3-allyl-4-hydroxy-4-phenylthiazolidine-2-thione | 1231773-08-2

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 唑烷类
• 英文名称: 3-allyl-4-hydroxy-4-phenylthiazolidine-2-thione
• 英文别名: 4-Hydroxy-4-phenyl-3-prop-2-enyl-1,3-thiazolidine-2-thione
• CAS: 1231773-08-2
• 化学式: C₁₂H₁₃NOS₂
• 分子量: 251.373
• InChiKey: ICSKMOLYHUEFCI-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.4
• 重原子数：
  16
• 可旋转键数：
  3
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.25
• 拓扑面积：
  80.9
• 氢给体数：
  1
• 氢受体数：
  3

反应信息

• 作为产物：
  描述：

  苯甲酰氯 在 potassium tert-butylate 作用下， 以 四氢呋喃 、 水 为溶剂， 反应 15.0h， 生成 3-allyl-4-hydroxy-4-phenylthiazolidine-2-thione
  参考文献：
  名称：

  CS2、胺和氧化亚硝叶立德在水中的多组分反应：直接获得 β-酮基二硫代氨基甲酸酯、噻唑烷-2-硫酮和噻唑-2-硫酮

  摘要：

  已经描述了通过 CS 2 、胺和氧化硫叶立德的多组分反应合成 β-酮基二硫代氨基甲酸酯、噻唑烷-2-硫酮和噻唑-2-硫酮的简单、通用且无催化剂的合成方法。β-酮基亚砜叶立德在 CS 2和仲胺存在下生成 β-酮基二硫代氨基甲酸酯，而伯胺在酸性环境中脱水后生成噻唑烷-2-硫酮或噻唑-2-硫酮。反应过程简单，底物范围广，官能团耐受性好。

  DOI：

  10.1021/acs.joc.2c02763

文献信息

• Water-Mediated Multicomponent Reaction: A Facile and Efficient Synthesis of Multisubstituted Thiazolidine-2-thiones
  作者：Cui-Rong Sun、Shi-Feng Gan、Jie-Ping Wan、Yuan-Jiang Pan

  DOI：10.1055/s-0029-1219558

  日期：2010.4

  A facile, efficient, and green method for the synthesis of multisubstituted thiazolidine-2-thione derivatives via a three-component reaction of amine, carbon disulfide, and α-bromoketone is described. By using water as the reaction medium, the reaction proceeds smoothly to give corresponding products in good to excellent yields.

  本文介绍了一种便捷、高效且环保的方法，通过胺、二硫化碳和α-溴代酮的三组分反应合成多取代噻唑烷-2-硫酮衍生物。采用水作为反应介质，反应顺利进行，得到相应产物，产率良好至优。
• Utility of N-Bromosuccinimide–Water Combination as a Green Reagent for Synthesis of N,S-Heterocycles and Dithiocarbamates from Styrenes
  作者：Firouz Matloubi Moghaddam、Mehri Goudarzi

  DOI：10.1055/s-0040-1707258

  日期：2020.11

  An efficient and unprecedented green protocol has been developed for the synthesis of N,S-heterocycles from styrenes and alkyl dithiocarbamates with high to excellent yields. The reaction of primary or secondary amines, CS2, and styrenes was carried out in water in the presence of a catalytic amount of an inorganic base. All products were made by using an N-bromosuccinimide–H2O combination as a green

  已开发出一种高效且前所未有的绿色方案，用于从苯乙烯和二硫代氨基甲酸烷基酯合成 N,S-杂环，收率高至极好。在催化量的无机碱存在下，伯胺或仲胺、CS2和苯乙烯的反应在水中进行。所有产品均使用 N-溴代琥珀酰亚胺-H2O 组合作为绿色且廉价的试剂制成。
• [EN] METHODS AND COMPOSITIONS TO MODIFY GSK-3 ACTIVITY<br/>[FR] PROCÉDÉS ET COMPOSITIONS POUR MODIFIER L'ACTIVITÉ DE GSK-3
  申请人：UNIV OHIO

  公开号：WO2016010611A1

  公开（公告）日：2016-01-21

  Methods for modulating GSK-3 activity and methods for treating a GSK-3 -mediated disorder in a subject in need thereof. The methods include contacting a cell expressing GSK-3 with or administering to the subject in need a therapeutically effective amount of one or more compounds of General Formula (I) or General Formula (II): or pharmaceutically-acceptable salts or solvates thereof.

