Synthesis of 2-phenylbenzothiazoles
Double C-S bond formation Via C-H bond functionalization Synthesis of benzothiazoles and naphtho[2,1- d] thiazoles from N -substituted arylamines and elemental sulfur
Table 3
To further expand the substrate scope, arylamines such as anilines, 1-naphthylamines, and 2-anthranylamine instead of 2-naphthylamines were examined in this cyclization reaction (Table 3). Under optimized reaction conditions, only electron-donating groups such as methyl, methoxyl, and N, N-dimethylamino substituted anilines could smoothly be transformed into the target products, and a close examination of the results shows that the product yield decreases in the order: (Me)2N-> MeO- > Me-.
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