AR062526A1 - DERIVADOS DE 4-(3-METILMORFOLIN-4-IL)PIRIMIDINA Y MORFOLIN-4-IL-PIRIMIDINA COMO INHIBIDORES DE MTOR QUINASA Y PI3K, UNA COMPOSICIoN FARMACEUTICA QUE LOS COMPRENDE Y EL USO DE LOS MISMOS EN LA FABRICACION DE MEDICAMENTOS PARA EL TRATAMIENTO DE DIVERSOS TIPOS DE CANCER. - Google Patents
DERIVADOS DE 4-(3-METILMORFOLIN-4-IL)PIRIMIDINA Y MORFOLIN-4-IL-PIRIMIDINA COMO INHIBIDORES DE MTOR QUINASA Y PI3K, UNA COMPOSICIoN FARMACEUTICA QUE LOS COMPRENDE Y EL USO DE LOS MISMOS EN LA FABRICACION DE MEDICAMENTOS PARA EL TRATAMIENTO DE DIVERSOS TIPOS DE CANCER.Info
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- alkyl
- 6alkyl
- alkoxy
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- C07D401/04—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 directly linked by a ring-member-to-ring-member bond
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- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/506—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
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- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more 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, directly attached to ring carbon atoms
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- C07D239/42—One nitrogen atom
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- 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
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- C07D403/12—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 chain containing hetero atoms as chain links
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- 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
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- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
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Abstract
Un compuesto de formula (1) o una sal aceptable para uso farmacéutico del mismo, composiciones farmacéuticas que los comprenden y el uso do los mismos en terapia, por ejemplo, en el tratamiento de enfermedades proliferativas, tal como cáncer y, en particular, en enfermedades mediadas por una mTOR quinasa y/o uno o más enzimas PI3K. Reivindicacion 1: Un compuesto, caracterizado porque es de formula (1) o una sal aceptable para uso farmacéutico del mismo; donde m es 0, 1, 2, 3 o 4; Y1 e Y2 son independientemente N o CR8, con la condicion de que uno sea N y el otro sea CR8; X es un grupo ligador seleccionado entre -CR4=CR5-, -CR4=CR5CR6R7-, -CR6R7CR5=CR4-, -C:::C-, -C:::CCR6R7.-, -CR6R7C:::C-, -NR4CR6R7-, -OCR6R7-, - SCR6R7-, - S(O)CR6R7-, -S(O)2CR6R7-, -C(O)NR4CR6R7-, -NR4C(O)CR6R7-, -NR4C(O)NR5CR6R7-, -NR4S(O)2CR6R7-, -S(O)2NR4CR6R7-, -C(O)NR4-, - NR4C(O)-, -NR4C(O)NR5-, -S(O)2NR4- y -NR4S(O)2-; R1 es un grupo seleccionado entre hidrogeno, alquilo C1-6, alquenilo C2-6, alquinilo C2-6, carbociclilo, carbociclil C1-6alquilo, heterociclilo y heterociclil C1-6alquilo, donde dicho grupo se encuentra opcionalmente sustituido con uno o más grupos seleccionados entre halo, ciano, nitro, R9, -OR9, -SR9, -SOR9, -SO2R9, - COR9, -CO2R9, -CONR9R10, -NR9R10, -NR9COR10, -NR9CO2R10, -NR9CONR10R15, -NR9COCONR10R15 y -NR9SO2R10; R2 es un grupo seleccionado entre alquilo C1-6, carbociclilo y heterociclilo, donde dicho grupo se encuentra sustituido con -NR17CONR18R19 y, opcionalmente, con uno o más grupos seleccionados independientemente entre halo, ciano, nitro, -R11, -OR11, -SR11, -SOR11, -SO2R11, -COR11, -CO2R11, -CONR11R12, -NR11R12, -NR11COR12, y -NR11COCONR12R16; cada R3, cuando está presente, es seleccionado independientemente entre halo, ciano, nitro, -R13, -OR13, -SR13, -SOR13 -SO2R13, -COR13, -CO2R13, -CONR13R14, -NR13R14, -NR13COR14, -NR13CO2R14 y -NR13SO2R14; R4 y R5 son independientemente hidrogeno o alquilo C1-6; o R1 y R4, junto con el átomo o átomos al cual están unidos, forman un anillo carbociclilo o heterociclilo de 4 a 10 miembros, donde 1, 2 o 3 átomos de carbono del anillo son opcionalmente reemplazados por N, O o S y donde dicho anillo se encuentra opcionalmente sustituido con uno o más grupos seleccionados entre halo, ciano, nitro, hidroxi, oxo, alquilo