IN WHICH N 1 OR O, G is a member of the group formed by the furoyl, thenoyl, nitrothenoyl and carbobenzoxy radicals and R, when n 1, is a member of the group formed by hydrogen, the methyl, butyl, isobutyl, delta -(2-furoyl) amino-butyl, hydroxymethyl, benzyl and p-hydroxybenzyl radicals, are endowed with antibacterial properties, and are useful in bacteriocidal compositions.
摘要:
The present invention relates to substituted tetrahydrofurfuryl aminoesters. The novel tetrahydrofurfuryl dialkyl aminoesters are represented by the formula
IN WHICH R is a member of the group formed by the 2-naphthyl, 2naphthyl substituted with methoxy in the 6-position and 5,6,7,8tetrahydro-1-naphthyl radicals. The addition salts with the terapeutically acceptable acids, the starting and intermediate products of these aminoesters, also form the subject of the invention. The novel aminoesters and their salts, endowed with peripheral and cerebral vasodilatory properties, are of particular interest in human therapeutics.
摘要:
The present invention relates to substituted tetrahydrofurfuryl aminoesters. The novel tetrahydrofurfuryl dialkyl aminoesters are represented by the formula
in which R is a member of the group formed by the 2-naphthyl, 2naphthyl substituted in the 6-position with alkoxy and 5,6,7,8tetrahydro-1-naphthyl radicals. The addition salts with the therapeutically acceptable acids, the starting and intermediate products of these aminoesters, also form the subject of the invention.
摘要:
ACID SALTS OF ESTERS OF A-(1-NAPHTHYL)-DELTA-PENT-4-ENOIC ACID ARE OBTAINED BY THE REACTION OF THE ACID WITH AN AMINO DERIVATIVE OF THE FORMULA
Y-(CH2)2-N(-R2)-R3
WHEREIN R2 AND R3 ARE LOWER ALKYL RADICALS AND Y IS SELECTED FROM THE GROUP CONSISTING OF THE HALOGENS AND THE HYDROXY RADICAL TO OBTAIN ESTERS OF THE FORMULA