Skip to main content

Thank you for visiting nature.com. You are using a browser version with limited support for CSS. To obtain the best experience, we recommend you use a more up to date browser (or turn off compatibility mode in Internet Explorer). In the meantime, to ensure continued support, we are displaying the site without styles and JavaScript.

  • Article
  • Published:

Decarboxylative C(sp3)–N cross-coupling via synergetic photoredox and copper catalysis

Abstract

Amines are a quintessential moiety in bioactive molecules, pharmaceuticals and organic materials. Transition-metal-catalysed C–N coupling of aryl electrophiles has been established as a powerful and reliable method for amine synthesis. However, the analogous C–N coupling of alkyl electrophiles is largely under-developed due to the decomposition of metal alkyl intermediates by β-hydrogen elimination and difficulty in C(sp3)–N reductive elimination. Here, we provide a general strategy for amination of alkyl electrophiles by merging photoredox and copper catalysis. Photoredox catalysis allows the use of alkyl redox-active esters, recently established as a superior class of alkyl electrophiles, whereas copper catalysis enables C(sp3)–N cross-coupling. Decarboxylative amination can be used for the synthesis of a diverse set of alkyl anilines with high chemoselectivity and functional-group compatibility. Rapid functionalization of amino acids, natural products and drugs is demonstrated.

This is a preview of subscription content, access via your institution

Access options

Buy this article

Prices may be subject to local taxes which are calculated during checkout

Fig. 1: Reaction development.
Fig. 2: Synthetic applications.
Fig. 3: Control reactions. 
Fig. 4: Reactions of copper amine complexes with a redox-active ester.

Similar content being viewed by others

References

  1. Lawrence, S. A. Amines: Synthesis Properties and Applications (Cambridge Univ. Press, Cambridge, 2004).

  2. Ricci, A. Amino Group Chemistry: From Synthesis to the Life Sciences (Wiley-VCH, Weinheim, 2008).

  3. Edwards, M. G.et al Borrowing hydrogen: a catalytic route to C–C bond formation from alcohols.Chem. Commun. 90–91 (2004)..

  4. Watson, A. J. A. & Williams, J. M. J. The give and take of alcohol activation. Science 329, 635–636 (2010).

    Article  CAS  Google Scholar 

  5. Hollmann, D., Tillack, A., Michalik, D., Jackstell, R. & Beller, M. An improved ruthenium catalyst for the environmentally benign amination of primary and secondary alcohols. Chem. Asian J. 2, 403–410 (2007).

    Article  CAS  Google Scholar 

  6. Sorribes, I., Junge, K. & Beller, M. Direct catalytic N-alkylation of amines with carboxylic acids. J. Am. Chem. Soc. 136, 14314–14319 (2014).

    Article  CAS  Google Scholar 

  7. Yang, Q., Wang, Q. & Yu, Z. Substitution of alcohols by N-nucleophiles via transition metal-catalyzed dehydrogenation. Chem. Soc. Rev. 44, 2305–2329 (2015).

    Article  CAS  Google Scholar 

  8. Ley, S. V. & Thomas, A. W. Modern synthetic methods for copper-mediated C(aryl)–O, C(aryl)–N, and C(aryl)–S bond formation. Angew. Chem. Int. Ed. 42, 5400–5449 (2003).

    Article  CAS  Google Scholar 

  9. Sambiagio, C., Marsden, S. P., Blacker, A. J. & McGowan, P. C. Copper catalysed Ullmann type chemistry: from mechanistic aspects to modern development. Chem. Soc. Rev. 43, 3525–3550 (2014).

    Article  CAS  Google Scholar 

  10. Hartwig, J. F. Evolution of a fourth generation catalyst for the amination and thioetherification of aryl halides. Acc. Chem. Res. 41, 1534–1544 (2008).

    Article  CAS  Google Scholar 

  11. Surry, D. S. & Buchwald, S. L. Dialkylbiaryl phosphines in Pd-catalyzed amination: a user’s guide. Chem. Sci. 2, 27–50 (2011).

    Article  CAS  Google Scholar 

  12. Choi, J. & Fu, G. C. Transition metal-catalyzed alkyl–alkyl bond formation: another dimension in cross-coupling chemistry. Science 356, eaaf7230 (2017).

    Article  Google Scholar 

  13. Hu, X. Nickel-catalyzed cross coupling of non-activated alkyl halides: a mechanistic perspective. Chem. Sci. 2, 1867–1886 (2011).

    Article  CAS  Google Scholar 

  14. Tasker, S. Z., Standley, E. A. & Jamison, T. F. Recent advances in homogeneous nickel catalysis. Nature 509, 299–309 (2014).

