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Pol J Pharmacol Pharm ; 38(3): 309-19, 1986.
Article in English | MEDLINE | ID: mdl-3490658

ABSTRACT

The synthesis of two Schiff bases of aryl methyl ketones and ethylenediamine 1c, 1d, symmetric adducts of aryl isothiocyanates with Schiff bases 2d-2m and 2-thioxopyrrolidine-4,5-dione derivatives 4d-4m obtained by condensation of oxalyl chloride with Schiff bases of aroylthioacetic acid anilides and ethylenediamine is described. Some of 13 investigated compounds 4a, 4b, 4d-4l, 5a, 5b of 2-thioxopyrrolidine-4,5-dione type showed sedative and analgesic action.


Subject(s)
Analgesics , Pyrrolidines/pharmacology , 5-Hydroxytryptophan/pharmacology , Analgesics/chemical synthesis , Analgesics/toxicity , Animals , Anticonvulsants , Drug Interactions , Helplessness, Learned , Lethal Dose 50 , Male , Mice , Motor Activity/drug effects , Pyrrolidines/chemical synthesis , Pyrrolidines/toxicity , Rats , Rats, Inbred Strains , Sleep/drug effects , Stereotyped Behavior/drug effects
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