首页> 外国专利> A conventional method for the preparation of new precursor of no-carrier-adde O-(2-18Ffluoroethyl)-L-tyrosine

A conventional method for the preparation of new precursor of no-carrier-adde O-(2-18Ffluoroethyl)-L-tyrosine

机译:制备无载体的邻位O-(2- [18F]氟乙基)-L-酪氨酸新前体的常规方法

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.Formula 1 : Synthesis precursors for O-(2-[18F]fluoroethyl)-L-Tyrosine.
机译:这是合成无载体的 O -(2-[ 18 F]氟乙基)-L-酪氨酸的一种新的前驱体和新方法。合适的用于肿瘤诊断成像的PET(位置发射断层扫描)探针。标题化合物的制备从具有化学式1的前体开始,其中R 1 是羧基的保护基官能团,R 2 是氨基的保护基,R 3 是离去基团。 R 1 代表芳基烷基,R 2 代表羧基,R 3 代表 p -甲苯磺酰氧基,甲磺酰氧基或三氟甲磺酰氧基或溴。本发明包括一种用于合成具有化学式1的化学结构的新的前体的方法。 <图像文件=“ IMGA0001.GIF” he =“ 24” id =“ ia01” imgContent =“ chem” imgFormat =“ GIF” wi =“ 70” /> 式1: O -(2-[ 18 F]氟乙基)-L-酪氨酸的合成前体。

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