Synthesis of azepinoindolone derivative using Larock’s heteroannulation as key step

Authors

  • Amrita Chakraborty Department of Chemistry, Anugrah Narayan College (A constituent unit of Patliputra University), Boring Road, Patna, Bihar 800013, India
  • Ankita Department of Chemistry, Anugrah Narayan College (A constituent unit of Patliputra University), Boring Road, Patna, Bihar 800013, India
  • Nisha Kumari Department of Chemistry, Anugrah Narayan College (A constituent unit of Patliputra University), Boring Road, Patna, Bihar 800013, India
  • Ratnesh Kumar Department of Chemistry, Anugrah Narayan College (A constituent unit of Patliputra University), Boring Road, Patna, Bihar 800013, India

DOI:

https://doi.org/10.31305/rrijm.2023.v08.n03.008

Keywords:

Azepinoindolone, lactamization, Larock’s heteroannulation, internal alkyne, 2,3-disubstituted indole

Abstract

Synthesis of tetrahydroazepino[4,5-b] indol-2(1H)-one derivative was achieved via intramolecular lactamization of the corresponding amine prepared from suitably designed 2,3-disubstituted indole. Larock’s heteroannulation was employed to get 2,3-disubstituted indole from tosyl protected 2-iodoaniline and internal alkyne which was prepared according to the methodology reported by Greg Fu.  

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Published

14-03-2023

How to Cite

Chakraborty, A., Ankita, Nisha Kumari, & Ratnesh Kumar. (2023). Synthesis of azepinoindolone derivative using Larock’s heteroannulation as key step . RESEARCH REVIEW International Journal of Multidisciplinary, 8(3), 52–64. https://doi.org/10.31305/rrijm.2023.v08.n03.008