Abstract

Environmentally Benign Synthesis of Tetrahydroindeno[1,2-b]Pyrrole-3-carboxylate Derivatives as Potential Antiinflammatory Agents

Author(s): M. Srinivas Reddy* and S. Ramakrishna
Department of Pharmaceutical Chemistry, Vaageswari College of Pharmacy, Karimnagar-505 001, Department of Chemistry, Kakatiya University, Warangal-506 002, India

Correspondence Address:
Department of Pharmaceutical Chemistry, Vaageswari College of Pharmacy, Karimnagar-505 001, India E-mail: [email protected]


A new series of tetrahydroindeno[1,2-b]pyrrole-3-carboxylate derivatives(4) were synthesized by reaction of 5-amino-2-mercapto benzimidazole with 1,3-dicarbonyls and activated carbonyl compounds using ceric ammonium nitrate catalyst by a three component one-pot reaction. Structures of these compounds were established on the basis of infrared spectroscopy, proton nuclear magnetic resonance, carbon-13 nuclear magnetic resonance, mass spectrometry and elemental analyses. The title compounds 4a-h were evaluated for antiinflammatory activity using the carrageenan-induced paw edema method at a dose of 100 mg/kg in comparison to ibuprofen as a reference drug. Compounds 4a, 4b, 4c and 4d exhibited potent antiinflammatory activity comparable to that of ibuprofen.



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