N-(2-硫苯基)苯甲酰胺 | 1020-40-2

• 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-硫苯基)苯甲酰胺
• 英文名称: N-(2-mercaptophenyl)benzamide
• 英文别名: 2-Benzamino-thiophenol；Benzamidobenzenethiol；N-(2-sulfanylphenyl)benzamide
• CAS: 1020-40-2
• 化学式: C₁₃H₁₁NOS
• 分子量: 229.302
• InChiKey: YGJHOWOEBFBOSF-UHFFFAOYSA-N

物化性质

• 熔点：
  116-117 °C(Solv: ligroine (8032-32-4))
• 沸点：
  291.4±23.0 °C(Predicted)
• 密度：
  1.267±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  2.8
• 重原子数：
  16
• 可旋转键数：
  2
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.0
• 拓扑面积：
  30.1
• 氢给体数：
  2
• 氢受体数：
  2

安全信息

• 海关编码：
  2930909090

反应信息

• 作为反应物：
  描述：

  N-(2-硫苯基)苯甲酰胺 在 molybdenum hexacarbonyl 作用下， 以 丙酮 为溶剂， 反应 6.0h， 以67%的产率得到N-苯甲酰替苯胺
  参考文献：
  名称：

  钼介导的硫醇和二硫化物脱硫

  摘要：

  我们已经成功地实现了六羰基钼 [Mo(CO)6] 介导的硫醇和二硫化物的脱硫。在该反应中，芳基、苄基、伯和仲烷基硫醇的巯基 (SH) 巯基以及二硫化物的 S-S 单键可以被去除。该反应具有高官能团耐受性且不受空间位阻影响。丙酮-d 6 反应的结果表明，硫醇和二硫化物脱硫中的氢源分别是巯基和丙酮（溶剂）的氢原子，脱硫通过形成一种有机钼物种。

  DOI：

  10.1055/s-0034-1378315
• 作为产物：
  描述：

  双(2-氨基苯基)二硫 在 sodium tetrahydroborate 、 N,N-二异丙基乙胺 作用下， 以 四氢呋喃 、 乙醇 、 二氯甲烷 为溶剂， 反应 1.5h， 生成 N-(2-硫苯基)苯甲酰胺
  参考文献：
  名称：

  Discovery of new low-molecular-weight p53–Mdmx disruptors and their anti-cancer activities

  摘要：

  Although several p53-Mdm2-binding disruptors have been identified to date, few studies have been published on p53-Mdmx-interaction inhibitors. In the present study, we demonstrated that o-aminothiophenol derivatives with molecular weights of 200-300 selectively inhibited the p53-Mdmx interaction. S-2-Isobutyramidophenyl 2-methylpropanethioate (K-178) (1c) activated p53, up-regulated the expression of its downstream genes such as p21 and Mdm2, and preferentially inhibited the growth of cancer cells with wild-type p53 over those with mutant p53. Furthermore, we found that the S-isobutyryl-deprotected forms 1b and 3b of 1c and S-2-benzamidophenyl 2-methylpropanethioate (K-181) (3c) preferentially inhibited the p53-Mdmx interaction over the p53-Mdm2 interaction, respectively, by using a Flag-p53 and glutathione S-transferase (GST)-fused protein complex (Mdm2, Mdmx, DAPK1, or PPID). In addition, the interaction of p53 with Mdmx was lost by replacing a sulfur atom with an oxygen atom in 1b and 1c. These results suggest that sulfides such as 1b, 3b, 4b, and 5b interfere with the binding of p53-Mdmx, resulting in the dissociation of the two proteins. Furthermore, the results of oral administration experiments using xenografts in nude mice indicated that 1c reduced the volume of tumor masses to 49.0% and 36.6% that of the control at 100 mg/kg and 150 mg/kg, respectively, in 40 days. (C) 2016 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmc.2016.03.021

文献信息

• Zeolite-catalyzed simple synthesis of different heterocyclic rings, part 2
  作者：Adrienn Hegedüs、Ilona Vígh、Zoltán Hell

  DOI：10.1002/hc.20036

  日期：——

  A simple and environmentally friendly synthesis was developed for the preparation of 2-arylimidazoline derivatives and 2-arylbenzoxazole derivatives using a small pore size zeolite. The similar reaction was not applicable to the preparation of the sulfur-containing analogs cysteamine or 2-aminothiophenol, probably because of a disadvantageous reaction between the zeolite and the thio compound. © 2004

