilo C1-4, aminocarbonilo-alquilo C1-4, alquenilo C2-4, alquil (C1-4)sulfonilo, trifluorometilsulfonilo, alquenil(C2-4)sulfonilo, alcoxi(C1-4)carbonilo, alquil(C1-4)carbonilo, alquenil(C2-4)oxicarbonilo o alquenil(C2-4)carbonilo; ciano, tetrazolilo; 2-oxo-oxazolidinilo opcionalmente sustituido con R10; 3-hidroxi-3-ciclobuteno-1,2-diona-4-ilo; 2,4-tioazolidinadiona-5-ilo; tetrazol-5-ilaminocarbonilo; 1,2,4-triazol-5-ilo opcionalmente sustituido con R10; 5-oxo-1,2,4-oxadiazol-3-ilo; halógeno; alquil(C1-4)tio; trifluorometilo, hidroxi opcionalmente sustituido con alquilo C1-4, alquenilo C2-4, alcoxi(C1-4)carbonilo, alquil(C1-4)carbonilo, alquenil(C2-4)oxicarbonilo, alquenil(C2-4)carbonilo; oxo; alquil(C1-4)sulfonilo; alquenil(C2-4)sulfonilo; o aminosulfonilo en donde el grupo amino está opcionalmente sustituido con alquilo C1-4 o alquenilo C2-4; R3 es H, o cuando Rv y Rw son un enlace, R3 está en posición 3 o 4 y cuando Rv y Rw no son un enlace, R3 está en posición 1, 2, 3 o 4 y R3 es: carboxi; alcoxi(C1-6)carbonilo; aminocarbonilo en donde el grupo amino está opcionalmente sustituido con hidroxi, alquilo C1-6, hidroxialquilo C1-6, aminocarbonil alquilo C1-6, alquenilo C2-6, alquil(C1-6)sulfonilo, trifuorometilsulfonilo, alquenil(C2-6)sulfonilo, alcoxi(C1-6)carbonilo, alquil(C1-6)carbonilo, alquenil(C2-6)oxicarbonilo o alquenil(C2-6)carbonilo y además opcionalmente sustituido con alquilo C1-6, hidroxialquilo C1-6, aminocarbonilalquilo C1-6 o alquenilo C2-6; ciano, tetrazolilo; 2-oxo-oxazolidinilo opcionalmente sustituido con R10; 3-hidroxi-3-ciclobuteno-1,2-diona-4-ilo; 2,4-tiazolidinadiona-5-ilo; tetrazol-5-ilaminocarbonilo; 1,2,4-triazol-5-ilo opcionalmente sustituido con R10; o 5-oxo-1,2,4-oxadiazol-3-ilo; o alquilo C1-4 o etenilo opcionalmente sustituido con cualquiera de los grupos enunciados anteriormente para R3 y/o 0 a 2 grupos R12 independientemente seleccionados entre halógeno, alquil(C1-6)tio; trifluorometilo; alcoxi(C1-6)carbonilo, alquil(C1-6)carbonilo; alquenil(C2-6)oxicarbonilo; alquenil(C2-6)carbonilo; hidroxi opcionalmente sustituido con alquilo C1-6; alquenilo C2-6, alcoxi(C1-6)carbonilo, alquil(C1-6)carbonilo, alquenil(C2-6)oxicarbonilo, alquenil(C2-6)carbonilo o aminocarbonilo en donde el grupo amino está opcionalmente sustituido con alquilo C1-6; alquenilo C2-6, alquil(C1-6)carbonilo o alquenil(C2-6)carbonilo; amino opcionalmente mono- o di-sustituido con alcoxi(C1-6)carbonilo, alquil(C1-6)carbonilo, alquenil(C2-6)oxicarbonilo, alquenil(C2-6)carbonilo, alquilo C1-6, alquenilo C2-6, alquil(C1-6)sulfonilo, alquenil(C2-6)sulfonilo o aminocarbonilo en donde el grupo amino está opcionalmente sustituido con alquilo C1-6 o alquenilo C2-6; aminocarbonilo en donde el grupo amino está opcionalmente sustituido con alquilo C1-6, hidroxialquilo C1-6, aminocarbonilalquilo C1-6, alquenilo C2-6, alcoxi (C1-6)carbonilo, alquil(C1-6)carbonilo, alquenil(C2-6)oxicarbonilo o alquenil(C2-6)carbonilo y además opcionalmente sustituido con alquilo C1-6, hidroxialquilo C1-6, aminocarbonilalquilo C1-6 o alquenilo