期刊
NEW JOURNAL OF CHEMISTRY
卷 45, 期 7, 页码 3479-3484出版社
ROYAL SOC CHEMISTRY
DOI: 10.1039/d0nj05878e
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资金
- Research Council of Shahid Beheshti University
- RUDN University Strategic Academic Leadership Program
An efficient one-pot reaction for the synthesis of a new class of pseudopeptides connected to sulfonamide via a tandem N-sulfonylation/Ugi four-component reaction strategy is reported in this study. The reaction is carried out using readily available starting materials in ethanol/water at room temperature. The synthesized compounds have the potential for designing modern drugs with highly desirable features.
In this study, an efficient one-pot reaction is reported for the synthesis of a new class of pseudopeptide connected to sulfonamide via a tandem N-sulfonylation/Ugi four-component reaction (Ugi-4CR) strategy under mild conditions in high yields. This five-component reaction strategy is carried out by readily available starting materials, sulfonyl chlorides, glycines, benzylamines, benzaldehydes, and isocyanides, in ethanol/water at room temperature. The generation of carboxylic acid that is a key component in Ugi-4CR could be accomplished by performing the N-sulfonylation reaction, and it could be used in the next step without further purification. The as-synthesized compounds that are constructed from pseudopeptide connected to a sulfonamide scaffold have the potential to be used in designing modern drugs with the highly desirable feature.
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