2-氨基-6-氟-N-(5-氟-4-(4-(4-(噁丁环烷-3-基)哌嗪-1-羰基)哌啶-1-基)吡啶-3-基)吡唑并[1,5-A]嘧啶-3-甲酰胺 | 1613191-99-3

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 吡唑并嘧啶类
• 中文名称: 2-氨基-6-氟-N-(5-氟-4-(4-(4-(噁丁环烷-3-基)哌嗪-1-羰基)哌啶-1-基)吡啶-3-基)吡唑并[1,5-A]嘧啶-3-甲酰胺
• 英文名称: 2-amino-6-fluoro-N-[5-fluoro-4-(4-{[4-(oxetan-3-yl)piperazin-1-yl]carbonyl}piperidin-1-yl)pyridin-3-yl]pyrazolo[1,5-a]pyrimidine-3-carboxamide
• 英文别名: VX-803；2-amino-6-fluoro-N-[5-fluoro-4-[4-[4-(oxetan-3-yl)piperazine-1-carbonyl]-1-piperidyl]-3-pyridyl]pyrazolo[1,5-a]pyrimidine-3-carboxamide；2-amino-6-fluoro-N-(5-fluoro-4-{4-[4-(oxetan-3-yl)piperazine-1-carbonyl]piperidin-1-yl}pyridin-3-yl)pyrazolo[1,5-a]pyrimidine-3-carboxamide；Gartisertib；2-amino-6-fluoro-N-[5-fluoro-4-[4-[4-(oxetan-3-yl)piperazine-1-carbonyl]piperidin-1-yl]pyridin-3-yl]pyrazolo[1,5-a]pyrimidine-3-carboxamide
• CAS: 1613191-99-3
• 化学式: C₂₅H₂₉F₂N₉O₃
• 分子量: 541.561
• InChiKey: QAYHKBLKSXWOEO-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  0.1
• 重原子数：
  39
• 可旋转键数：
  5
• 环数：
  6.0
• sp3杂化的碳原子比例：
  0.48
• 拓扑面积：
  134
• 氢给体数：
  2
• 氢受体数：
  11

反应信息

• 作为产物：
  描述：

  5-溴-3-氟吡啶 在 吡啶 、 二苯甲酮亚胺 、 tris-(dibenzylideneacetone)dipalladium(0) 、 正丁基锂 、 N-[(6-chlorobenzotriazol-1-yl)oxy-(dimethylamino)methylene]-dimethyl-ammonium tetrafluoroborate 、 sodium carbonate 、 caesium carbonate 、 N,N-二异丙基乙胺 、 4,5-双二苯基膦-9,9-二甲基氧杂蒽 作用下， 以 四氢呋喃 、 1,4-二氧六环 、 正己烷 、 乙腈 、 环己醇 为溶剂， 反应 18.5h， 生成 2-氨基-6-氟-N-(5-氟-4-(4-(4-(噁丁环烷-3-基)哌嗪-1-羰基)哌啶-1-基)吡啶-3-基)吡唑并[1,5-A]嘧啶-3-甲酰胺
  参考文献：
  名称：

  COMPOUNDS USEFUL AS INHIBITORS OF ATR KINASE

  摘要：

  本发明涉及作为ATR蛋白激酶抑制剂的化合物。该发明涉及包括本发明化合物的药学上可接受的组合物；使用本发明化合物治疗各种疾病、疾病和症状的方法；制备本发明化合物的方法；制备本发明化合物的中间体；以及本发明化合物的固体形式。 本发明的化合物具有式I-A或I-B： 其中变量如本文所定义。

  公开号：

  US20150158872A1

文献信息

• Compounds useful as inhibitors of ATR kinase
  申请人：Vertex Pharmaceuticals Incorporated

  公开号：US09340546B2

  公开（公告）日：2016-05-17

  The present invention relates to compounds useful as inhibitors of ATR protein kinase. The invention also relates to pharmaceutically acceptable compositions comprising the compounds of this invention; methods of treating of various diseases, disorders, and conditions using the compounds of this invention; processes for preparing the compounds of this invention; intermediates for the preparation of the compounds of this invention; and methods of using the compounds in in vitro applications, such as the study of kinases in biological and pathological phenomena; the study of intracellular signal transduction pathways mediated by such kinases; and the comparative evaluation of new kinase inhibitors. The compounds of this invention have formula I: or a pharmaceutically acceptable salt, wherein the variables are as defined herein. Moreover, The compounds of this invention have formula I-A: or a pharmaceutically acceptable salt, wherein the variables are as defined herein.

