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Synthesis 2004(11): 1799-1805
DOI: 10.1055/s-2004-829127
DOI: 10.1055/s-2004-829127
PAPER
© Georg Thieme Verlag Stuttgart · New York
Synthesis of Mono- and N,N-Disubstituted Thioureas and N-Acylthioureas
Further Information
Received
12 February 2004
Publication Date:
01 July 2004 (online)
Publication History
Publication Date:
01 July 2004 (online)
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.
Key words
thioureas - benzotriazole - acylations - nucleophilic substitution - substituent effects
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