Premaletha Sethulekshmy, Ghosh Arghya, Joseph Sumi, Yetra Santhivardhana Reddy, Biju Akkattu T
Organic Chemistry Division, CSIR-National Chemical Laboratory (CSIR-NCL), Dr. Homi Bhabha Road, Pune-411008, India.
Chem Commun (Camb). 2017 Jan 26;53(9):1478-1481. doi: 10.1039/c6cc08640c.
A mild, general, and high yielding synthesis of N-acyl 2-aminobenzothiazoles has been demonstrated by N-heterocyclic carbene (NHC)-organocatalyzed direct amidation of aldehydes with 2-aminobenzothiazoles proceeding via acyl azolium intermediates. The carbene generated from the triazolium salt under oxidative conditions was the key for the success of this reaction. The method was subsequently applied to the synthesis of various biologically important N-acyl 2-aminobenzothiazoles.
通过N-杂环卡宾(NHC)-有机催化醛与2-氨基苯并噻唑经酰基唑鎓中间体进行直接酰胺化反应,已证明了一种温和、通用且高产率的N-酰基-2-氨基苯并噻唑的合成方法。在氧化条件下由三唑鎓盐生成的卡宾是该反应成功的关键。该方法随后被应用于各种具有重要生物学意义的N-酰基-2-氨基苯并噻唑的合成。