3,3'-(2,4,6-trimethyl-1,4-dihydropyridine-3,5-diyl)bis(5-(4-chlorophenyl)-4,5-di-hydroisoxazole) | 1447968-07-1

• 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: 3,3'-(2,4,6-trimethyl-1,4-dihydropyridine-3,5-diyl)bis(5-(4-chlorophenyl)-4,5-di-hydroisoxazole)
• CAS: 1447968-07-1
• 化学式: C₂₆H₂₅Cl₂N₃O₂
• 分子量: 482.409
• InChiKey: CCNJEBURUXQCID-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  7.12
• 重原子数：
  33.0
• 可旋转键数：
  4.0
• 环数：
  5.0
• sp3杂化的碳原子比例：
  0.31
• 拓扑面积：
  55.21
• 氢给体数：
  1.0
• 氢受体数：
  5.0

反应信息

• 作为产物：
  描述：

  3,5-丁二酮-2,4,6-三甲基-1,4-羟基吡啶 在 吡啶 、 盐酸羟胺 、 potassium hydroxide 作用下， 反应 6.0h， 生成 3,3'-(2,4,6-trimethyl-1,4-dihydropyridine-3,5-diyl)bis(5-(4-chlorophenyl)-4,5-di-hydroisoxazole)
  参考文献：
  名称：

  Synthesis, antibacterial and antifungal evaluation of novel 1,4-dihydropyridine derivatives

  摘要：

  3,5-Diacetyl-1,4-dihydro-2,4,6-trimethylpyridine (1) has been condensed with aromatic aldehydes to give the corresponding cinnamoyl derivatives IIa-e. the behavior of IIc, d towards thiourea, hydroxylamine hydrochloride, hydrazine hydrate and other bifunctional reagents has been investigated. The newly synthesized compounds were screened for their antimicrobial activity against Gram-positive bacteria, Gram-negative bacteria and as antifungal reagent. Among all the tested compounds, it was found that compounds IIIa and Vila, b revealed better activity against the Gram-positive rather than the Gram-negative bacteria. (C) 2013 Elsevier B.V. All rights reserved.

  DOI：

  10.1016/j.saa.2012.12.069