CC BY 4.0 · Pharmaceutical Fronts 2022; 04(04): e244-e249
DOI: 10.1055/s-0042-1755195
Original Article

Novel and Practical Industrial Process Scale-Up of 5-Bromo-2-chloro-4-(methoxycarbonyl)benzoic acid, a Key Intermediate in the Manufacturing of Therapeutic SGLT2 Inhibitors

Yi Zhang
1   Novel Technology Center of Pharmaceutical Chemistry, Shanghai Institute of Pharmaceutical Industry Co., Ltd., China State Institute of Pharmaceutical Industry Co., Ltd., Shanghai, People's Republic of China
2   Shanghai Engineering Research Center of Pharmaceutical Process, Shanghai Institute of Pharmaceutical Industry Co., Ltd., China State Institute of Pharmaceutical Industry, Shanghai, People's Republic of China
,
Xiao Ma
1   Novel Technology Center of Pharmaceutical Chemistry, Shanghai Institute of Pharmaceutical Industry Co., Ltd., China State Institute of Pharmaceutical Industry Co., Ltd., Shanghai, People's Republic of China
2   Shanghai Engineering Research Center of Pharmaceutical Process, Shanghai Institute of Pharmaceutical Industry Co., Ltd., China State Institute of Pharmaceutical Industry, Shanghai, People's Republic of China
,
Xiao-Hui Shan
3   Shandong Shenghua New Material Technology Co., Ltd., Laiyang, People's Republic of China
,
Xiao-Wen Zhang
1   Novel Technology Center of Pharmaceutical Chemistry, Shanghai Institute of Pharmaceutical Industry Co., Ltd., China State Institute of Pharmaceutical Industry Co., Ltd., Shanghai, People's Republic of China
2   Shanghai Engineering Research Center of Pharmaceutical Process, Shanghai Institute of Pharmaceutical Industry Co., Ltd., China State Institute of Pharmaceutical Industry, Shanghai, People's Republic of China
,
Jian-Qi Li
1   Novel Technology Center of Pharmaceutical Chemistry, Shanghai Institute of Pharmaceutical Industry Co., Ltd., China State Institute of Pharmaceutical Industry Co., Ltd., Shanghai, People's Republic of China
2   Shanghai Engineering Research Center of Pharmaceutical Process, Shanghai Institute of Pharmaceutical Industry Co., Ltd., China State Institute of Pharmaceutical Industry, Shanghai, People's Republic of China
,
Yu Liu
1   Novel Technology Center of Pharmaceutical Chemistry, Shanghai Institute of Pharmaceutical Industry Co., Ltd., China State Institute of Pharmaceutical Industry Co., Ltd., Shanghai, People's Republic of China
2   Shanghai Engineering Research Center of Pharmaceutical Process, Shanghai Institute of Pharmaceutical Industry Co., Ltd., China State Institute of Pharmaceutical Industry, Shanghai, People's Republic of China
› Author Affiliations


Abstract

5-Bromo-2-chloro-4-(methoxycarbonyl)benzoic acid (1) is a key intermediate for the synthesis of a family of promising SGLT2 inhibitors currently in preclinical and phase I studies for diabetes therapy. In this investigation, cheap, easily available dimethyl terephthalate was used as the raw starting material, and compound 1 was prepared effectively in six steps, including nitration, hydrolysis, hydrogenation, esterification, bromination, and diazotization. The preparation was run successfully on approximately 70 kg/batch with the total yield of 24%. This practical process was demonstrated to be scalable with a great yield and significant cost reduction.

