2-苯基喹啉-3-甲酰胺 | 856196-10-6

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 喹啉及其衍生物
• 中文名称: 2-苯基喹啉-3-甲酰胺
• 英文名称: 2-phenylquinoline-3-carboxamide
• 英文别名: 2-phenyl-quinoline-3-carboxylic acid amide；2-Phenyl-chinolin-3-carbonsaeure-amid
• CAS: 856196-10-6
• 化学式: C₁₆H₁₂N₂O
• 分子量: 248.284
• InChiKey: VHVLFCBCBAVXQR-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.7
• 重原子数：
  19
• 可旋转键数：
  2
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.0
• 拓扑面积：
  56
• 氢给体数：
  1
• 氢受体数：
  2

反应信息

• 作为反应物：
  描述：

  2-苯基喹啉-3-甲酰胺 在 alkaline KBrO 、 硫酸 、 sodium nitrite 作用下， 生成 3-bromo-2-phenylquinoline
  参考文献：
  名称：

  John, Journal fur praktische Chemie (Leipzig 1954), 1931, vol. <2> 131, p. 346,347

  摘要：

  DOI：
• 作为产物：
  描述：

  2-苯基-喹啉-3-羧酸 在 ammonium hydroxide 、 氯化亚砜 作用下， 生成 2-苯基喹啉-3-甲酰胺
  参考文献：
  名称：

  John, Journal fur praktische Chemie (Leipzig 1954), 1931, vol. <2> 131, p. 314,318

  摘要：

  DOI：

文献信息

• Palladium-Catalyzed Sequential Formation of CC Bonds: Efficient Assembly of 2-Substituted and 2,3-Disubstituted Quinolines
  作者：Xiaochen Ji、Huawen Huang、Yibiao Li、Huoji Chen、Huanfeng Jiang

  DOI：10.1002/anie.201202412

  日期：2012.7.16

  A series of substituted quinolines was prepared from arylamines, aldehydes, and terminal olefins (see scheme). The palladium‐catalyzed sequential formation of CC bonds proceeds smoothly with both electron‐deficient and electron‐rich olefins. When acrylic acid is used as terminal olefin, decarboxylation occurs to provide 2‐substituted quinolines.

  由芳基胺，醛和末端烯烃制得一系列取代的喹啉（参见方案）。钯催化的CC键的顺序形成与贫电子烯烃和富电子烯烃均能顺利进行。当丙烯酸用作末端烯烃时，会发生脱羧反应，提供2个取代的喹啉。
• [EN] METHOD FOR MANUFACTURING OF QUINOLINE-3-CARBOXAMIDES<br/>[FR] PROCÉDÉ POUR LA FABRICATION DE QUINOLÉINE-3-CARBOXAMIDES
  申请人：ACTIVE BIOTECH AB

  公开号：WO2012004338A1

  公开（公告）日：2012-01-12

  A method for preparing a compound of formula (I) by reacting the appropriate alkyl ester and an aniline derivative, in a refluxing mixture containing an aliphatic solvent or a mixture of aliphatic solvents having a boiling point in the range of 68-191 °C; condensing vapors of the refluxing mixture; treating the condensed vapors with an alcohol scavenging agent or a mixture of alcohol scavenging agents; and returning the condensed vapors back to the reaction mixture.

  一种制备式（I）化合物的方法，通过反应适当的烷基酯和苯胺衍生物，在含有沸点在68-191°C范围内的脂肪溶剂或脂肪溶剂混合物的回流混合物中，将回流混合物的蒸汽凝结；用醇清除剂或醇清除剂混合物处理凝结的蒸汽；并将凝结的蒸汽返回到反应混合物中。
• Novel polyamine analogues as therapeutic and diagnostic agents
  申请人：ORIDIGM CORPORATION

  公开号：EP1085011A1

  公开（公告）日：2001-03-21

  Novel inhibitors of polyamine transport having inhibition constants two orders of magnitude lower than those of known compounds are disclosed. These polyamine analogues are useful pharmaceutical agents for treating disease where it is desired to inhibit polyamine transport or other polyamine binding proteins, for example cancer and post-angioplasty injury. Novel chemical synthetic methods to obtain polyamine analogues are disclosed, including the production of a combinatorial polyamine library. These approaches yield analogues with desirable activities both for diagnostic and research assays and therapy. The assays of the invention are useful for high throughput screening of targets in the discovery of drugs that interact with the polyamine system.

  本发明揭示了具有比已知化合物低两个数量级的抑制常数的多胺转运抑制剂。这些多胺类似物是治疗需要抑制多胺转运或其他多胺结合蛋白的疾病的有用药物，例如癌症和血管成形术后的损伤。揭示了获得多胺类似物的新的化学合成方法，包括制备组合多胺库。这些方法产生的类似物具有理想的诊断和研究测定和治疗活性。本发明的测定方法对于高通量筛选与多胺系统相互作用的药物发现目标非常有用。
• Polyamine analogues as therapeutic and diagnostic agents
  申请人：MediQuest Therapeutics, Inc.

  公开号：EP1867633A1

  公开（公告）日：2007-12-19

  Novel inhibitors of polyamine transport having inhibition constants two orders of magnitude lower than those of known compounds are disclosed. These polyamine analogues are useful pharmaceutical agents for treating diseases where it is desired to inhibit polyamine transport or other polyamine binding proteins, for example cancer and post-angioplasty injury. Novel chemical synthetic methods to obtain polyamine analogues are disclosed, including the production of a combinatorial polyamine library. These approaches yield analogues with desirable activities both for diagnostic and research assays and therapy. The assays of the invention are useful for high throughput screening of targets in the discovery of drugs that interact with the polyamine system.

  本研究公开了新型多胺转运抑制剂，其抑制常数比已知化合物的抑制常数低两个数量级。这些多胺类似物是治疗需要抑制多胺转运或其他多胺结合蛋白的疾病（如癌症和血管成形术后损伤）的有用药物。公开了获得多胺类似物的新型化学合成方法，包括组合多胺库的生产。这些方法产生的类似物具有理想的活性，既可用于诊断和研究测定，也可用于治疗。本发明的检测方法可用于高通量筛选目标，以发现与多胺系统相互作用的药物。
• Full-length human cDNAs encoding potentially secreted proteins
  申请人：——

  公开号：US20020102604A1

  公开（公告）日：2002-08-01

  The invention concerns GENSET polynucleotides and polypeptides. Such GENSET products may be used as reagents in forensic analyses, as chromosome markers, as tissue/cell/organelle-specific markers, in the production of expression vectors. In addition, they may be used in screening and diagnosis assays for abnormal GENSET expression and/or biological activity and for screening compounds that may be used in the treatment of GENSET-related disorders.

  本发明涉及 GENSET 多核苷酸和多肽。这些 GENSET 产品可用作法医分析试剂、染色体标记、组织/细胞/器官特异性标记以及表达载体的生产。此外，它们还可用于筛选和诊断 GENSET 异常表达和/或生物活性的检测，以及筛选可用于治疗 GENSET 相关疾病的化合物。