Synthesis of Thieno[2,3-c]pyridine Derivatives by 1,2,3-Triazole-Mediated Metal-Free Denitrogenative Transformation Reaction.

IF 2.5 4区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY
Kumsal Eroğlu, Ömer Tahir Günkara, Wim Dehaen
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引用次数: 0

Abstract

In this study, we report the synthesis of thieno[2,3-c]pyridine derivatives by a metal-free method via fused 1,2,3-triazoles. In the synthesis of this skeleton using a three-step method, we first obtained 1-(2,2-dimethoxyethyl)-5-(thiophen-2-yl)-1H-1,2,3-triazole through a one-pot triazolation reaction and in the next step, we synthesized the thieno[2,3-c][1,2,3]triazolo[1,5-ɑ]pyridine compound using a modified Pomeranz-Fritsch reaction. In the final step, the synthesis of thieno[2,3-c]pyridine derivatives was achieved in good yield via acid-mediated denitrogenative transformation reactions. This mild condition synthetic process has enabled access to the title compounds, of which limited examples have been reported until now in the literature. Thus, the syntheses of 7-(substituted methyl)thieno[2,3-c]pyridine, thieno[2,3-c]pyridine-7-ylmethyl esters, and imidazo[1,5-ɑ]thieno[2,3-c]pyridine derivatives have been successfully achieved.

1,2,3-三唑介导的无金属脱氮转化反应合成噻吩[2,3-c]吡啶衍生物
本文报道了以1,2,3-三唑为原料,采用无金属法合成噻吩[2,3-c]吡啶衍生物。在该骨架的合成中,我们首先通过一锅三唑化反应得到了1-(2,2-二甲氧基乙基)-5-(噻吩-2-基)- 1h -1,2,3-三唑,然后通过改进的Pomeranz-Fritsch反应合成了噻吩[2,3-c][1,2,3]三唑[1,5-]吡啶化合物。最后一步,通过酸介导的脱氮转化反应,获得了产率较高的噻吩[2,3-c]吡啶衍生物。这种温和的条件合成过程使标题化合物,其中有限的例子已经报道,直到现在在文献中。因此,成功地合成了7-(取代甲基)噻吩[2,3-c]吡啶、噻吩[2,3-c]吡啶-7-基甲酯和咪唑[1,5-]噻吩[2,3-c]吡啶衍生物。
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
ChemistryOpen
ChemistryOpen CHEMISTRY, MULTIDISCIPLINARY-
CiteScore
4.80
自引率
4.30%
发文量
143
审稿时长
1 months
期刊介绍: ChemistryOpen is a multidisciplinary, gold-road open-access, international forum for the publication of outstanding Reviews, Full Papers, and Communications from all areas of chemistry and related fields. It is co-owned by 16 continental European Chemical Societies, who have banded together in the alliance called ChemPubSoc Europe for the purpose of publishing high-quality journals in the field of chemistry and its border disciplines. As some of the governments of the countries represented in ChemPubSoc Europe have strongly recommended that the research conducted with their funding is freely accessible for all readers (Open Access), ChemPubSoc Europe was concerned that no journal for which the ethical standards were monitored by a chemical society was available for such papers. ChemistryOpen fills this gap.
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