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pubmed-article:2163373pubmed:abstractTextTwo [18F]fluoroalkyl analogs of a neuroleptic YM-09151-2 were synthesized via nucleophilic [18F]fluorination of methanesulfonyloxy- or p-toluenesulfonyloxyalkyl derivatives using no-carrier-added [18F]fluoride. Although 3-[18F]fluoropropylaminobenzamide was obtained in good yield, the yield of 2-[18F]fluoroethyl derivative was severalfold lower. The product, N-[(2RS,3RS)-1-benzyl-2-methylpyrrolidin-3-yl]-5- chloro-2-methoxy-4-(3-[18F]fluoropropyl)-aminobenzamide, was shown to have a striatum-to-cerebellum ratio comparable to that of 11C labeled YM-09151-2 and thus to be a good candidate for measuring D2-receptors in vivo.lld:pubmed
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pubmed-article:2163373pubmed:articleTitleSynthesis of omega-[18F]fluoroalkyl analogs of YM-09151-2 for the measurement of D2-dopamine receptors with PET.lld:pubmed
pubmed-article:2163373pubmed:affiliationDivision of Radiopharmaceutical Chemistry, School of Medicine, Tohoku University, Sendai, Japan.lld:pubmed
pubmed-article:2163373pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:2163373pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed