AR065932A1 - Derivados de imidazolidinacarboxamida como inhibidores de lipasas y fosfolipasas - Google Patents
Derivados de imidazolidinacarboxamida como inhibidores de lipasas y fosfolipasasInfo
- Publication number
- AR065932A1 AR065932A1 ARP080101389A ARP080101389A AR065932A1 AR 065932 A1 AR065932 A1 AR 065932A1 AR P080101389 A ARP080101389 A AR P080101389A AR P080101389 A ARP080101389 A AR P080101389A AR 065932 A1 AR065932 A1 AR 065932A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkyl
- alkylene
- cycloalkyl
- aryl
- different way
- Prior art date
Links
- 102000004882 Lipase Human genes 0.000 title 1
- 108090001060 Lipase Proteins 0.000 title 1
- 239000004367 Lipase Substances 0.000 title 1
- 102000015439 Phospholipases Human genes 0.000 title 1
- 108010064785 Phospholipases Proteins 0.000 title 1
- 239000003112 inhibitor Substances 0.000 title 1
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 23
- 125000000217 alkyl group Chemical group 0.000 abstract 15
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 11
- 229910052739 hydrogen Inorganic materials 0.000 abstract 10
- 239000001257 hydrogen Substances 0.000 abstract 10
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 9
- 125000003118 aryl group Chemical group 0.000 abstract 9
- 125000002947 alkylene group Chemical group 0.000 abstract 7
- 125000000304 alkynyl group Chemical group 0.000 abstract 7
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 7
- 125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 abstract 7
- 125000003342 alkenyl group Chemical group 0.000 abstract 6
- 125000000896 monocarboxylic acid group Chemical group 0.000 abstract 6
- 125000004209 (C1-C8) alkyl group Chemical group 0.000 abstract 5
- 125000005843 halogen group Chemical group 0.000 abstract 5
- 125000001072 heteroaryl group Chemical group 0.000 abstract 4
- 229920006395 saturated elastomer Polymers 0.000 abstract 4
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 3
- HCMJWOGOISXSDL-UHFFFAOYSA-N (2-isothiocyanato-1-phenylethyl)benzene Chemical compound C=1C=CC=CC=1C(CN=C=S)C1=CC=CC=C1 HCMJWOGOISXSDL-UHFFFAOYSA-N 0.000 abstract 2
- -1 CH2-aryl Chemical group 0.000 abstract 2
- 125000004429 atom Chemical group 0.000 abstract 2
- 125000004432 carbon atom Chemical group C* 0.000 abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 2
- 125000000623 heterocyclic group Chemical group 0.000 abstract 2
- 125000004182 2-chlorophenyl group Chemical group [H]C1=C([H])C(Cl)=C(*)C([H])=C1[H] 0.000 abstract 1
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 abstract 1
- 125000003545 alkoxy group Chemical group 0.000 abstract 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 abstract 1
- 125000004122 cyclic group Chemical group 0.000 abstract 1
- 125000000392 cycloalkenyl group Chemical group 0.000 abstract 1
- 229940079593 drug Drugs 0.000 abstract 1
- 239000003814 drug Substances 0.000 abstract 1
- 125000001188 haloalkyl group Chemical group 0.000 abstract 1
