Abstract
It has been found that 2,3-dioxopyrrolo[2,1-a]isoquinolines react with aromatic amines in glacial acetic acid and with heteroaromatic and secondary aliphatic amines in the absence of acid with opening of the pyrroledione ring to give 1,2,3,4-tetrahydroisoquinoline enamino ketoamides.
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REFERENCES
A. G. Mikhailovskii and M. O. Dekaprilevich, Khim. Geterotsikl. Soedin., 1111 (1998).
A. G. Mikhailovskii, N. N. Polygalova, T. S. Turova, G. A. Lobashova, and M. I. Vakhrin, Khim. Geterotsikl. Soedin., 1357 (2004).
A. G. Mikhailovskii, Khim. Geterotsikl. Soedin., 685 (1996).
V. S. Shklyaev, B. B. Aleksandrov, A. G. Mikhailovskii, and M. I. Vakhrin, Khim. Geterotsikl. Soedin., 963 (1987).
A. G. Mikhailovskii and V. S. Shklyaev, Khim. Geterotsikl. Soedin., 946 (1994).
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Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 9, pp. 1378–1382, September, 2005.
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Polygalova, N.N., Mikhailovskii, A.G. Reaction of 2,3-Dioxopyrrolo-[2,1-a]isoquinolines with Aromatic and Secondary Aliphatic Amines. Chem Heterocycl Compd 41, 1173–1177 (2005). https://doi.org/10.1007/s10593-005-0298-x
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DOI: https://doi.org/10.1007/s10593-005-0298-x