Molybdenum‐Promoted Synthesis of Benzo[4,5]imidazo[1,2‐ <i>c</i> ]quinazolin‐6(5 <i>H</i> )‐ones <i>via</i> Nitro Reduction and Ring Expansion

Abstract A simple and efficient method to construct benzo[4,5]imidazo[1,2‐ c ]quinazolin‐6(5 H )‐one skeleton was reported. A powerful functional group transformation strategy of −NO 2 transformed into −NH 2 was involved in this method. Only Mo(CO) 6 was used in the reaction, which acted as both reductant and cyclization accelerator. And a series of benzo[4,5]imidazo[1,2‐ c ]quinazolin‐6(5 H )‐one derivatives were obtained.

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Publication Details

Journal
ChemistrySelect
Published
2024-09-09
DOI
https://doi.org/10.1002/slct.202403399
Citations
2
Primary Topic
Quinazolinone synthesis and applications
Type
article
Field-Weighted Citation Impact
0.50
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article

Molybdenum‐Promoted Synthesis of Benzo[4,5]imidazo[1,2‐ c ]quinazolin‐6(5 H )‐ones via Nitro Reduction and Ring Expansion

Zerui Meng, Caixia Xie, Ran Zhao, Xiangwei Meng et al.
2 citations
ChemistrySelect
Quinazolinone synthesis and applications
0.50
article

Molybdenum‐Promoted Synthesis of Benzo[4,5]imidazo[1,2‐ c ]quinazolin‐6(5 H )‐ones via Nitro Reduction and Ring Expansion

Zerui Meng, Caixia Xie, Ran Zhao, Xiangwei Meng, Xiaoru Meng, Xinrui Huang
article en
2 citations

Abstract

Abstract A simple and efficient method to construct benzo[4,5]imidazo[1,2‐ c ]quinazolin‐6(5 H )‐one skeleton was reported. A powerful functional group transformation strategy of −NO 2 transformed into −NH 2 was involved in this method. Only Mo(CO) 6 was used in the reaction, which acted as both reductant and cyclization accelerator. And a series of benzo[4,5]imidazo[1,2‐ c ]quinazolin‐6(5 H )‐one derivatives were obtained.

ChemistrySelectVol. 9(34)
Shandong University of Technology (CN), Binzhou Medical University (CN)
Openalex Percentile: Top 39%
Quinazolinone synthesis and applications
0.50
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