Abstract

The present invention relates to a process for the preparation of 1-(3-Chloro-5-{[4-(4-chlorothiophen-2-yl)-5-(4-cyclohexylpiperazin-1-yl)-1,3-thiazol-2-yl] carbamoyl} pyridin-2-yl) piperidine-4-carboxylic acid which is represented by the following structural formula-1 or its pharmaceutically acceptable salts.

Formula-1.

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