Organic and Biomolecular Chemistry Division and ‡Center for X-ray Crystallography, CSIR-Indian Institute of Chemical Technology , Hyderabad 500007, India.
J Org Chem. 2017 May 19;82(10):5310-5316. doi: 10.1021/acs.joc.7b00646. Epub 2017 May 4.
A novel and expeditious approach for the synthesis of N-fused and 3,4-disubstituted 5-imino-1,2,4-thiadiazole derivatives has been achieved through the molecular iodine-catalyzed oxidative cyclization of 2-aminopyridine/amidine and isothiocyanate via N-S bond formation at ambient temperature. The present one-pot transition-metal-free protocol provides the facile and highly efficient regiospecific synthesis of various 1,2,4-thiadiazole derivatives in a scaled-up manner with good to excellent yields using inexpensive I as a catalyst.
一种新颖、快速的方法,通过分子碘催化 2-氨基吡啶/脒和异硫氰酸酯的 N-S 键形成,在室温下进行氧化环化,合成了 N-稠合和 3,4-二取代的 5-亚氨基-1,2,4-噻二唑衍生物。本一锅无过渡金属的方法使用廉价的 I 作为催化剂,以良好至优异的收率,高效、高区域选择性地规模化合成了各种 1,2,4-噻二唑衍生物。