Decyclization of substituted 2-[2-oxofuran-3(2<i>h</i>)-ylidene)furan-2-carbohydrazides by the action of alcohols and analgesic activity of the obtained compounds

Author:

Igidov S. N12,Turyshev A. Yu.1,Makhmudov R. R3,Shipilovskikh D. A4,Dmitriev M. V3,Zvereva O. V1,Silaichev P. S3,Igidov N. M1,Shipilovskikh S. A35

Affiliation:

1. Perm State Pharmaceutical Academy

2. Merck LLC

3. Perm State University

4. Perm National Research Polytechnic University

5. ITMO University

Abstract

A new series of substituted 4-oxo-2-[2-(furan-2-ylcarbonyl)hydrazinylidene]butanoic acids and 2-[2-oxofuran3(2 H )-ylidene]furan-2-carbohydrazides was synthesized. A methodology was developed for their decyclization under the action of primary and secondary alcohols with the formation of substituted alkyl 4-oxo-2-[2-(furan-2ylcarbonyl)hydrazinylidene]butanoates, which exist in the form of three isomeric forms. Among the synthesized compounds, substances with pronounced analgesic activity were found.

Publisher

The Russian Academy of Sciences

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