HETEROCYCLIC ANALOGS OF 5,12-NAPHTHACENEQUINONE. 6. SYNTHESIS OF 4,11-DIMETHOXY DERIVATIVES OF ANTHRA[2,3-<i>b</i>]THIOPHENE-5,10-DIONE AND ANTHRA[2,3-<i>d</i>]ISOTHIAZOLE-5,10-DIONE
DOI:
https://doi.org/10.1007/7548Keywords:
3-chloro-1, 4-dimethoxyanthracene-9, 10-dione-2-carbaldehyde, 4, 11-dimethoxyanthra[2, 3-d]isothiazole-5, 10-dione, 3-b]thiophene-5, 10-dione derivatives, fluorescence spectra, Stokes shiftAbstract
Condensation of 2-formyl- or 2-cyano-3-chloro-1,4-dimethoxyanthraquinone with methyl thioglycolate in the presence of base gave methyl 4,11-dimethoxyanthra[2,3-b]thiophene-5,10-dione-2-carboxylate and its 3-amino derivative respectively. Hydrolysis of the ester group in methyl 4,11-dimethoxy-anthra[2,3-b]thiophene-5,10-dione-2-carboxylate and subsequent decarboxylation of the carboxylic acid formed gave 4,11-dimethoxyanthra[2,3-b]thiophene-5,10-dione. Condensation of 3-chloro-2-formyl-1,4-dimethoxyanthraquinone with ammonia in the presence of sulfur gave 4,11-dimethoxy-anthra[2,3-d]isothiazole-5,10-dione.How to Cite
Shchekotikhin, A. E.; Lusikov, Yu. N.; Buyanov, V. N.; Preobrazhenskaya, M. N. Chem. Heterocycl. Compd. 2007, 43, 439. [Khim. Geterotsikl. Soedin. 2007, 538.]
For this article in the English edition see DOI 10.1007/s10593-007-0063-4