Efficient synthesis of 5′-O-laurate of 1-β-d-arabinofuranosylcytosine via highly regioselective enzymatic acylation in binary solvent mixtures
作者:Xiao-feng Li、Min-hua Zong、Guang-lei Zhao
DOI:10.1016/j.bmcl.2010.05.077
日期:2010.7
Regioselective enzymatic acylations of 1-beta-D-arabinofuranosylcytosine (ara-C) with vinyl laurate (VL) in binary organic solvents were explored for the preparation of 5'-O-laurate of ara-C. Among the nine kinds of enzymes, Novozym 435 showed the highest regioselectivity (>99.9%) towards the 5'-OH of ara-C. This lipase showed higher catalytic activity in hexane-pyridine than in other tested solvent mixtures. The most suitable VL to ara-C molar ratio, initial water activity, and reaction temperature were shown to be 15: 1, 0.07, and 50 degrees C, respectively, under which the initial reaction rate and the maximum substrate conversion were as high as 84.0 mmol L (1) h (1) and 98.1%, respectively. The product of Novozym 435-catalyzed acylation was characterized by C-13 NMR and con. rmed to be 5'-O-laurate of ara-C. (C) 2010 Elsevier Ltd. All rights reserved.