S-phenyl 2-(4-methoxyphenyl)ethanethioate | 86211-05-4

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯硫酚酯
• 英文名称: S-phenyl 2-(4-methoxyphenyl)ethanethioate
• CAS: 86211-05-4
• 化学式: C₁₅H₁₄O₂S
• 分子量: 258.341
• InChiKey: FVUODDYGVWSSAY-UHFFFAOYSA-N

物化性质

• 沸点：
  403.3±28.0 °C(Predicted)
• 密度：
  1.19±0.1 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  3.8
• 重原子数：
  18
• 可旋转键数：
  5
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.13
• 拓扑面积：
  51.6
• 氢给体数：
  0
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  N-亚苄基-4-甲基苯磺酰胺 、 S-phenyl 2-(4-methoxyphenyl)ethanethioate 在 1-[3,5-bis(trifluoromethyl)phenyl]-3-[4-[(S)-[(2R,4S,5R)-5-ethenyl-1-azabicyclo[2.2.2]octan-2-yl]-(naphthalen-1-ylmethoxy)methyl]quinolin-6-yl]urea 作用下， 以 乙醚 为溶剂， 反应 72.08h， 以90%的产率得到S-phenyl (2S,3S)-2-(4-methoxyphenyl)-3-[(4-methylphenyl)sulfonamido]-3-phenylpropanethioate
  参考文献：
  名称：

  双功能有机催化剂催化S-苯基硫代酸酯的立体选择性曼尼希反应

  摘要：

  AbstractA highly stereoselective Mannich reaction of S‐phenyl thioesters was achieved by using bifunctional thiourea catalysts. Using a quinine‐derived C6′‐urea catalyst, the direct Mannich products of N‐tosyl imines and S‐phenyl thioesters were obtained in high yields and excellent diastereo‐ and enantioselectivities.magnified image

  DOI：

  10.1002/adsc.201400735
• 作为产物：
  描述：

  苯硫酚 、 4-甲氧基苯乙酰氯 在 三乙胺 作用下， 以 甲苯 为溶剂， 以97%的产率得到S-phenyl 2-(4-methoxyphenyl)ethanethioate
  参考文献：
  名称：

  β-内酯是多种细菌酶类活性部位标记的优先结构。

  摘要：

  DOI：

  10.1002/anie.200705768

文献信息

• Palladium-Catalyzed Thiocarbonylation of Aryl, Vinyl, and Benzyl Bromides
  作者：Mia N. Burhardt、Andreas Ahlburg、Troels Skrydstrup

  DOI：10.1021/jo5009965

  日期：2014.12.19

  A catalytic protocol for synthesis of thioesters from aryl, vinyl, and benzyl bromides as well as benzyl chlorides was developed using only stoichiometric amounts of carbon monoxide, produced from a solid CO precursor inside a two-chamber system. As a catalytic system, the combination of bis(benzonitrile) palladium(II) chloride and Xantphos furnished the highest yields of the desired compounds, along

  使用芳烃，乙烯基和苄基溴化物以及苄基氯来合成硫酯的催化方案仅使用化学计量量的一氧化碳开发，该一氧化碳是由两室系统中的固态CO前驱体产生的。作为催化体系，双（苄腈）氯化钯（II）和Xantphos的组合在120°C的苯甲醚溶液中提供了所需化合物以及弱碱NaOAc的最高收率。为了确保反应中的高化学选择性，催化体系和溶剂的选择被证明是重要的。富电子和缺电子的芳基溴在此反应中均能很好地发挥作用。向反应中加入1当量的碘化钠可改善缺电子的芳基溴化物的化学选择性。硫醇范围包括芳基和烷基硫醇，包括2-巯基二苯甲酮，其中通过硫羰基化和随后的McMurry偶联生成不同取代的苯并噻吩。事实证明，该方法可以适用于13 C引入噻吩环。
• Neutral Sulfur Nucleophiles: Synthesis of Thioethers and Thioesters by Substitution Reactions of N-Heterocyclic Carbene Boryl Sulfides and Thioamides
  作者：Xiangcheng Pan、Dennis P. Curran

