AR072458A2 - Derivados de azol-pirimidina condensados, composiciones farmaceuticas que los contienen y su uso para inhibir la actividad pi3k-? - Google Patents
Derivados de azol-pirimidina condensados, composiciones farmaceuticas que los contienen y su uso para inhibir la actividad pi3k-?Info
- Publication number
- AR072458A2 AR072458A2 ARP090102458A ARP090102458A AR072458A2 AR 072458 A2 AR072458 A2 AR 072458A2 AR P090102458 A ARP090102458 A AR P090102458A AR P090102458 A ARP090102458 A AR P090102458A AR 072458 A2 AR072458 A2 AR 072458A2
- Authority
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- Argentina
- Prior art keywords
- amino
- alkyl
- optionally substituted
- alkoxycarbonyl
- halogen
- Prior art date
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- 239000008194 pharmaceutical composition Substances 0.000 title 1
- DDWJFSYHYPDQEL-UHFFFAOYSA-N pyrimidine;1h-pyrrole Chemical class C=1C=CNC=1.C1=CN=CN=C1 DDWJFSYHYPDQEL-UHFFFAOYSA-N 0.000 title 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 83
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 50
- 229910052736 halogen Inorganic materials 0.000 abstract 28
- 125000004454 (C1-C6) alkoxycarbonyl group Chemical group 0.000 abstract 23
- 125000004076 pyridyl group Chemical group 0.000 abstract 22
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 abstract 18
- 125000001424 substituent group Chemical group 0.000 abstract 13
- 125000002252 acyl group Chemical group 0.000 abstract 12
- 125000004390 alkyl sulfonyl group Chemical group 0.000 abstract 12
- 125000002485 formyl group Chemical group [H]C(*)=O 0.000 abstract 12
- 150000002367 halogens Chemical group 0.000 abstract 12
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 12
- 125000002883 imidazolyl group Chemical group 0.000 abstract 12
- -1 nitro, cyano, carboxy, amino Chemical group 0.000 abstract 12
- 125000003226 pyrazolyl group Chemical group 0.000 abstract 12
- 125000000335 thiazolyl group Chemical group 0.000 abstract 12
- 125000006295 amino methylene group Chemical group [H]N(*)C([H])([H])* 0.000 abstract 11
- 125000004397 aminosulfonyl group Chemical group NS(=O)(=O)* 0.000 abstract 11
- 125000004193 piperazinyl group Chemical group 0.000 abstract 11
- 125000000719 pyrrolidinyl group Chemical group 0.000 abstract 11
- 125000000168 pyrrolyl group Chemical group 0.000 abstract 11
- 125000006700 (C1-C6) alkylthio group Chemical group 0.000 abstract 10
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 abstract 10
- 125000002768 hydroxyalkyl group Chemical group 0.000 abstract 10
- 125000006296 sulfonyl amino group Chemical group [H]N(*)S(*)(=O)=O 0.000 abstract 10
- 125000000217 alkyl group Chemical group 0.000 abstract 3
- 125000006577 C1-C6 hydroxyalkyl group Chemical group 0.000 abstract 2
- 125000004502 1,2,3-oxadiazolyl group Chemical group 0.000 abstract 1
- 125000004511 1,2,3-thiadiazolyl group Chemical group 0.000 abstract 1
- 125000004504 1,2,4-oxadiazolyl group Chemical group 0.000 abstract 1
- 125000004514 1,2,4-thiadiazolyl group Chemical group 0.000 abstract 1
- 125000004506 1,2,5-oxadiazolyl group Chemical group 0.000 abstract 1
- 125000004517 1,2,5-thiadiazolyl group Chemical group 0.000 abstract 1
