Synthesis 2001(6): 0929-0933
DOI: 10.1055/s-2001-13419
PAPER
© Georg Thieme Verlag Stuttgart · New York

Synthesis of 3′-Deoxy-3′-difluoromethyluridine and 2′-Deoxy-2′-difluoromethyluridine

Stéphane Marcotte, Baudoin Gérard, Xavier Pannecoucke, Christian Feasson, Jean-Charles Quirion*
Laboratoire d’Hétérochimie Organique associé au CNRS, IRCOF, INSA et Université de Rouen, Rue Tesnière, 76821 Mont Saint-Aignan cedex, France
Fax: +33(2)35522959; e-Mail: quirion@ircof.insa-rouen.fr;
Further Information

Publication History

Received 12 December 2000
Publication Date:
15 October 2004 (online)

Abstract

The synthesis of 3’-deoxy-3’-difluoromethyluridine (9) and 2’-deoxy-2’-difluoromethyluridine () by hydrogenation of the corresponding difluoromethylene derivatives is described. A second synthesis of the latter has been performed. Starting from thymidine, a two-step procedure affords the benzylated furanoid glycal 12. Addition of dibromodifluoromethane gives the α-2’-deoxy-2’-bromodifluoromethylarabinose (13). This compound allowed an access to α- or β -2’-deoxy-2’-difluoromethyluridine via a SN2 type reaction on a α-halodeoxyarabinose species.