Ostrowski Tomasz, Zeidler Joanna
Institute of Bioorganic Chemistry, Polish Academy of Sciences, PL-61704 Poznan, Poland.
Nucleic Acids Symp Ser (Oxf). 2008(52):585-6. doi: 10.1093/nass/nrn296.
The synthesis of 5-ethynyl-1H-[1,2,3]triazole-4-carboxylic acid amide riboside 1 and its derivatives exploits Pd(0)-catalyzed cross-coupling reactions. The iodinated key intermediate 3a, when coupled with alkynes affords 5-alkynylated products 1b,c,e,f in diverse yields. Methanolysis of 1b and 1c provides the title compound 1 and the 5-propynyl derivative 1d, respectively. When coupled with methyl acrylate, 3a gives the E-isomer 4c, although in low yield, while the other 5-iodo precursor 3b undergoes reduction to 4b.
5-乙炔基-1H-[1,2,3]三唑-4-羧酸酰胺核糖苷1及其衍生物的合成利用了钯(0)催化的交叉偶联反应。碘化关键中间体3a与炔烃偶联时,能以不同产率得到5-炔基化产物1b、c、e、f。1b和1c的甲醇解分别得到标题化合物1和5-丙炔基衍生物1d。3a与丙烯酸甲酯偶联时,虽然产率较低,但能得到E-异构体4c,而另一种5-碘代前体3b则发生还原反应生成4b。