Abstract
The starting materials thiazolo[2,3-
b]quinazolines (
5a,
b) were obtained in one pot synthesis by treating octahydroquinazoline (
2) with chloroacetic acid and aromatic aldehydes. Thiazoloquinazoline (
5) was reacted with CH
2(CN)
2/piperidine and CH
2(CN)
2/NaOH (CH
3OH), to furnish pyrano[2′,3′:4,5]thiazolo[2,3-
b]quinazolines (
6a,
b) and pyrido[2′,3′:4,5]thiazolo[2,3-
b]quinazoline (
7), respectively. Refluxing of
5a with NH
2CSNH
2/KOH and hydrazines in ethanol furnished the corresponding, [1,3]thiazino[4′5′:4,5]thiazolo[2,3-
b]quinazoline (
10) and pyrazolo[3′,4′:4,5]thiazolo[2,3-
b]quinazolines (
11a,
b), respectively. Antifungal activity was shown for some of the synthesized compounds.