  本发明涉及用作ATR蛋白激酶抑制剂的化合物。本发明还涉及包含本发明化合物的药学上可接受的组合物；使用本发明化合物治疗各种疾病、紊乱和状况的方法；制备本发明化合物的过程；用于制备本发明化合物的中间体；以及在体外应用中使用化合物的方法，例如研究生物和病理现象中的激酶、由这些激酶介导的细胞内信号转导途径的研究；以及新的激酶抑制剂的比较评估。本发明的化合物具有公式I：或药学上可接受的盐，其中变量如本文所定义。此外，本发明的化合物具有公式I-A：或药学上可接受的盐，其中变量如本文所定义。
• [EN] COMBINATION THERAPIES INCLUDING MYT1 INHIBITORS<br/>[FR] POLYTHÉRAPIES COMPRENANT DES INHIBITEURS DE MYTL
  申请人：REPARE THERAPEUTICS INC

  公开号：WO2022213204A1

  公开（公告）日：2022-10-13

  The use of inhibitors of tyrosine and threonine- specific cdc2-inhibitory kinase (Mytl) in the treatment of cancer is disclosed. In preferred embodiments, the Mytl inhibitor is a carboxamide pyrrolopyrazine or carboxamide pyrrolopyridine of Formula I. The Mytl inhibitors may be used in combination with a variety of other anti-cancer agents. Such agents include a WEE1 inhibitor, TOPI or TOP2A inhibitor, RRM1 or RRM2 inhibitor, AURKA or AURKB inhibitor, ATR inhibitor, TTK inhibitor, SOD1 or SOD2 inhibitor, BUB1 inhibitor, CDC7 inhibitor, SAE1 inhibitor, PLK1 inhibitor, UBA2 inhibitor, DUT inhibitor, HDAC3 inhibitor, CHEK1 inhibitor, MEN1 inhibitor, DOT1L inhibitor, CREBBP inhibitor, EZH2 inhibitor, PLK4 inhibitor, HASPIN inhibitor, METTL3 inhibitor, nucleoside analogs, and platinum-based DNA alkylating agents.

  本发明公开了在治疗癌症中使用酪氨酸和苏氨酸特异性cdc2抑制性激酶（Mytl）抑制剂的方法。在优选实施例中，Mytl抑制剂是式I的羧酰胺吡咯吡嗪或羧酰胺吡咯吡啶。Mytl抑制剂可以与各种其他抗癌药物联合使用。这些药物包括WEE1抑制剂、TOPI或TOP2A抑制剂、RRM1或RRM2抑制剂、AURKA或AURKB抑制剂、ATR抑制剂、TTK抑制剂、SOD1或SOD2抑制剂、BUB1抑制剂、CDC7抑制剂、SAE1抑制剂、PLK1抑制剂、UBA2抑制剂、DUT抑制剂、HDAC3抑制剂、CHEK1抑制剂、MEN1抑制剂、DOT1L抑制剂、CREBBP抑制剂、EZH2抑制剂、PLK4抑制剂、HASPIN抑制剂、METTL3抑制剂、核苷类似物和铂基DNA烷基化剂。
• COMPOUNDS USEFUL AS INHIBITORS OF ATR KINASE FOR THE TREATMENT OF CANCER DISEASES
  申请人：Vertex Pharmaceuticals Inc.

  公开号：EP3418281A1

  公开（公告）日：2018-12-26

  The present invention relates to compounds useful as inhibitors of ATR protein kinase. The invention also relates to pharmaceutically acceptable compositions comprising the compounds of this invention; methods of treating of various diseases, disorders, and conditions using the compounds of this invention; processes for preparing the compounds of this invention; intermediates for the preparation of the compounds of this invention; and methods of using the compounds in in vitro applications, such as the study of kinases in biological and pathological phenomena; the study of intracellular signal transduction pathways mediated by such kinases; and the comparative evaluation of new kinase inhibitors. The compounds of this invention have formula I: or a pharmaceutically acceptable salt, wherein the variables are as devined herein. Moreover, The compounds of this invention have formula I-A: or a pharmaceutically acceptable salt, wherein the variables are as defined herein.

