trans-4,5-diphenylimidazolidine-2-thione | 139237-78-8

• 分子结构分类: 有机化合物 - 苯丙烷和聚酮 - 二苯乙烯类
• 英文名称: trans-4,5-diphenylimidazolidine-2-thione
• 英文别名: trans-4,5-diphenylimidazoline-2-thione；4,5-diphenylimidazolidine-2-thione；trans-4,5-diphenylimidazolidin-2-thion；(4R,5R)-4,5-Diphenyl-2-imidazolidinethione；(4R,5R)-4,5-diphenylimidazolidine-2-thione
• CAS: 139237-78-8
• 化学式: C₁₅H₁₄N₂S
• 分子量: 254.356
• InChiKey: HJYSGEJLUSZCTF-ZIAGYGMSSA-N

物化性质

• 沸点：
  384.7±52.0 °C(Predicted)
• 密度：
  1.25±0.1 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  2.8
• 重原子数：
  18
• 可旋转键数：
  2
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.13
• 拓扑面积：
  56.2
• 氢给体数：
  2
• 氢受体数：
  1

反应信息

• 作为反应物：
  描述：

  trans-4,5-diphenylimidazolidine-2-thione 在 吡啶 、 4-二甲氨基吡啶 、 mercury(II) diacetate 作用下， 以 二氯甲烷 为溶剂， 生成 1,3-di(3-phenylpropionyl)-trans-4,5-diphenylimidazolidin-2-one
  参考文献：
  名称：

  Bifunctional chiral auxiliaries 2: the synthesis of 1,3-diacylimidazolidin-2-ones from 1,2-diamines

  摘要：

  The title compounds are readily prepared in three steps via the corresponding 1,3-diacylimidazolidine-2-thiones. The final step involves the novel use of mercury (II) acetate for the conversion of thioureas to ureas.

  DOI：

  10.1016/s0040-4039(00)92309-8
• 作为产物：
  描述：

  二硫化碳 、 1,2-二苯基乙烷-1,2-二胺 在 盐酸 作用下， 生成 trans-4,5-diphenylimidazolidine-2-thione
  参考文献：
  名称：

  Bifunctional chiral auxiliaries 5: The synthesis of 1,3-diacylimidazolidine-2-thiones and 1,3-diacylimidazolidin-2-ones from 1,2-diamines

  摘要：

  Although 1,2-diamines fail to cyclise with urea, phosgene or 1,1'-carbonyl diimidazole, they react with carbon disulphide to give the corresponding imidazolidine-2-thiones. These undergo clean diacylation to give 1,3-diacylimidazolidine-2-thiones which are readily converted to 1,3-diacylimidazolidin-2-ones on treatment with mercury (II) acetate. An alternative two-step route to 1,3-diacylimidazolidin-2-ones uses carbonyl sulphide to effect cyclisation of the 1,2-diamine to the imidazolidin-2-one, which is subsequently diacylated. The ability to convert homochiral 1,2-diamines to homochiral 1,3-diacylimidazolidin-2-ones has also been demonstrated.

  DOI：

  10.1016/s0040-4020(01)85757-4

文献信息

• Reaction of Thiocarbonyl Fluoride Generated from Difluorocarbene with Amines
  作者：Jiao Yu、Jin-Hong Lin、Ji-Chang Xiao

  DOI：10.1002/anie.201710186

  日期：2017.12.22

  The reaction of thiocarbonyl fluoride, generated from difluorocarbene, with various amines under mild conditions is described. Secondary amines, primary amines, and o‐phenylenediamines are converted to thiocarbamoyl fluorides, isothiocyanates, and difluoromethylthiolated heterocycles, respectively. Thiocarbamoyl fluorides were further transformed into trifluoromethylated amines by using a one‐pot process

  描述了在温和条件下由二氟卡宾生成的硫代羰基氟化物与各种胺的反应。仲胺，伯胺和邻苯二胺分别转化为硫代氨基甲酰氟，异硫氰酸酯和二氟甲基硫代杂环。硫氨甲酰氟通过一锅法进一步转化为三氟甲基化胺。硫代羰基氟化物在原位生成，并在温和条件下在一锅中迅速完全转化；因此，不需要特殊的安全预防措施。
• Heterocyclic compounds as P2X7 ion channel blockers
  申请人：Shum Patrick

  公开号：US20050026916A1

  公开（公告）日：2005-02-03

  The present invention relates to a novel series of 4,5-diphenyl-2-amino-4,5-dihydro-imidazole derivatives of the formula II: wherein R, R 1 , R 2 , R 3 , R 4 , R 5 , X and Y are as defined herein. This invention also relates to methods of making these compounds. The compounds of this invention are P2X7 ion channel blockers and are therefore useful as pharmaceutical agents, especially in the treatment and/or prevention of a variety of diseases having an inflammatory component, including inflammatory bowel disease, rheumatoid arthritis and disease conditions associated with the central nervous system, such as stroke, Alzheimer's disease, etc.

