Base‐promoted Oxidative Sulfuration/Cyclization to Construct Naphtho[2,3‐d]thiazole through Three‐component Reaction Using S₈ as the Sulfur Source

Abstract

Abstract A base‐promoted three‐component oxidative sulfuration/cyclization reaction of 2‐amino‐1,4‐naphthoquinone, aldehyde and elemental sulfur was developed. The naphtho[2,3‐d]thiazole ring was determined by forming two C−S bonds and one C=N bond, which demonstrates the advantages of cheap raw materials, no transition metal, and economic efficiency. The substrate scope was broad with aromatic and aliphatic aldehydes. The mechanistic study might promote the reaction design for a oxidative sulfuration/cyclization reaction.