喹啉酮類化合物的簡便合成
發(fā)布時間:2019-01-10 17:25
【摘要】:設計以簡單易得合成子β-烯胺酮1為原料,以氰基乙酸2為;噭,得到烯胺酮的α-C區(qū)域選擇性氰基乙;a(chǎn)物3.進而從化合物3出發(fā),以乙腈為溶劑,哌啶為催化劑,在40℃下,通過分子內環(huán)合反應,簡潔、高效合成了一類結構新穎的喹啉酮類雜環(huán)化合物4a~4t,產(chǎn)率82~95%.該方法具有操作簡便、原子經(jīng)濟、原料易得、后處理簡單等優(yōu)點.
[Abstract]:The 偽 -C region-selective cyanoacetylation product 3of enamine ketone was prepared by using simple and easy synthesis of 尾 -enamine ketone 1 as raw material and cyanoacetic acid 2 as acylation reagent. From compound 3, using acetonitrile as solvent and piperidine as catalyst, a class of novel quinolinone heterocyclic compounds 4a1 4t was synthesized by intramolecular cyclization at 40 鈩,
本文編號:2406589
[Abstract]:The 偽 -C region-selective cyanoacetylation product 3of enamine ketone was prepared by using simple and easy synthesis of 尾 -enamine ketone 1 as raw material and cyanoacetic acid 2 as acylation reagent. From compound 3, using acetonitrile as solvent and piperidine as catalyst, a class of novel quinolinone heterocyclic compounds 4a1 4t was synthesized by intramolecular cyclization at 40 鈩,
本文編號:2406589
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