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Abstract
The reaction of N-(2-cyanophenyl) benzimidoyl chloride with reagents containing a thioamide moiety,i.e.thioacetamide, benzylthiourea, symmetrical
dialkyl- and diarylthioureas gave different cyclic products: 3,1-benzothiazine, 1,3,5-benzotriazocine and quinazoline. The reaction pathways of prepared compounds are discussed.
References
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