Metal-Free Synthesis of 1,5-Disubstituted 1,2,3-Triazoles
Andrey Bubyrev, Ksenia Malkova, Grigory Kantin, Dmitry Dar’in, Mikhail Krasavin
Abstract
A three-component synthesis of 1,5-disubstituted 1,2,3-triazoles from α-acetyl-α-diazomethane sulfonamides, primary aliphatic amines, and aromatic aldehydes is presented. The 1,2,3-triazoles can be accessed in two alternative variants, depending on the substitutions in the sulfonamide portion of the diazo reagent. In one variant, intermediate 1,2,3-triazoline-4-sulfonamides are isolated chromatographically and then subjected to thermally promoted aromatization with elimination of sulfur(IV) oxide and amine. In the other variant, both chemical transformations take place in a single step conducted at room temperature.
Topics & Concepts
ChemistryDiazomethaneAromatizationDiazoReagentSulfonamideAmine gas treatingSulfurCombinatorial chemistryOrganic chemistryPrimary (astronomy)AstronomyPhysicsCatalysisClick Chemistry and ApplicationsCyclopropane Reaction MechanismsSynthesis and Biological Evaluation