spiro[(2H,3H)-3-(4-(5-p-N,N-dimethylaminophenyl-4,5-dihydro-1-acetylpyrazol-3-yl)phenyl)quinazoline-2,1'-cyclohexan]-4(1H)-one | 1229716-05-5

• 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: spiro[(2H,3H)-3-(4-(5-p-N,N-dimethylaminophenyl-4,5-dihydro-1-acetylpyrazol-3-yl)phenyl)quinazoline-2,1'-cyclohexan]-4(1H)-one
• 英文别名: 3-[4-[2-acetyl-3-[4-(dimethylamino)phenyl]-3,4-dihydropyrazol-5-yl]phenyl]spiro[1H-quinazoline-2,1'-cyclohexane]-4-one
• CAS: 1229716-05-5
• 化学式: C₃₂H₃₅N₅O₂
• 分子量: 521.662
• InChiKey: URUBMRSLOMVHRR-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  5.3
• 重原子数：
  39
• 可旋转键数：
  4
• 环数：
  6.0
• sp3杂化的碳原子比例：
  0.34
• 拓扑面积：
  68.2
• 氢给体数：
  1
• 氢受体数：
  5

反应信息

• 作为产物：
  描述：

  3-[4-[3-[4-(dimethylamino)phenyl]prop-2-enoyl]phenyl]spiro[1H-quinazoline-2,1'-cyclohexane]-4-one 、 溶剂黄146 在 hydrazine hydrate 作用下， 反应 4.0h， 以60%的产率得到spiro[(2H,3H)-3-(4-(5-p-N,N-dimethylaminophenyl-4,5-dihydro-1-acetylpyrazol-3-yl)phenyl)quinazoline-2,1'-cyclohexan]-4(1H)-one
  参考文献：
  名称：

  Synthesis, biological evaluation and molecular docking of novel series of spiro [(2H,3H) quinazoline-2,1′- cyclohexan]-4(1H)- one derivatives as anti-inflammatory and analgesic agents

  摘要：

  Three series of Spiro 1(2H,3H) quinazoline-2,1'-cyclohexan1-4(1H)-one derivatives have been synthesized. Some of the novel quinazolinone derivatives IIe, VIIIc, XIc, XIIb, XIIc, XVIb showed considerable potent anti-inflammatory and analgesic activity of superior G.I.T. safety profile in experimental rats in comparing to indomethacin and tramadol as reference drugs. Docking study into COX-2 has been made for derivatives of highest anti-inflammatory activity. The compound XVIb showed the nearest RMSD value to that of indomethacin.

  DOI：

  10.1016/j.ejmech.2009.12.078