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Efficient Synthesis of Hydroxy-Substituted 2-Aminobenzo[d]thiazole-6-carboxylic Acid Derivatives as New Building Blocks in Drug Discovery
Author(s) -
Martina Durcik,
Žan Toplak,
Nace Zidar,
Janez Ilaš,
Anamarija Zega,
D. Kikelj,
Lucíja Peterlin Mašič,
Tihomir Tomašič
Publication year - 2020
Publication title -
acs omega
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.779
H-Index - 40
ISSN - 2470-1343
DOI - 10.1021/acsomega.0c00768
Subject(s) - thiazole , ether , drug discovery , chemistry , molecule , carboxylic acid , combinatorial chemistry , stereochemistry , chemical space , ligand (biochemistry) , organic chemistry , receptor , biochemistry
Benzo[ d ]thiazole is widely used in synthetic and medicinal chemistry, and it is a component of many compounds and drugs that have several different bioactivities. Herein, we describe an elegant pathway for synthesis of methyl 4- and 5-hydroxy-2-amino-benzo[ d ]thiazole-6-carboxylates as building blocks that can be substituted at four different positions on the bicycle and thus offer the possibility to thoroughly explore the chemical space around the molecule studied as a ligand for the chosen target. A series of 12 new compounds was prepared using the described methods and Williamson ether synthesis.

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