Synthesis of mono-and N, N-disubstituted thioureas and N-acylthioureas
AR Katritzky, N Kirichenko, BV Rogovoy, J Kister…
Index: Katritzky, Alan R.; Kirichenko, Nataliya; Rogovoy, Boris V.; Kister, Jeremy; Tao, Hui Synthesis, 2004 , # 11 p. 1799 - 1805
Full Text: HTML
Citation Number: 13
Abstract
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, fj and acyl-5a-f, ik or arylaminocarbonyl-5g, h (benzotriazol-1-yl) carboximidamides with hydrogen sulfide give the corresponding thioureas 3a-d, fj, and N- acylthioureas 6a-f, ik or N-carbamoylthioureas 6g, h, respectively.
Related Articles:
[Kodomari, Mitsuo; Suzuki, Masato; Tanigawa, Keiko; Aoyama, Tadashi Tetrahedron Letters, 2005 , vol. 46, # 35 p. 5841 - 5843]
[Herr; Kuhler; Meckler; Opalka Synthesis, 2000 , # 11 p. 1569 - 1574]
[Ouwerkerk, Niels; Van Boom, Jacques; Lugtenburg, Johan; Raap, Jan European Journal of Organic Chemistry, 2002 , # 14 p. 2356 - 2362]
[Mohanta, Pramod K.; Dhar, Sanchita; Samal; Ila; Junjappa Tetrahedron, 2000 , vol. 56, # 4 p. 629 - 637]
[Journal of Medicinal Chemistry, , vol. 48, # 7 p. 2509 - 2517]