Formation of the imidazolinone ring under mild conditions in the presence of sodium hydride

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Abstract

Substituted imidazolinones containing heterocyclic carboxylic acids as substituents and possessing herbicidal properties were synthesized by cyclization of 2-amino-2,3-dimethylbutyramide with heterocyclic ethyl dicarboxylates under mild conditions. The use of NaH as base leads to a significant increase in the reaction rate and allows the preparation of the target compounds in high yields.

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Vasiliev, A. N., Lopez, A. F., Fernandez, J. D., & Mocchi, A. J. (2004). Formation of the imidazolinone ring under mild conditions in the presence of sodium hydride. Molecules, 9(7), 535–540. https://doi.org/10.3390/90700535

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