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.
Authors
- Gui‐Fa Su (ORCID: https://orcid.org/0000-0003-3128-2381)
- Dong‐Liang Mo (ORCID: https://orcid.org/0000-0002-4005-2249)
- Shan Chen (ORCID: https://orcid.org/0000-0002-2750-5063)
- Yan Li (ORCID: https://orcid.org/0000-0003-1963-839X)
- Chunhua Chen (ORCID: https://orcid.org/0000-0001-9589-6329)
- Yanjie Chen
Institutions
- Minzu University of China (CN)
- State Ethnic Affairs Commission (CN)
- Guangxi Normal University (CN)
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
- Field-Weighted Citation Impact
- 0.00