Synthesis of 2-Pyrazolines with a CF3- and Alkyne-Substituted Quaternary Carbon Center via [3+2] Cycloaddition of β-CF3-1,3-enynes and Diazoacetates

Given the importance of both the CF3 group and the alkyne moiety in synthetic/medicinal chemistry, we report here the first example of efficient synthesis of 2-pyrazolines with a CF3- and alkyne-substituted quaternary carbon center. This methodology has the advantages of high functional group compatibility, the avoidance of base and open-flask conditions, easily available and easy to handle reagent, and broad substrate scope. Notably, this protocol allows for the late-stage functionalization of biologically active molecules and the gram-scale synthesis.

Automated summary

In this study, an efficient method for synthesizing 2-pyrazolines with a CF3- and alkyne-substituted quaternary carbon center is reported. This methodology offers high functional group compatibility, easily accessible reagents, and broad substrate scope.