80276-25-1Relevant articles and documents
Synthesis, study of the structure, and modification of the products of the reaction of 4-aryl-4-oxobut-2-enoic acids with thiourea
Kolos, Nadezhda N.,Nazarenko, Nikolai V.,Shishkina, Svetlana V.,Doroshenko, Andrey O.,Shvets, Elena G.,Kolosov, Maksim A.,Yaremenko, Fedor G.
, p. 1202 - 1209 (2020)
[Figure not available: see fulltext.] A number of previously undescribed derivatives of 2-amino-5-(2-aryl-2-oxoethyl)thiazol-4(5H)-one containing electron-donating substituents in the aromatic ring were synthesized by the reaction of (E)-4-aryl-4-oxobut-2
Synthesis of new thiazolidine and imidazolidine derivatives of pharmacological interest
El-Aasar, Nadia K.,Saied, Khaled F.
, p. 645 - 652 (2008/09/21)
(Chemical Equation Presented) The hitherto unknown 5-(2-aryl-2-oxoethyl)-4- oxo-1,3-thiazolidines 1a-l have been synthesized via cycloaddition process between thiourea and/or its derivatives with 3-aroylpropenoic acids. 1H NMR spectra revealed the presence of 1a-c as a tautmeric mixture. The presence of the thiazoline tautmers (1a-c)′ was confirmed by methylating the tautmeric mixture, to the respective methylated derivatives 2-N-methylanilino-5-(2-aryl-2-oxoethyl)-4-oxo-1,3-thiazolines 2a-c and 1g-i. Acidic treatment of 1 provided the respective 2-oxo homologues 3a-i. When 1a-d, k were refluxed with DMF, molecular rearrangement was achieved, providing the 4-oxo-2-thioxoimidazolidine isomers 4a-d, k. Bromination of 4a and 4d in hot acetic acid afforded the respective (E,Z)-5-benzoylmethylene derivatives 5a, d which were prepared authentically. Thiation of 1a-c and 4a-c gave 5-aryl-2,3-dihydro-2-phenyliminothieno[2,3-d]thiazoles 6a-c and 1-phenyl-5-aryl-2,3-dihydro-2-thioxothieno[2,3-d]imidazoles 7a-c, respectively. The proposed structures have been confirmed by elemental analysis and spectroscopic data. The selected products showed different antimicrobial effect.
