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 language | English |
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Pages (from-to) | 4076-4082 |
Number of pages | 7 |
Journal | Molecules |
Volume | 19 |
Issue number | 4 |
DOIs | |
Publication status | Published - 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