SYNTHESIS OF CERTAIN CYCLOPENTYLbPYRIDIN-5-ONES OF ANTICIPATED ANTI- INFLAMMATORY, ANTICOAGULANT AND ANTIMICROBIAL ACTIVITIES

Document Type : Original Article

Authors

1 Organic Chemistry Department, Faculty of Pharmacy, Cairo University,

2 Organic Chemistry Department, Faculty of Pharmacy, Suez Canal University

3 Clinical Pharmacology Department, Faculty of Medicine, Menofia University

4 Microbiology Department, Faculty of Medicine, Menofia University

Abstract

The reaction of quinolinic anhydride (2) with α-(or ɣ-) picoline yielded 6-(2-pyridinyl) cyclopentylbpyridine-5,7-dione (3) or 6-(4- pyridinyl) analogue 4 Compounds 3 and 4 were changed into the chloro derivatives 5 and 6 respectively by using mixture of phosphorus pentachloride and phosphorus oxychloride. The chloro compounds (5 and 6) underwent nucleophilic substitution condensed with different amines to produce compound 7 and 8 respectively. The hydrazino derivatives 7i and 8i respectively were with different aromatic aldehydes to produce 9 and 10 respectively.
Compounds  8g and 10f, which showed a significant antiinflammatory action compared to Indomethacine. Also compounds 8h and 9h were  active as anticoagulant as phenindione. Finally, 9f, and 9c. showed antimicrobial activity especially against Staphlococoue aureus and Escherichica coli.