A One-Step Microwave-Assisted Synthetic Method for an O/S-Chemoselective Route to Derivatives of the First Adenosine A3 PET Radiotracer

Karem Shanab (Corresponding author), Catharina Neudorfer, Wolfgang Holzer, Markus Mitterhauser, Wolfgang Wadsak, Helmut Spreitzer

Publications: Contribution to journalArticlePeer Reviewed

Abstract

The synthesis of reference standards and expected in vivo metabolites of the first adenosine A3 PET radiotracer [18F]FE@SUPPY ([18F]fluoroethyl 4,6-diethyl-5-[(ethylsulfanyl) carbonyl]-2-phenylpyridine-3-carboxylate) was achieved by using a straightforward microwave assisted alkylation method, which allowed O/S-chemoselective alkylation of the starting material 1 to give each target compound 2-8 in a single step.

Original languageEnglish
Pages (from-to)4076-4082
Number of pages7
JournalMolecules
Volume19
Issue number4
DOIs
Publication statusPublished - Apr 2014

Austrian Fields of Science 2012

  • 104015 Organic chemistry
  • 301207 Pharmaceutical chemistry
  • 301305 Medical chemistry

Keywords

  • chemoselective
  • alkylation
  • microwave
  • adenosine A3
  • PET
  • radiotracer
  • RECEPTOR
  • TARGET
  • Adenosine A3
  • Microwave
  • Radiotracer
  • Alkylation
  • Chemoselective

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