N-(2-氨基苯基)-3-(三氟甲基)苯甲酰胺 | 400073-82-7

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 中文名称: N-(2-氨基苯基)-3-(三氟甲基)苯甲酰胺
• 英文名称: N-(2-aminophenyl)-3-(trifluoromethyl)benzamide
• CAS: 400073-82-7
• 化学式: C₁₄H₁₁F₃N₂O
• mdl: MFCD02656545
• 分子量: 280.249
• InChiKey: GHMQDKBUBCXCIU-UHFFFAOYSA-N

物化性质

• 沸点：
  311.9±42.0 °C(Predicted)
• 密度：
  1.373±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  3
• 重原子数：
  20
• 可旋转键数：
  2
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.07
• 拓扑面积：
  55.1
• 氢给体数：
  2
• 氢受体数：
  5

安全信息

• 海关编码：
  2924299090

反应信息

• 作为产物：
  描述：

  N-(2-nitrophenyl)-3-trifluoromethylbenzamide 在 palladium on activated charcoal 氢气 作用下， 以 乙酸乙酯 为溶剂， 以65%的产率得到N-(2-氨基苯基)-3-(三氟甲基)苯甲酰胺
  参考文献：
  名称：

  Cyclooxygenase-1-Selective Inhibitors Are Attractive Candidates for Analgesics That Do Not Cause Gastric Damage. Design and in Vitro/in Vivo Evaluation of a Benzamide-Type Cyclooxygenase-1 Selective Inhibitor

  摘要：

  Although cyclooxygenase-1 (COX-1) inhibition is thought to be a major mechanism of gastric damage by nonsteroidal anti-inflammatory drugs (NSAIDs), some COX-1-selective inhibitors exhibit strong analgesic effects without causing gastric damage. However, it is not clear whether their analgesic effects are attributable to COX-1-inhibitory activity or other bioactivities. Here, we report that N-(5-amino-2-pyridinyl)-4(trifluoromethyl)benzamide (18f, TFAP), which has a structure clearly different from those of currently available COX-1-selective inhibitors, is a potent COX-1-selective inhibitor (COX-1IC(50) = 0.80 +/- 0.05 mu M, COX-2IC(50) = 210 I mu M). This compound causes little gastric damage in rats even at an oral dose of 300 mg/kg, though it has an analgesic effect at as low a dose as 10 mg/kg. Our results show that COX-1-selective inhibitors can be analgesic agents without causing gastric damage.

  DOI：

  10.1021/jm701191z

文献信息

• Copper-catalyzed regioselective 2-amination of o-haloanilides with aqueous ammonia
  作者：Yan-Ling Tang、Mei-Ling Li、Jin-Chun Gao、Yun Sun、Lu Qu、Feng Huang、Ze-Wei Mao

  DOI：10.1016/j.tetlet.2021.153001

  日期：2021.4

  An efficient Cu(II)-vasicine catalytic system has been developed for intramolecular CN bond formation. In this way, regioselective 2-amination of o-haloanilides with aqueous ammonia in EtOH has been achieved. This strategy provides several advantages, such as good regioselectivity, high yields and functional group tolerance.

  已经开发出用于分子内C N键形成的有效Cu（II）-水杨碱催化体系。以这种方式，已经实现了在EtOH中用氨水进行邻卤代苯胺的区域选择性2-胺化。该策略具有几个优点，例如良好的区域选择性，高产率和官能团耐受性。