2-chloro-N-(5-phenyl-3-thienyl)acetamide | 1253594-45-4

• 分子结构分类: 有机化合物 - 有机氮化合物
• 英文名称: 2-chloro-N-(5-phenyl-3-thienyl)acetamide
• 英文别名: 2-chloro-N-(5-phenylthiophen-3-yl)acetamide
• CAS: 1253594-45-4
• 化学式: C₁₂H₁₀ClNOS
• 分子量: 251.737
• InChiKey: PMCZWCIKCSOCBD-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.1
• 重原子数：
  16
• 可旋转键数：
  3
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.08
• 拓扑面积：
  57.3
• 氢给体数：
  1
• 氢受体数：
  2

反应信息

• 作为反应物：
  描述：

  硫氰酸铵 、 2-chloro-N-(5-phenyl-3-thienyl)acetamide 以 乙醇 为溶剂， 反应 3.0h， 以58%的产率得到2-(5-phenyl-3-thienylimino)-1,3-thiazolidin-4-one
  参考文献：
  名称：

  Synthesis of Novel 2-Thienylimino-1,3-thiazolidin-4-ones

  摘要：

  本文介绍了用 3-氨基噻吩-2-羧酸酯通过简单的四步程序制备新的 2-噻吩亚氨基-1,3-噻唑烷-4-酮的方法。

  DOI：

  10.1055/s-0029-1218780
• 作为产物：
  描述：

  5-phenyl-3-thiopheneamine 、 氯乙酰氯 以 N,N-二甲基甲酰胺 为溶剂， 反应 2.0h， 以71%的产率得到2-chloro-N-(5-phenyl-3-thienyl)acetamide
  参考文献：
  名称：

  Synthesis of Novel 2-Thienylimino-1,3-thiazolidin-4-ones

  摘要：

  本文介绍了用 3-氨基噻吩-2-羧酸酯通过简单的四步程序制备新的 2-噻吩亚氨基-1,3-噻唑烷-4-酮的方法。

  DOI：

  10.1055/s-0029-1218780

文献信息

• Synthesis of Novel 2-Thienylimino-1,3-thiazolidin-4-ones
  作者：Gilbert Kirsch、Ismail Abdillahi、Germain Revelant、Yazid Datoussaid

  DOI：10.1055/s-0029-1218780

  日期：2010.8

  The preparation of new 2-thienylimino-1,3-thiazolidin-4-ones from 3-aminothiophene-2-carboxylate using an easy four-step procedure is described.

  本文介绍了用 3-氨基噻吩-2-羧酸酯通过简单的四步程序制备新的 2-噻吩亚氨基-1,3-噻唑烷-4-酮的方法。
• Synthesis and biological evaluation of novel 2-heteroarylimino-1,3-thiazolidin-4-ones as potential anti-tumor agents
  作者：Germain Revelant、Sophie Huber-Villaume、Sandrine Dunand、Gilbert Kirsch、Hervé Schohn、Stéphanie Hesse

  DOI：10.1016/j.ejmech.2015.02.053

  日期：2015.4

  A series of 35 heteroarylimino-1,3-thiazolidinones with three sites of functionalization were synthesized and their antiproliferative properties were studied. The in vitro screening by MTT assay was performed against five cancer cell lines (human colon cancer cell lines HT29, HCT116 and SW620 and breast cancer cell lines MCF7 and MDA-MB-231). It was observed that N3-substituted thiazolidinones had moderate activities whereas 5-benzylidene thiazolidinones showed promising activities. To investigate the mechanism of action, detailed biological studies of six selected compounds (those presenting the lower mitotic index) were carried out on the human colon cancer HT29 cell line. Cell cycle assay revealed that those compounds induced cell accumulation in G2/M and in subG0/G1 phases of cell cycle. Moreover, dissipation of mitochondria membrane potential was observed as well as redox changes in treated cells. (C) 2015 Elsevier Masson SAS. All rights reserved.