Abstract A simple synthesis of novel N-(2-[N’-acetamidomethyl])benzanilides derivatives from 2-nitrobenzaldehyde in a four steps process is described. The ¹H-NMR and ¹³C-NMR spectra were meticulously analyzed to characterize their structure and it was observed that derivatives with an ortho-substituted phenyl group exhibited detectable atropisomerism. The ADME/toxicity analyses was performed and several of these acetamidobenzanilides were tested in vitro against the epimastigote form of Trypanosoma cruzi, demonstrating significant activity.
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Ortellado et al. (2024) studied this question.
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