6533b857fe1ef96bd12b4d4a
RESEARCH PRODUCT
Synthesis and characterization of a new spirooxindole grafted pyrrolidino/piperidine moiety
El Sayed H. El AshrySaied M. SolimanMatti HaukkaYasmine M. Abdel AzizGehad LotfyAssem BarakatEl Sayed H. El TamanyMohamed M. Saidsubject
chemistry.chemical_compoundCrystallographychemistryHydrogen bondChemical polarityIsatinStackingProton NMRCyclohexanoneMoietyGeneral MedicinePiperidinedescription
In this text, we synthesized and characterized a new spirooxindole grafted pyrrolidino/piperidine moieties. The new hit obtained via one-pot reaction of the chalcone based cyclohexanone with the isatin and (R)-piperidine-2-carboxylic acid in MeOH under reflux for 48 h. The compound exclusively obtained in regio-selective and diastereo-selective manner. The chemical feature of the target compound is confirmed by 1H NMR and 13C NMR spectroscopy. In addition, we reported for the first time the X-ray single crystal structure of isatin. Its molecular packing depends mainly on strong O…H hydrogen bonds and π-π stacking interactions as well as weak H…H and H…C contacts. Using DFT calculations, isatin is a polar molecule with a net dipole moment of 5.912 Debye. Also, the calculated structure agreed very well with the experimental one. The charge distribution at the different atomic sites is calculated using NBO calculations.
year | journal | country | edition | language |
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2021-01-01 | Records of Pharmaceutical and Biomedical Sciences |