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John Stephenson † , Christopher Jones †† , Victor Snieckus ††

Directed ortho Metalation (DoM) of Naphthalene 1-8-bis-diethylamide: Research Towards Nerve Growth Factor Inhibitors. John Stephenson † , Christopher Jones †† , Victor Snieckus †† † Department of Chemical Engineering, Queen’s University †† Department of Chemistry, Queen’s University

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John Stephenson † , Christopher Jones †† , Victor Snieckus ††

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  1. Directed ortho Metalation (DoM) of Naphthalene 1-8-bis-diethylamide:Research Towards Nerve Growth Factor Inhibitors John Stephenson†, Christopher Jones††, Victor Snieckus†† † Department of Chemical Engineering, Queen’s University †† Department of Chemistry, Queen’s University Kingston, ON, Canada. K7L 3N6 stephensonj@cogeco.ca

  2. Nerve Growth Factor (NGF) • Involved with the neuronal development in the Central Nervous System and Peripheral Nervous System. • Nerve Growth Factor is implicated in Alzheimer’s, epilepsy, stroke and pain. • Production of protein is stimulated in patients suffering from Arthritis pain. • Inhibition of NGF causes reduction in pain levels. Shamovsky,et al. J Am Chem Soc, 1999, 121, 9797-9806

  3. Previously Identified NGF Inhibitors Target Molecules Marone, S. and Ross, G. 2000, World Patent No. WO0069829

  4. Directed ortho Metalation • Original Work • Gilman et al. J. Am. Chem. Soc.1939, 61, 106-109. • Wittig et al. Chem. Ber.1940, 73, 1197. Recent Work 1. Kalinin,A.; Snieckus, V. et al. J Org Chem, 2003, 68, 5992 2. Chauder, B.; Snieckus, V. et al. Org Lett, 2002, 4, 815

  5. Directed ortho Metalation (DoM) Reactions in Organic Synthesis E+ Hartung, C, Snieckus, V. Modern Arene Chemistry, Wiley-VCH, Weinheim. 2002, p. 330

  6. Examples of double DoM Chemistry of Naphthalene 1,8-bis(diethylamide) E+ E Equiv % Yield CF3CH2I I 4.4 86% TMSCl TMS 4.4 50% DMF CHO 2.2 40% (MeS)2 SMe 2.2 74%

  7. Examples of mono DoM Chemistry of Naphthalene 1,8-bis(diethylamide) E+ E Equiv Mono% Bis% SM% TMSCl TMS 1.1 ?% ?% ?% (SMe)2 SMe 1.1 ?% ?% ?% CF3CH2I I 1.1 ?% ?% ?% Snieckus, V.; Jones, C.; Stephenson, J., 2003, unpublished results.

  8. Mono or Di Deprotonation of Naphthalenebis-Diethylamide.What pathway does the deprotonation follow? • Determined by CD3OD Quench Experiments

  9. What Role Does the Equivalents of Base Have on formation of Mono or Bis? [M+-NEt2] Peak at 254 2.2 Eqv 1.1 Eqv 3.3 Eqv 4.4 Eqv Starting Material • Equilibrium can be seen for 1.1 equivalents

  10. Suzuki-Miyaura Cross Coupling • Background slide, perhaps containing: • Coupling of an aryl boronic acid with an acryl halide • Oxidative cycle: oxidative add, transmetalation, reductive elim ? Or other suggestions

  11. Suzuki-Miyaura Cross Coupling of 2,7-diHalo Naphthalene 1,8-Bis-Diethylamide

  12. Future Work Cross Coupling of Mono Product Cyclization of Mono Product

  13. Acknowledgements • Dr. Victor Snieckus • Chris Jones • Snieckus Group

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