Synthesis of mono- and N,N-disubstituted thioureas and N-acylthioureas

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Abstract

1-Benzotriazole-1-carbothioamide (2), prepared from 1-cyanobenzotriazole (1) and hydrogen sulfide, reacts with amines to give thioureas 3a-e. Reactions of (benzotriazol-1-yl)carboximidamides 4a-d,f-j and acyl- 5a-f,i-k or arylaminocarbonyl- 5g,h (benzotriazol-1-yl)carboximidamides with hydrogen sulfide give the corresponding thioureas 3a-d,f-j, and N-acylthioureas 6a-f,i-k or N-carbamoylthioureas 6g,h, respectively.

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Katritzky, A. R., Kirichenko, N., Rogovoy, B. V., Kister, J., & Tao, H. (2004). Synthesis of mono- and N,N-disubstituted thioureas and N-acylthioureas. Synthesis, (11), 1799–1805. https://doi.org/10.1055/s-2004-829127

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