Issue 58, 2015

Vilsmeier reagent-mediated synthesis of 6-[(formyloxy)methyl]-pyrazolopyrimidines via a one-pot multiple tandem reaction

Abstract

A new Vilsmeier reagent-mediated one-pot reaction using 5-(2-chloroacetylamino)pyrazoles as the starting material was developed for the efficient synthesis of 6-[(formyloxy)methyl]-1H-pyrazolo[3,4-d]pyrimidine. This new multiple tandem reaction, involving the Vilsmeier–Haack reaction, the Morgan–Walls reaction, sequential elimination, substitution, and final hydrolysis, afforded formyloxymethyl pyrazolo[3,4-d]pyrimidine products in good yields.

Graphical abstract: Vilsmeier reagent-mediated synthesis of 6-[(formyloxy)methyl]-pyrazolopyrimidines via a one-pot multiple tandem reaction

Supplementary files

Article information

Article type
Paper
Submitted
28 Apr 2015
Accepted
13 May 2015
First published
14 May 2015

RSC Adv., 2015,5, 47098-47107

Author version available

Vilsmeier reagent-mediated synthesis of 6-[(formyloxy)methyl]-pyrazolopyrimidines via a one-pot multiple tandem reaction

S. Lu, P. Liu and F. F. Wong, RSC Adv., 2015, 5, 47098 DOI: 10.1039/C5RA07707A

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