Synthesis ( IF 2.6 ) Pub Date : 2018-02-14 , DOI: 10.1055/s-0036-1591936 Hakjune Rhee 1, 2 , Yuri Jeong 1 , Jaeyoung Ban 1 , Minkyung Lim 1
‡ These authors contributed equally to this work
Abstract
N-Sulfonylformamidines were synthesized from N-sulfonylsulfonamides by reacting with p-toluenesulfonyl chloride (TsCl) and N,N -disubstituted formamides. In this reaction, it was expected that mixing TsCl with the N,N-disubstituted formamide would generate an iminium salt (Vilsmeier reagent). The reaction avoids the use of metal catalysts and hazardous reagents, and the desired N-sulfonylformamidines were obtained in 60% to quantitative yields.
N-Sulfonylformamidines were synthesized from N-sulfonylsulfonamides by reacting with p-toluenesulfonyl chloride (TsCl) and N,N -disubstituted formamides. In this reaction, it was expected that mixing TsCl with the N,N-disubstituted formamide would generate an iminium salt (Vilsmeier reagent). The reaction avoids the use of metal catalysts and hazardous reagents, and the desired N-sulfonylformamidines were obtained in 60% to quantitative yields.
中文翻译:
由N-磺酰基磺酰胺合成N-磺酰基甲am的新方法
‡这些作者对这项工作做出了同等的贡献
抽象的
Ñ -Sulfonylformamidines从合成Ñ -sulfonylsulfonamides通过与反应p甲苯磺酰氯(的TsCl)和Ñ,ñ -二取代的甲酰胺。在该反应中,预期将TsCl与N,N-二取代的甲酰胺混合将产生亚胺盐(Vilsmeier试剂)。该反应避免了使用金属催化剂和有害试剂,并且以60%至定量收率获得了所需的N-磺酰基甲am。
Ñ -Sulfonylformamidines从合成Ñ -sulfonylsulfonamides通过与反应p甲苯磺酰氯(的TsCl)和Ñ,ñ -二取代的甲酰胺。在该反应中,预期将TsCl与N,N-二取代的甲酰胺混合将产生亚胺盐(Vilsmeier试剂)。该反应避免了使用金属催化剂和有害试剂,并且以60%至定量收率获得了所需的N-磺酰基甲am。