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Preparation and Some Reactions with 3-(Quinolin-3-yl)-3-Oxopropanoic Acid
Preparation of quinolinyl-3-oxopropanoic acid 2 was accomplished by hydrolysis of pyranoquinolinedione 1 in aqueous alkaline medium. The chemical behavior of this β-keto acid 2 towards nitrosation, coupling with a diazonium salt, esterification, condensation with 2,2-dimethoxyethanamine, hydrazinoly...
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Published in: | Journal of the Mexican Chemical Society 2011-10, Vol.55 (4), p.224-232 |
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Main Authors: | , , , |
Format: | Article |
Language: | eng ; por |
Subjects: | |
Online Access: | Get full text |
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Summary: | Preparation of quinolinyl-3-oxopropanoic acid 2 was accomplished by hydrolysis of pyranoquinolinedione 1 in aqueous alkaline medium. The chemical behavior of this β-keto acid 2 towards nitrosation, coupling with a diazonium salt, esterification, condensation with 2,2-dimethoxyethanamine, hydrazinolysis, Knoevenagel condensation with isatine, salisyaldehyde, 3-formylquinolones, and 3-formylchromone, was investigated. Also many of the products of these reactions were found obtainable using either pyranoquinolinedione 1 or β-keto acid 2, under the same conditions. |
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ISSN: | 1870-249X |