CO6220908A2 - Derivados de 2,3 -dihidroimizazo[1,2-c]quinazolina sustituidos de utilidad en el tratamiento de trastornos hiperproliferativos y enfermedades asociadas con la angiogenesis - Google Patents
Derivados de 2,3 -dihidroimizazo[1,2-c]quinazolina sustituidos de utilidad en el tratamiento de trastornos hiperproliferativos y enfermedades asociadas con la angiogenesisInfo
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- CO6220908A2 CO6220908A2 CO09057915A CO09057915A CO6220908A2 CO 6220908 A2 CO6220908 A2 CO 6220908A2 CO 09057915 A CO09057915 A CO 09057915A CO 09057915 A CO09057915 A CO 09057915A CO 6220908 A2 CO6220908 A2 CO 6220908A2
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Abstract
1.- Un compuesto que tiene la fórmula:o una sal aceptable fisiológicamente, solvato, hidrato oestereoisómero del mismo, donde: R1 es -(CH2)n-(CHR4)-(CH2)m-N(R5)(R5'); R2 es un heteroarilo opcionalmente sustituido con 1, 2 o 3 grupos R6; R3 es alquilo o cicloalquilo; R4 es hidrógeno, hidroxi o alcoxi y R5 y R5´ pueden ser iguales o diferentes y son independientemente, hidrógeno, alquilo, cicloalquilalquilo, o alcoxialquilo o R5 y R5´ se pueden tomar junto con el átomo de nitrógeno al cual se encuentran unidos para formar un anillo heterocíclico que contiene nitrógeno de 3 a 7 miembros que contiene opcionalmente al menos un heteroátomo adicional seleccionado entre oxígeno, nitrógeno o azufre y que se puede sustituir opcionalmente con 1 o más grupos R6', o R4 y R5 se pueden tomar junto con los átomos a los cuales se encuentran unidos para formar un anillo heterocíclico que contiene nitrógeno de 5 o 6 miembros que contiene opcionalmente 1 o más átomos n es un entero entre 1-4 y m es un entero entre 0-4 con la condición de que cuando R4 y R5 se toman junto con los átomos a los cuales se encuentran unidos para formar un anillo que contiene nitrógeno de 3 a 7 miembros, n + m < 4. 2.- El compuesto de la reivindicación 1, donde R2 es un heteroarilo que contiene nitrógeno opcionalmente sustituido con 1, 2 o 3 grupos R6. 3.- El compuesto de la reivindicación 1, donde R5 y R5´ son independientemente alquilo.4.- El compuesto de la reivindicación 1, donde R5 y R5' se toman junto con el átomo de nitrógeno al cual se encuentran unidos para formar un anillo heterocíclico que contiene nitrógeno de 5 o 6 miembros que contiene al menos un heteroátomo adicional seleccionado entre oxígeno, nitrógeno o azufre y que se puede sustituir opcionalmente con 1 o más grupos R6´. 5.- El compuesto de la reivindicación 1, donde R4 es hidroxi.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US87309006P | 2006-12-05 | 2006-12-05 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CO6220908A2 true CO6220908A2 (es) | 2010-11-19 |
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ID=39492563
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CO09057915A CO6220908A2 (es) | 2006-12-05 | 2009-06-04 | Derivados de 2,3 -dihidroimizazo[1,2-c]quinazolina sustituidos de utilidad en el tratamiento de trastornos hiperproliferativos y enfermedades asociadas con la angiogenesis |
