SYNTHESIS AND PROPERTIES OF SUBSTITUTED ISOXAZOLO[3',4':4,5]THIENO[2,3-<i>b</i>]PYRIDINES
Keywords:
3-aminothieno[2,3-b]pyridines, 3-azidothieno[2,3-b]pyridines, isoxazolo[3',4':4,5]thieno[2,3-b]pyridines, 2-(2-R-ethylthio-2-oxo)-3-pyridyl cyanides, 3-cyano-2(1H)pyridinethionesAbstract
We synthesized derivatives of a novel heterocyclic system, isoxazolo[3',4':4,5]thieno[2,3-b]pyridine by sequential conversions in three steps: isomerization of 2-(2-R-ethylthio-2-oxo)-3-pyridyl cyanides obtained by alkylation from substituted 3-cyano-2(1H)-pyridinethiones by α-halomethyl ketones in alkaline medium, to form 3-aminothieno[2,3-b]pyridines; diazotization of the amino group followed by nucleophilic substitution of the diazonium group by an azido group, bypassing the step of isolating the diazonium salts; and thermolysis of the azides formed.
How to Cite
Vasilin, V. K.; Kaigorodova, E. A.; Firgang, S. I.; Krapivin, G. D. Chem. Heterocycl. Compd. 2004, 40, 377. [Khim. Geterotsikl. Soedin. 2004, 462.]
For this article in the English edition, see DOI 10.1023/B:COHC.0000028636.31350.c0