Journal article
Synthesis and radiosynthesis of a novel PET fluorobenzyl piperazine for melanoma tumour imaging; [18F]MEL054
SR Taylor, MP Roberts, NA Wyatt, TQ Pham, D Stark, T Bourdier, P Roselt, A Katsifis, I Greguric
Australian Journal of Chemistry | CSIRO PUBLISHING | Published : 2013
DOI: 10.1071/CH12489
Abstract
2-{2-[4-(4-[18F]-Fluorobenzyl)piperazin-1-yl]-2-oxoethyl}isoindolin-1-one ([18F]MEL054), is a new potent indolinone-based melanin binder designed to target melanotic tumours. [18F]MEL054 was prepared by an automated two-step radiosynthesis, comprising of the preparation of 4-[18F]fluorobenzaldehyde from 4-formyl-N,N,N-trimethylanilinium triflate, followed by reductive alkylation with 2-(2-oxo-2-piperazin-1-ylethyl)isoindolin-1-one. 4-[18F]Fluorobenzaldehyde was prepared on a GE TRACERlab FXFN module in 68±8% radiochemical yield (RCY, non-decay corrected), purified by a Sep-Pak Plus C18 cartridge and eluted into the reactor of an in-house modified Nuclear Interface [18F]FDG synthesis module f..
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Funding Acknowledgements
The authors gratefully acknowledge Tim Jackson for technical assistance and Christian Wichmann for his contribution. They thank the Commonwealth Government of Australia for their financial support to the Collaborative Research Centre for Biomedical Imaging Development (CRC-BID).