C2-6; oxo, alquil(C1-6)sulfonilo, alquenil(C2-6)sulfonilo; o aminosulfonilo en donde el grupo amino está opcionalmente sustituido con alquilo C1-6 o alquenilo C2-6; o hidroxi opcionalmente sustituido con alquilo C1-6, alquenilo C2-6, alcoxi(C1-6)carbonilo, alquil(C1-6)carbonilo, alquenil(C2-6)oxicarbonilo, alquenil(C2-6)carbonilo o aminocarbonilo en donde el grupo amino está opcionalmente sustituido con alquilo C1-6, alquenilo C2-6, alquil(C1-6)carbonilo o alquenil(C2-6)carbonilo; o amino opcionalmente mono- o di-sustituido con alcoxi(C1-6)carbonilo, alquil(C1-6)carbonilo, alquenil(C2-6)oxicarbonilo, alquenil(C2-6)carbonilo, alquilo C1-6, alquenilo C2-6, alquil(C1-6)sulfonilo, alquenil(C2-6)sulfonilo o aminocarbonilo en donde el grupo amino está opcionalmente sustituido con alquilo C1-6 o alquenilo C2-6, con la condición de que, cuando R3 está en posición 4 no sea hidroxilo o amino opcionalmente sustituido; además, cuando R3 está disustituido con un sustituyente que contiene hidroxi o amino y un sustituyente que contiene carboxi, estos juntos opcionalmente pueden formar un enlace de tipo éster o amida cíclico, respectivamente; R10 se selecciona entre alquilo C1-4 y alquenilo C2-4 cualquiera de los cuales puede estar opcionalmente sustituido con un grupo R12 como se ha definido anteriormente; carboxi, aminocarbonilo en donde el grupo amino está opcionalmente sustituido con hidroxi, alquilo C1-6, alquenilo C2-6, alquil(C1-6)sulfonilo, trifluorometilsulfonilo, alquenil(C2-6)sulfonilo, alcoxi(C1-6)carbonilo, alquil(C1-6)carbonilo, alquenil(C2-6)oxicarbonilo o alquenil(C2-6)carbonilo y además opcionalmente sustituido con alquilo C1-6 o alquenilo C2-6, alquil(C1-6)sulfonilo; trifluorometilsulfonilo, alquenil(C2-6)sulfonilo; alcoxi(C1-6)carbonilo; alquil(C1-6)carbonilo, alquenil(C2-6)oxicarbonilo, y alquenil(C2-6)carbonilo; R4 es un grupo -CH2-R51 en que R51 se selecciona entre: alquilo C4-8; hidroxialquilo C4-8, alcoxi(C1-4)-alquilo(C4-8); alcanoiloxi(C1-4)-alquilo(C4-8); cicloalquil(C3-8)alquilo(C4-8), hidroxi-, alcoxi C1-6- o alcanoiloxi(C1-6)-cicloalquil(C3-8)-alquilo(C4-8), cianoalquilo(C4-8); alquenilo(C4-8); alquinilo(C4-8); tetrahidrofurilo; mono- o di-alquil(C1-6)-aminoalquilo(C4-8), acilamino-alquilo(C4-8), alquil (C1-6)- o acil-aminocarbonil-alquilo(C4-8); mono- o di-alquil(C1-6)-amino(hidroxi)-alquilo(C4-8); o R4 es un grupo -U-R52 en donde R52 es un sistema bicíclico de fórmula (2) de anillos carbocíclicos o heterocíclicos, opcionalmente sustituido; que contiene hasta 4 heteroátomos en cada anillo, en que al menos uno de los anillos (a) y (b) es aromático; X1 es C o N cuando forma parte de un anillo aromático o CR14 cuando forma parte de un anillo no aromático; X2 es N, NR13, O, S(O)x, CO o CR14 cuando forma parte de un anillo aromático o no aromático o puede ser además CR14R15 cuando forma parte de un anillo no aromático; X3uy X5 son independientemente N o C; Y1 es un grupo enlazador de 0 a 4 átomos y cada átomo del mismo se selecciona independientemente entre N, NR13, O, S(O)x, CO, y CR14 cuando forma parte