6-bromo-4-(tetrahydro-2H-pyran-4-yl)-3,4-dihydropyrazino[2,3-b]pyrazin-2(1H)-one | 1228014-16-1

• 分子结构分类: 有机化合物 - 有机酸及其衍生物 - 羧酸及其衍生物
• 英文名称: 6-bromo-4-(tetrahydro-2H-pyran-4-yl)-3,4-dihydropyrazino[2,3-b]pyrazin-2(1H)-one
• 英文别名: 6-Bromo-4-(tetrahydro-2H-pyran-4-yl)-3,4-dihydropyrazino[2,3-b]pyrazin-2(1H)-one；2-bromo-8-(oxan-4-yl)-5,7-dihydropyrazino[2,3-b]pyrazin-6-one
• CAS: 1228014-16-1
• 化学式: C₁₁H₁₃BrN₄O₂
• 分子量: 313.154
• InChiKey: UGNVJEFFXOAVDT-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1
• 重原子数：
  18
• 可旋转键数：
  1
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.55
• 拓扑面积：
  67.4
• 氢给体数：
  1
• 氢受体数：
  5

反应信息

• 作为反应物：
  描述：

  6-bromo-4-(tetrahydro-2H-pyran-4-yl)-3,4-dihydropyrazino[2,3-b]pyrazin-2(1H)-one 、 六甲基二锡 在 四(三苯基膦)钯 作用下， 以 1,4-二氧六环 为溶剂， 反应 3.0h， 以42.3%的产率得到4-(tetrahydro-2H-pyran-4-yl)-6-(trimethylstannyl)-3,4-dihydropyrazino[2,3-b]pyrazin-2(1H)-one
  参考文献：
  名称：

  [EN] MTOR KINASE INHIBITORS FOR ONCOLOGY INDICATIONS AND DISEASES ASSOCIATED WITH THE MTOR/P13K/AKT PATHWAY
  [FR] INHIBITEURS DE mTOR KINASE ET LEUR EMPLOI DANS LES CAS D'INDICATIONS ONCOLOGIQUES ET POUR DES MALADIES EN RAPPORT AVEC LA VOIE mTOR/P13K/AKT

  摘要：

  本文提供具有以下结构的杂环芳基化合物：R2 N（I）或（II），其中R1-R4如本文所定义，包含有效量杂环芳基化合物的组合物，以及治疗或预防癌症、炎症性疾病、免疫疾病、神经退行性疾病、糖尿病、肥胖症、神经系统疾病、与年龄相关的疾病或心血管疾病的方法，包括向需要的患者施用有效量的杂环芳基化合物。

  公开号：

  WO2010062571A1
• 作为产物：
  描述：

  2-chloro-N-(3,5-dibromo-pyrazin-2-yl)-acetamide 在 N,N-二异丙基乙胺 、 sodium iodide 作用下， 以 乙腈 为溶剂， 反应 17.5h， 生成 6-bromo-4-(tetrahydro-2H-pyran-4-yl)-3,4-dihydropyrazino[2,3-b]pyrazin-2(1H)-one
  参考文献：
  名称：

  Discovery of Mammalian Target of Rapamycin (mTOR) Kinase Inhibitor CC-223

  摘要：

  We report here the synthesis and structure-activity relationship (SAR) of a novel series of mammalian target of rapamycin (mTOR) kinase inhibitors. A series of 4,6- or 1,7-disubstituted-3,4-dihydropyrazino[2,3-b]pyrazine-2(1H)-ones were optimized for in vivo efficacy. These efforts resulted in the identification of compounds with excellent mTOR kinase inhibitory potency, with exquisite kinase selectivity over the related lipid kinase PI3K. The improved PK properties of this series allowed for exploration of in vivo efficacy and ultimately the selection of CC-223 for clinical development.

  DOI：

  10.1021/acs.jmedchem.5b00626

文献信息

• mTOR KINASE INHIBITORS FOR ONCOLOGY INDICATIONS AND DISEASES ASSOCIATED WITH THE mTOR/PI3K/AKT PATHWAY
  申请人：Perrin-Ninkovic Sophie

  公开号：US20100216781A1

  公开（公告）日：2010-08-26

  Provided herein are Heteroaryl Compounds having the following structure: wherein R 1 -R 4 are as defined herein, compositions comprising an effective amount of a Heteroaryl Compound and methods for treating or preventing cancer, inflammatory conditions, immunological conditions, neurodegenerative diseases, diabetes, obesity, neurological disorders, age-related diseases, or cardiovascular conditions, comprising administering an effective amount of a Heteroaryl Compound to a patient in need thereof.

