AR057990A1 - Imidazolinas 4,4,5,5 tetrasustituidas y un proceso para su sintesis - Google Patents
Imidazolinas 4,4,5,5 tetrasustituidas y un proceso para su sintesisInfo
- Publication number
- AR057990A1 AR057990A1 ARP060105272A ARP060105272A AR057990A1 AR 057990 A1 AR057990 A1 AR 057990A1 AR P060105272 A ARP060105272 A AR P060105272A AR P060105272 A ARP060105272 A AR P060105272A AR 057990 A1 AR057990 A1 AR 057990A1
- Authority
- AR
- Argentina
- Prior art keywords
- ch2ch3
- piperidinyl
- och3
- morpholinyl
- ch2ch2oh
- Prior art date
Links
- 230000015572 biosynthetic process Effects 0.000 title 1
- 238000000034 method Methods 0.000 title 1
- 238000003786 synthesis reaction Methods 0.000 title 1
- -1 -CI Chemical group 0.000 abstract 25
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 16
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 abstract 13
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 abstract 8
- 125000004573 morpholin-4-yl group Chemical group N1(CCOCC1)* 0.000 abstract 8
- 125000000587 piperidin-1-yl group Chemical group [H]C1([H])N(*)C([H])([H])C([H])([H])C([H])([H])C1([H])[H] 0.000 abstract 8
- 229910052739 hydrogen Inorganic materials 0.000 abstract 6
- 239000001257 hydrogen Substances 0.000 abstract 6
- 125000004214 1-pyrrolidinyl group Chemical group [H]C1([H])N(*)C([H])([H])C([H])([H])C1([H])[H] 0.000 abstract 5
- 125000004200 2-methoxyethyl group Chemical group [H]C([H])([H])OC([H])([H])C([H])([H])* 0.000 abstract 5
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 5
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 abstract 5
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 abstract 5
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 4
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 4
- 125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 abstract 3
- 125000000175 2-thienyl group Chemical group S1C([*])=C([H])C([H])=C1[H] 0.000 abstract 3
- 125000001541 3-thienyl group Chemical group S1C([H])=C([*])C([H])=C1[H] 0.000 abstract 3
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 abstract 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N methanol Substances OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 abstract 3
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 abstract 3
- 125000002941 2-furyl group Chemical group O1C([*])=C([H])C([H])=C1[H] 0.000 abstract 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N EtOH Substances CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 2
- 229910052736 halogen Inorganic materials 0.000 abstract 2
- 125000001160 methoxycarbonyl group Chemical group [H]C([H])([H])OC(*)=O 0.000 abstract 2
- RWRDLPDLKQPQOW-UHFFFAOYSA-N tetrahydropyrrole Natural products C1CCNC1 RWRDLPDLKQPQOW-UHFFFAOYSA-N 0.000 abstract 2
- 125000003682 3-furyl group Chemical group O1C([H])=C([*])C([H])=C1[H] 0.000 abstract 1
- 125000000590 4-methylphenyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)C([H])([H])[H] 0.000 abstract 1
- 102000012199 E3 ubiquitin-protein ligase Mdm2 Human genes 0.000 abstract 1
