4-(2,5-Dimethyl-1H-pyrrol-1-yl)-1,2,5-oxadiazol-3-amine

IF 0.4 Q4 CHEMISTRY, ORGANIC
Molbank Pub Date : 2023-07-20 DOI:10.3390/m1700
N. V. Obruchnikova, O. Rakitin
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引用次数: 0

Abstract

1,2,5-Oxadiazol-3-amines with a heterocyclic substituent in the 4-position are being intensively investigated as compounds with valuable pharmacological activity. In this communication, the reaction of 1,2,5-oxadiazole-3,4-diamine with 2,5-hexanedione was shown to selectively give 4-(2,5-dimethyl-1H-pyrrol-1-yl)-1,2,5-oxadiazol-3-amine as a product of the Paal–Knorr reaction. The structure of the synthesized compound was established by elemental analysis, high-resolution mass spectrometry, 1H and 13C NMR, and IR spectroscopy.
4-(2,5-二甲基-1H-吡咯-1-基)-1,2,5-恶二唑-3-胺
在4-位具有杂环取代基的1,2,5-恶二唑-3-胺作为具有宝贵药理活性的化合物正在被深入研究。在该通信中,1,2,5-恶二唑-3,4-二胺与2,5-己二酮的反应显示选择性地得到4-(2,5-二甲基-1H-吡咯-1-基)-1,2,5恶二唑-3-胺,作为Paal–Knorr反应的产物。通过元素分析、高分辨率质谱、1H和13C NMR以及IR光谱确定了合成化合物的结构。
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
Molbank
Molbank Chemistry-Physical and Theoretical Chemistry
CiteScore
0.70
自引率
33.30%
发文量
174
审稿时长
11 weeks
期刊介绍: •organic synthesis •biosynthesis •extraction and purification •natural product derivatives •structural elucidation (X-ray crystallography, NMR, etc.)
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