One-pot synthesis of 6-l-[18f] fluoro-3,4-dihydroxyphenylalanine (6-l-[18f] fdopa).

Geert Luurtsema (Inventor), Chantal Kwizera (Inventor), Simon Niels Blok (Inventor), Ines Farinha Antunes (Inventor), Philippus Hein Elsinga (Inventor), Erik de Vries (Inventor)

Research output: Patent

128 Downloads (Pure)

Abstract

The invention relates to the field of medicinal chemistry and radiopharmaceuticals, in particular to means, methods and cassettes for the automated synthesis of the radiotracer 6-L-[18F]fluoro-3,4- dihydroxyphenylalanine (6-L-[18F]FDOPA). Provided is a method for the one-pot synthesis of 6-L-[18F]FDOPA comprising contacting a BOC- protected stannyl precursor of the formula I with [18F] Tetraethylammonium fluoride ([18F]Et4NF) in the presence of the Cu-catalyst Cu(Impy)4(OTf)2.
Original languageEnglish
Patent numberWO2024058665
Priority date15/09/2022
Filing date14/09/2023
Publication statusPublished - 21-Mar-2024

Fingerprint

Dive into the research topics of 'One-pot synthesis of 6-l-[18f] fluoro-3,4-dihydroxyphenylalanine (6-l-[18f] fdopa).'. Together they form a unique fingerprint.

Cite this