A novel route to acyl ureas: Syntheses of N-[5-(2-chlorophenyl)-2- furoyl]-N'-arylthioureas and ureas

Article abstract of DOI:10.1080/00397910008087430

A novel route to acyl ureas is described. Reaction of 5-(2- chlorophenyl)-2-furoyl chloride with ammonium thiocyanate first, then arylamine under phase transfer catalysis gives N-[5-(2-chlorophenyl)-2- furoyl]-N'-arylthioureas (1a-o). Compounds 1a-o on ox

Full text of DOI:10.1080/00397910008087430

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Synthetic Communications: An
International Journal for Rapid
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Organic Chemistry
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A Novel Route to Acyl
Ureas: Syntheses of N-[5-(2-
Chlorophenyl)-2-Furoyl]-N'-
Arylthioureas and Ureas
Zheng Li a , Xicun Wang a , Yuxia Da a & Jichou Chen
a
a Department of Chemistry , Northwest Normal
University, Lanzhou , Gansu, 730070, P.R., China
Published online: 04 Dec 2007.
To cite this article: Zheng Li , Xicun Wang , Yuxia Da & Jichou Chen (2000) A Novel
Route to Acyl Ureas: Syntheses of N-[5-(2-Chlorophenyl)-2-Furoyl]-N'-Arylthioureas and
Ureas, Synthetic Communications: An International Journal for Rapid Communication
of Synthetic Organic Chemistry, 30:14, 2635-2645, DOI: 10.1080/00397910008087430
To link to this article: http://dx.doi.org/10.1080/00397910008087430
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