Abstract
The alkylation of 2-amino-6-nitro- and 2,6-diaminobenzothiazoles by ethylene chlorohydrin has been studied. A comparative analysis has been made of the composition of these reaction mixtures and of those obtained from other 2-aminobenzothiazoles using this reaction. The structure of the synthesized compounds was confirmed using IR and 1H NMR spectroscopy, mass spectrometry, and X-ray diffraction and via alternative syntheses.
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Ambartsumova, R.F., Tashkhodzhaev, B., Antipin, M.Y. et al. Regularities and Features of the Reaction of 2-Amino-6-nitro- and 2,6-Diaminobenzothiazoles with Ethylene Chlorohydrin. Chemistry of Heterocyclic Compounds 38, 1397–1405 (2002). https://doi.org/10.1023/A:1022194829594
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DOI: https://doi.org/10.1023/A:1022194829594