Synthesis and properties of sym-triazines. 10 Synthesis of 2,4-diamino-sym-triazines containing a sterically hindered phenol substituent

Condensation of N-(4-hydroxy-3,5-di-tert-butylphenyl)biguanide with esters in the presence of catalytic amounts of sodium ethylate gives 2-amino-4-(4-hydroxy-3,5-di-tert-butylanilino)-6-substituted sym-triazines. When the trichloroacetate ester is used the main product is 2-amino-4-(4-hydroxy-3,5-di-tert-butylanilino)-6-oxo-1(5)H-sym-triazine.For communication 9 see [1]Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 10, pp. 1395–1399, October, 1992.     

Synthesis and properties of furan derivatives. 3. Synthesis of 1,2-disubstituted δ2-imidazolines containing furfuryl and tetrahydrofurfuryl groups

The condensation of N-furfuryl- and N-tetrahydrofurfurylethylenediamines with hydrochloride salts of iminoesters of carboxylic acids gives 1,2-disubstituted ²-imidazolines containing furfuryl or tetrahydrofurfuryl groups at N¹.For communication 2, see [1]Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 10, pp. 1312–1315, October, 1992.