CYCLOCONDENSATION OF 3-AMINO-2-IMINONAPHTHO[1,2-D]THIAZOLE WITH ALPHA-KETOCARBOXYLIC ACID-DERIVATIVES - SYNTHESIS OF 2-SUBSTITUTED 3-OXO-3H-NAPHTHO[1',2'-4,5]THIAZOLO[3,2-B][1,2,4]TRIAZINES AS POTENTIAL ANTI-HIV AGENTS

The cyclocondensation of 3-amino-2-iminonaphtho[1,2-d]thiazole (1) with a series of alpha-keto mono- and dicarboxylic acid derivatives 5a-i under different conditions was investigated. When the experiments were performed by refluxing in glacial acetic acid, the corresponding cyclized products, 2-substituted 3-oxo-3H-naphtho[1',2':4,5]thiazolo[3,2-b][1,2,4]triazines 4 were obtained in fair to good yields. On the other hand, when the reaction was conducted in boiling ethanol, it gave only the open chain condensates 6, or in rare cases, together with minor amount of 4. Since the intermediates 6 exist as mixture of both E- and Z-isomers, cyclization through heating was found insufficient. In any event representative compounds 4b,g,i have been evaluated for anti-HIV activity, but none of them were active.