N-(4H-indeno[1,2-b]thiophen-4-yl)-4-methylbenzenesulfonamide | 1292302-55-6

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 英文名称: N-(4H-indeno[1,2-b]thiophen-4-yl)-4-methylbenzenesulfonamide
• CAS: 1292302-55-6
• 化学式: C₁₈H₁₅NO₂S₂
• 分子量: 341.455
• InChiKey: BTTNDRNSGHZVQB-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.9
• 重原子数：
  23
• 可旋转键数：
  3
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.11
• 拓扑面积：
  82.8
• 氢给体数：
  1
• 氢受体数：
  4

反应信息

• 作为产物：
  描述：

  在 copper(II) bis(trifluoromethanesulfonate) 作用下， 以 甲苯 为溶剂， 反应 12.0h， 以88%的产率得到N-(4H-indeno[1,2-b]thiophen-4-yl)-4-methylbenzenesulfonamide
  参考文献：
  名称：

  Facile Cu(OTf)2-catalyzed preparation of 9-tosylaminofluorene derivatives from o-arylated N-tosylbenzaldimines

  摘要：

  The 9-tosylaminofluorene derivatives were synthesized conveniently by Cu(OTf)(2)-catalyzed aza-Friedel-Crafts reaction of o-arylated N-tosylbenzaldimines in high yields. This is an efficient, atom-economic, and green method. (C) 2010 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tetlet.2010.10.110

文献信息

• Efficient Synthesis of 9-Tosylaminofluorene Derivatives by Boron Trifluoride Etherate-Catalyzed Aza-Friedel-Crafts Reaction of in situ Generated N-Tosylbenzaldimines
  作者：Xufen Yu、Xiyan Lu

  DOI：10.1002/adsc.201000732

  日期：2011.3.7

  An efficient and expeditious boron trifluoride etherate (BF3⋅Et2O) catalyzed one‐pot reaction for the synthesis of N‐tosyl‐9‐aminofluorenes and anthracene derivatives from in situ generated N‐tosylbenzaldimines via an aza‐Friedal–Crafts reaction has been developed. The catalytic reaction shows high substrate tolerance with excellent yields.

  一种有效的和迅速的三氟化硼醚（BF 3 ⋅Et 2 O）催化的一锅用于合成反应Ñ甲苯磺酰基-9- aminofluorenes和蒽衍生物从原位生成Ñ -tosylbenzaldimines经由氮杂Friedal-Crafts反应具有已开发。催化反应显示出高的底物耐受性和优异的产率。
• Facile Cu(OTf)2-catalyzed preparation of 9-tosylaminofluorene derivatives from o-arylated N-tosylbenzaldimines
  作者：Xufen Yu、Xiyan Lu

  DOI：10.1016/j.tetlet.2010.10.110

  日期：2011.4

  The 9-tosylaminofluorene derivatives were synthesized conveniently by Cu(OTf)(2)-catalyzed aza-Friedel-Crafts reaction of o-arylated N-tosylbenzaldimines in high yields. This is an efficient, atom-economic, and green method. (C) 2010 Elsevier Ltd. All rights reserved.