Photocatalytic One-Pot Three-Component Reaction for the Regioselective Synthesis of Bromo-Substituted Pyrazoles

IF 3.3 2区 化学 Q1 CHEMISTRY, ORGANIC
Zhiying Zhang, Yinyin Li, Yatang Wang, Xiaofeng Hua, Chuanyu Zheng, Qianlan Shi, Zhiyong Tan, Lvyin Zheng* and Wei Guo*, 
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引用次数: 0

Abstract

A photocatalytic three-component cascade reaction of readily available enaminones, hydrazines, and CBr4 for the synthesis of bromo-substituted pyrazoles in one pot has been demonstrated. This strategy involves intermolecular C-N/C-Br bond formation and represents an efficient approach to the construction of 4-bromo-substituted pyrazoles with high regioselectivity, broad substrate scope, good functional group tolerance, convenient operation, and mild reaction conditions. Mechanistic investigations show that this reaction proceeds via intermolecular cyclization of enaminones with hydrazines, followed by a regioselective bromination of pyrazoles using CBr4 as a “Br” source.

Abstract Image

用于溴代吡唑的区域选择性合成的光催化一锅三组分反应
研究人员展示了一种光催化三组分级联反应,即在一个反应器中利用容易获得的烯氨酮、肼和 CBr4 来合成溴代吡唑。该策略涉及分子间 C-N/C-Br 键的形成,是构建 4-溴代吡唑的有效方法,具有高区域选择性、广泛的底物范围、良好的官能团耐受性、便捷的操作和温和的反应条件。机理研究表明,该反应通过烯氨酮与肼的分子间环化进行,然后以 CBr4 作为 "Br "源对吡唑进行区域选择性溴化。
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来源期刊
The Journal of Organic Chemistry
The 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: The 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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