C1-6, alcoxilo C1-6, haloC1-6alquilo, haloC1-6alcoxilo, hidroxiC1-6alquilo, hidroxiC1-6alcoxilo, alcoxi C1-6-alquilo C1-6, alcoxi C1-6-alcoxilo C1-6, amino, alquilamino C1-6, bi(alquil C1-6)amino, aminoC1-6alquilo, alquil C1-6-aminoC1-6alquilo, bi(alquil C1-6)aminoC1-6alquilo, cianoC1-6alquilo, alquilsulfonilo C1-6, alquilsulfonilamino C1-6, alquilsulfonil C1-6-alquilC1-6amino, sulfamoilo, alquilsulfamoilo C1-6, bi(alquil C1-6)sulfamoilo, alcanoilamino C1-6, alcanoil C1-6-alquil C1-6amino, carbamoilo, alquilcarbamoilo C1-6 y bi(alquil C1-6)carbamoilo; R6 y R7 se seleccionan independientemente entre hidrogeno, halo, ciano, nitro y alquilo C1-6; R8 se selecciona entre hidrogeno, halo, ciano y alquilo C1-6; R9 y R10 son independientemente hidrogeno o un grupo seleccionado entre alquilo C1-6, carbociclilo, carbociclilC1-6alquilo, heterociclilo y heterociclilC1-6alquilo, donde dicho grupo se encuentra opcionalmente sustituido con uno o más grupos seleccionados entre halo, ciano, nitro, hidroxi, alquilo C1-6, alcoxilo C1-6, haloC1-6alquilo, haloC1-6alcoxilo, hidroxiC1-6alquilo, hidroxiC1-6alcoxilo, alcoxi C1-6-alquilo C1-6, alcoxi C1-6- alcoxilo C1-6, amino, alquilamino C1-6, bi(alquil C1-6)amino, aminoC1-6alquilo, alquil C1-6-aminoC1-6alquilo, bi(alquil C1-6)aminoC1-6alquilo, cianoC1-6alquilo, alquilsulfonilo C1-6, alquilsulfonilamino C1-6, alquilsulfonil C1-6-alquilC1-6amino, sulfamoilo, alquilsulfamoilo C1-6, bi(alquil C1-6)sulfamoilo, alcanoilamino C1-6, alcanoil C1-6-alquilC1-6amino, carbamoilo, alquilcarbamoilo C1-6 y bi(alquil C1-6)carbamoilo; R11, R12, R17 y R18 son independientemente hidrogeno o un grupo seleccionado entre alquilo C1-6, carbociclilo, carbociclilC1-6alquilo, heterociclilo y heterociclilC1-6alquilo, donde dicho grupo se encuentra opcionalmente sustituido con uno o más grupos seleccionados entre halo, ciano, nitro, hidroxi, alquilo C1- 6, alcoxilo C1-6, haloC1-6alquilo, haloC1-6alcoxilo, hidroxiC1-6alquilo, hidroxiC1-6alcoxilo, alcoxi C1-6-alquilo C1-6, alcoxi C1-6-alcoxilo C1-6, amino, alquilamino C1-6, bi(alquil C1-6)amino, aminoC1-6alquilo, alquil C1-6-aminoC1-6alquilo, bi(alquil C1-6)aminoC1-6alquilo, cianoC1-6alquilo, alquilsulfonilo C1-6, alcanoilamino C1-6, alcanoil C1-6-alquil C1-6amino, carbamoilo, alquilcarbamoilo C1-6 y bi(alquil C1-6)carbamoilo; R13, R14, R15, R16 y R19 son independientemente hidrogeno o un grupo seleccionado entre alquilo C1-6, carbociclilo, carbociclilC1-6alquilo, heterociclilo y heterociclilC1-6alquilo, donde dicho grupo se encuentra opcionalmente sustituido con uno o más grupos seleccionados entre halo, ciano, nitro, hidroxi, alquilo C1-6, alcoxilo C1-6, haloC1-6alquilo, haloC1-6alcoxilo, hidroxiC1-6alquilo, hidroxiC1-6alcoxilo, alcoxi C1-6-alquilo C1-6, alcoxi C1-6-alcoxilo C1-6, amino, alquilamino C1-6, bi(alquil C1-6)amino, aminoC1-6alquilo, alquil C1-6-aminoC1- 6alquilo, bi(alquil C1-6)aminoC1-6alquilo, cianoC1-6alquilo, alquilsulfonilo C1-6, alquilsulfonilamino C1-6, alquilsulfonil C1-6-alquilC1-6amino, sulfamoilo, alquilsulfamoilo C1-6, bi(alquil C1-6)sulfamoilo, alcanoilamino C1-6, alcanoil C1-6-alquil C1-6amino, carbamoilo, alquilcarbamoilo C1-6 y bi(alquil C1-6)carbamoilo; o R18 y R19 forman, junto con el átomo de nitrogeno al cual se encuentran unidos, un anillo heterociclilo de 3 a 10 miembros, donde 1 o 2 átomos de carbono del anillo son opcionalmente reemplazados por N, O o S y donde dicho anillo se encuentra opcionalmente sustituido con uno o más grupos seleccionados entre halo, ciano, nitro, hidroxi, alquilo C1-6, alcoxilo C1-6, haloC1-6alquilo, haloC1-6alcoxilo, hidroxiC1- 6alquilo, hidroxiC1-6alcoxilo, alcoxi C1-6-alquilo C1-6, alcoxi C1-6-alcoxilo C1-6, amino, alquilamino C1-6, bi(alquil C1-6)amino, aminoC1-6alquilo, alquil C1-6-aminoC1-6alquilo, bi(alquil C1-6)aminoC1-6alquilo, cianoC1-6alquilo, alquilsulfonilo C1- 6, alquilsulfonilamino C1-6, alquilsulfonil C1-6-alquilC1-6amino, sulfamoilo, alquilsulfamoilo C1-6, bi(alquil C1-6)sulfamoilo, alcanoilamino C1-6, alcanoil C1-6-alquil C1-6amino, carbamoilo, alquilcarbamoilo C1-6 y bi(alquil C1-6)carbamoilo.
