N-(3,5-dimethoxyphenyl)-4-(1-morpholino)-6-(prop-2-ynyloxy)-1,3,5-triazin-2-amine | 1335447-88-5

• 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-(3,5-dimethoxyphenyl)-4-(1-morpholino)-6-(prop-2-ynyloxy)-1,3,5-triazin-2-amine
• CAS: 1335447-88-5
• 化学式: C₁₈H₂₁N₅O₄
• 分子量: 371.396
• InChiKey: WGJWBIGGHDVQBY-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.48
• 重原子数：
  27.0
• 可旋转键数：
  7.0
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.39
• 拓扑面积：
  90.86
• 氢给体数：
  1.0
• 氢受体数：
  9.0

反应信息

• 作为反应物：
  描述：

  3-[(7-chloroquinolin-4-yl)amino]azidopropane 、 N-(3,5-dimethoxyphenyl)-4-(1-morpholino)-6-(prop-2-ynyloxy)-1,3,5-triazin-2-amine 在 copper(ll) sulfate pentahydrate 、 sodium ascorbate 作用下， 以 水 、 叔丁醇 为溶剂， 反应 3.0h， 以57%的产率得到(7-chloroquinolin-4-yl)-(3-{4-[(4-(3,5-dimethoxyphenylamino)-6-(morpholin-4-yl)-[1,3,5]triazin-2-yl)oxymethyl]-[1,2,3]triazol-1-yl}propyl)amine
  参考文献：
  名称：

  Synthesis of 4-aminoquinoline-1,2,3-triazole and 4-aminoquinoline-1,2,3-triazole-1,3,5-triazine Hybrids as Potential Antimalarial Agents

  摘要：

  We report herein synthesis of a series of 4‐aminoquinoline‐1,2,3‐triazole and 4‐aminoquinoline‐1,2,3‐triazole‐1,3,5‐triazine hybrids and evaluate their antimalarial activity against D6 and W2 strains of Plasmodium falciparum. To study the structure–activity relationship of substituted 4‐aminoquinoline–based hybrids, 34 structurally diverse compounds were synthesized and tested against D6 and W2 strains of P. falciparum. Some of the compounds have shown promising antimalarial activity without toxicity against Vero cells.

  DOI：

  10.1111/j.1747-0285.2011.01115.x
• 作为产物：
  描述：

  3,5-二甲氧基苯胺 在 碳酸氢钠 、 potassium carbonate 作用下， 以 四氢呋喃 为溶剂， 反应 4.0h， 生成 N-(3,5-dimethoxyphenyl)-4-(1-morpholino)-6-(prop-2-ynyloxy)-1,3,5-triazin-2-amine
  参考文献：
  名称：

  Synthesis of 4-aminoquinoline-1,2,3-triazole and 4-aminoquinoline-1,2,3-triazole-1,3,5-triazine Hybrids as Potential Antimalarial Agents

  摘要：

  We report herein synthesis of a series of 4‐aminoquinoline‐1,2,3‐triazole and 4‐aminoquinoline‐1,2,3‐triazole‐1,3,5‐triazine hybrids and evaluate their antimalarial activity against D6 and W2 strains of Plasmodium falciparum. To study the structure–activity relationship of substituted 4‐aminoquinoline–based hybrids, 34 structurally diverse compounds were synthesized and tested against D6 and W2 strains of P. falciparum. Some of the compounds have shown promising antimalarial activity without toxicity against Vero cells.

  DOI：

  10.1111/j.1747-0285.2011.01115.x