3-(phenylsulfanyl)-2H-isoindole-1-carboxaldehyde | 1285620-97-4

• 分子结构分类: 有机化合物 - 有机硫化合物 - 硫醚类
• 英文名称: 3-(phenylsulfanyl)-2H-isoindole-1-carboxaldehyde
• 英文别名: 1-carbaldehyde-3-phenylsulfanyl-2H-isoindole；3-phenylsulfanyl-2H-isoindole-1-carbaldehyde
• CAS: 1285620-97-4
• 化学式: C₁₅H₁₁NOS
• 分子量: 253.324
• InChiKey: BZUFIYBRDWTYFA-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4.2
• 重原子数：
  18
• 可旋转键数：
  3
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.0
• 拓扑面积：
  58.2
• 氢给体数：
  1
• 氢受体数：
  2

反应信息

• 作为产物：
  描述：

  异吲哚啉-1-酮 在 水 、 三乙胺 、 sodium hydroxide 、 三氯氧磷 作用下， 以 乙醇 、 二氯甲烷 、 N,N-二甲基甲酰胺 为溶剂， 反应 3.08h， 生成 3-(phenylsulfanyl)-2H-isoindole-1-carboxaldehyde
  参考文献：
  名称：

  Nucleophilic substitutions in the isoindole series as a valuable tool to synthesize derivatives with antitumor activity

  摘要：

  A novel synthetic approach to the synthesis of 3-substituted isoindoles through nucleophilic substitution of 3-halo derivatives by charged carbon, and neutral nitrogen, oxygen, and sulfur nucleophiles, assisted by a 1-acyl group, is reported. Aryl-thio-isoindoles, obtained through a direct nucleophilic substitution with sulfur nucleophiles, showed cytotoxic activity, with GI(50) values from micromolar to sub-micromolar concentrations, against the total number of cell lines investigated. (C) 2011 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tet.2011.01.056

文献信息

• Nucleophilic substitutions in the isoindole series as a valuable tool to synthesize derivatives with antitumor activity
  作者：Patrizia Diana、Annamaria Martorana、Paola Barraja、Alessandra Montalbano、Anna Carbone、Girolamo Cirrincione

  DOI：10.1016/j.tet.2011.01.056

  日期：2011.3

  A novel synthetic approach to the synthesis of 3-substituted isoindoles through nucleophilic substitution of 3-halo derivatives by charged carbon, and neutral nitrogen, oxygen, and sulfur nucleophiles, assisted by a 1-acyl group, is reported. Aryl-thio-isoindoles, obtained through a direct nucleophilic substitution with sulfur nucleophiles, showed cytotoxic activity, with GI(50) values from micromolar to sub-micromolar concentrations, against the total number of cell lines investigated. (C) 2011 Elsevier Ltd. All rights reserved.