Serendipitous discovery of nitrogen bridgehead fused pyridines: photophysical properties and live-cell imaging potential

A novel synthetic route to fluorescent nitrogen bridgehead fused pyridines (NBFPs) was discovered serendipitously during attempts to synthesize a thiazole derivative via a Hantzsch-type thiazole reaction from 2-cyanoethanethioamide and chloroacetone. A mechanism was proposed to rationalize the formation of NBFPs, which guided the subsequent expansion of the reaction scope and optimization of reaction conditions. The scope of the reaction was extended to include arylacetonitriles and esters of 2-(heteroaryl)acetic acids bearing an ortho-positioned pyridine-type nitrogen as a starting material. The structures of selected compounds were confirmed by single-crystal X-ray diffraction. All synthesized NBFPs exhibited pH-sensitive fluorescence and Stokes shifts exceeding 100 nm in several cases. Two compounds, methylthiazole derivative 1 and quinoline derivative 8 , displayed pH-dependent emission suitable for lysosomal labelling. However, live-cell microscopy revealed limited colocalization with lysosomal probe Lysotracker Red, suggesting that these probes may localize to other acidic environments as well. Both compounds showed pronounced spectral responsiveness and fluorescence lifetime variations, indicating potential for use as environment-sensitive intracellular sensors. The methyl thiazole derivative 1 exhibited particularly favourable properties, including high photostability, low background fluorescence, minimal cytotoxicity and polarity sensitivity. These findings position NBFPs as a promising class of fluorophores for live-cell imaging and intracellular sensing applications, and warrant further investigation into their structure–function relationships and environmental responsiveness. • New acid-promoted synthesis of nitrogen bridgehead fused pyridines (NBFPs). • NBFPs exhibit strong pH-dependent emission and large Stokes shifts. • Two derivatives show environment-sensitive fluorescence in live cells. • Compound 1 combines low toxicity, photostability, and low background signal.

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Publication Details

Journal
Journal of Photochemistry and Photobiology A Chemistry
Published
2026-01-26
DOI
https://doi.org/10.1016/j.jphotochem.2026.117068
Primary Topic
Molecular Sensors and Ion Detection
Type
article
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article

Serendipitous discovery of nitrogen bridgehead fused pyridines: photophysical properties and live-cell imaging potential

Janez Mravljak, Jakob Kljun, Hana Kokot, Aljoša Bolje et al.
Journal of Photochemistry and Photobiology A Chemistry
Molecular Sensors and Ion Detection
article

Serendipitous discovery of nitrogen bridgehead fused pyridines: photophysical properties and live-cell imaging potential

Janez Mravljak, Jakob Kljun, Hana Kokot, Aljoša Bolje, Andraž Bevk, Stane Pajk, Lucija Peterlin Mašič, Natalija Trunkelj
article en

Abstract

A novel synthetic route to fluorescent nitrogen bridgehead fused pyridines (NBFPs) was discovered serendipitously during attempts to synthesize a thiazole derivative via a Hantzsch-type thiazole reaction from 2-cyanoethanethioamide and chloroacetone. A mechanism was proposed to rationalize the formation of NBFPs, which guided the subsequent expansion of the reaction scope and optimization of reaction conditions. The scope of the reaction was extended to include arylacetonitriles and esters of 2-(heteroaryl)acetic acids bearing an ortho-positioned pyridine-type nitrogen as a starting material. The structures of selected compounds were confirmed by single-crystal X-ray diffraction. All synthesized NBFPs exhibited pH-sensitive fluorescence and Stokes shifts exceeding 100 nm in several cases. Two compounds, methylthiazole derivative 1 and quinoline derivative 8 , displayed pH-dependent emission suitable for lysosomal labelling. However, live-cell microscopy revealed limited colocalization with lysosomal probe Lysotracker Red, suggesting that these probes may localize to other acidic environments as well. Both compounds showed pronounced spectral responsiveness and fluorescence lifetime variations, indicating potential for use as environment-sensitive intracellular sensors. The methyl thiazole derivative 1 exhibited particularly favourable properties, including high photostability, low background fluorescence, minimal cytotoxicity and polarity sensitivity. These findings position NBFPs as a promising class of fluorophores for live-cell imaging and intracellular sensing applications, and warrant further investigation into their structure–function relationships and environmental responsiveness. • New acid-promoted synthesis of nitrogen bridgehead fused pyridines (NBFPs). • NBFPs exhibit strong pH-dependent emission and large Stokes shifts. • Two derivatives show environment-sensitive fluorescence in live cells. • Compound 1 combines low toxicity, photostability, and low background signal.

Journal of Photochemistry and Photobiology A ChemistryVol. 476
University of Ljubljana (SI), Jožef Stefan Institute (SI)
Life in Land
Openalex Percentile: Top 78%
Molecular Sensors and Ion Detection
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