Faculty of Chemistry, Wroclaw University of Science and Technology, Wybrzeże Wyspiańskiego 27, 50 370 Wrocław, Poland.
Institute of Medical Biology PAS, 106 Lodowa St., 93-232 Łódź, Poland.
Biomed Pharmacother. 2022 Sep;153:113473. doi: 10.1016/j.biopha.2022.113473. Epub 2022 Aug 1.
Chiral sulfonamides with aromatic fragments are important chemical building blocks found widely in many natural products, catalysts, and molecules of biological importance. In this report, we describe the efficient synthesis of a series of chiral sulfonamides which, in addition to the aromatic part (phenyl, biphenyl, and dansyl units), possess N-heterocyclic systems. The described compounds were obtained by nucleophilic substitution of chiral N-heterocyclic amines and commercially available aromatic sulfonyl chlorides under mild conditions. All derivatives were examined in antiviral assay against AdV5, HSV-1, HPIV-3, HCMV, and EMCV viruses.
手性芳基磺酰胺是许多天然产物、催化剂和生物重要分子中广泛存在的重要化学结构单元。在本报告中,我们描述了一系列手性磺酰胺的有效合成方法,这些磺酰胺除了芳基部分(苯基、联苯基和丹磺酰基单元)外,还具有杂环系统。所述化合物是通过在温和条件下用手性杂环胺和亲电试剂商业可得的芳基磺酰氯进行亲核取代反应得到的。所有衍生物都在抗 AdV5、HSV-1、HPIV-3、HCMV 和 EMCV 病毒的抗病毒测定中进行了测试。