Synthesis of Mono- and N,N-Disubstituted Thioureas and N-Acylthioureas

Alan R. Katritzky; Nataliya Kirichenko; Boris V. Rogovoy; Jeremy Kister; Hui Tao

doi:10.1055/s-2004-829127

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Synthesis of Mono- and N,N-Disubstituted Thioureas and N-Acylthioureas

Journal article

Peer reviewed

Synthesis of Mono- and N,N-Disubstituted Thioureas and N-Acylthioureas

Alan R. Katritzky, Nataliya Kirichenko, Boris V. Rogovoy, Jeremy Kister and Hui Tao

Synthesis (Stuttgart), Vol.2004(11), pp.1799-1805

03/08/2004

DOI: https://doi.org/10.1055/s-2004-829127

Abstract

paper

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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Title: Synthesis of Mono- and N,N-Disubstituted Thioureas and N-Acylthioureas
Creators - without role: Alan R. Katritzky
Nataliya Kirichenko
Boris V. Rogovoy
Jeremy Kister
Hui Tao
Publication Details: Synthesis (Stuttgart), Vol.2004(11), pp.1799-1805
Identifiers: 9939590608331
Academic Unit: King Abdulaziz University
Language: English
Resource Type: Journal article