ethyl 2-(5-bromo-3-(ethylamino)pyrazin-2-ylamino)acetate | 1228014-20-7

• 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: ethyl 2-(5-bromo-3-(ethylamino)pyrazin-2-ylamino)acetate
• 英文别名: Ethyl 2-(5-bromo-3-(ethylamino)pyrazin-2-ylamino)acetate；ethyl 2-[[5-bromo-3-(ethylamino)pyrazin-2-yl]amino]acetate
• CAS: 1228014-20-7
• 化学式: C₁₀H₁₅BrN₄O₂
• 分子量: 303.159
• InChiKey: PVQYIZJADZBWRR-UHFFFAOYSA-N

物化性质

• 沸点：
  390.1±42.0 °C(Predicted)
• 密度：
  1.512±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  2.1
• 重原子数：
  17
• 可旋转键数：
  7
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.5
• 拓扑面积：
  76.1
• 氢给体数：
  2
• 氢受体数：
  6

反应信息

• 作为反应物：
  描述：

  ethyl 2-(5-bromo-3-(ethylamino)pyrazin-2-ylamino)acetate 在 盐酸 、 1,1'-双(二苯膦基)二茂铁二氯化钯(II)二氯甲烷复合物 、 溶剂黄146 作用下， 以 1,4-二氧六环 、 甲醇 、 水 为溶剂， 反应 20.33h， 生成 1-乙基-7-[2-甲基-6-(4H-1,2,4-三唑-3-基)吡啶-3-基]-3,4-二氢吡嗪并[2,3-b]吡嗪-2(1H)-酮
  参考文献：
  名称：

  Optimization of a Series of Triazole Containing Mammalian Target of Rapamycin (mTOR) Kinase Inhibitors and the Discovery of CC-115

  摘要：

  We report here the synthesis and structure activity relationship (SAR) of a novel series of triazole containing mammalian target of rapamycin (mTOR) kinase inhibitors. SAR studies examining the potency, selectivity, and PK parameters for a series of triazole containing 4,6- or 1,7-disubstituted-3,4-dihydropyrazino[2,3-b]pyrazine-2(1H)-ones resulted in the identification of triazole containing mTOR kinase inhibitors with improved PK properties. Potent compounds from this series were found to block both mTORC1(p56) and mTORC2(pAktS473) signaling in PC-3 cancer cells, in vitro and in vivo. When assessed in efficacy models, analogs exhibited dose-dependent efficacy in tumor xenograft models. This work resulted in the selection of CC-115 for clinical development.

  DOI：

  10.1021/acs.jmedchem.5b00627
• 作为产物：
  描述：

  2-(3,5-二溴吡嗪-2-基氨基)乙酸乙酯 以77的产率得到ethyl 2-(5-bromo-3-(ethylamino)pyrazin-2-ylamino)acetate
  参考文献：
  名称：

  J. Med. Chem. 2015, 58, 5599-5608

  摘要：

  DOI：

文献信息

• [EN] ANTI-CANCER NUCLEAR HORMONE RECEPTOR-TARGETING COMPOUNDS<br/>[FR] COMPOSÉS CIBLANT DES RÉCEPTEURS HORMONAUX NUCLÉAIRES ANTICANCÉREUX
  申请人：NUVATION BIO INC

  公开号：WO2020232119A1

  公开（公告）日：2020-11-19

  The disclosure relates to anti-cancer compounds derived from nuclear steroid receptor binders, to products containing the same, as well as to methods of their use and preparation.

  该披露涉及从核类固醇受体结合物中衍生的抗癌化合物，以及含有这些化合物的产品，以及它们的使用和制备方法。
• [EN] MTOR KINASE INHIBITORS FOR ONCOLOGY INDICATIONS AND DISEASES ASSOCIATED WITH THE MTOR/P13K/AKT PATHWAY<br/>[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
  申请人：SIGNAL PHARM LLC

  公开号：WO2010062571A1

  公开（公告）日：2010-06-03

  Provided herein are Heteroaryl Compounds having the following structure: R2 N (I) or (II) 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：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。
• [EN] METHODS OF SYNTHESIS AND PURIFICATION OF HETEROARYL COMPOUNDS<br/>[FR] PROCÉDÉS DE SYNTHÈSE ET DE PURIFICATION DE COMPOSÉS HÉTÉROARYLES
  申请人：SIGNAL PHARM LLC

  公开号：WO2011053518A1

  公开（公告）日：2011-05-05

  Provided herein are methods to prepare Heteroaryl Compounds having the following structure: Forumula (I) or Formula (II): 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：Forumula（I）或Formula（II）：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、老年病或心血管疾病。
• 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。