2016
DOI: 10.1016/j.tetlet.2016.06.103
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Direct and facile synthesis of 9-aminoacridine and acridin-9-yl-ureas

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Cited by 11 publications
(3 citation statements)
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“…The synthesized compound 3 showed complex NMR spectra (see ESI, Supporting information, Figure S1) which is typical for the 9‐amido acridine derivatives due to their existence in tautomeric equilibrium 41 (Scheme 2).…”
Section: Experimental Section/methodsmentioning
confidence: 99%
“…The synthesized compound 3 showed complex NMR spectra (see ESI, Supporting information, Figure S1) which is typical for the 9‐amido acridine derivatives due to their existence in tautomeric equilibrium 41 (Scheme 2).…”
Section: Experimental Section/methodsmentioning
confidence: 99%
“…Various attempts to functionalize compound 2 at its 16-position proved unsuccessful. For example, our efforts to introduce an amino group, as reported for the conversion of acridine into its 9-amino derivative (urea and sodium hydride in dimethylsulfoxide), 32 only led to the recovery of the starting material. Similarly, our attempt to oxidize 2 into the corresponding acridone, as reported in the case of acridines (sodium hydride in dimethylsulfoxide), 33 failed (starting material recovered, even after heating at 80 °C overnight).…”
Section: Articlementioning
confidence: 99%
“…Compound 6 was synthesized according to the published literature [11] and the characterization data was consistent with the literature.…”
Section: Synthesis Of 2-mercapto-4-hydroxyquinazoline (6)mentioning
confidence: 99%