Synthesis 2025; 57(12): 1997-2003
DOI: 10.1055/a-2567-4644
paper

Ag(I)/Au(I)-Catalyzed Domino Propargylation/Aza-Annulation to Access Coumarino[4,3-b]pyridines

a   Department of Organic Synthesis & Process Chemistry, CSIR-Indian Institute of Chemical Technology (CSIR-IICT), Hyderabad 500007, India
b   Academy of Scientific and Innovative Research (AcSIR), Ghaziabad 201002, India
,
Venkatareddy Edhara
a   Department of Organic Synthesis & Process Chemistry, CSIR-Indian Institute of Chemical Technology (CSIR-IICT), Hyderabad 500007, India
b   Academy of Scientific and Innovative Research (AcSIR), Ghaziabad 201002, India
,
Ankita Kumari
a   Department of Organic Synthesis & Process Chemistry, CSIR-Indian Institute of Chemical Technology (CSIR-IICT), Hyderabad 500007, India
b   Academy of Scientific and Innovative Research (AcSIR), Ghaziabad 201002, India
,
Adla Vijender
a   Department of Organic Synthesis & Process Chemistry, CSIR-Indian Institute of Chemical Technology (CSIR-IICT), Hyderabad 500007, India
› Institutsangaben

C.R.R. thanks the CSIR-Indian Institute of Chemical Technology Hyderabad for funding the project. V.E. thanks Uquifa India Pvt. Ltd. for supporting the doctoral research program. A.K. thanks the Council of Scientific and Industrial Research (CSIR), New Delhi, for the research fellowship. [CSIR-IICT Communication no. IICT/Pubs./2025/048].


Abstract

An approach for the synthesis of diversely substituted coumarino[4,3-b]pyridines (5H-[1]benzopyrano[4,3-b]pyridin-5-ones), involving the annulation of 4-aminocoumarins with propargylic alcohols, is reported. The reaction proceeds through C-3 propargylation followed by an aza-annulation in a domino manner in the presence of AgSbF6/AuCl(PPh3) as the catalytic system. The products can be synthesized from a broad range of propargylic alcohols, demonstrating the compatibility with different functional groups.

Supporting Information



Publikationsverlauf

Eingereicht: 05. Februar 2025

Angenommen nach Revision: 26. März 2025

Accepted Manuscript online:
26. März 2025

Artikel online veröffentlicht:
14. April 2025

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