Synthesis and Properties of 1,3-Disubstituted Ureas and Their Isosteric Analogs Containing Polycyclic Fragments: VII. Synthesis and Properties 1-[(Adamantan-1-yl)methyl]-3-(fluoro, chlorophenyl) Ureas
作者:D. V. Danilov、V. S. D’yachenko、Y. P. Kuznetsov、V. V. Burmistrov、G. M. Butov
DOI:10.1134/s1070428021020020
日期:2021.2
Abstract A series of 1,3-disubstituted ureas containing a lipophilic adamantane moiety tethered to the ureido group by a methylene bridge were synthesized by the reaction of 1-(isocyanatomethyl)adamantane with monohalo- and dihaloanilines in yields of up to 92%. The synthesized ureas are target oriented inhibitors of human soluble epoxide hydrolase (sEH).
摘要 通过1-(异氰酸根合甲基)金刚烷与单卤代和二卤代苯胺的反应,合成了一系列包含通过亚甲基桥连接到脲基的亲脂性金刚烷部分的1,3-二取代脲,产率高达92%。合成的脲是人类可溶性环氧化物水解酶(sEH)的靶向抑制剂。