- 125000001781 1,3,4-oxadiazolyl group Chemical group 0.000 abstract 1
- 125000004520 1,3,4-thiadiazolyl group Chemical group 0.000 abstract 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 abstract 1
- 125000003545 alkoxy group Chemical group 0.000 abstract 1
- 125000004414 alkyl thio group Chemical group 0.000 abstract 1
- 229910052801 chlorine Inorganic materials 0.000 abstract 1
- 239000000460 chlorine Substances 0.000 abstract 1
- 125000002541 furyl group Chemical group 0.000 abstract 1
- 125000000623 heterocyclic group Chemical group 0.000 abstract 1
- 125000001786 isothiazolyl group Chemical group 0.000 abstract 1
- 125000002971 oxazolyl group Chemical group 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 239000000126 substance Substances 0.000 abstract 1
- 125000001544 thienyl group Chemical group 0.000 abstract 1
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- C07D471/12—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 three hetero rings
- C07D471/14—Ortho-condensed systems
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- 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
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- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Abstract
Un derivado de azolpirimidina condensado de la formula (1), su forma tautomérica o estereoisomérica, o una sal del mismo, donde X representa NH; Y1 representa N; Y2 e Y3 representan CR3R4; el enlace químico entre Y2- - -Y3 representa un enlace simple; Z3 y Z4 representan CH; Z1 y Z2 representan independientemente CH o CR2; R1 representa: uno de los siguientes anillos heterocíclicos seleccionados del grupo que consiste en: pirazolilo sustituido con 1 a 3 sustituyentes seleccionados del grupo que consiste en hidroxi, halogeno, nitro, ciano, carboxi, amino, N-(alquil C1-6)amino, N-(hidroxialquil C1-6)amino, N,N-di(alquil C1-6)amino, N-(acil C1-6)amino, N-(alcoxicarbonil C1-6)amino, N-(formil)-N-(alquil C1-6)amino, N,N-di(alquil C1-6)amino (alquenil C2-6)amino, N-(alcansulfonil C1-6)amino, N-[N,N-di(alquil C1-6)amino metilen]amino, alquiltio C1-6, alcanosulfonilo C1-6, sulfamoilo, alcoxi C1-6, alcoxicarbonilo C1-6, pirrolilo, imidazolilo, pirazolilo, pirrolidinilo, piridilo, fenil alcoxicarbonilo C1-6, tiazolilo opcionalmente sustituido con piridilo, piperazinilo opcionalmente sustituido con alquilo C1-6 o alcoxi C1-6; o con 1 o 2 sustituyentes alquilo C1-6 sustituidos con mono-, di- o tri-halogeno; o con 3 sustituyentes alquilo C1-6 opcionalmente sustituidos con mono-, di- o tri- halogeno; furilo sustituido con 1 a 3 sustituyentes seleccionados del grupo que consiste en hidroxi, halogeno, nitro, ciano, carboxi, amino, N-(alquil C1-6)amino, N-(hidroxialquil C1-6)amino, N,N-di(alquil C1-6)amino, N-(acil C1-6)amino. N-(alcoxicarbonil C1-6)amino, N-(formil)-N-(alquil C1-6)amino, N,N-di(alquil C1-6)amino (alquenil C2-6)amino, N-(alcan C1-6)sulfonil amino, N-[N,N-di(alquil C1-6)aminometilen]amino, alquiltio C1-6, alcansulfonilo C1-6, sulfamoilo, alcoxi C1-6, alcoxicarbonilo C1-6, pirrolilo, imidazolilo, pirazolilo, pirrolidinilo, piridilo, fenil alcoxicarbonilo C1-6, tiazolilo opcionalmente