    Article  CAS  Google Scholar 

  15. Macgregor, S. A., Neave, G. W. & Smith, C. Theoretical studies on C–heteroatom bond formation via reductive elimination from group 10 M(PH3)2(CH3)(X) species (X=CH3, NH2, OH, SH) and the determination of metal–X bond strengths using density functional theory. Faraday Discuss. 124, 111–127 (2003).

    Article  CAS  Google Scholar 

  16. Bissember, A. C., Lundgren, R. J., Creutz, S. E., Peters, J. C. & Fu, G. C. Transition-metal-catalyzed alkylations of amines with alkyl halides: photoinduced, copper-catalyzed couplings of carbazoles. Angew. Chem. Int. Ed. 52, 5129–5133 (2013).

    Article  CAS  Google Scholar 

  17. Do, H.-Q., Bachman, S., Bissember, A. C., Peters, J. C. & Fu, G. C. Photoinduced, copper-catalyzed alkylation of amides with unactivated secondary alkyl halides at room temperature. J. Am. Chem. Soc. 136, 2162–2167 (2014).

    Article  CAS  Google Scholar 

  18. Kainz, Q. M. et al. Asymmetric copper-catalyzed C–N cross-couplings induced by visible light. Science 351, 681–684 (2016).

    Article  CAS  Google Scholar 

  19. Zhao, W., Wurz, R. P., Peters, J. C. & Fu, G. C. Photoinduced, copper-catalyzed decarboxylative C–N coupling to generate protected amines: an alternative to the Curtius rearrangement. J. Am. Chem. Soc. 139, 12153–12156 (2017).

    Article  CAS  Google Scholar 

  20. Cheung, C. W. & Hu, X. Amine synthesis via iron-catalysed reductive coupling of nitroarenes with alkyl halides. Nat. Commun. 7, 12494 (2016).

    Article  Google Scholar 

  21. Gui, J. et al. Practical olefin hydroamination with nitroarenes. Science 348, 886–891 (2015).

    Article  CAS  Google Scholar 

  22. Cornella, J. et al. Practical Ni-catalyzed aryl–alkyl cross-coupling of secondary redox-active esters. J. Am. Chem. Soc. 138, 2174–2177 (2016).

    Article  CAS  Google Scholar 

  23. Qin, T. et al. A general alkyl–alkyl cross-coupling enabled by redox-active esters and alkylzinc reagents. Science 352, 801–805 (2016).

    Article  CAS  Google Scholar 

  24. Toriyama, F. et al. Redox-active esters in Fe-catalyzed C–C coupling. J. Am. Chem. Soc. 138, 11132–11135 (2016).

    Article  CAS  Google Scholar 

  25. Li, C. et al. Decarboxylative borylation. Science 356, eaam7355 (2017).

    Article  Google Scholar 

  26. Fawcett, A. et al. Photoinduced decarboxylative borylation of carboxylic acids. Science 357, 283–286 (2017).

    Article  CAS  Google Scholar 

  27. Candish, L., Teders, M. & Glorius, F. Transition-metal-free, visible-light-enabled decarboxylative borylation of aryl N-hydroxyphthalimide esters. J. Am. Chem. Soc. 139, 7440–7443 (2017).

    Article  CAS  Google Scholar 

  28. Hu, D., Wang, L. & Li, P. Decarboxylative borylation of aliphatic esters under visible-light photoredox conditions. Org. Lett. 19, 2770–2773 (2017).

    Article  CAS  Google Scholar 

  29. Xue, W. & Oestreich, M. Copper-catalyzed decarboxylative radical silylation of redox-active aliphatic carboxylic acid derivatives. Angew. Chem. Int. Ed. 56, 11649–11652 (2017).

    Article  CAS  Google Scholar 

  30. Zuo, Z. et al. Merging photoredox with nickel catalysis: coupling of α-carboxyl sp 3-carbons with aryl halides. Science 345, 437–440 (2014).

    Article  CAS  Google Scholar 

  31. Zuo, Z. & MacMillan, D. W. Decarboxylative arylation of α-amino acids via photoredox catalysis: a one-step conversion of biomass to drug pharmacophore. J. Am. Chem. Soc. 136, 5257–5260 (2014).

    Article  CAS  Google Scholar 

  32. Fang, Z., Feng, Y., Dong, H., Li, D. & Tang, T. Copper(i)-catalyzed radical decarboxylative imidation of carboxylic acids with N-fluoroarylsulfonimides. Chem. Commun. 52, 11120–11123 (2016).

