Synthesis of novel tryptophan derivatives of potential biological activity

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Abstract

Tryptophan methyl ester 2 reacts with ethyl cyanoacetate to form acetonitrilocarbonyltryptophan methylester 3. The latter reacts with cyanomethylene reagents, hydrazines, cyanomethylenes and sulfur to form the corresponding α-pyrido-3-indolopropanoate derivatives 6a,b, pyrazolyltryptophan methyl ester derivatives 8a,b and thiophenotryptophan methyl ester derivatives 10a,b, respectively. Also compound 3 reacts with benzaldehyde to give the condensated product 12. The reactivity of the latter product towards chemical reagents was studied to form pyridine, pyrazole and isoxazole derivatives.

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Mohareb, R. M., Louca, N. A., Elmegeed, G. A., & Hana, H. Y. (2009). Synthesis of novel tryptophan derivatives of potential biological activity. Journal of the Chilean Chemical Society, 54(2), 175–179. https://doi.org/10.4067/S0717-97072009000200018

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