Copper‐mediated annulation of 2‐aminoacetophenones and 2‐bromopyridines-Reference-Cited by-同舟云学术

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Copper‐mediated annulation of 2‐aminoacetophenones and 2‐bromopyridines

Published:2022-04 Issue:2 Volume:60 Page:164-168
ISSN:2572-8288
Container-title:Vietnam Journal of Chemistry
language:en
Short-container-title:Vietnam Journal of Chemistry

Author:

Hai Pham Hoang¹²,Nam Phan Thanh Son¹²,Tung Nguyen Thanh¹²^ORCID

Affiliation:

1. Faculty of Chemical Engineering, Ho Chi Minh City University of Technology (HCMUT) 268 Ly Thuong Kiet Street, District 10 Ho Chi Minh City 70000 Viet Nam

2. Vietnam National University Ho Chi Minh City Linh Trung Ward, Thu Duc District Ho Chi Minh City 70000 Viet Nam

Abstract

AbstractA simple, practical method for synthesis of pyrido‐fused quinazolinones is herein developed. Reactions of 2’‐aminoacetophenones and 2‐bromopyridines proceeded in the presence of Cu(OAc)2 catalyst, NaOAc base, TEMPO co‐oxidant, and DMSO solvent. Simple functional groups were compatible with reaction conditions.

Publisher

Wiley

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/vjch.202100091

Reference18 articles.

1. Benzimidazo[2,1-b]quinazolin-12-ones. New class of potent immunosuppressive compounds

2. Luotonin A. A Naturally Occurring Human DNA Topoisomerase I Poison

3. Base-Controlled Selectivity in the Synthesis of Linear and Angular Fused Quinazolinones by a Palladium-Catalyzed Carbonylation/Nucleophilic Aromatic Substitution Sequence

4. Condensation of anthranilic acids with pyridines to furnish pyridoquinazolones via pyridine dearomatization

5. Palladium‐Catalyzed Carbonylative Cyclization of Arenes by CH Bond Activation with DMF as the Carbonyl Source

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