Events The 24th International Electronic Conference on Synthetic Organic Chemistry

Event submissions

Published

This submission belongs to the session A. General Organic Synthesis of the event The 24th International Electronic Conference on Synthetic Organic Chemistry

Published date

14 Nov, 2020

Citation

MANUEL ALEJANDRO RENTERIA GOMEZ, MARIA DEL ROCÍO GÁMEZ MONTAÑO, MAHANANDAIAH KURVA, Synthesis of triphenylamine-imidazo[1,2-a]pyridine via Groebke-Blackburn-Bienaymé Reaction, in Proceedings of The 24th International Electronic Conference on Synthetic Organic Chemistry, 15 November–15 December 2020, MDPI: Basel, Switzerland, doi: 10.3390/ecsoc-24-08422

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Synthesis of triphenylamine-imidazo[1,2-a]pyridine via Groebke-Blackburn-Bienaymé Reaction

MANUEL ALEJANDRO RENTERIA GOMEZ ¹

MAHANANDAIAH KURVA ²

MARIA DEL ROCÍO GÁMEZ MONTAÑO ²

1. Universidad de Guanajuato, División de Ciencias Naturales y Exactas, Departamento de Química, Mexico

2. Universidad de Guanajuato, División de Ciencias Naturales y Exactas, Departamento de Química

Abstract

A series of triphenylamine-imidazo[1,2-a]pyridine were synthesized in moderate yields (34-67%) by Groebke–Blackburn–Bienaymé reaction (GBBR) under eco-friendly conditions (20 mol% ammonium chloride catalyst in EtOH). Triphenylamine and imidazo[1,2-a]pyridines are a privileged core exhibited fluorescence and medicinal properties.

Keywords

Groebke–Blackburn–Bienaymé reaction

triphenylamine-imidazo[1,2-a]pyridine

fluorescence

Manuscript

GeneralOrganicSynthesis_8422-done.pdf

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