Abstract
The bromination of 2-amino-and 2-acetylamino-4-(2-furyl)thiazoles has been studied, and it has been shown that bromination takes place first in the furan ring and then, with an excess of bromine, also in the thiazole ring in position 5.
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Perkone, A.Y., Saldabol, N.O. & Miller, S.A. The bromination of 2-amino- and 2-acetylamino-4-(2-furyl)-thiazoles. Chem Heterocycl Compd 5, 372–373 (1969). https://doi.org/10.1007/BF00471147
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DOI: https://doi.org/10.1007/BF00471147