1-(4-(methylthio)oxazol-2-yl)-7-phenylheptan-1-ol | 1096535-76-0

• 分子结构分类: 有机化合物 - 有机硫化合物 - 硫醚类
• 英文名称: 1-(4-(methylthio)oxazol-2-yl)-7-phenylheptan-1-ol
• 英文别名: 1-(4-Methylsulfanyl-1,3-oxazol-2-yl)-7-phenylheptan-1-ol
• CAS: 1096535-76-0
• 化学式: C₁₇H₂₃NO₂S
• 分子量: 305.441
• InChiKey: JTTNMWLHJDKMML-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4.7
• 重原子数：
  21
• 可旋转键数：
  9
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.47
• 拓扑面积：
  71.6
• 氢给体数：
  1
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  1-(4-(methylthio)oxazol-2-yl)-7-phenylheptan-1-ol 在 戴斯-马丁氧化剂 作用下， 以 二氯甲烷 为溶剂， 反应 1.0h， 以85%的产率得到1-(4-(methylthio)oxazol-2-yl)-7-phenylheptan-1-one
  参考文献：
  名称：

  Exploration of a fundamental substituent effect of α-ketoheterocycle enzyme inhibitors: Potent and selective inhibitors of fatty acid amide hydrolase

  摘要：

  A series of C4 substituted alpha-ketooxazoles were examined as inhibitors of the serine hydrolase fatty acid amide hydrolase in efforts that further de. ne and generalize a fundamental substituent effect on enzyme inhibitory potency. Thus, a plot of the Hammett sigma(m) versus -log K-i provided a linear correlation (R-2 = 0.90) with a slope of 3.37 (rho = 3.37), that is of a magnitude that indicates that of the electron-withdrawing character of the substituent dominates its effects (a one unit change in sigma(m) provides a > 1000-fold change in Ki). (C) 2008 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2008.06.084
• 作为产物：
  描述：

  2-(1-(tert-butyldimethylsilyloxy)-7-phenylheptyl)-4-(methylthio)oxazole 在 四丁基氟化铵 作用下， 以 四氢呋喃 为溶剂， 反应 0.5h， 以90%的产率得到1-(4-(methylthio)oxazol-2-yl)-7-phenylheptan-1-ol
  参考文献：
  名称：

  Exploration of a fundamental substituent effect of α-ketoheterocycle enzyme inhibitors: Potent and selective inhibitors of fatty acid amide hydrolase

  摘要：

  A series of C4 substituted alpha-ketooxazoles were examined as inhibitors of the serine hydrolase fatty acid amide hydrolase in efforts that further de. ne and generalize a fundamental substituent effect on enzyme inhibitory potency. Thus, a plot of the Hammett sigma(m) versus -log K-i provided a linear correlation (R-2 = 0.90) with a slope of 3.37 (rho = 3.37), that is of a magnitude that indicates that of the electron-withdrawing character of the substituent dominates its effects (a one unit change in sigma(m) provides a > 1000-fold change in Ki). (C) 2008 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2008.06.084

文献信息

• C4-SUBSTITUTED ALPHA-KETO OXAZOLES
  申请人：Boger Dale L.

  公开号：US20110184026A1

  公开（公告）日：2011-07-28

  The invention provides a series of C4-substituted oxazole compounds having an alpha keto side chain at the 2 position, for example, compounds of formula I. The compounds can inhibit fatty acid amide hydrolase and can be useful for treatment of malconditions modulated by fatty acid amide hydrolase. The invention further provides methods of making compounds of formula I, useful intermediates in the preparation of compounds of formula I, and methods of using compounds of formula I and compositions thereof.

  该发明提供了一系列C4取代的噁唑化合物，其在2位具有α酮侧链，例如，公式I的化合物。这些化合物可以抑制脂肪酸酰胺水解酶，并可用于治疗受脂肪酸酰胺水解酶调节的疾病。该发明还提供了制备公式I化合物的方法，用于制备公式I化合物的有用中间体，以及使用公式I化合物及其组成物的方法。
• [EN] C4-SUBSTITUTED ALPHA-KETO OXAZOLES<br/>[FR] APHA-CÉTO OXAZOLES SUBSTITUÉES EN C4
  申请人：SCRIPPS RESEARCH INST

  公开号：WO2009154785A2

  公开（公告）日：2009-12-23

  The invention provides a series of C4-substituted oxazole compounds having an alpha keto side chain at the 2 position, for example, compounds of formula I. The compounds can inhibit fatty acid amide hydrolase and can be useful for treatment of malconditions modulated by fatty acid amide hydrolase. The invention further provides methods of making compounds of formula I, useful intermediates in the preparation of compounds of formula I, and methods of using compounds of formula I and compositions thereof.