4.8 Article

Synthesis of Triazenes with Nitrous Oxide

Journal

ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
Volume 54, Issue 1, Pages 302-305

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/anie.201408597

Keywords

amides; coupling reactions; Grignard reagents; nitrous oxide; triazenes

Funding

  1. Swiss National Science Foundation
  2. EPFL

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Triazenes are valuable compounds in organic chemistry and numerous applications have been reported. Furthermore, triazenes have been investigated extensively as potential antitumor drugs. Here, we describe a new method for the synthesis of triazenes. The procedure involves a reagent which is rarely used in synthetic organic chemistry: nitrous oxide (N2O, laughing gas). Nitrous oxide mediates the coupling of lithium amides and organomagnesium compounds while serving as a nitrogen donor. Despite the very inert character of nitrous oxide, the reactions can be performed in solution under mild conditions. A key advantage of the new procedure is the ability to access triazenes with alkynyl and alkenyl substituents. These compounds are difficult to prepare by conventional methods because the required starting materials are unstable. Some of the new alkynyltriazenes were found to display high cytotoxicity in invitro tests on ovarian and breast cancer cell lines.

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