  本发明涉及一种新的4,5-二苯基-2-氨基-4,5-二氢咪唑衍生物系列，其化学式为II： 其中R、R1、R2、R3、R4、R5、X和Y如本文所定义。本发明还涉及制备这些化合物的方法。本发明的化合物是P2X7离子通道阻断剂，因此在作为药用剂方面具有用途，特别是在治疗和/或预防具有炎症成分的各种疾病方面，包括炎症性肠病、类风湿关节炎以及与中枢神经系统相关的疾病状况，如中风、阿尔茨海默病等。
• Thiocarbonyl Surrogate via Combination of Sulfur and Chloroform for Thiocarbamide and Oxazolidinethione Construction
  作者：Wei Tan、Jianpeng Wei、Xuefeng Jiang

  DOI：10.1021/acs.orglett.7b00819

  日期：2017.4.21

  An efficient and practical thiocarbonyl surrogate via combination of sulfur and chloroform has been developed. A variety of thiocarbamides and oxazolidinethiones have been established, including chiral thiourea catalysts and chiral oxazolidinethione auxiliaries with high selectivity. Meanwhile, pesticides Diafenthiuron (an acaricide), ANTU (a rodenticide), and Chloromethiuron (an insecticide) were

  已经开发了通过硫和氯仿的组合的有效和实用的硫代羰基替代物。已经建立了多种硫代脲和恶唑烷硫酮，包括具有高选择性的手性硫脲催化剂和手性恶唑烷硫酮助剂。同时，实际上通过克方法通过该方法合成了杀虫剂DiafeNThiuron（一种杀螨剂），ANTU（一种灭鼠剂）和Chloromethiuron（一种杀虫剂）。通过卡宾捕集控制实验进一步确认了作为主要中间体的双氯卡宾。
• Bifunctional chiral auxiliaries 6: Alkylations of enolates derived from 1,3-diacylimidazolidine- 2-thiones and 1,3-diacylimidazolidin-2-ones
  作者：Stephen G. Davies、Gary B. Evans、Andrew A. Mortlock

  DOI：10.1016/0957-4166(94)80022-7

  日期：1994.4

  Sodium and potassium enolates of 1,3-diacylimidazolidin-2-ones undergo clean alkylation reactions with reactive alkyl halides; the latter enolates reacting generally more stereoselectively due, it is proposed, to the lower temperature at which the reactions proceed. The reactions are all stereoregular, with the diastereoisomeric identity of products being established unambiguously by the synthesis

  1,3-二酰基咪唑烷基-2-酮的烯醇钠和钾盐与反应性烷基卤化物进行干净的烷基化反应；提议的是，后者由于反应进行的较低温度而通常更立体选择性地发生反应。反应都是立体有规的，通过（2S）-3-苯基-2-甲基丙烷-1-醇的合成可以明确地确定产物的非对映异构身份。在这些反应中的不对称诱导的意义上是与螯合的中间性一致的顺式烯醇化物其中亲电子从面部优先接近外在五元环上的最接近的烷基/芳基上。相反，由于烯醇盐的分解，在烷基化反应中1，3-二酰基咪唑烷-2-硫酮不能作为双官能手性助剂。
• 2,4,5-Trisubstituted imidazolines and pharmaceutical compositions
  申请人：Ciba-Geigy Corporation

  公开号：US04308277A1

  公开（公告）日：1981-12-29

  Compounds of the formula ##STR1## in which R.sub.1 and R.sub.2 independently of one another are substituted or unsubstituted aryl or hetero-aryl groups, R.sub.3 is hydrogen or lower alkyl and R.sub.4 is a substituted or unsubstituted aliphatic hydrocarbon radical, and their pharmaceutically usable salts. These compounds possess immunoregulatory, antithrombotic and antiinflammatory properties and can be used as active ingredients in medicaments. They are prepared, for example, by reacting compounds of the formulae ##STR2## in which one of the radicals X and Y is mercapto, which can be in the form of a salt, and the other is a radical replaceable by etherified mercapto, with one another.

  公式为##STR1##的化合物，其中R.sub.1和R.sub.2分别是取代或未取代的芳基或杂环芳基，R.sub.3是氢或低碳烷基，R.sub.4是取代或未取代的脂肪烃基，以及它们的药用盐。这些化合物具有免疫调节、抗血栓和抗炎性能，并可用作药物的活性成分。例如，它们可通过将公式为##STR2##的化合物进行反应制备，其中X和Y中的一个基团是巯基，可以是盐的形式，另一个是可由醚化巯基取代的基团。