Abstract
The synthesis of two series of N-substituted 4,7,7-trimethyl-3-(1-piperidinyl)bicyclo[2.2.1]hept-2-ene 2-carboxamides (I d-h) and 2-carbothioamides (I i-o), as well as of some N-aryl 4,7,7-trimethyl-3-(1-pyrrolidinyl)bicyclo[2.2.1]hept-2-ene 2-carboxamides (I a-c), by reaction of camphor piperidinoenamine and pyrrolidinoenamine with aryl isocyanates and isothiocyanates is described. On the whole compounds (I d-h) showed a weak hypotensive activity in rats.
Publication types
-
Research Support, Non-U.S. Gov't
MeSH terms
-
Animals
-
Antihypertensive Agents / chemical synthesis*
-
Antihypertensive Agents / pharmacology
-
Blood Glucose / metabolism
-
Blood Pressure / drug effects
-
Bridged Bicyclo Compounds / chemical synthesis*
-
Bridged Bicyclo Compounds / pharmacology
-
Bridged-Ring Compounds / chemical synthesis*
-
Chemical Phenomena
-
Chemistry
-
Heart Rate / drug effects
-
Hypoglycemic Agents / pharmacology
-
Piperidines / chemical synthesis*
-
Piperidines / pharmacology
-
Rats
Substances
-
Antihypertensive Agents
-
Blood Glucose
-
Bridged Bicyclo Compounds
-
Bridged-Ring Compounds
-
Hypoglycemic Agents
-
Piperidines