sustituido con piridilo, piperazinilo opcionalmente sustituido con alquilo C1-6 o alcoxi C1-6 y alquilo C1-6 opcionalmente sustituido con mono, di- o tri-halogeno, tienilo sustituido con 1 a 3 sustituyentes seleccionados del grupo que consiste en hidroxi, halogeno (aunque no cloro), carboxi, amino, N-(alquil C1-6)amino, N-(hidroxialquil C1-6)amino, N,N-di(alquil C1-6)amino, N-(acil C1-6)amino, N-(alcoxicarbonil C1-6)amino, N-(formil)-N-(alquil C1-6)amino, N,N-di(alquil C1-6)amino (alquenil C2-6)amino, N-(alcan C1-6)sulfonil amino, N-[N,N-di(alquil C1-6)aminometilen]amino, alquiltio C1-6, alcansulfonilo C1-6, sulfamoilo, alcoxi C1-6, alcoxicarbonilo C1-6, pirrolilo, imidazolilo, pirazolilo, pirrolidinilo, piridilo, fenil alcoxicarbonilo C1-6, tiazolilo opcionalmente sustituido con piridilo, piperazinilo opcionalmente sustituido con alquilo C1-6 o alcoxi C1-6; o con 1 sustituyente alquilo C1-6 sustituido con mono-, di- o tri-halogeno; o con 2 o 3 sustituyentes alquilo C1-6 opcionalmente sustituidos con mono-, di- o tri-halogeno; tiazolilo sustituido con 1 a 3 sustituyentes seleccionados del grupo que consiste en hidroxi, halogeno, nitro, ciano, carboxi, amino, N-(alquil C1-6)amino, N-(hidroxialquil C1-6)amino, N,N-di(alquil C1-6)amino, N-(acil C1-6)amino, N-(formil)-N-(alquil C1-6)amino, N,N-di(alquil C1-6)amino (alquenil C2-6)amino, N-(alcan C1-6)sulfonil amino, N-[N,N-di(alquil C1-6)aminometilen]amino, alquiltio C1-6, alcansulfonilo C1-6, sulfamoilo, alcoxi C1-6, alcoxicarbonilo C1-6, pirrolilo, imidazolilo, pirazolilo, pirrolidinilo, piridilo, fenil alcoxicarbonilo C1-6, tiazolilo opcionalmente sustituido con piridilo, piperazinilo opcionalmente sustituido con alquilo C1-6, o alcoxi C1-6 y alquilo C1-6 opcionalmente sustituido con mono-, di- o tri-halogeno; o con 1 o 2 sustituyentes alquilo C1-6 sustituido con mono-, di- o tri-halogeno; o con 3 sustituyentes alquilo C1-6 opcionalmente sustituidos con mono-, di- o tri-halogeno; o con 3 sustituyentes piridilo; o con 3 sustituyentes N-(alcoxicarbonil C1-6)amino; isotiazolilo opcionalmente sustituido con 1 a 3 sustituyentes seleccionados del grupo que consiste en hidroxi, halogeno, nitro, ciano, carboxi, amino, N-(alquil C1-6)amino, N-(hidroxialquil C1-6)amino, N,N-di(alquil C1-6)amino, N-(acil C1-6)amino, N-(alcoxicarbonil C1-6)amino, N-(formil)-N-(alquil C1-6)amino, N,N-di(alquil C1-6)amino (alquenil C2-6)amino, N-(alcan C1-6)sulfonil amino, N-[N,N-di(alquil C1-6)aminometilen]amino, alquiltio C1-6, alcansulfonilo C1-6, sulfamoilo, alcoxi C1-6, alcoxicarbonilo C1-6, pirrolilo, imidazolilo, pirazolilo, pirrolidinilo, piridilo, fenil alcoxicarbonilo C1-6, tiazolilo opcionalmente sustituido con piridilo, piperazinilo opcionalmente sustituido con alquilo C1-6 o alcoxi C1-6 y alquilo C1-6 opcionalmente sustituido con mono-, di- o tri-halogeno; oxazolilo opcionalmente sustituido con 1 a 3 sustituyentes seleccionados del grupo que consiste en hidroxi, halogeno, nitro, ciano, carboxi, amino, N-(alquil C1-6)amino, N-(hidroxialquil C1-6)amino, N,N-di(alquil C1-6)amino, N-(acil C1-6)amino, N-(alcoxicarbonil C1-6)amino, N-(formil)-N-(alquil C1-6)amino, N,N-di(alquil C1-6)amino (alquenil