The reaction of β-(thio-morpholin-1-yl)propio-amidoxime with tosyl chloride in CHCl in the presence of DIPEA when heated at 343 K for 8 h afforded the title hydrated salt, CHNS·Cl·HO, 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 (2021). , , 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 topology.
Download full-text PDF |
Source |
---|---|
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8819427 | PMC |
http://dx.doi.org/10.1107/S2056989022000111 | DOI Listing |
Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!