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第 34 卷第 1 期Vol. 34 No. 1
2004 年 2 月Feb 2004

所屬欄目:其它

5-取代-1H-1,2,4-三氮唑-3-羧酸的合成及結構表征
李德江; 孫碧海; 李斌(湖北省丹江口市鄖陽(yáng)師范專(zhuān)科學(xué);瘜W(xué)系; 武漢化工學(xué)院制藥工程系; 湖北丹江口市; 湖北武漢)
摘 要:以5 氯基 1H 1,2,4 三氮唑 3 羧酸乙酯為原料,經(jīng)Sandmeyer反應合成了5 取代 1H 1,2,4 三氮唑 3 羧酸乙酯,其中取代基為氯、溴、碘、氰基等。并通過(guò)UV,IR,1HNMR和元素分析對所有產(chǎn)物的結構進(jìn)行了表征。
關(guān)鍵詞:5-氨基-1H-1; 2; 4-三氮唑-3-羧酸乙酯; Sandmeyer反應; 合成; 表征
中圖分類(lèi)號:TQ252.6  文獻標識碼:A  文章編號:1009-9212(2004)01-0035-03
The Synthesis of 5-Substituting group-1H-1,2,4-Triazole-3-Carboxylic Acid Ethyl Ester
LI De-jiang~1; SUN Bi-hai~2; LI Bin~2 (1.Department of Chemistry; Yunyang Teachers College; Danjiangkou 442700; China; 2.Department of Pharmaceutical Technology; Wuhan Institute of Chemical Technology; Wuhan 430073; China)
Abstract:1H-1,2,4-triazole derivatives,owing to their extensive uses in pharmaceutical synthesis,in an effort to search for more useful reaction intermediates containing 1H-1,2,4-triazole, four new 5-substituted-1H-1,2,4-triazoles were synthesized from 5-amino-1H-1,2,4-triazole-3-carboxylic acid ethyl ester by Sandmeyer reaction. Their structures were confirmed by elementl analysis, IR, UV and ~1 HNM.
Key words:5-amino-1H-1; 2; 4-triazole-3-carboxylic acid ethyl ester; Sandmeyer reactipn; synthesis; characterization
收稿日期:2003-08-22
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