Organocatalytic Enantioselective [3+2] Cycloaddition of para ‐Quinamines with Cyclic N ‐Sulfonyl Ketimines: Access to Imidazolidine‐Fused Benzosultam Derivatives

Comprehensive Summary Given the well‐established pharmacological significance of both imidazolidine derivatives and benzosultam analogues, the imidazolidine‐fused benzosultam scaffold, which is accessible through molecular hybridization, represents an architecturally novel N ‐heterocyclic framework with substantial potential for medicinal chemistry research. Herein, we report an efficient protocol for the synthesis of highly substituted imidazolidine‐fused benzosultams via a mild, catalyst‐free [3+2] cycloaddition between readily available para ‐quinamines and cyclic N ‐sulfonyl ketimines. This transformation enables the convergent assembly of two privileged pharmacophoric motifs into a single polycyclic scaffold, and is characterized by high yields (up to 99%), remarkably broad substrate scope, excellent functional group tolerance, exceptionally fast reaction rates (complete within 5 min), and high diastereoselectivity. Notably, the purification can be accomplished simply by trituration, which significantly enhances both operational simplicity and environmental sustainability. Furthermore, for the first time, a bifunctional amine‐thiourea catalyst has been successfully applied to the cycloaddition of para ‐quinamines, enabling a catalytic asymmetric variant that delivers structurally unprecedented enantioenriched 6/5/6/6‐fused benzosultams in up to 90% yields with excellent diastereo‐ and enantiocontrol (up to 97.5 : 2.5 er). The practical utility of this methodology is demonstrated through scale‐up synthesis and late‐stage modification. Mechanistic investigations suggest the involvement of a single amine‐thiourea catalyst in the enantiodetermining transition state, and two plausible mechanisms, along with their corresponding asymmetric induction models, are proposed. Collectively, this methodology provides a versatile platform for the rapid construction of imidazolidine and benzosultam bioisosteres, and holds great promise for applications in medicinal chemistry.

Authors

Institutions

Publication Details

Journal
Chinese Journal of Chemistry
Published
2026-08-27
DOI
https://doi.org/10.1002/cjoc.70762
Primary Topic
Asymmetric Synthesis and Catalysis
Type
article
Field-Weighted Citation Impact
0.00

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Organocatalytic Enantioselective [3+2] Cycloaddition of para ‐Quinamines with Cyclic N ‐Sulfonyl Ketimines: Access to Imidazolidine‐Fused Benzosultam Derivatives

Yang Ma, Ting Xiao, Zhe Liu, Feng Lv et al.
Chinese Journal of Chemistry
Asymmetric Synthesis and Catalysis
article

Organocatalytic Enantioselective [3+2] Cycloaddition of para ‐Quinamines with Cyclic N ‐Sulfonyl Ketimines: Access to Imidazolidine‐Fused Benzosultam Derivatives

Yang Ma, Ting Xiao, Zhe Liu, Feng Lv, Yan Ding, Weiwei Xia, Anhui Liao, Shiru Li, Zengwei Lai
article en

Abstract

Comprehensive Summary Given the well‐established pharmacological significance of both imidazolidine derivatives and benzosultam analogues, the imidazolidine‐fused benzosultam scaffold, which is accessible through molecular hybridization, represents an architecturally novel N ‐heterocyclic framework with substantial potential for medicinal chemistry research. Herein, we report an efficient protocol for the synthesis of highly substituted imidazolidine‐fused benzosultams via a mild, catalyst‐free [3+2] cycloaddition between readily available para ‐quinamines and cyclic N ‐sulfonyl ketimines. This transformation enables the convergent assembly of two privileged pharmacophoric motifs into a single polycyclic scaffold, and is characterized by high yields (up to 99%), remarkably broad substrate scope, excellent functional group tolerance, exceptionally fast reaction rates (complete within 5 min), and high diastereoselectivity. Notably, the purification can be accomplished simply by trituration, which significantly enhances both operational simplicity and environmental sustainability. Furthermore, for the first time, a bifunctional amine‐thiourea catalyst has been successfully applied to the cycloaddition of para ‐quinamines, enabling a catalytic asymmetric variant that delivers structurally unprecedented enantioenriched 6/5/6/6‐fused benzosultams in up to 90% yields with excellent diastereo‐ and enantiocontrol (up to 97.5 : 2.5 er). The practical utility of this methodology is demonstrated through scale‐up synthesis and late‐stage modification. Mechanistic investigations suggest the involvement of a single amine‐thiourea catalyst in the enantiodetermining transition state, and two plausible mechanisms, along with their corresponding asymmetric induction models, are proposed. Collectively, this methodology provides a versatile platform for the rapid construction of imidazolidine and benzosultam bioisosteres, and holds great promise for applications in medicinal chemistry.

Chinese Journal of Chemistry
Jiangnan University (CN)
National Natural Science Foundation of China
Life in Land, Responsible consumption and production
Openalex Percentile: Top 19%
Asymmetric Synthesis and Catalysis
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.