Crystal structure and hirshfeld surface analysis of a β-Carboline derivative

The title compound was synthesized in redox neutral C–H functionalization method. The resultant compound was characterized by 1H NMR and X-ray diffraction. The X-ray diffraction study reveals that the sample has crystallized in the triclinic crystal system with the space group P1. The asymmetric unit cell contains two molecules. The lattice parameters are a = 9.6544(3) A, b = 11.1048(4) A, c = 14.1787(5) A, α = 87.2370(10)˚, β = 70.5310(10)˚, γ = 65.3700(10)˚ and V = 1295.48(8) A3. The molecule is stabilized by both intra and intermolecular interactions of the type C-H...O, C-H...N and N-H...O hydrogen bonds.