Synthesis of hexaprofen [2-(4-cyclohexylphenyl) propionic acid] |
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Authors: | Hong Dae Choi Jun Joo Ma Byeng Wha Son |
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Affiliation: | 1. Department of Chemistry, Dongeui University, 614-714, Pusan, Korea 2. Department of Chemistry, National Fisheries University of Pusan, 608-023, Pusan, Korea
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Abstract: | A novel preparative method for hexaprofen, which is a potent antiinflammatory agent, is described. Friedel-Crafts reaction of cyclohexylbenzene with ethyl α-chloro-α-(methylthio) acetate1 and α-chloro-α-(methylthio) acetonitrile2 afforded ethyl 2-(methylthio)-2-(4-cyclohexylphenyl) acetate7 and 2-methylthio-2-(4-cyclohexylphenyl) acetonitrile8, respectively. Compounds7 and8 were converted into the corresponding ethyl 2-methylthio-2-(4-cyclohexylphenyl) propionate9 and 2-methylthio-2-(4-cyclohexylphenyl) propionitrile10 by methylation with sodium hydride and methyl iodide. Hexaprofen13 was prepared by hydrolysis of ethyl 2-(4-cyclohexylphenyl) propionate11 and of 2-(4-cyclohexylphenyl) propionitrile12 followed by desulfurization of compounds9 and10. |
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