Green Multicomponent‐Click Strategy for One‐Pot Synthesis of Polyheterocyclic Estazolam Aza‐Analogs and Their Symmetrical Polyheterocycles

ABSTRACT A novel one‐pot synthesis of polyheterocyclic compounds (PHCs) incorporating fused 1,5‐disubstituted 1,2,3‐triazole‐1,4‐benzodiazepines (fused 1,5‐Ds‐1,2,3‐T‐1,4‐BZD) bound to 1,5‐disubstituted tetrazoles (1,5‐Ds‐Ts) was developed via Ugi‐azide four‐component reaction (UA‐4CR), followed by an intramolecular alkyne–azide cycloaddition (IAAC). The strategy features overall yields up to 92%, the construction of three heterocycles, broad applicability to UA‐4CR products, a single purification step via flash column chromatography, green solvent conditions (water or EtOH), and scalability. The secondary amine functional group in PHCs enabled further structural diversification in the synthesis of symmetrical polyheterocycles (SPHs) and structurally aza‐analogs of estazolam. This is the first report of an alternative energy sources (AES)‐assisted UA‐4CR/IAAC strategy for the synthesis of fused 1,5‐Ds‐1,2,3‐T‐1,4‐BZD, applied to the synthesis of SPHs that allow the construction of six heterocyclic rings.

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Publication Details

Journal
Asian Journal of Organic Chemistry
Published
2026-04-01
DOI
https://doi.org/10.1002/ajoc.70382
Primary Topic
Click Chemistry and Applications
Type
article
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article

Green Multicomponent‐Click Strategy for One‐Pot Synthesis of Polyheterocyclic Estazolam Aza‐Analogs and Their Symmetrical Polyheterocycles

Rocío Gámez‐Montaño, Manuel A. Rentería‐Gómez, Alejandro Corona‐Díaz, Diana García‐García
Asian Journal of Organic Chemistry
Click Chemistry and Applications
article

Green Multicomponent‐Click Strategy for One‐Pot Synthesis of Polyheterocyclic Estazolam Aza‐Analogs and Their Symmetrical Polyheterocycles

Rocío Gámez‐Montaño, Manuel A. Rentería‐Gómez, Alejandro Corona‐Díaz, Diana García‐García
article en

Abstract

ABSTRACT A novel one‐pot synthesis of polyheterocyclic compounds (PHCs) incorporating fused 1,5‐disubstituted 1,2,3‐triazole‐1,4‐benzodiazepines (fused 1,5‐Ds‐1,2,3‐T‐1,4‐BZD) bound to 1,5‐disubstituted tetrazoles (1,5‐Ds‐Ts) was developed via Ugi‐azide four‐component reaction (UA‐4CR), followed by an intramolecular alkyne–azide cycloaddition (IAAC). The strategy features overall yields up to 92%, the construction of three heterocycles, broad applicability to UA‐4CR products, a single purification step via flash column chromatography, green solvent conditions (water or EtOH), and scalability. The secondary amine functional group in PHCs enabled further structural diversification in the synthesis of symmetrical polyheterocycles (SPHs) and structurally aza‐analogs of estazolam. This is the first report of an alternative energy sources (AES)‐assisted UA‐4CR/IAAC strategy for the synthesis of fused 1,5‐Ds‐1,2,3‐T‐1,4‐BZD, applied to the synthesis of SPHs that allow the construction of six heterocyclic rings.

Asian Journal of Organic ChemistryVol. 15(4)
Universidad de Guanajuato (MX)
Affordable and clean energy
Openalex Percentile: Top 24%
Click Chemistry and Applications
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