- 108050002772 E3 ubiquitin-protein ligase Mdm2 Proteins 0.000 abstract 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 1
- 229910006074 SO2NH2 Inorganic materials 0.000 abstract 1
- 125000000217 alkyl group Chemical group 0.000 abstract 1
- HSFWRNGVRCDJHI-UHFFFAOYSA-N alpha-acetylene Natural products C#C HSFWRNGVRCDJHI-UHFFFAOYSA-N 0.000 abstract 1
- 239000002246 antineoplastic agent Substances 0.000 abstract 1
- 229910052801 chlorine Inorganic materials 0.000 abstract 1
- 239000000460 chlorine Substances 0.000 abstract 1
- 125000001309 chloro group Chemical group Cl* 0.000 abstract 1
- 125000001995 cyclobutyl group Chemical group [H]C1([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 abstract 1
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 abstract 1
- GLUUGHFHXGJENI-UHFFFAOYSA-N diethylenediamine Natural products C1CNCCN1 GLUUGHFHXGJENI-UHFFFAOYSA-N 0.000 abstract 1
- 230000000694 effects Effects 0.000 abstract 1
- 150000002148 esters Chemical class 0.000 abstract 1
- 125000002534 ethynyl group Chemical group [H]C#C* 0.000 abstract 1
- 150000002367 halogens Chemical class 0.000 abstract 1
- 150000002431 hydrogen Chemical class 0.000 abstract 1
- CBOIHMRHGLHBPB-UHFFFAOYSA-N hydroxymethyl Chemical compound O[CH2] CBOIHMRHGLHBPB-UHFFFAOYSA-N 0.000 abstract 1
- 150000002462 imidazolines Chemical class 0.000 abstract 1
- 239000003112 inhibitor Substances 0.000 abstract 1
- 230000003993 interaction Effects 0.000 abstract 1
- YYERFRCBHRNMTB-UHFFFAOYSA-N n,n-diethylpiperidine-1-carboxamide Chemical compound CCN(CC)C(=O)N1CCCCC1 YYERFRCBHRNMTB-UHFFFAOYSA-N 0.000 abstract 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 1
- IWELDVXSEVIIGI-UHFFFAOYSA-N piperazin-2-one Chemical class O=C1CNCCN1 IWELDVXSEVIIGI-UHFFFAOYSA-N 0.000 abstract 1
- 150000004885 piperazines Chemical class 0.000 abstract 1
- JSPCTNUQYWIIOT-UHFFFAOYSA-N piperidine-1-carboxamide Chemical compound NC(=O)N1CCCCC1 JSPCTNUQYWIIOT-UHFFFAOYSA-N 0.000 abstract 1
- 150000003053 piperidines Chemical class 0.000 abstract 1
- 102000004169 proteins and genes Human genes 0.000 abstract 1
- 108090000623 proteins and genes Proteins 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- NQRYJNQNLNOLGT-UHFFFAOYSA-N tetrahydropyridine hydrochloride Natural products C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 abstract 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/04—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
- C07D233/20—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member with substituted hydrocarbon radicals, directly attached to ring carbon atoms
- C07D233/22—Radicals substituted by oxygen atoms
-
- A—HUMAN NECESSITIES
- 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
- A61K31/41—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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/04—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
- C07D233/20—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member with substituted hydrocarbon radicals, directly attached to ring carbon atoms
- C07D233/26—Radicals substituted by carbon atoms having three bonds to hetero atoms
-
