A new and facile synthetic approach to substituted 2-thioxoquinazolin-4-ones by the annulation of a pyrimidine derivative
A new and facile synthesis of 2-thioxoquinazolin-4-ones by introducing a benzenoid system in the pyrimidine moiety by reacting ethoxymethylene derivatives of 1,3-diarylthiobarbituric acids (DTBA) with active methylene compounds, such as malononitrile and ethyl cyanoacetate, in presence of ZnCl2 has...
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Format: | Article |
Language: | English |
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Beilstein-Institut
2010-11-01
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Series: | Beilstein Journal of Organic Chemistry |
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Online Access: | https://doi.org/10.3762/bjoc.6.120 |
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author | Nimalini D. Moirangthem Warjeet S. Laitonjam |
author_facet | Nimalini D. Moirangthem Warjeet S. Laitonjam |
author_sort | Nimalini D. Moirangthem |
collection | DOAJ |
description | A new and facile synthesis of 2-thioxoquinazolin-4-ones by introducing a benzenoid system in the pyrimidine moiety by reacting ethoxymethylene derivatives of 1,3-diarylthiobarbituric acids (DTBA) with active methylene compounds, such as malononitrile and ethyl cyanoacetate, in presence of ZnCl2 has been developed. |
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format | Article |
id | doaj.art-418578a3ff744fec91b14c5f5ce8f4a1 |
institution | Directory Open Access Journal |
issn | 1860-5397 |
language | English |
last_indexed | 2024-12-17T00:18:58Z |
publishDate | 2010-11-01 |
publisher | Beilstein-Institut |
record_format | Article |
series | Beilstein Journal of Organic Chemistry |
spelling | doaj.art-418578a3ff744fec91b14c5f5ce8f4a12022-12-21T22:10:38ZengBeilstein-InstitutBeilstein Journal of Organic Chemistry1860-53972010-11-01611056106010.3762/bjoc.6.1201860-5397-6-120A new and facile synthetic approach to substituted 2-thioxoquinazolin-4-ones by the annulation of a pyrimidine derivativeNimalini D. Moirangthem0Warjeet S. Laitonjam1Department of Chemistry, Manipur University, Canchipur 795 003, Manipur, IndiaDepartment of Chemistry, Manipur University, Canchipur 795 003, Manipur, IndiaA new and facile synthesis of 2-thioxoquinazolin-4-ones by introducing a benzenoid system in the pyrimidine moiety by reacting ethoxymethylene derivatives of 1,3-diarylthiobarbituric acids (DTBA) with active methylene compounds, such as malononitrile and ethyl cyanoacetate, in presence of ZnCl2 has been developed.https://doi.org/10.3762/bjoc.6.120benzenoidethylcyanoacetatemalononitrilepyrimidine2-thioxoquinazolin-4-ones |
spellingShingle | Nimalini D. Moirangthem Warjeet S. Laitonjam A new and facile synthetic approach to substituted 2-thioxoquinazolin-4-ones by the annulation of a pyrimidine derivative Beilstein Journal of Organic Chemistry benzenoid ethylcyanoacetate malononitrile pyrimidine 2-thioxoquinazolin-4-ones |
title | A new and facile synthetic approach to substituted 2-thioxoquinazolin-4-ones by the annulation of a pyrimidine derivative |
title_full | A new and facile synthetic approach to substituted 2-thioxoquinazolin-4-ones by the annulation of a pyrimidine derivative |
title_fullStr | A new and facile synthetic approach to substituted 2-thioxoquinazolin-4-ones by the annulation of a pyrimidine derivative |
title_full_unstemmed | A new and facile synthetic approach to substituted 2-thioxoquinazolin-4-ones by the annulation of a pyrimidine derivative |
title_short | A new and facile synthetic approach to substituted 2-thioxoquinazolin-4-ones by the annulation of a pyrimidine derivative |
title_sort | new and facile synthetic approach to substituted 2 thioxoquinazolin 4 ones by the annulation of a pyrimidine derivative |
topic | benzenoid ethylcyanoacetate malononitrile pyrimidine 2-thioxoquinazolin-4-ones |
url | https://doi.org/10.3762/bjoc.6.120 |
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