Synthesis of new 3-(2-aminothiazol-4-yl)-4-hydroxy-2H-chromen-2-one derivatives
Aminothiazole derivatives of 4-hydroxy-2H-chromen-2-one were prepared by the Hantzsch reaction1 using 3-(2-bromoacetyl)-4-hydroxy-2H-chromen-2-one and thiourea derivatives. Starting compound for this synthesis 3-(2-bromoacetyl)-4-hydroxy- 2H-chromen-2-one (1) was prepared previously.2 Also, for this...
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doaj-cbff64da4b2a49a394ad7fd9a0e1ba4d2020-12-24T14:30:36ZengSerbian Chemical Society Journal of the Serbian Chemical Society0352-51391820-74212006-01-0171658158510.2298/JSC0606581S0352-51390606581SSynthesis of new 3-(2-aminothiazol-4-yl)-4-hydroxy-2H-chromen-2-one derivativesSukdolak S.0Vuković N.1Solujić S.2Milošev M.3Manojlović N.4Krstić Lj.5Prirodno-matematički fakultet, Institut za hemiju, KragujevacPrirodno-matematički fakultet, Institut za hemiju, KragujevacPrirodno-matematički fakultet, Institut za hemiju, KragujevacPrirodno-matematički fakultet, Institut za hemiju, KragujevacPrirodno-matematički fakultet, Institut za hemiju, KragujevacIHTM, Centar za hemiju, BeogradAminothiazole derivatives of 4-hydroxy-2H-chromen-2-one were prepared by the Hantzsch reaction1 using 3-(2-bromoacetyl)-4-hydroxy-2H-chromen-2-one and thiourea derivatives. Starting compound for this synthesis 3-(2-bromoacetyl)-4-hydroxy- 2H-chromen-2-one (1) was prepared previously.2 Also, for this synthesis we used thiourea derivatives (2a-j) as compounds which possess groups with biological activity. Reactions are carried out in refluxing ethanol for a period of 30 - 45 min. Final products (3a-j) are obtained in a high yield. Chemical structure of the obtained compounds was confirmed by elemental and structural analysis (IR and 1H NMR spectroscopy).http://www.doiserbia.nb.rs/img/doi/0352-5139/2006/0352-51390606581S.pdfhantzsch reaction3-(2-aminothiazol-4-yl)-4-hydroxy-2h-chromen-2-onederivatives |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Sukdolak S. Vuković N. Solujić S. Milošev M. Manojlović N. Krstić Lj. |
spellingShingle |
Sukdolak S. Vuković N. Solujić S. Milošev M. Manojlović N. Krstić Lj. Synthesis of new 3-(2-aminothiazol-4-yl)-4-hydroxy-2H-chromen-2-one derivatives Journal of the Serbian Chemical Society hantzsch reaction 3-(2-aminothiazol-4-yl)-4-hydroxy-2h-chromen-2-onederivatives |
author_facet |
Sukdolak S. Vuković N. Solujić S. Milošev M. Manojlović N. Krstić Lj. |
author_sort |
Sukdolak S. |
title |
Synthesis of new 3-(2-aminothiazol-4-yl)-4-hydroxy-2H-chromen-2-one derivatives |
title_short |
Synthesis of new 3-(2-aminothiazol-4-yl)-4-hydroxy-2H-chromen-2-one derivatives |
title_full |
Synthesis of new 3-(2-aminothiazol-4-yl)-4-hydroxy-2H-chromen-2-one derivatives |
title_fullStr |
Synthesis of new 3-(2-aminothiazol-4-yl)-4-hydroxy-2H-chromen-2-one derivatives |
title_full_unstemmed |
Synthesis of new 3-(2-aminothiazol-4-yl)-4-hydroxy-2H-chromen-2-one derivatives |
title_sort |
synthesis of new 3-(2-aminothiazol-4-yl)-4-hydroxy-2h-chromen-2-one derivatives |
publisher |
Serbian Chemical Society |
series |
Journal of the Serbian Chemical Society |
issn |
0352-5139 1820-7421 |
publishDate |
2006-01-01 |
description |
Aminothiazole derivatives of 4-hydroxy-2H-chromen-2-one were prepared by the Hantzsch reaction1 using 3-(2-bromoacetyl)-4-hydroxy-2H-chromen-2-one and thiourea derivatives. Starting compound for this synthesis 3-(2-bromoacetyl)-4-hydroxy- 2H-chromen-2-one (1) was prepared previously.2 Also, for this synthesis we used thiourea derivatives (2a-j) as compounds which possess groups with biological activity. Reactions are carried out in refluxing ethanol for a period of 30 - 45 min. Final products (3a-j) are obtained in a high yield. Chemical structure of the obtained compounds was confirmed by elemental and structural analysis (IR and 1H NMR spectroscopy). |
topic |
hantzsch reaction 3-(2-aminothiazol-4-yl)-4-hydroxy-2h-chromen-2-onederivatives |
url |
http://www.doiserbia.nb.rs/img/doi/0352-5139/2006/0352-51390606581S.pdf |
work_keys_str_mv |
AT sukdolaks synthesisofnew32aminothiazol4yl4hydroxy2hchromen2onederivatives AT vukovicn synthesisofnew32aminothiazol4yl4hydroxy2hchromen2onederivatives AT solujics synthesisofnew32aminothiazol4yl4hydroxy2hchromen2onederivatives AT milosevm synthesisofnew32aminothiazol4yl4hydroxy2hchromen2onederivatives AT manojlovicn synthesisofnew32aminothiazol4yl4hydroxy2hchromen2onederivatives AT krsticlj synthesisofnew32aminothiazol4yl4hydroxy2hchromen2onederivatives |
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1724371805212246016 |