## Abstract [^11^C]paclitaxel, a potential solid tumor imaging agent, was synthesized by reacting [__ฮฑ__โ^11^C]benzoyl chloride with the primary amine precursor of paclitaxel. The time for synthesis, purification, and formulation was 38 min from end of bombardment with an average specific radioacti
Solid-phase radiosynthesis of [11C]WAY 100635
โ Scribed by Alan A. Wilson; Jean N. DaSilva; Sylvain Houle
- Publisher
- John Wiley and Sons
- Year
- 1996
- Tongue
- French
- Weight
- 301 KB
- Volume
- 38
- Category
- Article
- ISSN
- 0022-2135
No coin nor oath required. For personal study only.
โฆ Synopsis
An efficient, fast and simple method is described for the radiosynthesis of the potent and selective ~-
[11C]Iodomethane was effectively trapped on a C18 reverse-phase cartridge at ambient temperature where it reacted rapidly with the normethyl precursor, N-[2-[4-(2- hydroxypheny1)-1 -piperazinyl]ethyl]-N-(2-pyridinyl)cyclohexane carboxamide. Following high performance liquid chromatography purification and formulation, [IICIWAY 100635 was obtained in high radiochemical yields (40%, uncorrected from [11C]Iiodomethane) in a synthesis time of 25 min with an average specific actvity of (at end-ofsynthesis) 33 GBq/pmole (900 mCi/pmole).
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