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Microwave‐Assisted Cobalt‐Catalyzed Synthesis of Quinazolinones via Acceptorless Dehydrogenative Coupling under Neat Condition
Author(s) -
Pal Adwitiya,
Majumdar Adrija,
Sau Subham,
Thakur Arunabha
Publication year - 2025
Publication title -
chemistry – an asian journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.18
H-Index - 106
eISSN - 1861-471X
pISSN - 1861-4728
DOI - 10.1002/asia.202401690
Subject(s) - catalysis , chemistry , combinatorial chemistry , quinazolinone , atom economy , cobalt , derivative (finance) , solvent , organic chemistry , financial economics , economics
Abstract Herein, we present a sustainable and atom‐economical approach for the synthesis of quinazolinones via acceptorless dehydrogenative coupling (ADC) using earth‐abundant Co‐salt, (CoCl 2 ) as the catalyst under neat condition. This method is distinguished by its green credentials, like, solvent‐free, microwave‐assisted heating, cost‐effective, use of renewable alcohols, and generating only H 2 and water as byproducts. Remarkably, this protocol achieves quinazolinone synthesis without the need for external ligands, oxidants, or additional additives. Two synthetic pathways were developed: one involving the coupling of alcohols with 2‐aminobenzamide, and the other with N ‐phenyl‐substituted 2‐aminobenzamides and its derivative. The scalability of this method, demonstrated through gram‐scale synthesis, highlights its potential for industrial applications. Mechanistic insights were explored through control experiments, intermediate detection by HRMS, and Hammett analysis, shedding light on the plausible reaction pathway.

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