Synthesis and Evaluations of “1,4-Triazolyl Combretacoumarins” and Desmethoxy Analogs

Authors

Tashrique A. Khandaker, CUNY City CollegeFollow
Jessica D. Hess, University of Texas at El Paso
Renato Aguilera, University of Texas at El Paso
Graciela Andrei, Rega Institute of Medical Research
Robert Snoeck, Rega Institute of Medical Research
Dominique Schols, Rega Institute of Medical Research
Padmanava Pradhan, CUNY City CollegeFollow
Mahesh K. Lakshman, CUNY City CollegeFollow

Document Type

Article

Publication Date

8-7-2019

Abstract

1,4-Triazolyl combretacoumarins have been prepared by linking the trimethoxyarene unit of combretastatin A4 with coumarins, via a 1,2,3-triazole. For this, 4-azidocoumarins were accessed by a sequential two-step, one-pot reaction of 4-hydroxycoumarins with (benzotriazol-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate (BOP), followed by reaction with NaN₃. In the reaction with BOP, a coumarin-derived phosphonium ion intermediate seems to form, leading to an O⁴-(benzotriazolyl)coumarin derivative. For the CuAAC reaction of azidocoumarins with 5-ethynyl-1,2,3-trimethoxybenzene, catalytic [(MeCN)₄Cu]PF₆ in CH₂Cl₂/MeOH with 2,6-lutidine, at 50 ^oC, was suitable. The 4-azidocoumarins were less reactive as compared to PhN₃ and the NBO coefficients of the azido groups were compared by DFT analysis. Compound solubility was a problem in biological assays. On the basis of the biological and solubility data of one 1,4-triazolyl combretacoumarin, four analogs lacking one or two methoxy groups were synthesized. Reactivity differences among the phenylacetylenes were noted and the NBO coefficients of the alkynes were compared by DFT analysis. In cytotoxicity assays, 1-phenyl-4-(3,4,5-trimethoxyphenyl)-1H-1,2,3-triazole showed activity in CEM and MDA-MB-231 cell lines by apoptosis. The desmethoxy 6-bromo-4-(4-(4-methoxyphenyl)-1H-1,2,3-triazol-1-yl)-2H-chromen-2-one also showed cytotoxicity against the two cell lines, but this did not appear to be consistent with apoptosis. The antiviral activity of the compounds was unremarkable.

Comments

This work was originally published in the European Journal of Organic Chemistry, available at https://doi.org/10.1002/ejoc.201900569.

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