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Synfacts 2014; 10(1): 0012
DOI: 10.1055/s-0033-1340329
Synthesis of Natural Products and Potential Drugs
© Georg Thieme Verlag Stuttgart · New York

Synthesis of a SIRT1 Inhibitor

Contributor(s):
Philip Kocienski
Gritsch PJ, Stempel E, Gaich T * Leibniz University, Hannover, Germany
Enantioselective Synthesis of Cyclohepta[b]indoles: Gram-Scale Synthesis of (S)-SIRT1-Inhibitor IV.

Org. Lett. 2013;
15: 5472-5475
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Further Information

Publication History

Publication Date:
13 December 2013 (online)

 
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Key words

SIRT1 inhibitor - [3,3]-sigmatropic rearrangement - Cope rearrangement - asymmetric cyclopropanation - cascade reaction

Significance

SIRT1 deacetylates the p53 tumor suppressor protein, a key transcriptional regulator of genes involved in cell cycle regulation, apoptosis, and DNA repair. The target molecule is a potent SIRT1 inhibitor. The key step in the synthesis of the (S)-eutomer depicted is the stereospecific [3,3]-sigmatropic rearrangement of the divinyl­cylopropane intermediate F derived from aldehyde D via a Horner–Wadsworth–Emmons (HWE) reaction.


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Comment

Twelve examples of the HWE–[3,3]-sigmatropic rearrangement cascade leading to cyclohepta[b]indoles are described. The temperature required for the [3,3]-sigmatropic rearrangement varies from room temperature to 140 °C, depending on the structure of the indole divinylcyclopropane. For an earlier synthesis of the racemic target and its chiral HPLC resolution, see: A. D. Napper et al. J. Med. Chem. 2005, 48, 8045.


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