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Sociedade Brasileira de Química, Química Nova, 7(35), p. 1477-1481

DOI: 10.1590/s0100-40422012000700033

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Biomimetic oxidation of carbamazepine with hydrogen peroxide catalyzed by a manganese porphyrin

This paper is made freely available by the publisher.
This paper is made freely available by the publisher.

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Abstract

This laboratory project is planned for an undergraduate chemistry laboratory in which students prepare a manganese porphyrin able to mimic the oxidative metabolism of carbamazepine, one of the most frequently prescribed drugs in the treatment of epilepsy. The in vitro oxidation of carbamazepine results in the formation of the corresponding 10,11-epoxide, the main in vivo metabolite. The reaction is catalyzed by manganese porphyrin in the presence of H2O2, an environmentally-friendly oxidant. Through this project students will develop their skills in organic synthesis, coordination chemistry, chromatographic techniques such as TLC and HPLC, UV-visible spectrophotometry, and NMR spectroscopy.