de un anillo aromático o no aromático o puede ser además CR14R15 cuando forma parte de un anillo no aromático; Y2 es un grupo enlazador de 0 a 4 átomos, y cada átomo de Y2 se selecciona independientemente entre N, NR13, O, S(O)x, CO, y CR14 cuando forma parte de un anillo aromático o no aromático o puede ser además CR14R15 cuando forma parte de un anillo no aromático; cada uno de R14 y R15 se selecciona independientemente entre H, alquil(C1-4)tio, halo, carboxi-alquilo(C1-4); haloalcoxi(C1-4); haloalquilo(C1-4); alquilo C1-4; alquenilo C2-4; alcoxi(C1-4)carbonilo; formilo; alquil(C1-4)carbonilo; alquenil(C2-4)oxicarbonilo; alquenil(C2-4)carbonilo; alquil(C1-4)carboniloxi; alcoxi(C1-4)carbonil-alquilo(C1-4); hidroxi; hidroxialquilo C1-4; mercapto-alquilo C1-4; alcoxi C1-4; nitro; ciano; carboxi; amino o aminocarbonilo opcionalmente sustituido como en el caso de los sustituyentes correspondientes en R3; alquil(C1-4)sulfonilo; alquenil(C2-4)sulfonilo, o aminosulfonilo en donde el grupo amino está opcionalmente sustituido con alquilo C1-4 o alquenilo C2-4; arilo; aril(C1-4)alquilo; aril(C1-4)alcoxi; cada R13 es independientemente H, trifluorometilo; alquilo C1-4 opcionalmente sustituido con hidroxi, carboxi, alcoxi (C1-6)carbonilo, alcoxi(C1-6), alquil(C1-6)tio, halo, o trifluorometilo; alquenilo C2-4, arilo, aril-alquilo(C1-4); arilcarbonilo, heteroarilcarbonilo, alcoxi(C1-4)carbonilo; alquil(C1-4)carbonilo; formilo, alquil(C1-6)sulfonilo; o aminocarbonilo en donde el grupo amino está opcionalmente sustituido con alcoxi(C1-4)carbonilo, alquil(C1-4)carbonilo, alquenil(C2-4)oxicarbonilo, alquenil(C2-4)carbonilo, alquilo C1-4 o alquenilo C2-4 y además opcionalmente sustituido con alquilo C1-4 o alquenilo C2-4; cada x es independientemente 0, 1, o 2; U es CO, SO2 o CH2; o R4 es un grupo -X1a-X2a-X3a-X4a en que: X1a es CH2, CO, o SO2; X2a es CR14aR15a; X3a es NR13a, O, S, SO2 o SR14aR15a; en donde: cada uno de R14a y R15a se selecciona independientemente entre los grupos enunciados anteriormente para R14 y R15, con la condición de que, R14a y R15a en el mismo átomo de C no sean ambos seleccionados entre hidroxi opcionalmente sustituido y amino opcio
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| GBGB0112834.7A GB0112834D0 (en) | 2001-05-25 | 2001-05-25 | Medicaments |
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| ARP020101914A AR038172A1 (es) | 2001-05-25 | 2002-05-23 | Compuesto de ciclohexano y ciclohexeno, su uso para preparar una composicion farmaceutica, dicha composicion farmaceutica, procedimiento para preparar el compuesto y compuestos intermediarios en dicho procedimiento |
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| EP (1) | EP1399443B1 (es) |
| JP (2) | JP4463565B2 (es) |
| KR (1) | KR20040010654A (es) |
| CN (1) | CN1535272A (es) |
| AR (1) | AR038172A1 (es) |
| AT (1) | ATE380812T1 (es) |
| AU (1) | AU2002367697A1 (es) |
| BR (1) | BR0210016A (es) |
| CA (1) | CA2448525A1 (es) |
| CO (1) | CO5540344A2 (es) |
| CZ (1) | CZ20033202A3 (es) |
| DE (1) | DE60224039T2 (es) |
