Abstract
treatment of 2-mercapto benzothiazole with hydrazine hydrate to obtain the intermediate of 2-hydrazinobenzothiazole (S1). A series of (S1-S13) compound has been prepared after treatment compound (S1) with phthalic anhydride two derivatives of pyridazinone and phthalazinone has been obtained (S3). The reaction (S1) with phenylisothiocyanate and ethyl chloroacetate afforded 3-phenyl-1, 3-thiazolidin-2,4-dione-2-(benzothiazole-2yl-hydrazone) (S13). The reaction of (S1) with aromatic aldehyde synthesized azomethines (S6-S8) then treated with mercaptoacetic acid to obtained (S9-S11). The reaction of (S1) with p-bromophenacyl bromide afforded another 1, 2, 4-triazole (S2). The reaction between (S1) and chloroacetic acid gave (S4). The compound (S4) been reacted with ortho- A minoaniline result the benzimidazole (S5). Using M.P and FT-IR to test all compounds and using H1-NMR & C13-NMR spectra for some of them.
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Al-Khazraji, S. I. C. (2020). Synthesis and characterization of some heterocyclic compounds derived from 2-mercapto benzothiazole. In AIP Conference Proceedings (Vol. 2290). American Institute of Physics Inc. https://doi.org/10.1063/5.0027534
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