  开发了一种简单且环保的合成方法，用于使用小孔径沸石制备 2-芳基咪唑啉衍生物和 2-芳基苯并恶唑衍生物。类似的反应不适用于含硫类似物半胱胺或2-氨基苯硫酚的制备，可能是因为沸石与硫代化合物之间的反应不利。© 2004 Wiley Periodicals, Inc. 杂原子化学 15:428–431, 2004; 在线发表于 Wiley InterScience (www.interscience.wiley.com)。DOI 10.1002/hc.20036
• Trifluoromethylation of thiophenols and thiols with sodium trifluoromethanesulfinate and iodine pentoxide
  作者：Jing-Jing Ma、Wen-Bin Yi、Guo-Ping Lu、Chun Cai

  DOI：10.1039/c5cy01561h

  日期：——

  facile trifluoromethylation process for a wide range of thiophenols and thiols under metal free conditions has been developed using two simple and safe solids, sodium trifluoro-methanesulfinate and iodine pentoxide, via the radical process.

  通过自由基方法，使用两种简单且安全的固体，即三氟甲亚磺酸钠和五氧化二碘，开发了一种选择性，简便的三氟甲基化方法，用于在无金属条件下处理多种苯酚和硫醇。
• Synthesis of <i>C</i> ‐ and <i>N</i> ‐Substituted 1,5,2,6‐Dithiadiazocanes –Electrophilic‐Nucleophilic Thioamination (ENTA) Reagents
  作者：Tomas Javorskis、Arminas Jurys、Gintautas Bagdžiūnas、Edvinas Orentas

  DOI：10.1002/adsc.202100424

  日期：2021.7

  A synthetic method is presented for S−N bond formation starting from cheap and affordable materials. We show that (un)substituted N-protected cyclic eight-membered C2-symmetric sulfenamides have been prepared in a few steps using this procedure. The synthetic utility of these ambipolar derivatives was demonstrated in a variety of synthetic transformations affording different S,N-heterocyles of pharmaceutical

  提出了一种从廉价且负担得起的材料开始形成 S-N 键的合成方法。我们表明，已使用此程序在几个步骤中制备了（未）取代的N保护的环状八元C 2对称次磺酰胺。这些双极性衍生物的合成效用已在各种合成转化中得到证明，这些合成转化可在一个或两个步骤中从简单的起始材料提供具有药物相关性的不同S,N-杂环。
• Copper-Catalyzed Arylation of Benzothiazoles with Toluene Derivatives­: Synthesis of 2-Arylbenzothiazole
  作者：Hongmei Deng、Xueshun Jia、Jian Li、Chengliang Li、Tao Jin、Zhiqiang Liu、Ruolan Jiang、Chunju Li

  DOI：10.1055/s-0036-1588487

  日期：2017.9

  Abstract A copper-catalyzed reaction of benzothiazole and readily available toluene derivatives has been disclosed. This protocol is proposed to proceed through the oxidation of toluene and ring opening of benzothiazole, thus providing a new pathway for the synthesis of 2-arylbenzothiazoles. A copper-catalyzed reaction of benzothiazole and readily available toluene derivatives has been disclosed. This

  摘要 已经公开了苯并噻唑和容易获得的甲苯衍生物的铜催化反应。建议该方案通过甲苯的氧化和苯并噻唑的开环进行，从而为合成2-芳基苯并噻唑提供了一条新途径。 已经公开了苯并噻唑和容易获得的甲苯衍生物的铜催化反应。建议该方案通过甲苯的氧化和苯并噻唑的开环进行，从而为合成2-芳基苯并噻唑提供了一条新途径。
• 3,6-Di(pyridin-2-yl)-1,2,4,5-tetrazine (pytz) mediated metal-free mild oxidation of thiols to disulfides in aqueous medium
  作者：Suvendu Samanta、Shounak Ray、Abhisek Brata Ghosh、Papu Biswas

  DOI：10.1039/c6ra01509c

  日期：——

  Thiols are efficiently oxidized to disulfides (RSSR) in presence of 3, 6-Di(pyridin-2-yl)-1,2,4,5-tetrazine (pytz) in aqueous medium, as well as in absence of solvent under mild and metal-free conditions. A broad...

  在3，6-二（吡啶-2-基）-1,2,4,5-四嗪（pytz）的存在下，在温和的条件下以及无溶剂的情况下，硫醇可有效地氧化为二硫化物（RSSR）。和无金属的条件。国外...