| Literature DB >> 35145744 |
Lyudmila A Kayukova1, Elmira M Yergaliyeva1, Anna V Vologzhanina2.
Abstract
The reaction of β-(thio-morpholin-1-yl)propio-amidoxime with tosyl chloride in CHCl3 in the presence of DIPEA when heated at 343 K for 8 h afforded the title hydrated salt, C7H14N3S+·Cl-·H2O, in 84% yield. This course of the tosyl-ation reaction differs from the result of tosyl-ation obtained for this substrate at room temperature, when only 2-amino-8-thia-1,5-di-aza-spiro-[4.5]dec-1-ene-5-ammonium tosyl-ate was isolated in 56% yield. The structure of the reaction product was established by physicochemical methods, spectroscopy, and X-ray diffraction. The single-crystal data demonstrated that the previously reported crystal structure of this compound [Kayukova et al. (2021). Chem. J. Kaz, 74, 21-31] had been refined in a wrong space group. In the extended structure, the chloride anions, water mol-ecules and amine groups of the cations form two-periodic hydrogen-bonded networks with the fes topology. © Kayukova et al. 2022.Entities:
Keywords: crystal structure; hydrogen bonding; redetermination; spiro[4.5]dec-1-en-5-ium; tosylation
Year: 2022 PMID: 35145744 PMCID: PMC8819427 DOI: 10.1107/S2056989022000111
Source DB: PubMed Journal: Acta Crystallogr E Crystallogr Commun