Literature DB >> 35145744

Redetermination of the structure of 2-amino-8-thia-1,5-di-aza-spiro-[4.5]dec-1-en-5-ium chloride monohydrate.

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


  9 in total

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Authors:  Lyudmila Kayukova; Anna Vologzhanina; Kaldybai Praliyev; Gulnur Dyusembaeva; Gulnur Baitursynova; Asem Uzakova; Venera Bismilda; Lyailya Chingissova; Kydyrmolla Akatan
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  9 in total
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1.  Reaction Products of β-Aminopropioamidoximes Nitrobenzenesulfochlorination: Linear and Rearranged to Spiropyrazolinium Salts with Antidiabetic Activity.

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Journal:  Molecules       Date:  2022-03-28       Impact factor: 4.411

  1 in total

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