Functional sulfur-containing compounds

The Thorpe-Ziegler intramolecular cyclization of 2-RCH₂S-, 2-RCH₂S(O)-, and 2-RCH₂SO₂-substituted nicotinic acid esters and nitriles (R is alkyl, aryl, and 2-thienyl) upon the action of potassium tert-butoxide has been studied. The reaction results in the formation of the corresponding 2-R-substituted 3-aminothieno2,3-b]pyridines, 3-aminothieno2,3-b]pyridine 1-oxides, and 3-aminothieno2,3-b]pyridine 1,1-dioxides with the reaction taking place only in the case if R is aryl or 2-thienyl. Methyl esters of 2-RCH₂S-, 2-RCH₂S(O)-, and 2-RCH₂SO₂-substituted nicotinic acids also undergo the intramolecular cyclization of the Dieckmann type to form the corresponding 2-R-substituted 3-hydroxythieno2,3-b]pyridines, thieno2,3-b]pyridin-3(2H)-one 1-oxides, and thieno2,3-b]pyridin-3(2H)-one 1,1-dioxides. Such a reaction takes place for all the R groups except when R = AlkCH₂S and AlkCH₂S(O).