发明授权
US5510522A Synthesis of N-formyl-3,4-di-t-butoxycarbonyloxy-6-(trimethylstannyl)-L-phenylalanine ethyl ester and its regioselective radiofluorodestannylation to 6- .sup.18 F!fluoro-1-dopa 失效
N-甲酰基-3,4-二叔丁氧基羰基氧基-6-(三甲基甲锡烷基)-L-苯丙氨酸乙酯的合成及其对6- [18 F]氟-1-多巴的区域选择性全氟代去甲硅烷基化

Synthesis of
N-formyl-3,4-di-t-butoxycarbonyloxy-6-(trimethylstannyl)-L-phenylalanine
ethyl ester and its regioselective radiofluorodestannylation to
6- .sup.18 F!fluoro-1-dopa
摘要:
A process for forming a 6-fluoro derivative of compounds in the L-Dopa family comprising the steps of protecting the groups attached to the benzene ring in the compound followed by serially reacting the protected compound with (a) iodine and silver trifluoroacetic acid; (b) Bb.sub.3 ; (c) dit-butyldicarbonate; (d) hexamethyltin; (e) a fluoro compound; (f) hydrobromic acid; and (g) raising the pH to .ltoreq.7.
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