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Effective method for the synthesis of azolo[1,5-a]pyrimidin-7-amines

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Chemistry of Heterocyclic Compounds Aims and scope

Condensation of aminoazoles with (2E)-(3-morpholin-4-yl)acrylonitrile and 3,3-diethoxypropionitrile was used to synthesize a series of azolo[1,5-a]pyrimidin-7-amines. It was established that the reactions with certain aminotriazoles gave mixtures of regioisomers: azolo[1,5-а]pyrimidin-7-amines and azolo[4,3-а]pyrimidin-5-amines.

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The results were obtained within the framework of State Assignment of the Ministry of Education and Science of the Russian Federation (No. 4.6351.2017/8.9).

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Correspondence to Denis A. Gazizov.

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Supplementary information file containing 1Н, 13С NMR and 1H–13C HSQC, 1H–13С HMBC spectra of compounds 3ah, 5a is available at the journal website at http://link.springer.com/journal/10593.

Translated from Khimiya Geterotsiklicheskikh Soedinenii, 2019, 55(6), 573–577

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Gazizov, D.A., Fedotov, V.V., Gorbunov, E.B. et al. Effective method for the synthesis of azolo[1,5-a]pyrimidin-7-amines. Chem Heterocycl Comp 55, 573–577 (2019). https://doi.org/10.1007/s10593-019-02498-2

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  • DOI: https://doi.org/10.1007/s10593-019-02498-2

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