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METHOD FOR SYNTHESIZING 2-THIOURIDINE ANALOG

机译:2-硫代鸟嘌呤类似物的合成方法

摘要

PROBLEM TO BE SOLVED: To provide a method for efficiently synthesizing a 2-thiouridine analog in large quantities from inexpensive compounds.;SOLUTION: This method for synthesizing a 2-thiouridine analog is characterized by comprising the respective protective steps 10, 11 and 12 of introducing respective protective groups onto the hydroxy group at the 3'-position, the hydroxy group at the 5'-position, and the carbonyl group at the 4-position of an uridine analog, the functional group substitution step 13 of converting the carbonyl group at the 2-position of the uridine analog into a thiocarbonyl group, and the respective deprotecting steps 14 and 8 of eliminating the protective groups introduced in the protective steps after the functional group substitution.;COPYRIGHT: (C)2002,JPO
机译:解决的问题:提供一种从廉价的化合物中有效地大量合成2-硫代尿苷类似物的方法。解决方案:该合成2-硫代尿苷类似物的方法的特征在于包括相应的保护步骤10、11和12在尿苷类似物的3'-位置的羟基,5'-位置的羟基和4-位的羰基上引入各自的保护基,将羰基转化的官能团取代步骤13在尿苷类似物的2位上形成一个硫代羰基,以及分别在官能团取代后消除在保护步骤中引入的保护基的脱保护步骤14和8.COPYRIGHT:(C)2002,JPO

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