作者:Zienab M. Nofal、Elsyed A. Soliman、Somaia S. Abd El-Karim、Magdy I. El-Zahar、Aladdin M. Srour、Shalini Sethumadhavan、Timothy J. Maher
DOI:10.1002/jhet.1886
日期:2014.11
reacted with different reagents such as acid anhydrides, malononitrile, chloroacetyl chloride, and aromatic aldehydes to produce the corresponding benzimidazole products 2, 3, 4, 5, 6, 7, 8, 9, respectively. Also, 2‐chloro‐N‐(4‐(1‐methyl‐1H‐benzo[d]imidazol‐2‐yl)thiazol‐2‐yl) acetamide (6) was reacted with diaminoethane, ortho‐substituted aniline, thioglycolic acid, thiosemicarbazide derivatives, secondary
使4-(1 H-苯并[d]咪唑-2-基)噻唑-2-胺及其1-甲基衍生物(1)与不同的试剂如酸酐,丙二腈,氯乙酰氯和芳香醛反应生成苯并咪唑产品相应的2,3,4,5,6,7,8,9分别。同样,使2-氯-N-(4-(1-甲基-1 H-苯并[d]咪唑--2-基)噻唑-2-基)乙酰胺(6)与二氨基乙烷,邻苯二甲酸酯反应。取代的苯胺,巯基乙酸,硫脲衍生物,仲胺,和异硫氰酸钾,得到相应的衍生物10,11,12,13,14,15,16,17,分别。研究了一些新合成的衍生物对两种不同细胞系HepG2和PC12的细胞毒活性。化合物9和15b显示出针对两种类型的测试癌细胞系的有希望的抗癌活性。