Supplementary Material



Publication History

Received: 28 February 2022

Accepted: 16 June 2022

Article published online:
22 August 2022

© 2022. The Author(s). This is an open access article published by Thieme under the terms of the Creative Commons Attribution License, permitting unrestricted use, distribution, and reproduction so long as the original work is properly cited. (https://creativecommons.org/licenses/by/4.0/)

Georg Thieme Verlag KG
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  • References

  • 1 Manoj A, Das S, Kunnath Ramachandran A, Alex AT, Joseph A. SGLT2 inhibitors, an accomplished development in field of medicinal chemistry: an extensive review. Future Med Chem 2020; 12 (21) 1961-1990
  • 2 Xu B, Lv B, Feng Y. et al. O-Spiro C-aryl glucosides as novel sodium-dependent glucose co-transporter 2 (SGLT2) inhibitors. Bioorg Med Chem Lett 2009; 19 (19) 5632-5635
  • 3 Lv B, Xu B, Feng Y. et al. Exploration of O-spiroketal C-arylglucosides as novel and selective renal sodium-dependent glucose co-transporter 2 (SGLT2) inhibitors. Bioorg Med Chem Lett 2009; 19 (24) 6877-6881
  • 4 Prous JR, Serradell N, Munoz R. et al. Preparation of pyrano[3,2-c]benzopyran-6(2h)-one derivatives as SGLT2 antidiabetic agents. WO Patent 2013045495 A1. April 2013
  • 5 Liu H, Li J, Wang J. Process for preparation of C,O-spiro aryl glycoside compounds and use thereof. WO Patent 2016206604 A1. December, 2016
  • 6 Kroh C, Lang IU, Rose H. et al. Use of sodium-dependent glucose transporter SGLT2 inhibitors for the prevention and/or treatment of cardiac diseases in felines. WO Patent 2021165177 A1. August, 2021
  • 7 Chen YW, Feng Y, Xu BH. et al. Preparation of benzylic glycoside derivatives and their inhibitory effect on sodium-dependent glucose co-transporter SGLT. US Patent 20080242596 A1. October, 2008
  • 8 Liu YH, Fu TM, Ou CY. et al. Improved preparation of (1S,3′R,4‘S,5′S,6’R)-5-chloro-6-[(4-ethylphenyl)methyl]-3′,4′,5′,6′-tetrahydro-6′-(hydroxymethyl)-spiro[isobenzofuran-1(3H),2′-[2H]pyran]-3′,4′,5′-triol. Chin Chem Lett 2013; 24 (02) 131-133
  • 9 Lee SH, Kim MJ, Lee SH, Kim J, Park HJ, Lee J. Thiazolylmethyl ortho-substituted phenyl glucoside library as novel C-aryl glucoside SGLT2 inhibitors. Eur J Med Chem 2011; 46 (07) 2662-2675
  • 10 Qin ZW, Liu C, Shi YL. et al. Method for preparing 2-amino-4-methanesulfonamide methylbenzoate. CN Patent 103524386 A. January, 2014
  • 11 Li Z, Zhang X, Zhang X. et al. 18F-Labeled benzyldiamine derivatives as novel flexible probes for positron emission tomography of cerebral β-amyloid plaques. J Med Chem 2016; 59 (23) 10577-10585
  • 12 Skibo EB, Gilchrist JH. Synthesis and electrochemistry of pyrimidoquinazoline-5,10-diones. Design of hydrolytically stable high potential quinones and new reductive alkylation systems. J Org Chem 1988; 53 (18) 4209-4218
  • 13 Ursuegui S, Yougnia R, Moutin S. et al. A biotin-conjugated pyridine-based isatoic anhydride, a selective room temperature RNA-acylating agent for the nucleic acid separation. Org Biomol Chem 2015; 13 (12) 3625-3632
  • 14 Bauer E, Gerlach K, Pfau R. et al. Novel substituted nitrogen-containing heterobicycles and use thereof as factor Xa inhibitors. CA Patent 2511349 A1. July, 2004
  • 15 Kim M, Boissonnault JA, Dau PV, Cohen SM. Metal-organic framework regioisomers based on bifunctional ligands. Angew Chem Int Ed Engl 2011; 50 (51) 12193-12196
  • 16 Chen YW, Feng Y, Xu BH. et al. Glucose transport inhibitors and methods of use. US Patent 2007275907 A1. November, 2007