C2-6)amino, N-(alcan C1-6)sulfonil amino, N-[N,N-di(alquil C1-6)aminometilen]amino, alquiltio C1-6, alcansulfonilo C1-6, sulfamoilo, alcoxi C1-6, alcoxicarbonilo C1-6, pirrolilo, imidazolilo, pirazolilo, pirrolidinilo, piridilo, fenil alcoxicarbonilo C1-6, tiazolilo opcionalmente sustituido con piridilo, piperazinilo opcionalmente sustituido con alquilo C1-6 o alcoxi C1-6 y alquilo C1-6 opcionalmente sustituido con mono-, di- o tri-halogeno; isoxazoliIo sustituido con 1 a 3 sustituyentes seleccionados del grupo que consiste en hidroxi, halogeno, nitro, ciano, carboxi, amino, N-(alquil C1-6)amino, N-(hidroxialquil C1-6)amino, N,N-di(alquil C1-6)amino, N-(acil C1-6)amino, N-(alcoxicarbonil C1-6)amino, N-(formil)-N-(alquil C1-6)amino, N,N-di(alquil C1-6)amino (alquenil C2-6)amino, N-(alcan C1-6)sulfonil amino, N-[N,N-di(alquil C1-6)aminometilen]amino, alquiltio C1-6, alcansulfonilo C1-6, sulfamoilo, alcoxi C1-6, alcoxicarbonilo C1-6, pirrolilo, imidazolilo, pirazolilo, pirrolidinilo, piridilo, fenil alcoxicarbonilo C1-6, tiazolilo opcionalmente sustituido con piridilo, piperazinilo opcionalmente sustituido con alquilo C1-6 o alcoxi C1-6; o con 1 o 2 sustituyentes alquilo C1-6 sustituidos con mono-, di- o tri-halogeno; o con 3 sustituyentes alquilo C1-6 opcionalmente sustituidos con mono-, di- o tri-halogeno; imidazolilo sustituido con 1 a 3 sustituyentes seleccionados del grupo que consiste en hidroxi, halogeno, nitro, ciano, carboxi, amino, N-(alquil C1-6)amino, N-(hidroxialquil C1-6)amino, N,N-di(alquil C1-6)amino, N-(acil C1-6)amino, N-(alcoxicarbonil C1-6)amino, N-(formil)-N-(alquil C1-6)amino, N,N-di(alquil C1-6)amino (alquenil C2-6)amino, N-(alcan C1-6)sulfonil amino, N-[N,N-di(alquil C1-6)aminometilen]amino, alquiltio C1-6, alcansulfonilo C1-6, sulfamoilo, alcoxi C1-6, alcoxicarbonilo C1-6 , pirrolilo, imidazolilo, pirazolilo, pirrolidinilo, piridilo, fenil alcoxicarbonilo C1-6, tiazolilo opcionalmente sustituido con piridilo, piperazinilo opcionalmente sustituido con alquilo C1-6 o alcoxi C1-6 y alquilo C1-6 opcionalmente sustituidos con mono-, di- o tri-halogeno; isoimidazolilo opcionalmente sustituido con 1 a 3 sustituyentes seleccionados del grupo que consiste en hidroxi, halogeno, nitro, ciano, carboxi, amino, N-(alquil C1-6)amino, N-(hidroxialquil C1-6)amino, N,N-di(alquil C1-6)amino, N-(acil C1-6)amino, N-(alcoxicarbonil C1-6)amino, N-(formil)-N-(alquil C1-6)amino, N,N-di(alquil C1-6)amino (alquenil C2-6)amino, N-(alcan C1-6)sulfonil amino, N-[N,N-di(alquil C1-6)aminometilen]amino, alquiltio C1-6, alcansulfonilo C1-6, sulfamoilo, alcoxi C1-6, alcoxicarbonilo C1-6, pirrolilo, imidazolilo, pirazolilo, pirrolidinilo, piridilo, fenil alcoxicarbonilo C1-6, tiazolilo opcionalmente sustituido con piridilo, piperazinilo opcionalmente sustituido con alquilo C1-6 o alcoxi C1-6 y alquilo C1-6 opcionalmente sustituido con mono-, di- o tri-halogeno; 1,2,3-tiadiazolilo sustituido con 1 a 3 sustituyentes seleccionados del grupo que consiste en hidroxi, halogeno, nitro, ciano, carboxi, amino, N-(alquil C1-6)amino, N-(hidroxialquil C1-6)amino, N,N-di(alquil C1-6)amino, N-(acil C1-6)amino, N-(alcoxicarbonil C1-6)amino, N-(formil)-N-(alquil