Hantzsch pyrrole synthesis The Hantzsch Pyrrole Synthesis , named for Arthur Rudolf Hantzsch , is the chemical reaction of β-ketoesters with ammonia and α-haloketones to give substituted pyrroles. Pyrroles are found in a variety of natural products with biological activity , so the synthesis of substituted pyrroles has important applications in medicinal chemistry . Alternative methods for synthesizing pyrroles exist, such as the Knorr Pyrrole Synthesis and Paal-Knorr Synthesis .Mechanism Below is one published mechanism for the reaction: The mechanism starts with the amine attacking the β carbon of the β-ketoesters, and eventually forming an enamine . The enamine then attacks the carbonyl carbon of the α-haloketone. This is followed by the loss of H2 O, giving an imine . This intermediate undergoes an intramolecular nucleophilic attack , forming a 5-membered ring. Finally, a hydrogen is eliminated and the pi-bonds are rearranged in the ring , yielding the final product . An alternative mechanism has been proposed in which the enamine attacks the α-carbon of the α-haloketone as part of a nucleophilic substitution , instead of attacking the carbonyl carbon.Generalized Reaction Under Mechanochemical Conditions A generalization of the Hantzsch pyrrole synthesis was developed by Estevez, et al . In this reaction highly substituted pyrroles can be synthesized in a one-pot reaction , with relatively high yields. This reaction involves the high-speed vibration milling of ketones with N -iodosuccinimide and p -toluenesulfonic acid, to form an α-iodoketone in situ . This is followed by addition of a primary amine , a β-dicarbonyl compound, cerium ammonium nitrate and silver nitrate , as shown in the scheme below:Applications 2,3-dicarbonylated pyrroles 2,3-dicarbonylated pyrroles can be synthesized by a version of the Hantzsch Pyrrole Synthesis. These pyrroles are particularly useful for total synthesis because the carbonyl groups can be converted into a variety of other functional groups . The reaction can also occur between an enamine and an α-haloketone to synthesize substituted indoles, which also have biological significance. A library of substituted pyrrole analogs can be quickly produced by using continuous flow chemistry . The advantage of using this method, as opposed to the in-flask synthesis, is that this one does not require the work-up and purification of several intermediates, and could therefore lead to a higher percent yield .
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