Abstract
A convenient three-step synthesis of the title compound from commercially available 3,4-dimethoxyphenethylamine is described. The title compound is a stable, crystalline, organic-soluble solid which reacts with carrier-added [ 18F]acetyl hypofluorite to yield 6-[ 18F]fluorodopamine (20 Âą 7% radiochemical yield EOS, n = 3) following deprotection with hydriodic acid.
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