Synthesis 2016; 48(01): 73-78
DOI: 10.1055/s-0035-1560708
paper
© Georg Thieme Verlag Stuttgart · New York

Asymmetric Synthesis and Absolute Configuration of (+)- and (–)-Perhexiline

Chih-Chung Tseng*
a   Kosterlitz Centre for Therapeutics, Institute of Medical Sciences, University of Aberdeen, Aberdeen, AB25 2ZD, Scotland, UK   Email: c.c.tseng@abdn.ac.uk   Email: m.zanda@abdn.ac.uk
,
Iain R. Greig
a   Kosterlitz Centre for Therapeutics, Institute of Medical Sciences, University of Aberdeen, Aberdeen, AB25 2ZD, Scotland, UK   Email: c.c.tseng@abdn.ac.uk   Email: m.zanda@abdn.ac.uk
,
William T. A. Harrison
b   Department of Chemistry, University of Aberdeen, AB24 3UE, Scotland, UK
,
Matteo Zanda*
a   Kosterlitz Centre for Therapeutics, Institute of Medical Sciences, University of Aberdeen, Aberdeen, AB25 2ZD, Scotland, UK   Email: c.c.tseng@abdn.ac.uk   Email: m.zanda@abdn.ac.uk
c   CNR–ICRM, via Mancinelli 7, 20131 Milan, Italy
› Author Affiliations
Further Information

Publication History

Received: 13 August 2015

Accepted after revision: 21 September 2015

Publication Date:
27 October 2015 (online)


This work is dedicated to Professor Iwao Ojima on the occasion of his 70th birthday.

Abstract

Racemic perhexiline has been used (or is currently undergoing clinical trials) for the treatment of a variety of cardiovascular disorders. Increasing evidence suggests that the (–)-enantiomer should be used, as opposed to the racemic mixture. Here, we report the first asymmetric synthesis of both enantiomers of perhexiline in high enantiomeric excess and the assignment of their (–)-S/(+)-R absolute stereochemistry by X-ray crystallography.

Supporting Information

 
  • References

    • 1a Tamargo J, López-Sendón J. Nat. Rev. Drug Discovery 2011; 10: 536
    • 1b Lee L, Campbell R, Scheuermann-Freestone M, Taylor R, Gunaruwan P, Williams L, Ashrafian H, Horowitz J, Fraser AG, Clarke K, Frenneaux M. Circulation 2005; 112: 3280
    • 1c Abozguia K, Elliott P, McKenna W, Phan TT, Nallur-Shivu G, Ahmed I, Maher AR, Kaur K, Taylor J, Henning A, Ashrafian H, Watkins H, Frenneaux M. Circulation 2010; 122: 1562
  • 2 Inglis S, Stewart S. Eur. J. Cardiovasc. Nurs. 2006; 5: 175
    • 3a Ashrafian H, Horowitz JD, Frenneaux MP. Cardiovasc. Drug Rev. 2007; 25: 76
    • 3b Rouhi AM. Chem. Eng. News 2003; 81 (18): 56
    • 4a Kennedy JA, Unger SA, Horowitz JD. Biochem. Pharmacol. 1996; 52: 273
    • 4b Ceccarelli SM, Chomienne O, Gubler M, Arduini A. J. Med. Chem. 2011; 54: 3109
  • 5 Samudio I, Harmancey R, Fiegl M, Kantarjian H, Konopleva M, Korchin B, Kaluarachchi K, Bornmann W, Duvvuri S, Taegtmeyer H, Andreeff M. J. Clin. Invest. 2010; 120: 142
  • 6 Vander Heiden MG. Nat. Rev. Drug Discovery 2011; 10: 671
  • 7 Galluzzi L, Kepp O, Vander Heiden MG, Kroemer G. Nat. Rev. Drug Discovery 2013; 12: 829
  • 8 Davies BJ, Herbert MK, Culbert JA, Pyke SM, Coller JK, Somogyi AA, Milne RW, Sallustio BC. J. Chromatogr., Biomed. Appl. 2006; 832: 114
    • 9a Horgan SW, Palopoli FP, Schwoegler EJ. US 4069222, 1978
    • 9b Schou SC. J. Labelled Compd. Radiopharm. 2010; 53: 31
  • 10 Glorius F, Spielkamp N, Holle S, Goddard R, Lehmann CW. Angew. Chem. Int. Ed. 2004; 43: 2850
  • 11 Scheiper B, Glorius F, Leitner A, Fürstner A. Proc. Natl. Acad. Sci. U.S.A. 2004; 101: 11960
  • 12 Heitbaum M, Fröhlich R, Glorius F. Adv. Synth. Catal. 2010; 352: 357
  • 13 Müller T, Dettner K, Seifert K. Eur. J. Org. Chem. 2011; 6032
  • 14 Klapars A, Huang X, Buchwald SL. J. Am. Chem. Soc. 2002; 124: 7421
  • 15 Kunz K, Scholz U, Ganzer D. Synlett 2003; 2428
  • 16 Because perhexiline 1 is not UV-detectable, the enantiomeric excesses of perhexiline samples were determined by chiral HPLC analysis of the corresponding UV-detectable benzamide derivatives 7. See the experimental section for details on the preparation of 7 from perhexiline.
  • 17 Crystallographic data for compound 6 have been deposited with the accession number CCDC 1057017, and can be obtained free of charge from the Cambridge Crystallographic Data Centre, 12 Union Road, Cambridge CB2 1EZ, UK; Fax: +44(1223)336033; E-mail: deposit@ccdc.cam.ac.uk; Web site: www.ccdc.cam.ac.uk/ conts/retrieving.html.
  • 18 Still WC, Kahn M, Mitra A. J. Org. Chem. 1978; 43: 2923