A Facile and Green Synthesis of Novel Imide and Amidic Acid Derivatives of Phenacetin as Potential Analgesic and Anti-Pyretic Agents

Author(s): Yervala D. Reddy, Padam P. Kumar, Bhoomireddy R. Devi, Pramod K. Dubey, Yalamanchili B. Kumari

Journal Name: Letters in Organic Chemistry

Volume 10 , Issue 1 , 2013

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Facile and green syntheses of potential analgesic and antipyretic compounds, N-(4-ethoxy-phenyl)-2-(1,3- dioxo-1,3-dihydroisoindol-2-yl)acetamide derivatives 6a-g and N-[(4-ethoxy-phenylcarbamoyl)methyl]phthalamic acid derivatives 10a-g have been developed. Two synthetic routes (A and B) have been established for the preparation of 6a-g. In the route-A, 4-ethoxyaniline 2 was reacted with chloroacetyl chloride 3 in a solution of potassium acetate and acetic acid to yield N-(4-ethoxyphenyl)-2-chloroacetamide 4. The latter was reacted with imide compounds 5a-g either in triethanolamine as a green solvent or in solid phase in the presence of TEBAC and KI to yield 6a-g. Alternatively, in the route-B, reaction of anhydrides 7a-g with glycine 8 yielded the (1, 3-dioxo-1, 3-dihydroisoindol-2-yl)acetic acid derivatives 9a-g which on reaction with 2 either in triethnolamine and DCC as a dehydrating agent or in solid phase in the presence of DCC gave 6a-g. The latter were hydrolyzed in 0.5N ethanolic KOH to afford 10a-g.

Keywords: Anhydrides, imides, 4-ethoxyaniline, phenacetin, Analgesic & Antipyretic, erythrocytes, triethanolamine, TEBAC, Perkin – Elmer 1000, capillary tubes, structural

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Article Details

Year: 2013
Published on: 04 February, 2013
Page: [70 - 76]
Pages: 7
DOI: 10.2174/1570178611310010016

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