Abstract:
THIS INVENTION IS CONCERNED WITH THE PREPARATION OF CYCLOPENTENE - 1,1 - DICARBOXAMIDES; 1,3-DIAZASPIRO (4,4) NONENE-2,4 - DIONES; 1 - AMINOCYCLOPENTENE-1-CARBOXYLIC ACIDS; 1-(N - ALKYLAMINO) CYCLOPENTENE - 1 - CARBOXYLIC ACIDS; AND 3-OXA-1-AZASPIRO (4,4) NONENE-2,4-DIONES WHICH ARE INTERMEDIATE IN THE PREPARATION OF 6-(1-AMINOCYCLOPENTENE-1-CARBOXAMIDO) PENICILLANIC ACIDS WHICH ARE USEFUL ANTIBACTERIAL AGENTS.
Abstract:
ALICYCLIC ACIDS HAVING A HYDRAZINE SUBSTITUENT ARE PREPARED BY REACTING ACETYL HYDRAZINE WITH AN ALICYCLIC COMPOUND, THE CYCLOAKYLIDENE COMPOUND FORMED BEING THEN REACTED TO ADD A CYANO GROUP AND THE CYANO ALICYCLIC HYDRAZIDE FORMED IS THEN HYDROLYZED TO PRODUCE THE DESIRED COMPOUND. THE COMPOUNDS HAVE BIOCHEMICAL ACTIVITY.
Abstract:
THE COMPOUNDS ARE BIALICYCLIC AMINO ACIDS WHICH ARE USEFUL AS ANTI-INFLAMMATORY AGENTS IN WARMBLOODED ANIMALS. THE COMPOUNDS ARE ALSO USEFUL, WHEN THEIR AMINO GROUPS ARE PROPERLY BLOCKED, FOR REACTING WITH 6-AMINOPENICILLANIC ACID, OR DERIVATIVES THEREOF, TO PREPARE PENICILLINS HAVING ANTIBIOTIC ACTIVITY, OR AS INTERMEDIATES IN THE PREPARATION OF THEIR CORRESPONDING N-CARBOXYANHYDRIDES WHICH MAY BE REACTED DIRECTLY WITH 6-AMINOPENICILLANIC ACID, OR DERIVATIVES THEREOF, TO PREPARE SAID PENICILLINS.