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机构地区:[1]吉林化工学院精细化工系 [2]延边大学化学系,吉林诞吉133002
出 处:《有机化学》1991年第6期626-631,共6页Chinese Journal of Organic Chemistry
摘 要:吖啶类化合物在抗疟和抗癌的药用研究中具有显著的作用[1,2],尤其在临床抗疟中广泛地应用了该类药物.Some 6,7-Methylenedioxy-thio-1(2 H,4 H) acridine-fused heterocycles and ami-no derivatives of thio-acridone were synthesized.The title compound 1 reacted with hydrox-yamine hydrochloride to give the oxmine of 1 in good yiela.The oximc reacteu with variousacyl chloride to give the corresponding O-acyl-thio-acrioone oxime 4 a-c.The aooition ofisonicotan and arylhydrazine to 1 gave the hydrazone 2 b-f.Cyclization of led toindole-fused thia-acridine, a-c Reaction of with thiosemicarbazice gave pyrazole-fused thio-acridine (5),while pyrazoles 7-9 were obtained by condensation of hydrazine and diketoester 6.Furanodione and isoxazole-fusef thio-acridine (10 anf 11) were also synthesizedfrom diketo ester 6.-substituted thio-acridione (12) obtained by treatment of 6 with 1,2-diaminobenzene was converted to thio-acridine-fused furanoquinoxaline 1) in PPA.
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