An improved synthesis of (3-N-[11C]methyl)spiperone
β 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
No coin nor oath required. For personal study only.
β¦ 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.
π SIMILAR VOLUMES
## Abstract Toluene derivatives are often found in drugβlike molecules, and are therefore desirable as radiolabelled moieties. The desire for an alternate to the Stille coupling led us to investigate the feasibility of the Suzuki coupling. We have found the Suzuki coupling route to be a robust alte
## Abstract An high yield synthesis of the title compound from ^13^CO~2~ is described. A key to the success is direct formation of the ester from the intermediate lithium propiolateβ^13^C~3~.