NEW METHODOLOGY TO SYNTHESIS 3- SECONDARY AMINES OF IMIDAZOBENZOTHIAZOLE DERIVATIVES WITH STUDY THEIR BIOLOGICAL ACTIVITIES

Abdul Gabar Abdul Maged, Naeemah Al-lami
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引用次数: 0

Abstract

In this research, new derivatives of bicyclic fused rings containing bridgehead nitrogen atom imidazo/benzothiazole were prepared from 2-aminobenzothiazole with 2-bromo-1-(4-bromophenyl)ethan-1-one to form compound A1. Then, through the Mannich reaction, compound A2 was prepared from compound A1 with formaldehyde and 4-aminoacetophenone. Schiff bases A3-A6 were prepared from condensation reaction between compound A2 with different amines. Finally, the reduction reaction was accomplished by using NaBH4 to reduce the imine group to forming new compounds A7-A10. These compounds were characterized by FTIR, 1HNMR, and 13CNMR. The prepared compounds showed biological activity against some microorganisms.
新方法合成咪唑苯并噻唑衍生物3-仲胺并研究其生物活性
本研究以2-氨基苯并噻唑与2-溴-1-(4-溴苯基)乙烷-1-酮为原料,合成了含有桥头堡氮原子的双环稠环的新衍生物咪唑/苯并噻唑,形成化合物A1。然后,通过Mannich反应,由化合物A1与甲醛和4-氨基苯乙酮制备化合物A2。由化合物A2与不同胺的缩合反应制备了席夫碱A3-A6。最后,通过使用NaBH4将亚胺基团还原成新的化合物A7-A10来完成还原反应。通过FTIR、1HNMR和13CNMR对这些化合物进行了表征。所制备的化合物显示出对某些微生物的生物活性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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