摘要
利用相转移催化法在超声辐射下合成了 8种未见文献报道的 5 ,7 二取代 2 (5 芳基 2 呋喃甲酰亚胺 ) [1,2 ,4] 噻二唑并 [2 ,3 a]嘧啶衍生物 .其结构经元素分析、IR和1HNMR得到确证 .该法具有操作简便 ,反应时间短等优点 .初步的生物活性测试结果表明部分化合物具有一定除草活性 .
Eight new 5,7-disubstituted-2-(5-aryl-2-furoylimino)-[1,2,4]-thiadiazolo[2,3-a]pyrimidine derivatives were synthesized under ultrasonic irradiation. All of them are new compounds and their structures were exactly confirmed by IR, 1H NMR spectra and elemental analysis. Our method using the ultrasonic irradiation under the condition of phase transfer catalyst (PTC) has the advantages of short reaction time and good yield. The preliminary biological tests show that some of the target compounds have some inhibitory activities against weeds.
出处
《有机化学》
SCIE
CAS
CSCD
北大核心
2004年第12期1610-1613,共4页
Chinese Journal of Organic Chemistry
基金
国家"十.五"重点科技攻关计划 (No.2 0 0 4BA30 8A2 2 8)资助项目
关键词
芳基
噻二唑
酰亚胺
取代
合成
衍生物
呋喃
嘧啶
超声辐射
元素分析
acyl thiourea, [1,2,4]-thiadiazolo[2,3-a]pyrimidine, ultrasonic irradiation, phase transfer catalysis, synthesis, bioactivity