  DOI：10.1021/ol5010164

  日期：2014.5.16

  Newly discovered boryl sulfides and N-borylthioamides are shown to serve as neutral sources of sulfur nucleophiles in substitutions reactions. For example, heating of diMe-Imd-BH(SPh)2 with benzyl bromides, primary bromides, or acid chlorides provides the corresponding thioethers or thioesters in high yields. Likewise, N-phenyltetrazole thioethers/esters are made from a readily available N-borylthionotetrazole

  已显示新发现的硼烷基硫化物和N-硼烷基硫代酰胺可在取代反应中用作硫亲核试剂的中性来源。例如，将diMe-Imd-BH（SPh）2与苄基溴化物，伯溴化物或酰氯一起加热可提供高收率的相应硫醚或硫酯。同样地，Ñ -phenyltetrazole硫醚/酯由容易获得的制造Ñ -borylthionotetrazole。可以将硼烷基硫化物的形成及其向前的亲核取代反应向下进行一锅反应，该反应的成分为NHC-硼烷（NHC-BH 3），二硫化物和亲电试剂。
• BETA-LACTONES AS ANTIBACTERIAL AGENTS
  申请人：Sieber Stephan A.

  公开号：US20110196027A1

  公开（公告）日：2011-08-11

  The present invention relates to specific beta-lactone compounds and compositions thereof for the treatment of infections, such as, e.g., infections with bacteria or infections with protozoa, in particular infections with Gram-positive and/or Gram-negative bacteria and of infectious diseases caused by or related to Gram-positive and/or Gram-negative bacteria, and to the modulation of virulence of Gram-positive and/or Gram-negative bacteria or of protozoa by specific beta-lactone compounds. The invention further relates to the use of the compounds or compositions for preventing or eliminating biofilms.

  本发明涉及特定的β-内酰胺类化合物及其组合物，用于治疗感染，例如细菌感染或原虫感染，特别是革兰氏阳性和/或革兰氏阴性细菌感染以及由革兰氏阳性和/或革兰氏阴性细菌引起或相关的传染病，并且涉及通过特定的β-内酰胺类化合物调节革兰氏阳性和/或革兰氏阴性细菌或原虫的毒力。本发明还涉及使用这些化合物或组合物预防或消除生物膜。
• Beta-lactones as antibacterial agents
  申请人：Sieber Stephan A.

  公开号：US08563598B2

  公开（公告）日：2013-10-22

  The present invention relates to specific beta-lactone compounds and compositions thereof for the treatment of infections, such as, e.g., infections with bacteria or infections with protozoa, in particular infections with Gram-positive and/or Gram-negative bacteria and of infectious diseases caused by or related to Gram-positive and/or Gram-negative bacteria, and to the modulation of virulence of Gram-positive and/or Gram-negative bacteria or of protozoa by specific beta-lactone compounds. The invention further relates to the use of the compounds or compositions for preventing or eliminating biofilms.

  本发明涉及特定的β-内酰胺类化合物及其组合物，用于治疗感染，例如细菌感染或原虫感染，特别是革兰氏阳性和/或革兰氏阴性细菌感染和由革兰氏阳性和/或革兰氏阴性细菌引起或相关的传染病，并且涉及通过特定的β-内酰胺类化合物调节革兰氏阳性和/或革兰氏阴性细菌或原虫的毒力。本发明还涉及使用上述化合物或组合物预防或消除生物膜。
• A highly convenient procedure for the hydrolysis of terminal phenyl vinyl sulfides
  作者：Vichai Reutrakul、Patcharin Poochaivatananon

  DOI：10.1016/s0040-4039(00)81457-4

  日期：1983.1