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Families Citing this family (68)
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| EP2184276A1 (en) | 2008-11-07 | 2010-05-12 | Universite Paul Cezanne Aix-Marseille Iii | Process to prepare new substituted 1H-Benzo(d) imidazol-2(3h)-Ones, New intermediates and their use as bace 1 inhibitors |
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| TWI533871B (zh) | 2014-03-11 | 2016-05-21 | 國立中央大學 | 萘并［２，３－ｆ］喹喔啉－７，１２－二酮化合物緩解疼痛的應用 |
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| FR3018813B1 (fr) * | 2014-03-18 | 2016-04-15 | Maco Pharma Sa | Procede de synthese d'un derive de psoralene |
| WO2016059220A1 (en) | 2014-10-16 | 2016-04-21 | INSERM (Institut National de la Santé et de la Recherche Médicale) | Tcr-activating agents for use in the treatment of t-all |
| EP3018127A1 (en) * | 2014-11-07 | 2016-05-11 | Bayer Pharma Aktiengesellschaft | Synthesis of copanlisib and its dihydrochloride salt |
| EP3018131A1 (en) * | 2014-11-07 | 2016-05-11 | Bayer Pharma Aktiengesellschaft | Synthesis of copanlisib and its dihydrochloride salt |
| US20180042929A1 (en) * | 2015-03-09 | 2018-02-15 | Bayer Pharma Aktiengesellschaft | Use of substituted 2,3-dihydroimidazo[1,2-c]quinazolines |
| BR112017019188A2 (pt) * | 2015-03-09 | 2018-04-24 | Bayer Pharma Aktiengesellschaft | Combinações contendo 2,3-di-hidroimidazo[1,2-c] quinazolina substituídas |
| FR3033499A1 (fr) * | 2015-03-11 | 2016-09-16 | Centre Leon-Berard | Composition pour le traitement des tumeurs neuroendocrines pancreatiques |
| CN112062778B (zh) * | 2015-07-02 | 2024-04-19 | 豪夫迈·罗氏有限公司 | 苯并氧氮杂䓬噁唑烷酮化合物及其使用方法 |
| CN105130998B (zh) * | 2015-09-25 | 2017-07-28 | 苏州立新制药有限公司 | 库潘尼西的制备方法 |
| CN105130997B (zh) * | 2015-09-25 | 2017-12-05 | 苏州明锐医药科技有限公司 | 一种库潘尼西的制备方法 |
| EP3426657B1 (en) | 2016-03-08 | 2022-07-13 | Bayer Pharma Aktiengesellschaft | 2 amino n [7 methoxy 2, 3-dihydroimidazo-[1, 2-c]quinazolin-5-yl]pyrimidine 5 carboxamides |
| EP3219329A1 (en) | 2016-03-17 | 2017-09-20 | Bayer Pharma Aktiengesellschaft | Combinations of copanlisib |
| KR20220120711A (ko) * | 2016-05-26 | 2022-08-30 | 유니버시티 오브 피츠버그 - 오브 더 커먼웰쓰 시스템 오브 하이어 에듀케이션 | 폐혈관 질환 치료용 조성물 및 방법 |
| WO2017211248A1 (zh) * | 2016-06-08 | 2017-12-14 | 深圳市塔吉瑞生物医药有限公司 | 一种取代的咪唑并喹唑啉化合物及其药物组合物 |
| CN109729716B (zh) | 2016-09-23 | 2022-03-15 | 拜耳制药股份公司 | Pi3k-抑制剂的组合产品 |
| CN106177918A (zh) * | 2016-09-30 | 2016-12-07 | 广州赛莱拉干细胞科技股份有限公司 | 一种间充质干细胞注射液及其制备方法和应用 |
| US11241500B2 (en) | 2016-12-14 | 2022-02-08 | Tarveda Therapeutics, Inc. | HSP90-targeting conjugates and formulations thereof |
| US11684672B2 (en) | 2017-02-24 | 2023-06-27 | Bayer Pharma Aktiengesellschaft | Combinations of copanlisib with anti-PD-1 antibody |
| WO2018215282A1 (en) | 2017-05-26 | 2018-11-29 | Bayer Pharma Aktiengesellschaft | Combination of bub1 and pi3k inhibitors |
| US11185549B2 (en) | 2017-06-28 | 2021-11-30 | Bayer Consumer Care Ag | Combination of a PI3K-inhibitor with an androgen receptor antagonist |
| US11253594B2 (en) * | 2017-07-07 | 2022-02-22 | University Of Pittsburgh-Of The Commonwealth System Of Higher Education | Drug combinations for protecting against neuronal cell death |
