p-TSA catalyzed 6- endo-trig/ dig cyclization of 5-aminopyrazoles and 3°/2°-propargylic alcohols: access to pyrazolo[1,5- a]dihydropyrimidines and pyrazolo[3,4- b]pyridines

Org Biomol Chem. 2024 Oct 2;22(38):7854-7859. doi: 10.1039/d4ob01255k.

Abstract

A facile, straightforward synthesis of fused pyrazolo[1,5-a]dihydropyrimidines and pyrazolo[3,4-b]pyridines is accomplished by using 5-aminopyrazoles, 3°/2°-propargylic alcohols and ynones in the presence of p-TSA. The reaction proceeds through allenylation (N-alkylation)/propargylation (C-alkylation) of 5-aminopyrazoles, followed by intramolecular 6-endo-trig/dig cyclization leading to the title products with the formation of new C-N and C-C bonds. Operationally simple reaction conditions, inexpensive reagents, better yields, and gram-scale synthesis are the advantages of this protocol.