DOI QR코드

DOI QR Code

A Novel Synthetic Method for Bepotastine, a Histamine H1 Receptor Antagonist

  • Received : 2012.10.10
  • Accepted : 2012.11.22
  • Published : 2013.02.20

Abstract

An efficient and alternative synthesis of enantiomerically pure (+)-(S)-4-(4-((4-chlorophenyl)(pyrid-2-yl)methoxy]piperidin-1-yl)butanoic acid, bepotastine (1) is described. The key resolution of (R/S)-bepotastine l-menthyl ester (3) is achived via diastereomeric salt crystallization using N-benzyloxycarbonyl-L-aspartic acid (NCbzLAA) as the resolving agent to provide (S)-bepotastine l-menthyl ester (S)-3. Hydrolysis of (S)-bepotastine l-menthyl ester (S)-3 afforded the desired bepotastine (1) with good yields and enantiopurity (> 99%). Finally, bepotastine besilate (4) and bepotastine calcium (5) are achived by salt formation of bepotastine (1) with benzene sulfonic acid and calcium salt respectively. The reaction conditions were optimized to make suitable for commercial scale production.

Keywords

References

  1. Yato, N.; Murata, T.; Saito, N.; Sakai, A.; Kikuchi, M.; Tsuzurahara, K. Folia Pharmacol. Jpn. 1997, 110, 19. https://doi.org/10.1254/fpj.110.19
  2. Kida, T.; Fujii, A.; Sakai, O.; Iemura, M.; Atsumi, I.; Wada, T.; Sakaki, H. Exp. Eye Res. 2010, 91, 85. https://doi.org/10.1016/j.exer.2010.04.006
  3. Nakahara, T.; Urabe, K.; Moroi, Y.; Morita, K.; Furue, M. J. Dermatol. Sci. 2003, 32, 237. https://doi.org/10.1016/S0923-1811(03)00130-0
  4. Protzko, E. E.; Gomes, P. J.; Williams, J. I.; Gow, J. A.; McNamara, T. R. J. Allergy Clin. Immun. 2009, 123, S50.
  5. Simons, E. R.; Simons, K. J. J. Allergy Clin. Immunol. 2011, 128, 1139. https://doi.org/10.1016/j.jaci.2011.09.005
  6. Tomson Pharma: Drug Report: Bpotastine, Sep., 2012.
  7. Graul, A.; Castaner, J. Drug Future 1998, 23, 256. https://doi.org/10.1358/dof.1998.023.03.448876
  8. Froimowitz, M.; Gu, Y. A. Dakin, L. A.; Kelley, C. J.; Parrish, D.; Deschamps, J. R. Bioorg. Med. Chem. Lett. 2005, 15, 3044. https://doi.org/10.1016/j.bmcl.2005.04.034
  9. Chen, C.; Reamer, R. A.; Chilenski, J. R.; McWilliams, C. J. Org. Lett. 2003, 5, 5039. https://doi.org/10.1021/ol0360795
  10. Takemoto, M.; Achiwa, K. Chem. Pharm. Bull. 1996, 44, 853. https://doi.org/10.1248/cpb.44.853
  11. Corey, E. J.; Helal, C. J. Tetrahedron Lett. 1996, 37, 5675. https://doi.org/10.1016/0040-4039(96)01198-7
  12. Bojadziev, S. E.; Tsankov, D. T.; Ivanov, P. M.; Berova, N. D. Bull. Chem. Soc. Jpn. 1987, 60, 2651. https://doi.org/10.1246/bcsj.60.2651
  13. Ogura, H.; Mineo, S.; Nakagawa, K.; Shiba, S. Yakuga. Zasshi 1981, 101, 329.
  14. Hiroshi, Y.; Kiyoshi, O.; Yasuyuki, Y.; Kensaku, F. JP 1998, 10120677.
  15. Kita, J.; Yoshioka, R.; Ozaki, Y.; Takemura, S.; Fujiwara, H.; Yamada, S. JP 1998-237070.
  16. Kita, J.; Yoshioka, R.; Ozaki, Y.; Takemura, S.; Fujiwara, H.; Yamada, S. JP 2000-198784
  17. Kita, J.; Yoshioka, R.; Ozaki, Y.; Takemura, S.; Fujiwara, H.; Yamada, S. WO 982940.
  18. Zhiquan, Z.; Zongyi, Z.; Lizeng, P. Chinese J. Pharm. 2006, 37, 726.
  19. Collet, A. Encyclopedia of Separation 2000, 5, 2326.
  20. Dyer, U. C.; Henderson, D. A.; Mitchell, M. B. Org. Process Res. Dev. 1999, 3, 161. https://doi.org/10.1021/op9800818
  21. Afraz, M. C.; Ariaans, G. J. A.; Broxterman, Q. B.; Bruggink, A. ARKIVOC 2004, 64.

Cited by

  1. -Heteroaryl Ketones vol.19, pp.8, 2017, https://doi.org/10.1021/acs.orglett.7b00691
  2. Rhodium Catalyzed Asymmetric Hydrogenation of 2-Pyridine Ketones vol.17, pp.17, 2013, https://doi.org/10.1021/acs.orglett.5b01878
  3. Structural Insight into Enantioselective Inversion of an Alcohol Dehydrogenase Reveals a “Polar Gate” in Stereorecognition of Diaryl Ketones vol.140, pp.39, 2013, https://doi.org/10.1021/jacs.8b08640
  4. Iridium-Catalyzed Highly Enantioselective Transfer Hydrogenation of Aryl N-Heteroaryl Ketones with N-Oxide as a Removable ortho-Substituent vol.20, pp.4, 2013, https://doi.org/10.1021/acs.orglett.7b03878
  5. Highly Enantioselective Hydrogenation of Non-ortho-Substituted 2-Pyridyl Aryl Ketones via Iridium-f-Diaphos Catalysis vol.21, pp.14, 2019, https://doi.org/10.1021/acs.orglett.9b01415
  6. Light-induced metal-free transformations of unactivated pyridotriazoles vol.10, pp.36, 2019, https://doi.org/10.1039/c9sc02448d