[1,2,5]Thiadiazolo[3,4-b]pyrazine-5,6(4H,7H)-dione

Fused 1,2,5-chalcogenadiazoles are often used as biologically active compounds and organic optovoltaic materials. [1,2,5]Thiadiazolo[3,4-b]pyrazines are much less studied due to difficulties in their preparation. In this communication, [1,2,5]thiadiazolo[3,4-b]pyrazine-5,6(4H,7H)-dione, a key precursor for the synthesis of 5,6-dihalo-[1,2,5]thiadiazolo[3,4-b]pyrazines, was prepared via condensation of 1,2,5-thiadiazole-3,4-diamine with oxalic acid or oxalyl chloride. The structure of the newly synthesized compound was established by elemental analysis, high-resolution mass spectrometry, 1H and 13C NMR, IR spectroscopy, and mass spectrometry.

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Publication Details

Journal
Molbank
Published
2025-07-01
DOI
https://doi.org/10.3390/m2030
Primary Topic
Synthesis and Characterization of Heterocyclic Compounds
Type
article
Field-Weighted Citation Impact
0.00

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article

[1,2,5]Thiadiazolo[3,4-b]pyrazine-5,6(4H,7H)-dione

Natalia V. Obruchnikova, Олег А. Ракитин, Lidia S. Konstantinova
Molbank
Synthesis and Characterization of Heterocyclic Compounds
article

[1,2,5]Thiadiazolo[3,4-b]pyrazine-5,6(4H,7H)-dione

Natalia V. Obruchnikova, Олег А. Ракитин, Lidia S. Konstantinova
article en

Abstract

Fused 1,2,5-chalcogenadiazoles are often used as biologically active compounds and organic optovoltaic materials. [1,2,5]Thiadiazolo[3,4-b]pyrazines are much less studied due to difficulties in their preparation. In this communication, [1,2,5]thiadiazolo[3,4-b]pyrazine-5,6(4H,7H)-dione, a key precursor for the synthesis of 5,6-dihalo-[1,2,5]thiadiazolo[3,4-b]pyrazines, was prepared via condensation of 1,2,5-thiadiazole-3,4-diamine with oxalic acid or oxalyl chloride. The structure of the newly synthesized compound was established by elemental analysis, high-resolution mass spectrometry, 1H and 13C NMR, IR spectroscopy, and mass spectrometry.

MolbankVol. 2025(3)
N.D. Zelinsky Institute of Organic Chemistry (RU)
Russian Science Foundation
Openalex Percentile: Top 88%
Synthesis and Characterization of Heterocyclic Compounds
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