Metal-Free Annulation of Arenes with 2-Aminopyridine Derivatives: The Methyl Group as a Traceless Non-Chelating Directing Group†
Correction(s) for this article
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Corrigendum: Metal-Free Annulation of Arenes with 2-Aminopyridine Derivatives: The Methyl Group as a Traceless Non-Chelating Directing Group
- Volume 53Issue 37Angewandte Chemie International Edition
- pages: 9695-9695
- First Published online: September 2, 2014
Srimanta Manna
Abteilung Chemische Biologie, Max-Planck-Institut für Molekulare Physiologie, Otto-Hahn-Strasse 11, 44227 Dortmund (Germany)
Fakultät Chemie und Chemische Biologie, Technische Universität Dortmund, Otto-Hahn-Strasse 6, 44221 Dortmund (Germany)
Search for more papers by this authorDr. Kiran Matcha
Abteilung Chemische Biologie, Max-Planck-Institut für Molekulare Physiologie, Otto-Hahn-Strasse 11, 44227 Dortmund (Germany)
Search for more papers by this authorCorresponding Author
Dr. Andrey P. Antonchick
Abteilung Chemische Biologie, Max-Planck-Institut für Molekulare Physiologie, Otto-Hahn-Strasse 11, 44227 Dortmund (Germany)
Fakultät Chemie und Chemische Biologie, Technische Universität Dortmund, Otto-Hahn-Strasse 6, 44221 Dortmund (Germany)
Abteilung Chemische Biologie, Max-Planck-Institut für Molekulare Physiologie, Otto-Hahn-Strasse 11, 44227 Dortmund (Germany)===Search for more papers by this authorSrimanta Manna
Abteilung Chemische Biologie, Max-Planck-Institut für Molekulare Physiologie, Otto-Hahn-Strasse 11, 44227 Dortmund (Germany)
Fakultät Chemie und Chemische Biologie, Technische Universität Dortmund, Otto-Hahn-Strasse 6, 44221 Dortmund (Germany)
Search for more papers by this authorDr. Kiran Matcha
Abteilung Chemische Biologie, Max-Planck-Institut für Molekulare Physiologie, Otto-Hahn-Strasse 11, 44227 Dortmund (Germany)
Search for more papers by this authorCorresponding Author
Dr. Andrey P. Antonchick
Abteilung Chemische Biologie, Max-Planck-Institut für Molekulare Physiologie, Otto-Hahn-Strasse 11, 44227 Dortmund (Germany)
Fakultät Chemie und Chemische Biologie, Technische Universität Dortmund, Otto-Hahn-Strasse 6, 44221 Dortmund (Germany)
Abteilung Chemische Biologie, Max-Planck-Institut für Molekulare Physiologie, Otto-Hahn-Strasse 11, 44227 Dortmund (Germany)===Search for more papers by this authorWe thank Prof. Dr. Herbert Waldmann for his generous support.
Graphical Abstract
Disappearing Me: A novel selective annulation between 2-aminopyridine derivatives and arenes under metal-free conditions provides the important pyrido[1,2-a]benzimidazole scaffold under mild reaction conditions. In this intermolecular reaction the methyl group of methylbenzenes serves as a traceless, non-chelating, and highly regioselective directing group.
Abstract
A novel annulation reaction between 2-aminopyridine derivatives and arenes under metal-free conditions is described. The presented intermolecular transformation provided straightforward access to the important pyrido[1,2-a]benzimidazole scaffold under mild reaction conditions. The unprecedented application of the methyl group of methylbenzenes as a traceless, non-chelating, and highly regioselective directing group is reported.
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References
- 1For medicinal properties of benzimidazole compounds, see:
- 1aR. S. Begunov, G. A. Ryzvanovicha, Russ. Chem. Rev. 2013, 82, 77–97;
- 1bH. Takeshita, J. Watanabe, Y. Kimura, K. Kawakami, H. Takahashi, M. Takemura, A. Kitamura, K. Someya, R. Nakajima, Bioorg. Med. Chem. Lett. 2010, 20, 3893–3896;
- 1cM. Sedic, M. Poznic, P. Gehrig, M. Scott, R. Schlapbach, M. Hranjec, G. Karminski-Zamola, K. Pavelic, S. K. Pavelic, Mol. Cancer Ther. 2008, 7, 2121–2132;
- 1dM. Hranjec, I. Piantanida, M. Kralj, L. Šuman, K. i. Pavelić, G. Karminski-Zamola, J. Med. Chem. 2008, 51, 4899–4910;
- 1eM. Hranjec, M. Kralj, I. Piantanida, M. Sedić, L. Šuman, K. Pavelić, G. Karminski-Zamola, J. Med. Chem. 2007, 50, 5696–5711;
- 1fS. K. Kotovskaya, Z. M. Baskakova, V. N. Charushin, O. N. Chupakhin, E. F. Belanov, N. I. Bormotov, S. M. Balakhnin, O. A. Serova, Pharm. Chem. J. 2005, 39, 574–578.
