A novel strategy for synthesis of 5-iodo ((125/131)I)-1, 2, 3-triazoles via click chemistry.
- Author:
Cheng WANG
1
;
Jilin YIN
;
Wei ZHOU
;
Lan ZHANG
;
Zheng ZHOU
Author Information
1. PET-CT Center, Guangzhou General Hospital of Guangzhou Military Command, Guangzhou 510010, China. wangch628@163.com
- Publication Type:Journal Article
- MeSH:
Click Chemistry;
Iodine Radioisotopes;
Radiopharmaceuticals;
chemical synthesis;
Triazoles;
chemical synthesis
- From:
Journal of Southern Medical University
2013;33(6):779-784
- CountryChina
- Language:English
-
Abstract:
We report a facile and effective method for radioiodine-labeled radiopharmaceuticals via copper (I)-catalyzed click chemistry route. In the novel radioiodination method, 5-iodo ((125/131)I)-1, 2, 3-triazoles were synthesized after a 24-h click reaction in organic solvent with a radiochemical yield of 13%. However, in the aqueous phase, the radiochemical yield of the conjugation radioiodine to RGD via click chemistry was 0. This suggested an exchange between hydrogen ion and iodine ion in aqueous phase so that no enough radioiodine was left to conjugate with RGD. We propose different mechanisms of Cu (I)-catalyzed cycloaddition of organic azides and 1-iodo-alkynes in organic phase and aqueous phase.
