ethyl 2-(cyclopropanecarbonyl)-3-(dimethylamino)acrylate | 344615-37-8

• 分子结构分类: 有机化合物 - 脂质和类脂质分子 - 脂肪酰基
• 英文名称: ethyl 2-(cyclopropanecarbonyl)-3-(dimethylamino)acrylate
• 英文别名: (Z)-ethyl 2-(cyclopropanecarbonyl)-3-(dimethylamino)acrylate；ethyl (Z)-2-(cyclopropanecarbonyl)-3-(dimethylamino)prop-2-enoate
• CAS: 344615-37-8
• 化学式: C₁₁H₁₇NO₃
• 分子量: 211.261
• InChiKey: YRPHQFNJRONNNY-CLFYSBASSA-N

物化性质

• 沸点：
  289.8±30.0 °C(Predicted)
• 密度：
  1.125±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  1.2
• 重原子数：
  15
• 可旋转键数：
  6
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.64
• 拓扑面积：
  46.6
• 氢给体数：
  0
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  ethyl 2-(cyclopropanecarbonyl)-3-(dimethylamino)acrylate 在 sodium hydroxide 、 三乙胺 作用下， 以 甲醇 、 乙醇 为溶剂， 反应 2.0h， 生成 5-环丙基-1-(5-喹啉基)-1H-吡唑-4-羧酸
  参考文献：
  名称：

  Discovery of zoniporide: A potent and selective sodium–hydrogen exchanger type 1 (NHE-1) inhibitor with high aqueous solubility

  摘要：

  Zoniporide (CP-597,396) is a potent and selective inhibitor of NHE-1, which exhibits high aqueous solubility and acceptable pharmacokinetics for intravenous administration. The discovery, synthesis, activities, and rat and dog pharmacokinetics of this compound are presented. The potency and selectivity of zoniporide may be due to the conformation that the molecule adopts due to the presence of a cyclopropyl and a 5-quinolinyl substituent on the central pyrazole ring of the molecule. (C) 2001 Elsevier Science Ltd. All rights reserved.

  DOI：

  10.1016/s0960-894x(01)00059-2
• 作为产物：
  描述：

  乙基三甲基硅基丙二酸 在 正丁基锂 作用下， 以 正己烷 为溶剂， 反应 20.25h， 生成 ethyl 2-(cyclopropanecarbonyl)-3-(dimethylamino)acrylate
  参考文献：
  名称：

  Discovery of zoniporide: A potent and selective sodium–hydrogen exchanger type 1 (NHE-1) inhibitor with high aqueous solubility

  摘要：

  Zoniporide (CP-597,396) is a potent and selective inhibitor of NHE-1, which exhibits high aqueous solubility and acceptable pharmacokinetics for intravenous administration. The discovery, synthesis, activities, and rat and dog pharmacokinetics of this compound are presented. The potency and selectivity of zoniporide may be due to the conformation that the molecule adopts due to the presence of a cyclopropyl and a 5-quinolinyl substituent on the central pyrazole ring of the molecule. (C) 2001 Elsevier Science Ltd. All rights reserved.

  DOI：

  10.1016/s0960-894x(01)00059-2

文献信息

• SUBSTITUTED PYRIMIDIN-5-CARBOXAMIDES 281
  申请人：GILL Adrian Liam

  公开号：US20090264401A1

  公开（公告）日：2009-10-22

  A compound of formula (I): and pharmaceutically-acceptable salts thereof wherein the variable groups are defined within; their use in the inhibition of 11βHSD1, processes for making them and pharmaceutical compositions comprising them are also described.

  一种具有化学式（I）的化合物： 及其药用盐，其中变量基团在其中定义；还描述了它们在抑制11βHSD1中的应用，制备它们的方法以及包含它们的药物组合物。
• Pyrid-2-one derivatives and methods of use
  申请人：——

  公开号：US20040147561A1

  公开（公告）日：2004-07-29

  Selected compounds are effective for treatment of diseases, such as cell proliferation or apoptosis mediated diseases. The invention encompasses novel compounds, analogs, prodrugs and pharmaceutically acceptable derivatives thereof, pharmaceutical compositions and methods for prophylaxis and treatment of diseases and other maladies or conditions involving stroke, cancer and the like. The subject invention also relates to processes for making such compounds as well as to intermediates useful in such processes.

  所选化合物对于治疗疾病，如细胞增殖或凋亡介导的疾病，具有有效性。该发明涵盖了新颖的化合物、类似物、前药和其药学上可接受的衍生物，以及用于预防和治疗涉及中风、癌症等疾病和其他疾病或病况的药物组合物和方法。该主题发明还涉及制备此类化合物的方法，以及在这些过程中有用的中间体。
• PYRAZOLE DERIVATIVES AS 11-BETA-HSD1 INHIBITORS
  申请人：Packer Martin John

  公开号：US20090221663A1

  公开（公告）日：2009-09-03

  A compound of Formula (I): and pharmaceutically-acceptable salts thereof wherein the variable groups are defined within; their use in the inhibition of 11βHSD1, processes for making them and pharmaceutical compositions comprising them are also described.

  公式（I）的化合物及其药学上可接受的盐，其中可变基团在其内部定义；还描述了它们在抑制11βHSD1方面的用途，制造它们的过程以及包含它们的制药组合物。
• Pyrazole Derivatives as 11-Beta-HSD1 Inhibitors
  申请人：Packer Martin John

  公开号：US20110224273A1

  公开（公告）日：2011-09-15

  A compound of formula (I): and pharmaceutically-acceptable salts thereof wherein the variable groups are defined within; their use in the inhibition of 11βHSD1, processes for making them and pharmaceutical compositions comprising them are also described.

  化合物I的式子及其药用可接受的盐，其中变量基团在定义范围内；还描述了它们在抑制11βHSD1方面的使用，制造它们的过程以及包含它们的制药组合物。
• Pyrazole derivatives as 11-beta-HSD1 inhibitors
  申请人：AstraZeneca AB (Publ)

  公开号：EP2292228A1

  公开（公告）日：2011-03-09

  A compound of formula (I): and pharmaceutically -acceptable salts thereof wherein the variable groups are defined within; their use in the inhibition of 11βHSD1, processes for making them and pharmaceutical compositions comprising them are also described.

  式 (I) 的化合物： 及其药学上可接受的盐，其中的可变基团在其中定义；还描述了它们在抑制 11βHSD1 中的用途、制造工艺以及包含它们的药物组合物。