由3-氨基茚唑和两种不同氨基酸一锅合成2,3-二取代嘧啶[1,2-b]茚唑骨架。

IF 3.6 2区 化学 Q1 CHEMISTRY, ORGANIC
Yingying Zheng, Xiaotian Wu, Xueyan Lv and Chen Ma*, 
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引用次数: 0

摘要

以3-氨基吲哚唑和两个氨基酸为原料,合成了2,3-二取代嘧啶[1,2-b]吲哚唑。该策略已在多种3-氨基吲哚唑和氨基酸中得到验证,并已成功扩大到克级合成,突出了该方案的实用性和应用价值。此外,氨基酸的利用不仅减少了副产物的形成,而且使反应更加环保。机制研究表明,I2促进了氨基酸的脱羧和随后的氧化环化过程。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

One-Pot Synthesis of 2,3-Disubstituted Pyrimido[1,2-b]indazole Skeletons from 3-Aminoindazole and Two Distinct Amino Acids

One-Pot Synthesis of 2,3-Disubstituted Pyrimido[1,2-b]indazole Skeletons from 3-Aminoindazole and Two Distinct Amino Acids

An effective synthesis for 2,3-disubstituted pyrimido[1,2-b]indazole from 3-aminoindazole and two amino acids was developed. This strategy has been demonstrated with a variety of 3-aminoindazole and amino acids, and it has been successfully scaled up to gram-scale synthesis, highlighting the practicality and application value of the protocol. Furthermore, the utilization of amino acids not only reduces the formation of byproducts but also renders the reaction more environmentally friendly. Mechanistic studies revealed that I2 promoted the decarboxylation of amino acids and the subsequent oxidative cyclization process.

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来源期刊
Journal of Organic Chemistry
Journal of Organic Chemistry 化学-有机化学
CiteScore
6.20
自引率
11.10%
发文量
1467
审稿时长
2 months
期刊介绍: Journal of Organic Chemistry welcomes original contributions of fundamental research in all branches of the theory and practice of organic chemistry. In selecting manuscripts for publication, the editors place emphasis on the quality and novelty of the work, as well as the breadth of interest to the organic chemistry community.
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