Synthesis and Antiarrhythmic and Anticonvulsant Activities of Amino Amides and Amino Esters Based on 1-(4-Fluorophenyl)- and 1-[3-(Trifluoromethyl)phenyl]cyclopentane-1-carboxylic Acids
The alkylation of 2-(4-fluorophenyl)- and 2-[3-(trifluoromethyl)phenyl]acetonitriles with 1,4-dibromobutane gave 1-(substituted phenyl)cyclopentane-1-carbonitriles which were hydrolyzed to the corresponding carboxylic acids by the action of potassium hydroxide in ethylene glycol. The resulting ac...
Uloženo v:
| Vydáno v: | Russian journal of organic chemistry Ročník 60; číslo 6; s. 1028 - 1035 |
|---|---|
| Hlavní autoři: | , , , , , , , |
| Médium: | Journal Article |
| Jazyk: | angličtina |
| Vydáno: |
Moscow
Pleiades Publishing
01.06.2024
PLEIADES PUBLISHING LTD Springer Nature B.V |
| Témata: | |
| ISSN: | 1070-4280, 1608-3393 |
| On-line přístup: | Získat plný text |
| Tagy: |
Přidat tag
Žádné tagy, Buďte první, kdo vytvoří štítek k tomuto záznamu!
|
| Shrnutí: | The alkylation of 2-(4-fluorophenyl)- and 2-[3-(trifluoromethyl)phenyl]acetonitriles with 1,4-dibromobutane gave 1-(substituted phenyl)cyclopentane-1-carbonitriles which were hydrolyzed to the corresponding carboxylic acids by the action of potassium hydroxide in ethylene glycol. The resulting acids were converted to acid chlorides, and the latter reacted with
N
,
N
-dialkylaminoalkylamines, as well as with
N
,
N
-dialkylaminoalkanols, to produce new amino amide and amino ester derivatives of 1-(4-fluorophenyl)- and 1-[3-(trifluoromethyl)phenyl]cyclopentane-1-carboxylic acids, which were characterized as hydrochlorides. The synthesized compounds were evaluated for their antiarrhythmic and anticonvulsant activities. |
|---|---|
| Bibliografie: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 |
| ISSN: | 1070-4280 1608-3393 |
| DOI: | 10.1134/S1070428024060071 |