A New Approach to the Synthesis of Sydnonimines Carboxyethylated at the Exocyclic Nitrogen Atom

Objective: A new library of sydnonimines containing a carboxyethyl group at the exocyclic nitrogen atom was presented. Methods: Four-step synthesis including cyanomethylation, N-nitrosation, cyclization, and final introduction of a carboxyethyl group was used to obtain new sydnonimines. Results and Discussion: We discovered that the proposed approach can be optimized for a gram-scale synthesis with a single chromatographic step. Our method can be applied to obtain libraries of potential biologically active compounds of this class. Conclusions: We designed a new series of sydnonimines with a carboxyethyl group at the exocyclic nitrogen atom. Going forward, the synthesized substances can be potentially used in new promising drug design.

Authors

Institutions

Publication Details

Journal
Russian Journal of Bioorganic Chemistry
Published
2026-01-29
DOI
https://doi.org/10.1134/s1068162025602551
Primary Topic
Synthesis and Reactivity of Heterocycles
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

A New Approach to the Synthesis of Sydnonimines Carboxyethylated at the Exocyclic Nitrogen Atom

N. S. Popov, D. S. Ivanov, V. Yu. Balaban’yan, M. S. Baranov et al.
Russian Journal of Bioorganic Chemistry
Synthesis and Reactivity of Heterocycles
article

A New Approach to the Synthesis of Sydnonimines Carboxyethylated at the Exocyclic Nitrogen Atom

N. S. Popov, D. S. Ivanov, V. Yu. Balaban’yan, M. S. Baranov, I. N. Myasnyanko, S. A. Krasnova
article en

Abstract

Objective: A new library of sydnonimines containing a carboxyethyl group at the exocyclic nitrogen atom was presented. Methods: Four-step synthesis including cyanomethylation, N-nitrosation, cyclization, and final introduction of a carboxyethyl group was used to obtain new sydnonimines. Results and Discussion: We discovered that the proposed approach can be optimized for a gram-scale synthesis with a single chromatographic step. Our method can be applied to obtain libraries of potential biologically active compounds of this class. Conclusions: We designed a new series of sydnonimines with a carboxyethyl group at the exocyclic nitrogen atom. Going forward, the synthesized substances can be potentially used in new promising drug design.

Russian Journal of Bioorganic ChemistryVol. 52(1)
Pirogov Russian National Research Medical University (RU), Tver State Medical University (RU), Institute of Bioorganic Chemistry (RU)
Openalex Percentile: Top 73%
Synthesis and Reactivity of Heterocycles
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.