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作 者:阿布拉江·克依木[1] 阿娜姑·托合提[1] 刘方明[2]
机构地区:[1]新疆大学化学与化工学院,新疆乌鲁木齐830046 [2]杭州师范大学材料与化学化工学院,浙江杭州310036
出 处:《合成化学》2012年第5期591-595,共5页Chinese Journal of Synthetic Chemistry
基 金:新疆自然科学基金资助项目(2009211A02)
摘 要:以3,5-二取代异噁唑-4-甲酰肼为基本原料制备关键中间体1-(3-对甲氧基苯基-5-甲基异噁唑-4-基)-4-芳基氨基硫脲(3a~3c);3在不同条件下经关环反应制得含有3,5-二取代异噁唑的2-芳氨基噻二唑(4a~4c),2-芳氨基噁二唑(5a~5c)和3-[3'-(4″-甲氧基苯基)-5'-甲基-异噁唑-4'-基)-4-芳基-1,2,4-三唑-5-硫酮(6a~6c);6与碘甲(乙)烷反应合成了4-芳基-5-[3'-(4″-甲氧基苯基)-5'-甲基异噁唑-4'-基]-3-甲(乙)硫基-1,2,4-三唑(7a~8c),其结构经1H NMR,IR,MS和元素分析表征,其中4,5,7和8未见文献报道。Key intermediate,1-(3-p-methoxyphenyl-5-methylisoxazole-4-yl)-4-arylthiosemicarbazides(3a~3c),were prepared by the reaction of 3,5-disubstituted isoxazole-4-formylhidrizine with arylisothiocyanates.1,3,4-Thiadiazole(4a~4c),1,3,4-oxadiazole(5a~5c) and the corresponding 5-methyl/ethylthiotriazole(6a~6c) were synthesized by the cyclization of 3 in different reaction conditions.5-Methyl/ethylthiotriazole derivatives(7a~8c) were synthesized by the reaction of 6 with MeI or EtI.The structures were characterized by 1H NMR,IR,MS and elemental analysis.4,5,7 and 8 were new compound.
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