2-Benzazepines. 5. Synthesis of pyrimido[5,4-d][2]benzazepines and their evaluation as anxiolytic agents

A series of 5H-pyrimido[5,4-d][2]benzazepines has been synthesized, starting from the corresponding 2-benzazepin-5-ones, and evaluated as potential anxiolytic agents. Selected compounds from this series show a pharmacological profile of action different than that of diazepam. They are more potent th...

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Veröffentlicht in:Journal of medicinal chemistry 1983-11, Vol.26 (11), p.1589-1596
Hauptverfasser: Trybulski, Eugene J, Benjamin, Louis E, Earley, James V, Fryer, R. Ian, Gilman, Norman W, Reeder, Earl, Walser, Armin, Davidson, Arnold B, Horst, W. Dale
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Sprache:eng
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Zusammenfassung:A series of 5H-pyrimido[5,4-d][2]benzazepines has been synthesized, starting from the corresponding 2-benzazepin-5-ones, and evaluated as potential anxiolytic agents. Selected compounds from this series show a pharmacological profile of action different than that of diazepam. They are more potent than diazepam in the anti-pentylenetetrazole test and in the [3H]diazepam binding assay, yet show less activity in the inclined screen test. A pharmacological data profile is given for 9-chloro-7-(2-chlorophenyl)-5H-pyrimido[5,4-d] [2]benzazepine (7c). The structure-activity relationships of these potential anxiolytic agents are discussed.
ISSN:0022-2623
1520-4804
DOI:10.1021/jm00365a008