    Article  CAS  Google Scholar 

  33. Liu, Z. J. et al. Directing group in decarboxylative cross-coupling: copper-catalyzed site-selective C–N bond formation from nonactivated aliphatic carboxylic acids. J. Am. Chem. Soc. 138, 9714–9719 (2016).

    Article  CAS  Google Scholar 

  34. Huihui, K. M. et al. Decarboxylative cross-electrophile coupling of N-hydroxyphthalimide esters with aryl iodides. J. Am. Chem. Soc. 138, 5016–5019 (2016).

    Article  CAS  Google Scholar 

  35. Jamison, C. R. & Overman, L. E. Fragment coupling with tertiary radicals generated by visible-light photocatalysis. Acc. Chem. Res. 49, 1578–1586 (2016).

    Article  CAS  Google Scholar 

  36. Okada, K., Okamoto, K., Morita, N., Okubo, K. & Oda, M. Photosensitized decarboxylative Michael addition through N-(acyloxy)phthalimides via an electron-transfer mechanism. J. Am. Chem. Soc. 113, 9401–9402 (1991).

    Article  CAS  Google Scholar 

  37. Zhang, H., Zhang, P., Jiang, M., Yang, H. & Fu, H. Merging photoredox with copper catalysis: decarboxylative alkynylation of α-amino acid derivatives. Org. Lett. 19, 1016–1019 (2017).

    Article  CAS  Google Scholar 

  38. Tellis, J. C., Primer, D. N. & Molander, G. A. Single-electron transmetalation in organoboron cross-coupling by photoredox/nickel dual catalysis. Science 345, 433–436 (2014).

    Article  CAS  Google Scholar 

  39. Skubi, K. L., Blum, T. R. & Yoon, T. P. Dual catalysis strategies in photochemical synthesis. Chem. Rev. 116, 10035–10074 (2016).

    Article  CAS  Google Scholar 

  40. Corcoran, E. B. et al. Aryl amination using ligand-free Ni(ii) salts and photoredox catalysis. Science 353, 279–283 (2016).

    Article  CAS  Google Scholar 

  41. Yoo, W.-J., Tsukamoto, T. & Kobayashi, S. Visible-light-mediated Chan–Lam coupling reactions of aryl boronic acids and aniline derivatives. Angew. Chem. Int. Ed. 54, 6587–6590 (2015).

    Article  CAS  Google Scholar 

  42. Zhang, Y., Yang, X., Yao, Q. & Ma, D. CuI/DMPAO-catalyzed N-arylation of acyclic secondary amines. Org. Lett. 14, 3056–3059 (2012).

    Article  CAS  Google Scholar 

  43. Zhou, W., Fan, M., Yin, J., Jiang, Y. & Ma, D. CuI/Oxalic diamide catalyzed coupling reaction of (hetero)aryl chlorides and amines. J. Am. Chem. Soc. 137, 11942–11945 (2015).

    Article  CAS  Google Scholar 

  44. Collins, K. D. & Glorius, F. A robustness screen for the rapid assessment of chemical reactions. Nat. Chem. 5, 597–601 (2013).

    Article  CAS  Google Scholar 

  45. Keenan, M. et al. Two analogues of fenarimol show curative activity in an experimental model of Chagas disease. J. Med. Chem. 56, 10158–10170 (2013).

    Article  CAS  Google Scholar 

Download references

Acknowledgements

This work is supported by the NoNoMeCat Marie Skłodowska-Curie training network funded by the European Union under the Horizon 2020 Programme (675020-MSCA-ITN-2015-ETN). We thank R. Scopelliti (École Polytechnique Fédérale de Lausanne) for assistance with X-ray crystallography of 9a.

Author information

Authors and Affiliations

Authors

Contributions

R.M. and X.H. conceived and designed the study. R.M. designed and optimized the synthetic method, and studied the scope, application and mechanism. A.F. and J.B. contributed to the scope and application. R.M. and X.H. wrote the manuscript. X.H. directed the research.

Corresponding author

Correspondence to Xile Hu.

Ethics declarations

Competing interests

The authors declare no competing financial interests.

Additional information

Publisher’s note: Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Supplementary information

Supplementary Information

Supplementary Methods, Supplementary Tables 1–10, Supplementary Figures 1–100, Supplementary References.

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Mao, R., Frey, A., Balon, J. et al. Decarboxylative C(sp3)–N cross-coupling via synergetic photoredox and copper catalysis. Nat Catal 1, 120–126 (2018). https://doi.org/10.1038/s41929-017-0023-z

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1038/s41929-017-0023-z

This article is cited by

Search

Quick links

Nature Briefing

Sign up for the Nature Briefing newsletter — what matters in science, free to your inbox daily.

Get the most important science stories of the day, free in your inbox. Sign up for Nature Briefing