| ES2930081T3 (es) * | 2017-08-11 | 2022-12-07 | Teligene Ltd | Pirazolopirimidinas sustituidas útiles como inhibidores de quinasas |
| TWI794288B (zh) | 2017-09-08 | 2023-03-01 | 德商拜耳製藥公司 | 科帕利普(copanlisib)調配物 |
| EP3498266A1 (en) | 2017-12-15 | 2019-06-19 | Bayer Consumer Care AG | Formulations of copanlisib |
| WO2019105734A1 (en) | 2017-11-28 | 2019-06-06 | Bayer Consumer Care Ag | Combinations of copanlisib |
| WO2019105835A1 (en) | 2017-11-29 | 2019-06-06 | Bayer Consumer Care Ag | Combinations of copanlisib and anetumab ravtansine |
| WO2019197269A1 (en) | 2018-04-11 | 2019-10-17 | Bayer Aktiengesellschaft | Combinations of copanlisib with triazolone derivatives and their use in the treatment of cancer |
| CN108383849B (zh) * | 2018-04-26 | 2020-11-06 | 浙江大学 | 咪唑并喹唑啉衍生物及其在抗肿瘤抗炎中的应用 |
| CN108841318A (zh) * | 2018-07-12 | 2018-11-20 | 中国科学院海洋研究所 | 一种自修复壳聚糖水凝胶防腐涂料及其合成方法 |
| CA3110754A1 (en) | 2018-08-28 | 2020-03-05 | Bayer As | Combination of pi3k-inhibitors and targeted thorium conjugates |
| EP3866805A1 (en) | 2018-10-16 | 2021-08-25 | Bayer Aktiengesellschaft | Combination of atr kinase inhibitors with 2,3-dihydroimidazo[1,2-c]quinazoline compounds |
| CN109516961B (zh) * | 2018-12-25 | 2021-01-01 | 浙江大学 | 氨基喹唑啉酮和氨基异喹啉酮衍生物及其应用 |
| WO2020164997A1 (en) | 2019-02-12 | 2020-08-20 | Bayer Aktiengesellschaft | Combination of pi3k-inhibitors |
| WO2023139125A1 (en) | 2022-01-18 | 2023-07-27 | Synthon B.V. | Improved process for preparation of copanlisib |
| WO2023218032A1 (en) | 2022-05-13 | 2023-11-16 | Synthon B.V. | Solid forms of copanlisib salts |
Family Cites Families (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3644354A (en) | 1968-09-16 | 1972-02-22 | Sandoz Ag | 5-substituted-2 3-dihydroimidazo(1 2-c)quinazolines |
| US4146718A (en) | 1978-04-10 | 1979-03-27 | Bristol-Myers Company | Alkyl 5,6-dichloro-3,4-dihydro-2(1h)-iminoquinazoline-3-acetate hydrohalides |
| KR100830859B1 (ko) * | 2000-04-27 | 2008-05-21 | 아스텔라스세이야쿠 가부시키가이샤 | 이미다조피리딘 유도체 및 이를 함유하는 의약 조성물 |
| US6608053B2 (en) | 2000-04-27 | 2003-08-19 | Yamanouchi Pharmaceutical Co., Ltd. | Fused heteroaryl derivatives |
| PA8578001A1 (es) * | 2002-08-07 | 2004-05-07 | Warner Lambert Co | Combinaciones terapeuticas de inhibidores de quinasa de erb b y terapias antineoplasicas |
| ATE411996T1 (de) * | 2002-09-30 | 2008-11-15 | Bayer Healthcare Ag | Kondensierte azolpyrimidinderivate |
| AT412873B (de) | 2004-02-20 | 2005-08-25 | Aop Orphan Pharmaceuticals Ag | Verfahren zur herstellung von anagrelid hydrochlorid |
| WO2007143483A2 (en) | 2006-06-01 | 2007-12-13 | Smithkline Beecham Corporation | Combination of pazopanib and lapatinib for treating cancer |
| WO2008002039A1 (en) | 2006-06-28 | 2008-01-03 | Hanmi Pharm. Co., Ltd. | Quinazoline derivatives for inhibiting the growth of cancer cell |
| EP2508525A1 (en) | 2011-04-05 | 2012-10-10 | Bayer Pharma Aktiengesellschaft | Substituted 2,3-dihydroimidazo[1,2-c]quinazoline salts |
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