Abstract
A simple one-pot procedure for the preparation of [ 11C-carbonyl]-WAY100635, a potent 5HT1A receptor antagonist, was developed. The procedure involves the trapping of 11CO 2 in a tetrahydrofuran (THF) solution of cyclohexylmagnesium chloride, elimination of excess Grignard reagents with anhydrous HCl, reaction with SOCl 2, and the reaction of the resulting acid chloride with WAY100634 (2 mg) and triethylamine (20 μL) in THF. The total synthesis time is 45 min. Starting from 1326 ± 173 mCi of 11CO 2, the average amount of [ 11C-carbonyl]-WAY100635 ( n =40 ) at end-of-synthesis (EOS) was 30 ± 13 mCi (2.3% radiochemical yield), or 148 ± 61 mCi (11%) at end-of-bombardment (EOB). The radiochemical purity was >99%, and the specific activity was 3.6 ± 1.9 Ci/μmol (EOS, n =40 ), or 21.3 ± 9.8 Ci/μmol at EOB. This method is reliable and flexible for routine clinical studies.
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