{"title":"NEW METHODOLOGY TO SYNTHESIS 3- SECONDARY AMINES OF IMIDAZOBENZOTHIAZOLE DERIVATIVES WITH STUDY THEIR BIOLOGICAL ACTIVITIES","authors":"Abdul Gabar Abdul Maged, Naeemah Al-lami","doi":"10.28936/jmracpc15.1.2023.(17)","DOIUrl":null,"url":null,"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.","PeriodicalId":32906,"journal":{"name":"lmjl@ l`rqy@ lbHwth lswq wHmy@ lmsthlk","volume":" ","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2023-06-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"lmjl@ l`rqy@ lbHwth lswq wHmy@ lmsthlk","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.28936/jmracpc15.1.2023.(17)","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
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.