Abstract
A simple and novel route for the synthesis of new spirocyclic propionamide derivative is developed. The present work involves N-arylation of pyrazolone (1) using copper(I) iodide catalyst followed by reduction to give amine (2). The coupling of 2 with 3-(4-fluorophenyl)propionic acid and deprotection of Boc group yields the title compound (3). © 2012 by the authors; licensee MDPI, Basel, Switzerland.
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Srinivasan, R., Narayana, B., Samshuddin, S., & Sarojini, B. K. (2012). 3-(4-fluorophenyl)-n-[4-(4-furan-2-yl-1-oxo-2,3,7-triazaspiro[4.5]dec-3-en-2-yl)phenyl]propionamide hydrochloride. MolBank, 2012(3). https://doi.org/10.3390/M771
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