- 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
- C07D401/06—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 carbon chain containing only aliphatic carbon atoms
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/06—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
-
- 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
- C07D405/06—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 carbon chain containing only aliphatic carbon atoms
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D407/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00
- C07D407/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00 containing two hetero rings
- C07D407/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
- C07D409/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
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- 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
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- 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
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Public Health (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Abstract
Los compuestos descriptos muestran actividad como agentes antitumorales. Estas imidazolinas son inhibidores de la interaccion entre P53 y MDM2 (proteínas). Reivindicacion 1: Un compuesto de formula (1), en la que X1 y X2 son halogeno, acetileno, ciano, trifluorometilo o nitro; R1 y R2 se seleccionan de entre el grupo que consiste en -H, -CH3, - CH2CH3, -CH2OH y -CH2OCH3 con la condicion de que y no sean ambos hidrogeno; R3 es -H o -C(=O)-R7; y cuando R6 es hidrogeno entonces, R4 es -OCH3, - OCH2CH3, -OCH2CH2F, -OCH2CH2OCH3, u -OCH(CH3)2; R5 es -H, -halogeno, -CH3, -CF3, -OCH3, -C(CH3)2, -ciclopropilo, ciano, -C(CH3)3, -C(CH3)2OR (en la que R es -H, -CH3, -CH2-CH3, -C(CH3)2CH-OR (en la que R es -H, -CH3, -CH(CH3)2, -CH2CH2OH o - CH2CH2OCH3), -C(CH3)2CN, -C(CH3)2COR (en la que R es -CH3), -C(CH3)2COOR (en la que R es -H, -CH3, -CH2CH3 o -CH-(CH3)2), -C(CH3)2CONRaRb (en la que Ra es -H, -CH3, y Rb es -H o -CH3), -SR (en la que R es -CH3 o -CH2CH3),o -SO2R (en la que R es - CH3, -CH2CH3, 1-pirrolidina, -NH-terc-butilo o -N(CH3)2); y cuando R6 no es hidrogeno entonces R4 es -OCH3, -OCH2CH3, -OCH2CH2F, -OCH2CH2OCH3, o -OCH(CH3)2; R5 es hidrogeno, -CI, -OCH3, terc-butiIo o -N(CH3)2; R6 es -CI, ciclopropilo, -SO2R (en la que R es -CH3, -CH2CH3, 1-pirrolidina, -NH-terc-butilo, -NH2, o -N(CH3)2); y R7 se selecciona del grupo que consiste en i) -CH3, -CH(CH3)2, -CH2CH(CH3)2, ciclopropilo, ciclobutilo, -CH2CH2Ph, 2-furanilo, fenilo o fenilo sustituido por cloro, -OCH3 o ciano, ii) 4-morfolinilo, 1-piperidinilo, 4-tiomorfolinilo o 4-tiomorfolinil-1,1-dioxido, iii) -NRc2 (en la que Rc es hidrogeno, -CH3, -CH2CH3. -CH2CH2OH, -CH2CH2OCH3 o -CH2CH(OH)CH2OH), iv) una piperazina sustituida de la formula (2), en la que R se selecciona del grupo que consiste en a) hidrogeno, b) alquilo inferior, c) -CH(CH3)2, d) -CH(CH2CH3)2, e) ciclopentilo, f) -CH2CH(OH)CH3, g) -CH2CF3, h) -CH2CH(OH)CF3, i) -CH2C(CH3)2OH, j) -CH2-[4-N-metilpiperidinilo], k) -CH2CH2Rd (en la