Abstract
2-Alkyl-3-(1-methyl-2-benzimidazolyl)-7-acyloxychromones were synthesized by the reaction of substituted or unsubstituted 2-(2,4-dihydroxyphenacyl)-1-methylbenzimidazoles with the acid chlorides and anhydrides of carboxylic acids. The products were converted into 2-alkyl-7-hydroxychromones as a result of acid hydrolysis.
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Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 1, pp. 26–30, January, 2008.
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Frasinyuk, M.S., Khilya, V.P. Chemistry of hetero analogs of isoflavones 25. Synthesis of 2-alkyl-3-(2-benzimidazolyl)-chromones. Chem Heterocycl Comp 44, 20–24 (2008). https://doi.org/10.1007/s10593-008-0015-7
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DOI: https://doi.org/10.1007/s10593-008-0015-7