N-(benzenesulfonyl)-4-[[4-[[1-(4-chlorophenyl)cyclopropyl]amino]-6-(2,2,2-trifluoroethoxy)-1,3,5-triazin-2-yl]amino]benzamide | 1360828-04-1

• 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-(benzenesulfonyl)-4-[[4-[[1-(4-chlorophenyl)cyclopropyl]amino]-6-(2,2,2-trifluoroethoxy)-1,3,5-triazin-2-yl]amino]benzamide
• CAS: 1360828-04-1
• 化学式: C₂₇H₂₂ClF₃N₆O₄S
• 分子量: 619.024
• InChiKey: QDAHXJOCDHKYCA-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  6.5
• 重原子数：
  42
• 可旋转键数：
  10
• 环数：
  5.0
• sp3杂化的碳原子比例：
  0.19
• 拓扑面积：
  144
• 氢给体数：
  3
• 氢受体数：
  12

反应信息

• 作为产物：
  描述：

  苯磺酰胺 、 4-(4-(1-(4-chlorophenyl)cyclopropylamino)-6-(2,2,2-trifluoroethoxy)-1,3,5-triazin-2-ylamino)benzoic acid 在 4-二甲氨基吡啶 、 盐酸-N-乙基-Nˊ-(3-二甲氨基丙基)碳二亚胺 、 N,N-二异丙基乙胺 作用下， 以 N,N-二甲基甲酰胺 为溶剂， 反应 16.0h， 生成 N-(benzenesulfonyl)-4-[[4-[[1-(4-chlorophenyl)cyclopropyl]amino]-6-(2,2,2-trifluoroethoxy)-1,3,5-triazin-2-yl]amino]benzamide
  参考文献：
  名称：

  Functionalized triazines as potent HCV entry inhibitors

  摘要：

  A series of potent and novel acylsulfonamide-bearing triazines were synthesized and the structure-activity relationships (SARs) as HCV entry inhibitors were evaluated. This acylsulfonamide series was derived from an early lead, 4-(4-(1-(4-chlorophenyl)cyclopropylamino)-6-(2,2,2-trifluoroethoxy)-1,3,5-triazin-2-ylamino)benzoic acid wherein the carboxylic acid was replaced with an acylsulfonamide moiety. This structural modification provided a class of compounds which projected an additional vector off the terminus of the acylsulfonamide functionality as a means to drive activity. This effort led to the discovery of potent analogues within this series that demonstrated sub-nanomolar EC50 values in the HCV pseudotype particle (HCVpp) assay. (C) 2016 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2016.12.038

文献信息

• Compounds for the Treatment of Hepatitis C
  申请人：Sun Li-Qiang

  公开号：US20120213729A1

  公开（公告）日：2012-08-23

  The disclosure provides compounds of formula I, including pharmaceutically acceptable salts, as well as compositions and methods of using the compounds. The compounds have activity against hepatitis C virus (HCV) and may be useful in treating those infected with HCV.

  本公开提供了I式化合物，其中包括药用可接受的盐，以及使用该化合物的组合物和方法。这些化合物对丙型肝炎病毒（HCV）具有活性，并可用于治疗HCV感染者。
• US8765944B2
  申请人：——

  公开号：US8765944B2

  公开（公告）日：2014-07-01
• Functionalized triazines as potent HCV entry inhibitors
  作者：Eric S. Mull、Li-Qiang Sun、Qian Zhao、Betsy Eggers、Kevin Pokornowski、Guangzhi Zhai、Ramkumar Rajamani、Susan Jenkins、Melissa Kramer、Ying-Kai Wang、Hua Fang、Daniel Tenney、Carl J. Baldick、Mark I. Cockett、Nicholas A. Meanwell、Paul M. Scola

  DOI：10.1016/j.bmcl.2016.12.038

  日期：2017.2

  A series of potent and novel acylsulfonamide-bearing triazines were synthesized and the structure-activity relationships (SARs) as HCV entry inhibitors were evaluated. This acylsulfonamide series was derived from an early lead, 4-(4-(1-(4-chlorophenyl)cyclopropylamino)-6-(2,2,2-trifluoroethoxy)-1,3,5-triazin-2-ylamino)benzoic acid wherein the carboxylic acid was replaced with an acylsulfonamide moiety. This structural modification provided a class of compounds which projected an additional vector off the terminus of the acylsulfonamide functionality as a means to drive activity. This effort led to the discovery of potent analogues within this series that demonstrated sub-nanomolar EC50 values in the HCV pseudotype particle (HCVpp) assay. (C) 2016 Elsevier Ltd. All rights reserved.