以腺苷为原料,利用Mitsunobu反应分别采用三步法(总收率69.6%)和一步法(收率68.4%)合成了5′-脱氧-5′-乙酰硫代腺苷,其结构经1HNMR和MS表征。Mitsunobu反应一步法对腺苷5′-OH有较高的化学选择性,并根据这一事实提出了可能的反应机理。
5′-Acetylthio-5′-deoxynucleoside was synthesised from adenosine by Mitsunobu reaction of three steps(total yield of 69.6%) and one step(yield of 68.4%),respectively.The structrue was characterized by 1H NMR and MS.The possible reaction mechanism was provided according to the fact that 5′-OH exhibited more selective replaced by acetylthio group in the one step method.