Synthesis of 2-Thio-Substituted Benzothiazoles via a Domino Condensation/<i>S</i>-Arylation/Heterocyclization Process
作者:Liu Shi、Xiangqian Liu、Hui Zhang、Yongwen Jiang、Dawei Ma
DOI:10.1021/jo200535e
日期:2011.5.20
Condensation of carbon disulfide with thiols in the presence of K2CO3 generates carbonotrithioate salts in situ, which undergo coupling with 2-iodoanilines and subsequent intramolecular condensation and elimination under assistance of CuBr to afford 2-thio-substituted benzothiazoles. Both aliphatic and aromatic thiols are compatible with this process, delivering the corresponding heterocycles with
在K 2 CO 3存在下,二硫化碳与硫醇的缩合原位生成三硫代碳酸盐,将其与2-碘苯胺偶联,随后在CuBr的帮助下进行分子内缩合和消除,得到2-硫基取代的苯并噻唑。脂族和芳族硫醇均与该过程相容,从而提供具有良好多样性的相应杂环。
A Convenient Method for the Preparation of Alkyl Aryl Sulfides from Alcohols and (Chloromethylene)dimethylammonium Chloride
(Chloromethylene)dimethylammonium chloride (Vilsmeier reagent), prepared easily from DMF and oxalyl chloride, works as an efficient condensation reagent for the thioetherification of alcohols in on...