New polysubstituted monoterpenic thiazolidinones: synthesis, spectroscopic and crystal structure studies

The synthesis of three new polysubstituted monoterpenic thiazolidin-4-ones, namely (Z)-3-methyl-2-{(E)-[(1R, 4R)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-yl-idene]hydrazinylidene}thiazolidin-4-one, C14H21N3OS (2), (2Z, 5Z)-5-[(dimethylamino)methylidene]-2-{(E)-[(1R, 4R)-1,7,7-trimethylbicyclo[2.2.1]heptan2- ylidene]hydrazinylidene}thiazolidin-4-one, C16H24N4OS (3), and (2Z, 5Z)-5[(dimethylamino)methylidene]-3-methyl-2-{(E)-[(1R, 4R)-1,7,7-trimethylbicyclo[ 2.2.1]heptan-2-ylidene]hydrazinylidene}thiazolidin-4-one, C17H26N4OS (4), is reported, starting from the corresponding thiosemicarbazones obtained from naturally occurring (R)-camphor. All the newly obtained thiazolidin-4-ones have been fully characterized by HRMS and H-1 and C-13 (1D and 2D) NMR spectroscopy. Two of them, i.e. 2 and 3, were identified by single-crystal X- ray crystallography, confirming the synthetic pathway and the spectroscopic analyses. In 3, there are two roughly identical molecules within the asymmetric unit with the same absolute configuration. These two molecules are linked through N-H center dot center dot center dot O hydrogen bonds, building an R-2(2)(8) graph-set motif.