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Total Synthesis of an Experimental Antitubercular Drug CDRI-830
Authors:Uma Reddy Pailla  L. K. Ravindranath
Affiliation:1. Research and Development , Suven Life Sciences Ltd. , Hyderabad , India;2. Department of Chemistry , Sri Krishnadevaraya University , Ananthapur , Andhra Pradesh , India;3. Department of Chemistry , Sri Krishnadevaraya University , Ananthapur , Andhra Pradesh , India
Abstract:The triarylmethane antituberculosis drug CDRI-830 is synthesized. The triarylmethane derivative 4 is prepared from ether 6 by a rearrangement process. The total synthesis of the drug CDRI-830 is achieved in a good overall yield of 35% from a simple thiophene derivative 8.
Keywords:CDRI-830  ether rearrangement  Friedel–Crafts reaction
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