摘要
用2-苯基-1,2,3-三唑基-4-甲醛(1)或喹喔啉基-2-甲醛(2)与乙二胺缩合成双席夫碱3或4,然后与α-氯代肟在三乙胺条件下发生1,3-偶极环加成得到双-4,5-二氢-1,2,4-噁二唑啉衍生物6a~6f或7a~7f.目标化合物的结构经元素分析,IR,1HN MR和MS确认.
Condensation of ethylenediamine with 2-phenyl- 1,2,3-triazole-4-carboxaldehyde (1) or quinoxa- line-2-carboxaldehyde (2) gave bis-Schiff base 3 or 4, which then reacted with a-chloro-oximes to afford bis- bis-4,5-dihydro-1,2,4-oxadiazoline derivatives 6a-6f or 7a-7f by 1,3-dipolar cycloaddition. The structures of new compounds were confirmed by elemental analysis, IR, ^1H NMR and MS spectra.
出处
《有机化学》
SCIE
CAS
CSCD
北大核心
2007年第9期1162-1166,共5页
Chinese Journal of Organic Chemistry
基金
国家自然科学基金(No20562011)
新疆大学青年启动基金资助项目