  本发明涉及可用作 ATR 蛋白激酶抑制剂的化合物。本发明还涉及包含本发明化合物的药学上可接受的组合物；使用本发明化合物治疗各种疾病、失调和病症的方法；制备本发明化合物的工艺；制备本发明化合物的中间体；以及在体外应用中使用本发明化合物的方法，例如研究生物和病理现象中的激酶；研究由这些激酶介导的细胞内信号转导途径；以及比较评估新的激酶抑制剂。 本发明的化合物具有式 I： 或药学上可接受的盐，其中变量如本文所设计。 此外，本发明的化合物具有式 I-A： 或药学上可接受的盐，其中变量如本文所定义。
• 2-AMINO-N-(PIPERIDIN-1-YL-PYRIDIN-3-YL) PYRAZOLO[1,5ALPHA]PYRIMIDINE-3-CARBOXAMID AS INHIBITOR OF ATR KINASE
  申请人：Vertex Pharmaceuticals Incorporated

  公开号：EP3486245A1

  公开（公告）日：2019-05-22

  The present invention relates to compounds useful as inhibitors of ATR protein kinase. The invention also relates to pharmaceutically acceptable compositions comprising the compounds of this invention; methods of treating of various diseases, disorders, and conditions using the compounds of this invention; processes for preparing the compounds of this invention; intermediates for the preparation of the compounds of this invention; and methods of using the compounds in in vitro applications, such as the study of kinases in biological and pathological phenomena; the study of intracellular signal transduction pathways mediated by such kinases; and the comparative evaluation of new kinase inhibitors. The compounds of this invention have formula I: or a pharmaceutically acceptable salt, wherein the variables are as devined herein. Moreover, The compounds of this invention have formula I-A: or a pharmaceutically acceptable salt, wherein the variables are as defined herein.

  本发明涉及可用作 ATR 蛋白激酶抑制剂的化合物。本发明还涉及包含本发明化合物的药学上可接受的组合物；使用本发明化合物治疗各种疾病、失调和病症的方法；制备本发明化合物的工艺；制备本发明化合物的中间体；以及在体外应用中使用本发明化合物的方法，例如研究生物和病理现象中的激酶；研究由这些激酶介导的细胞内信号转导途径；以及比较评估新的激酶抑制剂。 本发明的化合物具有式 I： 或药学上可接受的盐，其中变量如本文所设计。 此外，本发明的化合物具有式 I-A： 或药学上可接受的盐，其中变量如本文所定义。
• Method for treating cancer using a combination of Chk1 and ATR inhibitors
  申请人：Vertex Pharmaceuticals Incorporated

  公开号：US11179394B2

  公开（公告）日：2021-11-23

  The present invention relates to methods of treating cancer in a patient by administering a compound useful as an inhibitor of ATR protein kinase in combination with a compound useful as an inhibitor of Chk1 protein kinase. The aforementioned combination displays a surprising synergistic effect in treating cancer despite the targeted protein kinases being within the same biological pathway. Moreover, the present invention also relates to methods of treating cancer by administering a compound useful as an inhibitor of ATR protein kinase; administering a compound useful as an inhibitor of Chk1 protein kinase; as well as administering a DNA damaging agent to a patient. The compounds utilized in this invention are represented by formula I and formula II: wherein the variables are as defined herein.

  本发明涉及通过施用一种可作为 ATR 蛋白激酶抑制剂的化合物和一种可作为 Chk1 蛋白激酶抑制剂的化合物来治疗患者癌症的方法。尽管靶向蛋白激酶属于同一生物通路，但上述组合在治疗癌症方面显示出惊人的协同效应。此外，本发明还涉及治疗癌症的方法，即给患者施用一种可作为 ATR 蛋白激酶抑制剂的化合物；给患者施用一种可作为 Chk1 蛋白激酶抑制剂的化合物；以及给患者施用一种 DNA 损伤剂。 本发明中使用的化合物由式I和式II表示： 其中变量如本文所定义。