The current situation of cancer and the classification of anticancer agents were briefly introduced in this thesis.The present development of Capecitabine was particularly introduced.After analyzing the 4 reported routes,two of them were chosen to study further,and then identified the best one.After got through 3 reported synthetic routes to obtain Capecitabine,an unreported route was designed and finished.Based on these four routes,finally the most economical one was picked up.5-deoxy-1,2,3-tri-O-acetyl-D-ribofuranoside(9)was obtained from D-ribofura -noside through 6 steps like acetalation protection,paratoluensulfonylation,bromation,reduction, deprotection and acetylation.The structure of Capecitabine and 5-deoxy-1,2,3-tri-O-acetyl-D-ribo -furanoside had been confirmed by MS and ~1H-NMR.The mechanism of Silyl reaction had also been discussed in this thesis. |