| 摘要 |
Substituted phenyl N-(2,6-dichlorophenyl)benzymidate, obtained by condensation of a salt of 2,6-dichlorophenol with the imidoyl chloride, is converted by the Chapman rearrangement to the compound of formula <IMAGE> in which Q is a radical chosen from the cyano and alkoxycarbonyl groups and Z is a substituted or unsubstituted phenyl group. By hydrolysis of the compound (III), o-(2,6-dichloroanilino)phenylacetic acid is obtained. This compound is useful as an analgesic and non-steroidal anti-inflammatory agent.
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