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Synthetic Communications
An International Journal for Rapid Communication of Synthetic Organic Chemistry
Volume 42, 2012 - Issue 18
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Original Articles

Practical Demethylation of Podophyllotoxin and Efficient Preparation of 4-Amino-4-deoxy-4′-demethylepipodophyllotoxin

, , &
Pages 2780-2789 | Received 20 Feb 2011, Published online: 29 May 2012
 

Abstract

4′-Demethylepipodophyllotoxin (4′-DMEP) was readily available through demethylation of podophyllotoxin using methionine in methanesulfonic acid in the presence of TFA (or acetone/water). Thus, 4-amino-4-deoxy-4′-demethylepipodophyllotoxin was obtained in three steps in excellent yield by a Ritter reaction on 4′-DMEP, followed by treatment with thiourea in AcOH.

GRAPHICAL ABSTRACT

ACKNOWLEDGMENTS

We thank Daniel Dauzonne and Claude Monneret from Institut Curie (Paris) for their interest and exploitation of the demethylation procedure.

Notes

a Presence of 2% of 4c (4-epimer of starting material).

b Presence of di- and tri-demethylated compounds 5a (1%) and 5b (0.5%).

c Presence of di-demethylated compound 5a (0.5%).

d In the absence of acetone/water.

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