Chin. J. Org. Chem. ›› 2012, Vol. 32 ›› Issue (11): 2187-2192.DOI: 10.6023/cjoc201206006 Previous Articles     Next Articles



王晶, 丁丽, 肖笛, 薛思佳   

  1. 上海师范大学生命与环境科学学院化学系 上海 200234
  • 收稿日期:2012-06-06 修回日期:2012-06-27 发布日期:2012-07-04
  • 通讯作者: 薛思佳
  • 基金资助:

    “十二五”国家科技支撑计划(No. 2011BAE06B01-17)、国家自然科学基金(Nos. 21042010, 21102092, 30870560)资助项目.

Synthesis and Preliminary Anticancer Activity Evaluation of Tetrahydropyrido[4,3-d]dihydropyrimidine-2-one Derivatives

Wang Jing, Ding Li, Xiao Di, Xue Sijia   

  1. College of Life and Environment Sciences, Shanghai Normal University, Shanghai 200234
  • Received:2012-06-06 Revised:2012-06-27 Published:2012-07-04
  • Supported by:

    Project supported by the Key Scientific “Twelfth Five-Year” National Technology Support Program (No. 2011BAE06B01-17), and the National Natural Science Foundation of China (Nos. 21042010, 21102092, 30870560).

In search of more effective anticancer agents, sixteen novel tetrahydropyrido[4,3-d]dihydropyrimidine-2-one derivatives 2a2p were synthesized by reacting N-(4-substituted benzyl)-3,5-bisbenzylidene-4-piperidone with urea in EtONa/EtOH under reflux condition. The structures were confirmed by 1H NMR, IR, MS and elemental analysis. The preliminary bioassay indicated that some title compounds exhibited good antiproliferative activities against K562 cells, certain antiproliferative activities against ovarian cancer HO-8910 cells and liver cancer SMMC-7721 cells.

Key words: tetrahydropyrido[4,3-d]dihydropyrimidine-2-one, derivative, synthesis, leukemic K562 cells, anticancer activities