10-(4-(2-(4-methoxyphenyl)-2H-tetrazol-5-yl)butyl)-10H-phenothiazine | 1387626-76-7

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 苯并噻嗪类
• 英文名称: 10-(4-(2-(4-methoxyphenyl)-2H-tetrazol-5-yl)butyl)-10H-phenothiazine
• 英文别名: 10-[4-[2-(4-Methoxyphenyl)tetrazol-5-yl]butyl]phenothiazine
• CAS: 1387626-76-7
• 化学式: C₂₄H₂₃N₅OS
• 分子量: 429.546
• InChiKey: KIHOJZCALKBJBN-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  6.3
• 重原子数：
  31
• 可旋转键数：
  7
• 环数：
  5.0
• sp3杂化的碳原子比例：
  0.21
• 拓扑面积：
  81.4
• 氢给体数：
  0
• 氢受体数：
  6

反应信息

• 作为产物：
  描述：

  吩噻嗪 在 palladium on activated charcoal 、 氢气 、 sodium hydride 、 三乙胺 作用下， 以 四氢呋喃 、 甲醇 、 二氯甲烷 、 mineral oil 为溶剂， 20.0 ℃ 、101.33 kPa 条件下， 反应 72.33h， 生成 10-(4-(2-(4-methoxyphenyl)-2H-tetrazol-5-yl)butyl)-10H-phenothiazine
  参考文献：
  名称：

  Selective hydroboration of dieneamines. Formation of hydroxyalkylphenothiazines as MDR modulators

  摘要：

  N-dienylphenothiazines synthesized from tetrazolo[1,5-a]pyridinium salts by treatment with phenothiazine were subjected to catalytic hydrogenation to yield N-butylphenothiazines, whereas transformation of these dienes with borane dimethyl sulfide (BH3 x Me2S) resulted in selective hydroboration of one double bond and full reduction of the other double bond to give 2-hydroxybutylphenothiazines. Position of the hydroxyl group was supported by NMR spectroscopy and verified by X-ray analysis. Comparison of MDR modulatory activity of the new derivatives revealed that the hydroxybutyl compounds are promising candidates for development of novel MDR inhibitors. (C) 2012 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmc.2012.05.065

文献信息

• Selective hydroboration of dieneamines. Formation of hydroxyalkylphenothiazines as MDR modulators
  作者：Daniella Takács、Ildikó Nagy、Petra Bombicz、Orsolya Egyed、Katalin Jemnitz、Zsuzsanna Riedl、József Molnár、Leonard Amaral、György Hajós

  DOI：10.1016/j.bmc.2012.05.065

  日期：2012.7

  N-dienylphenothiazines synthesized from tetrazolo[1,5-a]pyridinium salts by treatment with phenothiazine were subjected to catalytic hydrogenation to yield N-butylphenothiazines, whereas transformation of these dienes with borane dimethyl sulfide (BH3 x Me2S) resulted in selective hydroboration of one double bond and full reduction of the other double bond to give 2-hydroxybutylphenothiazines. Position of the hydroxyl group was supported by NMR spectroscopy and verified by X-ray analysis. Comparison of MDR modulatory activity of the new derivatives revealed that the hydroxybutyl compounds are promising candidates for development of novel MDR inhibitors. (C) 2012 Elsevier Ltd. All rights reserved.