4-(10-METHYL-10H-PHENOTHIAZIN-3-YL)-1,4-DIHYDROPYRIDINES, 4,5-DIHYDROINDENO[1,2-<i>b</i>]- AND 5,5-DIOXO-4,5-DIHYDROBENZOTHIENO[3,2-<i>b</i>]PYRIDINES
DOI:
https://doi.org/10.1007/7687Keywords:
10-methyl-10H-phenothiazin-3-carbaldehyde, 1, 4-dihydropyridine, Hantzsch synthesis, 4-(10-methyl-10H-phenothiazin-3-yl)-5-oxo-1H-4, 5-dihydroindeno[1, 2-b]pyridineAbstract
Different modifications of the Hantzsch synthesis using 10-methyl-10H-phenothiazine-3-carbaldehyde gave 4-(10-methyl-10H-phenothiazin-3-yl)-substituted 1,4-dihydropyridine-3,5-di-, 5-oxo-4,5-dihydro-1H-indeno[1,2-b]pyridine-, and 5,5-dioxo-4,5-dihydro-1H-5λ<sup>6</sup>-benzo[4,5]thieno[3,2-b]pyridine-3-carboxylic esters.How to Cite
Vigante, B.; Tirzitis, G.; Tirzite, D.; Chekavichus, B.; Uldrikis, J.; Sobolev, A.; Duburs, G. Chem. Heterocycl. Compd. 2007, 43, 225. [Khim. Geterotsikl. Soedin. 2007, 280.]
For this article in the English edition see DOI 10.1007/s10593-007-0035-8