N-(4-methylbenzoyl)-N’-phenylthiourea | 65739-28-8

• 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: N-(4-methylbenzoyl)-N’-phenylthiourea
• 英文别名: 1-(4-methyl-benzoyl)-3-phenyl-thiourea；1-(4-methylbenzoyl)-3-phenylthiourea；4-methyl-N-(phenyl-thiocarbamoyl)-benzamide；N-<4-Methyl-benzoyl->-N'-phenyl-thioharnstoff；4-methyl-N-(phenylcarbamothioyl)benzamide
• CAS: 65739-28-8
• 化学式: C₁₅H₁₄N₂OS
• 分子量: 270.355
• InChiKey: XUXJIMPTMMWXPR-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4.4
• 重原子数：
  19
• 可旋转键数：
  2
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.07
• 拓扑面积：
  73.2
• 氢给体数：
  2
• 氢受体数：
  2

反应信息

• 作为反应物：
  描述：

  N-(4-methylbenzoyl)-N’-phenylthiourea 在 溴 、 三乙胺 作用下， 以 丙酮 为溶剂， 以73%的产率得到(4-Methylphenyl)-(4-methyl-3-phenyl-2-sulfanylideneimidazol-1-yl)methanone
  参考文献：
  名称：

  一些新的1-甲苯基-3-芳基-4-甲基咪唑-2-硫酮的合成和生物活性

  摘要：

  由2-，3-和4-甲基苯甲酰氯经异硫氰酸酯形成，然后用各种取代的苯胺处理，制备了三组新的1-（异构甲基）苯甲酰基-3-芳基 硫脲（1-3a-i） 。在溴存在下，进行硫脲 （1-3a-i） 与丙酮的碱催化缩合 反应，得到相应的1-（异构甲基）苯甲酰基-3-苯甲酰基-3-芳基-4-甲基咪唑-2-硫酮 （ 4–6a–i） 产量高。硫脲和相应的硫酮通过光谱数据和元素分析进行​​表征。还讨论了硫酮的质量裂解模式。评价了该硫酮的抗菌，抗真菌和杀虫活性，并显示出显着的抗菌活性和轻微但不显着的抗真菌和杀虫特性。

  DOI：

  10.1007/s00044-007-9017-8
• 作为产物：
  描述：

  1-乙酰基-3-苯基硫脲 、 对甲基苯甲酰氯 以 丙酮 为溶剂， 反应 3.0h， 以46%的产率得到N-(4-methylbenzoyl)-N’-phenylthiourea
  参考文献：
  名称：

  Kavalek, Jaromir; Jirman, Josef; Machacek, Vladimir, Collection of Czechoslovak Chemical Communications, 1988, vol. 53, # 3, p. 593 - 600

  摘要：

  DOI：

文献信息

• NOVEL THIOUREA OR UREA DERIVATIVE, PREPARATION METHOD THEREOF, AND PHARMACEUTICAL COMPOSITION FOR PREVENTING OR TREATING AIDS, CONTAINING SAME AS ACTIVE INGREDIENT
  申请人：You Ji Chang

  公开号：US20130096138A1

  公开（公告）日：2013-04-18

  Disclosed are novel thiourea or urea derivatives inhibitory of HIV activity. Also provided are a method for preparing the thiourea or urea derivatives, and a pharmaceutical composition for the prophylaxis or therapy of AIDS comprising the derivatives. Having high inhibitory activity against HIV, the thiourea or urea derivatives can be effectively used in the prophylaxis or therapy of AIDS.

  本文披露了一种新颖的硫脲或脲衍生物，具有抑制HIV活性的作用。还提供了一种制备硫脲或脲衍生物的方法，以及一种包含这些衍生物的用于预防或治疗艾滋病的药物组合物。由于硫脲或脲衍生物具有高抑制HIV活性，因此可以有效地用于艾滋病的预防或治疗。
• Aroylthioureas: new organic ionophores for heavy-metal ion selective electrodes
  作者：Elena Otazo-Sánchez、Leonel Pérez-Marín、Osvaldo Estévez-Hernández、Susana Rojas-Lima、Julián Alonso-Chamarro

  DOI：10.1039/b102029n

  日期：——

  Thiourea derivatives (46 aroylthioureas) having different substituents close to the sulfur atom were synthesized and their ionophore potential in ion selective electrodes (ISEs) was examined. Structural considerations were taken into account based on the corresponding heavy-metal ISE parameters. As ionophores, some 1-furoyl-3-substituted thioureas (series 2) gave the best results in Pb(II), Hg(II) and Cd(II) ISEs. The strong intramolecular hydrogen bond in series 2 allows ligand interaction only through the CS group. Substituents on the furan and phenyl rings give rise to low solubility in the membrane plasticizer. 3-Alkyl substituted furoylthioureas improve solubility but enhance oxidative processes with chain length. New X-ray diffraction (XRD) structures and theoretical DFT calculations were considered in the analysis of the substituent influence on the selectivity of ISEs. These new ionophores have advantages because of their stability, simple synthesis and easy modification of the sulfur binding ability resulting from substitution.

