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A series of pyrano-fused pyrazolo[3,4-b]pyridine derivatives with an aryl group presenting the 2-position of the pyridine nucleus have been synthesized by microwave-assisted three-component reactions of aldehydes, tetrahydropyran-4-one, and 3-methyl-1-phenyl-1H-pyrazol-5-amine in HOAc. This method is very efficient because of short reaction times and easy work-up, and it provides an efficient and promising synthetic strategy for the construction of the tricyclic pyrano-fused pyrazolo[3,4-b]pyridine skeleton.

A novel and efficient access to 2-(argio(3-methyl-5-oxo-1-phenyl-4,5-dihydro-1H-pyrazol-4-yl)methyl)-3-hydroxynaphthalene-1,4-dione derivatives from readily available substrates in neat water is described with aid of microwave irradiation. The results of our study provide a green, simple and practical one-pot approach to the synthesis of 3-hydroxynaphthalene-1,4-dione analogs in excellent yields without further purification.

A series of new functionalized thiopyrano-, pyrano[4,3-d]pyrimidine derivatives with benzyl group residing in 8-position of fused pyrimidine nucleus were synthesized through multicomponent reactions of aromatic aldehydes, tetrahydrothiopyran-4-one(tetrahydropyran-4-one), and aryl amidines using t-BuOK as a base under microwave heating. The procedure is facile, avoiding time-consuming and costly syntheses, tedious work-up, and purifications of precursors as well as protection/deprotection of functional groups. This method is very efficient due to short reaction times and easy work up and provides a four-component strategy for the construction of the thiopyrano-, and pyrano[4,3-d] pyrimidine skeletons.

A series of new functionalized pyrazolopyridine derivatives with different substituted patterns were synthesized via microwave-assisted multi-component divergent reactions of aldehydes, 5-aminopyrazoles, and cycloketones by controlling the reaction condition. The procedures are facile, avoiding time-consuming and costly syntheses, tedious work-up, and purifications of precursors as well as protection/deprotection of functional groups. This chemistry provides an efficient and promising synthetic strategy to construction of the pyrazolopyridine skeleton.

A series of pyrano-fused pyrazolo[3,4-b]pyridine derivatives with an aryl group presenting the 2-position of the pyridine nucleus have been synthesized by microwave-assisted three-component reactions of aldehydes, tetrahydropyran-4-one, and 3-methyl-1-phenyl-1H-pyrazol-5-amine in HOAc. This method is very efficient because of short reaction times and easy work-up, and it provides an efficient and promising synthetic strategy for the construction of the tricyclic pyrano-fused pyrazolo[3,4-b]pyridine skeleton.

A series of new functionalized pyrazolopyridine derivatives with different substituted patterns were synthesized via microwave-assisted multi-component divergent reactions of aldehydes, 5-aminopyrazoles, and cycloketones by controlling the reaction condition. The procedures are facile, avoiding time-consuming and costly syntheses, tedious work-up, and purifications of precursors as well as protection/deprotection of functional groups. This chemistry provides an efficient and promising synthetic strategy to construction of the pyrazolopyridine skeleton.

A novel pseudo four-component reaction of 4-pyranones or thiones with aromatic aldehydes and arylamidines is established to provide the anellated pyrimidines regioselectively.