76543-31-2Relevant academic research and scientific papers
Cyclocondensation of 2,2-dichloroethenylbenzamide and its analogs with amidines and hydrogen sulfide in the presence of bases
Demidchuk,Seferov,Vasilenko,Brovarets,Drach
experimental part, p. 500 - 504 (2009/07/18)
Available chlorine-containing enamides of the general formula Cl 2C=CHNHCOR (I) easily react with benzamidine and its derivatives to give 1:1 adducts which under heating with sodium methylate transform to 2-(methoxymethyl)-4,5-diaryl-s-triazines. Reaction of compounds (I) with hydrogen sulfide in the presence of triethylamine yields a mixture of products. Only the corresponding 3,5-bis(acylaminomethyl)-1,2,4-tritiolanes were isolated from the reaction mixture in moderate yield.
REACTION OF FUNCTIONAL DERIVATIVES OF 3,3-DICHLORO-2-ACYLAMINOACRYLIC ACIDS WITH BENZAMIDINE
Vinogradova, T. K.,Mis'kevich, G. N.,Drach, B. S.
, p. 1587 - 1592 (2007/10/02)
The methyl ester, amide, and azlactone of 3,3-dichloro-3-benzoylaminoacrylic acid react readily with benzamidine and give high yields of 4(5)-benzoylamino-4(5)-dichloromethyl-2-phenyl-4H(5H)-5(4)imidazolone.A similar reaction without participation of the
