Synthesis of C2-Alkyl Quinazolinones through Bis(pinacolato)diborane Mediated Transfer Hydrogenation Reaction of Alkynes to Alkanes

Herein, we report a facile approach to prepare a variety of C2-alkyl-substituted quinazolinones in good to excellent yields and high reduction selectivity through bis(pinacolato)diborane (B<sub>2</sub>Pin<sub>2</sub>)-mediated transfer hydrogenation of an alkyne to an alkane under mild reaction conditions. Control experiments revealed that MeOH as the green hydrogen source and B<sub>2</sub>Pin<sub>2</sub> was converted to nucleophilic species in the presence of MeOH and base. More importantly, the reaction was easily performed in gram scales and quinazolinone-derived estrone could be obtained in good yield over three steps. The present method features broad substrate scope, good functional group tolerance, green hydrogen source, and borate-mediated transfer hydrogenation.

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Publication Details

Journal
The Journal of Organic Chemistry
Published
2025-10-28
DOI
https://doi.org/10.1021/acs.joc.5c02134
Primary Topic
Quinazolinone synthesis and applications
Type
article
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article

Synthesis of C2-Alkyl Quinazolinones through Bis(pinacolato)diborane Mediated Transfer Hydrogenation Reaction of Alkynes to Alkanes

Gui‐Fa Su, Dong‐Liang Mo, Shan Chen, Yan Li et al.
The Journal of Organic Chemistry
Quinazolinone synthesis and applications
article

Synthesis of C2-Alkyl Quinazolinones through Bis(pinacolato)diborane Mediated Transfer Hydrogenation Reaction of Alkynes to Alkanes

Gui‐Fa Su, Dong‐Liang Mo, Shan Chen, Yan Li, Chunhua Chen, Yanjie Chen
article en

Abstract

Herein, we report a facile approach to prepare a variety of C2-alkyl-substituted quinazolinones in good to excellent yields and high reduction selectivity through bis(pinacolato)diborane (B<sub>2</sub>Pin<sub>2</sub>)-mediated transfer hydrogenation of an alkyne to an alkane under mild reaction conditions. Control experiments revealed that MeOH as the green hydrogen source and B<sub>2</sub>Pin<sub>2</sub> was converted to nucleophilic species in the presence of MeOH and base. More importantly, the reaction was easily performed in gram scales and quinazolinone-derived estrone could be obtained in good yield over three steps. The present method features broad substrate scope, good functional group tolerance, green hydrogen source, and borate-mediated transfer hydrogenation.

The Journal of Organic ChemistryVol. 90(44)
Minzu University of China (CN), State Ethnic Affairs Commission (CN), Guangxi Normal University (CN)
Openalex Percentile: Top 76%
Quinazolinone synthesis and applications
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