Abstract
5-((1-[11C]-methyl-2-(S)-pyrrolidinyl)methoxy)-2-chloro-3-((E)- 2-(2-fluoropyridin-4-yl)vinyl)pyridine ([11C]-FPVC) was synthesized from [11C]-methyl iodide and the corresponding normethyl precursor. The average time of synthesis, purification, and formulation was 42 min with an average non-decay-corrected radiochemical yield of 19%. The average specific radioactivity was 359 GBq/μmol (9691 mCi/μmole) at end of synthesis (EOS).
Original language | English (US) |
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Pages (from-to) | 459-462 |
Number of pages | 4 |
Journal | Journal of Labelled Compounds and Radiopharmaceuticals |
Volume | 49 |
Issue number | 5 |
DOIs | |
State | Published - Apr 2006 |
Keywords
- Carbon-11
- Positron emission tomography
- α4β2 nicotinic acetylcholine receptor
ASJC Scopus subject areas
- Analytical Chemistry
- Biochemistry
- Radiology Nuclear Medicine and imaging
- Drug Discovery
- Spectroscopy
- Organic Chemistry