Aim: The synthesis of diverse N-substituted pyrroles utilizing rice malt is identified. The reaction of hexane-2,5-dione with various primary amines develops the intriguing pyrrole scaffold in moderate to good yields.
Methods: The reaction was carried out at room to ambient temperature in an extremely environmentally benign condition, without the need for any additional solvents or catalysts.
Results: In the synthesis of N-derivatized pyrroles, several 1 amines, both cyclic and acyclic residue, have been accomplished.
Conclusion: To the best of my knowledge, no study has been reported so far based on Paal- Knorr pyrrole synthesis utilizing rice malt as a catalyst and solvent.
Keywords: Rice malt, polysaccharides, polyhydroxy-sugar, paal-knorr, pyrrole, chemotherapeutics, hexane-2, 5-dione, amine, cyclodehydration, cyclo-condensation, aromatization.