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2-氯-6-甲氧基-9-烷基嘌呤化合物的合成
Synthesis of 2-Chloro-6-methoxy-9-alkylpurine Compounds
【摘要】 以2-氨基-6-氯嘌呤为原料,通过烃基化反应、重氮化反应和烷氧基化反应,得到2-氯-6-甲氧基-9-烷基嘌呤化合物,其结构经MS、1HNMR和元素分析等方法确认。探讨了溶剂选择、原料配比、催化剂和反应温度等因素对N9-烃基化反应的影响,其最优反应条件为:以DMF为溶剂,碳酸钾为缚酸剂,苄基三乙基氯化铵为相转移催化剂,n(2-氨基-6-氯嘌呤)∶n(溴代烷)=1∶3,n(溴代烷)∶n(碳酸钾)=1∶1.5,与碳酸钾等物质的量的苄基三乙基氯化铵,反应温度为20℃,烃基化反应收率可达76%以上。
【Abstract】 An efficient procedure for the synthesis of 2-chloro-6-methoxy-9-alkylpurine compounds with better yield through alkylation,diazotization and oxyalkylation of 2-amino-6-chloropurine is reported.The target compounds were characterized by means of MS,1HNMR and elemental analysis.The effect of solvent,mole ratio of raw material,catalyst and reaction temperature on the alkylation reaction was discussed,and the yield of the target compounds was more than 76% under the following optimized conditions:n(2-amino-6-chloropurine)∶n(bromoalkane)=1∶3,n(bromoalkane)∶n(K2CO3)=1∶1.5,reaction temperature was 20 ℃ with DMF as solvent.
【Key words】 purine compounds; alkylation; diazotization; oxyalkylation; drug and cosmetic materials;
- 【文献出处】 精细化工 ,Fine Chemicals , 编辑部邮箱 ,2011年10期
- 【分类号】TQ463.53
- 【被引频次】2
- 【下载频次】163