Abstract
Benzimidic acid methyl esters on heating with glycine ester in toluene in presence of sodium acetate yield 4-(aminoaryl)-methylene-2-aryl-2-imidazolin-5-ones. They undergo acetylation and benzoylation on reaction with acetic anhydride and benzoyl chloride, respectively. The 1 3 C assignment of some of the carbon atoms of one of the acetyl derivatives has been done by HMQC and HMBC experiments.
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