## Abstract 2β‐Carbomethoxy‐3β‐(4‐fluorophenyl)‐[N‐^11^C‐methyl]tropane, a potent inhibitor of dopamine transport, was prepared by N‐methylation of the appropriate nor‐methyl precursor in DMF with [^11^C]iodomethane. After derivatization of unreacted precursor with a long chain acyl halide, the rad
New method for routine production of L-[methyl-11C]methionine: in loop synthesis
✍ Scribed by Vanessa Gómez; Juan Domingo Gispert; Víctor Amador; Jordi Llop
- Publisher
- John Wiley and Sons
- Year
- 2008
- Tongue
- French
- Weight
- 124 KB
- Volume
- 51
- Category
- Article
- ISSN
- 0022-2135
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✦ Synopsis
Abstract
A fast, clean and reproducible method for the manufacture of the radiotracer L‐[methyl‐^11^C]methionine is reported. The reaction at room temperature of the non‐radioactive precursor L‐homocysteine (1 mg solution in ethanol/water 50/50) with [^11^C]CH~3~I in an HPLC loop led to the formation of the desired radiotracer with a high radiochemical yield (38.4±4.1% end of synthesis) in a short production time (12 min). Radiochemical purity of the final radiotracer was 99.9±0.05%. Specific activities in the range 11–45 GBq/µmol were obtained. The presence of the undesired enantiomer (D‐[methyl‐^11^C]methionine) was not detected in any of the cases. Copyright © 2008 John Wiley & Sons, Ltd.
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