N-[2-[3-[3-[(2S)-2-[bis(ethylsulfanyl)methyl]pyrrolidine-1-carbonyl]-4-nitrophenoxy]propyl-(4-methylphenyl)sulfonylamino]ethyl]-4-methyl-N-(3-phenylmethoxypropyl)benzenesulfonamide | 271253-09-9

• 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-[2-[3-[3-[(2S)-2-[bis(ethylsulfanyl)methyl]pyrrolidine-1-carbonyl]-4-nitrophenoxy]propyl-(4-methylphenyl)sulfonylamino]ethyl]-4-methyl-N-(3-phenylmethoxypropyl)benzenesulfonamide
• CAS: 271253-09-9
• 化学式: C₄₅H₅₈N₄O₉S₄
• 分子量: 927.241
• InChiKey: RJAPNNPJOFNZGD-QLKFWGTOSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  8.4
• 重原子数：
  62
• 可旋转键数：
  24
• 环数：
  5.0
• sp3杂化的碳原子比例：
  0.44
• 拓扑面积：
  227
• 氢给体数：
  0
• 氢受体数：
  13

反应信息

• 作为反应物：
  描述：

  N-[2-[3-[3-[(2S)-2-[bis(ethylsulfanyl)methyl]pyrrolidine-1-carbonyl]-4-nitrophenoxy]propyl-(4-methylphenyl)sulfonylamino]ethyl]-4-methyl-N-(3-phenylmethoxypropyl)benzenesulfonamide 在 tin(ll) chloride 作用下， 以 四氢呋喃 、 甲醇 为溶剂， 生成
  参考文献：
  名称：

  Synthesis of Polyaminoalkyl Substituted Conjugates of Pyrrolo[2,1-c][1,4]benzodiazepine Involving SNAr Reaction of 2-Nitro-5-fluorobenzoate Precursors

  摘要：

  A synthetic procedure is described for conjugating polyaminoalkyl groups to the pyrrolo[2, 1-c][1,4]benzodiazepine pharmacophore in order to alter its characteristic DNA sequence binding preference. To this end SNAr reactions of 2-nitro-5-fluorobenzoate esters with different polyaminoalkyl side chains were examined and incorporated in the synthetic scheme.

  DOI：

  10.3987/com-99-s116
• 作为产物：
  描述：

  ethyl N-(2-nitro-5-fluorobenzoyl)pyrrolidine-2-carboxaldehyde 在 三甲基氯硅烷 、 sodium hydride 作用下， 以 四氢呋喃 为溶剂， 生成 N-[2-[3-[3-[(2S)-2-[bis(ethylsulfanyl)methyl]pyrrolidine-1-carbonyl]-4-nitrophenoxy]propyl-(4-methylphenyl)sulfonylamino]ethyl]-4-methyl-N-(3-phenylmethoxypropyl)benzenesulfonamide
  参考文献：
  名称：

  Synthesis of Polyaminoalkyl Substituted Conjugates of Pyrrolo[2,1-c][1,4]benzodiazepine Involving SNAr Reaction of 2-Nitro-5-fluorobenzoate Precursors

  摘要：

  A synthetic procedure is described for conjugating polyaminoalkyl groups to the pyrrolo[2, 1-c][1,4]benzodiazepine pharmacophore in order to alter its characteristic DNA sequence binding preference. To this end SNAr reactions of 2-nitro-5-fluorobenzoate esters with different polyaminoalkyl side chains were examined and incorporated in the synthetic scheme.

  DOI：

  10.3987/com-99-s116

文献信息

• Synthesis of Polyaminoalkyl Substituted Conjugates of Pyrrolo[2,1-c][1,4]benzodiazepine Involving SNAr Reaction of 2-Nitro-5-fluorobenzoate Precursors
  作者：Kiyoshi Matsumoto、Hirokazu Iida、J. William Lown

  DOI：10.3987/com-99-s116

  日期：——

  A synthetic procedure is described for conjugating polyaminoalkyl groups to the pyrrolo[2, 1-c][1,4]benzodiazepine pharmacophore in order to alter its characteristic DNA sequence binding preference. To this end SNAr reactions of 2-nitro-5-fluorobenzoate esters with different polyaminoalkyl side chains were examined and incorporated in the synthetic scheme.
• Iida, Hirokazu; Hayashi, Naoto; Lown, J. William, Heterocycles, 2004, vol. 62, p. 693 - 711
  作者：Iida, Hirokazu、Hayashi, Naoto、Lown, J. William、Matsumoto, Kiyoshi

  DOI：——

  日期：——