4.2 Article

Synthesis of polyfunctionalized pyrido[1,2-a]pyrazines and pyrazino[1,2-a]quinolines via one-pot multicomponent reactions

期刊

MONATSHEFTE FUR CHEMIE
卷 147, 期 12, 页码 2127-2133

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SPRINGER WIEN
DOI: 10.1007/s00706-016-1836-1

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Heterocycles; Methylidenepiperazine-2-ones; Pyrido[1,2-a]pyrazines; Multicomponent reactions; Cyclizations

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An efficient, straightforward, and general method for the synthesis of pyrido[1,2-a]pyrazine and pyrazino[1,2-a]quinoline derivatives via a one-pot three-component reaction between cyclic enamineones, aromatic aldehydes, and 1,3-dicarbonyl compound is reported. On our knowledge, this is the first reported one-pot multicomponent reaction for synthesis of pyrido[1,2-a]pyrazine and pyrazino[1,2-a]quinoline derivatives. A proposed reaction pathway for the synthesis has been proved experimentally, consisting in addition of 3-(alkoxycarbonylmethylidene)piperazine-2-ones to the products of condensation of aromatic aldehydes and 1,3-dicarbonyl compounds, followed by further cyclocondensation Michael addition. The structure of the thirteen new compounds was proven by elemental and spectral analysis (H-1 and C-13 NMR, HPLC/MS, and FT-IR).

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