Abstract
The corresponding 2-(2-furyl)- and 2-[β-(2-furyl)vinyl]imida zo[4,5-f]quinolines were obtained by condensation of 5,6-diaminoquinoline and 5-amino-6-rnethylaminoquinoline with furfural, furylacrolein, and their 5-bromo and 5-nitro derivatives and also with the hydrochlorides of imino esters of furancarboxylic and furylacrylic acids. Alkylation, acetylation, nitration, and substitution of the halogen in the furan ring by a nitro group were studied.
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Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 4, pp. 440–442, April, 1973.
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Pozharskii, F.T., Oleinikova, L.Y. Synthesis and transformations of 2-(2-furyl)- and 2-[β-(2-furyl)vinyl]imidazo[4,5-f]quinolines. Chem Heterocycl Compd 9, 406–408 (1973). https://doi.org/10.1007/BF00471512
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DOI: https://doi.org/10.1007/BF00471512