que Rd es -OH, -OCH3, -OCH2CH2OH, -OCH2CH2OCH3, -CN, -CF3, -SO2CH3, -SO2NH2, -SO2N(CH3)2, -CONH2, -CON(CH3)2, -NH2, -NHCOCH3, -NHSO2CH3, -N(CH3)2, -N(CH2CH3)2, -N(CH2CH2CH3)2, 1-pirrolidinilo, 1-piperidinilo, 4-morfolinilo, 2-isotiazolidinil-1 1-dioxido, o 2-tetrahidrofuranilo), l) -CH2CH2CH2Re (en la que Re es -OH, -OCH3, -SO2CH3, -SO2CH2CH3, -SO2N(CH3)2, -CN, -N(CH3)2, -N(CH2CH2CH3)2, 1-imidazolilo, 1-pirrolidinilo, 1-piperidinilo, 4-morfolinilo, -COOCH3, -COOCH2CH3, -COOC(CH3)3, -CON(CH3)2, -CO-Rf (en la que Rf es -CH3, -CH2CH3, ciclopropilo, fenilo, 2-tienilo, 3-tienilo, 2-furanilo, 3-furanilo), -COCH2-Rg (en la que Rg es 1-1, -NHCH2CH2OH, -NHCH2CH2OCH3, -NHCH2CH2N(CH3)2, 1-piperidinilo, 1-(piperidinil-4-metanol), 4-morfolinilo, o -N(CH3)-(3- (1-metilpirrolidinilo)), m) CH2CORh (en la que Rh es -OCH3, -OCH2CH3, -NH2, - NHCH2CH(CH3)2, -NHCH2CF3, -NH-ciclopropilo, -NH-terc-butilo, -NHCH2CH2CH2OH, -N(CH3)2, -N(CH2CH3)2, -N(CH2CH2OH)2, -N(CH2CH2OCH3)2, -N(CH3)CH2CH2OH, -N(CH3)CH2CH2OCH3, - NHCH2CH2OCH3, 1-pirrolidinilo, 1-piperidinilo, 1-(piperidinil-4-metanol), 1-(piperidinil-3-carboxamida), 4-morfolinilo, 4-tiomorfolinilo, 4-tiomorfolinil-1,1-dioxido, 1-piperazinilo, 1-(4-acetilpiperazinilo), 1-(3-oxopiperazinilo), n) -SO2Ri (en la que Ri es -CH3, -CH2CH3, -CH(CH3)2, fenilo, 4-metilfenilo, 4-propilfenilo, -CF3, 2-tienilo, 3-tienilo, -NH2, -NHCH3, -N(CH3)2, -NHCH2CH2OCH3, -N(CH2CH2OCH3)2, 1-pirrolidinilo, 1-piperidinilo, 4-morfolinilo, 1-piperazil-4-etanol, 1-(4- acetilpiperazinilo), 1-(3-oxopiperazinilo)), o) -CORj (en la que Rj es -CH3, -CH2CH3, -CH(CH3)2, 2-tetrahidrofuranilo, 2-tienilo, 3-tienilo, -NH2, -NHCH3, -N(CH3)2, 1-pirrolidinilo, 1-piperidinilo, 4-morfolinilo, 1-piperazinil-4-etanol, 1-(4- acetilpiperazinilo), o 1-(3-oxopiperazinilo)), p) 4-tetrahidro-2H-tiopiranil-1,1-dioxido, q) 4-piperidinil-1-acetilo, r) 4-piperidinil-1-dimetilcarboxamida, y s) 3-tetrahidro-tiofenil-1,1-dioxido; v) una oxopiperazina sustituida de la formula (3), en la que R es -H, -CH3, -CH2CH3, -CH2CH2CH3, -CH2CH2OH o - CH2CH2OCH3; y vi) una piperidina sustituida de la formula (4), en la que R es -H, -COOCH3, -COOCH2CH3, -CONH2, -OH, -CH2OH, -CH2CH2OH, -CH2N(CH2CH3)2, -CH2-(1-piperazinilo), -CH2-(1-(3- oxopiperazinilo)),-NH2, -NHCOCH3, -NHCOCH2NH2, -NHCOCH2NHCH3, -NHCOCH2N(CH3)2, -NHCOCH2N(CH2CH2OH)2, -NHCOCH2N(CH2CH2OCH3)2, -NHCOCH2NHCH2CH2OH, -NHCOCH2-(1-(4-acetilpiperazinilo)), -NHCOCH2-(1-(3-oxopiperazinilo)), -NHCOCH2-(1- piperidinacarboxamida), -NHCOCH2-(N,N-dietil-1-piperidinilcarboxamida), -NHCOCH2-(1-(3-hidroxipiperidinilo)), -NHCOCH2-(1-(piperidinil-4-metanol)), -NHCON(CH3)2, -NHCSNHCH3, -NHCSNHPh, -NHCH2CONH2, 1 -pirrolidinilo, 1-piperidinilo, 1-(4- metilpiperazinilo), o 4-morfolinilo; y las sales y ésteres farmacéuticamente aceptables de los mismos.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US74122305P | 2005-12-01 | 2005-12-01 | |
| US85274706P | 2006-10-19 | 2006-10-19 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR057990A1 true AR057990A1 (es) | 2008-01-09 |
Family
ID=37866229
