Synthesis
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

© 2025. Thieme. All rights reserved

Georg Thieme Verlag KG
Oswald-Hesse-Straße 50, 70469 Stuttgart, Germany

 
  • References


    • For selected papers, see:
    • 2a Adib M, Peytam F, Jazi MR, Khanaposhtani MM, Mahernia S, Bijanzadeh HR, Jahani M, Imanparast S, Faramarzi MA, Mahdavig M, Larijani B. New J. Chem. 2018; 42: 17268
    • 2b Encinas EM, Rubiales G, Knudssen BR, Palacios F, Alonso C. Eur. J. Med. Chem. 2019; 178: 752
    • 2c Liendo AR, Jiménez IA, Encinas EM, Sifaoui I, Batlle MR, Pellicer JC, Alonso C, Palacios F, Piñero JE, Morales JL. Pharmaceuticals 2021; 14: 1013
    • 2d Gouda MA. S, Salem MA. I, Marzouk MI, Mahmoud NF. H, Ismail MF. Chem. Biodiversity 2023; 20: e202300706
    • 2e Yu J, Gao M, Zhao R, Liu H, Fan H, Pan L, Jin J. Phytochem. Lett. 2023; 57: 5
  • 3 Wang XL, Dou M, Luo Q, Cheng LZ, Yan YM, Li RT, Cheng YX. Fitoterapia 2016; 12: 4
  • 4 Pang M, Lee J, Jeon JH, Song IS, Han YT, Choi MK. Mass Spectrom. Lett. 2021; 12: 200

    • For selected references, see:
    • 6a Mulakayala N, Rambabu D, Raja MR, Chaitanya M, Kumar CS, Kalle AM, Krishna GR, Reddy CM, Rao MV. B, Pal M. Bioorg. Med. Chem. 2012; 20: 759
    • 6b Ling F, Xiao L, Fang L, Lv Y, Zhong W. Adv. Synth. Catal. 2018; 360: 444
    • 6c Beccalli EM, Contini A, Trimarco P. Tetrahedron Lett. 2004; 45: 3447

      For selected papers, see:
    • 7a Yadav A, Biswas S, Mobin SM, Samanta S. Tetrahedron Lett. 2017; 58: 3634
    • 7b ref 2e.
    • 8a Ataee-Kachouei T, Nasr-Esfahani M, Mohammadpoor-Baltork I, Mirkhani V, Moghadam M, Tangestaninejad S, Notash B. Appl. Organomet. Chem. 2020; 34: e5948
    • 8b Jadhav G, Medhane V, Deshmukh D. Lett. Org. Chem. 2021; 18: 862
  • 9 Yoon JA, Han YT. Synthesis 2019; 51: 4611

    • For selected references, see:
    • 10a Reddy CR, Nair K, Srinivasu E, Subbarao M, Grée R. J. Org. Chem. 2024; 89: 2675
    • 10b Reddy CR, Aila M, Subbarao M, Warudikar K, Grée R. Org. Lett. 2021; 23: 4882
    • 10c Chada RR, Kajare RC, Bhandari MC, Mohammed SZ, Khatravath M, Warudikara K, Punna N. Org. Biomol. Chem. 2021; 19: 809
    • 10d Reddy CR, Subbarao M, Sathish P, Kolgave DH, Donthiri RR. Org. Lett. 2020; 22: 689
    • 10e Reddy CR, Valleti RR, Sathish P. J. Org. Chem. 2017; 82: 2345
  • 12 Sharma A, Gogoi P. Org. Biomol. Chem. 2019; 17: 9014
    • 13a Liu P, Deng C.-L, Lei X, Lin G.-q. Eur. J. Org. Chem. 2011; 7308
    • 13b Jeong Y, Kim BI, Lee JK, Ryu JS. J. Org. Chem. 2014; 79: 6444
    • 13c Schömberg F, Zi Y, Vilotijevic I. Chem. Commun. 2018; 54: 3266