A Gram Scale Synthesis of 3,4-Dihalogen Substituted 1,8-Naphthalimides

A general protocol for the synthesis of 3,4-dihalogen substituted 1,8-naphthalimides is proposed, starting from available and cheap 1,8-naphthalic anhydride. The reported new compounds have only bromine or chlorine atoms as substituents, in contrast to the known iodo-containing analogues. This is an advantage in possible aryl nucleophilic substitution or cross-coupling modifications, making them interesting and important building-block molecules in naphthalimide chemistry. Although the procedure includes five synthetic steps, they are quick and straightforward. The overall yields are relatively high (48–62%), and only one column of chromatographic purification is needed. All the reactions were carried out on a multigram scale to allow the target building-block compounds to be obtained in sufficient amounts for further derivatizations.

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Publication Details

Journal
Molbank
Published
2024-11-18
DOI
https://doi.org/10.3390/m1918
Citations
1
Primary Topic
Molecular Sensors and Ion Detection
Type
article
Field-Weighted Citation Impact
0.24

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article

A Gram Scale Synthesis of 3,4-Dihalogen Substituted 1,8-Naphthalimides

Irena Zagranyarska, Yulian Zagranyarski, Monika Mutovska, Zlatina Vlahova et al.
1 citations
Molbank
Molecular Sensors and Ion Detection
0.24
article

A Gram Scale Synthesis of 3,4-Dihalogen Substituted 1,8-Naphthalimides

Irena Zagranyarska, Yulian Zagranyarski, Monika Mutovska, Zlatina Vlahova, Stanimir Stoyanov, Natali Simeonova, Denitsa Anastasova
article en
1 citations

Abstract

A general protocol for the synthesis of 3,4-dihalogen substituted 1,8-naphthalimides is proposed, starting from available and cheap 1,8-naphthalic anhydride. The reported new compounds have only bromine or chlorine atoms as substituents, in contrast to the known iodo-containing analogues. This is an advantage in possible aryl nucleophilic substitution or cross-coupling modifications, making them interesting and important building-block molecules in naphthalimide chemistry. Although the procedure includes five synthetic steps, they are quick and straightforward. The overall yields are relatively high (48–62%), and only one column of chromatographic purification is needed. All the reactions were carried out on a multigram scale to allow the target building-block compounds to be obtained in sufficient amounts for further derivatizations.

MolbankVol. 2024(4)
Bulgarian Academy of Sciences (BG), Institute of Organic Chemistry with Centre of Phytochemistry (BG), Institute of Molecular Biology (BG), Sofia University "St. Kliment Ohridski" (BG)
European Commission, Bulgarian National Science Fund
Openalex Percentile: Top 48%
Molecular Sensors and Ion Detection
0.24
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