Abstract
A number of epinephrine analogs and corresponding 1-aryl-2-alkylaminoethyl chloride hydrochlorides and bromide hydrobromides have been prepared. The central intermediates of the syntheses were the 5-aryl-3-alkyl-2-oxazolidones (IV), accessible by alkylation of the product obtained using the Reformatzky reaction of an aromatic aldehyde with ethyl bromoacetate. The results of a pharmacological study of the products obtained are summarized.
Original language | English |
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Pages (from-to) | 1121-1125 |
Number of pages | 5 |
Journal | Journal of Medicinal Chemistry |
Volume | 11 |
Issue number | 6 |
DOIs | |
State | Published - 1 Sep 1968 |
Externally published | Yes |