^NQNHC Ligand-Enabled Cu(I)-Catalyzed Double Hydroamination: A Regio- and Chemoselective Bicyclization of <i>o</i>‑Amino 1,6-Diyne

In this work, we have developed an efficient method for the intramolecular double hydroamination of aniline by employing o-amino 1,6-diyne as a potential starting material. This protocol enables easy access to bioactive motif 3,4-dihydro-1H-[1,4]oxazino[4,3-a]indole through an intramolecular cascade bicyclization and concomitant isomerization pathway in one pot. This transformation has been effectively achieved by utilizing a stereoelectronically tuned, π-accepting NHC-supported copper(I) system. During ligand optimization trials, naphthoquinone-annulated N-heterocyclic carbene, Nq(IDipp) [1,3-bis(2,6-diisopropylphenyl)-4,5-naphthoquino-imidazolidene]-supported copper(I) complexes of the type Nq(IDipp)CuX (X = Cl or I) were synthesized and fully characterized using various spectroscopic techniques. For this conversion, NHC plays a crucial role in providing the optimum electron density around the metal center. It is a highly regio- and chemoselective transformation with a high atom economy and uses cheap, environmentally benign copper-based catalysts. Furthermore, a plausible mechanism has been proposed on the basis of experimental observations and literature support.