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吡唑类化合物的合成与药理活性研究 被引量:8

Synthesis and pharmacological activity of pyrazole
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摘要 目的:合成吡唑类衍生物并研究其抗流感病毒活性。方法:以1-甲氧甲酰基-5-氨基-1H-吡唑-3-甲酸乙酯为原料,同氯乙酰氯和取代哌嗪反应得到含氮化合物;同硫氰酸钠、酰氯反应得到酰氨基硫脲。结果与结论:合成了7个新化合物;其中部分化合物具有一定抗流感病毒活性。 Objective : To synthesize pyrazole and its analogs and evaluate their anti-influenza virus activity. Methods: pyrazole was reacted with chloroacetyl chloride and substituted piperazidine to obtain nitrogenous compounds and reacted with sodium thiocyanate and acyl chloride to obtain substituted thiourea. Results and Conclusion: 7 new compounds have been synthesized, among them 3b had antiinfluenza virus activity.
机构地区 天津药物研究院
出处 《中国新药杂志》 CAS CSCD 北大核心 2007年第24期2043-2044,2053,共3页 Chinese Journal of New Drugs
基金 天津市科技发展计划项目(043185111-7)
关键词 吡唑类 神经氨酸酶抑制剂 流感病毒 合成 pyrazole neuraminidase inhibitors influenza virus synthesis
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