| ES (1) | ES2298439T3 (es) |
| GB (1) | GB0112834D0 (es) |
| HU (1) | HUP0400017A2 (es) |
| IL (1) | IL158869A0 (es) |
| MX (1) | MXPA03010790A (es) |
| NO (1) | NO20035190D0 (es) |
| PL (1) | PL367079A1 (es) |
| TW (1) | TWI232219B (es) |
| WO (1) | WO2003087098A1 (es) |
| ZA (1) | ZA200308696B (es) |
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| HUP0300721A3 (en) | 2000-07-26 | 2006-02-28 | Smithkline Beecham Plc | Aminopiperidine quinolines and their azaisosteric analogues with antibacterial activity, process for producing them, pharmaceutical compositions containing them and use thereof |
| ATE327231T1 (de) | 2000-09-21 | 2006-06-15 | Smithkline Beecham Plc | Chinolinderivate als antibakterielle mittel |
| FR2816618B1 (fr) | 2000-11-15 | 2002-12-27 | Aventis Pharma Sa | Derives heterocyclylalcoyl piperidine, leur preparation et les compositions qui les contiennent |
| GB0031086D0 (en) * | 2000-12-20 | 2001-01-31 | Smithkline Beecham Plc | Medicaments |
| GB0031088D0 (en) | 2000-12-20 | 2001-01-31 | Smithkline Beecham Plc | Medicaments |
| GB0101577D0 (en) | 2001-01-22 | 2001-03-07 | Smithkline Beecham Plc | Compounds |
| FR2822154B1 (fr) | 2001-03-13 | 2005-10-21 | Aventis Pharma Sa | Derives de la quinolyl propyl piperidine, leur preparation et les compositions qui les contiennent |
| GB0112836D0 (en) | 2001-05-25 | 2001-07-18 | Smithkline Beecham Plc | Medicaments |
| GB0112834D0 (en) | 2001-05-25 | 2001-07-18 | Smithkline Beecham Plc | Medicaments |
| GB0118238D0 (en) * | 2001-07-26 | 2001-09-19 | Smithkline Beecham Plc | Medicaments |
| US7312212B2 (en) * | 2002-01-29 | 2007-12-25 | Glaxo Group Limited | Aminopiperidine derivatives |
| WO2003064431A2 (en) | 2002-01-29 | 2003-08-07 | Glaxo Group Limited | Aminopiperidine compounds, process for their preparation, and pharmaceutical compositions containing them |
| US6818772B2 (en) * | 2002-02-22 | 2004-11-16 | Abbott Laboratories | Antagonists of melanin concentrating hormone effects on the melanin concentrating hormone receptor |
| AR040335A1 (es) * | 2002-06-26 | 2005-03-30 | Glaxo Group Ltd | Compuesto de ciclohexano o ciclohexeno, uso del mismo para preparar un medicamento, composicion farmaceutica que lo comprende, procedimiento y compuestos intermediarios de utilidad para preparar dicho compuesto |
| FR2844270B1 (fr) | 2002-09-11 | 2006-05-19 | Aventis Pharma Sa | Derives de la quinolyl propyl piperidine, leur procede et intermediaires de preparation et les compositions qui les contiennent |
| FR2844268B1 (fr) | 2002-09-11 | 2004-10-22 | Aventis Pharma Sa | Derives de la quinolyl propyl piperidine, leurs procedes et intermediaires de preparation et les compositions qui les contiennent |
| BR0315221A (pt) | 2002-10-10 | 2005-08-23 | Morphochem Ag Komb Chemie | Compostos com atividade antibacteriana |
| TW200427688A (en) * | 2002-12-18 | 2004-12-16 | Glaxo Group Ltd | Antibacterial agents |
| DE10316081A1 (de) | 2003-04-08 | 2004-10-21 | Morphochem AG Aktiengesellschaft für kombinatorische Chemie | Neue Verbindungen mit antibakterieller Aktivität |
