Other formats:
BibTeX
LaTeX
RIS
@inproceedings{386931,
author = {Mohamed, Walid Fathalla and Pazdera, Pavel},
address = {Pardubice},
booktitle = {XXVth Conference of Organic Chemists},
edition = {1},
keywords = {Quinazolines; Thioureas; Benzimidoyl isothiocyanates},
language = {eng},
location = {Pardubice},
isbn = {80-7194-349-5},
pages = {KS 8},
publisher = {Publishing House of Pardubice University},
title = {The Synthesis of New N3-Aryl-N1-(2-phenylquinazolin-4-yl)thioureas},
year = {2001}
}
TY - JOUR
ID - 386931
AU - Mohamed, Walid Fathalla - Pazdera, Pavel
PY - 2001
TI - The Synthesis of New N3-Aryl-N1-(2-phenylquinazolin-4-yl)thioureas
PB - Publishing House of Pardubice University
CY - Pardubice
SN - 8071943495
KW - Quinazolines
KW - Thioureas
KW - Benzimidoyl isothiocyanates
N2 - The reactions of N2-1-(2-cyanophenyl)-N1-thioxomethylidenebenzene-1-carboximidamide with amines and anilines afforded N3,N3-di R-N1-(2-phenyl-3,4-dihydroquinazolin-4-yliden)thiourea and N3-R-N1-(2-phenyl-quinazolin-4-yl)thiourea. This reaction was applied to involve more anilines with large substituents in order to examine the effect of these large substituents on the reaction pathway and to obtain large number of quinazolines with a big variety of substituents for biological activity screening. This process took place in a one pot reaction starting from the easily available benzamide derivative, which subsequently converted to the imidoyl chloride by the reaction with PCl5 , then to the isothiocyanate. The additon reaction of the isothiocyanate with anilines undergoes a series of spontaneous step of reactions, which finally ends by the formation of the quinazoline derivative.
ER -
MOHAMED, Walid Fathalla and Pavel PAZDERA. The Synthesis of New N3-Aryl-N1-(2-phenylquinazolin-4-yl)thioureas. In \textit{XXVth Conference of Organic Chemists}. 1st ed. Pardubice: Publishing House of Pardubice University, 2001, p.~KS 8, 2 pp. ISBN~80-7194-349-5.
|
