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Synthesis of diversely 1,3,5-trisubstituted pyrazolesvia 5-exo-dig cyclization†
Dmitry A. Borkin,Mirela Puscau,Alena Carlson,Agnes Solan,Kraig A. Wheeler,Béla Török,Roman Dembinski
Organic & Biomolecular Chemistry Pub Date : 05/10/2012 00:00:00 , DOI:10.1039/C2OB25580D
Abstract

5-Exo-dig cyclocondensation of alk-3-yn-1-ones with hydrazines, in the presence of montmorillonite K-10, provides an effective method with a high atom economy for the synthesis of diversely 1,3,5-trisubstituted pyrazoles. The microwave-accelerated reaction proceeds in the absence of solvent and leads to 5-benzyl substituted pyrazoles with good yields (72–91%). The regiochemistry of the process was confirmed by the X-ray crystallographic structure determination of 1-(2-fluorophenyl)-5-(4-methylbenzyl)-3-phenyl-1H-pyrazole.

Graphical abstract: Synthesis of diversely 1,3,5-trisubstituted pyrazoles via 5-exo-dig cyclization
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