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Synthesis of Mono- and N,N<i>-</i>Disubstituted Thioureas and <i>N</i>-Acylthioureas
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2004
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BiosynthesisArylaminocarbonyl- 5GEngineeringOrganic ChemistryStereoselective SynthesisHeterocycle ChemistryPharmacologyHydrogen SulfideSynthetic ChemistryBiomolecular EngineeringN-carbamoylthioureas 6GNatural Product Synthesis
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.