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 |
|---|---|
| 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 |