  合成了46种不同取代基的噻唑衍生物（芳酰噻唑），并研究了它们在离子选择电极（ISEs）中的离子载体潜力。根据相应的重金属ISE参数，考虑了结构因素。作为离子载体，某些1-呋喃酰基-3-取代噻唑（系列2）在Pb(II)、Hg(II)和Cd(II) ISE中表现出最佳性能。系列2中的强内氢键使得配体只能通过CS基团进行相互作用。呋喃和苯环上的取代基导致在膜增塑剂中溶解度低。3-烷基取代的呋喃酰噻唑提高了溶解度，但随着链长的增加增强了氧化过程。在分析取代基对ISE选择性的影响时，考虑了新的X射线衍射（XRD）结构和理论DFT计算。这些新离子载体因其稳定性、简单合成和由于取代改变硫结合能力的易修改性而具有优势。
• Formal [3+2] Annulation Involving Allylic Bromides and Thioureas. Synthesis of 2-Iminothiazolidines through a Base-Catalyzed Intramolecular<i>anti</i>-Michael Addition
  作者：Misael Ferreira、Marcus M. Sá

  DOI：10.1002/adsc.201401026

  日期：2015.3.9

  A simple and efficient protocol was developed for the synthesis of 2‐iminothiazolidines through a base‐mediated [3+2] annulation involving substituted thioureas and allylic bromides bearing electron‐withdrawing groups. This domino process consists of nucleophilic displacement, followed by intramolecular anti‐Michael addition of the preformed allylic isothiourea under mild conditions to give the thiazolidine

  开发了一种简单有效的方案，用于通过碱介导的[3 + 2]环合反应合成2-亚氨基并噻唑烷，该环合反应涉及取代的硫脲和带有吸电子基团的烯丙基溴。该多米诺过程包括亲核取代，然后在温和条件下将预先形成的烯丙基异硫脲进行分子内抗迈克尔加成，得到噻唑烷核心。
• An Efficient Synthesis of Thiazolidine-4-ones with Antitumor and Antioxidant Activities
  作者：Ashraf A. Aly、Alan B. Brown、Mohamed Abdel-Aziz、Gamal El-Din A. A. Abuo-Rahma、Mohamed F. Radwan、Mohamed Ramadan、Amira M. Gamal-Eldeen

  DOI：10.1002/jhe.641

  日期：2012.7

  triphenylphosphine at −5°C led to (Z)‐methyl 2‐[(Z)‐2‐(4‐aroylimino)‐4‐oxo‐3‐aryl‐1,3‐thiazolidin‐5‐ylidene]acetates in good yields. The mechanism is discussed. X‐ray structure analysis of one thiazolidine derivative is described. Antitumor and antioxidant activities have been investigated. One derivative of 1,3‐thiazolidine showed moderate antiproliferative in vitro activity against hepatocellular carcinoma Hep‐G2

  3-芳酰基-1-芳基硫脲与二氯甲烷中的2-丁炔酸二甲酯在二氯甲烷中反应，并在-5°C下被三苯膦催化，生成（Z）-甲基2-[[（Z）-2-（4-芳基氨基）]-4 [-氧代-3-芳基-1,3-噻唑烷酮-5-亚萘基]乙酸酯的收率很高。讨论了该机制。描述了一种噻唑烷衍生物的X射线结构分析。已经研究了抗肿瘤和抗氧化活性。1,3-噻唑烷的一种衍生物在体外对肝细胞癌Hep-G2表现出中等的抗增殖活性，而另一种1,3-噻唑烷与抗坏血酸相比具有有效的抗氧化活性。
• Synthesis, crystal structure of some new 2-(4-methylbenzoylimino)-3-aryl-4-methyl-1,3-thiazolines
  作者：Aamer Saeed、Masood Parvez

  DOI：10.1002/jhet.5570430431

  日期：2006.7

  efficient, straightforward synthesis of some new 2-(4-methylbenzoylimino)-3-aryl-4-methyl-1,3-thiazolines (2a-i) is described. The methodology involves the cyclization of 1-(4-methylbenzoyl)-3-arylthioureas with acetone in the presence of bromine and triethylamine. The structures were confirmed by spectroscopic data, elemental analyses and in one case (2i) by the single crystal X-ray diffraction data.

  描述了一些新的2-（4-甲基苯甲酰亚氨基）-3-芳基-4-甲基-1,3-噻唑啉（2a-i）的有效，直接合成。该方法涉及在溴和三乙胺存在下用丙酮环化1-（4-甲基苯甲酰基）-3-芳基硫脲。通过光谱数据，元素分析以及在一种情况下（2i）通过单晶X射线衍射数据确认了结构。