  本文提供了以下结构的杂环芳基化合物：其中R1-R4的定义如下，包含有效量的杂环芳基化合物的组合物以及治疗或预防癌症、炎症性疾病、免疫性疾病、神经退行性疾病、糖尿病、肥胖症、神经系统疾病、与年龄相关的疾病或心血管疾病的方法，包括向需要此类治疗的患者施用有效量的杂环芳基化合物。
• PYRAZINO[2,3-b]PYRAZINE mTOR KINASE INHIBITOR FOR ONCOLOGY INDICATIONS AND DISEASES ASSOCIATED WITH THE mTOR/PI3K/AKT PATHWAY
  申请人：Perrin-Ninkovic Sophie

  公开号：US20120059164A1

  公开（公告）日：2012-03-08

  Provided herein are Heteroaryl Compounds having the following structure: wherein R 1 -R 4 are as defined herein, compositions comprising an effective amount of a Heteroaryl Compound and methods for treating or preventing cancer, inflammatory conditions, immunological conditions, neurodegenerative diseases, diabetes, obesity, neurological disorders, age-related diseases, or cardiovascular conditions, comprising administering an effective amount of a Heteroaryl Compound to a patient in need thereof.

  本文提供具有以下结构的杂环芳基化合物：其中R1-R4如本文所定义，包括有效量的杂环芳基化合物的组合物以及治疗或预防癌症、炎症病症、免疫病症、神经退行性疾病、糖尿病、肥胖症、神经系统疾病、与年龄相关的疾病或心血管病症的方法，包括向需要该药物的患者施用有效量的杂环芳基化合物。
• Pyrazino[2,3-b]pyrazine mTOR kinase inhibitors for oncology indications and diseases associated with the mTOR/PI3K/Akt pathway
  申请人：Signal Pharmaceuticals, LLC

  公开号：US08110578B2

  公开（公告）日：2012-02-07

  Provided herein are Heteroaryl Compounds having the following structure: wherein R1-R4 are as defined herein, compositions comprising an effective amount of a Heteroaryl Compound and methods for treating or preventing cancer, inflammatory conditions, immunological conditions, neurodegenerative diseases, diabetes, obesity, neurological disorders, age-related diseases, or cardiovascular conditions, comprising administering an effective amount of a Heteroaryl Compound to a patient in need thereof.

  本文提供具有以下结构的杂环芳基化合物：其中，R1-R4如本文所定义，包含有效量的杂环芳基化合物的组合物以及治疗或预防癌症、炎症疾病、免疫疾病、神经退行性疾病、糖尿病、肥胖症、神经系统疾病、老年疾病或心血管疾病的方法，包括向需要此类治疗的患者施用有效量的杂环芳基化合物。
• METHODS OF SYNTHESIS AND PURIFICATION OF HETEROARYL COMPOUNDS
  申请人：Harris Roy L.

  公开号：US20110137028A1

  公开（公告）日：2011-06-09

  Provided herein are methods to prepare Heteroaryl Compounds having the following structure: wherein R 1 -R 4 are as defined herein. The Heteroaryl compounds are useful for treating or preventing cancer, inflammatory conditions, immunological conditions, neurodegenerative diseases, diabetes, obesity, neurological disorders, age-related diseases, or cardiovascular conditions.

  本文提供制备具有以下结构的杂环芳基化合物的方法：其中R1-R4如本文所定义。这些杂环芳基化合物可用于治疗或预防癌症、炎症性疾病、免疫疾病、神经退行性疾病、糖尿病、肥胖症、神经系统疾病、与年龄相关的疾病或心血管疾病。
• Methods of synthesis and purification of heteroaryl compounds
  申请人：Harris Roy L.

  公开号：US08569494B2

  公开（公告）日：2013-10-29

  Provided herein are methods to prepare Heteroaryl Compounds having the following structure: wherein R1-R4 are as defined herein. The Heteroaryl compounds are useful for treating or preventing cancer, inflammatory conditions, immunological conditions, neurodegenerative diseases, diabetes, obesity, neurological disorders, age-related diseases, or cardiovascular conditions.

  本文提供了制备具有以下结构的杂环芳基化合物的方法：其中R1-R4如本文所定义。这些杂环芳基化合物可用于治疗或预防癌症、炎症性疾病、免疫性疾病、神经退行性疾病、糖尿病、肥胖症、神经系统疾病、与年龄相关的疾病或心血管疾病。