One-pot quinazolin-4-ylidenethiourea synthesis via N-(2-cyanophenyl)benzimidoyl isothiocyanate
One-pot quinazolin-4-ylidenethiourea synthesis via N-(2-cyanophenyl)benzimidoyl isothiocyanate
复制标题
DOI:
10.3390/60700574
复制
发表时间:
2001-07-01
期刊:
影响因子:
4.6
通讯作者:
Pazdera, P
中科院分区:
文献类型:
--
作者:
Fathalla, WM;Cajan, M;Pazdera, P
1,1-Disubstituted-3-(2-phenyl-3H-quinazolin-4-ylidene)thioureas (8) were synthesized in a one pot reaction of N-(2-cyanophenyl)benzimidoyl isothicyanate (3) with secondary amines. The products underwent transamination reactions. Compounds 8a-8g were identified by FTIR, H-1-NMR, C-13-NMR, mass spectroscopy and X-ray crystallography.