3-((Hetera)cyclobutyl)azetidines, “Stretched” Analogues of Piperidine, Piperazine, and Morpholine: Advanced Building Blocks for Drug Discovery

J. Org. Chem. 2019, 84 (3), 1363-1371

DOI: 10.1021/acs.joc.8b02822

Feskov I.; Chernykh A.; Kuchkovska Y.; Daniliuc C.; Kondratov I.; Grygorenko O.

Four 3-((hetera)cyclobutyl)azetidine-based isosteres of piperidine, piperazine, and morpholine were designed and synthesized on up to gram scale. The key step of the synthetic sequence included cyclization of N-protected 2-(azetidin-3-yl)propane-1,3-diol or the correspon notding 1,3-dibromide. X-ray diffraction studies of the products obtained, followed by exit vector plot analysis of their molecular geometry demonstrated their larger size and increased conformational flexibility as compared to the parent heterocycles, and confirmed their potential utility as building blocks for lead optimization programs.

3-((Hetera)cyclobutyl)azetidines, “Stretched” Analogues of Piperidine


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