C1-6)amino, N,N-di(alquil C1-6)amino (alquenil C2-6)amino, N-(alcan C1-6)sulfonil amino, N-[N,N-di(alquil C1-6)aminometilen]amino, alquiltio C1-6, alcansulfonilo C1-6, sulfamoilo, alcoxi C1-6, alcoxicarbonilo C1-6, pirrolilo, imidazolilo, pirazolilo, pirrolidinilo, piridilo, fenil alcoxicarbonilo C1-6, tiazolilo opcionalmente sustituido con piridilo, piperazinilo opcionalmente sustituido con alquilo C1-6 o alcoxi C1-6 y alquilo C1-6 opcionalmente sustituido con mono-, di- o tri-halogeno; 1,2,4-tiadiazolilo, 1,2,5-tiadiazolilo o 1,3,4-tiadiazolilo opcionalmente sustituidos con 1 a 3 sustituyentes seleccionados del grupo que consiste en hidroxi, halogeno, nitro, ciano, carboxi, amino, N-(alquil C1-6)amino, N-(hidroxialquil C1-6)amino, N,N-di(alquil C1-6)amino, N-(acil C1-6)amino, N-(alcoxicarbonil C1-6)amino, N-(formil)-N-(alquil C1-6)amino, N,N-di(alquil C1-6)amino (alquenil C2-6)amino, N-(alcan C1-6)sulfonil amino, N-[N,N-di(alquil C1-6)aminometilen]amino, alquiltio C1-6, alcansulfonilo C1-6, sulfamoilo, alcoxi C1-6, alcoxicarbonilo C1-6, pirrolilo, imidazolilo, pirazolilo, pirrolidinilo, piridilo, fenil alcoxicarbonilo C1-6, tiazolilo opcionalmente sustituido con piridilo, piperazinilo opcionalmente sustituido con alquilo C1-6 o alcoxi C1-6 y alquilo C1-6 opcionalmente sustituido con mono-, di- o tri-halogeno; 1,2,3-oxadiazolilo, 1,2,4-oxadiazolilo, 1,2,5-oxadiazolilo o 1,3,4-oxadiazolilo, opcionalmente sustituidos con 1 a 3 sustituyentes seleccionados del grupo que consiste en hidroxi, halogeno, nitro, ciano, carboxi, amino, N-(alquil C1-6)amino, N-(hidroxialquil C1-6)amino, N,N-di(alquil C1-6)amino, N-(acil C1-6)amino, N-(alcoxicarbonil C1-6)amino, N-(formil)-N-(alquil C1-6)amino,
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| ARP090102458A AR072458A2 (es) | 2002-09-30 | 2009-07-01 | Derivados de azol-pirimidina condensados, composiciones farmaceuticas que los contienen y su uso para inhibir la actividad pi3k-? |
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| NZ234186A (en) * | 1989-07-07 | 1991-10-25 | Janssen Pharmaceutica Nv | Imidazo quinazolin-one derivatives and pharmaceutical compositions |
| CN1033644C (zh) * | 1993-01-02 | 1996-12-25 | 瑞安大药厂股份有限公司 | 3-取代甲基-2,3-二氢咪唑并[1,2-c]喹唑啉衍生物,其制备与用途 |
| EP0771204A4 (en) | 1994-08-12 | 1999-10-20 | Pro Neuron Inc | METHOD FOR TREATING SEPSIS OR FLAMMABLE DISEASES WITH OXYPURINE NUCLEOSIDES |
| US6066642A (en) * | 1996-01-29 | 2000-05-23 | The United States Of America As Represented By The Department Of Health And Human Services | Dihydropyridine-, pyridine-, benzopyran-4-one- and triazoloquinazoline derivative, their preparation and their use as adenosine receptor antagonists |
| US5932584A (en) * | 1997-05-06 | 1999-08-03 | National Science Council | Optically active 2,3-dihydroimidazo(1,2-C) quinazoline derivatives, the preparation and antihypertensive use thereof |
| EP1278748B1 (en) | 2000-04-25 | 2011-03-23 | ICOS Corporation | Inhibitors of human phosphatidyl-inositol 3-kinase delta |
| WO2001083456A1 (en) * | 2000-04-27 | 2001-11-08 | Yamanouchi Pharmaceutical Co., Ltd. | Condensed heteroaryl derivatives |
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