2-phenyl-1-(2-thioxobenzo[d]oxazol-3(2H)-yl)ethanone | 312313-33-0

• 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: 2-phenyl-1-(2-thioxobenzo[d]oxazol-3(2H)-yl)ethanone
• 英文别名: N-(phenylacetyl)benzoxazoline-2-thione；N-Phenylacetylbenzoxazole-2-thione；2-Phenyl-1-(2-sulfanylidene-1,3-benzoxazol-3(2H)-yl)ethan-1-one；2-phenyl-1-(2-sulfanylidene-1,3-benzoxazol-3-yl)ethanone
• CAS: 312313-33-0
• 化学式: C₁₅H₁₁NO₂S
• 分子量: 269.324
• InChiKey: DRXWFEJOHOQSCK-UHFFFAOYSA-N

物化性质

• 沸点：
  418.3±38.0 °C(Predicted)
• 密度：
  1.37±0.1 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  3.3
• 重原子数：
  19
• 可旋转键数：
  2
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.07
• 拓扑面积：
  61.6
• 氢给体数：
  0
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  2-phenyl-1-(2-thioxobenzo[d]oxazol-3(2H)-yl)ethanone 以 苯 为溶剂， 20.0~180.0 ℃ 、399.97 Pa 条件下， 生成 2-(furan-3-yl)benzo[d]oxazole
  参考文献：
  名称：

  苯并恶唑-2（3 H）-硫酮与环烯烃和杂芳族化合物的光加成反应

  摘要：

  苯并恶唑-2-硫酮的光加成反应1与环烯烃2和杂芳族化合物3进行了检查。的照射Ñ -acylbenzoxazole -2-硫酮1A和1B，和3-（甲氧羰基） -苯并恶唑-2-和3-（苯氧基羰基）（3 ħ）-thiones（1F和1H。，RESP）在环烯烃的存在2A -图2c，环己-1,4-二烯（2D）和茚（2E），得到2-取代的苯并恶唑4 - 13，18和19，和iminothietanes 14- 17，由两性离子中间体的硫醇盐阴离子的酰基或MeOCO和PhOCO基团的分子内俘获我和由两性离子中间体的酚盐阴离子II，分别从螺环氨基thietanes衍生AT通过形成[2 + 2] 1的CS键和2的CC键的环加成。在杂芳族化合物3的存在下照射1只能得到2-取代的苯并恶唑20 – 33。

  DOI：

  10.1002/hlca.200390266
• 作为产物：
  描述：

  苯乙酰氯 、 2-巯基苯并恶唑 在 三乙胺 作用下， 以 丙酮 为溶剂， 反应 0.5h， 以31%的产率得到2-phenyl-1-(2-thioxobenzo[d]oxazol-3(2H)-yl)ethanone
  参考文献：
  名称：

  Design of benzimidazole- and benzoxazole-2-thione derivatives as inhibitors of bacterial hyaluronan lyase

  摘要：

  Bacterial hyaluronan lyases (Hyal) degrade hyaluronan, an important component of the extracellular matrix, and are involved in microbial spread. Hyal inhibitors may serve as tools to study the role of the enzyme, its substrates and products in the course of bacterial infections. Moreover, such enzyme inhibitors are potential candidates for antibacterial combination therapy. Based on crystal structures of Streptococcus pneumoniae Hyal in complex with a hexasaccharide substrate and with different inhibitors, 1-acylated benzimidazole-2-thiones and benzoxazole-2-thiones were derived as new leads for the inhibition of Streptococcus agalactiae strain 4755 Hyal. Structure-based optimization led to N-(3-phenylpropionyl)benzoxazole-2-thione, one of the most potent compounds known to date (IC50 values: 24 mu M at pH 7.4, 15 mu M at pH 5). Among the 27 new derivatives, other N-acylated benzimidazoles and benzoxazoles are just as active at pH 7.4, but not at pH 5. The results support a binding mode characterized by interactions with residues in the catalytic site and with a hydrophobic patch. (C) 2011 Elsevier Masson SAS. All rights reserved.

  DOI：

  10.1016/j.ejmech.2011.07.014

文献信息

• Photochemical reactions of N-acylbenzoxazole-2-thiones
  作者：Takehiko Nishio、Ikuo Iida、Kunio Sugiyama

  DOI：10.1039/b002548h

  日期：——

  presence of a variety of alkenes 2 yields 2-substituted benzoxazoles 3–20 and/or the unexpected products, iminothietanes 21–29 by intramolecular trapping of the acyl group by thiolate anion of the zwitterionic intermediate I and by the phenolate anion of the zwitterionic intermediate II, respectively, derived from the spirocyclic aminothietanes AT which are formed by regioselective [2+2] cycloaddition of

  研究了N-酰基苯并恶唑-2-硫酮1的光化学反应。在多种存在下辐照N-酰基苯并恶唑-2-硫酮1烯烃 2产生2取代苯并恶唑 3–20和/或意想不到的产物，通过分子内诱捕亚氨基噻吨21–29酰基 经过 硫醇根阴离子两性离子中间体I和酚盐阴离子分别由区域选择性形成的螺环氨基硫杂环丁烷AT衍生的两性离子中间体II[2 + 2]环加成的碳硫双键1与烯烃 双键。
• Acylation and Alkoxycarbony-lation of Benzoxazoline-2-thione and Benzothiazoline-2-thione
  作者：Takehiko Nishio、Kiyoko Shiwa

  DOI：10.3987/com-03-s(p)10

  日期：——

  Acylation of benzoxazoline-2-thione (1) and benzothiazoline-2-thione (2) with acetic anhydride (3) and acyl chlorides (4) gave N-acyl (5, 6) and/or S-acyl (7, 8) derivatives depending on the nature of acylating agents and bases used. Alkoxycarbonylation of 1 with aralkyl chlorocarbonates (9) gave N-alkoxycarbonyl derivatives (10) mainly, while that of 2 with aralkyl chloroccarbonates (9) gave S-alkoxycarbonyl derivatives (12) exclusively. Photolysis of N-acyl derivatives (5 or 6) in the presence of alcohols afforded 1 or 2, respectively, together with esters (16).