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A Domino Process for the Sustainable Synthesis of Quinazolin-4(3H)-ones with Direct Chemo- and Regioselective Bromination
Abstract An efficient approach is reported for the direct and sustainable construction of quinazolin-4(3 H )-ones through a three-component reaction of isatoic anhydride, primary amines, and bromoacetyl bromide or chloroacetyl chloride in the presence of K 2 CO 3 in DMSO. With bromoacetyl bromide, m...
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Published in: | Synlett 2018-09, Vol.29 (15), p.2046-2050 |
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Main Authors: | , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that cite this one |
Online Access: | Get full text |
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Summary: | Abstract
An efficient approach is reported for the direct and sustainable construction of quinazolin-4(3
H
)-ones through a three-component reaction of isatoic anhydride, primary amines, and bromoacetyl bromide or chloroacetyl chloride in the presence of K
2
CO
3
in DMSO. With bromoacetyl bromide, mono- or dibrominated quinazolinone scaffolds were obtainable in a chemo- and regioselective manner. |
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ISSN: | 0936-5214 1437-2096 |
DOI: | 10.1055/s-0037-1610226 |