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 1H, 13C NMR, 2D-NMR, 15N NMR spectroscopy in addition to elemental analyses. The possible mechanism for the reaction is also discussed.
| Original language | English |
|---|---|
| Article number | 128618 |
| Journal | Journal of Molecular Structure |
| Volume | 1219 |
| DOIs | |
| State | Published - 5 Nov 2020 |
Keywords
- 2-(Oxoindolinylidene)malononitrile
- Spiro[indoline-3,6'[1,3]thiazine
- Thiosemicarbazones
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