Interception of enamine intermediates in reductive functionalization of lactams by sodium hydride: Synthesis of 2-cyano-3-iodo piperidines and pyrrolidines. (21st May 2022)

• Record Type: Journal Article
• Authors: Chen, Jiahua; Lim, Jun Wei; Chiba, Shunsuke
• Is Part Of: Tetrahedron. Volume 114(2022)
• Publication Date: 2022-05-21
• Subjects: Sodium hydride -- Lactams -- Saturated nitrogen heterocycles -- Iodination -- Cyanation; Chemistry, Organic -- Periodicals; 547.005
• DOI: 10.1016/j.tet.2022.132779
• Languages: English
• ISSNs: 0040-4020

Abstract

Abstract: Facile conversion of 2-piperidones and 2-pyrrolidones into 2-cyano-3-iodo piperidines or pyrrolidines has been accomplished by the sequence of 1) controlled hydride reduction of lactams using sodium hydride (NaH) in the presence of sodium iodide (NaI); 2) silylation of anionic hemiaminal intermediates to facilitate deoxygenation to form an equilibrium mixture of iminium cations and enamines-silanol pair; 3) interception of enamine intermediates by electrophilic iodination to generate iodonium ions; 4) nucleophilic cyanation of the resultant iminium cations. The overall transformation proceeded in highly diastereoselective fashion. The resultant 2-cyano-3-iodo piperidines were converted into 2-cyanotetrahydropyridines, which could be used for [2 + 2]-annulation or ring-expansion reactions with reactive benzyne or alkyne species, respectively. Graphical abstract: Image 1