Abstract
The synthesis in excellent yields of 2,3-dihydro-6-mercapto-1,3,5-triphenyl-2-thioxo-4(3H)-pyrimidinone 3 and 5-ethoxycarbonyl-2,3-dihydro-6-mercapto-1,3-diphenyl-2-thioxo-4(3H )- pyrimidinone 4 by reaction of methyl phenylacetate or diethyl malonate, respectively, with phenyl isothiocyanate (3 molar equivalents) and sodium hydride (2 molar equivalents) in DMF solution is described. Acylation of 3 and 4 with acyl chlorides gave, generally in satisfactory yields, 6-acylthio derivatives 13 and 14. Some of the above compounds showed a platelet antiaggregating activity in vitro superior or comparable to that of acetylsalicylic acid, as well as remarkable antiinflammatory, antiarrhythmic, local anesthetic and antihyperlipidemic activities in rats and in mice. Weak anticonvulsant and hypoglycemic activities were also detected.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Anesthetics, Local / chemical synthesis
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Anesthetics, Local / pharmacology
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Animals
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Anti-Arrhythmia Agents / chemical synthesis*
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Anti-Arrhythmia Agents / pharmacology
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Anti-Inflammatory Agents, Non-Steroidal / chemical synthesis*
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Anti-Inflammatory Agents, Non-Steroidal / pharmacology
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Anticonvulsants / chemical synthesis
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Anticonvulsants / pharmacology
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Hypoglycemic Agents / chemical synthesis
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Hypoglycemic Agents / pharmacology
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Hypolipidemic Agents / chemical synthesis*
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Hypolipidemic Agents / pharmacology
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Mice
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Platelet Aggregation Inhibitors / chemical synthesis*
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Platelet Aggregation Inhibitors / pharmacology
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Pyrimidinones / chemical synthesis*
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Pyrimidinones / pharmacology
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Rats
Substances
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Anesthetics, Local
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Anti-Arrhythmia Agents
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Anti-Inflammatory Agents, Non-Steroidal
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Anticonvulsants
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Hypoglycemic Agents
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Hypolipidemic Agents
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Platelet Aggregation Inhibitors
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Pyrimidinones