- 150000002431 hydrogen Chemical class 0.000 abstract 1
- 125000001147 pentyl group Chemical group C(CCCC)* 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
Classifications
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- C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
- C07D233/66—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two 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
- C07D233/72—Two oxygen atoms, e.g. hydantoin
- C07D233/76—Two oxygen atoms, e.g. hydantoin with substituted hydrocarbon radicals attached to the third ring carbon atom
- C07D233/78—Radicals substituted by oxygen atoms
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- 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
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Abstract
Su uso como medicamentos y composiciones farmacéuticas. Reivindicacion 1: Un compuesto de la formula (1) en la que: X, Y de igual o diferente modo -C(R3)(R4)-, -(C=O)-, -(C=S), en la que al menos uno de X o Y es -(C=O)- o -(C=S)-; pero ambos nopueden ser simultáneamente -(C=O)- o -(C=S)-; o X e Y juntos son C(R3)=C(R3); R hidrogeno, alquilo (C1-8), halogenoalquilo (C1-5), (CR5R6)m-O(R7), alquiloxi(C1-3)-alquileno(C1-3, arilo, heterociclo, alquilen(C1-4)-arilo, alquilen(C1-4)-heteroarilo,alquilen(C1-4)-cicloalquilo (C5-12), en los que el cicloalquilo, arilo, heterociclo o heteroarilo pueden estar sustituidos una más veces con F, Cl, Br, I, OH, CF3, NO2, CN, OCF3, O-alquilo(C1-6), O-alcoxi(C1-4)-alquilo(C1-4), S-alquilo(C1-6),alquilo (C1-6), halogenoalquilo (C2-4), O-halogenoalquilo(C2-4), alquenilo (C2-6), cicloalquilo (C3-8), O-cicloalquilo(C3-8), alquinilo (C2-6), alquilen(C0-8)-arilo, O-alquilen(C0-8)-arilo, S-arilo, alquilen(C0-8)-heteroarilo, N-(R5)(R6), SO2-CH3,SO2-NH2, SF5, COOH, COO-alquilo(C1-6), CON(R5)(R6), N(R5)CO(R6), N(R5)SO2(R6), CO(R5), (CR5R6)m'-O(R7), O-CO-N(R5)(R6), O-CO-alquilen(C1-6)-CO-O-alquilo(C1-6), O-CO-alquilen(C1-6)-CO-OH, O-CO-alquilen(C1-6)-CO-N(R5)(R6), en los que el arilo yheteroarilo pueden estar a su vez sustituidos una o más veces con F, Cl, Br, I, OH, CF3, NO2, CN, OCF3, O-alquilo(C1-6), O-alcoxi(C1-4)-alquilo(C1-4), S-alquilo(C1-6), alquilo (C1-6), alquenilo (C2-6), cicloalquilo (C3-8), O-cicloalquilo(C3-8),alquinilo (C2-6), N(R8)(R9), SO2-CH3, SF5, COOH, COO-alquilo(C1-6), CON(R8)(R9), N(R8)CO(R9), N(R8SO2(R9), CO(R8), (CR8R9)m''-O(R10), O-CO-N(R8)(R9), O-CO-alquilen(C1-6)-CO-O-alquilo(C1-6), O-CO-alquilen(C1-6)-CO-OH, O-CO-alquilen(C1-6)-CO-N(R8)(R9); m, m', m'' 0, 1, 2, 3, 4, 5, 6; R5, R6, R7, R8, R9, R10 de igual o diferente modo hidrogeno, alquilo (C1-8); o -(C=O)-NR1aR2a; o -(C=O)-O-R1b; o Ry X para X = -C(R3)(R4)- forman un sistema anular monocíclico, de 4 a 7 miembros, saturadoso parcialmente insaturado o un sistema anular bibíblico, de 8 a 14 miembros, saturado o parcialmente insaturado, cuyos miembros individuales de los sistemas anulares se pueden sustituir por uno a tres átomos