An improved synthesis of TRβ-selective thyromimetic GC-1
Xiaohui Chu1, Jinjun Wang1,2, Yanzhong Li3,4
1School of Food and Bioengineering, Yantai Institute of Technology, Yantai, 264003, China.
None:
A new efficient synthesis of TRβ-selective thyromimetic GC-1 is described. The present strategy employs benzyl substituent as the exclusive protecting group, avoiding side reactions and simplifying the purification process in the last step. This paper reports 62% overall yield in six steps for total synthesis of GC-1 in multi-gram scale. The initial synthetic route is adaptable to analogue design and suitable for the preparation of other natural methylenebisphenols.
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