Evaluating N-difluoromethyltriazolium triflate as a precursor for the synthesis of high molar activity [¹⁸ F]fluoroform.

ABSTRACT: The trifluoromethyl group is a prominent motif in biologically active compounds and therefore of great interest for the labeling with the positron emitter fluorine-18 for positron emission tomography (PET) imaging. Multiple labeling strategies have been explored in the past; however, most of them suffer from low molar activity due to precursor degradation. In this study, the potential of 1-(difluoromethyl)-3-methyl-4-phenyl-1H-1,2,3-triazol-3-ium triflate as precursor for the synthesis of the [¹⁸ F]trifluoromethylation building block [¹⁸ F]fluoroform with high molar activity was investigated. The triazolium precursor was reacted under various conditions with [¹⁸ F]fluoride, providing [¹⁸ F]fluoroform with radiochemical yields (RCY) and molar acti

SUBMITTER: Pees A 

PROVIDER: S-EPMC9293032 | biostudies-literature | 2021 Oct

REPOSITORIES: biostudies-literature