Facile and diverse synthesis of indolyl substituted 4,5,6,7-tetrahydro-4H-indol-4-ones and 1,6-dihydropyrrolo[2,3-c]pyrazol via multi-component reactions

IF 1.5 4区 化学 Q3 CHEMISTRY, ORGANIC
Jing Wang , Lu Yu , Haoqiang Jiang , Songlei Zhu
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引用次数: 0

Abstract

An efficient and facile protocol for the synthesis of some novel 4,5,6,7-tetrahydro-4H-indol-4-ones, 1,6-dihydropyrrolo[2,3-c]pyrazol and 1,4-dihydrochromeno [4,3-b]pyrrol by one-pot three-component reaction of 3-cyanoacetyl indoles, arylglyoxal monohydrate and various enaminones, pyrazol-5-amines or 4-amino coumarin. The advantages of this method include the availability of starting materials, mild reaction conditions and good yields of products, operational simplicity.

Abstract Image

多组分反应合成吲哚取代4,5,6,7-四氢- 4h -吲哚-4-酮和1,6-二氢吡咯[2,3-c]吡唑的简便多样
以3-氰乙酰吲哚、芳基乙二醛一水和各种胺酮、吡唑-5胺或4-氨基香豆素为原料,通过一锅三组分反应合成新型4,5,6,7-四氢- 4h -吲哚-4-酮、1,6-二氢吡咯[2,3-c]吡唑和1,4-二氢色胺[4,3-b]吡咯。该方法的优点是原料容易获得,反应条件温和,产物收率高,操作简单。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Tetrahedron Letters
Tetrahedron Letters 化学-有机化学
CiteScore
3.50
自引率
5.60%
发文量
521
审稿时长
28 days
期刊介绍: Tetrahedron Letters provides maximum dissemination of outstanding developments in organic chemistry. The journal is published weekly and covers developments in techniques, structures, methods and conclusions in experimental and theoretical organic chemistry. Rapid publication of timely and significant research results enables researchers from all over the world to transmit quickly their new contributions to large, international audiences.
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