Facile Condensation of 2‐Aminobenzaldehydes into Azolo[4,5‐b]Quinolones-Reference-Cited by-同舟云学术

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Facile Condensation of 2‐Aminobenzaldehydes into Azolo[4,5‐b]Quinolones

Published:2024-07-12 Issue:27 Volume:9 Page:
ISSN:2365-6549
Container-title:ChemistrySelect
language:en
Short-container-title:ChemistrySelect

Author:

Opryshko Victoria E.¹,Zaitseva Elvira R.¹,Ivanov Dmitrii S.¹,Eshtukov‐Shcheglov Artur V.¹,Tyurin Anton P.¹,Mikhaylov Andrey A.¹,Smirnov Alexander Yu.¹²,Baranov Mikhail S.¹²^ORCID

Affiliation:

1. Institute of Bioorganic Chemistry Russian Academy of Sciences Miklukho-Maklaya 16/10 117997 Moscow Russia

2. Pirogov Russian National Research Medical University Ostrovitianov 1 117997 Moscow Russia

Abstract

AbstractAn operationally simple approach to azolo[4,5‐b]quinolines based on the condensation of 2‐aminobenzaldehydes with various azolones is developed. A series of 22 compounds was synthesized typically in good yields (40–92 %).

Funder

Russian Science Foundation

Publisher

Wiley

Reference15 articles.

1. Synthesis and Applications of Imidazoquinolines: A Review

2. Synthesis and Biological Activity Evaluation of Novel 5-Methyl-7-phenyl-3H-thiazolo[4,5-b]pyridin-2-ones

3. Docking Studies on Some Synthesized 5H-Chromeno[4,3-b]Pyridin-5-One Derivatives for Breast Cancer

4. Synthesis and herbicidal activity of 5-(haloalkyl)-substituted thiazolo[4,5-b]pyridine-3(2H)-acetic acid derivatives

5. Inhibitors of blood platelet cAMP phosphodiesterase. 2. Structure-activity relationships associated with 1,3-dihydro-2H-imidazo[4,5-b]quinolin-2-ones substituted with functionalized side chains

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