-
2001
- 2001-05-25 GB GBGB0112834.7A patent/GB0112834D0/en not_active Ceased
-
2002
- 2002-05-23 TW TW091110839A patent/TWI232219B/zh not_active IP Right Cessation
- 2002-05-23 AR ARP020101914A patent/AR038172A1/es not_active Application Discontinuation
- 2002-05-24 DE DE60224039T patent/DE60224039T2/de not_active Expired - Lifetime
- 2002-05-24 HU HU0400017A patent/HUP0400017A2/hu unknown
- 2002-05-24 KR KR10-2003-7015379A patent/KR20040010654A/ko not_active Withdrawn
- 2002-05-24 MX MXPA03010790A patent/MXPA03010790A/es unknown
- 2002-05-24 CN CNA028146689A patent/CN1535272A/zh active Pending
- 2002-05-24 CA CA002448525A patent/CA2448525A1/en not_active Abandoned
- 2002-05-24 JP JP2003584054A patent/JP4463565B2/ja not_active Expired - Fee Related
- 2002-05-24 AU AU2002367697A patent/AU2002367697A1/en not_active Abandoned
- 2002-05-24 ES ES02807202T patent/ES2298439T3/es not_active Expired - Lifetime
- 2002-05-24 IL IL15886902A patent/IL158869A0/xx unknown
- 2002-05-24 US US10/478,154 patent/US7141564B2/en not_active Expired - Fee Related
- 2002-05-24 CZ CZ20033202A patent/CZ20033202A3/cs unknown
- 2002-05-24 EP EP02807202A patent/EP1399443B1/en not_active Expired - Lifetime
- 2002-05-24 AT AT02807202T patent/ATE380812T1/de not_active IP Right Cessation
- 2002-05-24 WO PCT/EP2002/005708 patent/WO2003087098A1/en not_active Ceased
- 2002-05-24 BR BR0210016-9A patent/BR0210016A/pt not_active IP Right Cessation
- 2002-05-24 PL PL02367079A patent/PL367079A1/xx not_active Application Discontinuation
-
2003
- 2003-11-07 ZA ZA200308696A patent/ZA200308696B/en unknown
- 2003-11-18 CO CO03101671A patent/CO5540344A2/es not_active Application Discontinuation
- 2003-11-21 NO NO20035190A patent/NO20035190D0/no not_active Application Discontinuation
-
2006
- 2006-11-22 US US11/604,045 patent/US20070135422A1/en not_active Abandoned
-
2009
- 2009-11-13 JP JP2009259981A patent/JP2010031057A/ja active Pending
Also Published As
| Publication number | Publication date |
|---|---|
| KR20040010654A (ko) | 2004-01-31 |
| TWI232219B (en) | 2005-05-11 |
| ATE380812T1 (de) | 2007-12-15 |
| GB0112834D0 (en) | 2001-07-18 |
| NO20035190D0 (no) | 2003-11-21 |
| EP1399443A1 (en) | 2004-03-24 |
| ES2298439T3 (es) | 2008-05-16 |
| CZ20033202A3 (cs) | 2004-08-18 |
| JP2010031057A (ja) | 2010-02-12 |
| DE60224039D1 (de) | 2008-01-24 |
| US20070135422A1 (en) | 2007-06-14 |
| IL158869A0 (en) | 2004-05-12 |
| BR0210016A (pt) | 2004-06-15 |
| JP2005519981A (ja) | 2005-07-07 |
| JP4463565B2 (ja) | 2010-05-19 |
| WO2003087098A1 (en) | 2003-10-23 |
| MXPA03010790A (es) | 2004-03-02 |
| US7141564B2 (en) | 2006-11-28 |
| CO5540344A2 (es) | 2005-07-29 |
| HUP0400017A2 (hu) | 2004-06-28 |
| CA2448525A1 (en) | 2003-10-23 |
| US20040171620A1 (en) | 2004-09-02 |
| AU2002367697A1 (en) | 2003-10-27 |
| CN1535272A (zh) | 2004-10-06 |
| PL367079A1 (en) | 2005-02-21 |
| DE60224039T2 (de) | 2008-11-27 |
| EP1399443B1 (en) | 2007-12-12 |
| ZA200308696B (en) | 2004-05-21 |
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| FA | Abandonment or withdrawal |