- 2
- 2aJ. A. Adachi, H. L. DuPont, Clin. Infect. Dis. 2006, 42, 541–547;
- 2bE. Marchi, G. Mascellani, L. Montecchi, A. P. Venturini, M. Brufani, L. Cellai, J. Med. Chem. 1985, 28, 960–963.
- 3For the synthesis of pyrido[1,2-a]benzimidazoles through C–H amination, see:
- 3aY. He, J. Huang, D. Liang, L. Liu, Q. Zhu, Chem. Commun. 2013, 49, 7352–7354;
- 3bD. Liang, Y. He, L. Liu, Q. Zhu, Org. Lett. 2013, 15, 3476–3479;
- 3cN. Kutsumura, S. Kunimatsu, K. Kagawa, T. Otani, T. Saito, Synthesis 2011, 3235–3240;
- 3dH. Wang, Y. Wang, C. Peng, J. Zhang, Q. Zhu, J. Am. Chem. Soc. 2010, 132, 13217–13219.
- 4For other synthesis methods for pyrido[1,2-a]benzimidazoles, see:
- 4aZ. Wu, Q. Huang, X. Zhou, L. Yu, Z. Li, D. Wu, Eur. J. Org. Chem. 2011, 5242–5245;
- 4bK. Noriki, K. Shinichi, K. Kimiko, O. Takashi, S. Takao, Synthesis 2011, 3235–3240;
- 4cD. Zhao, J. Hu, N. Wu, X. Huang, X. Qin, J. Lan, J. You, Org. Lett. 2011, 13, 6516–6519;
- 4dC. G. Yan, Q. F. Wang, X. K. Song, J. Sun, J. Org. Chem. 2009, 74, 710–718;
- 4eC. Venkatesh, G. S. M. Sundaram, H. Ila, H. Junjappa, J. Org. Chem. 2006, 71, 1280–1283;
- 4fG. Morgan, S. Stewart, J. Chem. Soc. 1939, 1057–1066;
- 4gG. Morgan, S. Stewart, J. Chem. Soc. 1938, 1292–1305.
- 5For reviews on C–H amination, see:
- 5aM. L. Louillat, F. W. Patureau, Chem. Soc. Rev. 2014, 43, 901–910;
- 5bR. Samanta, A. P. Antonchick, Synlett 2012, 809–813;
- 5cF. Collet, C. Lescot, P. Dauban, Chem. Soc. Rev. 2011, 40, 1926–1936;
- 5dF. Collet, R. H. Dodd, P. Dauban, Chem. Commun. 2009, 5061–5074.
- 6For reviews on the chemistry of IIII compounds, see:
- 6aV. V. Zhdankin, Hypervalent Iodine Chemistry: Preparation, Structure and Synthetic Applications of Polyvalent Iodine Compounds, Wiley, Chichester, 2014;
- 6bM. S. Yusubov, V. V. Zhdankin, Curr. Org. Synth. 2012, 9, 247–272;
- 6cJ. L. F. Silva, Jr., B. Olofsson, Nat. Prod. Rep. 2011, 28, 1722–1754;
- 6dE. A. Merritt, B. Olofsson, Synthesis 2011, 517–538;
- 6eJ. P. Brand, D. F. Gonzalez, S. Nicolai, J. Waser, Chem. Commun. 2011, 47, 102–115;
- 6fV. V. Zhdankin, ARKIVOC 2009, 1–62;
- 6gM. Uyanik, K. Ishihara, Chem. Commun. 2009, 2086–2099;
- 6hT. Dohi, M. Ito, N. Yamaoka, K. Morimoto, H. Fujioka, Y. Kita, Tetrahedron 2009, 65, 10797–10815;
- 6iV. V. Zhdankin, P. J. Stang, Chem. Rev. 2008, 108, 5299–5358;
- 6jS. Quideau, L. Pouysegu, D. Deffieux, Synlett 2008, 467–495.
