Nickel( <scp>II</scp> ) Assisted One‐Pot Synthesis of Quinazolinones From Alcohols

ABSTRACT An efficient, eco‐friendly one‐pot synthesis of 2‐aryl quinazolinone derivatives through the dehydrogenative coupling of alcohols and 2‐aminobenzonitriles in the presence of a Ni(II) catalyst. The catalytic protocol was eco‐friendly, straightforward and provided the desired quinazolinone products with moderate to excellent yields (12 examples, yields ≤ 91%). The catalytic reaction was operated in low catalyst loading (5 mol%) water and hydrogen gas are the only by‐products. The control experiments and mechanistic studies confirm that the reaction proceeds via an aldehyde and cyclic aminol intermediate. Additionally, large‐scale synthesis of 2‐(p‐tolyl)quinazolin‐4(3H)‐one (72%) demonstrates the robustness of the present method.

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Publication Details

Journal
Journal of Heterocyclic Chemistry
Published
2025-11-23
DOI
https://doi.org/10.1002/jhet.70135
Primary Topic
Quinazolinone synthesis and applications
Type
article
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article

Nickel( II ) Assisted One‐Pot Synthesis of Quinazolinones From Alcohols

Pennamuthiriyan Anandaraj
Journal of Heterocyclic Chemistry
Quinazolinone synthesis and applications
article

Nickel( II ) Assisted One‐Pot Synthesis of Quinazolinones From Alcohols

Pennamuthiriyan Anandaraj
article en

Abstract

ABSTRACT An efficient, eco‐friendly one‐pot synthesis of 2‐aryl quinazolinone derivatives through the dehydrogenative coupling of alcohols and 2‐aminobenzonitriles in the presence of a Ni(II) catalyst. The catalytic protocol was eco‐friendly, straightforward and provided the desired quinazolinone products with moderate to excellent yields (12 examples, yields ≤ 91%). The catalytic reaction was operated in low catalyst loading (5 mol%) water and hydrogen gas are the only by‐products. The control experiments and mechanistic studies confirm that the reaction proceeds via an aldehyde and cyclic aminol intermediate. Additionally, large‐scale synthesis of 2‐(p‐tolyl)quinazolin‐4(3H)‐one (72%) demonstrates the robustness of the present method.

Journal of Heterocyclic ChemistryVol. 63(2)
Anna University, Chennai (IN)
Openalex Percentile: Top 73%
Quinazolinone synthesis and applications
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