Condensation of 2-amino-3-cyano-4,5,6,7-tetrahydroindole with Β-dicarbonyl compounds |
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Authors: | M. V. Mezentseva A. N. Grinev O. S. Anisimova L. M. Alekseeva Yu. N. Sheinker |
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Affiliation: | (1) S. Ordzhonikidze All-Union Scientific Research Chemical Pharmaceutical Institute, 119815 Moscow |
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Abstract: | Depending on conditions, the condensation of 2-amino-3-cyano-4,5,6,7-tetrahydroindole with -dicarbonyl compounds leads to 2-methyl-4-oxo- or 4-methyl-2-oxo-10-cyano-6,7,8,9-tetrahydropyrimido[1,2-a]indoles via the intermediate compounds: 2-(3-ethoxy-carbonyl-prop-2-en-2-yl amino) and 2-(1,3-dioxobutylamino)-3-cyano-4,5,6,7-tetrahydroindoles, respectively.Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 6, pp. 833–838. June, 1989. |
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