A one-pot synthesis of pyrido[2,3-d]- and quinolino[2,3-d]pyrimidines
The in situ formed methylene derivatives of 1,3-dicarbonyl compounds; ethyl cyanoacetate; malononitrile and ketones; react with 6-amino-1,3-dimethyluracil as activated alkenyl derivatives, affording Michael adducts. The adduts simultaneously undergo cyclization to furnish pyrido[2,3-d]- or quinolino...
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Published in | Heterocycles Vol. 55; no. 7; pp. 1315 - 1322 |
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Main Authors | , , |
Format | Journal Article |
Language | English |
Published |
OXFORD
Elsevier
01.07.2001
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Subjects | |
Online Access | Get more information |
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Summary: | The in situ formed methylene derivatives of 1,3-dicarbonyl compounds; ethyl cyanoacetate; malononitrile and ketones; react with 6-amino-1,3-dimethyluracil as activated alkenyl derivatives, affording Michael adducts. The adduts simultaneously undergo cyclization to furnish pyrido[2,3-d]- or quinolino[2,3-d]pyrimidine derivatives in high yield. |
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ISSN: | 0385-5414 |
DOI: | 10.3987/com-01-9209 |