  调节GSK-3活性的方法和治疗需要的主体中GSK-3介导的疾病的方法。该方法包括将表达GSK-3的细胞与或向需要的主体施用一种或多种通用式(I)或通用式(II)的化合物的治疗有效量接触，或其药用接受的盐或溶剂。
• Imidazole and thiazole compositions for modifying biological signaling
  申请人：Ohio University

  公开号：US10023567B2

  公开（公告）日：2018-07-17

  Compounds having General Formula (I) or General Formula (II): in which R1 is chosen from C1 to C10 aliphatic or heteroaliphatic groups, optionally substituted with one or more aryl groups, substituted aryl groups, heteroaryl groups, substituted heteroaryl groups, or combination thereof; R2 is chosen from aromatic moieties, substituted aromatic moieties, heteroaromatic moieties substituted heteroaromatic moieties, and coumarin; R3 is chosen from —H, C1 to C10 aliphatic or heteroaliphatic groups, phenyl, or substituted phenyl, wherein the aliphatic or heteroaliphatic groups are optionally substituted with one or more phenyl groups, aryl groups, heteroaryl groups, substituted heteroaryl groups, or combination thereof, and wherein the aliphatic or heteroaliphatic groups are optionally bonded to R2 to form a ring; X is S or O; and Y is S or NH, may be used in pharmaceutical compositions that modify of biological signaling processes or as reagents for biological assays.

  具有通式(I)或通式(II)的化合物：其中 R1 选自 C1 至 C10 脂肪族或杂脂肪族基团，任选被一个或多个芳基、取代芳基、杂芳基、取代杂芳基或其组合取代；R2 选自芳香族基团、取代芳香族基团、杂芳香族基团、取代杂芳香族基团和香豆素；R3 选自-H、C1 至 C10 脂肪族或杂脂肪族基团、苯基或取代苯基，其中脂肪族或杂脂肪族基团可选择被一个或多个苯基、芳基、杂芳基、取代杂芳基或其组合取代，并且其中脂肪族或杂脂肪族基团可选择与 R2 键合形成环；X 是 S 或 O；Y 是 S 或 NH，可用于改变生物信号转导过程的药物组合物或用作生物检测试剂。
• Prevention and treatment of non-alcoholic fatty liver disease
  申请人：Ohio University

  公开号：US10392381B2

  公开（公告）日：2019-08-27

  Methods for preventing, treating, and/or reducing the risk of developing non-alcoholic fatty liver disease in a subject in need thereof and pharmaceutical compositions for the prevention or treatment of non-alcoholic fatty liver disease. Methods for inhibiting excessive accumulation of fat in liver tissue. The methods include administering to the subject or contacting the liver tissue with a therapeutically effective amount of at least one compound of General Formula (I) or General Formula (II): or pharmaceutically-acceptable salts or solvates thereof. The pharmaceutical composition includes at least one compound of the General Formula (I) or the General Formula (II) for administration to a subject for the prevention or treatment of non-alcoholic fatty liver disease.

  预防、治疗和/或降低有需要者患非酒精性脂肪肝风险的方法，以及预防或治疗非酒精性脂肪肝的药物组合物。抑制脂肪在肝组织中过度积累的方法。这些方法包括向受试者施用或用治疗有效量的至少一种通式（I）或通式（II）化合物：或其药学上可接受的盐或溶解物接触肝组织。药物组合物包括至少一种通式(I)或通式(II)化合物，用于给受试者用药，以预防或治疗非酒精性脂肪肝。