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Merck

Highly efficient and facile synthesis of 5-azido-2'-deoxyuridine.

Nucleosides, nucleotides & nucleic acids (2010-07-01)
Stephanie Gourdain, Christian Petermann, Dominique Harakat, Pascale Clivio
ZUSAMMENFASSUNG

Previously reported syntheses of the photoaffinity label 5-azido-2'-deoxyuridine are rather inefficient and involve the tedious preparation of a 5-nitro intermediate. To overcome these inconveniences, we have developed a new approach from the commercially available 5-bromo-2'-deoxyuridine nucleoside. Our synthetic route makes use of a benzylamination reduction sequence. Using this strategy, the 5-azido-2'-deoxyuridine photolabel is prepared in three steps and quantitative yields.

MATERIALIEN
Produktnummer
Marke
Produktbeschreibung

Sigma-Aldrich
Benzylamin, ReagentPlus®, 99%
Sigma-Aldrich
Benzylamin, purified by redistillation, ≥99.5%
Sigma-Aldrich
Benzylamin -hydrochlorid
Supelco
Benzylamin, derivatization grade (GC derivatization), LiChropur, ≥99.0%