An improved method for the synthesis of radiolabeled McN5652 via thioester precursors

Makiko Suehiro, John L. Musachio, Robert F. Dannals, William B. Mathews, Hayden T Ravert, Ursula Scheffel, Henry N. Wagner

Research output: Contribution to journalArticlepeer-review

21 Scopus citations


An improved procedure that facilitates routine production and increases the radiochemical yield of [11C]McN5652 (trans - 1,2,3,5,6,10b-hexahydro-6-[4-([11C]methylthio)-phenyl]pyrrolo-[2,1-a]-isoquinoline) is presented. Specifically, thiol acetate, butyrate, and benzoate derivatives of McN5652 were prepared as the precursors for the [11C]McN5652 synthesis. These thioesters offer greater stability than the previously used thiol precursor (desmethyl McN5652) and enable a single batch of material to be used for multiple radiolabelings. Hydrolysis of the thioester functionality (tetrabutylammonium hydroxide, 10 min) unmasked the free thiol which, without purification, was reacted with [11C]iodomethane in DMF at 40-45 °C for 1 min. The average decay-corrected radiochemical yield for [11C]McN5652 was 26% with an average specific activity of 2290mCi/μmol (end of synthesis). This facile radiolabeling method, utilizing the butyrate thioester of McN5652, was also employed in the preparation of [3H](+)- and (-)McN5652 [trans-1,2,3,5,6S (or 6R),10bR, (or 10bS)-hexahydro-6-[4-([3H]methylthio)phenyl] pyrrolo-[2,1,a]-iso-quinoline] from [3H]iodomethane.

Original languageEnglish (US)
Pages (from-to)543-545
Number of pages3
JournalNuclear Medicine and Biology
Issue number4
StatePublished - May 1995

ASJC Scopus subject areas

  • Molecular Medicine
  • Radiology Nuclear Medicine and imaging
  • Cancer Research


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