Synthesis of Heterocycles Based on 4,5-Dichlorophthalonitrile

The SNAr reaction of 4,5-dichlorophthalonitrile with various bifunctional nucleophiles was carried out in anhydrous DMF in the presence of K2CO3 as a deprotonating agent. It was shown that 4,5-dichlorophthalonitrile can be successfully employed in the synthesis of heterocyclic compounds; however, in some cases, these reactions may either give product mixtures or result in an unexpected rearrangement.

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Publication Details

Journal
Russian Journal of Organic Chemistry
Published
2025-05-01
DOI
https://doi.org/10.1134/s1234567825600932
Primary Topic
Synthesis and biological activity
Type
article
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article

Synthesis of Heterocycles Based on 4,5-Dichlorophthalonitrile

V. V. Bukhalin, V. V. Aleksandriiskii, V. L. Baklagin, И. Г. Абрамов
Russian Journal of Organic Chemistry
Synthesis and biological activity
article

Synthesis of Heterocycles Based on 4,5-Dichlorophthalonitrile

V. V. Bukhalin, V. V. Aleksandriiskii, V. L. Baklagin, И. Г. Абрамов
article en

Abstract

The SNAr reaction of 4,5-dichlorophthalonitrile with various bifunctional nucleophiles was carried out in anhydrous DMF in the presence of K2CO3 as a deprotonating agent. It was shown that 4,5-dichlorophthalonitrile can be successfully employed in the synthesis of heterocyclic compounds; however, in some cases, these reactions may either give product mixtures or result in an unexpected rearrangement.

Russian Journal of Organic ChemistryVol. 61(5)
Ivanovo State University of Chemistry and Technology (RU), Yaroslavl State Technical University (RU)
Openalex Percentile: Top 87%
Synthesis and biological activity
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