首页> 外国专利> Convenient method for the preparation of new precursor of no-carrier-added O-(2-18Ffluoroethyl)-L-Tyrosine)

Convenient method for the preparation of new precursor of no-carrier-added O-(2-18Ffluoroethyl)-L-Tyrosine)

机译:方便的制备无载体的O-(2- [18F]氟乙基)-L-酪氨酸的新前体的方法

摘要

This is a new precursor and new method for the synthesis of no-carrier-added O-(2-[18F]fluoroethyl)-L-Tyrosine which has been proved a suitable PET (position emission tomography) probe for tumor diagnosis imaging, the preparation of the title compound starts from precursors with the chemical structures as in Formula 1, wherein R1 is a protective group for the carboxyl functional group, R2 is a protective group for the amino group, and R3 acts as a leaving group. R1 represents an arylalkyl group, R2 represents a carboxyl group, and R3 represents a p-tosyloxy, methane sulfonyloxy or trifluoromethane sulfonyloxy or bromine, the invention includes a method for the syntheses of new precursors with the chemical structures as in Formula 1.
机译:这是合成无载体的O-(2-[ 18 F]氟乙基)-L-酪氨酸的新前驱物和新方法,已被证明是一种适合的PET(位置发射断层扫描) )用于肿瘤诊断成像的探针,从具有化学式1的前体开始制备标题化合物,其中R 1 是羧基官能团的保护基,R 2 是氨基的保护基,R 3 充当离去基团。 R 1 代表芳基烷基,R 2 代表羧基,R 3 代表对甲苯磺酰氧基,甲烷磺酰氧基或三氟甲烷磺酰氧基或溴,本发明包括具有化学式如式1的新的前体的合成方法。

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