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP060105272A AR057990A1 (es) | 2005-12-01 | 2006-11-29 | Imidazolinas 4,4,5,5 tetrasustituidas y un proceso para su sintesis |
Country Status (17)
| Country | Link |
|---|---|
| US (1) | US7851626B2 (es) |
| EP (3) | EP2130822A1 (es) |
| JP (1) | JP4870778B2 (es) |
| KR (2) | KR20100129331A (es) |
| CN (1) | CN101316823B (es) |
| AR (1) | AR057990A1 (es) |
| AU (1) | AU2006319248B2 (es) |
| BR (1) | BRPI0619236A2 (es) |
| CA (1) | CA2630410C (es) |
| CR (1) | CR9980A (es) |
| ES (1) | ES2538714T3 (es) |
| MA (1) | MA31550B1 (es) |
| NO (1) | NO20082389L (es) |
| NZ (1) | NZ568285A (es) |
| RU (1) | RU2442779C2 (es) |
| TW (1) | TWI326681B (es) |
| WO (1) | WO2007063013A1 (es) |
Families Citing this family (50)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA2666489C (en) * | 2006-10-19 | 2012-10-02 | F. Hoffmann-La Roche Ag | Imidazolone and imidazolidinone derivatives as 11b-hsd1 inhibitors for diabetes |
| CA2666762C (en) * | 2006-10-19 | 2014-12-30 | F. Hoffmann-La Roche Ag | Aminomethyl-4-imidazoles |
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- 2006-11-22 WO PCT/EP2006/068748 patent/WO2007063013A1/en not_active Ceased
- 2006-11-22 RU RU2008126383/04A patent/RU2442779C2/ru active
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- 2006-11-22 NZ NZ568285A patent/NZ568285A/en not_active IP Right Cessation
- 2006-11-22 BR BRPI0619236-0A patent/BRPI0619236A2/pt not_active Application Discontinuation
- 2006-11-22 JP JP2008542723A patent/JP4870778B2/ja not_active Expired - Fee Related
- 2006-11-22 ES ES06819663.3T patent/ES2538714T3/es active Active
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- 2006-11-22 CN CN2006800448100A patent/CN101316823B/zh not_active Expired - Fee Related
- 2006-11-22 KR KR1020107024025A patent/KR20100129331A/ko not_active Ceased
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- 2008-05-26 NO NO20082389A patent/NO20082389L/no not_active Application Discontinuation
- 2008-06-02 MA MA30992A patent/MA31550B1/fr unknown
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| RU2442779C2 (ru) | 2012-02-20 |
| CA2630410C (en) | 2014-02-25 |
| RU2008126383A (ru) | 2010-01-10 |
| JP2009517439A (ja) | 2009-04-30 |
| CA2630410A1 (en) | 2007-06-07 |
| HK1126216A1 (en) | 2009-08-28 |
| NO20082389L (no) | 2008-08-18 |
| EP2311814A1 (en) | 2011-04-20 |
| US7851626B2 (en) | 2010-12-14 |
| KR20100129331A (ko) | 2010-12-08 |
| MA31550B1 (fr) | 2010-08-02 |
| TW200804297A (en) | 2008-01-16 |
| EP1960368B1 (en) | 2015-05-06 |
| AU2006319248A1 (en) | 2007-06-07 |
| CN101316823A (zh) | 2008-12-03 |
| KR20080072894A (ko) | 2008-08-07 |
| US20070129416A1 (en) | 2007-06-07 |
| BRPI0619236A2 (pt) | 2011-09-20 |
| AU2006319248B2 (en) | 2012-09-27 |
| NZ568285A (en) | 2011-08-26 |
| CR9980A (es) | 2008-06-18 |
| CN101316823B (zh) | 2013-05-22 |
| JP4870778B2 (ja) | 2012-02-08 |
| EP1960368A1 (en) | 2008-08-27 |
| WO2007063013A1 (en) | 2007-06-07 |
| ES2538714T3 (es) | 2015-06-23 |
| EP2130822A1 (en) | 2009-12-09 |
| KR101109437B1 (ko) | 2012-01-31 |
| TWI326681B (en) | 2010-07-01 |
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