- 7For selected C–H amination reactions using IIII reagents, see:
- 7aS. K. Alla, R. K. Kumar, P. Sadhu, T. Punniyamurthy, Org. Lett. 2013, 15, 1334–1337;
- 7bG. Jacquemot, M.-A. Menard, C. L. Homme, S. Canesi, Chem. Sci. 2013, 4, 1287–1292;
- 7cC. Röben, J. A. Souto, E. C. Escudero-Adán, K. Muñiz, Org. Lett. 2013, 15, 1008–1011;
- 7dJ. A. Souto, D. Zian, K. Muñiz, J. Am. Chem. Soc. 2012, 134, 7242–7245;
- 7eX. Ban, Y. Pan, Y. Lin, S. Wang, Y. Du, K. Zhao, Org. Biomol. Chem. 2012, 10, 3606–3609;
- 7fU. Farid, T. Wirth, Angew. Chem. 2012, 124, 3518–3522;
10.1002/ange.201107703 Google ScholarAngew. Chem. Int. Ed. 2012, 51, 3462–3465;
- 7gY. Du, R. Liu, G. Linn, K. Zhao, Org. Lett. 2006, 8, 5919–5922;
- 7hH. J. Kim, S. H. Cho, S. Chang, Org. Lett. 2012, 14, 1424–1427;
- 7iA. A. Kantak, S. Potavathri, R. A. Barham, K. M. Romano, B. DeBoef, J. Am. Chem. Soc. 2011, 133, 19960–19965;
- 7jH. J. Kim, J. Kim, S. H. Cho, S. Chang, J. Am. Chem. Soc. 2011, 133, 16382–16385.
- 8For a review on the work of our group, see:
- 8aR. Samanta, K. Matcha, A. P. Antonchick, Eur. J. Org. Chem. 2013, 5769–5804; and for recent work, see:
- 8bR. Samanta, J. O. Bauer, C. Strohmann, A. P. Antonchick, Org. Lett. 2012, 14, 5518–5521;
- 8cR. Samanta, J. Lategahn, A. P. Antonchick, Chem. Commun. 2012, 48, 3194–3196;
- 8dA. P. Antonchick, R. Samanta, K. Kulikov, J. Lategahn, Angew. Chem. 2011, 123, 8764–8767;
10.1002/ange.201102984 Google ScholarAngew. Chem. Int. Ed. 2011, 50, 8605–8608.
- 9For leading reviews on coupling without chelating, see:
- 9aN. Kuhl, M. N. Hopkinson, J. Wencel-Delord, F. Glorius, Angew. Chem. 2012, 124, 10382–10401;
10.1002/ange.201203269 Google ScholarAngew. Chem. Int. Ed. 2012, 51, 10236–10254;
- 9bJ. A. Ashenhurst, Chem. Soc. Rev. 2010, 39, 540–548.
- 10For reviews on the development of traceless directing groups, see:
- 10aG. Rousseau, B. Breit, Angew. Chem. 2011, 123, 2498–2543;
10.1002/ange.201006139 Google ScholarAngew. Chem. Int. Ed. 2011, 50, 2450–2494; for selected recent works, see:
- 10bJ. M. Neely, T. Rovis, J. Am. Chem. Soc. 2014, 136, 2735–2738;
- 10cJ. Luo, S. Preciado, I. Larrosa, J. Am. Chem. Soc. 2014, 136, 4109–4112;
- 10dC. Wang, Y. Huang, Org. Lett. 2013, 15, 5294–5297;
- 10eS. M. Preshlock, D. L. Plattner, P. E. Maligres, S. W. Krska, R. E. Maleczka, M. R. Smith, Angew. Chem. 2013, 125, 13153–13157;
10.1002/ange.201306511 Google ScholarAngew. Chem. Int. Ed. 2013, 52, 12915–12919;
- 10fX. Huang, J. Huang, C. Du, X. Zhang, F. Song, J. You, Angew. Chem. 2013, 125, 13208–13212; Angew. Chem. Int. Ed. 2013, 52, 12970–12974;
- 10gA. V. Gulevich, F. S. Melkonyan, D. Sarkar, V. Gevorgyan, J. Am. Chem. Soc. 2012, 134, 5528–5531;
- 10hL. Ackermann, E. Diers, A. Manvar, Org. Lett. 2012, 14, 1154–1157;
- 10iR. Samanta, A. P. Antonchick, Angew. Chem. 2011, 123, 5323–5326; Angew. Chem. Int. Ed. 2011, 50, 5217–5220.
- 11
- 11aD. Sharma, C. B. Reddy, A. K. Shil, R. P. Saroach, P. Das, Mol. Diversity 2013, 17, 651–659;
- 11bA. Jha, ARKIVOC 2006, 13–20;
- 11cC. Wu, J. Org. Chem. 1998, 63, 2348–2350;
- 11dR. A. Olofson, J. T. Martz, J. P. Senet, M. Piteau, T. Malfroot, J. Org. Chem. 1984, 49, 2081–2082.