3-(3-methylphenyl)-2-(propylsulfanyl)quinazolin-4(3H)-one | 25477-44-5

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 二氮杂萘
• 英文名称: 3-(3-methylphenyl)-2-(propylsulfanyl)quinazolin-4(3H)-one
• 英文别名: 2-propylsulfanyl-3-m-tolyl-3H-quinazolin-4-one；2-Propylmercapto-3-m-tolyl-4(3H)-chinazolinon；3-(3-Methylphenyl)-2-propylsulfanylquinazolin-4-one
• CAS: 25477-44-5
• 化学式: C₁₈H₁₈N₂OS
• 分子量: 310.42
• InChiKey: XLWYUOILPFTJDH-UHFFFAOYSA-N

物化性质

• 沸点：
  485.0±38.0 °C(Predicted)
• 密度：
  1.18±0.1 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  4.3
• 重原子数：
  22
• 可旋转键数：
  4
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.22
• 拓扑面积：
  58
• 氢给体数：
  0
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  邻苯二胺 、 3-(3-methylphenyl)-2-(propylsulfanyl)quinazolin-4(3H)-one 以 melt 为溶剂， 反应 6.0h， 以69%的产率得到6H-苯并咪唑并[2,1-b]喹唑啉-12-酮
  参考文献：
  名称：

  New general synthesis of benzo[4,5]imidazo[1,2-a]pyrimidine and benzo[4,5]imidazo[2,1-b]quinazoline derivatives

  摘要：

  The reactions of benzene-1,2-diamine with 5-substituted 2-(alkylsulfanyl)-4-methylpyrimidin-6(1H)-ones and 2-(propylsulfanyl)- and 5-iodo-2-(propylsulfanyl)-3,4-dihydroquinazolines at 175-185A degrees C under solvent-free conditions unexpectedly afforded benzo[4,5]imidazo[1,2-a]pyrimidine, benzo[4,5]imidazo[2,1-b]-quinazoline, and 2,2'-(benzene-1,2-diyldiimino)bis[pyrimidin-4(3H)-ones]. The described reaction is the first example of synthesis of these heterocyclic systems by fusion of benzimidazole to pyrimidine or quinazoline and is likely to follow ANRORC mechanism.

  DOI：

  10.1134/s1070428016070150
• 作为产物：
  描述：

  溴丙烷 、 2-疏基-3-间甲苯-3H-喹唑啉-4-酮 在 sodium hydroxide 作用下， 以 水 为溶剂， 反应 15.0h， 以79%的产率得到3-(3-methylphenyl)-2-(propylsulfanyl)quinazolin-4(3H)-one
  参考文献：
  名称：

  New general synthesis of benzo[4,5]imidazo[1,2-a]pyrimidine and benzo[4,5]imidazo[2,1-b]quinazoline derivatives

  摘要：

  The reactions of benzene-1,2-diamine with 5-substituted 2-(alkylsulfanyl)-4-methylpyrimidin-6(1H)-ones and 2-(propylsulfanyl)- and 5-iodo-2-(propylsulfanyl)-3,4-dihydroquinazolines at 175-185A degrees C under solvent-free conditions unexpectedly afforded benzo[4,5]imidazo[1,2-a]pyrimidine, benzo[4,5]imidazo[2,1-b]-quinazoline, and 2,2'-(benzene-1,2-diyldiimino)bis[pyrimidin-4(3H)-ones]. The described reaction is the first example of synthesis of these heterocyclic systems by fusion of benzimidazole to pyrimidine or quinazoline and is likely to follow ANRORC mechanism.

  DOI：

  10.1134/s1070428016070150

文献信息

• New general synthesis of benzo[4,5]imidazo[1,2-a]pyrimidine and benzo[4,5]imidazo[2,1-b]quinazoline derivatives
  作者：A. A. Harutyunyan

  DOI：10.1134/s1070428016070150

  日期：2016.7

  The reactions of benzene-1,2-diamine with 5-substituted 2-(alkylsulfanyl)-4-methylpyrimidin-6(1H)-ones and 2-(propylsulfanyl)- and 5-iodo-2-(propylsulfanyl)-3,4-dihydroquinazolines at 175-185A degrees C under solvent-free conditions unexpectedly afforded benzo[4,5]imidazo[1,2-a]pyrimidine, benzo[4,5]imidazo[2,1-b]-quinazoline, and 2,2'-(benzene-1,2-diyldiimino)bis[pyrimidin-4(3H)-ones]. The described reaction is the first example of synthesis of these heterocyclic systems by fusion of benzimidazole to pyrimidine or quinazoline and is likely to follow ANRORC mechanism.