A Convenient Synthesis of Fluoroalkylated Benzimidazole‐ or Indole‐fused Benzoxazines

Abstract Fluoroalkyl group is of particular interest in pharmaceutical chemistry. Since benzimidazole‐ or indole‐fused benzoxazines are important motifs in numerous biologically active molecules, the incorporation of a fluoroalkyl group into these molecules may provide more opportunities for drug developments. Herein we describe the first synthesis of fluoroalkylated benzimidazole‐ or indole‐fused benzoxazines by using fluoroalkylated propiolates as building blocks. The reactions proceeded smoothly under mild conditions to give the desired products in moderate to high yields. Notably, benzimidazole‐fused products were obtained by a convenient one‐pot two‐step process.