o grupos de átomos de la serie -CHR11-, -CR11R12-, -(C=R11)-, =C(R11)-, -NR11-, -C(=O)-, -O-, -S-, -SO-, -SO2-, con la condicion de que dos unidades de la serie -O-, -S-, -SO-, -SO2- no pueden ser adyacentes; R11, R12 de igual o diferente modo hidrogeno, alquilo (C1-6), arilo, cicloalquilo(C3-12), alquilen(C1-4)-arilo, alquilen(C1-3)-cicloalquilo(C3-12); en los que el arilo o cicloalquilo pueden estar sustituidos con F, Cl, Br, I, OH, CF3, NO2, CN, OCF3, O-alquilo(C1-6), O-alcoxi(C1-4)-alquilo(C1-4), S-alquilo(C1-6), alquilo (C1-6),halogenoalquilo(C2-4), O-halogenoalquilo(C2-4), alquenilo (C2-6), alquinilo (C2-6), N(R13)(R14), SO2-CH3, SO2-NH2, SF5, COOH, COO-alquilo(C1-6), CON(R13)(R14), N(R13)CO(R14), N(R13)SO2(R14), CO(R13), (CR13R14)n-O(R15), O-CO-N(R13)(R14), O-CO-alquilen(C1-6)-CO-O-alquilo(C1-6), O-CO-alquilen(C1-6)-CO-OH, O-CO-alquilen(C1-6)-CO-N(R13)(R14); n 0, 1, 2, 3, 4, 5, 6; R13, R14, R15 de igual o diferente modo hidrogeno, alquilo (C1-8); R1, R1a, R1b de igual o diferente modo alquilo (C5-16), CH2-arilo, alquilen(C1-2)-heteroarilo, CH2-cicloalquilo(C5-12), en los que el arilo, heteroarilo o cicloalquilo pueden estar sustituidos una o más veces con F, Cl, Br, I, OH, CF3, NO2, CN, OCF3, O-alquilo(C1-6), O-alcoxi(C1-4)-alquilo(C1-4), S-alquilo(C1-6), alquilo (C1-6), halogenoalquilo (C2-4), O-halogenoalquilo(C2-4), alquenilo (C2-6), cicloalquilo (C3-8), O-cicloalquilo(C3-8), alquinilo (C2-6), alquilen(C0-8)-arilo, O-alquilen(0-8)-arilo, S-arilo, alquilen(C0-8)-heteroarilo,N(R16)(R17), SO2-CH3, SO2-NH2, SF5, COOH, COO-alquilo(C1-6), CON(R16)(R17), N(R16)CO(R17), N(R16)SO2(R17), CO(R16), (CR16R17)o-O(R18), O-CO-N(R16)(R17), O-CO-alquilen(C1-6)-CO-O-alquilo(C1-6), O-CO-alquilen(C1-6)-CO-OH, O-CO-alquilen(C1-6)-CO-N(R16)(R17), en los que el arilo o heteroarilo a su vez pueden estar sustituidos una o más veces con F, Cl, Br, I, OH, CF3, NO2, CN, OCF3, O-alquilo(C1-6), O-alcoxi(C1-4)-alquilo(C1-4), S-alquilo(C1-6), alquilo (C1-6), alquenilo (C2-6), cicloalquilo(C3-8), O-cicloalquilo(C3-8), alquinilo (C2-6), N(R19)(R20), SO2-CH3, SF5, COOH, COO-alquilo(C1-6), CON(R19)(R20), N(R19)CO(R20), N(R19)SO2(R20), CO(R19), (CR19R20)o'-O(R21), O-CO-N(R19)(R20), O-CO-alquilen(C1-6)-CO-O-alquilo(C1-6), O-CO-alquilen(C1-6)-CO-OH, O-CO-alquilen(C1-6)-CO-N(R19)(R20); o, o' 0, 1, 2, 3, 4, 5, 6; R16, R17, R18, R19, R20, R21 de igual o diferente modo hidrogeno, alquilo (C1-8); o un radical de formula (2), con W -C(R28)(R29)-, -C(R28)(R29)-C(R28a)(R29a)-, -C(R28)(R29)-O-; R22, R23, R24, R25, R26, R27, R28, R29, R28a, R29a de igual o diferente modo hidrogeno, F, Cl, Br, I, OH, CF3, NO2, CN, OCF3, SF5, O-alquilo(C1-6), O-alcoxi(C1-4)-alquilo(C1-4), S-alquilo(C1-6), alquilo (C1-6), halogenoalquilo (C2-4), O-halogenoalquilo(C2-4), alquenilo (C2-6), cicloalquilo (C3-8), O-cicloalquilo(C3-8), cicloalquenilo (C3-8), alquinilo (C2-6), N(R30)(R31), SO2-CH3, COOH, COO-alquilo(C1-6), CON(R30)(R31), N(R30)CO(R31), N(R30)SO2(R31), CO(R30), (CR30R31)p-O(R32), O-CO-N(R30)(R31), O-CO-alquilen(C1-6)-CO-O-alquilo(C1-6), O-CO-alquilen(C1-6)-CO-OH, O-CO-alquilen(C1-6)-CO-N(R30)(R31); p 0, 1, 2, 3, 4, 5, 6; R30, R31, R32 de igual o diferente modo hidrogeno, alquilo (C1-6); o R22 y R28 o R23 y R29 junto con losátomos de carbono que los llevan forman un sistema anular monocíclico, de 5 o 6 miembros, saturado, parcialmente insaturado o aromático, cuyos miembros individuales se pueden sustituir por -CHR33-, -CR33R34-, =(C-R33)-; o R24 y R26 o R25 y R27 juntocon los átomos de carbono que los llevan forman un sistema anular monocíclico, de 5 o 6 miembros, saturado, parcialmente insaturado o aromático, cuyos miembros individuales se pueden sustituir por -CHR33-, -CR33R34-, =(C-R33)-; R33, R34 de igual odiferente modo F, Cl, Br, I, OH, CF3, NO2, CN, OCF3, SF5, O-alquilo(C1-6), O-alcoxi(C1-4)-alquilo(C1-4), S-alquilo(C1-6), alquilo (C1-6), halogenoalquilo (C2-4)-, O-halogenoalquilo(C2-4), alquenilo (C2-6), cicloalquilo (C3-8), O-cicloalquilo (C3-8),alquinilo (C2-6), N-(R35)(R36), SO2-CH3, COOH, COO-alquilo(C1-6), CON(R35)(R36), N(R35)CO(R36), N(R35)SO2(R36), CO(R35), CR35R36)q-O(R37), O-CO-N(R35)(R36), O-CO-alquilen(C1-6)-CO-O-alquilo(C1-6), O-CO-alquilen(C1-6)-CO-OH, O-CO-alquilen(C1-6)-CO-N(R35)(R36); q 0, 1, 2, 3, 4, 5, 6; R35, R36, R37 de igual o diferente modo hidrogeno, alquilo (C1-6); R2, R2a de igual o diferente modo hidrogeno, alquilo (C1-8); R3, R4 de igual o diferente modo hidrogeno, alquilo (C1-6), bencilo; las formastautomeras del compuesto y las sales fisiologicamente toleradas del mismo; con la condicion de que R1 no es pentilo, CH2-fenilo, -CH2-(2-Cl-fenilo), cilohexilo, -(2-metilciclohexilo) si X = CH2, Y = CO, R = metilo, R2 = H.
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| WO2011107494A1 (de) | 2010-03-03 | 2011-09-09 | Sanofi | Neue aromatische glykosidderivate, diese verbindungen enthaltende arzneimittel und deren verwendung |
| EP2582709B1 (de) | 2010-06-18 | 2018-01-24 | Sanofi | Azolopyridin-3-on-derivate als inhibitoren von lipasen und phospholipasen |
| US8530413B2 (en) | 2010-06-21 | 2013-09-10 | Sanofi | Heterocyclically substituted methoxyphenyl derivatives with an oxo group, processes for preparation thereof and use thereof as medicaments |
| TW201215388A (en) | 2010-07-05 | 2012-04-16 | Sanofi Sa | (2-aryloxyacetylamino)phenylpropionic acid derivatives, processes for preparation thereof and use thereof as medicaments |
| TW201221505A (en) | 2010-07-05 | 2012-06-01 | Sanofi Sa | Aryloxyalkylene-substituted hydroxyphenylhexynoic acids, process for preparation thereof and use thereof as a medicament |
| TW201215387A (en) | 2010-07-05 | 2012-04-16 | Sanofi Aventis | Spirocyclically substituted 1,3-propane dioxide derivatives, processes for preparation thereof and use thereof as a medicament |
| WO2013037390A1 (en) | 2011-09-12 | 2013-03-21 | Sanofi | 6-(4-hydroxy-phenyl)-3-styryl-1h-pyrazolo[3,4-b]pyridine-4-carboxylic acid amide derivatives as kinase inhibitors |
