methyl N-(2-fluorophenyl)ethanimidothioate | 374889-97-1

• 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: methyl N-(2-fluorophenyl)ethanimidothioate
• 英文别名: N-(2-fluorophenyl) thioacetoimidate methyl ester
• CAS: 374889-97-1
• 化学式: C₉H₁₀FNS
• 分子量: 183.25
• InChiKey: TYSSCFXHCPNRAU-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.6
• 重原子数：
  12
• 可旋转键数：
  2
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.22
• 拓扑面积：
  37.7
• 氢给体数：
  0
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  methyl N-(2-fluorophenyl)ethanimidothioate 以89%的产率得到3-(4-bromophenyl)-4-(2-fluorophenyl)-5-methyl-4H-1,2,4-triazole
  参考文献：
  名称：

  Triazole derivatives

  摘要：

  该发明涉及一种三唑衍生物，具有抑制甘氨酸转运体活性，并用作药物，以及一种新颖的三唑衍生物。这种创新的三唑衍生物具有出色的抑制甘氨酸转运体活性，并可用作治疗痴呆症、精神分裂症、认知障碍或涉及各种疾病如阿尔茨海默病、帕金森病、亨廷顿病等的认知障碍，或涉及神经退行性疾病和脑血管疾病等疾病的痉挛。特别是，这种药物对改善痴呆症等学习障碍非常有用。

  公开号：

  US20030216385A1
• 作为产物：
  描述：

  2-氟乙酰苯胺 在 劳森试剂 、 potassium carbonate 作用下， 以 甲苯 、 乙腈 为溶剂， 反应 2.0h， 生成 methyl N-(2-fluorophenyl)ethanimidothioate
  参考文献：
  名称：

  Synthesis and Biological Evaluation of 3-Biphenyl-4-yl-4-phenyl-4H-1,2,4-triazoles as Novel Glycine Transporter 1 Inhibitors

  摘要：

  We describe the preparation and evaluation of a novel series of glycine transporter 1 (GlyT1) inhibitors derived from a high-throughput screening hit The SAR studies resulted in the discovery of 3-biphenyl-4-yl-4-(2 fluorophenyl)-5-isopropyl-4H-1,2,4-triazole (6p) A pharmacokinetic study was also conducted and revealed that 6p had excellent oral bioavailability and ameliorated learning impairment in passive avoidance tasks in mice

  DOI：

  10.1021/jm101031u

文献信息

• Atropisomeric 4-Phenyl-4<i>H</i>-1,2,4-triazoles as Selective Glycine Transporter 1 Inhibitors
  作者：Takashi Sugane、Takahiko Tobe、Wataru Hamaguchi、Itsuro Shimada、Kyoichi Maeno、Junji Miyata、Takeshi Suzuki、Tetsuya Kimizuka、Shuichi Sakamoto、Shin-ichi Tsukamoto

  DOI：10.1021/jm400383w

  日期：2013.7.25

  We report on the optimization of 4H-1,2,4-triazole derivatives to increase their activity and selectivity as glycine transporter 1 (GlyT1) inhibitors. Structure-activity relationship exploration resulted in the identification of a 3-[3-ethyl-5-(6-phenylpyridin-3-yl)-4H-1,2,4-triazol-4-yl]-2-methyl-benzonitrile (14u) compound with markedly higher selectivity for GlyT1. Physiochemical studies revealed that 14u exists as a stable pair of atropisomers under physiological conditions. We successfully separated the atropisomers to obtain active enantiomer (R)-14u, which displayed favorable pharmacokinetic properties, as well as positive results in the mice Y-maze test.