Radiosynthesis of a selective dopamine D-1 receptor antagonist: R(+)-7-chloro-8-hydroxy-3-[11C]methyl-1-phenyl-2,3,4,5-tetrah ydro-1H-3-benzazepine ([11C]SCH 23390)

  • Hayden T. Ravert
  • , Alan A. Wilson
  • , Robert F. Dannals
  • , Dean F. Wong
  • , Henry N. Wagner

Research output: Contribution to journalArticlepeer-review

21 Scopus citations

Abstract

Carbon-11 labeled SCH 23390, a selective dopamine D-1 receptor antagonist (Fig. 1b), was prepared by N-alkylation of the nor-methyl precursor with [11C]iodomethane. The product was purified by semi-preparative HPLC and shown to be radiochemically pure at the end of synthesis. The synthesis was completed in approximately 22 min with an average radiochemical yield of 28% (based on [11C]iodomethane) and an average specific activity of approximately 1950 mCi/μmol calculated at the end of synthesis.

Original languageEnglish
Pages (from-to)305-306
Number of pages2
JournalInternational Journal of Radiation Applications and Instrumentation. Part
Volume38
Issue number4
DOIs
StatePublished - 1987

Fingerprint

Dive into the research topics of 'Radiosynthesis of a selective dopamine D-1 receptor antagonist: R(+)-7-chloro-8-hydroxy-3-[11C]methyl-1-phenyl-2,3,4,5-tetrah ydro-1H-3-benzazepine ([11C]SCH 23390)'. Together they form a unique fingerprint.

Cite this