| EP2760862B1 (en) | 2011-09-27 | 2015-10-21 | Sanofi | 6-(4-hydroxy-phenyl)-3-alkyl-1h-pyrazolo[3,4-b]pyridine-4-carboxylic acid amide derivatives as kinase inhibitors |
| WO2013048982A1 (en) * | 2011-09-27 | 2013-04-04 | Bristol-Myers Squibb Company | Pyrrolinone carboxamide compounds useful as endothelial lipase inhibitors |
| US9249096B2 (en) | 2011-09-27 | 2016-02-02 | Bristol-Myers Squibb Company | Pyrrolinone carboxamide compounds useful as endothelial lipase inhibitors |
| US9493412B2 (en) | 2011-09-27 | 2016-11-15 | Bristol-Myers Squibb Company | Pyrrolinone carboxamide compounds useful as endothelial lipase inhibitors |
| US8933235B2 (en) | 2011-09-30 | 2015-01-13 | Bristol-Myers Squibb Company | Pyridinedione carboxamide inhibitors of endothelial lipase |
| EP2847174B1 (en) | 2012-04-03 | 2017-05-17 | Bristol-Myers Squibb Company | Pyrimidinone carboxamides as inhibitors of endothelial lipase |
| EP2844643B1 (en) * | 2012-04-03 | 2016-11-30 | Bristol-Myers Squibb Company | Pyrimidinedione carboxamide inhibitors of endothelial lipase |
| AR102942A1 (es) | 2014-12-11 | 2017-04-05 | Bayer Cropscience Ag | Derivados de arilsulfuro y arilsulfóxido de cinco miembros c-n-conectados, como plaguicidas |
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| JP3227976B2 (ja) | 1993-02-26 | 2001-11-12 | 松下電器産業株式会社 | 光学的情報記録部材、記録再生方法、及び記録再生装置 |
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| US20060211755A1 (en) | 2003-03-31 | 2006-09-21 | Eli Lilly And Company Patent Division | 3-oxo-1, 3-dihydro-indazole-2-carboxylic acid amide derivatives as phospholipase inhibitors |
| EP1613608A1 (en) | 2003-04-01 | 2006-01-11 | Eli Lilly And Company | Phospholipase inhibitors |
| US7595403B2 (en) | 2003-04-01 | 2009-09-29 | Eli Lilly And Company | Benzisothiazol-3-one-carboxylic acid amides as phospholipase inhibitors |
| JP2007528420A (ja) * | 2004-03-11 | 2007-10-11 | グラクソ グループ リミテッド | 新規m3ムスカリン性アセチルコリン受容体アンタゴニスト |
| DE102005018389A1 (de) | 2005-04-20 | 2006-10-26 | Sanofi-Aventis Deutschland Gmbh | Azolderivate als Inhibitoren von Lipasen und Phospholipasen |
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| CN101646655A (zh) | 2010-02-10 |
| AU2008235066A1 (en) | 2008-10-16 |
| CA2682875A1 (en) | 2008-10-16 |
| WO2008122352A1 (de) | 2008-10-16 |
| BRPI0809693A2 (pt) | 2014-10-07 |
| MA31296B1 (fr) | 2010-04-01 |
| TW200904804A (en) | 2009-02-01 |
| EP2144885B1 (de) | 2016-06-29 |
| UY31001A1 (es) | 2008-11-28 |
| NZ580127A (en) | 2011-03-31 |
| EP2144885A1 (de) | 2010-01-20 |
| RU2009140761A (ru) | 2011-05-10 |
| MX2009010485A (es) | 2009-10-19 |
| US8735437B2 (en) | 2014-05-27 |
| US20100105719A1 (en) | 2010-04-29 |
| KR20090126293A (ko) | 2009-12-08 |
| CL2008000981A1 (es) | 2008-10-10 |
| ZA200906211B (en) | 2010-05-26 |
| CO6220934A2 (es) | 2010-11-19 |
| JP2010523503A (ja) | 2010-07-15 |
| IL201255A0 (en) | 2010-05-31 |
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