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Application Number | Priority Date | Filing Date | Title |
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GB0616747A GB0616747D0 (en) | 2006-08-24 | 2006-08-24 | Novel compounds |
US94854407P | 2007-07-09 | 2007-07-09 |
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AR062526A1 true AR062526A1 (es) | 2008-11-12 |
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ARP070103775A AR062526A1 (es) | 2006-08-24 | 2007-08-24 | DERIVADOS DE 4-(3-METILMORFOLIN-4-IL)PIRIMIDINA Y MORFOLIN-4-IL-PIRIMIDINA COMO INHIBIDORES DE MTOR QUINASA Y PI3K, UNA COMPOSICIoN FARMACEUTICA QUE LOS COMPRENDE Y EL USO DE LOS MISMOS EN LA FABRICACION DE MEDICAMENTOS PARA EL TRATAMIENTO DE DIVERSOS TIPOS DE CANCER. |
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US (1) | US7750003B2 (es) |
EP (1) | EP2057140B1 (es) |
JP (1) | JP5534811B2 (es) |
KR (1) | KR101435231B1 (es) |
AR (1) | AR062526A1 (es) |
AU (1) | AU2007287428B2 (es) |
CA (1) | CA2660758A1 (es) |
CL (1) | CL2007002446A1 (es) |
CO (1) | CO6150160A2 (es) |
HK (1) | HK1130776A1 (es) |
IL (1) | IL196998A0 (es) |
MX (1) | MX2009002046A (es) |
NO (1) | NO20090631L (es) |
PE (1) | PE20081362A1 (es) |
UY (1) | UY30559A1 (es) |
WO (1) | WO2008023159A1 (es) |
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MX2009002046A (es) | 2006-08-24 | 2009-03-06 | Astrazeneca Ab | Derivados de morfolino pirimidina utiles en el tratamiento de trastornos proliferativos. |
AU2007300295A1 (en) | 2006-09-25 | 2008-04-03 | Boehringer Ingelheim International Gmbh | Compounds which modulate the CB2 receptor |
US7759344B2 (en) * | 2007-01-09 | 2010-07-20 | Amgen Inc. | Bis-aryl amide derivatives and methods of use |
KR20090108124A (ko) * | 2007-02-06 | 2009-10-14 | 노파르티스 아게 | Pi 3-키나제 억제제 및 그의 사용 방법 |
JP2010533158A (ja) * | 2007-07-09 | 2010-10-21 | アストラゼネカ アクチボラグ | 化合物類−945 |
JP5508260B2 (ja) | 2007-07-09 | 2014-05-28 | アストラゼネカ アクチボラグ | mTORキナーゼおよび/またはP13Kに関連する病気に用いられるモルホリノピリミジン誘導体 |
EP2217565B1 (en) | 2007-11-07 | 2013-05-22 | Boehringer Ingelheim International GmbH | Compounds which modulate the cb2 receptor |
EP2250160B1 (en) | 2008-01-25 | 2015-11-11 | Millennium Pharmaceuticals, Inc. | Thiophenes and their use as phosphatidylinositol 3-kinase (pi3k) inhibitors |
CN104058999A (zh) | 2008-02-29 | 2014-09-24 | 伊沃泰克股份公司 | 酰胺化合物、组合物及其应用 |
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WO2008023159A1 (en) | 2008-02-28 |
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AU2007287428B2 (en) | 2011-08-11 |
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PE20081362A1 (es) | 2008-11-14 |
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