Abstract
Structurally diverse annulated benzothiazoloquinazolines have been synthesized by an environmentally benign, efficient, and convenient synthesis involving three-component domino reaction of 2-aminobenzothiazoles, α-tetralone, and furan-2-carbaldehyde/p-methoxybenzaldehyde using an SO3H-functionalized halogen-free ionic liquid ([MIM(CH2)4SO3H][HSO4]) as a catalyst and a reaction medium.
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