Microwave-Promoted Synthesis of 4-Arylpyrimidines by Pd-Catalysed Suzuki–Miyaura Coupling of 4-Pyrimidyl Tosylates in Water
Abstract The Suzuki–Miyaura coupling reaction of 4-pyrimidyl tosylates was investigated with aryl, heteroaryl and alkyl boronic acids. The reaction provided 4-substituted pyrimidines in good-to-excellent yields after one-hour microwave irradiation in water at 100 °C. The method constitutes a fast op...
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Georg Thieme Verlag KG
2017-03-01
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Online Access: | http://www.thieme-connect.de/DOI/DOI?10.1055/s-0036-1588810 |
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doaj-b6443a597c94415da133bc01e4411b2c2020-11-25T03:12:45ZengGeorg Thieme Verlag KGSynOpen2509-93962017-03-0101010024002810.1055/s-0036-1588810Microwave-Promoted Synthesis of 4-Arylpyrimidines by Pd-Catalysed Suzuki–Miyaura Coupling of 4-Pyrimidyl Tosylates in WaterJosé Rodríguez-AguilarBeatriz OrdóñezMatías VidalMarcos Caroli RezendeMoisés DomínguezAbstract The Suzuki–Miyaura coupling reaction of 4-pyrimidyl tosylates was investigated with aryl, heteroaryl and alkyl boronic acids. The reaction provided 4-substituted pyrimidines in good-to-excellent yields after one-hour microwave irradiation in water at 100 °C. The method constitutes a fast option for the synthesis of these heterocyclic systems.http://www.thieme-connect.de/DOI/DOI?10.1055/s-0036-1588810suzuki–miyaura couplingpyrimidinestosylatesmicrowave-accelerated synthesiscross-coupling |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
José Rodríguez-Aguilar Beatriz Ordóñez Matías Vidal Marcos Caroli Rezende Moisés Domínguez |
spellingShingle |
José Rodríguez-Aguilar Beatriz Ordóñez Matías Vidal Marcos Caroli Rezende Moisés Domínguez Microwave-Promoted Synthesis of 4-Arylpyrimidines by Pd-Catalysed Suzuki–Miyaura Coupling of 4-Pyrimidyl Tosylates in Water SynOpen suzuki–miyaura coupling pyrimidines tosylates microwave-accelerated synthesis cross-coupling |
author_facet |
José Rodríguez-Aguilar Beatriz Ordóñez Matías Vidal Marcos Caroli Rezende Moisés Domínguez |
author_sort |
José Rodríguez-Aguilar |
title |
Microwave-Promoted Synthesis of 4-Arylpyrimidines by Pd-Catalysed Suzuki–Miyaura Coupling of 4-Pyrimidyl Tosylates in Water |
title_short |
Microwave-Promoted Synthesis of 4-Arylpyrimidines by Pd-Catalysed Suzuki–Miyaura Coupling of 4-Pyrimidyl Tosylates in Water |
title_full |
Microwave-Promoted Synthesis of 4-Arylpyrimidines by Pd-Catalysed Suzuki–Miyaura Coupling of 4-Pyrimidyl Tosylates in Water |
title_fullStr |
Microwave-Promoted Synthesis of 4-Arylpyrimidines by Pd-Catalysed Suzuki–Miyaura Coupling of 4-Pyrimidyl Tosylates in Water |
title_full_unstemmed |
Microwave-Promoted Synthesis of 4-Arylpyrimidines by Pd-Catalysed Suzuki–Miyaura Coupling of 4-Pyrimidyl Tosylates in Water |
title_sort |
microwave-promoted synthesis of 4-arylpyrimidines by pd-catalysed suzuki–miyaura coupling of 4-pyrimidyl tosylates in water |
publisher |
Georg Thieme Verlag KG |
series |
SynOpen |
issn |
2509-9396 |
publishDate |
2017-03-01 |
description |
Abstract
The Suzuki–Miyaura coupling reaction of 4-pyrimidyl tosylates was investigated with aryl, heteroaryl and alkyl boronic acids. The reaction provided 4-substituted pyrimidines in good-to-excellent yields after one-hour microwave irradiation in water at 100 °C. The method constitutes a fast option for the synthesis of these heterocyclic systems. |
topic |
suzuki–miyaura coupling pyrimidines tosylates microwave-accelerated synthesis cross-coupling |
url |
http://www.thieme-connect.de/DOI/DOI?10.1055/s-0036-1588810 |
work_keys_str_mv |
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