Research Article
Synthesis and Antimicrobial Evaluation of Some Novel Trisubstituted s-Triazine Derivatives Based on Isatinimino, Sulphonamido, and Azacarbazole
Scheme 2
Disubstitution (ii) dry THF, 30–35°C, K2CO3. 5a, R = morpholinyl, R′ = thiazolyl, 5b, R = morpholinyl, R′ = methyl pyrimidinyl, 5c, R = piperidinyl, R′ = thiazolyl, 5d, R = piperidinyl, R′ = methyl pyrimidinyl, 5e, R = pyrrolidinyl, R′ = thiazolyl, 5f, R = pyrrolidinyl, R′ = methyl pyrimidinyl, 5 g, R = N-methyl piperazinyl, R′ = thiazolyl, 5 h, R = N-methyl piperazinyl, R′ = methyl pyrimidinyl, 5i, R = N-ethyl piperazinyl, R′ = thiazolyl, 5j, R = N-ethyl piperazinyl, R′ = methyl pyrimidinyl, 5k, R = N-phenyl piperazinyl R′ = thiazolyl, 5l, R = N-phenyl piperazinyl, R′ = methyl pyrimidinyl.