Abstract
A series of N-acyl-4,7,7-trimethyl-N-phenyl-3-(1-piperidinyl or dimethylamino)bicyclo[2.2.1]hept-2-ene-2-carbothioamides was prepared in excellent yields by reaction of 4,7,7-trimethyl-N-phenyl-3-(1-piperidinyl or dimethylamino)bicyclo[2.2.1]hept-2-ene-2-carbothioamides with a number of aromatic or heterocyclic acyl chlorides in dry pyridine solution and in the presence of sodium hydride. Some of the above compounds showed a platelet antiaggregating activity in vitro superior or comparable to that of acetylsalicylic acid; moreover, some compounds exhibited moderate analgesic, antiinflammatory and hypotensive activities in mice or rats.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Acetylcholine / antagonists & inhibitors
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Animals
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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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Antihypertensive Agents / chemical synthesis
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Antihypertensive Agents / pharmacology
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Bridged Bicyclo Compounds / chemical synthesis*
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Bridged Bicyclo Compounds / pharmacology
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Guinea Pigs
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Histamine H1 Antagonists / chemical synthesis
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Histamine H1 Antagonists / pharmacology
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Humans
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In Vitro Techniques
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Mice
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Piperidines / chemical synthesis*
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Piperidines / pharmacology
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Platelet Aggregation Inhibitors / chemical synthesis*
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Platelet Aggregation Inhibitors / pharmacology
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Rats
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Thioamides / chemical synthesis*
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Thioamides / pharmacology
Substances
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Anti-Inflammatory Agents, Non-Steroidal
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Antihypertensive Agents
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Bridged Bicyclo Compounds
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Histamine H1 Antagonists
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Piperidines
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Platelet Aggregation Inhibitors
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Thioamides
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Acetylcholine