The title compound, C10H11NOS2, crystallizes with Z' = 2 in space group C2/c. The molecules are linked by two N-H...S hydrogen bonds [H...S = 2.60 and 2.62 A, N...S = 3.350 (2) and 3.490 (2) A, and N-H...S = 143 and 172 degrees] into two distinct types of R(2)2(8) dimer, viz. one generated by inversion and the other by a twofold rotation axis. A single C-H...pi(arene) hydrogen bond links the two types of dimer into chains.
Molecules of the title compound, C10H10ClNOS2, are linked into C4 chains by an N-H...O hydrogen bond [H...O = 2.16 A, N...O = 3.013 (3) A and N-H...O = 176 degrees ], and the chains are linked into sheets by a centrosymmetric pi-pi stacking interaction.
Regioselective Synthesis of Novel 4-Aryl-2-ethylthio-7-methyl Pyrazolo[1,5-a]-[1,3,5]-triazines. -The title compounds (III) represent purine analogues and are of biological interest. They can be synthesized either directly starting from the dithiocarbonates (I) or by a two-step sequence starting from isothiocyanates (IV) which includes the thiourea derivatives (V). Their reaction with EtBr in DMF at room temperature proceeds via intermediates of type (VII). -(INSUASTY*, H.; ESTRADA, M.; CORTES, E.; QUIROGA, J.; INSUASTY, B.; ABONIA, R.; NOGUERAS, M.; COBO, J.; Tetrahedron Lett. 47 (2006) 31, 5441-5443; Dep. Quim., Univ. Narino, Pasto, Colombia; Eng.) -S. Adam 46-205
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.