Cobalt(<scp>iii</scp>)-catalyzed redox-neutral [4+2]-annulation of <i>N</i>-chlorobenzamides/acrylamides with alkylidenecyclopropanes at room temperature

Abstract

An efficient synthesis of substituted 3,4-dihydroisoquinolinones through [4+2]-annulation of N-chlorobenzamides/acrylamides having a monodentate directing group with alkylidenecyclopropanes in the presence of a less expensive, highly abundant and air stable Co(iii) catalyst via a C-H activation is demonstrated. In this reaction, the N-Cl bond of N-chlorobenzamide serves as an internal oxidant and thus an external metal oxidant is avoided. The 3,4-dihydroisoquinolinone derivatives are converted successfully into the highly useful imidoyl chloride derivatives. The deuterium labeling and kinetic isolabelling studies reveal that the C-H activation is a rate-determining step in this cyclization reaction.

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