Synthesis p. 412 - 416 (1988)
Update date:2022-07-30
Topics:
Kimny, Tan
Gasquez, Francoise
Compagnon, Paul-Louis
N1-(1,2-Diarylethenyl)-N2-(alkyl- or arylaminocarbonyl)benzamidines are easily prepared in good to high yields (61-90percent) by reaction of various isocyanates with N1-(1,2-diarylethenyl)benzamidines in tetrahydrofuran.When this addition reaction of the isocyanates (and also of phenyl isothiocyanate) with the amidines is performed in boiling toluene in the presence of catalytic amounts of quinuclidine the resultant N1,N2-disubstituted benzamidines are cyclized to give substituted 2-oxo- or 2-thioxo-1,2,3,4-tetrahydro-1,3,5-triazines in yields of 31-92percent.
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