Volume 132, Issue 5 pp. 1873-1878
Forschungsartikel

Imidazotetrazines as Weighable Diazomethane Surrogates for Esterifications and Cyclopropanations

Riley L. Svec

Riley L. Svec

Department of Chemistry and Carl R. Woese Institute for Genomic Biology, University of Illinois at Urbana-Champaign, Urbana, IL, 61801 USA

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Prof. Paul J. Hergenrother

Corresponding Author

Prof. Paul J. Hergenrother

Department of Chemistry and Carl R. Woese Institute for Genomic Biology, University of Illinois at Urbana-Champaign, Urbana, IL, 61801 USA

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First published: 02 December 2019
Citations: 9

Abstract

Diazomethane is one of the most versatile reagents in organic synthesis, but its utility is limited by its hazardous nature. Although alternative methods exist to perform the unique chemistry of diazomethane, these suffer from diminished reactivity and/or correspondingly harsher conditions. Herein, we describe the repurposing of imidazotetrazines (such as temozolomide, TMZ, the standard of care for glioblastoma) for use as synthetic precursors of alkyl diazonium reagents. TMZ was employed to conduct esterifications and metal-catalyzed cyclopropanations, and results show that methyl ester formation from a wide variety of substrates is especially efficient and operationally simple. TMZ is a commercially available solid that is non-explosive and non-toxic, and should find broad utility as a replacement for diazomethane.

Conflict of interest

The authors declare no conflict of interest.

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