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An improved synthesis of (3-N-[11C]methyl)spiperone

✍ Scribed by Robert F. Dannals; Hayden T. Ravert; Alan A. Wilson; Henry N. Wagner Jr


Book ID
103919631
Publisher
Elsevier Science
Year
1986
Weight
154 KB
Volume
37
Category
Article
ISSN
0883-2889

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✦ Synopsis


An improved radiochemical synthesis of (3-N-[11C]methyl) spiperone is reported. The radiotracer was prepared by N-alkylation of spiperone in dimethylformamide in the presence of equimolar aqueous tetrabutylammonium hydroxide and was purified by semi-preparative reversed phase high performance liquid chromatography (C-18 HPLC). The average radiochemical yield was approximately 21% end-of-synthesis (EOS) with an average specific activity of over 2750 mCi/mumol EOS. The total time for synthesis and specific activity determination was approximately 21 min.


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