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A convenient route for the synthesis of adenosine

机译:合成腺苷的便捷途径

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A convenient route for the synthesis of adenosine uses hypoxanthine, which is obtained easily and low prices, and phosphorus oxychloride as starting materials was proposed. The route involved three steps as chlorination, condensation and aminolysis, respectively. The reaction condition is mild and the overall yield is higher than other conventional chemical synthesis methods. Firstly, 6-chloropurine was obtained from hypoxanthine and phosphorus oxychloride by chlorination with 90.0% yield. Then, adenosine was produced from 6-chloropurine and tetraacetyl-ribofuranose without separation by condensation and ammonolysis with 75.0% and 66.7% yields, respectively. The total yield of three steps is 45%, the optimum reaction temperature of condensation and ammonolysis are 135 °C and 100 °C, respectiveely. The structures of the compounds were confirmed by TLC, IR, NMR and MS analysis.
机译:提出了一种简便易行,价格低廉的次黄嘌呤合成腺苷的简便方法,并提出了以三氯氧磷为起始原料的方法。该路线分别包括氯化,缩合和氨解三个步骤。反应条件温和,总收率高于其他常规化学合成方法。首先,从次黄嘌呤和氯氧化磷中氯化得到6-氯嘌呤,收率为90.0%。然后,由6-氯嘌呤和四乙酰基-呋喃核糖生产腺苷,而没有通过缩合和氨解分离而分离,产率分别为75.0%和66.7%。三个步骤的总产率为45%,缩合和氨解的最佳反应温度分别为135°C和100°C。通过TLC,IR,NMR和MS分析证实了化合物的结构。

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