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Labelable compounds for the simple synthesis of 3 '- 18F fluoro-3'-deoxythymidine and process for their preparation

机译:用于简单合成3'- [18F]氟-3'-脱氧胸苷的可标记化合物及其制备方法

摘要

The invention relates to compounds, which are suitable for use as labelling precursor substances for producing 3'-[18F]-fluoro-3'-deoxy thymidine and are structured as per formula (1). In said formula, R represents triphenylmethyl, triphenylmethyl substituted on the phenyl group, trialkylmethyl, triphenylsilyl, triphenylsilyl substituted on the phenyl group, or trialkylsilyl; R' represents R1-SO2, whereby R1 stands for an unsubstituted or substituted C1-C5 alkyl or an unsubstituted or substituted phenyl and R" represents a C2-C10 alkyloxy carbonyl, with the exception of 3-N-Boc-1-(3-O-nosyl-5-O-trityl-2 deoxy- beta -D lyxofuranosyl)thymine. The invention also relates to a method for producing said compounds and to the use thereof for synthesising 3'-[18F]-fluoro-3'-deoxy thymidine.
机译:本发明涉及化合物,其适合用作用于生产3'-[[18 F]]-氟-3'-脱氧胸苷的标记前体物质,并且根据式(1)进行结构化。上述式中,R表示在苯基上取代的三苯基甲基,三苯基甲基,在苯基上取代的三烷基甲基,三苯基甲硅烷基,三苯基甲硅烷基或三烷基甲硅烷基。 R′代表R 1 -SO 2,其中R 1代表未取代或取代的C 1 -C 5烷基或未取代或取代的苯基,R”代表C 2 -C 10烷氧基羰基,但3-N- Boc-1-(3-O-壬基-5-O-三苯甲基-2脱氧-β-D-呋喃呋喃糖基)胸腺嘧啶。本发明还涉及制备所述化合物的方法及其在合成3'-[< 18> F]-氟-3'-脱氧胸苷。

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