1207452-03-6Relevant articles and documents
Facile and efficient approach for the synthesis of N2-dimethylaminomethylene-2′-O-methylguanosine
Mukobata, Tsuyoshi,Ochi, Yosuke,Ito, Yuji,Wada, Shun-ichi,Urata, Hidehito
scheme or table, p. 129 - 131 (2010/04/05)
A convenient method for the synthesis of N2-dimethylaminomethylene-2′-O-methylguanosine (1), which is a useful intermediate for oligonucleotide construction, was developed. We chose the di-tert-butylsilyl group and the triisopropylbenzenesulfonyl group as sugar and base protecting groups, respectively. These protecting groups were stable during the 2′-O-methylation step with MeI and NaH. Our six-step synthesis of 1 is easy to perform using commercially available reagents, and requires only three chromatographic purifications. Compound 1 was obtained in 56% yield from guanosine.