A method has been developed for the preparation of new pyrazolo[3,4-b]pyridines and tetrahydropyrazolo[3,4-b]quinolinones by the reactions of 5-amino-1-aryl-1H-pyrazole-4-carbonitriles with aliphatic and cyclic 1,3-dicarbonyl compounds in the presence of anhydrous tin(IV) chloride.
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Translated from Khimiya Geterotsiklicheskikh Soedinenii, 2017, 53(2), 207–212
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Potapov, A.Y., Vandyshev, D.Y., Kosheleva, Y.A. et al. Cyclization of 5-amino-1-aryl-1H-pyrazole-4-carbonitriles with β-dicarbonyl compounds. Chem Heterocycl Comp 53, 207–212 (2017). https://doi.org/10.1007/s10593-017-2041-9
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DOI: https://doi.org/10.1007/s10593-017-2041-9
Keywords
- acetylacetone
- acetoacetic ester
- 4-amino-1-aryl-6-methyl-1H-pyrazolo[3,4-b]pyridines
- 4-amino-1-aryl-6-oxo-6,7-dihydro-1H-pyrazolo[3,4-b]pyridines
- 5-amino-1-aryl-1H-pyrazole-4-carbonitriles
- benzoylacetone
- 1,3-cyclohexanediones
- 1,6-diaryl-5-methane-sulfonyl-1H-pyrazolo[3,4-b]pyridines
- malonic ester
- 1,6,7,8-tetrahydro-5H-pyrazolo[3,4-b]quinolinones