Abstract
A series of new spiro[indoline-3,6'-[1,3]thiazines] were synthesized in modest yields by refluxing of substituted (1,2-dihydroquinolin-3-yl)-methylene)hydrazinecarbothioamides with 2-(2-oxoindolin-3-ylidene)malononitrile in pyridine as a solvent. The structure assignment of all obtained products has been confirmed by H-1, C-13 NMR, 2D-NMR, N-15 NMR spectroscopy in addition to elemental analyses. The possible mechanism for the reaction is also discussed. (C) 2020 Published by Elsevier B.V.