Issue 2, 2022

Unexpected ring opening of pyrazolines with activated alkynes: synthesis of 1H-pyrazole-4,5-dicarboxylates and chromenopyrazolecarboxylates

Abstract

1H-Pyrazole-4,5-dicarboxylates and chromenopyrazole carboxylates were prepared by reacting pyrazolines with activated alkynes under neat conditions without a catalyst. The products were formed via unexpected ring opening of pyrazolines with the elimination of styrene/ethylene. These types of transformations are unknown and the products formed were confirmed using their spectral/analytical data. In addition, the structures of compounds 5e and 5n were confirmed by single-crystal X-ray analysis. Control experiments were conducted to support the proposed reaction mechanism.

Graphical abstract: Unexpected ring opening of pyrazolines with activated alkynes: synthesis of 1H-pyrazole-4,5-dicarboxylates and chromenopyrazolecarboxylates

Supplementary files

Article information

Article type
Communication
Submitted
02 Sep 2021
Accepted
06 Dec 2021
First published
07 Dec 2021

Org. Biomol. Chem., 2022,20, 334-338

Unexpected ring opening of pyrazolines with activated alkynes: synthesis of 1H-pyrazole-4,5-dicarboxylates and chromenopyrazolecarboxylates

S. T. Kolla, N. R. Rayala, B. Sridhar and C. R. Bhimapaka, Org. Biomol. Chem., 2022, 20, 334 DOI: 10.1039/D1OB01727F

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