2-{4-[(4-butylphenylamino)(1-cyclohexyl-1H-tetrazol-5-yl)methyl]phenyl}-3-cyclohexylamino-5-methylimidazo[1,2-a]pyridine | 1440522-54-2

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 唑类
• 英文名称: 2-{4-[(4-butylphenylamino)(1-cyclohexyl-1H-tetrazol-5-yl)methyl]phenyl}-3-cyclohexylamino-5-methylimidazo[1,2-a]pyridine
• 英文别名: 2-[4-[(4-butylanilino)-(1-cyclohexyltetrazol-5-yl)methyl]phenyl]-N-cyclohexyl-5-methylimidazo[1,2-a]pyridin-3-amine
• CAS: 1440522-54-2
• 化学式: C₃₈H₄₈N₈
• 分子量: 616.853
• InChiKey: QHIVUQYXIVDSHJ-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  10.4
• 重原子数：
  46
• 可旋转键数：
  11
• 环数：
  7.0
• sp3杂化的碳原子比例：
  0.47
• 拓扑面积：
  85
• 氢给体数：
  2
• 氢受体数：
  6

反应信息

• 作为产物：
  描述：

  对苯二甲醛 在 叠氮基三甲基硅烷 、 氯化铋 作用下， 以 neat (no solvent) 为溶剂， 反应 0.17h， 生成 2-{4-[(4-butylphenylamino)(1-cyclohexyl-1H-tetrazol-5-yl)methyl]phenyl}-3-cyclohexylamino-5-methylimidazo[1,2-a]pyridine
  参考文献：
  名称：

  Three Novel Sequential Reactions for the Facile Synthesis of a Library of Bisheterocycles Possessing the 3-Aminoimidazo[1,2-a]pyridine Core Cata­lyzed by Bismuth(III) Chloride

  摘要：

  Novel, one-pot, two-step, sequential protocols for the synthesis of 1,4-phenylene bisheterocyclic compounds have been developed. Successive sequencing of the Groebke-Blackburn-Bienayme reaction with Ugi-azide, Hantzsch and Biginelli reactions results in rapid and efficient formation of bisheterocyclic compounds. A simple, fast and high yielding method for the synthesis of 3-aminoimidazo[1,2-a]pyridines catalyzed by bismuth(III) chloride under solvent-free conditions is reported. Bismuth(III) chloride is also an efficient catalyst for the Ugi-azide reaction under solvent free conditions.

  DOI：

  10.1055/s-0032-1318221