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新型薁并[1,2-f]苯并[1,4]二氮卓类衍生物的合成与表征

Efficient synthesis of novel azuleno [1,2-f][1,4]benzodiazepines
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摘要 以1-甲酰基-2-甲氧基薁-3-甲酸甲酯为反应底物,通过与邻苯二胺缩合、烷基化、脱羧等过程,成功地制备了新型薁并[1,2-f]苯并[1,4]二氮卓类衍生物.反应收率良好、操作简单、条件温和.产物结构通过红外光谱、核磁共振谱、质谱及元素分析证实. Azuleno[1,2-f][1,4]benzodiazepine derivatives were synthesized by the three steps(condensation,alkylation and decarboxylation) of ethyl 1-formyl-2-methoxyazulene-3-carboxylate with o-phenylenediamine.This method provides several advantages such as good yield and simple work-up procedure.All the products were fully characterized by 1 H NMR,IR,MS spectra and elemental analyses.
出处 《渤海大学学报(自然科学版)》 CAS 2013年第2期161-165,共5页 Journal of Bohai University:Natural Science Edition
基金 辽宁省科技厅项目(No:2011220022)
关键词 2-甲氧基薁 邻苯二胺 薁并[1 2-f]苯并[1 4]二氮卓类衍生物合成 2-methoxyazulene o-phenylenediamine azuleno[1,2-f][1,4]benzodiazepine
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