Multicomponent synthesis and preliminary anti-inflammatory activity of lipophilic diphenylamines

Non-Steroidal Anti-inflammatory Drugs (NSAIDs) are some of the most prescribed medications for pain but the incidence of adverse effects-especially during chronic treatment-points out the requirement of new analgesics. In this study, we showed an efficient two-steps synthesis of diphenylamine-containing dipeptides consisting of a multicomponent process followed by a Buchwald-Hartwig cross-coupling reaction. We prepared 16 diphenylamine derivatives and evaluated their in vivo anti-inflammatory activity through an ear edema model using 12-O-tetradecanoylpholbol-13-acetate. Furthermore, the toxicity of the more potent compounds in the Artemia salina model and their cell viability using murine RAW 264.7 cells is reported. The fluorinated compound 10k becomes a reliable candidate since it reduced the TPA-induced edema to 92%, lacked cytotoxicity against murine macrophages, and had minimal toxicity in Artemia salina.

Automated summary

In this study, an efficient two-step synthesis of diphenylamine-containing dipeptides was demonstrated, with fluorinated compound 10k showing promising anti-inflammatory activity, no cytotoxicity against murine cells, and minimal toxicity in Artemia salina.