Lewis Acid‐Catalyzed Substituted spiro 4‐thia‐1,2,6,9 tetraazaspiro[4.4]non‐2‐ene‐7,8‐diones via 1,3‐dipolar [3+2]cycloaddition

Author:

Lingareddy Eeda12ORCID,Nadagouda Aishwarya12,Sai Lokavarapu12ORCID,Pardha Saradhi Todeti32,Bansod Sudhakar12ORCID,Tangutur Anjana Devi32ORCID,Nanubolu Jagadeesh Babu42ORCID,Kumbhare Ravindra M.12ORCID

Affiliation:

1. Fluoro-Agrochemicals Department CSIR-Indian Institute of Chemical Technology Hyderabad 500007(TS) India

2. Academy of Scientific and Innovative Research (AcSIR) Ghaziabad 201002(UP) India

3. Department of Applied Biology CSIR-Indian Institute of Chemical Technology Hyderabad 500007(TS) India

4. Centre for X-ray Crystallography CSIR-Indian Institute of Chemical Technology Hyderabad 500007(TS) India

Abstract

AbstractA series of substituted spiro 4‐thia‐1,2,6,9‐tetraazaspiro[4.4]non‐2‐ene‐7,8‐diones were synthesized with good yields through 1,3‐dipolar substituted hydrazonoylchloride's substituted 2‐thioxoimidazolidin‐4,5‐diones under mild conditions as described. This switchable C−S and C−N bond connection with simple execution and broad substrate scope. In this study, the synthesized compounds 3 aq were screened against four distinct cancer cell lines (PANC‐1, MIA PaCa‐2, MDA MB231 and DU145) along with a standard cell line HEK‐293, to determine their in vitro anticancer activities, and assessed using the Sulphorhodamine B assay to determine their viability

Publisher

Wiley

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