96730-35-7Relevant articles and documents
New one-pot synthesis of 1,3,5-triazines: three-component condensation, dimroth rearrangement, and dehydrogenative aromatization
Junaid, Ahmad,Lim, Felicia Phei Lin,Tiekink, Edward R. T.,Dolzhenko, Anton V.
supporting information, p. 548 - 555 (2019/06/25)
A new, effective one-pot synthesis of the 6,N2-diaryl-1,3,5-triazine-2,4-diamines under microwave irradiation was developed. The method involved an initial three-component condensation of cyanoguanidine, aromatic aldehydes, and arylamines in the presence of hydrochloric acid. Without isolation, the resulting 1,6-diaryl-1,6-dihydro-1,3,5-triazine-2,4-diamines were treated with a base to initiate Dimroth rearrangement and spontaneous dehydrogenative aromatization, affording the desired compounds. The developed method was found to be sufficiently general in scope, tolerating various aromatic aldehydes and amines; by using their combinations in the first step, a representative library of 110 compounds was successfully prepared and screened for anticancer properties.
1-Aryl-4,6-diamino-1,2-dihydrotriazine as antimalarial agent: A new synthetic route
Kidwai,Mothsra,Mohan,Biswas
, p. 915 - 917 (2007/10/03)
Some novel derivatives of 1-aryl-4,6-diamino-1,2-dihydrotriazines have been synthesized using neat technology under microwaves. These were tested in vitro against both sensitive and resistant Plasmodium falciparum strains for antimalarial activity.
An efficient synthesis of 1-aryl-4,6-diamino-1,2-dihydro-1,3,5-triazines
Saesaengseerung, Neungruthai,Vilaivan, Tirayut,Thebtaranonth, Yodhathai
, p. 2089 - 2100 (2007/10/03)
1-Aryl-4,6-diamino-1,2-dihydro-1,3,5-triazines bearing diverse substituents at C2 and on the aromatic ring have been synthesized in good yield from an acid-catalyzed reaction between corresponding arylbiguanide and carbonyl compound in the presence of triethyl orthoacetate as a water scavenger.